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Biotech Manufacturing Associate Jobs in Delaware

$15.50 - $21.25/hr

In this role, the Associate Director ensures equipment reliability, safe work practices, and ... biotech manufacturing or equivalent military experience At least three (3) years in a supervisory ...

OR Associate's degree with four (4) years of relevant leadership experience within a manufacturing environment or military service or three (3) years' experience in a direct GMP, biotechnology ...

OR Associate's degree with four (4) years of relevant leadership experience within a manufacturing environment or military service or three (3) years' experience in a direct GMP, biotechnology ...

... biotechnology manufacturing setting with demonstrated leadership skillsOR Associate's degree with four (4) years of relevant leadership experience within a manufacturing environment or military ...

Lab Tech - I (Associate)

Millsboro, DE · On-site

$41K - $46K/yr

Responsibilities Join a Manufacturing Operations team responsible for producing high-quality biotechnology products in a regulated manufacturing environment. Team members work with a Safety First ...

Associate Director, Facilities Operations & Integrated Services Wilmington Biologics Site Position ... biotechnology, healthcare, or regulated manufacturing. * 5+ years of leadership experience managing ...

Associate Director, Facilities Operations & Integrated Services Wilmington Biologics Site Position ... biotechnology, healthcare, or regulated manufacturing. * 5+ years of leadership experience managing ...

QC Microbiology Scientist

Middletown, DE · On-site

$24 - $31.50/hr

Mentor and train QC Analysts and Associates on microbiological methods and best practices. * Other ... biotechnology environment; OR * Master's degree with 3+ years or PhD with 1+ years of relevant QC ...

QC Microbiology Scientist

Middletown, DE · On-site

$24 - $31.50/hr

Mentor and train QC Analysts and Associates on microbiological methods and best practices. * Other ... biotechnology environment; OR * Master's degree with 3+ years or PhD with 1+ years of relevant QC ...

QC Microbiology Scientist

Middletown, DE · On-site

$24 - $31.50/hr

Mentor and train QC Analysts and Associates on microbiological methods and best practices. * Other ... biotechnology environment; OR * Master's degree with 3+ years or PhD with 1+ years of relevant QC ...

Strategic Sourcing Manager

Wilmington, DE · On-site

$125K - $162K/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 ...

... safe manufacture of new drug therapies. When you join our family, you will have a significant ... S.) or Associates Degree in Biology or related discipline required. * 0-2 years of experience in ...

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Biotech Manufacturing Associate information

See Delaware salary details

$12

$20

$33

How much do biotech manufacturing associate jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for biotech manufacturing associate in Delaware is $20.86, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 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 Delaware?

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

What job categories do people searching Biotech Manufacturing Associate jobs in Delaware look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Delaware are:

What cities in Delaware are hiring for Biotech Manufacturing Associate jobs?

Cities in Delaware with the most Biotech Manufacturing Associate job openings:

Infographic showing various Biotech Manufacturing Associate job openings in Delaware as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $43,379 per year, or $20.9 per hour.

Associate Director, Maintenance (Hiring Our Heroes Corporate Fellow)

On-site


Merck & Co.
Pharmaceutical Product Wholesalers • 10K+ employees

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by parents


$15.50 - $21.25/hr

Part-time

Posted 17 days ago


Job description

Job Requirements This posting is for the Hiring Our Heroes, Corporate Fellowship 2026 - Cohort 3. Candidates must be transitioning service member fellows who will complete the program within the last 180 days of transition from military service. The fellowship will be 12 weeks long. - The Associate Director, Maintenance provides operational leadership and technical oversight of maintenance activities for the sterile product manufacturing site. In this role, the Associate Director ensures equipment reliability, safe work practices, and regulatory compliance while supporting production needs and continuous improvement initiatives. In addition, this role will support the development and execution of the site's Integrated Facilities Management (IFM) strategy and will actively participate throughout the project life cycle in Factory Acceptance Tests (FATs) for utilities, facilities, and process equipment to ensure maintainability, reliability, and lifecycle considerations are incorporated into equipment and system design. Key Responsibilities - Capital Projects & Equipment Lifecycle Support - Participate as the maintenance representative in major capital project design, execution, and start-up, with primary emphasis on start-up readiness-ensuring maintenance strategies, CMMS build-out, spare parts, diagnostic capabilities, SOPs, training, and reliable systems turnover are fully in place prior to qualification and initial manufacturing-along with participation in future capital equipment installations and small- to mid-scale upgrade projects, coordinating contractors and internal resources under engineering or project management leadership. - Attend and actively participate in utility, facility, and process equipment Factory Acceptance Tests (FATs) throughout the project life cycle. - Provide maintenance and reliability input during FATs to ensure: Maintainability and accessibility are considered Spare parts strategies are optimized Standardization, diagnostics, and serviceability are aligned with site practices - Support equipment turnover to maintenance, including documentation review, CMMS asset setup, and maintenance strategy development. Maintenance Operations & Leadership Oversee day-to-day maintenance operations for assigned production areas, including preventive, predictive, and corrective maintenance activities. Supervise, coach, and develop maintenance staff; ensure adherence to safe work practices and OSHA/GMP requirements. Coordinate maintenance priorities with production, quality, and engineering teams to minimize downtime and support production schedules. Ensure accurate and timely execution and documentation of maintenance activities within the CMMS. Maintain key maintenance performance metrics for assigned areas and communicate operational status to site leadership. Integrated Facilities Management (IFM) Support Support the development, deployment, and ongoing execution of the site IFM strategy in alignment with site leadership objectives. Serve as a key maintenance interface with IFM service providers, ensuring alignment with maintenance standards, safety expectations, and GMP requirements. Participate in defining maintenance scopes of work, service-level expectations, and performance metrics related to IFM services. Support monitoring of IFM performance and identification of continuous improvement opportunities at the operational level. Reliability & Continuous Improvement Implement and sustain preventive and predictive maintenance tasks as defined by site strategy and reliability programs. Support troubleshooting and root-cause analysis for major equipment or system failures; coordinate corrective actions with engineering and subject-matter experts. Apply Lean and continuous improvement principles at the area or equipment level to reduce downtime and improve maintenance efficiency. Support reliability improvement initiatives by providing operational insights on equipment performance and maintainability. Compliance & Regulatory Readiness Ensure all maintenance activities comply with GMP requirements, safety regulations, and site procedures. Prepare, maintain, and provide maintenance records and documentation to support internal reviews and regulatory inspections. Support inspection readiness activities by ensuring assigned areas meet compliance and documentation expectations. Qualifications Required Bachelor's degree in Engineering, Facilities Management, or a related technical field with Seven (7) years of maintenance experience in pharmaceutical, biotech manufacturing or equivalent military experience At least three (3) years in a supervisory or team-lead role with responsibility for maintenance technicians or supervisors. Practical experience with CMMS, preventive maintenance, and predictive maintenance programs. Familiarity with GMP, safety regulations, and industry standards applicable to sterile manufacturing. Proven experience troubleshooting process equipment and coordinating corrective actions with cross-functional teams. Working knowledge of Lean principles or continuous improvement methods. Strong communication skills and ability to collaborate across production, quality, engineering, and facilities teams. Preferred Experience with potent compound manufacturing Experience supporting or interfacing with Integrated Facilities Management (IFM) organizations. Experience participating in or supporting FATs, SATs, and equipment qualification activities. Exposure to predictive maintenance technologies (vibration analysis, ultrasound, thermography) or coordination with Predictive Maintenance (PdM) service providers. Demonstrated ability to develop, coach, and retain maintenance technicians. - Eligibility Requirements: Must be an active participant in the current cohort of the Hiring Our Heroes (HOH) Corporate Fellowship Program. Candidates must meet all eligibility criteria as defined by the Hiring Our Heroes program. Please ensure you are registered with the HOH program to be considered. - US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts This is an unpaid, 12-week training fellowship hosted by our company, aligned with DoD SkillBridge guidelines. This is not an offer of employment. This opportunity is exclusively for active participants in the Hiring Our Heroes (HOH) Corporate Fellowship Program. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance - Salary: . Date posted: 08/21/2026


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