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Process Validation Engineer Jobs in Grand Rapids, MI

Actalent

Process Engineer

Zeeland, MI

$40 - $50/hr

Process Engineer - R&D Manufacturing This Process Engineer role sits within a research and ... Apply statistical analysis and validation techniques to assess process capability, identify ...

Celia Corporation

Process Engineer

Sparta, MI

Perform testing, experimentation, and validation of manufacturing processes and equipment ... Create engineering drawings, process flow diagrams, P&IDs, and project documentation. * Develop and ...

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All JobsProcess Validation Engineer JobsProcess Validation Engineer Jobs in Grand Rapids, MI

Process Validation Engineer information

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$7

$37

$66

How much do process validation engineer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for process validation engineer in Grand Rapids, MI is $37.97, according to ZipRecruiter salary data. Most workers in this role earn between $22.16 and $49.42 per hour, depending on experience, location, and employer.

What are some common challenges faced by process validation engineers during product scale-up?

Process Validation Engineers often encounter challenges when scaling up products from development to full-scale manufacturing. These can include ensuring process consistency, managing variations in equipment or raw materials, and troubleshooting unexpected deviations that may not have surfaced during small-scale trials. Effective communication with cross-functional teams—such as quality assurance, production, and R&D—is essential to quickly address issues and maintain compliance with regulatory requirements. Being proactive and detail-oriented helps navigate these complexities and ensures successful validation outcomes.

What is a process validation engineer?

Process Validation Engineers are professionals responsible for ensuring that manufacturing processes consistently produce products that meet predetermined quality standards. They design, execute, and document validation protocols to verify that equipment, systems, and processes operate effectively and efficiently. These engineers play a crucial role in regulated industries such as pharmaceuticals, biotechnology, and medical devices, where compliance with industry standards and regulatory requirements is essential. Their work helps to minimize risks, ensure product safety, and maintain regulatory compliance.

What is the difference between Process Validation Engineer vs Quality Assurance Engineer?

AspectProcess Validation EngineerQuality Assurance Engineer
Primary FocusValidating manufacturing processes to ensure product quality and complianceDeveloping and implementing quality systems and procedures to prevent defects
CertificationsGMP, ISO, Six Sigma often preferredISO, Six Sigma, CQE certifications common
Work EnvironmentManufacturing, pharmaceutical, biotech facilitiesQuality departments across various industries
Key ResponsibilitiesProcess validation, protocol development, troubleshootingAudits, quality audits, process improvements

While both roles aim to ensure product quality, the Process Validation Engineer primarily focuses on validating manufacturing processes, whereas the Quality Assurance Engineer oversees overall quality systems and compliance. Both roles often collaborate but serve distinct functions within the quality management framework.

What does a process validation engineer do?

A process validation engineer is responsible for developing, executing, and documenting validation protocols to ensure manufacturing processes meet quality and regulatory standards. They analyze process data, identify risks, and implement improvements using tools like statistical analysis and validation software. Their work helps ensure products are consistently safe, effective, and compliant with industry regulations.

Do process validation engineers make good money?

Process validation engineers typically earn competitive salaries that vary by industry, experience, and location. They often have specialized skills in quality assurance, regulatory compliance, and validation tools, which can lead to higher compensation levels. Overall, the role is considered well-paying within manufacturing, pharmaceutical, and biotech sectors.

What are the key skills and qualifications needed to thrive as a process validation engineer?

To thrive as a Process Validation Engineer, you need a solid background in engineering or life sciences, a thorough understanding of validation protocols, and knowledge of industry regulations such as GMP. Experience with validation software, statistical analysis tools, and familiarity with regulatory documentation systems are typically required. Strong analytical thinking, attention to detail, and effective communication skills help you resolve issues and coordinate cross-functional teams. These skills and qualities are essential to ensure processes are compliant, efficient, and produce high-quality, safe products.
What are popular job titles related to Process Validation Engineer jobs in Grand Rapids, MI? For Process Validation Engineer jobs in Grand Rapids, MI, the most frequently searched job titles are:
Process Validation Engineer jobs near you
Infographic showing various Process Validation Engineer job openings in Grand Rapids, MI as of August 2026, with employment types broken down into 71% Full Time, and 29% Contract. Highlights an 100% In-person job distribution, with an average salary of $78,982 per year, or $38 per hour.

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

Grand River Aseptic Manufacturing, Inc.

Grand Rapids, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago

Job description

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