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Biotech Manufacturing Associate Jobs in Michigan

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Biotech Manufacturing Associate information

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$10

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How much do biotech manufacturing associate jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for biotech manufacturing associate in Michigan is $18.16, according to ZipRecruiter salary data. Most workers in this role earn between $14.23 and $20.34 per hour, depending on experience, location, and employer.

What are Biotech Manufacturing Associates?

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 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 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 role of a manufacturing associate?

A Biotech Manufacturing Associate is responsible for performing tasks related to the production of biopharmaceutical products, including operating equipment, following strict safety and quality protocols, and documenting processes. They work in controlled environments and often require knowledge of Good Manufacturing Practices (GMP) and attention to detail. The role supports ensuring the efficient and compliant manufacturing of biotech products.

What are 5 careers in biotechnology?

Biotech manufacturing associates work in roles such as research scientist, quality control analyst, process development engineer, regulatory affairs specialist, and bioprocess technician. These careers involve working with laboratory equipment, manufacturing processes, and compliance standards in a biotech production environment.

What is the highest paying job in biotech?

In biotech manufacturing, senior roles such as Biotech Manufacturing Director or Vice President of Manufacturing tend to be the highest paying positions, often earning six-figure salaries. These roles require extensive experience, leadership skills, and knowledge of regulatory compliance and process optimization.

What are the key skills and qualifications needed to thrive as a Biotech Manufacturing Associate, and why are they important?

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.

How to get into biotech sales with no experience?

Biotech sales roles typically require knowledge of the industry and strong communication skills. To enter with no experience, candidates can pursue relevant certifications, such as in biology or sales, and gain familiarity with biotech products through online courses or networking. Entry-level positions often value transferable skills like customer service or technical aptitude, and internships or entry-level roles can provide valuable industry exposure.
What are popular job titles related to Biotech Manufacturing Associate jobs in Michigan? For Biotech Manufacturing Associate jobs in Michigan, the most frequently searched job titles are:
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What cities in Michigan are hiring for Biotech Manufacturing Associate jobs? Cities in Michigan with the most Biotech Manufacturing Associate job openings:
Infographic showing various Biotech Manufacturing Associate job openings in Michigan as of June 2026, with employment types broken down into 90% Full Time, 5% Part Time, 3% Contract, and 2% Nights. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $37,776 per year, or $18.2 per hour.
Assistant Manufacturing Associate

Assistant Manufacturing Associate

Emergent Biosolutions

Lansing, MI • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

 Preparedness today, safer tomorrow.

 Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world.  Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.

I.    JOB SUMMARY 

Execute tasks per CGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing training program. Actively incorporate the Shared Values set out by Emergent BioSolutions while performing day to day activities.

II.    ESSENTIAL FUNCTIONS
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.

General

  • Complete training and demonstrate competency on Assistant Manufacturing Associate qualification blocks in accordance with the training progression pathway
  • Execute and document procedural steps in compliance with CGMP standards, clean room behavior and Standard Operating Procedures
  • Comply with all applicable rules and regulations of Emergent and the Pharmaceutical / Biotech industry. This includes FDA regulations such as CGMP, GDP, EH&S regulations, and company regulations such as the employee handbook
  • Maintain state of facility environmental control including preparation of defined concentrations of cleaning solutions, daily, monthly, quarterly, and annual cleaning of manufacturing areas per Standard Operating Procedures
  • Review all documentation for accuracy and completeness of process signature steps as each step is completed. Perform “real time” review of all documentation (BPRs, forms, logs, etc.) in the area throughout the shift
  • Stock gowning and consumable supplies in the controlled areas maintaining Kanban inventory control of manufacturing materials


Lean Concepts

  • Follow standard work guidelines
  • Collaborate with applicable Integrated Process Teams to participate in continuous improvement and learn new Lean concepts
  • Actively participate in Kanban and 6S programs


Inspection and Packaging

  • Successfully complete inspector qualification requirements to identify, classify and cull product defects, including those defects which could impact patient safety (inspector qualification)
  • Independently operate labeling equipment with minimal supervision (Qualification)
  • Apply traceability and expiration information to secondary packaging components such as cartons and cases. Confirm suitability of secondary packaging components during printing processes through 100% inspection (carton printing, case creation)
  • Package product in secondary and final packaging components while performing 100% reconciliation of product rejects (Packaging)
  • Complete ambient tracking documentation
  • Execute material issuance and confirmation of process steps using specific SAP modules

Building 55 Operations – Prep

  • Execute material issuance and confirmation of process steps using specific SAP modules
  • Precisely weigh and hydrate media components
  • Load, run and unload parts washer and sterilization/decontamination using specific validated load configurations per Standard Operating Procedures
  • Assemble clean process glassware configurations and portable tanks utilizing sanitary connections, quick connects and stainless-steel ancillary parts
  • Perform Cleaning (COP/CIP) and Sterilizing (SOP/SIP) of production vessels through interface with automated control system (DeltaV)
  • Prepare and dispense intermediate materials. 


Behavior/Cultural Responsibilities

  • Standing Shoulder to Shoulder (no matter what):
    • working collaboratively with others, communicating, and managing conflict effectively
  • Break Through Thinking:
    • cultivating innovation and nimble learning
  • Own It Always:
    • ensuring accountability, and making good and timely decisions
  • Compete Where It Counts:
    • demonstrating courage and focusing on customers
  • Integrity and Instills Trust:
    • gaining the confidence and trust of others through honesty, integrity and authenticity
  • Manages Complexity:
    • making sense of complex, high quantity, and sometimes contradictory information to effectively solve problem
  • Plans and Aligns:
    • plan and prioritize work to meet commitments aligned with organizational goals
  • Drives Engagement:
    • creating a climate where people are motivated to do their best to help the organization achieve its objectives
      The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time which reflects management’s assignment of essential functions. 


III. MINIMUM EDUCATION, EXPERIENCE, SKILLS

  • HS Diploma
  • 0–1-year experience working in a CGMP environment
  • Knowledge of CGMP and CFR requirements preferred but not required
  • Personal Competencies: Self-awareness, Integrity, Team Player, Creative, and Culturally aware

If the hiring manager expresses an interest in interviewing you for the open position, you must discuss your interest in the open position with your current manager prior to an interview being scheduled.

U.S. Base Pay Ranges and Benefits Information

The estimated annual base salary as a new hire for this position ranges from $34,000 to $41,200. Individual base pay depends on various factors such as applicant’s education, experience, skills, and abilities, as well as internal equity and alignment with market data.  The salary may also be adjusted based on applicant’s geographic location.  Certain roles are eligible for additional incentive compensation, including merit increases, annual bonus, [and/or long-term incentives in the form of stock options.]

Additionally, Emergent offers a comprehensive benefits package*.  Information regarding additional benefits can be found here:  https://www.emergentbiosolutions.com/careers/life-at-emergent

(*Eligibility for benefits is governed by the applicable plan documents and policies).

If you are selected for an interview, please feel welcome to speak to a Human Resources Partner about our compensation philosophy and available benefits.