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Pharma Validation Engineer Jobs in Michigan (NOW HIRING)

Deloitte

System Test and Validation Lead

Midland, MI · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Deloitte

System Test and Validation Lead

Detroit, MI · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Deloitte

System Test and Validation Lead

Midland, MI · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Deloitte

System Test and Validation Lead

Detroit, MI · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Deloitte

System Test and Validation Lead

Midland, MI · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Deloitte

System Test and Validation Lead

Detroit, MI · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

TriMas Corporation

Quality Engineer

Clinton, MI · On-site

$71K - $91K/yr

... client pharma or device phase of development and assess device application Coordinate quality ... Validation protocol approval Completion and approval of risk assessments support NCRs, CCRs and ...

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How much do pharma validation engineer jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for pharma validation engineer in Michigan is $45.32, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $55.10 per hour, depending on experience, location, and employer.

What is a pharma validation engineer?

A Pharma Validation Engineer ensures that manufacturing processes, equipment, and systems in the pharmaceutical industry comply with regulatory standards such as FDA, GMP, and ISO. They develop validation protocols, conduct tests, analyze data, and generate reports to ensure consistent product quality and safety. Their role is critical in minimizing risks, maintaining compliance, and supporting regulatory audits.

What does a pharma validation engineer do?

A typical day for a Pharma Validation Engineer involves developing and executing validation protocols for manufacturing equipment, laboratory instruments, or processes, ensuring they meet all regulatory and quality standards. You might collaborate closely with QA teams, production staff, and external vendors to troubleshoot issues, review data, and document results for compliance audits. Preparing detailed reports, participating in cross-functional meetings, and staying updated with current regulatory changes are also common responsibilities. This dynamic environment offers opportunities to work on diverse projects and continually expand your technical expertise while supporting product safety and efficacy.

What skills and qualifications are needed to be a pharma validation engineer?

To thrive as a Pharma Validation Engineer, you need a solid background in engineering or life sciences, with expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and Good Manufacturing Practices (GMP). Experience with validation software (like ValGenesis or MasterControl), statistical analysis tools, and relevant certifications (such as Six Sigma or ISPE) is highly valued. Strong attention to detail, project management abilities, and effective communication skills are crucial for this role. These competencies ensure validation activities meet strict regulatory standards, support product quality, and facilitate seamless cross-functional collaboration in the pharmaceutical industry.

What are the most commonly searched types of Pharma Validation Engineer jobs in Michigan?

The most popular types of Pharma Validation Engineer jobs in Michigan are:

What are popular job titles related to Pharma Validation Engineer jobs in Michigan?

For Pharma Validation Engineer jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Pharma Validation Engineer jobs in Michigan look for?

The top searched job categories for Pharma Validation Engineer jobs in Michigan are:

Pharma Validation Engineer jobs near you
Infographic showing various Pharma Validation Engineer job openings in Michigan as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $94,265 per year, or $45.3 per hour.

Sterility Assurance Validation Engineer/Specialist I/II/III

Grand Rapids, MI • On-site

Grand River Aseptic Manufacturing
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Grand River Aseptic Manufacturingexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Job description

Sterility Assurance Validation Engineer/Specialist I/II/III
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 Sterility Assurance Validation Engineer/Specialist I/II/III is responsible for supporting validation of cGMP equipment, facilities and processes as it relates to sterility assurance. These duties will include, but are not limited to validation of autoclaves, depyrogenation equipment, critical utilities, cleaning, production equipment, and manufacturing processes (aseptic process simulation, decontamination, etc).
Non-Negotiable Requirements:
  • For Sterility Assurance Validation Engineer/Specialist I: Up to 3 years' related work experience in a pharma, biopharma, and/or biotech manufacturing environment
  • For Sterility Assurance Validation Engineer/Specialist II: 3 to 5 years' related work experience in a pharma, biopharma, and/or biotech manufacturing environment.
  • For Sterility Assurance Validation Engineer/Specialist III: More than 5 years' related work experience in a pharma, biopharma, and/or biotech manufacturing environment.
  • Bachelor's degree in Engineering is required for the Engineer role. Bachelor's degree in life sciences or other related field is required for the Specialist role.
  • Proficient computer skills in Microsoft Word, Excel, and Outlook.
  • Must be open to working onsite and supporting a 24/7 manufacturing environment.
  • Work is occasionally performed in a cleanroom environment as required to support sterility assurance validation activities.

Preferred Requirements:
  • Knowledge of cGMPs for API facilities, pharmaceutical manufacturing processes (primarily filling activities, but drug product/substance knowledge is beneficial as well), 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):
  • Support and maintain sterility assurance strategies, policies, and procedures applicable to all sterile processing facilities at GRAM.
  • Establish and maintain good practices with regards to processes and/or internal conditions leading to an aseptic environment.
  • Assure that all validation is performed to conform to GRAM's and cGMP requirements.
  • Provide sterility assurance support to internal customers such as Technical Services, Quality Control, Manufacturing and other users of validation services.
  • Support validation and requalification of equipment and systems as related to sterilization.
  • Write, review, and execute studies for sterilization processes, aseptic processing simulations, and cleaning.
  • Maintains equipment logbooks and other forms to document use, proper cleaning and sterilization.
  • Open to a flexible and fluid work environment. Work on any assignment as directed and flexibility to support limited multi-shift operations, training and testing.
  • Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practice.
  • 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!

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