Supervisor, Central Services

Position Summary

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.

The Supervisor, Central Services is responsible for supporting the overall cGMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk products from microbial and cell culture systems for Phase I/II GMP manufacturing. The Supervisor, Central Services performs production operations including but not limited to preparation of media and buffer solutions as well as being involved in both start-up and product changeover activities, and completing daily manufacturing tasks as well as supporting more in-depth, long term projects.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

The Role

• Completes daily manufacturing tasks per standard operating procedures and batch document instructions and monitors critical process parameters.

• During technical transfer and the start-up activities, provide input on design and operation of equipment and effectively troubleshoot equipment and processing problems.

• Lead resolution of technical and process problems, initiate change control for equipment/process modifications. Identify, develop, and implement process improvements, equipment improvements/upgrades.

• Actively participates in the creation and revision of Batch Records, Standard Operating Procedures and other GMP documents.

• Receive, stage and track materials.

• Ensures all production activities are completed in a safe and compliant manor.

• Communicate assignments, milestones and deadlines to the team and individuals based on supervisor's instructions.

• Monitor and audit work processes to ensure compliance and completion of targets.

• Trains new and less experienced team members.

• Other duties as assigned.

The Candidate

• Bachelor’s Degree with 5+ years of directly related experience OR Associate Degree with 7+ years of directly related experience.

• 5+ years prior manufacturing experience in the pharmaceutical or biotechnology industry, with the demonstration of a high level of performance.

• Proficient and a high level of understanding of the basic FDA cGMP regulations.

• Must be team-oriented (proactively builds healthy working relationships between peers, their department and other groups).

• Able to fluently communicate in English. Exhibits excellent written and oral communication skills.

Why You Should Join Catalent

• Competitive medical benefits and 401K

• 152 Hours of PTO + 8 Paid Holidays

• Dynamic, fast-paced work environment

• Opportunity to work on Continuous Improvement Processes

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.