Quality Control Job at Catalent in the USA
Catalent is hiring an Associate Scientist, QC Microbiology for its Harmans, Maryland location. This is a full-time, 100% onsite role. The candidate selected for the Quality Control Job at Catalent Careers should support Phase I/II GMP manufacturing through environmental monitoring, microbiological testing, and aseptic process support. If you are experienced in cGMP cleanrooms and quality control microbiology, this opportunity offers competitive pay, strong benefits, and career growth in a leading CDMO.
Job Details:
- Job Title: Associate Scientist, QC Microbiology
- Location: Harmans, Maryland, United States (21077)
- Job ID: 0093195
- Shift: Monday – Friday, 12:00 AM – 8:30 AM
- Work Type: Full-time, 100% On-site
- Department: Quality Control – Microbiology
- Salary Range: $58,240 – $80,080 per year + annual bonus
About the Company:
Catalent is a leading global Contract Development and Manufacturing Organization (CDMO) dedicated to developing, manufacturing, and supplying products that help people live better and healthier lives. With more than 40 global sites and thousands of scientists and technicians, Catalent supports pharma, biotech, and consumer health companies in accelerating product development and bringing over 7,000 life-saving and life-enhancing products to market. The company produces more than 70 billion doses annually and plays a critical role in advancing global healthcare.
Educational Requirements for this Job:
- B.S. or A.S. in a Life Sciences discipline
- 0–4 years of relevant experience working in cGMP cleanrooms
- Experience in cGMP Quality Control – Good Manufacturing Practices
Key Responsibilities:
- Perform Environmental Monitoring (EM) of cleanrooms, including viable surface, viable air, and non-viable particulate sampling in the Quality Control Job at Catalent Careers
- Conduct routine sampling and testing of clean utilities such as USP water (WFI) and clean steam
- Perform bioburden testing on buffers, solutions, equipment cleaning samples, in-process, and release drug product samples
- Isolate and subculture microorganisms for identification as a Scientist
- Perform aseptic process simulations (media fills) and fill/finish monitoring
- Monitor air quality, aseptic technique, and environmental integrity
- Compile and trend Environmental Monitoring data
- Assist in SOP revisions and protocol creation
- Coordinate with Manufacturing and QA teams
- Communicate results through documentation and discussions in the Quality Control Job
Skills Required:
- Strong knowledge of cGMP and regulatory principles
- Experience in Quality Control microbiology
- Ability to analyze data and revise SOPs
- Proficiency in Microsoft Excel and Microsoft Word
- Strong attention to detail
- Ability to work in a fast-paced environment
- Flexibility for off-hour and weekend work if required
- Ability to work with minimal supervision
- Strong communication and teamwork skills
Benefits of the Quality Control Job:
- Competitive medical benefits
- 401K retirement plan
- 152 hours PTO
- 8 Paid Holidays
- Annual bonus opportunity
- Exposure to continuous improvement processes
- Opportunity to work on life-saving biologics and sterile drug products
- Career growth in a global pharmaceutical CDMO
- Dynamic and fast-paced work environment
