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En tant qu’analyste QA pour JurisÉvolution — notre logiciel phare destiné aux cabinets juridiques — tu seras au cœur du développement qualité.
Ton travail sera essentiel pour garantir la fiabilité, la performance et la convivialité de notre produit.
Tu collaboreras étroitement avec les développeurs, analystes et chefs de produit pour t’assurer que chaque nouvelle fonctionnalité respecte nos standards de qualité… et ceux de nos clients !
Ce que tu feras au quotidien:
* Participer à l’analyse des spécifications fonctionnelles pour comprendre les besoins à tester
* Concevoir, documenter et exécuter des plans de tests (fonctionnels, régressions, exploratoires, etc.)
* Identifier, documenter et suivre les anomalies jusqu’à leur résolution
* Collaborer avec les développeurs pour comprendre les enjeux techniques et assurer une couverture optimale des tests
* Participer à l’amélioration continue des processus QA (automatisation, outils, documentation)
* Contribuer activement aux revues d’exigences et aux démos d’équipe
* Tester sur différentes plateformes (web, desktop) et navigateurs
Ce qu’on cherche chez toi:
* Expérience pertinente en assurance qualité logicielle (minimum 2 ans)
* Bonne connaissance des méthodologies Agile/Scrum
* Connaissance des outils de gestion de tests (ex.
: TestRail, Xray, Zephyr) et/ou de tickets (ex.
: Azure Devops)
* Expérience avec les tests manuels et automatisés
* Esprit analytique, rigueur et souci du détail
* Excellente capacité à communiquer (écrit/oral), autant avec les développeurs qu’avec le reste de l’équipe
* Capacité à apprendre rapidement et à s’adapter à un environnement en constante évolution
* Une bonne maîtrise du français et de l’anglais est requise, car le titulaire du poste aura à communiquer fréquemment dans les deux langues, tant oralement que par écrit, car nous avons des collègues, des clients et des partenaires au Québec, ainsi que dans le reste du Canada et aux États-Unis.
Atouts supplémentaires (mais pas obligatoires):
* Expérience dans un environnement SaaS ou logiciel B2B
* Expérience avec un logiciel ERP et/ou un logiciel de comptabilité
* Connaissance du domaine juridique ou intérêt marqué pour celui-ci
* Expérience avec des outils d’automatisation comme Cypress, Selenium ou Playwright
* Connaissances en SQL ou en lecture de logs pour diagnostiquer des erreurs
Nous pouvons vous offrir:
* Un salaire et des avantages très compétitifs
* Une organisation multinationale avec la possibilité de travailler à l'étranger
* Un ordinateur portable et tous les accessoires pour être bien installé chez soi
* 5 jours de congé personnel par année, en plus des vacances
* Des plans d'épargne-retraite et un programme de bonification d’achat d’actions (CSU.TO)
* Un plan d'assuran...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 60000
Posted: 2025-07-01 08:47:50
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
To be added
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-07-01 08:47:37
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Functions, Duties, Tasks:
* Provide statistical input to the design, analysis, reporting and interpretation of clinical studies and contribution to publications.
* Use SAS or other software to develop custom programming code to generate tables, data listings, graphs and derived datasets as specified in the protocol/statistical analysis plan.
* Ensure that outputs meet quality standards and project requirements.
* Perform validation programming and work with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
* Keep project team members informed of programming progress and issues requiring their attention.
* Follow applicable SOPs and relevant regulatory guidelines.
* Manage scheduling and time constraints across multiple projects at a time, set goals based on priorities from management, and adapt to timeline or priority changes by reorganizing daily workload.
* Prepare in advance for internal meetings, contribute ideas, and demonstrate respect for opinions of others.
* Display willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
* Negotiate and establish accurate time estimates for completion of study activities with internal team members and statistical management, and complete project activities within timeframe allotted.
* Assist in drafting regulatory submissions.
* Effectively utilize current technologies and available tools for conducting the analyses.
* Keeping up-to-date with current literature and research new methodologies.
* Identifying, developing and implementing novel statistical methodologies in support of medicine development
* Ensure scientific integrity and animal welfare in all activities.
* Interact with global statisticians and implement recommendations locally.
* Create and maintain standard macros and applications to improve the efficiency of the department.
* Proactively participate in and/or lead process/quality impro...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-07-01 08:47:35
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.
The Environmental, Health & Safety Manager has the responsibility for managing the Environmental, Health & Safety programs.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits.
* Manage WPDES permits.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager.
* Work cooperatively with outside consultants.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs.
* Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
* Perform fit testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks.
* Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations.
* Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corporate EHS department using the RCI reporting program.
* Complete a first report of injury with Workers Compensation Carrier if required for a workplace injury.
* Monitor return to work instructions given by health care provider and advise area man...
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Type: Permanent Location: Sparta, US-WI
Salary / Rate: Not Specified
Posted: 2025-07-01 08:30:01
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
Job Description:
The Analyst, Global Finance Master Data, is responsible for service delivery of specific Global Finance Master Data process functions serviced by GS Finance-Manila in J&J.
Key Responsibilities:
* Perform day to day operations of Financial Master Data team which includes maintenance of GL Accounts, Profit Center, Cost Center, Internal Order and Exchange Rate in line with Global DTP and defined standards
* Proactively identify, rectify and follow-up errors and causes of errors.
* Ensure timeliness, accuracy and quality of work and service by Finance Master Data team through regular review, checks and approval.
* Resolve complex or critical process issues which go beyond Finance Master Data team member’s capabilities.
* Handle risks through mitigation.
* Ensure that documentations are complete and up-to-date.
* Initiate, monitor and review systems’ accesses of the team.
Identified gaps are to be
* Support auditors and legal authorities with the execution of required activities – ensure staff are available as required.
* Ensure strong internal controls are in place, in order to achieve “adequate” internal and external audit ratings.
* Accurate and timely month-end reporting.
Meet all corporate and regional deadlines.
Qualifications
Education:
* Candidates must have at least a university degree in finance or any related field or equivalent
Experience and Skills:
Required:
* At least 1-2 years experience in the ATR or Finance Master Data function
* Experience in shared services center of a multinational corporation is desirable
* Excellent oral and written communication skills
* Ability to read, understand and verbally exchange information and compose written material for business purposes in English
* Ability to express ideas and information in an organized and logical manner
* Quantitative and analytical skills for problem solving and issue /risk mitigation
* Innovates and takes part in continuous improvement
* Strong knowledge of finance and accounting principles and processes
* Strong knowledge of concepts, principles and procedures for ATR process and most specific focus on the MRCs/function in scope
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-07-01 08:19:29
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
The position is located in the Lead Identification Department, within the Discovery unit of the pRED’s Large Molecules Research, where the discovery of next generation biotherapeutics is the primary focus.
We closely collaborate with our therapeutic areas and other functions to convert therapeutic hypotheses into innovative therapeutics.
Job mission
We are offering an outstanding opportunity for an experienced Lab Scientist (m/f/d) in High Throughput Screening for therapeutic antibodies.
Your main focus will be the evaluation and implementation of innovative cell-based and biochemical high throughput technologies for phenotypic antibody screenings.
Together with our diverse team of screening specialists, you will contribute to the generation of new therapeutic molecules for our drug discovery projects using your knowledge to design and execute experiments within your area of expertise.
Your impact
* With your expertise in hands-on assay development, execution and troubleshooting of cell-based and biochemical high-throughput assays you enable the identification of novel state-of-the art assay systems
* You actively strive to stay current with the latest assay technology and trends to enhance assay efficiency and output.
* Shaping and evolving our portfolio projects by discovering and characterizing next generation protein therapeutics is part of your mission
* You build strong relationships and collaborate effectively with internal and external partners to develop new screening systems and drive technical innovation.
Your profile
* You are dedicated to a collaborative, learning-oriented, and self-organized culture to achieve project goals.
Thrives in a dynamic, inclusive environment with full accountability and focus on priorities.
* We are looking for an experienced Lab Scientist and antibody screening expert with a strong creative and 3+ years in the pharmaceutical or biotech industry or equivalent experience in driving the evolution of cell-based and biochemical ...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-07-01 08:19:27
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Buenos Aires, Argentina
Job Description:
About Oncology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for MSL Oncology to be in Buenos Aires.
Purpose
The Lung MSL Mission is to, through customized interactions, discuss our treatments with physicians and other customers to shape behaviors and support informed decision making whilst identifying and bringing medical insights into the organization as inputs to medical strategy.
You will be responsible for:
• Be TA scientific experts, considered a trusted scientific counterpart and partner by external and internal stakeholders.
• Be focused on Customer Interactions, engaged in high scientific quality peer-to-peer communication on products, treatment trends and studies with defined audience of Leading Specialists (LS) , Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders.
• Contribute to other activities in line with the local Medical Affairs Plan: insight collection, evidence generation and Medical Education.
RESPONSIBILITIES
TA Knowledge
• Continuously update own and customer’s knowledge of products, patient’s treatment
trends, clinical activities and studies, local healthcare environment
• Identify evolving scientific concepts with future clinical implications
• Through scientific interactions, gain valuable insights into treatment patterns and scientific activities and collaborate effectively with MAF team and CVT to share insights with the MAF team Collaborate with sales force and other field-based roles (respond to queries, share insights and TA knowledge)
• Contribute to medical training and provide scientific supp...
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Type: Permanent Location: Buenos Aires, AR-B
Salary / Rate: Not Specified
Posted: 2025-06-30 08:14:41
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Marketing
Job Sub Function:
Product Management
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, Diegem, Flemish Brabant, Belgium
Job Description:
Position Summary:
We are seeking a Senior Brand Manager to lead the development and execution of marketing strategies for two areas within our rare diseases team: Pulmonary Arterial Hypertension (PAH) and Autoantibody Diseases (Nipocalimab/Imaavy).
This role combines critical thinking with operational delivery, with a strong focus on crafting brand plans that resonate with healthcare professionals and drive impact in sophisticated, specialty markets.
The ideal candidate is someone who takes ownership, brings their own perspective to strategic and tactical discussions, and is comfortable challenging the status quo when needed.
We’re looking for someone who is hands-on, yet forward-looking—capable of delivering on today’s priorities while contributing to the strategic direction of the brands.
Key Responsibilities:
* Develop and implement marketing plans for PAH and Nipocalimab (Imaavy), in close alignment with cross-functional teams and regional/global partners.
* Lead positioning, messaging, and content development tailored to the needs of specialist audiences.
* Bring market insights and field feedback into strategy discussions and identify opportunities to differentiate and improve brand performance.
* Design and roll out omnichannel campaigns and promotional initiatives, ensuring consistency and compliance across channels.
* Collaborate closely with medical, market access & sales to drive coordinated execution.
* Propose and implement new ideas to improve customer engagement or strengthen brand relevance.
* Measure the impact of marketing activities and contribute to business reviews with clear, data-driven insights.
* PAH: actively identify and implement creative brand strategies & tactics to differentiate the portfolio from competitors, ensuring a strong and sustainable competitive edge in the PAH market.
* Nipocalimab (Imaavy) launch: Play a key role in the development & execution of our launch plan and build impactful marketing assets for Nipocalimab/Imaavy, striving to deliver an outstanding product introduction in Myasthenia Gravis.
Candidate Profile:
* Demonstrated ability in pharmaceutical marketing.
* Strong understanding of brand planning, camp...
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Type: Permanent Location: Diegem, BE-VBR
Salary / Rate: Not Specified
Posted: 2025-06-30 08:14:23
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
New Brighton, Minnesota, United States of America
Job Description:
Johnson & Johnson is hiring for a Facilities & EHS Specialist - Shockwave Medical to join our team located in New Brighton, MN.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Facilities Specialist will oversee all activities for our office facilities located in New Brighton MN. This position will act as the office administrator and will also support the EH&S, Supply Chain, & Operations teams.
Essential Job Functions
* Oversee the planning and scheduling of routine, preventative maintenance, repair, and shutdown maintenance activities.
* Acts as the primary site security administrator.
* Administer access control badging system.
* Handle any safety issues or concerns in a timely manner.
* Coordinate and lead new hire and internal move activities, including office space management.
* Helps to ensure all building and maintenance policies, procedures, SOP’s, codes, regulations, etc.
are followed and enforced including safety systems and standards.
* Lead & support daily facilities maintenance and vendor oversight.
* Maintains appropriate logs and records for ISO 14001 compliance.
* Initiate, complete and close our facility work orders in CMMS.
* Assists the facilities management team by coordinating with vendors for special projects as needed/assigned and coordinates all operations initiatives (e.g.
signage projects, special inspections, data collection)
* Maintain compliance documentation for ISO, OSHA, CDP.
ESG etc., including records/logs of regulatory actions.
* Conduct regular inspections and audits of facilities to ensure complian...
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Type: Permanent Location: New Brighton, US-MN
Salary / Rate: Not Specified
Posted: 2025-06-30 08:14:17
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Project/Program Management Group
Job Sub Function:
Project/Program Management
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America, Juarez, Chihuahua, Mexico, Raritan, New Jersey, United States of America, Zuchwil, Switzerland, Zug, Switzerland
Job Description:
Johnson & Johnson Medical Devices Companies a member of Johnson & Johnson's Family of Companies is recruiting for a Process Analyst MAKE/Quality.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/ (https://www.jnj.com/
The Johnson & Johnson Medical Devices Companies have been working to make surgery better for more than a century.
With substantial breadth and depth in surgical technologies, orthopedic and interventional solutions, we aspire to improve and enhance medical care for people worldwide.
Together, we are working to shape the future of health through differentiated products and services.
The Electrophysiology & Neurovascular Business unit, part of the Medical Devices sector within Johnson & Johnson is recruiting for a Make/Quality Process Analyst for the Transcend Program.
Reporting to the Electrophysiology & Neurovascular Make/Quality Workstream Lead for the Transcend Program, the Process Analyst supports the Make/Quality functional teams by providing inputs reflective of business needs and requirements in alignment with Transcend Program.
This position offers a unique opportunity to play a pivotal role in the successful deployment of a new ERP system that will streamline processes within J&J and enhance efficiency across the J&J MedTech organizations.
The successful candidate will have in-depth knowledge of Manufacturing and/or Quality processes for both Electrophysiology and Neurovascular, demonstrated experience in process design, end to end process improvement, change management, as well as ability to translate and write/offer the business requirements.
Key Role Responsibilities
* Collaborate with Pro...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-30 08:14:14
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
The Experienced Statistical Programmer is an individual contributor with in-depth knowledge of statistical programming methods, languages and data structures who supports data analysis and reporting activities within the Statistical Programming functional area in accordance with departmental processes and procedures.
This position is accountable for the development, verification, and documentation of code used for the analysis and reporting of clinical data and is responsible for the timeliness and the quality of assigned deliverables supporting clinical projects and submissions.
This position is a member of a programming team, capable of supporting programming activities of medium to high complexity with minimal guidance.
* Designs and develops statistical programs in support of clinical research analysis and reporting activities.
* Performs appropriate quality control and verification in support of assigned clinical research analysis and reporting activities.
* Maintains statistical programming documentation as appropriate.
* Completes programming tasks of medium to high complexity with high quality and timeliness of deliverables.
* Performs activities in compliance with departmental processes and procedures.
* Collaborates effectively with statistical programming and cross-functional team members and counterparts to achieve project goals.
* Critically reviews requirements and data, identifies gaps, proposes solutions, and applies expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.
* Ensures continued compliance with required company and departmental training, time reporting and other business/operational processes as required for position.
* May contribute to departmental innovation and process improvement projects.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-06-30 08:14:11
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
We are searching for the best talent for Director, Global Commercial Strategy Neurodegeneration to be in Raritan, NJ.
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
This is a newly created role responsible for leading the commercial strategy and launch readiness for select pipeline assets in neurodegeneration, including Alzheimer’s and Parkinson’s Diseases. This role will work across the enterprise to ensure development of a cohesive strategy and product and launch readiness. The Director, Global Strategic Marketing reports to the Global Commercial Disease Area Strategy Lead for Neurodegeneration and will be part of the team that leads creation of commercial strategy, launch excellence, and market shaping plans. This role will contribute to optimizing the value of our global J&J portfolio by collaborating with key functions across the Global Commercial Strategy Organization (GCSO), J&J Research and Development (R&D), and J&J business regions.
Tasks/Duties/Responsibilities
* Lead commercial strategy, launch excellence, market shaping and a competitive go-to-market model.
* Represent commercial view in cross-functional teams such as CDT to ensure development plans and market shaping activities are reflective of stakeholder needs and will drive approval, access and adoption.
* Collaborate with GCSO Medical and Market Access partners to ensure clear and cohesive strategic input to GCT, launch readiness teams and market shaping initiatives
* Coordinate with key cross-functional partners (Analytics, Finance, Competitive Intelligence, etc.) to develop differentiating value proposition and commercial forecast valuation models
* Partner across a diverse matrix of collaborators to deliver results and projects/initiatives (e.g.
Supply Chain, Data Sciences, etc.)
* Perform other work-related duties as assigned...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-30 08:13:50
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
Horsham, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for Director, Clinical Operations & Program Management to be in Horsham, PA.
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Are you ready to lead innovative medical affairs initiatives and drive impactful clinical trials for patients? Are you an experienced clinical operations leader looking to join a growing & diverse team?
Purpose: This role will be accountable and responsible for start-up and execution of medical affairs data generation efforts including company sponsored studies (CSS), investigator-initiated studies (IIS), collaborative studies, and post marketing commitments in assigned therapeutic areas.
This individual will be the line manager for the Clinical Operations and Program Management (PM) team and will ensure consistent Clinical Project Scientist (CPS) and PM support for key activities in their respective therapeutic areas.
This person will assist the head of the Strategic Operations group in running the departmental budgets and will be a primary contributor to annual budget planning process.
Working with their peers & partners on the clinical teams, they will take part in the development of therapeutic area strategic plans, including the Business Plan (BP) and Integrated Evidence Generation Plan (IEGP).
Responsibilities will also include the development & maintenance of critical internal & external alliances for their assigned Therapeutic Area (TA) portfolio.
You will be responsible for:
* Leading a team of Program Managers & Clinical Project Scientists who support assigned therapeutic areas with franchise strategy and planning, clinical programs & other key projects.
* Collaborating with Global Development leaders, including trial and contracting staff, to ensure appropriate support to enable study success within portfolio aligned timelines.
* Coordin...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-30 08:13:35
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Sr.
Regulatory Affairs Specialist (Remote) â Shockwave Medical to join our team located in Santa Clara, CA and Remote US.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, weâre developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team thatâs pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position OverviewÂ
The Sr.
Regulatory Affairs Specialist is an individual contributor that works closely and partners with internal departments to efficiently and effectively meet assigned regulatory requirements for Shockwave Medical, Inc.
(SWMI).
 The Sr.
Regulatory Affairs Specialist combines knowledge of scientific, regulatory and business issues to ensure that products are developed, manufactured and distributed to meet regulatory requirements with a focus on the United States and the EU.
Under direction of responsible Regulatory Affairs Management, acts as a decision-maker on regulatory issues, assures that registration/renewal deadlines are met, and supports new product development.
Â
Essential Job Functions
â¢Â   Collaboratively interface with a variety of levels on significant matters, often requiring the coordination of activity across organizational units.
â¢Â   Outline submission and approval requirements in assigned geographies.
â...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-30 08:13:19
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Chemical Research
Job Category:
Scientific/Technology
All Job Posting Locations:
San Diego, California, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Senior Scientist, Discovery Chemistry role to be in San Diego, CA.
Purpose:
We are seeking an experienced, highly skilled, and motivated analytical and separation scientist to work in our laboratories in La Jolla, CA, for the position of Senior Scientist in Discovery Chemistry.
This position will require the candidate to possess and leverage deep knowledge and capabilities in Analytical Chemistry and Separation Sciences as part of the Analytical Chemistry and High Throughput Purification (AC-HTP) team to provide support to discovery chemists.
Strong communication skills and the ability to thrive in a team and results oriented environment are key attributes.
The candidate must also have strong interpersonal skills to influence in a collaborative multidisciplinary environment.
You will be responsible for:
* Applying chiral and achiral chromatography methods and capabilities to accelerate Janssen small molecule discovery research.
* Evaluating and implementing new chromatography methods and apply them across different modalities and/or capabilities, such as small molecule drug discovery, peptide drug discovery, DNA-encoded library, target protein degradation and Direct-to-biology.
* Presenting at internal and external scientific meetings as appropriate.
* Working with the vendors, when needed, to implement new instrumentation and maintain the smooth operation of instruments.
* Routinely interacting with colleagues from therapeutic area project teams and core technology groups to develop and implement strategies on analytical chemistry to help advance programs.
Qualifications / Requirements:
Education:
* a minimum of a Masters degree in chemistry or related discipline is required
...
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Type: Permanent Location: San Diego, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-30 08:13:01
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Senior Scientist, Protein Characterization, Mass Spectrometry to be in Malvern, PA
Purpose:
The Therapeutics Discovery & Supply-Analytical Development (TDS-AD) is recruiting for a Senior Scientist located in Malvern, PA.
We discover and develop creative large molecule solutions to address significant unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases.
The Analytical Development organization is continuing to build key scientific expertise in protein and vaccine characterization, and primary structure elucidation! We need a hardworking scientist willing to bring their expertise to exciting efforts in novel areas of protein characterization.
You will join the Primary Structure team within the Characterization group in the TDS-AD department to conduct product characterization and process development activities.
You will be responsible for:
* Operating state-of-the-art LC and MS instrumentation
* Learning and applying different software packages for LCMS/protein analysis
* Performing LCMS-based quantitation of post-translational modifications
* Designing and implement peptide mapping / MS experiments on monoclonal antibodies and recombinant proteins to assess sequence coverage and sites of modification
* Participating in IND, IMPD, BLA, and other regulatory filings
* Developing test methods, provide documentation and write scientific reports.
* Conducting testing to support analytical development, manufacturing process development, process validations, and manufacturing investigations
* Leading or facilitating technical discussions and participate in cross-functional teams at project-rela...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-30 08:12:45
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ERM is seeking highly motivated Principal Consultant, Archaeologist to join our global consulting firm as part of our Cultural Resources Services team.
This is a full-time, salary-based position that can be based from a local ERM office or fully remote.
Applicants are preferred to be local to Austin, Dallas, Houston, or New Orleans, as well as be familiar with the relevant regional regulatory processes (i.e., federal, state, and municipal). Demonstrated regional high-level consulting experience is required.
Successful candidates must be flexible and responsive to a challenging and changing work environment where schedules and tasks fluctuate according to the needs of the projects and clients.
The hire will be attached to an ERM office in Texas or Louisiana.
Other geographies may be considered for the ideal candidate.
The successful candidate will also provide technical assistance for clients throughout the United States while also focusing on project needs and business development within their region.
RESPONSIBILITIES:
* Oversee a team performing literature review, field reconnaissance, field surveys, and excavation for archaeological studies and projects.
* Provide technical consulting skills to support the growth of ERM’s business and client base in the area of archaeology and cultural heritage.
* Interact with other ERM practice areas to share multi-disciplinary resources and best practices across the country.
* Represent ERM through communications and at meetings with state, federal and local agencies.
* Communicate regularly with clients via email and phone conferences.
* Oversee and manage subcontractors.
* Assist with preparing proposals to meet client needs.
* Manage multiple projects within scope/budget/schedule expectations and ensure quality standards on project deliverables.
* Lead, manage performance, hire and retain, inspire and mentor personnel for overall success of the technical team.
* Capitalize on existing ERM client relationships to expand ERM’s profile and market share in the Cultural Resource market (through a combination of excellence in technical delivery and business development). Work with other ERM resources to deepen relationships with ERM key clients and establish new client relationships that result in significant net revenue growth.
* Participate on teams comprised of impact assessment professionals from multiple offices around the global ERM organization.
* Interact with various State Historic Preservation Offices, federal agencies, and access online cultural resource databases.
* Lead and supervise staff in an office setting and/or during fieldwork.
* Perform research and write technical reports.
* Provide technical consulting skills to support the growth of ERM’s business and client base in the area of archaeology and cultural heritage.
* Interact with other ERM practice areas to share multi-disciplin...
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Type: Permanent Location: Metairie, US-LA
Salary / Rate: Not Specified
Posted: 2025-06-30 08:10:22
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ERM is hiring a Utility Safety Advisor in Fort Worth, Texas.
As a Utility Safety Advisor, you will engage with client and contractor team members in the field to facilitate safe work practices, identify hazards and advise mitigations, embrace client safety culture expectations, adhere to applicable project permits, and maintain compliance with the client’s Contractor Safety Program elements and other applicable safety regulations/requirements by local, state, and federal safety agencies.
This position works to promote a safe work environment by confirming that contractors and the project team, at a minimum, clearly understand the roles and responsibilities related to reviewing drawings, identifying known hazards, and communicating policies, standards, and procedures applicable to the work.
The role includes the responsibility of timely notification to management and the safety team about any safety issues.
This is a full-time (40+ hours a week) limited-term role for a duration of 3 months, extendable.
RESPONSIBILITIES:
* Provide quality assurance and quality control observation for electrical safety inspectors.
Observe contractor safety inspectors and conduct audits and reviews of work practices, work products, and skillsets of contractors’ safety inspectors.
* Promote high-voltage electrical safety during site inspection and the implementation of medium and high-risk scope activities.
* Initiate and/or participate in safety kick-off, periodic or daily safety meetings with contractors.
* Function as Subject Matter Expert (SME) on Federal, State, and local laws, rules, and regulations (including, but not limited to, DOT and OSHA) as well as industry best practices.
* Perform contractor safety observations as established by the frequency and level for each contractor and subcontractor.
* Provide on-site occupational safety support to identify, prevent, and mitigate safety risks.
* Document and retain safety documents in accordance with client requirements.
* Assign and/or coordinate with team members to address corrective actions, and communicate as appropriate with team members to prevent repeat occurrences.
* Receive safety-related questions and provide reliable feedback and instruction.
* Share safety information to all in an impactful, constructive, and results-oriented manner.
* Communicate safety trends and recommend safety corrective actions.
* Prepare safety observation and improvement reports to Management and/or client following an incident or high-potential consequence near miss.
* Support compliance with applicable programs (PPE, rubber gloving, and hot stick procedures).
* Capable of identifying existing and predictable hazards in the surroundings or working conditions that are unsanitary or dangerous.
REQUIREMENTS:
* High School Diploma or GED.
* Minimum of 5 years of experience as a journeyman lineman in construction within the power utility sect...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-06-30 08:10:20
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Ardurra is seeking a full-time Senior Ecologist to join our team in Orlando, FL.
This role focuses on environmental permitting, regulatory compliance, and database management for transportation-related projects.
The ideal candidate will possess strong ecological assessment skills and a solid understanding of permitting requirements for both state and federal agencies.
Primary Function:
We are seeking a motivated and knowledgeable Sr Ecologist to play a key role in the planning, execution, and management of wetland and natural resource projects throughout our Orlando Projects.
This is an exciting opportunity to work on diverse watershed projects in a collaborative and supportive work environment.
Primary Duties:
* Review roadway plans to determine permitting requirements for minor and major transportation projects, including identification and assessment of wetlands and protected species affected, and assessment of stormwater impacts
* Prepare state and federal permit application packages that describe the site assessments, stormwater data, agency jurisdiction, the measures necessary to satisfy permit requirements, and summaries of meetings with the regulatory agencies
* Conduct wetland inventories and Environmental Assessments, including a focus on protected species
* Assist in preparing and reviewing reports in support of projects, including protected species, natural habitat, environmental impacts, biological evaluations, minor NEPA/NMSA, and related regulatory requirements and compliance guidelines
* Review documents for projects prepared by others, including pre-design environmental documents, permit application packages, exemption verifications, or need for additional wildlife surveys
* Perform QA/QC reviews to ensure completeness, accuracy, and conformity to established industry standards and local, state, or federal criteria
* Provide practical solutions to project challenges by applying accepted procedures and methodologies and collaborating with others
* Support the preparation of draft environmental scope, units, and staff hours for projects based on existing transportation permitting policies and guidelines
* Monitor project budgets and schedules to ensure profitability and timeliness of deliverables
* Mentor junior-level team members while being a positive leader for the team
* Contribute to business development efforts by supporting proposals and identifying new opportunities
Education and Experience Requirements:
* Bachelor’s degree in physical or natural sciences or a related field such as Environmental Science, Biology, or Ecology
* 10+ years of prior practical experience (or 7+ with a relevant Master’s degree)
* Familiarity or established relationships with FDOT, regulatory agencies, and other municipal clients is strongly preferred
* In-depth knowledge of FDOT and regulatory agency criteria, standards, and plans preparation requirements
*...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: Not Specified
Posted: 2025-06-30 08:06:37
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Senior Bioanalytical Scientist
Join Elanco’s RBI Discovery Science team as a Senior Bioanalytical Scientist, where you'll play a key role in developing and validating cutting-edge bioanalytical assays to support the advancement of our biologic's portfolio, including therapeutic proteins and vaccines.
You’ll combine hands-on laboratory expertise with strategic leadership, working across internal teams and managing collaborations with external CROs.
This role offers an exciting opportunity to innovate, lead cross-functional initiatives, and contribute to the development of new bioanalytical technologies, driving products from discovery to clinical development.
We’re looking for expertise in ligand-binding assays (e.g., MSD, ELISA), cell-based assays, immunogenicity assessments, and ideally, assay automation.
A strong background in large molecules like monoclonal antibodies and complex proteins is highly desired.
Success in this role will require a collaborative mindset, leadership skills, and a proven ability to solve problems and communicate effectively in cross-functional environments.
Your Responsibilities:
* Lead the development, validation, and optimization of bioanalytical assays (e.g., MSD, ELISA, cell-based) for therapeutic proteins and vaccines.
* Independently design, execute, troubleshoot, and interpret laboratory studies, contributing directly to data generation and analysis.
* Manage and mentor junior scientists, fostering talent and ensuring excellence in internal and external (CRO) bioanalytical activities.
* Oversee CRO activities, including assay transfer, study monitoring, data review, and issue resolution, ensuring timelines and data quality.
* Drive innovation by developing creative solutions for bioanalytical challenges and implementing new technologies and platforms.
* Collaborate across teams (Discovery, PK, Pharmacology, Toxicology, Clinical) to align on assay design, development, and implementation.
* Design and execute assays for PK/TK studies, immunogenicity assessments (incl...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 171000
Posted: 2025-06-29 08:35:56
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Actus Nutrition is an industry-leading manufacturer of innovative dairy-based nutritional ingredients designed to optimize health and nutrition.
We are currently seeking a Quality Assurance Technician to be based out of our facility in Visalia, CA.
This is a 12-hour shift working on a rotating schedule.
Wages $22.50 - $25.00
QA Techs are responsible for:
Environmental sampling, performing microbiological tests for a dairy food production facility
Reporting results, validations, data entry and general sanitation for the lab
Requirements:
Individuals who would like to be considered for this opportunity will have at lease 1-2 years of manufacturing experience, preferably in a food grade facility and/or quality/auditing department.
Experience with petrifilm plating, moisture, Mojonnier fat testing, yeast/mold, ash and kjeldahl testing is a plus.
Ideal candidates will have excellent analytical, organizational and leadership skills with proven ability to manage multiple priorities in a fast-paced environment.
Must be detail oriented and customer focused with exceptional communication and computer skills.
The company is committed to identifying and recruiting only the highest caliber of talented individuals to join its team of passionate and dedicated employees.
It offers a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
OPEN
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Type: Permanent Location: Visalia, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-29 08:23:54
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The VP of R&D at NorthStar is a hybrid business / technical position and requires a blend of management and project management skills, product vision, financial savvy, excellent communication skills, and understanding of the agile process.
The Vice President of R&D is responsible for a continuous flow of product research and innovation leading to the improvement of existing products, incorporation of newly acquired product sets into the current list of corporate assets, and integration of third-party solutions with Harris’ product sets.
As the VP of R&D, the ideal candidate will be responsible for inspiring a diverse team of developers located in multiple offices throughout the US and Canada and across multiple products.
The VP of R&D is a highly motivated self-starter and team player; with a focus on team and client success, and business operations efficiency.
The candidate will manage and inspire a team of between 20-30 people and holds P&L responsibility and forecasting for their team.
This is a remote opportunity within Canada or USA.
What your impact will be:
* Translating business goals & product requirements into actionable development plans.
* Ensuring that development projects are delivered on time and within budget.
* Strategic planning, direction and control of product development activities; as well as technical input into the overall business strategy.
* Managing both onsite & offshore development teams.
* Proactively nurturing and building channels of communication across business units to ensure collaboration and achievement of organizational goals.
* Providing technical direction and guidance for all product development needs throughout the organization.
* Continually evaluating the organizational structure and current technology as a means to enhance productivity and implementing appropriate changes.
* Communicating industry trends and emerging new technologies that can provide the organization with an advantage.
* Managing strategic partnerships with vendors and suppliers.
* Conceive, develop, and drive all critical product road map offerings to position the NorthStar division for long term success and minimize attrition risks from competitors who claim to have a more complete product .
* Be an effective liaison between the NorthStar customer base and the internal NorthStar departments (i.e.
Sales, Professional Services and Support Services).
What we are looking for:
* Bachelor’s degree in a technical discipline or relevant experience.
* 10+ years of management experience at the product or people level.
* Exceptional written and verbal communication; communicating clearly and comprehensively to senior executives and technical experts.
* Organization and time-management skills, with a can-do attitude.
* Excellent team player able to manage and prioritize work for self and staff.
* Advanced analytical, diagnostic, and troubleshooting ...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-28 10:02:18
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Nous sommes à la recherche d’un·e Chef d’équipe Assurance Qualité Logicielle pour rejoindre notre équipe dynamique.
Relevant directement du Vice-président à la Recherche et au Développement, vous jouerez un rôle central dans l’assurance de la qualité, de la fiabilité et de la performance de nos produits.
À la tête d’une équipe composée de 5 spécialistes QA, vous serez responsable de l’encadrement, de la motivation et du développement professionnel de vos collaborateurs.
Vous veillerez à la mise en œuvre et au respect des meilleures pratiques de l’industrie en matière d’assurance qualité.
Vous superviserez l’ensemble des processus de tests automatisés, assurerez le maintien d’une pyramide de tests équilibrée et garantirez que chaque nouvelle version de nos produits respecte nos standards d’excellence.
Votre objectif : des livraisons impeccables, à chaque fois.
Responsabilités principales:
* Assumer la responsabilité complète de la qualité des livraisons logicielles.
* Définir et implanter les meilleures pratiques de l’industrie en matière d’assurance qualité logicielle.
* Élaborer et mettre en œuvre des stratégies de test robustes, incluant une pyramide de tests bien équilibrée (tests unitaires, d’intégration, end-to-end, etc.).
* Superviser l’équipe QA : définir les objectifs, évaluer les compétences, identifier les besoins de développement et soutenir la croissance professionnelle des membres.
* Identifier, documenter et suivre les anomalies et défauts logiciels.
* Collaborer étroitement avec les équipes de développement, produit et opérations pour résoudre les problèmes et améliorer les processus.
* Assurer la conformité aux normes de qualité internes et externes.
* Réaliser des tests de performance, de sécurité, de compatibilité et de régression.
* Produire des rapports de test clairs et formuler des recommandations pour l’amélioration continue.
* Prioriser les éléments à automatiser dans le cadre du processus CI/CD (intégration et déploiement continus), incluant les tests QA, afin d’assurer des livraisons fiables jusqu’en production.
Qualifications requises:
* Minimum de 10 ans d’expérience en assurance qualité logicielle, dont plusieurs années dans un environnement Agile/DevOps.
* Diplôme en informatique, en génie logiciel ou dans un domaine connexe.
* Expérience significative en assurance qualité logicielle, idéalement dans un environnement Agile/DevOps.
* Maîtrise des méthodologies de test (manuelles et automatisées) et des outils associés.
* Solides compétences en gestion d’équipe, leadership et communication.
* Capacité à travailler sous pression, à gérer les priorités et à respecter les échéanciers.
* Esprit analytique, rigueur et souci du détail.
Compétences techniques souhaitées:
* Expérience avec les test...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 85000
Posted: 2025-06-28 10:02:09
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: SIAM Analyst
As Elanco grows, the SIAM Business Systems Analyst will play a key role in stabilizing and optimizing the IT Operating Model through data-driven process improvement, service integration, and reporting.
This role is responsible for developing IT governance reports, managing dashboards in ServiceNow and Power BI, supporting vendor management reporting, and driving continuous improvement initiatives.
By partnering across IT and vendor teams, the analyst ensures process alignment, monitors performance metrics, and contributes to the ongoing evolution of Elanco’s IT governance, collaboration and processes.
Your Responsibilities:
* Generate, validate, and distribute monthly IT governance reports
* Develop and maintain ServiceNow Performance Analytics (PA) dashboards and Power BI (PBI) reports
* Assist in the development and delivery of vendor management reports for the VMO
* Contribute to the creation and tracking of ServiceNow enhancement stories and platform upgrade initiatives
* Set up, monitor, and manage ServiceNow SLA definitions and reporting
What You Need to Succeed (minimum qualifications):
* Minimum of three to five years of IT Service Desk experience.
* Minimum of three to five years of experience in data aggregation and reporting.
* Minimum of three to five years of experience and demonstrable proficiency using and developing reports within ServiceNow
* Education: A bachelor’s degree in IT, computer science, business, management or a related field is required
What will give you a competitive edge (preferred qualifications):
* Comprehensive understanding of an ITSM/ITIL governed support model.
* Proficiency in the analysis and interpretation of data and how to effectively utilize that information to drive efficiencies, maturation, and improvement.
* A solid understanding of IT Vendor deliverables and obligations through contracted SOWs, SLA/KPI measurement, and contractually binding credit generating stipulations
Additional Information:
* Travel: 0%
...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-06-28 10:01:45
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Technical Consultant, Swine
As a Technical Consultant within Elanco’s SBU team, you will be a trusted technical partner to customers and internal teams across the food animal health space.
You will position Elanco as the partner of choice by delivering exceptional technical expertise, market-leading product solutions, scientifically sound research, and value beyond product - including consulting, diagnostics, analytics, and market access support.
This role is field-based and requires travel up to 50%.
You will work cross-functionally within account teams, train Elanco colleagues, engage with industry stakeholders, and influence the long-term direction of our food animal portfolio through research, innovation, and customer-centric solutions.
Your Responsibilities:
Sales and Marketing Support
* Collaborate directly with customers and account teams to support Elanco’s commercial goals
* Identify opportunities and position Elanco products as solutions for customer challenges
* Participate in account planning and help implement Elanco’s value strategy at the customer level
* Support training efforts and contribute to product launch readiness
* Develop and deliver educational events and technical materials for internal and external stakeholders
Customer and Technical Leadership
* Train and coach Elanco teams on disease, product knowledge, and industry practices
* Build strong relationships with external veterinarians, consultants, and academic partners
* Serve as a technical authority to influence decisions at customer and industry levels
* Represent Elanco in key industry organizations and maintain thought leadership presence
Research and Innovation
* Conduct applied research with Elanco-approved products to generate field-relevant data
* Align technical research with business priorities and lifecycle planning for key brands
* Contribute to peer-reviewed publications and present at scientific meetings
* Support R&D efforts, including product line extensions and innovation ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 155000
Posted: 2025-06-28 10:01:41
