Group Leader QC - Equipment & Support
Who we are
The opportunity
The Quality Control Analytical Laboratory is responsible for all analytical testing to support the production of Cytotoxic injectable products. The laboratory executes a wide variety of analytical tests on active substances, excipients, packaging materials and drug products for release and stability purposes. The department is also responsible for introduction and qualification, maintenance and calibration of equipment, maintaining GMP documentation and stock keeping. In order to strengthen this responsibility, the Quality Control Analytical Laboratory is searching for a Group/Team leader Quality Control Analytical Laboratories Equipment & Support.
The group leader QC- Analytical Laboratory Equipment & Support is supported by an enthusiastic and diverse team, which closely collaborates with different stakeholders, like Procurement, E&M and Quality Systems to implement new analytical equipment and maintain existing equipment, update documentation and make sure all needed materials are available. It is your role to plan the various activities in close collaboration with stakeholders, while remaining aligned with the strategy, commitments and goals of the QC organization. You will be is a subject matter expert in equipment qualification and an expert in problem solving.
How you’ll spend your day
Manage Activities
- Guide the team in equipment implementation strategies
- Manage the team in establishing and maintaining quality at the lab in accordance with Site SOP’s, regulatory guidelines and cGXP compliance requirements.
- Maintain a culture of enhancing quality throughout the entire Laboratory.
- Performance of in-depth root cause analyses and problem solving
- Act as a Subject Matter Expert during regulatory and internal audits.
- Is a Subject Matter Expert with respect to equipment qualification.
- Responsible for implementation of equipment which meets the business needs and current regulations.
- Responsible for cross-departmental communication with stakeholders like Procurement and Quality Systems to meet project demands
- Responsible for equipment maintenance and Calibration
- Responsible for GMP documentation and ordering of materials
Manage Team and Resources
- Manage own team through talent identification, active performance management, succession planning, employee development, mentoring and modeling behavior according to Teva values.
- Run an efficient and effective QC team through managing the team budget and resources.
Manage of Culture of Safety
- Maintain a culture of enhancing safety throughout the entire Laboratory.
- Review and provide options to meet business needs without compromising health & safety.
Your experience and qualifications
- You will have a BS/master or PHD degree in analytical chemistry, pharmacy or similar field.
- You have some experience in leading a team or willing to develop your leadership skills.
Next to that you will have/ you are:
- Able to act as a liaison between stakeholders
- Good Knowledge with the use of ICH guidelines
- Excellent organizational skills and a strong analytical oriented mindset.
- Solid experience with analytical equipment implementation and qualification
- Good knowledge of Pharmaceutical quality systems and production processes
- Good scientific analytical attitude
- Excellent written and verbal communication skills
- Pro-active team player
- Results oriented
What will we offer?
- 25 paid holidays with 11,5 extra days (based on fulltime) with option to use for other purposes like education, cycle plan, etc.
- Competitive salary
- A number of health benefits including like Accident Assurance and Income protection
- 9 weeks of fully paid parenteral leave
- Flexible working conditions with hybrid working policy
- Competitive Pension
- Fully covered public transport contribution
Contact person
Ivo Huijskens - Senior Recruiter, Europe
Reports To
Head of Analytical Lab
Already Working @TEVA?
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Pre employment screening
Teva will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process.