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Biotech Manufacturing Associate Jobs in Baltimore, MD

... manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to ... Associates / equivalency (60 or more college credit hours) in related field preferred.

... manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to ... Associate degree/equivalency (60+ college credit hours) plus 2 years of relevant experience in at ...

Quality Engineer

Baltimore, MD · On-site

$71K - $92K/yr

... Manufacturing, Mechatronics) or equivalent experience, OR an associate's degree with significant ... Biotech, Diagnostic, Cosmetic, and Cannabis industries for over 70 years. Our success is built on ...

Quality Engineer

Baltimore, MD · On-site

$85 - $115/hr

... Manufacturing, Mechatronics) or equivalent experience, OR an associate's degree with significant ... Biotech, Diagnostic, Cosmetic, and Cannabis industries for over 70 years. Our success is built on ...

... manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to ... Associate degree/equivalency (60+ college credit hours) plus 2 years of relevant experience in at ...

Strategic Sourcing Manager

Baltimore, MD · On-site

$128K - $165K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Reporting to the Associate Director of Strategic Sourcing, you will lead the global sourcing ...

Showing results 41-49

Biotech Manufacturing Associate information

See Baltimore, MD salary details

$12

$20

$33

How much do biotech manufacturing associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for biotech manufacturing associate in Baltimore, MD is $20.70, according to ZipRecruiter salary data. Most workers in this role earn between $16.25 and $23.17 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are popular job titles related to Biotech Manufacturing Associate jobs in Baltimore, MD?

For Biotech Manufacturing Associate jobs in Baltimore, MD, the most frequently searched job titles are:

What job categories do people searching Biotech Manufacturing Associate jobs in Baltimore, MD look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Baltimore, MD are:

What cities near Baltimore, MD are hiring for Biotech Manufacturing Associate jobs?

Cities near Baltimore, MD with the most Biotech Manufacturing Associate job openings:

Infographic showing various Biotech Manufacturing Associate job openings in Baltimore, MD as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $43,066 per year, or $20.7 per hour.

Senior Engineering Technician

Catalent Pharma Solutions

Harmans, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

62nd of 86 rated pharmaceutical


Job description

Senior Engineering Technician

Position Summary:

  • Work Schedule: 7pm-7am, Thursday - Saturday and every other Wednesday

  • 100% on-site

Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD-just minutes from BWI Airport-features EMA and FDA-approved manufacturing suites, fill/finish capabilities, labs, and warehousing to support Phase 3 through commercial production of advanced therapies, including AAV and other viral vector-based products.

We are currently seeking a Senior Engineering Technician to provide technical support to GMP manufacturing/testing operations for Phase I/II bulk, Phase III and finished biologics in our multi-product facility in Harmans, MD.

The Senior Engineering Technician will be responsible for the overall facilities including executing the preventative maintenance, repairs, and installation of process equipment.

The Engineering Technician will report to the Supervisor, Engineering Technician.

The Role:

  • Analyze and develop engineering solutions to maintenance, continuous improvement, quality and safety initiatives, and failure investigations for manufacturing equipment/systems and instrumentation.

  • Work independently on assigned projects and collaboratively in a multi-functional team environment supporting day-to-day manufacturing schedules and operations.

  • Will engage in hands-on work troubleshooting and lead the repairing of bioprocess equipment. Equipment includes fermenters, bioreactors, centrifuges, tangential flow filtration systems, chromatography systems, incubators, BSCs, controlled temperature units, and laboratory equipment.

  • Work within Computerized Maintenance Management Systems (CMMS) to complete preventive and responsive maintenance work orders.

  • Work within manual and electronic engineering documentation systems to maintain engineering drawings and equipment history files.

  • Work with subcontractors and vendors as needed on equipment preventive maintenance, calibrations, and repairs.

  • Assist in maintaining PM programs for the bioprocess equipment and instrumentation. This includes generating PM SOPs/records, establishing PM frequencies, specifying spare parts and recommending/maintaining inventory levels.

  • Work with equipment vendors and Catalent's purchasing department to quote/purchase/procure equipment parts and instrumentation.

  • Develop job aids, work instructions, and troubleshooting guides for performing routine maintenance and repairs. Will be responsible for generating and updating documentation throughout the life cycle of the equipment.

  • Work in cleanrooms that requires full gowning (tyvek coverall, gloves, hair cover, shoe covers.)

  • Other duties as assigned

The Candidate:

  • High School Diploma required; Associates/Bachelors degree preferred.

  • A minimum of 5 years of related work experience, specifically in GMP / Bio-Pharma maintenance and/or engineering experience; Clean room experience or experience in a similar GMP / FDA regulated industry.

  • Must demonstrate abilities in mechanical/electrical repairs and maintenance.

  • Automation and controls operation, repairs and maintenance are preferred.

  • Requires basic math and computer skills (eg. Word and Excel) and must be able to clearly communicate (verbal, written).

  • Must have the ability to lift/carry 40 lbs. and to work on ladders/step stools.

  • Requires working extended periods on his/her feet in a manufacturing environment and must follow all Catalent's Safety and Quality procedures and practices.

The anticipated hourly rate for this position in Maryland is $38.46 - $43.26 plus shift differential andannual bonus, when eligible. 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

  • 152 hours of paid time off annually + 8 paid holidays

  • Competitive salary with yearly bonus potential

  • Community engagement and green initiatives

  • Generous 401K match and Paid Time Off accrual

  • 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.


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About Catalent

Sourced by ZipRecruiter

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.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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