Entry Level QC Laboratory Technician Jobs
New grad qc laboratory technician jobs are open to recent graduates and entry level candidates with zero to two years of experience, where hands-on lab coursework or an internship can carry more weight than a lengthy resume. Most openings are on-site roles across Biotechnology & Pharmaceuticals, Consulting & Professional Services, and Chemicals & Materials, with employers like American Regent, Aldevron, and Artech hiring at this level now.
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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 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.
Position Summary
We have an opportunity for a Senior Scientist, QC Analytical to join our team. In this role, you will support analytical testing to ensure GMP manufacturing for clinical and commercial clients. You will apply your technical knowledge, regulatory understanding, and commitment to scientific excellence to deliver high-quality results. This position reports to the Sr. Manager, Quality and offers the chance to work in a dynamic, fast-paced environment.
Shift: Monday – Friday, 8am-5pm
Location: Harmans, MD - BWI
100% Onsite
The Role
- Perform and support a broad range of analytical and molecular biology assays, including ELISA, qPCR, ddPCR, HPLC, capillary electrophoresis, DNA/RNA extraction, and related quality control testing.
- Troubleshoot laboratory, testing, and instrumentation issues, escalate concerns as needed, and recommend solutions to support batch release, stability, and special testing programs.
- Serve as a subject matter expert for key analytical techniques, providing technical guidance to auditors, vendors, and cross-functional teams.
- Mentor, train, and develop laboratory staff while promoting technical excellence and adherence to quality standards.
- Lead and support continuous improvement initiatives to enhance laboratory efficiency, compliance, and operational performance.
- Create, revise, and maintain technical documentation, including assay protocols, SOPs, summary reports, and other GMP-controlled records.
- Review laboratory work, approve data packages, and ensure accurate data interpretation and reporting in accordance with quality requirements.
- Manage and support change controls (CRs), CAPAs, deviations, OOS investigations, and issue resolution activities to ensure product quality and compliance.
- Monitor laboratory equipment performance, including maintenance, troubleshooting, alarm response, and coordination of corrective actions.
- Communicate quality-impacting issues to management and maintain flexibility to support unique production campaigns, including off-hours and weekend operations when required.
- Other duties as assigned
The Candidate
Minimum Requirements
- Bachelor’s degree in a Life Sciences discipline with 4–6 years of experience in a cGMP QC laboratory, or Master’s degree in a Life Sciences discipline with at least 2 years of experience in a cGMP QC laboratory
- Knowledge and expertise in QC analytical methods used for protein chemistry and molecular biology
- Experience in the biologic, pharmaceutical, or medical device industry performing hands-on QC work with strong familiarity of GMP practices
- Experience in writing Standard Operating Procedures (SOPs)
- Broad experience with biochemistry and related documentation
- Proficient in applying basic scientific and regulatory principles to solve operational and quality tasks
- Experience with Microsoft Excel and Microsoft Word
- Strong attention to detail and organizational skills
- Ability to succeed in a team-oriented environment under dynamic conditions
- Ability to work a set shift with occasional overtime as required
Preferred Skills & Background
- Experience with techniques such as ELISA, qPCR, ddPCR, HPLC, and Capillary Electrophoresis
Pay
The anticipated hourly rate for this position in MD is $50.48 – $57.69 Plus Bonus. The final hourly rate 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.
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.
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.
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.
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 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.
Position Summary
We have an opportunity for a Senior Scientist, QC Analytical to join our team. In this role, you will support analytical testing to ensure GMP manufacturing for clinical and commercial clients. You will apply your technical knowledge, regulatory understanding, and commitment to scientific excellence to deliver high-quality results. This position reports to the Sr. Manager, Quality and offers the chance to work in a dynamic, fast-paced environment.
Shift: Monday – Friday, 8am-5pm
Location: Harmans, MD - BWI
100% Onsite
The Role
- Perform and support a broad range of analytical and molecular biology assays, including ELISA, qPCR, ddPCR, HPLC, capillary electrophoresis, DNA/RNA extraction, and related quality control testing.
- Troubleshoot laboratory, testing, and instrumentation issues, escalate concerns as needed, and recommend solutions to support batch release, stability, and special testing programs.
- Serve as a subject matter expert for key analytical techniques, providing technical guidance to auditors, vendors, and cross-functional teams.
- Mentor, train, and develop laboratory staff while promoting technical excellence and adherence to quality standards.
- Lead and support continuous improvement initiatives to enhance laboratory efficiency, compliance, and operational performance.
- Create, revise, and maintain technical documentation, including assay protocols, SOPs, summary reports, and other GMP-controlled records.
- Review laboratory work, approve data packages, and ensure accurate data interpretation and reporting in accordance with quality requirements.
- Manage and support change controls (CRs), CAPAs, deviations, OOS investigations, and issue resolution activities to ensure product quality and compliance.
- Monitor laboratory equipment performance, including maintenance, troubleshooting, alarm response, and coordination of corrective actions.
- Communicate quality-impacting issues to management and maintain flexibility to support unique production campaigns, including off-hours and weekend operations when required.
- Other duties as assigned
The Candidate
Minimum Requirements
- Bachelor’s degree in a Life Sciences discipline with 4–6 years of experience in a cGMP QC laboratory, or Master’s degree in a Life Sciences discipline with at least 2 years of experience in a cGMP QC laboratory
- Knowledge and expertise in QC analytical methods used for protein chemistry and molecular biology
- Experience in the biologic, pharmaceutical, or medical device industry performing hands-on QC work with strong familiarity of GMP practices
- Experience in writing Standard Operating Procedures (SOPs)
- Broad experience with biochemistry and related documentation
- Proficient in applying basic scientific and regulatory principles to solve operational and quality tasks
- Experience with Microsoft Excel and Microsoft Word
- Strong attention to detail and organizational skills
- Ability to succeed in a team-oriented environment under dynamic conditions
- Ability to work a set shift with occasional overtime as required
Preferred Skills & Background
- Experience with techniques such as ELISA, qPCR, ddPCR, HPLC, and Capillary Electrophoresis
Pay
The anticipated hourly rate for this position in MD is $50.48 – $57.69 Plus Bonus. The final hourly rate 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.
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.
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.
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.
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Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals11
- Consulting & Professional Services5
- Chemicals & Materials4
- Science & Research2
- Technology & Software2
Entry Level QC Laboratory Technician Jobs: Frequently Asked Questions
How do I get an entry level qc laboratory technician job?
Start by highlighting any lab experience you have, whether from coursework, internships, or volunteer work. Employers at this level look for familiarity with standard lab equipment, attention to detail, and a working knowledge of quality control documentation practices. Certifications like ASQ's Certified Quality Technician (CQT) can strengthen your application, and tailoring your resume to each job description helps you clear applicant tracking systems.
Which companies hire entry level qc laboratory technicians?
Companies hiring entry level qc laboratory technicians right now include American Regent, Aldevron, and Artech, based on current listings on Migrate Mate as of November 2026. At this level, manufacturers, food and beverage producers, pharmaceutical companies, and contract testing labs tend to hire most actively, since they maintain large QC teams with consistent turnover at the technician tier.
Are there remote entry level qc laboratory technician jobs?
Yes, though most qc laboratory technician roles require on-site work because of hands-on equipment and sample handling duties. About 11% of entry level qc laboratory technician openings are remote or hybrid as of November 2026, and those positions typically involve documentation review, data entry, or quality systems support rather than direct lab work.
Are these new grad qc laboratory technician jobs?
Yes, these listings include new grad, recent graduate, and junior qc laboratory technician roles. A new grad-friendly posting typically welcomes zero to two years of experience and treats completed coursework, lab practicums, or internships as qualifying background. If a job description mentions on-the-job training, mentorship, or a willingness to consider candidates without prior industry experience, it's aimed at this entry level audience.
Which industries hire the most entry level qc laboratory technicians?
Entry Level qc laboratory technician roles concentrate in Biotechnology & Pharmaceuticals, Consulting & Professional Services, and Chemicals & Materials, based on current listings on Migrate Mate as of November 2026. These sectors rely on consistent product testing and regulatory compliance, which creates steady demand for entry level technicians who can be trained on internal processes and quality standards from the ground up.