Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead and enhance contamination control strategies in a dynamic CDMO environment.
- Company: Join Piramal Pharma Solutions, a global leader in drug development and manufacturing.
- Benefits: Competitive salary, career growth, and opportunities to work with cutting-edge technologies.
- Other info: Collaborative culture with a focus on continuous improvement and innovation.
- Why this job: Make a real impact on contamination control in the pharmaceutical industry.
- Qualifications: Bachelor's degree in a relevant field and 7-10 years of experience in biologics manufacturing.
The predicted salary is between 60000 - 80000 £ per year.
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
The Contamination Control Manager is responsible for leading, developing, and continuously enhancing the company’s established integrated contamination control strategy within a biologics Contract Development and Manufacturing Organization (CDMO) environment. This role works closely with Manufacturing, MSAT, and Quality to drive proactive identification, reduction and elimination of contamination risks across multiple facilities, client products & processes. The role is responsible for ensuring that the CCS is dynamic, effective and evolves in alignment with business needs, regulatory expectations and future-state technologies.
Key Responsibilities- Contamination Control Strategy (CCS)
- Lead development and maintenance of the site Contamination Control Strategy (CCS) aligned with global regulatory expectations (including UK/EU GMP Annex 1, FDA & ICH guidelines).
- Ensure contamination control principles are embedded across:
- Supplier and Service Provider Selection and Management
- Facility and Equipment Design
- Process Flows (open and closed systems)
- Facility and Equipment cleaning, sanitisation, sterilisation, pyrogen reduction, and material/personnel/waste flows
- Learning & Development curricula
- Adapt contamination control strategies to effectively support diverse client processes, modalities and manufacturing technologies.
- Partner with Manufacturing to integrate contamination control into:
- Shift routines and pre-job briefs
- Aseptic behaviours and operator practices
- Day-to-day decision making on the floor
- Training and capability building
- Equipment detailed design and specification
- Tech transfer and scale-up activities
- Process characterization and control strategy development
- Introduction of new client processes and products
- Data utilisation and CCS integration
- Commissioning, qualification, and readiness activities
- Lead and facilitate contamination-focused risk assessments (using FMEA and other appropriate methodologies) across:
- Client-specific processes and modalities
- Shared equipment, utilities and multiproduct/dedicated facilities
- Changeovers, campaign manufacturing, and process transfers
- Design and deploy contamination control training programs tailored to a CDMO environment, addressing:
- Variability between client processes and modalities
- Operator experience levels
- Critical aseptic behaviours, interventions, and human factor risks
- Champion a strong site-wide contamination control culture and awareness where:
- Contamination prevention is everyone’s responsibility
- Teams proactively identify, communicate and escalate risks
- Near-misses and learning opportunities are shared and acted upon
- Provide governance level oversight of contamination related data. Ensure the site CCS is informed by robust, accurate and timely trends, including:
- Environmental and personnel monitoring
- Microbiological excursions and alert/actions
- Deviation themes, near misses and human-factor patterns
- Utility-related contamination risks
- Cleaning effectiveness and disinfectant performance trends
- Support preparation and readiness efforts for audits and regulatory inspections as the contamination control SME. Clearly articulate the site CCS, risk-based rationale, and operational controls to clients and inspectors. Partner with site and client teams to address contamination risks while maintaining compliance and operational flexibility.
- Bachelor’s degree in microbiology, biology, biochemistry, chemical engineering, or related discipline (Master’s Degree is preferred).
- 7–10+ years’ experience in biologics or sterile pharmaceutical manufacturing, preferably in a CDMO environment.
- Strong expertise in:
- Aseptic processing and cleanroom operations
- Microbiological contamination control
- Multi-product, multi-client manufacturing models
- Ability to influence without authority in a matrixed CDMO environment
- Strong facilitation, coaching, project management and communication skills
- Practical, operations-focused problem solving
- Comfort working between client expectations and internal execution
- High level of integrity and ownership
- Direct experience supporting tech transfer into commercial manufacturing
- Hands-on involvement with EU GMP Annex 1 implementation
- Experience preparing sites for regulatory inspections and client audits
- Background in facilities with shared equipment and campaign manufacturing
Contamination Control Manager in Grangemouth employer: Piramal Pharma Ltd
Contact Detail:
Piramal Pharma Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Contamination Control Manager in Grangemouth
✨Tip Number 1
Network like a pro! Get out there and connect with industry professionals on LinkedIn or at local events. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their contamination control strategies and be ready to discuss how your experience aligns with their needs. Show them you’re not just another candidate!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. Focus on articulating your experience in aseptic processing and cleanroom operations.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Contamination Control Manager in Grangemouth
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Contamination Control Manager role. Highlight your relevant experience in biologics or sterile pharmaceutical manufacturing, and don’t forget to showcase your expertise in contamination control strategies!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this role. Mention specific experiences that align with the key responsibilities, like leading FMEA or collaborating with cross-functional teams.
Showcase Your Skills: Don’t just list your skills; demonstrate them! Use examples from your past roles to show how you’ve influenced contamination control practices or improved operational standards. We love seeing real-world applications of your expertise!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!
How to prepare for a job interview at Piramal Pharma Ltd
✨Know Your Contamination Control Strategies
Make sure you’re well-versed in contamination control strategies, especially those relevant to biologics and CDMO environments. Brush up on UK/EU GMP Annex 1 and FDA guidelines, as these will likely come up during your interview.
✨Showcase Your Cross-Functional Collaboration Skills
Be prepared to discuss how you've partnered with different teams like Manufacturing and Quality in the past. Highlight specific examples where your collaboration led to successful contamination control outcomes or improved processes.
✨Demonstrate Your Risk Management Expertise
Familiarise yourself with FMEA and other risk assessment methodologies. Be ready to explain how you've applied these tools in previous roles to identify and mitigate contamination risks effectively.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills in real-time. Think of examples where you had to make quick decisions regarding contamination control and how you ensured compliance while maintaining operational flexibility.