Supervisor, Manufacturing

$10,000 Sign on Bonus Manufacturing Supervisor Summary The Manufacturing Supervisor is accountable for leading teams to execute procedures for upstream manufacturing and support area of manufacturing using SOP’s and batch records.
Operating production equipment for upstream processing that may include process monitoring, media prep and harvesting.
The Manufacturing Supervisor is accountable for ensuring all team members are trained and training is completed on time prior to entering the production floor.
Catalent is a growing Biotech Contract Development and Manufacturing Organization (CDMO) with an internationally recognized tradition of quality and service.
Catalent Cell and Gene Therapy provides process development, process characterization, and GMP manufacturing services to industry leaders utilizing novel technologies to produce state-of-the-art vaccines and gene therapies.
As a Catalent employee, you will actively contribute to delivery of services to our clients and impact the well-being of their patients.
The Role Ensure staff are fully trained on all cGMP manufacturing operations and documentation and adhering to safety guidelines Build effective teams that apply their diverse skills and perspectives to achieve common goals.
Oversee daily activity for the group to ensure quality results Performance management for direct reports.
Draft and revise official manufacturing documents, SOPs, Batch Records, Validation Protocols.
Lead initiation and closure of deviations; may serve as the lead in the departmental investigation and be responsible for closing out deviations and CAPAs GMP batch review and close-out with Quality Assurance group.
Collaborate with MST and development groups to assist with tech-transfer, scale-up, and translation activities.
Provide daily production updates to production managers, client representatives, and project managers.
Provide guidance for continuous improvement initiatives with Upstream team.
Represent the department to clients and on cross-functional project team The Candidate Masters’ degree in a Scientific, Engineering or Biotech field with 4 – 6 years’ experience with upstream (fermentation/bioreactor) biologic production processes under GMP compliance.
OR Bachelor’s degree in a Scientific, Engineering or Biotech field with 6 - 8 years’ experience with upstream (fermentation/bioreactor) biologic production processes under GMP compliance.
OR HS Diploma or Associate Degree with 8 – 10 years’ experience with upstream (fermentation/bioreactor) biologic production processes under GMP compliance.
Outstanding knowledge, and ability to apply scientific principles utilized to solve operational, as well as routine production tasks Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, GM Excellence, and GROW) may be considered in place of external experience.
Experience in mammalian or microbrial cell culture a required.
Solid experience with the following: large-scale centrifuges, washers, autoclaves Proficient knowledge and ability to apply scientific principles utilized to solve operational, as well as routine production tasks.
Proficient knowledge of documentation including comprehension, review & establishing Batch Production Records, SOP’s, deviation & summary reports.
Actively pursues learning of required skills, new skills, and new equipment.
Possesses proficient equipment understanding, including understanding equipment function and application.
Position Benefits: Opportunity to gain experience in the cutting-edge gene therapy space and help to develop critical lifesaving therapies for our clients 152 hours PTO & 8 Holidays Medical, Dental & Vision Benefits and 401k Employee Stock Purchase Plan Tuition Reimbursement 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.
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S.
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