New · posted Oct 20
Catalent · Biotechnology
Scientist, QC Analytical
- Harmans, MD
- On-site
- Full-time
- Senior & Principal
Closes Nov 23, 2026 · 34 days left
The role
We have an opportunity for a Scientist, QC Analytical to join our team supporting analytical testing for GMP manufacturing of clinical and commercial products. This role requires strong technical knowledge, familiarity with scientific and regulatory principles, and a commitment to scientific excellence. The Scientist, QC Analytical will report to the Supervisor, QC Analytical and contribute to maintaining high-quality standards in testing and documentation.
Shift: Monday – Friday, 8am-5pm
Location: Harmans, MD - BWI
100% Onsite
- Perform assays such as ELISA, DNA/RNA extraction and gel electrophoresis, qPCR, ddPCR, HPLC, Capillary Electrophoresis, Appearance, Osmo, and pH.
- Document testing in compliance with GMP/GDP procedures.
- Generate internal and external documents such as assay protocols, summary reports, and standard operating procedures (SOPs).
- Provide analytical support to QC method services for method verification of platform test methods.
- Support release and stability testing for raw materials, components, standards, and finished products.
- Review laboratory work and approve data packages as designated by the Supervisor.
- Maintain and troubleshoot instrumentation, ensuring accurate data interpretation.
- Write laboratory investigations, out-of-specification reports, deviations, corrective and preventive actions (CAPAs), and perform statistical analysis and trending.
- Review paper and electronic records for accuracy and compliance.
- Report issues to management and participate in issue resolution and investigations.
- Work under general supervision to meet project goals and adapt to off-hour or weekend work as needed.
- Participate actively in training activities and manage individual training plans.
- Perform other duties as assigned.
What you need
Minimum Requirements
- Bachelor’s degree in a Life Sciences discipline with at least 2 years of experience in a cGMP QC laboratory, or a Master’s degree in a Life Sciences discipline with at least 1 year of experience in a cGMP QC laboratory.
- Experience in the biologic, pharmaceutical, or medical device industry performing hands-on QC work with strong familiarity with GMP practices.
- Experience in writing standard operating procedures (SOPs).
- Strong foundation in biochemistry with hands-on experience reviewing documentation and applying scientific and regulatory principles to support quality and operational activities.
- Demonstrates excellent attention to detail, organizational skills, and the ability to work effectively in fast-paced, team-oriented environments.
- Proficient in Microsoft Excel and Word, leveraging these tools to manage documentation, analyze data, and support business processes.
- Ability to work a set shift with occasional overtime as required.
Preferred Skills & Backgroundnice to have
- Experience with techniques such as ELISA, qPCR, ddPCR, HPLC, and Capillary Electrophoresis.
Pay and benefits
$79,997 – $99,986 a year
Employer provided$38.46 – $48.07 an hour · yearly at 2,080 hours (40 a week)
How this comparesThe anticipated hourly rate for this position in MD is $38.46 – $48.07 plus bonus. The final hourly rate offered to a successful candidate may vary and will depend on factors such as experience, skillset, education, and business needs. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Medical, dental, and vision benefits effective day one
Competitive paid time off plus 8 paid holidays
Tuition reimbursement
Annual performance review and defined career path
Bonus
Community engagement and green initiatives
Where you'll work
Harmans, MDOn-siteOpen in Maps (opens in a new tab)
More jobs in Harmans, MD
From the posting
About Catalent
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 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.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- 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.
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.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Equal opportunity, accessibility and legal noticesCatalent's statements, word for word
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.
Job intelligence
The context around this role
Live data · October 20, 2026
Salary intelligence
How the pay compares
This role's midpoint is 6% below the US median for Quality Control roles at this level.
This roleEmployer provided
Senior & Principal roles in Maryland5 roles publishing pay
Senior & Principal roles in the US56 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $79,997 | — | $99,986 |
| Maryland (middle half) | $106,500 | $110,000 | $112,500 |
| All US (middle half) | $78,500 | $95,500 | $113,125 |
This role: Catalent's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 20, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 307 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Catalent's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods11
- Documentation and SOPs9
- GMP and compliance5
- Collaboration and leadership3
- Investigations and CAPA2
- Data and digital systems2
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
Company hiring pulse
Catalent on Regulatory Jobs
- 30
- Open roles
- 28
- Distinct roles
- 8
- Locations
By discipline
- Quality30 100%
By level
- Associate & Specialist12 40%
- Senior & Principal10 33%
- Manager6 20%
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Scientist, QC Analytical at Catalent
Applications close November 23. $80K–$100K a year, employer provided.