Reviewer Production Documentation jobs at Teva in Netherlands, Haarlem

At our Haarlem production site, we are dedicated to one of the most meaningful missions in healthcare: the fight against cancer. As aShift Manager, you’ll lead and support a team of operators who help produce chemotherapy treatments.

In this role, you’ll be responsible for overseeing day-to-day operations, ensuring product quality, and maintaining strict compliance with GMP and safety standards. This is a hands-on leadership position where collaboration with QA, Maintenance, Engineering, and Operational Excellence teams is key. Your focus will be on effective people management, efficient shift execution, and driving a culture of continuous improvement.

This role follows a, meaning you’ll work(2 morning shifts, 2 evening shifts), followed by. The schedule rotates throughout the full week to ensure continuous coverage.

• Team Leadership & People Management
  • Lead and support a team of 15–20 operators and specialists
  • Conduct performance and development discussions
  • Oversee shift planning, onboarding, and manage absence or performance-related issues
• Shift & Production Oversight
  • Manage daily production activities to ensure safety, quality, and timely output
  • Escalate operational issues and support root cause investigations
  • Ensure compliance with EHS and GMP guidelines during all shift activities
• Equipment & Process Reliability
  • Monitor equipment readiness and coordinate maintenance when needed
  • Support technicians in resolving breakdowns or process deviations
  • Suggest and implement improvements to reduce downtime and enhance reliability
• Documentation & Reporting
  • Ensure accurate and timely completion of batch documentation (Batch Records)
  • Initiate and follow up on incident reports and EHS observations
  • Track and report on key performance metrics such as output, quality, and delays
• Continuous Improvement
  • Contribute to LEAN and Operational Excellence efforts
  • Participate in cross-functional improvement projects
  • Promote a culture of learning, ownership, and teamwork within the shift

• A bachelor-level way of thinking, ideally in Life Sciences or a technical field.

• Solid understanding of pharmaceutical production processes and GMP guidelines

• Experience with production control systems and planning methodologies
• Familiarity with quality management systems
• Working knowledge of LEAN, Six Sigma (Yellow/Green Belt preferred), and Operational Excellence practices
• Proven track record in a leadership role within a production environment
• Strong communication and interpersonal skills
• Effective team leadership and coaching abilities
• Proficient in English (spoken and written) and it would be great if you can speak Dutch

• Competitive Salary: We offer a salary that matches your skills and experience.
• Bonus: Based on personal and company performance.
• Shift Allowance: Based on the 16/7 shift you will get 19,6% on top of your salary
• Flexible Working Conditions: Benefit from our hybrid work policy.
• Comprehensive Pension Plan: Including disability insurance and partner/orphan pension coverage.
• Generous Vacation Leave: 25 paid vacation days.
• Parental Leave: 9 weeks of fully paid parental leave.
• Wellbeing Initiatives: Take advantage of our bike plan, caregiver support policy, “I Feel Fit” program, fresh fruit, and more.

Ivo Huijskens - Senior Recruiter Europe

Associate Director Production

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

You'll be part of a global organization that values operational excellence, collaboration, and proactive problem-solving and you'll help us deliver medicines that make a real difference in patients’ lives.

• Lead & coach a team of 8–10 professionals, divided between Compliance and Documentation.
  • Own and continuously improve compliance processes, including:
  • Supplier qualification and Quality Technical Agreement (QTA) coordination
  • Inspection readiness, audit execution, and self-inspection programs
  • Handling vendor change notifications, data integrity initiatives, and Global Notification To Management (GNTM)
  • Managing corporate gap assessments and supporting CAPA implementation
• Oversee documentation systems, ensuring:
  • Controlled issuance of SOPs, logbooks, and production batch records
  • Effective use and governance of the Electronic Document Management System (EDMS)
  • High-quality, audit-ready documentation across teams
• Prepare for and lead third-party audits and act as a strategic support during government inspections, either in the front office or as back-office lead, depending on the situation.
• Monitor and report on quality KPIs relevant to your area, translating performance insights into improvement initiatives.
• Foster collaboration with cross-functional stakeholders and contribute to global knowledge-sharing across the Teva Quality network.

• A bachelor's degree in Life Sciences (e.g., Pharmacy, Chemistry, Biology) or a related field
• Proven track record managing inspections and audits.
• Strong interpersonal and problem-solving skills, you’re comfortable influencing without authority.
• Strategic thinker with the ability to move fluidly between details and the big picture.
• Experience with quality systems, compliance programs, and team development in a regulated environment.

• Competitive Salary: We offer a salary that reflects your skills and experience.
• Bonus based on personal and company performance.
• Flexible Working Conditions: Enjoy the benefits of our hybrid work policy.
• Comprehensive Pension Plan: Includes occupational disability insurance and partner and orphan insurance.
• Generous Vacation: 26 paid vacation days, plus a personal choice budget of 11.5 days based on full-time employment
• Parental Leave: Benefit from 9 weeks of fully paid parental leave.
• Wellbeing Initiatives: Take advantage of our bike plan, caregiver policy and more.

Head of Compliance Systems & Compliance

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

We are looking for a meticulous Reviewer Production Documentation to join our team. In this role, you will ensure the accuracy, completeness, and compliance of all documentation throughout the drug manufacturing process. Stationed in the production department, you will work closely with operators and collaborate with various departments, including Parenterals, Quality Assurance, and Packaging. Your responsibilities will include guiding operators in proper documentation practices according to ALCOA++ principles, compiling and organizing relevant documents, reviewing BMRs/CVPs for completeness, and driving continuous improvements in the documentation process. This role is essential in maintaining the highest standards of compliance and quality in our production operations.

• Provide real-time guidance and support to operators during production, ensuring that they complete Batch Manufacturing Records (BMR) and Cleaning Validation Protocols (CVP) according to ALCOA++ principles.
• Gather and meticulously organize all necessary documentation related to each batch, ensuring a complete and traceable BMR/CVP.
• Conduct thorough reviews of BMRs and CVPs immediately after batch production to confirm accuracy, completeness, and adherence to regulatory standards.
• Identify and address any discrepancies, missing information, or unclear documentation by collaborating with operators and other stakeholders to rectify issues promptly.
• Oversee and coordinate the entire BMR/CVP review process, ensuring timely completion and submission of all records to Quality Assurance.
• Engage in regular meetings with stakeholders across various departments to discuss the progress and alignment of the BMR/CVP review cycle.
• Contribute to the ongoing enhancement of the BMR/CVP review process by proposing and implementing improvements that streamline documentation practices and increase compliance.
• Facilitate training sessions for operators on GMP guidelines and best practices for completing BMRs and CVPs in line with ALCOA principles, fostering a culture of accuracy and compliance.
  

• Knowledge of GMP guidelines and ALCOA principles.
• Experience with quality management systems like Trackwise.
• Familiarity with BMR/CVP processes in pharmaceutical manufacturing.
• 2-4 years of experience as an operator or documentation specialist in a pharmaceutical setting preferred.
• Experience with MES and SAP is a plus.

• Competitive Salary: We offer a salary that matches your skills and experience.
• Bonus: Based on both personal performance and company results.
• Flexible Working Conditions: Enjoy the benefits of our hybrid work policy.
• Comprehensive Pension Plan: Includes occupational disability insurance and partner and orphan insurance.
• Generous Vacation Policy: 26 paid vacation days, plus a PKB Budget of 11.5 days based on full-time employment.
• Parental Leave: Benefit from 9 weeks of fully paid parental leave.
• Wellbeing Initiatives: Take advantage of our bike plan, caregiver policy, "I Feel Fit" program, fresh fruit, and more.

Ivo Huijskens - Senior Recruiter Europe

Supervisor Production

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.