At a Glance
- Tasks: Lead global sterility assurance and contamination control strategies in a dynamic biopharmaceutical environment.
- Company: Join Teva, a leading innovative biopharmaceutical company dedicated to improving health worldwide.
- Benefits: Enjoy generous leave, flexible schedules, tailored health support, and career development opportunities.
- Other info: Be part of a diverse and inclusive workplace that values fresh thinking.
- Why this job: Make a real impact on patient safety and product quality in a collaborative culture.
- Qualifications: 15+ years in sterile pharmaceutical manufacturing and strong leadership skills required.
We Are Teva
How You’ll Spend Your Day
We are looking for an experienced quality and compliance leader with deep expertise in sterility assurance, microbiology, and contamination control to join our Global Quality organization. In this highly visible global role, you will drive quality, compliance, and operational excellence across Teva's manufacturing network and external partners, supporting inspection readiness, regulatory compliance, modernization initiatives, and contamination prevention strategies. Working closely with Quality, Operations, R&D, Regulatory Affairs, Supply Chain, and Technical Operations teams, you will play a key role in advancing Teva's commitment to product quality and patient safety.
Travel Requirements: Up to 30% domestic and international travel.
Key Responsibilities
- Define and execute the global sterility assurance (SA) strategy across internal sites and CMOs.
- Own aspects of the global microbiology, CCS, aseptic processing, endotoxin control, sterilization, EM, water systems, and CCI governance frameworks.
- Lead global policy, standards, and procedural lifecycle management.
- Oversee modernization, harmonization, and digitalization efforts.
- Serve as primary SME for inspections (FDA, EMA, MHRA), readiness activities, and regulatory responses.
- Provide technical support to R&D programs, validation strategies, and regulatory submissions.
- Chair cross-functional sterility assurance councils and technical networks.
- Manage global risk assessments, mitigation strategies, and contamination/event investigations.
- Provide guidance to ensure compliance with Teva's global standards, regulatory guidelines, and cGMP requirements.
- Support/lead Global Quality Compliance Initiatives and contribute to Teva's Long Range Plan.
- Support critical product incident management events, including complex investigations and CAPA development.
- When needed, work collaboratively with the site compliance teams to perform walkthroughs and maturity assessments.
- Work with sites to ensure mock audits support a strong state of inspection readiness.
- When needed, write or execute protocol for deep dive quality compliance assessments and risk assessments.
- Help create, review and monitor the Quality Improvement Plans (QIP) to minimize compliance risk and improve quality performance.
- Ensure Quality Risk Management is implemented effectively to assess, control, communicate, and review risks.
- Contribute to Teva's Global Compliance Network through GxP interpretation, knowledge sharing, and regulatory guidance.
Your Skills and Experience
Do you have?
- Bachelor's degree in Chemistry, Microbiology, Pharmacy, Engineering, or another science-based discipline.
- 15+ years of experience in sterile/aseptic pharmaceutical manufacturing, microbiology, quality assurance, or quality compliance roles.
- Experience leading in both matrix and functional environments with technical, operational, and people leadership responsibilities.
- Extensive experience supporting health authority inspections, regulatory submissions, approvals, and lifecycle management.
- Strong knowledge of audit and inspection management, investigations, complaints, and CAPA programs.
- Deep aseptic processing expertise, including knowledge of isolators/RABS and Annex 1 requirements.
- Experience supporting Environmental Monitoring (EM), Contamination Control Strategies (CCS), and process simulations.
- Pharmaceutical quality manufacturing experience within sterile products, biologics, biosimilars, medical devices, or other highly regulated environments.
- Strong understanding of cGMP requirements, quality systems, microbiology, quality control, quality assurance, and quality compliance.
- Deep knowledge and experience in auditing, compliance, and quality oversight.
Are You?
- A recognized subject matter expert who can influence across a global organization.
- A strong problem solver with excellent analytical and technical writing skills.
- An effective communicator with strong presentation, collaboration, and negotiation skills.
- Comfortable operating in a complex, global matrix environment.
- Skilled in project management, prioritization, and change leadership.
- Proactive, self-motivated, and committed to continuous improvement.
- Able to navigate changing priorities while building strong partnerships across functions and cultures.
How We’ll Take Care of You
Already Working @Teva?
Make sure to apply through our internal career site on Twist—your one-stop shop for career development
The deadline for internal applications will be Monday 14th September 2026
Teva’s Equal Employment Opportunity Commitment
Director Sterility Assurance and Contamination Controls employer: Teva Pharmaceutical
At Teva, we pride ourselves on being a leading biopharmaceutical company that fosters a high-performing and inclusive culture. As an Associate Director – Category Manager Devices, you will enjoy generous benefits, flexible working arrangements, and ample opportunities for career development through our Twist platform, all while contributing to meaningful health solutions worldwide. Join us in a collaborative environment where your expertise will drive impactful procurement strategies and enhance supplier relationships.
StudySmarter Expert Advice🤫
We think this is how you could land Director Sterility Assurance and Contamination Controls
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Teva Pharmaceutical. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Teva Pharmaceutical.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Teva Pharmaceutical. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Teva Pharmaceutical is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Director Sterility Assurance and Contamination Controls
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Teva Pharmaceutical!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Teva Pharmaceutical that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Teva Pharmaceutical!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Teva Pharmaceutical, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Teva Pharmaceutical
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Teva Pharmaceutical that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Teva Pharmaceutical’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
