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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 PTD, we collaborate to develop robust manufacturing processes and quality control systems to efficiently transform scientific ideas into products.
We reliably deliver quality products to patients enrolled in clinical studies around the world.
We excel in our work by creating an engaging and inclusive environment where everyone can bring their skills and talents to developing innovative medicines.
This position is part of the Synthetic Molecule Pharmaceutical and Solid State Development organisation (PTDC-P).
Within PTDC-P, we transform molecules to medicines through particle engineering, and develop and deliver customised clinical formulations and robust commercial drug products that benefit patients.
The Opportunity
As a Senior Scientist / Principal Scientist in Drug Product Development, you are responsible for developing robust formulations and lean manufacturing processes for oral dosage forms of new chemical entities.
In this position, you work closely with international teams, including scientists and management from other disciplines (chemistry, analytics, quality, regulatory, and commercial production), and you represent the department on technical development teams (CMC) and scientific boards.
Furthermore, you are driving scientific initiatives to ensure the department's scientific and technical excellence.
The main responsibilities of this challenging position include:
* Development and optimisation of clinical as well as commercial formulations and manufacturing processes for oral solid drug products using various manufacturing technologies (i.e.
batch and continuous mode), including the scale-up and transfers to commercial manufacturing sites to facilitate the successful process validation at the sites.
* Development and implementation of new and innovative drug delivery technologies that can be applied in regular portfolio projects.
* Application of statistical tools (e.g.
DoEs), risk assessment tools for QbD (e.g.
QRA, FMEA) and Modelling and Simulation tools.
* Regular review of scientific literature to extract relevant trends and integrate innovative concepts and technologies in the scientific strategy of the department.
* Active participation in scientific teams at Roche as well as external consortia.
* Authorship and review of technical reports, manufacturing instructions, process validation documents, and the CMC parts of regulatory submissions to support market authorisation.
* Contributing actively to the i...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-03-10 07:26:52
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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 Biological Core Technologies, a department within the Discovery of the pREDs Large Molecules Research , where the design, supply and development of next generation biologics is the primary focus.
We closely collaborate with our therapeutic areas and functions to convert therapeutic hypotheses into innovative therapeutics.
Job mission
We are looking for a collaborative Senior Scientist (m/f/d) to join us in shaping the future of protein chemistry.
In this role, you will guide a dedicated team of molecular biology and protein chemistry specialists, leveraging state-of-the-art technology to solve complex biological challenges.
You will oversee our bioconjugation strategies—both automated and manual—and drive the design of next-generation engineered proteins through meaningful partnerships with internal and external collaborators.
Your impact
* Empower a Team: Support and mentor a team of 6 to 9 experts in molecular biology and protein chemistry, fostering an environment where high-throughput automation and bioconjugation innovation can thrive
* Drive Innovation: Shape our therapeutic portfolio by developing advanced bioconjugation and protein engineering approaches, specifically focusing on next-generation antibody-based therapies
* Build Partnerships: Cultivate a culture of trust and effective communication with global partners to ensure our collective projects succeed
Your profile
* A People-First Leader: You enjoy helping others build the skills and mindsets they need to thrive.
You bring clarity to complex projects and help your team stay focused on outcomes that truly matter for patients.
* Technically Grounded: You bring 5+ years of experience in (site-directed) Bioconjugation technology, ideally within the ADC field, drug discovery, and advanced protein engineering.
Your deep understanding of biochemistry allows you to champion our technology and portfolio projects.
* Innovation-Minded: You are curious about liquid-handling automation and...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-03-10 07:25:18
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ERM is seeking a Construction Safety Specialist to support day-to-day construction field verification activities in Abilene, Texas.
The Specialist will spend most of their time in the field observing work, verifying that contractor activities align with project safety requirements, identifying hazards, and strengthening safe work practices across all trade partners.
Experience in data center construction is a plus, but not required.
A strong working knowledge of LOTO (Lockout/Tagout) and electrical safety is essential.
This is a full-time (40+ hours a week), limited-term role for approximately 6 months, with the possibility of extension, averaging 45 hours per week.
Responsibilities:
Construction Field Oversight & Daily Verifications
* Conduct daily field walks to verify contractor adherence to project and regulatory safety requirements.
* Observe high-risk activities (LOTO, energized work, working at heights, heavy lifts, confined space, equipment operations) and identify hazards in real time.
* Provide direct coaching, guidance, and actionable feedback to support safe work practices.
* Review JHAs, permits, and activity briefings for completeness and alignment with the planned scope of work.
* Support contractor orientations, onboarding, and field-level safety interactions.
EHS Program Application
* Identify and assess construction-related H&S risks and field conditions.
* Evaluate current practices against regulatory requirements and client standards.
* Apply client EHS programs, procedures, and expectations during daily field engagement.
* Verify alignment with applicable local, state, and federal H&S regulations.
Training, Engagement & Communication
* Support or deliver H&S training based on job-site hazards and regulatory needs.
* Participate in toolbox talks, safety stand-downs, coordination meetings, and trade-partner engagements.
* Share lessons learned and contribute to Significant Event (SE) or Significant Potential Event (SPE) communication.
Incident Prevention, Reporting & Response
* Report incidents, near misses, hazards, and unsafe behaviors immediately.
* Assist with incident investigations, root cause analysis, and follow-up actions.
* Collaborate with contractors to address and resolve identified issues.
Documentation & Reporting
* Maintain detailed documentation of interactions, inspections, coaching, and field observations.
* Track corrective actions and follow up through closure.
* Support client and internal reporting requirements, including daily/weekly summaries as needed
Requirements:
* Bachelor’s degree in environmental science, occupational safety, construction management, engineering, or related field (equivalent experience considered).
* 3–5 years of H&S experience in construction or industrial environments.
* Strong knowledge of LOTO, electrical safety, and high-risk construction activities.
* O...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2026-03-10 07:23:11
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ERM is hiring experienced Construction Safety Specialist to provide on-site support for our key pharmaceutical client in Kenosha, WI.
In this critical role, you will be responsible for providing on-site observation of construction activities from an EHS perspective, ensuring health and safety compliance with applicable regulations and existing company standards, and contributing to an environment where employee health and safety are preserved.
You will be present during all site activities and responsible for all health and safety activities, and the delegation of duties to any other project team members.
This is a full-time (40 - 72 hours/week), limited-term role for a duration of 12 months, renewable.
RESPONSIBILITIES:
* Engage with general contractors and subcontractors on behalf of the owner, as the owner’s representative.
* Promote client’s safety culture across contractor and subcontractor groups.
* Proactively identify uncontrolled hazards and influence safe work practices of general contractors and subcontractors on behalf of the owner.
* On-site observation of construction activities from an EHS perspective.
* Documentation of activities with respect to required EHS performance.
* Train on-site workers on EHS oversight program requirements.
* Train on-site subcontractors on EHS oversight program requirements.
* Help administer project directives given by the Client’s Environmental, Health, and Safety (EH&S) personnel throughout the project.
* Report on whether project staff and trade contractors are complying with the Client’s safety procedures and are working in accordance with the approved project-specific safety plan.
* Maintain required safety-related documentation on the project site, including, but not limited to, safety orientation training, Job Hazard Analyses (JHA), SDSs, pre-task assessments, and toolbox talk summaries.
* Participate in daily pre-shift coordination meetings to include review of the day’s activities and associated hazards.
* Review and comment on the General Contractor’s JHAs with project trades and obtain signatures prior to commencement of work.
* Conduct daily site inspections, focusing on work site orderliness and compliance with safety procedures and protocols.
Proposed corrections of safety deviations will be discussed with the General Contractor’s Safety Manager, and support will be provided for implementing corrective actions.
* Issue daily site observation reports for each site inspection.
REQUIREMENTS:
* Bachelor's degree in construction management, safety, or occupational health and safety, or a related degree preferred.
* 3+ years of on-site experience in construction-specific project health & safety.
* Certification in the field: CHST, ASP, and/or CSP are preferred.
* Pharmaceutical or high-tech project experience is highly desired.
* Strong knowledge of OSHA General Industry and constru...
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Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2026-03-09 07:12:52
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ERM is hiring experienced Construction Safety Specialist to provide on-site support for our key pharmaceutical client in Lebanon, IN.
In this critical role, you will be responsible for providing on-site observation of construction activities from an EHS perspective, ensuring health and safety compliance with applicable regulations and existing company standards, and contributing to an environment where employee health and safety are preserved.
You will be present during all site activities and responsible for all health and safety activities, and the delegation of duties to any other project team members.
This is a full-time (40 - 72 hours/week), limited-term role for a duration of 12 months, renewable.
RESPONSIBILITIES:
* Engage with general contractors and subcontractors on behalf of the owner, as the owner’s representative.
* Promote client’s safety culture across contractor and subcontractor groups.
* Proactively identify uncontrolled hazards and influence safe work practices of general contractors and subcontractors on behalf of the owner.
* On-site observation of construction activities from an EHS perspective.
* Documentation of activities with respect to required EHS performance.
* Train on-site workers on EHS oversight program requirements.
* Train on-site subcontractors on EHS oversight program requirements.
* Help administer project directives given by the Client’s Environmental, Health, and Safety (EH&S) personnel throughout the project.
* Report on whether project staff and trade contractors are complying with the Client’s safety procedures and are working in accordance with the approved project-specific safety plan.
* Maintain required safety-related documentation on the project site, including, but not limited to, safety orientation training, Job Hazard Analyses (JHA), SDSs, pre-task assessments, and toolbox talk summaries.
* Participate in daily pre-shift coordination meetings to include review of the day’s activities and associated hazards.
* Review and comment on the General Contractor’s JHAs with project trades and obtain signatures prior to commencement of work.
* Conduct daily site inspections, focusing on work site orderliness and compliance with safety procedures and protocols.
Proposed corrections of safety deviations will be discussed with the General Contractor’s Safety Manager, and support will be provided for implementing corrective actions.
* Issue daily site observation reports for each site inspection.
REQUIREMENTS:
* Bachelor's degree in construction management, safety, or occupational health and safety, or a related degree preferred.
* 3+ years of on-site experience in construction-specific project health & safety.
* Certification in the field: CHST, ASP, and/or CSP are preferred.
* Pharmaceutical or high-tech project experience is highly desired.
* Strong knowledge of OSHA General Industry and constru...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2026-03-09 07:12:52
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ERM is seeking experienced Wetland Delineators to support large‑scale field programs across the Gulf and West Region.
This role is ideal for candidates who excel in intensive fieldwork, lead data collection efforts, and apply rigorous ecological and regulatory methods.
As part of ERM’s Biological Field Services team, you will serve as a lead or co‑lead on wetland and waterbody delineations, maintain high technical standards, and produce defensible data for major infrastructure and permitting projects. This is a full time (60+ hours per week) limited-term role with a duration of 3 months, extendable.
Key Responsibilities
* Conduct wetland delineations following the 1987 Corps Manual and applicable Regional Supplements.
* Identify and document OHWM, hydrologic indicators, and geomorphic features of waterbodies.
* Conduct T&E species habitat assessments, evaluating habitat suitability and relevant ecological conditions.
* Collect and manage field data using submeter GPS and digital data‑collection tools.
* Contribute to survey documentation, including data forms, field notes, photo logs, and map review.
* Support report inputs and permit‑related documentation.
* Work safely as part of a field crew under ERM and client safety protocols.
Required Qualifications
* Minimum two (2) field seasons of wetland delineation experience using the 1987 Manual and Regional Supplements.
* Familiarity with Arid West and Great Plains Regional Supplements (or other applicable regions).
* Ability to interpret soils, vegetation, hydrology, NWI maps, aerial imagery, and topographic data for accurate field calls.
* Experience with submeter GNSS/GPS units and digital field applications.
* Ability to work long days (60+ hours/week), weekends, and extended rotations in remote or challenging conditions.
* Strong organizational and communication skills with a focus on high‑quality data collection.
* Valid driver’s license and clean driving record.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues.
We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic an...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2026-03-09 07:12:39
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What will your job look like?
The Resolution Specialist is responsible for managing complaints, incidents and accidents for designated Clients, in accordance with Client requirements and MTM Policies and Procedures for Quality & Compliance.
This position is location on-site in Norton, VA.
What you’ll do:
* Document, review, investigate, resolve and provide follow up for all complaints and complaint issues reported for assigned clients within the specified timeframe
* Closely adhere to client service level agreements to ensure complaints do not go out of compliance
* Obtain responses within 24-48 hours from Transportation Providers to complaints and complaint issues
* Provide immediate follow up for complaint responses that are not submitted within the specified timeframe
* Respond to client, Program Director, or Account Executive inquiries sent via email, or fax, within the specified timeframe
* Ensure accuracy of information in report prior to deadline submission
* Triage issues and provide assistance to MTM’s internal departments with complaint issues
* Assist with monthly trending information in regards to potential network inadequacies, transportation provider deficiencies, and training opportunities to applicable departments; report trends to leadership for further review
* Monitor and report incident/accident issues
* Monitor and report issues of non-compliance to the leadership staff and Network Management as indicated
* Compile weekly/monthly summaries of incident/accident investigations, findings, and resolutions as required
* Send out monthly Quality & Compliance Tips to transportation providers and Network Management regarding prevention measures identified
* Ensure all training documents received per Q&C request
* Create relevant workflows, and tracking mechanisms as assigned
* Perform activities and participate in quality improvement projects for the Quality Improvement Program(s) as assigned to ensure ongoing compliance with URAC standards
* Compile daily/weekly/monthly complaint reports to be submitted to designated clients per contract
What you’ll need:
Experience, Education & Certifications:
* High School Diploma or G.E.D.
* 2 years of customer service experience
Skills:
* Proficient in Microsoft Suite
* Strong and effective communication skills, with an emphasis on grammar and spelling
* Ability to tactfully question and obtain information
* Excellent organizational skills
* Excellent interpersonal skills
* Ability to manage multiple priorities required
* Ability to handle confidential information in a professional manner
* Strong problem solving skills
Even better if you have...
* Previous Quality & Compliance experience preferred
* Some college preferred
* A minimum of six months in the MTM Customer Service Center preferred
* Working knowledge of MTM Customer Ser...
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Type: Permanent Location: Norton, US-VA
Salary / Rate: Not Specified
Posted: 2026-03-08 07:35:51
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General Summary
Administers health and safety programs, including environmental policies in accordance with State and Federal OSHA compliance.
Under limited supervision, oversees the health and safety of Reser’s employee personnel and plant property.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principle Duties and Responsibilities
1.
Promotes and supports a culture of safety within the plant and company and coordinates plant safety committee activities and meetings. Advises and assists employees in adherence to company and local, state and federal regulatory standards.
2.
Oversees incident investigation and reporting procedures in collaboration with plant and corporate leadership for follow up to closure including root cause analysis.
3.
Tracks corrective actions, loss sources and trends.
Develops, monitors and communicates to local site leadership the associated KPIs.
4.
Utilizing safety management system regular follow up with local site leadership on incident and case management.
5.
Provides training on use of safety management system to local site staff who will utilize system.
6.
Applying continuous improvement practices, identifies waste in current processes and programs.
Discusses findings with local site leadership and Corporate Risk Management.
7.
Utilizing corporate standards and templates, facilitates in the implementation of local and facility specific compliance programs.
8.
Assists with property risk improvement opportunities to identify gaps in life safety and facility protection obligations. Completes actions to established targets and objectives for the site and oversees actions through completion.
in collaboration with site and corporate management.
9.
Assists in conducting safety and security audits and observations both formally and informally.
10.
Partners with leadership on environmental compliance and training.
11.
Develops and provides safety related resources and training. Maintains related tracking documentation (LOTO, Powered Industrial Trucks, Hazard Communication, Machine Guarding etc.).
12.
Administers employee safety training in the company ...
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Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2026-03-08 07:19:20
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eScholar Customer Support is looking for an exceptional talent to become our Customer Support Intern.
In this role, our intern will participate in three rotations with three focus areas per rotation.
Focus areas are Customer Support, Data Analytics, and Data Integration.
What your impact will be:
* Work closely with the Director, Customer Succes and the PS Team Leader to develop a sound understanding of all eScholar products
* Provide technical support to eScholar customers and manage incoming support issues via eScholar’s incident management system.
* Publish eScholar Analytics content to the customer analytics portal
* Participate in functional and technical design sessions
* Use and execute test plans written
* Work with Technical BA, customers & source system experts to understand reporting needs, underlying source data and associated business rules
* Use and edit test scripts to thoroughly test the accuracy and completeness of loaded data
* Gather end-user requirements for data dissemination and reporting
* Use various applications to analyze source system data and identify data quality issues and anomalies that will need to be corrected and/or handled in ETL routines
* Using ETL tools and/or SQL, develop data extract routines from a variety of disparate data sources and conform them to the eScholar Complete Data Warehouse product format
* Develop data visualizations using a variety of applications such as Tableau, AWS Quicksight, Microsoft Power BI, and others.
What we are looking for:
* Proficient in SQL
* Experience with Tableau, AWS Quicksight, Microsoft Power BI, and others.
* Experience with JavaScript, Python, CSS, and others
* Experience with version control and functional testing
* Experience with SQL Server, Postgres and Oracle
* Experience creating technical documentation
* Experience with AWS or Azure cloud-hosted applications
* Some prior experience with the education sector through internships
* Availability to work up to 25 hours/week
What will help you stand out:
* Attention to detail
* Very strong verbal and written communication skills
* Ability to work collaboratively and independently
* Proficient in MS Office
* Pursuing a BA/BS degree in Computer Science or a related field
* Willingness and ability to learn new tools and concepts
Salary
25/hr
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Type: Contract Location: Albany, US-NY
Salary / Rate: Not Specified
Posted: 2026-03-07 08:10:40
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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 EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Port Edwards and Wautoma, Wisconsin facilities.
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.
* Develop and maintain company environmental, health and safety programs at the facility.
* 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 w...
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Type: Permanent Location: Wautoma, US-WI
Salary / Rate: Not Specified
Posted: 2026-03-07 07:42:25
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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, Â 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
Unsere Pharma-Vision
Medikamente schnell zu den Patienten zu bringen und das beste Ergebnis für unsere Kunden zu schaffen.
Das ist es, was uns in Sterile Drug Product Manufacturing (SDPM) in Mannheim antreibt.
So tragen wir auch dazu bei, bis 2029 unser Ziel zu erreichen: 20 bahnbrechende Medikamente zur Behandlung der Krankheiten mit der gröÃten gesellschaftlichen Belastung bereitzustellen.
Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele groÃe Hoffnung und Zuversicht und deswegen müssen wir anders denken und arbeiten.
Mit dem Patient im Fokus setzen wir auf eine neue Organisation und zwar #WIRGEMEINSAM in SDPM! â
Deine Aufgaben
Als Senior Quality Assurance Manager / Qualified Person (m/w/d) förderst Du aktiv die Umsetzung unserer Lean-Mindset Kultur unter Berücksichtigung der Pharma Technical Operations (PT) Behaviours und Lean-Methoden und lebst diese vor.
Du bist im Lead bzgl.
der Sicherstellung der Harmonisierung und kontinuierlicher Verbesserung einzelner Prozesse und Vorgehensweisen in Abstimmung und Koordination mit den anderen Value Streams am Standort.
Darüber hinaus übernimmst Du folgende spannenden Aufgaben:Â
Lokale QA-Tätigkeiten, hierfür bist Du primär in Mannheim vor Ort
* Du unterstützt aktiv die Patientenversorgung mit kommerziellen und klinischen Arzneimitteln durch Sicherstellung einer GMP-konformen und termingerechten Freigabe von Arzneimittelchargen.
Die Berücksichtigung der gesetzlichen, regulatorischen und Roche internen Vorgaben sind Dir hierbei besonders wichtig.
* Selbständige Bearbeitung und Qualitätsbewertung komplexer Unplanned Events (UPE)
* Bei Bedarf Leitung und Koordination des lokalen Triage Teams zur Bearbeitung und Root-Cause-Analyse (RCA) von UPS innerhalb des verantworteten VS
* Coaching und Feedback von/an (Nicht-)Quality Vertretern zur Bearbeitung von UPE sowie bei Bedarf selbständige Bearbeitung und Koordination mit beteiligten Funktionen zur Bearbeitung von Planned Events (PE)
* Erstellung, Aktualisierung und (in Absprache mit Schnittstellen und Kollegen) Umsetzung eines inspektionsfesten Konzepts zur Quality Oversight sowie Vertretung von Qualitätsaspekten, aktive Unterstützung und Teilnahme an Audits und Selbstinspektionen
* AbschlieÃende, zusammenfassende Qualitätsbewertung von Bulk- und FINP Chargen und Koordination zur Chargenfreigabe notwendiger Aktivitäten
* Aufgrund der arzneimittelrechtlichen Vorgaben ist für diese TÃ...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2026-03-07 07:39:07
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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
Unsere Pharma-Vision
Medikamente schnell zu den Patienten zu bringen und das beste Ergebnis für unsere Kunden zu schaffen.
Das ist es, was uns in Sterile Drug Product Manufacturing (SDPM) in Mannheim antreibt.
So tragen wir auch dazu bei, bis 2029 unser Ziel zu erreichen: 20 bahnbrechende Medikamente zur Behandlung der Krankheiten mit der größten gesellschaftlichen Belastung bereitzustellen. Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele große Hoffnung und Zuversicht und deswegen müssen wir anders denken und arbeiten.
Mit dem Patient im Fokus setzen wir auf eine neue Organisation und zwar #WIRGEMEINSAM in SDPM!
Deine Position
Als Senior Leiter der Qualitätskontrolle (LQK) bist Du für die QC Analytik (mit Hauptfokus auf die mikrobiologische Analytik für Drug Product, Drug Substance und Direct Material sowie EMT) und deren Bewertung verantwortlich und bist in QA Funktion für die operativen Bereiche der Qualitätskontrolle zuständig.
Du nimmst die Funktion gemäß AMWHV §12 und 14 wahr.
Dir ist eine nahtlose Zusammenarbeit innerhalb QC sowie mit den jeweiligen Drug Product Einheiten besonders wichtig.
Als Schnittstelle zu globalen Funktionen wie z.
B.
Control System Specialists (CSS) oder Product Stuarts vertrittst Du den Standort Mannheim im globalen Netzwerk u.a.
im Rahmen von Harmonisierungsaktivitäten und zum Wissensaustausch.
Darüber hinaus übernimmst Du folgende spannenden Aufgaben:
* Sicherstellung einer GMP-konformen, effizienten und termingerechten Qualitätskontrolle von Arzneimitteln unter Beachtung aller gesetzlichen Rahmenbedingungen (AMG, AMWHV, ICH, Arzneibücher)
* Verantwortlich für die QC Analytik (mit Hauptfokus auf die mikrobiologische Analytik für Drug Product, Drug Substance und Direct Material sowie EMT) und deren Bewertung.
Dies erfolgt in enger Zusammenarbeit mit den Drug Product Einheiten
* Du bewertest die Prüfergebnisse bzw.
Arzneimittelqualität und bist für lnvestigations bei OOT bzw.
OOS Ergebnissen in der Abteilung in Zusammenarbeit mit der Qualified Person verantwortlich
* Verantwortlich für die Bemusterung (einschl.
Musterlagerung und Musterverteilung) sowie alle Prüfungen innerhalb der QC unter Beachtung der gesetzlichen Rahmenbedingungen (GMP, AMWHV, Arzneibücher, Arbeitssicherheit etc.)
* Wahrnehmung der QA/Q-Sys Funktion für die operativen Bereiche der Qualitätskontrolle.
Hierzu zählt die Genehmigung von Vorgabedokumenten wie z.
B.:
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2026-03-07 07:38:30
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PD&E Planner
Ardurra has an exciting opportunity for a Planner in our Project Development and Environment (PD&E) group in Orlando, Florida.
The position includes working with senior staff to prepare planning studies, alternative analyses, environmental impact assessments, and technical reports, including preparation of National Environmental Policy Act (NEPA) documents.
The ideal candidate will provide engineering and planning services supporting PD&E studies.
Essential Tasks
* Reviewing development plans for transportation system effects, infrastructure requirements, or compliance with applicable transportation regulations
* Documenting existing conditions and performing, analyzing, and summarizing research
* Working with our roadway design group to develop conceptual alternatives and design ideas for new or improved transportation infrastructure, such as interchanges, intersection improvements, pedestrian projects, and multi-modal facilities
* Collaborating with a team to complete feasibility studies, Efficient Transportation Decision Making documentation, PD&E studies, and other technical materials
* Performing QA/QC reviews to ensure completeness, accuracy, and conformity to engineering standards and practices
* Assisting in the pursuit of PD&E projects and other business development activities
* Assisting in the development of meeting materials, set up and break down of meetings, attendance, and facilitation
* Coordinating community review and public involvement activities for PD&E projects
* Identifying and coordinating with key stakeholders, special populations, and the general public
* Coordinating activities across multiple disciplines, both in-house and externally
Preferred Qualifications
* Bachelor’s degree in civil engineering, urban planning, economics, environmental or social science, geography, or a related field
* Ability to obtain a PE license or ACIP certification in the state of Florida once qualified.
* Three or more years of prior practical experience working on PD&E and transportation planning projects
* Familiarity with NEPA and Florida PD&E project requirements
* Proficiency with Microsoft Office
* Ability to communicate technical and complex information and to work well with others
* Possess attention to detail, organizational skills, and a positive attitude
* Ability to work independently
* Ability to multi-task and apply critical thinking skills
* Ability to work outside of regular business hours as needed (in case of public meetings or pop-up events)
* Ability to represent the client in a professional manner and maintain composure in tense environments
* Experience working in customer service is a bonus
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers. We nurture a family-like culture, striving to create a...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: Not Specified
Posted: 2026-03-07 07:35:00
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Ardurra is seeking a motivated and knowledgeable Environmental Scientist to join our staff in Palmetto, FL.
Our full-service environmental and ecological capabilities include support of client services in the areas of municipal and private development, utility permitting support, and agricultural activities permitting. We know the importance of protecting the environment while achieving project goals.
We believe that innovative thinking and up-front planning can lead to more cost-effective and successful project outcomes.
Primary Function:
The Environmental Scientist specializing in Wetland Delineation and Endangered Species will lead field and regulatory efforts focused on habitat mapping and identifying at‑risk wildlife, with an emphasis on gopher tortoises.
The ideal candidate will combine strong biological expertise with excellent communication skills, supporting both on‑the‑ground habitat assessments and public engagement related to species protection.
This role supports statewide conservation programs, implements permitting standards, and collaborates with agency partners, landowners, and conservation organizations to ensure long-term viability of protected species.
Primary Duties:
* Perform Habitat Mapping and Wetland Delineations
* Perform Listed Species Surveys, Permitting and Relocation Activities
* Habitat and Land Management Plans
* May serve as team leader in small projects and help train junior-level staff.
* May assist more senior scientists/engineers on large, more complex projects.
* Assists in the collection and analysis of data from sampling, reports, maps, drawings, tests and aerial photographs to evaluation, plan and permit projects.
* Performs site visits, field observations, and field data collection and/or field assignments for clients.
* May oversee work performed by lower-level scientists but does not typically have supervisory responsibility.
Education and Experience Requirements:
* Requires a 4-year degree in biology, environmental science, or related science
* 5 years’ related experience with State and Federal Environmental Permitting Processes.
This includes considerable experience in utilizing technical software and computer-related tools within the discipline
* This position is out of the Palmetto, FL Office Location- Local day trips with occasional overnight travel are a possibility
* Experience with State and Federal Environmental Permitting Processes
* May specialize in environmental science, soil science, GIS (Global Information Systems)
* Experience with protected species such as the gopher tortoise
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers. We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun. We are acutely focused on developing ...
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Type: Permanent Location: Palmetto, US-FL
Salary / Rate: Not Specified
Posted: 2026-03-07 07:34:54
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As part of the continued growth and innovation of our North American Corporate Sustainability & Climate Change (CS&CC) team, ERM has an opportunity for an experienced leader to join our global consulting firm as a Partner and become a true owner and shareholder in a business with sustainability at its heart.
We are looking for an established leader interested in being part of ERM’s thriving global community – outstanding professionals who combine strong consulting and business development skills with a strong technical foundation – to foster and expand a network of excellent client relationships across a variety of sectors. We seek an individual to help us drive the continued growth of ERM’s business through selling and delivering world-class services, recruiting and developing our next generation of leaders, and further advancing our reputation for CS&CC solutions, coupled with value-creation programs based on the rapidly evolving Low Carbon Economy Transition (LCET).
ERM, as the world’s leading sustainability consultancy, is uniquely qualified to advise Fortune 500 companies on climate strategy, disclosure, investor demands and the transition to a lower carbon economy.
Our global CS&CC practice is a clear market leader, providing highly innovative advisory services from Board engagement to operationalizing sustainability and climate change strategy across our client’s business.
Our team provides strategic advice to clients, including conducting a wide range of carbon accounting analyses, assessing transition and physical risks and opportunities, setting and implementing ambitious climate goals (e.g., net-zero and science based targets), embedding climate considerations/decarbonization into business strategy and disclosing through reporting and responding to investor inquiries.
With a target of reaching $50 million in sales by 2023 in North America, ERM’s CS&CC practice is one of the fastest growing in a business with annual double-digit growth.
ERM is also committed to taking a climate leadership position through “walking the talk” in our own business.
We have committed to net-zero across our operations by 2025 and we are strengthening our Science Based Targets to align to a 1.5-degree Celsius target.
This is a Partner-level opportunity for a senior-level professional looking to further their career with an equity stake with a global sustainable business consulting leader that supports the world’s leading organizations. A career as an ERM Partner is unique. Our partnership model offers unparalleled opportunities for leaders with ambition, vision and proven expertise, providing:
* The opportunity to contribute significantly to key decisions, including the overall strategic direction of our organization.
* Meaningful equity ownership with significant financial and intangible rewards.
* The ability to provide “thought leadership” on a wide range of technical and business issues impacting our c...
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Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2026-03-07 07:33:54
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At Harris, our culture is the foundation of everything we do.
We believe in respect for the individual, straightforward communication, relentless discipline in pursuit of operational excellence, and empowering people to make decisions at the point of contact.
We value common-sense problem solving, accountability, and continuous learning.
We also support both personal and professional dream realization, knowing that engaged people build exceptional products and partnerships.
If these values resonate with you, you’ll feel at home here.
If they don’t—Harris is likely not the right fit.
We’re seeking a Site Reliability Engineer (SRE) to ensure the reliability, performance, and scalability of our production systems.
You’ll blend engineering skill with operational discipline to build resilient services, reduce toil through automation, and partner with development and customer-facing teams to deliver consistently excellent experiences.
A critical component of this role includes customer support and customer-facing collaboration.
You will work directly with support teams—and at times with customers themselves—to troubleshoot issues, communicate clearly, and help drive solutions forward.
Because we believe bad news does not get better with time, transparency and timely communication are essential.
This role fits someone who thrives in an environment that expects ownership, reality-based decision making, and solutions—not problems.
This remote role welcomes candidates anywhere in Canada and the US.
Up to 5% of travel is required within North America.
A valid passport/visa is required for the travel.
Salary:
60-100K USD
80-120K CAD
What your impact will be:
* Monitor, maintain, and improve the reliability, availability, and performance of production systems.
* Collaborate with Customer Support to address escalated cases, ensuring timely, respectful, and clear communication.
* Engage directly with customers when needed to diagnose issues, explain technical details, or gather context.
* Bring customer feedback and recurring patterns back to engineering teams to drive long-term improvements.
* Build and maintain CI/CD pipelines and infrastructure-as-code environments (Ansible, Terraform, CloudFormation, etc.).
* Participate in on-call rotations and incident response, communicating early, often, and transparently.
* Conduct root cause analysis with a focus on deep understanding, cause-action clarity, and shared learning.
* Develop automation that reduces manual work and accelerates issue resolution.
* Contribute to documentation and knowledge sharing—because communication is only real when understanding is achieved.
* Make decisions at the point of contact and take ownership of outcomes, avoiding finger-pointing.
* Apply disciplined, practical thinking to solve problems quickly and effectively.
What we are looking for:
* 5–8+ years in Site Reliability Engineering, DevOp...
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Type: Permanent Location: Montpelier, US-VT
Salary / Rate: 100000
Posted: 2026-03-06 08:24:08
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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.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
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: Associate Manager - Biostatistician
The role of Biostatistician is to support the biostatistics and statistical analysis in terms of analysis dataset creation, statistical analysis and creation of statistical analysis tables and summaries in collaboration with statistical and programming colleagues, physicians, veterinarians, and/or medical colleagues.
Your Responsibilities:
* Prepare statistical analysis plans, including table under the supervision of senior statistical staff.
* 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.
* Generate randomization schedules from provided specifications under guidance from senior statistical staff.
* With mentoring, provide sample size calculations and review protocols for completeness and appropriateness of statistical sections.
* 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 an...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2026-03-06 08:22:15
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Safety & Health Manager
Job Description
The Safety and Health (S&H) Manager is responsible for developing, implementing, and overseeing safety and health programs within a tissue production facility, ensuring that all employees work in a safe environment in compliance with safety standards and regulations.
This role involves identifying potential risks, implementing preventive measures, and investigating incidents to drive continuous improvement.
The Safety and Health Manager will collaborate with various departments to promote a culture of safety and facilitate ongoing improvements.
Primary Location
Taiwan-Chung-Li
Additional Locations
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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Type: Permanent Location: Hsin Wu Hsiang, TW-TAO
Salary / Rate: Not Specified
Posted: 2026-03-06 08:11:44
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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
Deine Abteilung
Wir freuen uns auf Unterstützung und Deine Ideen im Team des Regional Customer Support Centers in Mannheim.
Wir sind verantwortlich für den technischen und applikativen Kundenservice im Bereich Molekulardiagnostik und Pathologie: vom technischen Produktmanagement über Trainings zur Bedienung von Analysegeräten bis zur telefonischen Hotline.
Während Deines Praktikums arbeitest Du zusammen mit unseren Spezialisten im Bereich der Laborsysteme zur medizinischen Diagnostik.
Hier sammelst Du Erfahrungen direkt an der Schnittstelle zwischen Technik, IT, Naturwissenschaft und Medizin und lernst unsere teils internationalen Kunden aus Labor und Krankenhaus in Deutschland, Österreich, der Schweiz, Belgien, der Niederlande, Griechenland und der Türkei kennen.
Deine Aufgaben
* Du unterstützt uns in der technischen und applikativen Hotline für unsere Kunden in Deutschland, Österreich und der Schweiz im Bereich der Pathologie.
* Dabei bearbeitest du eigenständig Kundenanfragen und dokumentierst diese in einem CRM System.
* Du unterstützt außerdem bei applikativen und technischen Serviceprojekten.
* Du erstellst Analysen und Reports für Controlling-Zwecke.
Dein Profil
* Studienstatus: Du bist eingeschriebene/r Student/in einem technischen oder wirtschaftlichen Studiengang und befindest Dich bereits in einem fortgeschrittenen Bachelor- oder Masterstudium.
Auch ein Praktikum in Deinem Gap Year ist bei uns möglich.
* Du hast Spaß am Kundenkontakt, verfügst über gute kommunikative Kenntnisse und liebst es, Probleme zu lösen.
* Du hast Routine im Umgang mit dem Google-Office-Paket.
* Du überzeugst mit einer analytischen Herangehensweise, hinterfragst konventionelle Denkmuster und verfügst über ein hohes Maß an Eigenständigkeit und Koordinationsfähigkeit.
* Arbeiten im Team ist für dich selbstverständlich, speziell auch im internationalen Kontext.
* Fließende Deutschkenntnisse und gute Englischkenntnisse in Wort und Schrift.
Deine Vorteile
* Flexible Zeiteinteilung
* 2268 € Vergütung im Monat für ein Vollzeitpraktikum > 3 Monate
* Vergünstigte Essenspreise (-50 %) in unserer Mitarbeiterkantine
* Fitnesszentrum auf dem Roche-Campus
* Vernetzung mit anderen Studierenden (online/offline)
Deine Bewerbung
Bitte lade Deinen Lebenslauf und Anschreiben online hoch.
Denke daran, daß sich dieses Praktikum ausschließlich an Studierende (m/w/d) bei laufender Immatrikulat...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2026-03-06 07:54:47
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Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world's most in demand and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life's essentials - and creates lasting value for its colleagues, customers, and other stakeholders.
Learn more about the company's Customized Polymer, Sustainable Fiber, Durable Metal, and Integrated Solutions at www.greif.com and follow Greif on Instagram and LinkedIn.
OUR VISION:
Being the customer service company in the world.
OUR PURPOSE:
Creating packaging solutions for life’s essentials.
Job Requisition #:
033510 Auxiliar SST (Open)
Job Description:
Key Responsibilities
* Prepares and/or reviews specifications or orders for non-routine purchase of safety equipment, ensuring that proper features are present and that items conform to health and safety standards.
* Maintains logbooks of all daily activities, including areas visited or activities performed.
* Collects data regarding potential hazards from new equipment or products.
* Maintains all required environmental records and documentation.
* Recommends corrective measures to be applied based on inspection results.
* Supplies, operates, or maintains personal protective equipment.
* Verifies availability or monitor use of safety equipment.
* Provides guidance to less experienced team members.
* Follow safety regulations.
* Performs other duties as assigned.
Education and Experience
* Typically possesses a high school diploma (or equivalent) and 2-4 years of relevant experience.
Knowledge and Skills
* Demonstrated knowledge of relevant equipment, policies, procedures, and strategies to promote effective safety operations.
* Critical thinking skills.
* Using logic and reasoning to identify the strengths and weaknesses of alternative solutions.
* Good analytical skills.
* Determining how a system should work and how changes in conditions, operations, and the environment will affect outcomes.
* Good knowledge about production operation.
* Attention to detail.
* Solid interpersonal and communication skills.
At Greif, we believe that our colleagues are the center of our success.
Our Total Rewards have a comprehensive focus on well-being and offer a competitive package that enables you to thrive, be engaged, and reach your full potential.
Protect Yourself From Scams: We value the integrity of our recruitment process and prioritize the well-being of our candidates.
While you may find Greif job postings on various platforms, all legitimate opportunities can be verified on our official Careers page at www.greif.com.
All communication from Greif regarding job opportunities will also come from an @greif.com email address.
...
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Type: Permanent Location: Cota, CO-CUN
Salary / Rate: Not Specified
Posted: 2026-03-06 07:48:04
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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
Join us in Roche Pharma based in Midrand as a Pharmacovigilance (PV) Hub Partner.
This position is responsible for supporting PV activities within the PV hub coverage areas to ensure PV activities are completed consistently in a timely manner in accordance with internal processes and local and international regulatory requirements.
In this pivotal role, you will be at the heart of pharmacovigilance, collaborating with cross-functional teams to uphold the highest standards in drug safety and regulatory requirements.
Key Challenges
Your Primary Responsibilities and Accountabilities:
* Ensures collection, reporting and handling of safety information associated with Roche products is performed according to global Roche and local regulatory requirements within the assigned PV hub coverage areas.
* Proactively manages workload to ensure regulatory timelines are met.
* Records management coordinator for the PV unit.
Key Activities
* Performs accurate data capture of adverse event reports, for Roche products from Clinical trials, Post-Marketing Studies (PMS), Spontaneous Reports, Market Research and Patient Support Programs (MAPs), etc.
associated with Company products onto the safety database in accordance with internal processes and local and international regulatory requirements.
* Performs post surveillance activities such as literature review and media monitoring.
* Performs reconciliation activities associated with Pharmacovigilance Agreements and various other sources such as product complaints, medical information inquiries and MAPs.
* Assists and supports department with documentation management.
* Performs and documents contact tests for drug safety to test the mechanisms of reporting to Local Safety Unit.
* Responsible for keeping relevant databases up to date.
* Supports the PV-hub team in ensuring high standards are maintained and opportunities for departmental improvements are identified and implemented.
* Participates in PV project work when necessary and when deemed appropriate by the PV Hub manager.
Who You Are as an Ideal Candidate:
Education/Qualifications
Minimum: Health Care Professional Degree (e.g.
Pharmacist, Registered Nurse, Bachelor of Science in Nursing, Physician assistant, Nurse Practitioner) or Life Science Degree (e.g.
BSc Biology, BSc Neuroscience, etc.)
Experience, Skills, Knowledge:
* Previous operational experience in Drug Safety/Pharmacovigilance (preferred)
* Strong knowl...
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Type: Permanent Location: Johannesburg, ZA-GT
Salary / Rate: Not Specified
Posted: 2026-03-06 07:46:49
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General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
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Type: Permanent Location: Halifax, US-NC
Salary / Rate: Not Specified
Posted: 2026-03-06 07:43:25
