Anne Arundel County, Maryland, United States · On-site
$110k–$130k/yr
Job Description Supervisor, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilit…
Skills: Manufacturing supervision, GMP compliance, Upstream processing, Cell culture, Bioreactor operation
Anne Arundel County, Maryland, United States · On-site
$110k–$130k/yr
Job Description Supervisor, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilit…
Skills: Manufacturing supervision, GMP compliance, Upstream processing, Cell culture, Batch record review
Düsseldorf, North Rhine-Westphalia, Germany · On-site
Der Standort Langenfeld konzentriert sich auf die Entwicklung neuartiger Zelltherapien auf der Basis pluripotenter Stammzellen (iPS-Zellen). iPS-Zellen werden in der hauseigenen GMP-Anlage erzeugt und strengen Qualitätsk…
Skills: Quality Control, GMP, Cell Culture, Analytical Testing, Microbiology
Anne Arundel County, Maryland, United States · On-site
$43/hr–$52/hr
Job Description Group Lead, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilit…
Skills: Manufacturing leadership, cGMP compliance, Process optimization, Batch production records, SOP management
Anne Arundel County, Maryland, United States · On-site
$38/hr–$43/hr
Job Description Associate III, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing faci…
Skills: CGMP manufacturing, Upstream production, Bioreactor operation, Aseptic cell culture, Fermentation
Anne Arundel County, Maryland, United States · On-site
$105k–$120k/yr
Senior Specialist, Quality Systems About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is …
Skills: Quality Assurance, CAPA, Deviation Management, Change Control, GMP
Glen Burnie, Maryland, United States · On-site
$110k–$130k/yr
Job Description Supervisor, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilit…
Skills: Manufacturing supervision, GMP compliance, Upstream processing, Cell culture, Bioreactor operation
Schorndorf, Baden-Württemberg, Germany · On-site
Job Title: Director Operations, Pharma & Consumer Health Reports to: General Manager, Pharma & Consumer Health Location: Schorndorf, Germany Position Summary The Director Operations, Pharma & Consumer Health is responsib…
Skills: cGMP Compliance, EHS Compliance, Pharmaceutical Manufacturing, Solid Dosage Forms, Lean Manufacturing
Anne Arundel County, Maryland, United States · On-site
$105k–$120k/yr
Senior Specialist QA OTF About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 …
Skills: Quality Assurance, GMP compliance, Batch record review, Visual inspection, Standard Operating Procedures
San Diego, California, United States · On-site
$115k–$125k/yr
Scientist 3, Analytical Development Position Summary: Work Schedule: Monday-Friday, core hours 8am-4:30pm 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (C…
Skills: Analytical Method Development, HPLC, UPLC, Stability-Indicating Methods, GMP Compliance
Anne Arundel County, Maryland, United States · On-site
$80k–$110k/yr
Engineer, FacilitiesAbout Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles…
Skills: cGMP, Facility engineering, Utility systems, Water for injection, HVAC
Glen Burnie, Maryland, United States · On-site
$110k–$130k/yr
Job Description Supervisor, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilit…
Skills: Manufacturing supervision, GMP compliance, Upstream processing, Cell culture, Batch record documentation
Philadelphia, Pennsylvania, United States · On-site
Sr. Manager, Project Management Position Summary: Shift: M-F 8am-5pm Location: Philadelphia, PA 100% Onsite Catalent’s Philadelphia, Pennsylvania site serves as the company’s North American Center of Excellence for clini…
Skills: Project Management, Team Leadership, Client Management, Financial Oversight, Continuous Improvement
Windsor, Ontario, Canada · On-site
$48k–$57k/yr
Quality Assurance Associate About Site Windsor, Ontario is one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a b…
Skills: Quality assurance, cGMP compliance, Documentation review, Batch review, Standard operating procedures
Anne Arundel County, Maryland, United States · On-site
$50/hr–$6k
Senior Scientist, QC Analytical About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is loc…
Skills: ELISA, qPCR, ddPCR, HPLC, Capillary electrophoresis
Glen Burnie, Maryland, United States · On-site
$38/hr–$43/hr
Job Description Associate III, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing faci…
Skills: Upstream production, Bioreactor operation, Aseptic cell culture, Fermentation, Fill-finish manufacturing
Anne Arundel County, Maryland, United States · On-site
$145k–$165k/yr
Reliability Engineering ManagerAbout Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is loca…
Skills: Reliability engineering, Root cause analysis, Failure modes and effects analysis, Statistical process control, Fault tree analysis
Glen Burnie, Maryland, United States · On-site
$43/hr–$52/hr
Job Description Group Lead, Manufacturing About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilit…
Skills: Manufacturing leadership, cGMP compliance, Process optimization, Batch production records, SOP management
Anne Arundel County, Maryland, United States · On-site
$315k–$400k/yr
Vice President and General Manager, Cell and Gene Position Summary: Location: Field Base – 50% Travel We have an opportunity for a Vice President and General Manager, Cell and Gene to join our team. This role is accounta…
Skills: Commercial Strategy, P&L Leadership, Business Development, Operational Excellence, Matrix Management
Madison, Wisconsin, United States · On-site
Specialist II Environmental Biochemist – Environmental, Health, Safety & Security (EHS&S) Position Summary: Work Schedule: Monday – Friday, core hours 8am-5pm100% on-site (Madison, WI) Catalent, Inc. is a leading global …
Skills: OSHA Compliance, Biochemical Risk Assessment, Industrial Hygiene, Hazardous Waste Management, GMP Regulations
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Supervise daily manufacturing operations, personnel, and production activities to ensure safe, efficient, and compliant execution. Lead and develop teams while managing production documentation, quality investigations, and cross-functional collaboration.
Requires a degree in a scientific, engineering, or biotech field with 4 to 10 years of experience in upstream biologic production under GMP compliance. Candidates must possess solid experience with large-scale manufacturing equipment and cell culture processes.
Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.
The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse.
The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing.
Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.
We have an opportunity for a Supervisor, Manufacturing to join our team. In this role, you will lead teams to execute procedures for upstream manufacturing and support areas using standard operating procedures and batch records. You will oversee production equipment operations for upstream processing, including process monitoring, media preparation, and harvesting. You will ensure all team members are fully trained and compliant before entering the production floor, while maintaining high standards of quality and safety.
Shift: Day shift 7pm-7am on a 2-2-3 rotation
Location: Harmans, MD - BWI
100% Onsite
Supervise day-to-day manufacturing operations, personnel, and production activities to ensure safe, efficient, and compliant execution.
Lead, train, coach, and develop teams in GMP requirements, safety standards, and operational excellence.
Build high-performing, engaged teams by fostering collaboration, accountability, diversity, and continuous development.
Manage employee performance through coaching, performance reviews, hiring support, onboarding, and talent retention initiatives.
Ensure production batches meet quality, regulatory, and GMP requirements, including batch review and closeout with Quality Assurance.
Author, review, and maintain manufacturing documentation, including SOPs, batch records, logbooks, validation protocols, and related records.
Lead deviation investigations, CAPA activities, and compliance initiatives to drive quality improvements and regulatory readiness.
Partner with cross-functional groups, including QA, MS&T, Engineering,
Facilities, Project Management, and clients, to execute production campaigns and technology transfers.
Oversee critical manufacturing processes, equipment operation, maintenance coordination, validation activities, and accurate scientific data analysis.
Drive continuous improvement initiatives by identifying process efficiencies, resolving operational challenges, and providing regular production updates to stakeholders.
Other duties as assigned
Master’s degree in a Scientific, Engineering, or Biotech field with 4–6 years of experience in upstream biologic production processes under Good Manufacturing Practice compliance OR
Bachelor’s degree in a Scientific, Engineering, or Biotech field with 6–8 years of experience in upstream biologic production processes under Good Manufacturing Practice compliance OR
High School Diploma or Associate Degree with 8–10 years of experience in upstream biologic production processes under Good Manufacturing Practice compliance
Experience in mammalian or microbial cell culture is required
Solid experience with large-scale centrifuges, washers, and autoclaves
Apply scientific and technical knowledge to solve routine production challenges, operate equipment effectively, and support manufacturing operations.
Maintain accurate GMP documentation, including batch records, SOPs, deviations, summary reports, and related manufacturing records.
Demonstrate strong communication, collaboration, and teamwork skills while working effectively with both technical and non-technical stakeholders.
Exhibit continuous learning, adaptability, creativity, and multitasking abilities, with a commitment to professional growth and process improvement.
Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
Experience with bacterial fermentation processes in a Good Manufacturing Practice environment, including bioreactor setup and operation, aseptic processing, process monitoring, sampling, troubleshooting, and batch record documentation
The anticipated salary range for this position in MD is $110,000 – $130,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Defined career path with annual performance reviews and feedback
Diverse and inclusive culture
Opportunities for career growth within an organization dedicated to improving lives
Competitive paid time off plus 8 paid holidays
Community engagement and green initiatives
Medical, dental, and vision benefits effective day one
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.
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 [email protected]. 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 [email protected] for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year. Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe. At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter. Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
Offices: 101 E Kennedy Blvd, Tampa, Florida 33602, US · 14 Schoolhouse Road, Somerset, NJ 08873, US · Frankland Road, Blagrove, Swindon, Wiltshire SN5 8YG, GB · 4-9-17 Akasaka, Minato-ku, Tokyo 107-0052, JP · 160 Pharma Dr, Morrisville, NC 27560, US
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year. Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe. At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter. Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
Offices: 101 E Kennedy Blvd, Tampa, Florida 33602, US · 14 Schoolhouse Road, Somerset, NJ 08873, US · Frankland Road, Blagrove, Swindon, Wiltshire SN5 8YG, GB · 4-9-17 Akasaka, Minato-ku, Tokyo 107-0052, JP · 160 Pharma Dr, Morrisville, NC 27560, US
