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Biotech Manufacturing Jobs (NOW HIRING)

Integrated Resources INC

Process Associate

Andover, MA · On-site

Required a Manufacturing Process Technician in a large scale biotech manufacturing facility This position is a temporary contract working on a 12 hour shift (6am - 6pm.) Includes some weekend work ...

Eurofins

Mechatronics Engineer

Louisville, KY · On-site

Fast-paced biotech manufacturing environment operating multiple shifts * Opportunity to work on cutting-edge robotic automation systems for DNA/RNA synthesis * Collaborative and innovation-driven ...

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How much do biotech manufacturing jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for biotech manufacturing in the United States is $20.84, 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 the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

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

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.
More about Biotech Manufacturing jobs
What cities are hiring for Biotech Manufacturing jobs? Cities with the most Biotech Manufacturing job openings:
What are the most commonly searched types of Biotech Manufacturing jobs? The most popular types of Biotech Manufacturing jobs are:
What states have the most Biotech Manufacturing jobs? States with the most job openings for Biotech Manufacturing jobs include:
What job categories do people searching Biotech Manufacturing jobs look for? The top searched job categories for Biotech Manufacturing jobs are:
Biotech Manufacturing jobs near you
Infographic showing various Biotech Manufacturing job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 92% Full Time, 1% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $43,341 per year, or $20.8 per hour.
Process Validation Engineer or Specialist I, II, III, or Sr.

Process Validation Engineer or Specialist I, II, III, or Sr.

Grand River Aseptic Manufacturing

Grand Rapids, MI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago

Job description

Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!
Overview of this Position:
The Process Validation Engineer or Specialist supports validation of cGMP equipment, facilities, and processes. These duties will include but are not limited to: validation of manufacturing processes and production equipment.
Non-Negotiable Requirements:
  • Completion of a bachelor's degree in Engineering is required for the Engineer role. Completion of a bachelor's degree in life sciences or another related field is required for the Specialist role.
  • A minimum of 1-4 years' related work experience in a pharma, biopharma, and/or biotech manufacturing environment is required for a level I.
  • A minimum of 3-5 years' related work experience in a pharma, biopharma, and/or biotech manufacturing environment is required for a level II.
  • A minimum of 4-6 years' related work experience in a pharma, biopharma, and/or biotech manufacturing environment is required for a level III.
  • Senior level - 6 plus years of pharmaceutical industry experience or equivalent combination of education and experience required (4 years of experience with a master's degree in engineering or life sciences, or 2 years of experience with a PhD in engineering or life sciences).
  • Proficient computer skills in Microsoft Word, Excel, and Outlook.
  • Demonstrated project management and leadership skills.
  • Must be open to working in and supporting a 24/7 manufacturing environment.
  • Work is occasionally performed in a cleanroom environment as required to support process validation activities.

Preferred Requirements:
  • Knowledge of cGMPs for API facilities, pharmaceutical manufacturing processes, clean rooms, utility systems and packaging operations.
  • Knowledge of GAMP5, ISPE Baseline Guides for Commissioning and Qualification, Annex 1 and FDA process validation guidance preferred.

Responsibilities Include (but are not limited to):
  • Assist with maintaining and revising validation procedures.
  • Establish and maintain good practices with regards to processes and/or internal conditions leading to an aseptic environment.
  • Establish and execute programs covering manufacturing processes, equipment, and cleaning.
  • Assure that all validation is performed to conform to GRAM's and cGMP requirements.
  • Provide validation support to internal customers such as Technical Services, Quality Control, Manufacturing, and other users of validation services.
  • Provide validation support to external customers and attend client meetings.
  • Demonstrate knowledge of GRAM's tech transfer process and provide professional interactions with clients during tech transfer activities.
  • Write, review, and execute protocols.
  • Write, review, and execute studies for process improvement and scale up projects.
  • Provide technical support to Manufacturing - troubleshooting and resolving process related issues.
  • Proactively and regularly communicate with the project team to update on validation status.
  • Identify process improvement opportunities and equipment needs for manufacturing/packaging.
  • Develop and execute Deviations and CAPAs based on validation changes.
  • Maintains equipment logbooks and other forms for document use, proper cleaning, and sterilization.
  • Support Agency, customer, and vendor audits as needed.
Full job description available during formal interview process.
What Sets GRAM Apart from Other Employers:
BENEFITS starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PAID TIME OFF: You choose how to use this time for your vacation, sick, or mental health needs! PTO: Full-time employees accrue up to 104 hours of paid time off per calendar year, with this amount being prorated your first year. WELLNESS TIME OFF (WTO): In addition to PTO, employees earn 1 hour of wellness time off for every 30 hours worked, to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
PAY: Depends on Experience and is discussed during the interview process.
If you meet the required criteria listed above, GRAM welcomes you to apply today!

Apply