-
2406174064W Qualifications :
• Junior, Senior, or Grad student pursuing a degree in data science, computer science, computer engineering, software engineering or statistics.
Required :
* Strong machine learning background
* Proficient in at least one programming language (Python or C preferred) and solid understanding of datastructures & algorithms
* Solid understanding of statistics, strong analytical skills
* Self-motivated, execute tasks in a timely manner
* Demonstrated communication skills, both written and verbal
Strongly preferred :
• Knowledge in data science / machine learning libraries (numpy, pandas, matplotlib, sklearn, nltk)
• Deep learning experience (TensorFlow, Keras)
• Experience in signal processing
• Big data / cloud experience (AWS, Azure, Google Cloud, Hadoop, Spark, Hive)
• Displayed interest in medical device industry
Abiomed is an Equal Opportunity Employer committed to a diverse workforce.
Abiomed will not discriminate against any worker or jobapplicant on the basis of race, color, religion, gender, gender identity, national origin, ancestry, age, sexual orientation, genderidentity, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, geneticinformation, veteran status, military service, application
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:51
-
2406166863W REQUIRED QUALIFICATIONS:
* Junior, Senior, or Grad student pursuing a degree in computer science or an engineering field.
* Experience with modular programming, C programming experience is strongly preferred.
* Demonstrated communication skills, both written and verbal.
* Experience with electrical design software tools - schematic capture and board layout.
* Working knowledge of general equipment in an EE lab such as an oscilloscope.
* Self-motivated, hard worker.
Execute tasks in a timely manner with minimal supervision.
* Willingness and ability to travel domestically and/or internationally as needed.
PREFFERED QUALIFICATIONS:
* Junior, Senior, or Grad student pursuing a degree in computer science, computer engineering, electrical engineering, or biomedical engineering.
* Hands-on electrical circuit test and troubleshooting experience of analog, digital, and mixed signal systems.
* Demonstrated design, testing and analytical skills
* Desire to pursue a career in the healthcare/MedTech engineering field.
* Experience with Altium schematic capture and layout.
Abiomed is an Equal Opportunity Employer committed to a diverse workforce.
Abiomed will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, national origin, ancestry, age, sexual orientation, gender identity, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.
Abiomed maintains a drug-free workplace
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:50
-
Johnson & Johnson Philippines is searching for Human Resource Interns to join our APAC HR Recruitment & Onboarding team from mid August to early December 2024.
If you are strong in critical thinking, self-motivated and detail oriented, then we invite you to embark on an exciting internship journey with us! This role will play an integral role in assisting and executing various Onboarding processes and will work cross functionally with other teams across the organization.
Key Activities
* SFDC (Salesforce.com) task monitoring
* Due diligence initiation and monitoring
* Organize and maintain hire and onboarding tracker system and database
* Invoice coordination and PO (Purchase Order) reports preparation
* Currently pursuing a degree in Psychology, Human Resources, or any related field
* Amenable to working onsite at our Paranaque office at least 2x a week; Remote on other days
* Excellent communication skills in English - written and verbal
* Proficient in Microsoft Office - Excel
* Proactive and detail-oriented with advanced administrative and organizational skills
* Strong analytical, problem solving, sound judgment and decision-making skills
* Learning agility, adaptability to change with a growth mindset
....Read more...
Type: Permanent Location: Manila, PH-00
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:48
-
Johnson & Johnson is made up of two key pillars: Pharmaceuticals, and MedTech.
Here at MedTech, we're changing the trajectory of health for humanity, using technology to enhance healthcare providers' abilities and improve patients' diagnoses, treatments, and recovery times .
We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.
With a reach of more than a billion people every day, there's no limit to the impact you can make here.
Are you ready to reimagine healthcare?
Here, your career breakthroughs will change the future of health, in all the best ways.
And you'll change, too.
You'll be inspired, and you'll inspire people across the world to change how they care for themselves and those they love.
Amplify your impact.
Join us!
About Ethicon
Ethicon Surgery Technologies, formerly Ethicon Endo Surgery Inc.
was created 25 years ago, in Cincinnati, Ohio, developing creative devices that have driven the groundbreaking shift from open to minimally invasive surgery that continues to lead the industry today.
The Ethicon business offers a broad range of products, platforms, and technologies-including surgical staplers, advanced energy, robotic surgery, clip appliers, and trocars-that are used in a wide variety of minimally invasive and open surgical procedures.
Specialties include support for treatment of colorectal and thoracic conditions, women's health conditions, hernias, cancer and obesity.
About the Role
Ethicon Surgical Technologies is recruiting for an R&D Quality Engineering Co-op for the Fall 2024 term from August 26 th - December 13 th , term dates are flexible in accordance with school semesters.
As a Co-op in the Quality Engineering organization, you will have the chance to:
* Create and update risk management documents like FMEAs in order to drive product requirements
* Develop technical writing skills by authoring Quality Plans with external manufacturers or Competitive Complaint Analyses
* Perform testing, experimentation, verification, and validation to support product design.
* Lead the development of laboratory testing, interpreting data results, and recommending next steps
* Learn and perform various statistical analysis techniques.
* Strengthen communication and leadership skills.
* Take advantage of training courses offered on-site.
The Quality Engineering Co-op will:
* Work New Product Development/R&D, Lifecycle/Sustaining, or the Quality Systems group.
* Partner a diverse team of Design Engineers, Development Engineers, Quality Engineers, Regulatory Affairs, Marketing, and Clinical.
* Report directly to, and receive assignments from, the team Quality Engineer, while also working with the broader team for additional assignments.
* Participate in and/or lead on-campus activities such as learning committees, volunteer events, and meet and greet luncheons with full time as...
....Read more...
Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:46
-
Johnson & Johnson is currently recruiting for a Finance Intern - Invoice to Cash, from August to early December, located in Manila, Philippines
"Reimagine the possibilities" at Johnson and Johnson Global Finance! We live this motto every day by creating game-changing business solutions for the world's largest and most broadly-based healthcare company.
As a member of our Global Finance team, you will have exclusive access to a network of financial professionals located in over 60 countries.
This new network will help you build on your current skills and explore opportunities to grow your career in J&J.
At J&J Global Finance, we value ideas for innovation and improvement and are committed to diversity and inclusion.
Together we will reimagine business processes to become more effective, more efficient, and improve customer experience.
We are proud to be an equal opportunity employer.
Job Description:
The Finance Intern - Invoice to Cash is mainly responsible for providing customer credit risk assessment for specific business MRCs and markets serviced by JNJ Global Services- Manila.
This position reports to the Credit Manager.
Major Duties & Responsibilities:
Customer risk assessment and mitigation:
* Lead in customer credit risk assessment process, and review customer credit condition based on local business, sales forecast, credit agency report, financial statement analysis, bank collateral, and other available information.
* Assess customer type and establish credit limits based on a deep understanding of customer creditworthiness and industry tendency.
* Proactively work with internal business partners with a comprehensive understanding of local business and marketing, to update customer credit risk.
* Support review of credit applications and provide comments on credit risk assessment.
Others
* Ensure that adequate and effective internal controls are in place and that processes and policies are established and documented in compliance with WWP, ICH, DTP, and other control requirements.
* Work on continuous improvement programs to standardize and improve the efficiency, effectiveness, and customer experience across various entities.
* Support monitoring KPI results to meet the Service Level Agreement commitments, and deliver high-quality service.
* Other ad-hoc tasks assigned by the manager.
* Currently pursuing a Bachelor's degree in Finance, Accounting, or Business-related courses
* Excellent written communication skills, with the ability to collaborate with a variety of stakeholders
* Knowledge of SAP is ideal, but not necessary
* Good command of English, both oral and written
* Proficient in Microsoft Office
* Teamwork spirit and can work under pressure
* Strong analytical, problem solving, sound judgment and decision-making skills
* Learning agility, adaptability to change with a growth mindset
* Demonstrated passion in Finance
....Read more...
Type: Permanent Location: Manila, PH-00
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:45
-
The Manager Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned products.
The Manager SAS, in partnership with the Medical Safety Officer (MSO), is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.
The Manager SAS will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product's safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings, and interpret safety information to make a recommendation, supporting SMT deliverables as required.
The Manager SAS will assist the MSO with activities related to the SMT and with contributions to key safety and clinical documents.
The Manager SAS will have in-depth product knowledge, will serve as product point of contact, and will provide mentoring to, and oversight of deliverables prepared by, other team members as needed (for complex reports).
The Manager SAS will function independently, or with moderate guidance from the Director, SAS Therapeutic Area Lead (TAL), be able to link discussions to content, and deliver quality results with minimal guidance.
The Manager SAS will build alliances and be able to influence other safety partners to shape decisions/outcomes.
• Lead safety evaluations, including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary , data retrieval, data analysis, report writing, and report revision .
• Ensure high quality safety evaluations and reports with minimal-to-moderate comments from stakeholders and minimal-to-moderate revisions required.
• Provide support to AD SASs for novel projects without defined processes.
• Provide input and review to key regulatory or clinical documents as appropriate.
• Demonstrate leadership in the SMT and support the MSO.
• Support SMT activities (e.g.
preparing and presenting data, compiling meeting minutes, updating signal tracking information).
• Lead proactive safety data reviews, if applicable and form a safety position across GMS which can be leveraged for aggregate safety reports.
Provide support for Health Authority interactions regarding safety and risk management, both written and verbal.
• Contribute to cross-functional training of relevant stakeholders.
* Mentor other SASs on activities within the role.
* Participate in department and/or cross-functional initiatives and explore innovative ways of presenting data, preparing reports, and improving efficiencies.
Assist in the creation, review and implementation of controlled documents and other related tools.
Support audits/inspections.
* Bachelor's Degree Required: Healthcare-related or Biomedical Science (...
....Read more...
Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:43
-
At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world's the most significant healthcare challenges.
Our Corporate Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.
We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.
With a reach of more than a billion people every day, there's no limit to the impact you can make here.
Are you ready to reimagine healthcare?
Here, your career breakthroughs will change the future of health, in all the best ways.
And you'll change, too.
You'll be inspired, and you'll inspire people across the world to change how they care for themselves and those they love.
Amplify your impact.
Join us!
We are currently hiring for a Quality Engineering Data Science Co-Op for the Fall 2024 term (Aug 26 th - Dec 13 th ) as a part of Johnson & Johnson Medical Device companies located Cincinnati, OH.
Johnson & Johnson Medical Device Companies produce a broad range of innovative products and solutions used primarily by health care professionals.
As the most comprehensive devices business in the world, Johnson & Johnson Medical Devices is best suited to serve evolving customer needs, train more surgeons to improve standards of care, and treat more patients globally as access expands.
As a Co-op in the MD Quality and Compliance (Q&C) Digital Solutions organization, you will have the chance to:
* Use state of the art tools and take advantage of training courses offered at J&J.
* Collaborate with teams internal and external to the advanced analytics to implement customer-centric solutions for data analytics and process improvements
* Perform software development and validation to support medical device quality system digital solutions.
* Learn and apply various software development and lifecycle management techniques.
* Promote digital culture and capabilities across J&J medical devices
* Strengthen communication and leadership skills.
* Work with a diverse team of data scientists, analytics app developers, quality engineers, etc.
* Meet with Quality management to discuss risks and opportunities for the respective projects.
The Digital Solutions Co-op will:
* Have the opportunity to work at and support Ethicon, Inc in Cincinnati, Ohio
* Assigned to a team in one of the various franchises of each respective company.
* Work in MD Q&C Digital Solutions group.
* Report directly to, and receive assignments from, MD Q&C Digital Solutions Advanced Analytics Manager, while also working with the broader team for additional assignments.
* Participate in and/or lead on-campus activities such as learning committees, volunteer events, and meet and greet luncheons with full time associates.
Rotations are generally 3-5...
....Read more...
Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:42
-
Senior R&D Program Manager
Location: Ballybrit, Galway
Live Our Credo & Pursue Our Purpose:
As part of the Johnson & Johnson family of companies, Our Purpose is 'We blend heart, science and ingenuity to profoundly change the trajectory of health for humanity.' We are guided by the values in Our Credo.
With responsibility to patients, employees, communities, and stakeholders, Our Credo puts the needs of each of those first.
Diversity, Equity & Inclusion:
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences
That is why we in Ireland are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential.
No matter who they are.
Diversity, Equity & Inclusion at Johnson & Johnson means "You Belong".
Cerenovus:
CERENOVUS, part of Johnson & Johnson Medical Devices Companies, is a global leader in neurovascular care.
Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship.
CERENOVUS offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.
What is it like to work at CERENOVUS Galway?
* Culturally, we are putting the needs of Our Credo stakeholders first through pursuing the highest standards of quality, compliance, and ethics, ensuring everyday actions contribute to Our Purpose.
* We are continuing to better our understanding of clot science, through our Neuro Thromboembolic Initiative (NTI).
This is a commitment to advance the treatment of stroke through interdisciplinary collaboration and investment in clot and stroke research.
How we understand clots and their behaviour enhances our opportunity to design devices that improve patient outcomes and, overall, advance the treatment of acute ischemic stroke.
* Strong new product pipeline and the fastest growing medical device company within J&J in 2021.
* From a People perspective, we invest in our people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation.
This is empowered through our employee resource groups (ERGs) focused on further balances of gender, nationality, capability and more, including the additional attracting of qualified diverse candidates for our open roles.
Job Summary:
CERENOVUS a Johnson & Johnson company is recruiting for a Senior R&D Program Manager, located at it's Global In...
....Read more...
Type: Permanent Location: Galway, IE-G
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:38
-
Product Specialist Wound Closure - Ethicon
* Great Place to Work® Certified - 2022 & 2023
* Market leader in advanced surgical medical technology
* Get involved in complex medical procedures to truly save lives.
Join our dynamic Ethicon team, working with industry-leading products and driving your career forward.
We offer exceptional training and are proud to be Great Place to Work® Certified 2022 & 2023.
THE OPPORTUNITY
An opportunity has become available for an experienced Product Specialist to join our Ethicon Surgical team, managing a well-established and growing territory across a number of key hospitals in and around West Brisbane & Toowoomba.
You will be responsible for a range of cutting-edge medical products used in a variety of minimally invasive and open surgical procedures.
By partnering with surgeons, nurses and procurement staff within the hospital environment, you will focus on developing long term relationships with these customers to achieve sales growth and targets.
If you are a driven, organized and sales and service-oriented individual with a strong desire to learn and grow in the medical device field, we want to hear from you!
RESPONSIBILITIES
* Responsible to develop and maintain key clinical relationships which foster product adoption
* Sell designated clinical products (e.g.
NPI) within a specific geographical territory using surgeon or account based business plans which drive
* action and outcomes in a timely manner.
* Actively uses TVA (daily) to capture all customer interactions, report competitive activity and to optimise cross selling opportunities and support
* initiatives which build ONEMD
* Actively purse tender/ contract opportunities in a timely manner
* Complete 'boot stock' counts/ consignment counts in accordance with customer expectations and company policy
ITS ALL ABOUT YOU
* A track record of sales success within a hospital environment, ideally in medical devices
* Experience and confidence to work under pressure in the operating theatre environment.
* Tertiary education within Medical Science, Biomedical Engineering, or related fields
* Possess a natural aptitude and passion for technology.
* Exhibit an ability to trouble shoot and remain calm under pressure.
* Be passionate about delivering exemplary patient outcomes.
* Love working as part of a cohesive team, always willing to lend a hand and share the load.
COMPANY CULTURE
* Competitive remuneration package.
* Continuous training and support.
* Award-winning leadership development programs.
* Inclusive, flexible, and accessible working arrangements.
* Equal opportunity employer supporting diversity and inclusion.
WHY CHOOSE US:
* Competitive remuneration package and continuous training.
* Supportive environment with award-winning leadership development programs.
* Inclusive, flexible, and accessible working arrang...
....Read more...
Type: Permanent Location: Brisbane, AU-QLD
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:37
-
Job Description
Cilag AG is an international production company of the pharmaceutical division Janssen of the Johnson & Johnson Group and manufactures pharmaceutical and medical products as well as chemical agents (APIs) for the global markets at its production site in Schaffhausen.
Thanks to our innovative products, processes and technologies, Cilag AG is today one of the leading pharmaceutical companies in Switzerland and at the same time a strategic launch and growth site.
Within the Quality Control (QC) department, we seek a dedicated personality - entry immediately or as agreed on.
Main Tasks
• Deputy of the laboratory lead in administrative and professional management of the laboratory for Combination products.
• Responsible for meeting deadlines and correct execution of analysis orders and method transfers, processing of investigational testing and maintenance activities in the laboratory.
• Authorised for raw data review and verification of results in eLIMS as well as QC releases.
• Processing and review of Lab Events, Lab Deviations and CAPAs.
• Support implementation of New products introduction
• Change Control-Ownership, Action-Owner & Assessor in the Change Control system for the subordinate laboratory.
• Responsible for cleanliness, orderliness as well as compliance with GMP, safety and work regulations in the laboratory.
• Preparation of control regulations, work instructions and SOPs.
The offered job in the QC FF SM Combo laboratory team offers a responsible GMP position in the pharmaceutical industry.
Interfaces to numerous local and global departments (such as the development department, various QC departments, Quality assurance and pharmaceutical production departments) as well as the work for new equipment introduction on site make the daily activities extremely interesting and varied.Qualifications
Your Profile
In addition to an analytical thinking and structured way of working and strong team and communication skills, you can tackle challenges in a solution-oriented and systematic way, you can solve complex and multi-layered tasks and set your priorities in a correct manner.
In addition to your assertiveness, you are ready to take responsibility and enjoy driving projects forward.
You also have the following qualifications:
• You successfully completed your science or technology studies, preferably with a focus on the pharmaceutical, (bio-)medical engineering or life science fields, or you have several years of experience as a laboratory assistant in quality control, preferably in a GMP-environment.
• You have very good organizational and communication skills, a customer-oriented approach and "can do" mentality.
• You have very good knowledge of analytical/physical methods.
• You have first experience in project management
• You have experience in the review of analytical data and GMP documents.
Experience in dealing with eLIMS are beneficial.
• You have very good knowledge in the appli...
....Read more...
Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:36
-
Position Summary:
(Briefly state the objectives of this position)
A Site Manager II (SM II) serves as the primary contact point between the Sponsor and the Investigational Site.
A Site Manager II is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.
Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols.
A Site Manager II may contribute to process improvement, training and mentoring of other Site Managers.
Principal Responsibilities:
(List Major Responsibilities and duties of the position.
Describe scope of responsibilities.)
1.
Acts as primary local company contact for assigned sites for specific trials.
2.
May participate in site feasibility and/or pre-trial site assessment visits
3.
Attends/participates in investigator meetings as needed.
4.
Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
Responsible for the implementation of analytical risk based monitoring model at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
5.
Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
Responsible in close collaboration with LTM and central study team for the activities during site activation phase in order to speed up the process and activate the site in shortest possible timeframe.
6.
Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas.
7.
Ensures site study supplies(such as Non-Investigational Product (IP), lab kits, etc.) are adequate for trial conduct.
8.
Ensures that clinical drug supplies are appropriately used, handled and stored and returns are accurately inventoried and documented.
9.
Arranges for the appropriate destruction of clinical supplies.
10.
Ensures site staff complete data entry and resolve queries within expected timelines.
11.
Ensures accuracy, validity and completeness of data collected at trial sites
12.
Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs)/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropria...
....Read more...
Type: Permanent Location: Chengdu, CN-51
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:35
-
Business Development - Joint Reconstruction
• Work with industry renowned robotics
• Exceptional training provided to start a new chapter in your career.
• Great Place to Work® Certified - 2023
DePuy Synthes is driven by passionate and highly motivated individuals who create a fast and dynamic work environment.
Our QLD Joints business is growing with exciting new products, a focus on patient outcomes, service and education of the orthopedics community.
We offer exceptional training and are proud to be Great Place to Work® Certified 2023.
THE OPPORTUNITY
An opportunity has become available for a Business Development Manager, Orthopaedic joints to join our DePuy Synthes team.
In this position you will lead in executing surgeon conversions via the Smart surgery strategy and meet/exceed a planned number of surgeon conversions resulting in sales targets on a state-wide basis to grow business.
In this unique role, you will be required to work with the State Joint's sales leadership and sales teams to identify, prioritize and action surgeon conversion plans.
This is a position that will require an experienced marketing professional with exceptional leadership qualities to take on the challenges of growing the business, building customer relationships and managing and developing a high performing sales team.
RESPONSIBILITIES
• Proven success in a marketing position
• A successful track record in the orthopaedic or surgical medical device sector is preferred;
• A relevant background in Physiotherapy, Data Science would also be highly considered;
• Strong strategic thinking skills
• Demonstrable leadership qualities to motivate and engage a dynamic sales team
• Strong interpersonal and communication skills, both written and verbal
• Capacity to make commercial decisions based on sound business knowledge
• Ability to deal with ambiguity and change
• Decision making ability in complex situations
• Strong business planning, effective selling and negotiating skills
• Ability to build effective long-term relationships both internally & externallyITS ALL ABOUT YOU
• Tertiary qualification in a health-related field with knowledge of the anatomy and physiology.
• Proactive problem-solving and effective communication skills.
• Aptitude for understanding technical devices and technology.
• Comfortable working in a team environment, but also be extremely self-motivated when working alone.
• Ability to perform under pressure in an operating theatre environment.
• Excellent communication, organizational and customer relation skills.
COMPANY CULTURE
• Competitive remuneration package.
• Continuous training and support.
• Award-winning leadership development programs.
• Inclusive, flexible, and accessible working arrangements.
• Equal opportunity employer supporting diversity and inclusion.
WHY CHOOSE US:
• Competitive remuneration package and continuous training.
• Supportive environment with award-wi...
....Read more...
Type: Permanent Location: Brisbane, AU-QLD
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:33
-
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/ .
Johnson & Johnson is recruiting for an Associate Director, Clinical Project Scientist, Oncology.
The position can be located in Spring House, PA; Raritan, NJ; High Wycombe, UK; Beerse, Belgium; Breda, Netherlands.
Remote work options within the United States, United Kingdom and European Union may be considered on a case-by-case basis and if approved by the company.
As the Associate Director, Clinical Project Scientist, you are a responsible member of a clinical team dedicated to the development and execution of clinical strategies and the clinical and operational implementation of a complex compound program.
The Clinical Scientist provides active scientific contribution to a cross-functional clinical team developing a molecular entity.
The Clinical Scientist provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and clinical study reports and supports preparation of relevant documents for regulatory filings.
The Clinical Scientist will collaborate with Study Responsible Physician(s) in monitoring of clinical trial conduct.
This role involves extensive team matrix interactions with colleagues from a number of different disciplines.
Primary Responsibilities Include:
* Supports medical monitoring and reporting, evaluates clinical trial adverse events, reviews clinical laboratory results
* Participates in preparation of clinical development plans, trial protocols and clinical study reports
* Interacts with clinical investigators
* Support Clinical Operations during trial set up, conduct, monitoring, and closeout
Assists data management with the review of clinical data and query resolution
* Works closely with Quality Management & Assurance to ensure flawless execution of clinical trials
* Assists with drafting responses to questions from Ethics Committees and Health Authorities
* Supports integrated document development for marketing authorization filing
* Interprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions
* Supports preparation for the FDA Advisory Committee and EU Oral Explanation
* Assists Regulatory Affairs in the development of drug regulatory strategies
* Support general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillance
* R...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:32
-
Department:
The Bioprocessing Department of Operations is responsible for the quality and safety of processes and the equipment used by the Fermentation, Pre-culture, Bioreactor Assembly, Primary Recovery, Downstream Processing and Column Packing departments.
In addition, the department is responsible for investigating and immediately solving (technical and quality-related) deviations in the production process, including support in outside office hours as part of on-call duty.
The department leads and participates in various projects to optimize and implement new equipment and processes.
Job Description:
As a Manufacturing Process Specialist/ Equipment Engineer, you are responsible for the availability and functionality of the equipment required for the production purposes.
This includes:
* Work with cross functional team members, incorporating external manufacturing partners to ensure equipment meets varied quality, EHSS and compliance requirements
* Initiate and lead process and/or equipment improvement projects.
This includes leading and executing Change Control processes, managing Business Improvements and defining User Requirements in consultation with a multidisciplinary team.
Ensure that value-added improvements in the areas of capacity, safety (EHS&S) and quality (GMP) regarding equipment and/or process are implemented
* Participate in NPI projects and (global) multidisciplinary projects as an extended team member.
* Develop and sustain a long-term strategy for the asset such that manufacturing capacity remains adequate.
Ensure that an Asset Team is in place to ensure life cycle management of the equipment.
* Actively lead and/or participates in investigations into deviations in production processes, identifies corrective and/or preventive actions and ensures that these are dealt with adequately and within agreed timelines.
Provide first line support to manufacturing by, for example, providing expert advice to the shop floor in case of process issues.
Take part of on-call duty for troubleshooting of process disturbances in collaboration with team of Business System Owners.
Are you a hardworking team player, with a 'can-do' mentality and a good eye for technical challenges? Then we are looking for you!Qualifications:
* Higher professional education (HBO) or university education (WO) education, in a relevant field (e.g.
pharmaceutical sciences, biotechnology, biochemistry, life sciences, biological engineering, etc).
* 4-2 years' experience in a biotechnology or biopharmaceutical industry environment.
* Experience with downstream production processes and equipment.
Preferably experience with/knowledge of both upstream and downstream processing.
* Affinity for production equipment and automation systems (e.g.
DeltaV).
* Able to work in a high quality environment (GMP)
* Can work well both independently and in a team.
* Good Data Analysis skills
* Good organizational chan...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:32
-
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/.
Janssen Research & Development, L.L.C, a member of the Johnson & Johnson Family of Companies, is recruiting for a Director/Senior Director, Clinical Rseearch Physician for Late Development Oncology.
The preferred location for this position is Spring House, PA, but consideration could be given to other locations.
Up to 25% travel may be required.
The Medical Director/Senior Medical Director will contribute to the development and oversee the execution of oncology clinical research studies, ensuring consistency and quality, across the assigned development program.
This person will work closely with the clinical project scientist team and Clinical Leader in Late Development, in collaboration with other functional disciplines, including GCO, Data Management, Statistics, Regulatory, QMMC, and GMS to ensure flawless and integrated execution of study start-up planning, oversight, and reporting of clinical studies in Oncology.
Together with the Clinical Leader, the Study Responsible Physician will represent the clinical team in governance and committee meetings relating to the overall strategy and operational implementation of the clinical studies in the development plan.
ESSENTIAL FUNCTIONS:
• Lead the project scientists, ensuring appropriate training, mentoring, and supervision across the assigned study/studies within the clinical development program.
• Work closely with functional partners (Data Management, Biostatistics, Regulatory, GCO, QMMC, GMS) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in late development in close collaboration with key functional stakeholders.
• Provide support for clinical study/studies within a development program including:
• Working closely with the colleague study responsible physicians and clinical project scientists in collaboration with GCO and GMS to ensure comprehensive medical monitoring, thorough and timely responses to address site issues and eligibility questions, and detailed, real time review of serious adverse events and deaths.
• Working in partnership with colleague study responsible physicians and clinical project scientists to ensure development of high quality study protocols including use of consistent processes/standards across studies.
• Collaborate with the Clinical Leader, Clinical Project Scientists and Procurement on key study design elements including assessment of complexity and cost of p...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:29
-
Johnson & Johnson Global Services, the global shared services organization supporting the businesses of Johnson & Johnson, performs select functional work in a consistent manner across regions and sectors using simplified, standardized end-to-end processes and state-of-the-art technology.
The vision of Johnson & Johnson Global Services is "to be trusted business partners who deliver increasing value by creating and sustaining globally standard world-class services that enable the power of Johnson & Johnson."
There are more than 2,000 employees in Human Resources, Finance and Procurement who work for Johnson & Johnson Global Services in key service centers located in Manila, Suzhou, Prague, Bogota and Tampa, as well as in local country-based hubs.
SENIOR CASH COLLECTOR WITH GERMAN
Location: Prague
Contract: full time, permanent contract
The responsibilities & the impact YOU will have:
* Cash Collection for assigned region and customers according to the defined procedures and finance principles and legislation
* Management of Aging buckets
* Selected Accounts Receivables tasks
* Selected Credit Management tasks
* Respond to specific questions from local organizations, customer service, audit, finance reconciliation and invoice processing groups and clarify situations when necessary
* Making outbound calls and responding to inbound calls promptly according to processes
* Researching and resolving disputes and deductions that would otherwise delay or prevent payment of accounts receivable
* Placing accounts on credit hold, and releasing orders from credit hold within scope of authority
* Evaluating credit risk, making recommendations on and setting credit limits according to the defined procedures
* Work with credit reports and monitoring from credit agencies
* Meet dashboard metrics related to Cash Collection
* Perform all I2C procedures as required, in a timely manner
* Perform monthly analysis of DD customers
We would love to hear from YOU, if you have:
* Strong communication skills on the phone combined with customer and service orientation
* Experience in a similar job in finance / accounting / customer service environment
* Ability to solve difficult situations using own judgment and sense of initiative
* Eye for detail
* Strong analytical skills
* Proficient in German (written and oral) & good level of English (written and oral)
* Team player
This is what awaits YOU at J&J:
* An opportunity to be part of a global market leader.
* A dynamic and inspiring working environment.
* Many opportunities to work on challenging projects and assignments.
* An opportunity to participate in employee engagement activities on a voluntary basis based on individual preference
* Possibilities for further personal as well as professional development.
* Many employees benefits:
+ 5 weeks of vacation, home office, fle...
....Read more...
Type: Permanent Location: Prague, CZ-10
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:27
-
Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Engineer, Automation - CAR-T!
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We are Janssen.
We collaborate with the world for the health of everyone in it.
Learn more at www.janssen.com and follow us @JanssenGlobal.
Janssen Biotech, Inc.
is part of the Janssen Pharmaceutical Companies.
Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy.
This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR-T platform and investigational treatment.
Are you interested in joining a team that is passionate about improving the lives of cancer patients? We work on the most sophisticated treatment options available today.
To support the global CAR-T program, Janssen is rapidly growing its manufacturing and laboratory capabilities.
This position offers a perfect environment to transform CAR-T Cell Therapy manufacturing and the underlying supply chain systems, into something unique given the limited amount of Cell Therapy manufacturers worldwide.
Apply today for this exciting chance to be part of the #CAR-T team!
Our Raritan, NJ Cell Therapy facility is scaling up operational flows to serve more patients and meet the highest quality standards without compromising manufacturing efficiency.
This exciting new role reports to the Site Lead of CAR-T Supply Chain Systems and will be tasked with the enhancing Raritan's current Automation / OSI-PI capabilities.
The individual will design, plan, and implement Process Level Automation with the goal to transform the site into a paper-less manufacturing facility.
The Senior Engineer should be passionate about data and will collaborate with Janssen's CAR-T supply chain team to acquire business insights and propose data-driven solutions.
This is an outstanding opportunity to sit on an E2E Supply Chain team and develop next generation automation knowledge and business experience.
A fantastic role for high potential talent seeking accelerated career development and growth.
Key responsibilities:
* Act as Technical Business/Process Owner for the site's OSI-PI Data Historian.
* Lead and improve the capabilities of CAR-T Process Level Automation systems (OSI-PI, Equipment PLC/SCADA, BMS, EMS, IDP (Instrument Data Platform) in compliance with site local and global procedures.
* Configure and manage system integrations, user administration, performance monitoring, a...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:23
-
Caring for the world, one person at a time, inspires and unites Johnson & Johnson.
J&J embraces research and science - bringing innovative ideas, products and services to advance health and well-being.
Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
J&J has more than 250 companies located in 60 countries around the world.
At the Janssen Pharmaceutical Companies of Johnson & Johnson we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We are Janssen.
We collaborate with the world for the health of everyone in it.
Learn more at www.janssen.com and follow us @JanssenGlobal.
The ATSC New Site Project Leader is fully accountable from start to regulatory approval for leading the project team that will deliver a New Greenfield CART Manufacturing facility to be located in the USA (TBD).
This plant will supply lifesaving medicines for patients for J&JIM.
The new site startup leader will be responsible for shaping the overall planning of the project, development of a new manufacturing site location including engineering, construction, equipment delivery, commissioning & qualification, hiring and training program for all new J&J employees, startup and FDA regulatory approval of the first product.
The plant will employ ~850 FTE when in full operation (80%/20% - JNJ vs Contractor) and will require approximately 1000 engineers, equipment vendors and craftsman to design & build the facility.
Overall schedule for new facility from CAR) to commercial FDA approval is 5 years.
1.
Strategic Planning: Develop and implement the strategic vision for cell therapy site build engineering, aligning it with the organization's objectives and growth plans.
- Evaluate and recommend suitable sites for cell therapy facilities, considering factors such as location, infrastructure, regulatory compliance, and scalability.
- Work closely with cross-functional teams, including scientists, regulatory affairs, and operations, to ensure alignment of engineering activities with business goals.
2.
Project Management: Plan, coordinate, and oversee all aspects of cell therapy site build projects, including facility design, construction, commissioning, and validation.
- Collaborate with architects, contractors, vendors, and regulatory authorities to ensure compliance with relevant guidelines, codes, and regulations.
- Develop project budgets and timelines, monitor progress, and manage resources to ensure timely and within-budget project completion.
3.
Engineering and Design: Provide engineering expertise in the design and layout of cell therapy facilities, ensuring compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP), and other industry standards.
- R...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:23
-
Janssen Biotech, Inc., is recruiting for a Group Product Director (GPD), Professional Marketing, Multiple Myeloma (TALVEY) located in Horsham, PA.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/ .
This position is a critical part of the U.S.
multiple myeloma (TALVEY) marketing team.
The GPD, Professional Marketing, will be responsible for leading a team accountable for the development and execution of the U.S.
professional marketing launch strategy.
This role will function as a leader on the TALVEY marketing team and will report directly to the Director of Marketing.
The GPD will be responsible for the leadership of direct reports and must work closely with multiple functions including Business Analytics, Sales, Sales Training, Franchise Marketing, Finance, Medical Affairs, Real World Value & Evidence (HECOR), Strategic Customer Group, Corporate Communications, and outside vendors to effectively execute key commercial activities.
In addition, this GPD will also collaborate closely with the leaders across the Multiple Myeloma and Bispecific Portfolio.
Responsibilities include but limited to:
* Lead development of short- and long-term professional marketing strategies and tactics for TALVEY and maximize the growth of the business.
Set clear strategy to optimize execution.
* Manage professional agency of record and other specialty agencies to implement HCP tactics and training.
* Lead media and digital strategy and asset creation for HCP audience.
* Manage budget, including all aspects of agency and media spend.
* Partner with market research, competitive intelligence, and analytics to deepen key insights for the brand, market & current/future indications.
* Play a meaningful role partnering with cross functional partners including Global, US Medical Affairs, Commercial Excellence, Sales Leadership, Finance, Oncology Franchise marketing and agency partners to develop professional marketing plans and tactics for the U.S.
business.
* Lead HCP engagement strategy including collaboration with market development team to ensure strategic message alignment with KOLs and peer-to-peer programs and education.
* Provide input to forecasts for product line and updates throughout the year.
* Coordinate promotional activities with sales management and deliver strategic content for field meetings.
* Partner with Sales Training on product training requirements and execution to the field.
* Supports franchise team cross-functional initiativ...
....Read more...
Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:21
-
Johnson & Johnson's Global Tax Operations Team is seeking a Tax Manager - Global Tax Technology in New Brunswick, NJ.
The Tax Manager will be responsible for providing operational support to our Country Tax Centers as well as our business operations currently using our Corporate Vertex O Series Indirect Tax Engine.
This position will also drive new Vertex projects supporting Indirect Tax compliance, reporting & analytics.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/.
The Global Tax Technology Team partners with Tax Operations and Tax Planning as well as J&J IT and external vendors to identify technology solutions that enable efficient, accurate, and sustainable tax reporting, compliance and planning activities.
Key Responsibilities Include:
* Provide Operational Support of the Corporate Instance of Vertex O Series Tax Determination Engine and associated transactional ERP platforms and infrastructure
* Act as an administrator for the global Vertex O Series
* Manage functional design of Vertex O Series and accelerators
* Manage Vertex O Series functional and infrastructure upgrades
* Manage root cause analysis and solutioning in support of tax operations and deliver organizations incident reporting for Vertex O Series
* Create & Update Standard Operating Procedures and work instructions for Vertex O Series
* Manage SOX and operational controls related to Vertex O Series
* Perform Change Control, User Access Management and troubleshooting of issues related to Vertex O Series
* Perform Application Lifecycle Maintenance Activities related to Vertex O Series
* Develop and present recommendations related to new Vertex O Series Deployments and related applications
* Lead new Vertex O Series and related applications deployments including development of business case, deployment schedule, project plan & cross functional resource requirements
* Prepare and maintain project expense overviews, project status report and communication with key stakeholders for Vertex O Series deployments
* Perform data integration, data transformation specifications based on business rules, process methodology from source systems
* Provide Master data support for material and customers by interacting with the Tax COE and the SC Master Data Team
* Support special projects and automation opportunities
* A minimum of a bachelor's degree is required with a preference in Finance, Accounting, Information Technology or related fie...
....Read more...
Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:20
-
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/ .
Johnson & Johnson is recruiting for a Clinical Project Scientist, Oncology.
The position can be located in Spring House, PA; Raritan, NJ; High Wycombe, UK; Beerse, Belgium; Breda, Netherlands; or Issy-les-Moulineaux, France.
Remote work options within the United States, United Kingdom and European Union may be considered on a case-by-case basis and if approved by the company.
The Clinical Project Scientist (CPS) works in the Oncology Therapeutic Area Development group, and participates in the development, oversight, and execution of Ph I-IV clinical research trials working closely with Study Responsible Physicians and other Clinical Project Scientists.
The position reports to a more senior Clinical Project Scientist.
Primary Responsibilities Include:
• For ongoing clinical trials, this individual in collaboration with the Study Responsible Physician/other Clinical Project Scientists, will participate in or lead aspects of aggregate and participant level data, including patient screening/eligibility evaluation, PK/PD data, adverse events, efficacy, coding, and other data critical to study endpoints
• May participate in drafting protocol synopses, sections of full protocols, informed consent documents, and will review Case Report Forms (CRFs) and other data collection tools against draft protocols and central vendor scope of work
• May partner with the lead CPS/Cross Functional Trial Team to mitigate issues in initiation of clinical trials and may participate in review of Monitoring Guidelines, SET/IDMC Charter, Statistical Analysis Plan, Data Management, and Safety Management Plans
• May perform medical monitoring/reporting, evaluates ongoing clinical trial data
• May partner with the lead CPS drafting Medical Review Plan and Medical Review Forms
• May liaise with vendor laboratories, Translational Research lead, pharmacokinetic operations and/or biomarker operations to ensure sample collection, processing, and tracking
• May liaise with Integrated Data Analysis & Reporting team in set-up of data visualization tools (e.g., iDARTs)
• May participate in or lead aspects of training the central study team, local study team, site personnel or external vendors on protocol, disease evaluation criteria, or other specific aspects of the clinical study
• May participate in data review and drafting documents for Health Care Authority interactions.
• Will actively participate in mentorship and training oppor...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:19
-
About Johnson & Johnson
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 Descriptions:
We are looking for a dedicated Customer Services Specialist to ensure efficient order fulfilment and distribution of medical device supplies to hospitals and clinics.
The ideal candidate will facilitate smooth operations within the supply chain, contributing to the medical services community.
Responsibilities:
• Service as primary contact for healthcare customers, hospitals and clinics, ensuring their medical supplies needs are met.
• Collaborate with internal stakeholders on inventory readiness and price listing.
• Collaborate with warehouse and delivery team to deliver seamless supply chain distribution.
• Prepare invoicing, delivery documents and other administrative reports.
• Identify areas for policy and process improvement and make appropriate recommendations to management.
• Participate in project teams focused on developing, testing, implementing, and improving processes and procedures.
Key Qualifications & Requirements:
• 2-3 years of related experience.
Candidates with less experience may be considered for the role of Customer Service Assistant.
• Excellent customer service skills, with strong organizational abilities, prioritizing and multi-tasking in a fast-pace environment.
• Proficient in Microsoft Word, Excel, PowerPoint
• Good in spoken English and Chinese
• Experience in healthcare / medical industries is an advantage.
• Fresh graduates will be considered for this position.
This Is What Awaits YOU At J&J
• An opportunity to be part of a global market leader.
• A dynamic and inspiring working environment.
• Many opportunities to work on challenging pro jects and assignments.
• Possibilities for further personal as well as professional development.
• Many employees benefits:
• Supportive team culture, flexible working hours, employee development and wellness support,
• Refreshment in the workplace, company gym, JJ Club, corporate events
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
....Read more...
Type: Permanent Location: Mongkok, CN-91
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:18
-
Janssen Pharmaceuticals, Inc., Neuroscience, a member of Johnson & Johnson's Family of Companies, is recruiting for a Neuroscience Sales Specialist to support Northern Michigan including the entire Upper Peninsula and northern Lower Peninsula (Cadillac, Traverse City, Alpena, Mackinaw City).
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/.
The Sales Specialist, Neuroscience will:
* Devise and implement customer specific pre and post call selling approaches that evaluate and address the practitioners' perspectives and the institutions philosophies within compliance guidelines.
* Consistently use approved clinical studies and marketing aids to support the case for the value proposition when selling.
Position and adapt the message to meet the practitioner's, institutions, and company's objectives.
* Develop and execute on comprehensive business plan that includes but not limited to opportunities and challenges in local market, key strategies and tactics to drive the business, maximization of resources available as well partnership with key business partners and stakeholders in order to drive sales in local geography.
* Develop a territory coverage plan that maximizes selling time with all account professionals.
Adjust the schedule to increase access to key stakeholders, including coverage of all shifts.
Institute strategies to increase access to all key stakeholders.
* Maximize and customize the value proposition and influence contract implementation processes within the assigned institutions.
Hold hospital stakeholders accountable to the institutional contract.
* Develop and apply knowledge of payer access and affordability landscape in the territory regarding the company's products.
* Devise and institute an integrated business plan that includes clear strategies and tactics to target key accounts utilizing all available resources, while aligning the plan with the district's, regions, and company's goals.
* Analyze business analytics to recognize territory opportunities, strengths, and trends, and to monitor the effectiveness of the business plan.
Adjust the plan to minimize the impact of competition and to maximize sales opportunities.
#Neuroscience #Janssenbreakthrough #mycompanyRequired Qualifications:
* A minimum of a Bachelor's Degree
* A valid driver's license issued in one (1) of the fifty (50) United States
* A minimum oftwo (2) years of relevant work experience in healthcare sales/account management, or busi...
....Read more...
Type: Permanent Location: Traverse City, US-MI
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:16
-
Global Data Manager Specialist
Location: South Africa
At Johnson & Johnson Innovative Medicine, what matters most is helping people live full and healthy lives.
We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time.
Within Integrated Data Analytics & Reporting (IDAR), the Data Management and Central Monitoring (DTCM) team has a new opportunity for a Global Data Manager Specialist to be located South Africa.
As a Global Data Manager Specialist, you'll operate in a pivotal role, overseeing and ensuring the success of multiple trials across varying complexities.
This is an individual contributor role, and whether leading or participating in projects, you'll wield your expertise to guide decisions, influence processes, and foster collaboration among internal and external stakeholders.
Diversity & Inclusion are crucial to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions!
Are you ready to join our team? Then read further!
Key Responsibilities:
Strategic Leadership: Collaborate with CROs, trial stakeholders, and internal teams to define and align data management expectations for assigned trials.
Drive improvements in deliverables through proactive communication and feedback.
Requirements Gathering and Conventions: Lead the collection of content and integration requirements for electronic CRFs and data collection tools.
Establish quality expectations and standards for clinical data, ensuring clear structure and content alignment.
Oversight and Quality Assurance: Implement trial-level oversight controls as outlined in the oversight plan and QC process.
Ensure accuracy and compliance of clinical data management documents with regulatory guidelines and internal standards.
Inspection Readiness: Oversee real-time inspection readiness of data management deliverables.
Participate in regulatory agency audits and internal inspections as necessary.
Planning and Tracking: Lead the planning and tracking of data management deliverables, ensuring adherence to timelines and quality standards.
Collaborate with clinical working groups and stakeholders to meet trial needs optimally.
Best Practice Sharing: Spearhead the identification and dissemination of best practices within the organization.
Drive process, system, and tool improvement initiatives to enhance data management practices.
Education and Training: Deliver presentations and training sessions to investigators and site monitors.
Undertake responsibilities of a Clinical Data Manager as needed.Experience & Education Requirements:
* BA/BS degree or equivalent professional experience.
* Minimum 5 years' proven experience in data management
* Minimum 3 years as a Senior Global Data Manager, wi...
....Read more...
Type: Permanent Location: Johannesburg, ZA-GT
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:16
-
National Sales Manager (Oncology)
Location.: Poland
Full time job
The National Sales Manager is responsible for leading a sales team in the achievement of pharmaceutical product sales to new and established specialty accounts such as medical specialists, long-term care facilities, or hospitals to achieve sales objectives and greater market penetration.
Furthermore, the National Sales Manager has to ensure Execution Excellence when rolling out commercial strategy and tactics.
Essential duties and responsibilities:
* Execution of marketing strategy implementation to achieve both quantitative and qualitative sales targets
* Sales Force Efficiency - planning, deployment and analyzing of field activities, based on the CRM system and available data
* National territory management in collaboration with BI and CRM team
* Current, deepened analysis of sales results (effects) and activities related to sales representative's work - threats identification and proposing solutions to achieve both quantitative and qualitative targets.
* The Field Force team management, including coaching (frequent field visits), motivating, and preparing development & training plans.
* Providing constructive feedback and development of the team's sales skills, required to achieve set targets
* Building partnership relations with local KOLs and hospital decision-makers (hospital directors, medical directors, public orders departments)
* Co-creating marketing strategy for all products belonging to the Therapeutic Area
* Bottom-up planning in partnership with Brand Manager
* Cooperation with Brand Manager to deliver real data from the market to optimize marketing strategy
* Cooperation with Medical Affairs Managers to deliver information about medical education needs from the market
* Capturing Competitive Intelligence (CI) data and preparing monthly CI's reports
* Planning, monitoring, and realization of an operational budget
* Member of Country Value Team
Requirements (knowledge, education, skills):
* Proven experience in the pharmaceutical industry (sales or marketing), min.
6 years
* Willingness to travel (all over the country) and valid driver's license (category B)
* Experience in sales team management on the hospital market will be an advantage
* Knowledge of tender procedures and rules for the implementation of drug programs
* Experience in partnership with the Medical Department, Business Intelligence and Digital/CRM teams
* Education: University / Bachelor's Degree or Equivalent, preferably in a relevant business-related discipline
* Strong leadership skills, ability to structure and further develop a team of people, retain motivation, and infuse spirit relevant to the company culture, vision and business strategy
* Ability to challenge the "status quo" and recognize internal and external market complexity to act with courage promoting compliance to drive...
....Read more...
Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2024-04-14 08:48:15
