Manufacturing Associate Jobs in Maryland
Manufacturing Associate jobs in Maryland draw consistent demand across the state's defense manufacturing, biotech production, and food processing sectors, with openings at every level from entry-level assembly to senior process technician. The heaviest hiring concentrates in the Baltimore metro, Frederick, and the I-270 corridor, where established employers like Lockheed Martin, McCormick & Company, and Northrop Grumman maintain large production operations. The most in-demand specialties right now are quality control, GMP-regulated pharmaceutical manufacturing, and precision assembly. Scan the live roles below and apply to whichever ones fit.
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Associate II, 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 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 an Associate II, Manufacturing to join our team. In this role, you will support GMP upstream or downstream manufacturing processes for bulk biologics from microbial and cell culture systems. You will apply your knowledge to solve operational and routine tasks for Phase I/II and commercial GMP manufacturing. This position reports to the Supervisor, Manufacturing and plays a key role in ensuring compliance and operational excellence.
Shift: Day shift, 7am-7pm on a 2-2-3 rotation
Location: Harmans, MD - BWI
100% Onsite
The Role
- Complete Batch Production Records under current Good Manufacturing Practices and document processes using Standard Operating Procedures and Batch Production Records
- Generate operational protocols and internal or external documents including Standard Operating Procedures, Batch Production Records, deviations, and summary reports
- Collaborate with Process Development and Manufacturing Sciences and Technology teams to transfer new projects into GMP
- Generate and revise internal and external documents such as Standard Operating Procedures and Batch Records
- Support initiation and closure of deviations; may lead departmental investigations and close deviations and Corrective and Preventive Actions
- Troubleshoot process and equipment issues; work with Facilities and Validation to maintain manufacturing equipment
- Recommend equipment and supply purchases for production areas
- Develop creative solutions to operational problems using knowledge of available theories and proven solutions
- Work closely with production management on current and new manufacturing projects to develop processes and techniques to meet objectives and avoid delays
- Collaborate with various departments and assist other teams as needed
- Interact with clients during manufacturing campaigns; may oversee and escort person-in-plant during campaigns
- Participate in facility expansion and equipment validation activities
- Maintain full training in all GMP manufacturing operations and documentation while adhering to safety guidelines
- Perform other duties as assigned
The Candidate
Minimum Requirements
- High School diploma or General Education Diploma with 4+ years of experience in upstream (fermentation/bioreactor) or downstream (column chromatography, buffer/media skid) biologic production processes under GMP compliance OR Associate’s degree in a Scientific, Engineering, or Biotech field with 2+ years of experience in upstream or downstream biologic production processes under GMP compliance OR Bachelor’s degree in a Scientific, Engineering, or Biotech field with 1+ years of experience in upstream or downstream biologic production processes under GMP compliance
- Strong knowledge and ability to apply scientific principles to solve operational and routine production tasks
- Excellent documentation skills including comprehension, review, and establishing Batch Production Records, Standard Operating Procedures, deviations, and summary reports
- Team-oriented with the ability to collaborate effectively across Manufacturing, Quality Control, Quality Assurance, Regulatory, and Materials Management functions.
- Strong written and verbal communication skills with proficiency in English.
- Ability to work flexible schedules, including shift, overtime, and weekend coverage as required by production needs.
- Capable of performing physical requirements of the role, including lifting up to 40 pounds and extended periods of standing, walking, bending, reaching, pushing, and pulling.
- Ability to work safely and effectively in a manufacturing environment while maintaining a strong focus on quality, compliance, and operational excellence.
Pay
The anticipated hourly rate for this position in MD is $33.65 – $38.46 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.
Associate II, 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 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 an Associate II, Manufacturing to join our team. In this role, you will support GMP upstream or downstream manufacturing processes for bulk biologics from microbial and cell culture systems. You will apply your knowledge to solve operational and routine tasks for Phase I/II and commercial GMP manufacturing. This position reports to the Supervisor, Manufacturing and plays a key role in ensuring compliance and operational excellence.
Shift: Day shift, 7am-7pm on a 2-2-3 rotation
Location: Harmans, MD - BWI
100% Onsite
The Role
- Complete Batch Production Records under current Good Manufacturing Practices and document processes using Standard Operating Procedures and Batch Production Records
- Generate operational protocols and internal or external documents including Standard Operating Procedures, Batch Production Records, deviations, and summary reports
- Collaborate with Process Development and Manufacturing Sciences and Technology teams to transfer new projects into GMP
- Generate and revise internal and external documents such as Standard Operating Procedures and Batch Records
- Support initiation and closure of deviations; may lead departmental investigations and close deviations and Corrective and Preventive Actions
- Troubleshoot process and equipment issues; work with Facilities and Validation to maintain manufacturing equipment
- Recommend equipment and supply purchases for production areas
- Develop creative solutions to operational problems using knowledge of available theories and proven solutions
- Work closely with production management on current and new manufacturing projects to develop processes and techniques to meet objectives and avoid delays
- Collaborate with various departments and assist other teams as needed
- Interact with clients during manufacturing campaigns; may oversee and escort person-in-plant during campaigns
- Participate in facility expansion and equipment validation activities
- Maintain full training in all GMP manufacturing operations and documentation while adhering to safety guidelines
- Perform other duties as assigned
The Candidate
Minimum Requirements
- High School diploma or General Education Diploma with 4+ years of experience in upstream (fermentation/bioreactor) or downstream (column chromatography, buffer/media skid) biologic production processes under GMP compliance OR Associate’s degree in a Scientific, Engineering, or Biotech field with 2+ years of experience in upstream or downstream biologic production processes under GMP compliance OR Bachelor’s degree in a Scientific, Engineering, or Biotech field with 1+ years of experience in upstream or downstream biologic production processes under GMP compliance
- Strong knowledge and ability to apply scientific principles to solve operational and routine production tasks
- Excellent documentation skills including comprehension, review, and establishing Batch Production Records, Standard Operating Procedures, deviations, and summary reports
- Team-oriented with the ability to collaborate effectively across Manufacturing, Quality Control, Quality Assurance, Regulatory, and Materials Management functions.
- Strong written and verbal communication skills with proficiency in English.
- Ability to work flexible schedules, including shift, overtime, and weekend coverage as required by production needs.
- Capable of performing physical requirements of the role, including lifting up to 40 pounds and extended periods of standing, walking, bending, reaching, pushing, and pulling.
- Ability to work safely and effectively in a manufacturing environment while maintaining a strong focus on quality, compliance, and operational excellence.
Pay
The anticipated hourly rate for this position in MD is $33.65 – $38.46 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.
See All 8 Manufacturing Associate Jobs in Maryland
Find roles in Maryland that match your experience and apply in just a few clicks.
Find Manufacturing Associate JobsManufacturing Associate Jobs by City in Maryland
Where Maryland roles are concentrated, by current openings.
Manufacturing Associate Job Market in Maryland
A snapshot from current Maryland openings, updated as new roles post.
Who's Hiring
What Maryland Employers Look For
The qualifications that appear most often in manufacturing associate jobs across Maryland.
- High school diploma or GED required by most Maryland manufacturing employers
- Experience operating production equipment such as conveyors, presses, or assembly machinery
- Familiarity with Good Manufacturing Practice standards common in Maryland's biotech and pharma facilities
- Ability to read work orders, blueprints, or technical specifications accurately
- Demonstrated commitment to workplace safety protocols and OSHA compliance
- Basic quality inspection skills including measurement tools and defect identification
Manufacturing Associate Jobs in Maryland: Frequently Asked Questions
How do you become a manufacturing associate in Maryland?
Most Maryland manufacturing associate roles require a high school diploma or equivalent, with no state-issued license needed for general production work. Employers in regulated industries like pharmaceuticals and food processing typically require on-the-job GMP training, which they provide internally. Candidates who complete a certificate in manufacturing technology or industrial maintenance at a community college like Baltimore City Community College or Frederick Community College stand out in Maryland's competitive hiring pool.
Which companies hire manufacturing associates in Maryland?
Companies currently hiring manufacturing associates in Maryland include Miltenyi Biotec, Precigen, and Powrmatic, per current listings on Migrate Mate as of November 2026. Maryland's mix of defense contractors, life sciences manufacturers, and consumer goods producers means openings appear across a wide range of industries and facility types throughout the state.
Which Maryland cities have the most manufacturing associate jobs?
The cities with the most manufacturing associate openings in Maryland are Gaithersburg, Harmans, and Baltimore. Baltimore anchors the market with its large defense and food production facilities, while Frederick and the I-270 corridor attract biotech and pharmaceutical manufacturers drawn by proximity to federal research institutions, making even smaller suburban areas active hiring locations.
Are there remote manufacturing associate jobs in Maryland?
Yes, but they're rare. Manufacturing associate work is inherently hands-on and tied to a physical production floor, so most roles require on-site presence. About 0% of manufacturing associate openings tied to Maryland are remote or hybrid as of November 2026, and those tend to cover quality documentation, inventory coordination, or production scheduling rather than direct assembly or line work.
How can I get hired as a manufacturing associate in Maryland with little or no experience?
The most realistic entry path is applying directly to production technician trainee or manufacturing associate I postings at large Maryland facilities that run structured onboarding programs, including defense contractors and food manufacturers in the Baltimore region. Completing a short forklift certification or a manufacturing fundamentals certificate at a Maryland community college strengthens any application. Candidates from adjacent roles like warehouse associate, general laborer, or quality inspector frequently move into manufacturing associate positions without prior production floor experience.
Where can I find and apply to manufacturing associate jobs in Maryland?
You can find and apply to manufacturing associate jobs in Maryland on Migrate Mate, which lists current openings from employers hiring in the state right now. Search the listings, find the roles that match your background and location, and apply directly to the ones that fit.
See All 8 Manufacturing Associate Jobs in Maryland
Find roles in Maryland that match your experience and apply in just a few clicks.
Find Manufacturing Associate Jobs