Grand Rapids, MI · On-site
Mold Validation Engineer Locations: Grand Rapids, MI / Dexter, MI / Minneapolis, MN Role Summary ... Experience in regulated industry (Medical Device/Pharma) * Strong expertise in IQ/OQ/PQ, DOE, and ...
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Grand Rapids, MI · On-site
Mold Validation Engineer Locations: Grand Rapids, MI / Dexter, MI / Minneapolis, MN Role Summary ... Experience in regulated industry (Medical Device/Pharma) * Strong expertise in IQ/OQ/PQ, DOE, and ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
The Process Validation Engineer or Specialist supports validation of cGMP equipment, facilities ... A minimum of 1-4 years' related work experience in a pharma, biopharma, and/or biotech ...
The Process Validation Engineer or Specialist supports validation of cGMP equipment, facilities ... A minimum of 1-4 years' related work experience in a pharma, biopharma, and/or biotech ...
The Process Validation Engineer or Specialist supports validation of cGMP equipment, facilities ... A minimum of 1-4 years' related work experience in a pharma, biopharma, and/or biotech ...
The Process Validation Engineer or Specialist supports validation of cGMP equipment, facilities ... A minimum of 1-4 years' related work experience in a pharma, biopharma, and/or biotech ...
The Process Validation Engineer or Specialist supports validation of cGMP equipment, facilities ... A minimum of 1-4 years' related work experience in a pharma, biopharma, and/or biotech ...
The Process Validation Engineer or Specialist supports validation of cGMP equipment, facilities ... A minimum of 1-4 years' related work experience in a pharma, biopharma, and/or biotech ...
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
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
Grand Rapids, 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
Grand Rapids, 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
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
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
Grand Rapids, 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
Grand Rapids, 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
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
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
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
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
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
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
Grand Rapids, 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
Grand Rapids, 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
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
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
Riverview, MI · On-site
Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... Participates in and execute qualification and validation of equipment and processes Education ...
Riverview, MI · On-site
Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... Participates in and execute qualification and validation of equipment and processes Education ...
Riverview, MI · On-site
Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... Participates in and execute qualification and validation of equipment and processes Education ...
Riverview, MI · On-site
Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... Participates in and execute qualification and validation of equipment and processes Education ...
... validate outcomes with clients. Your ability to develop and sustain high-performing, diverse, and ... Aerospace Engineering, Automotive Engineering, Biomedical Engineering, Chemical Engineering ...
... validate outcomes with clients. Your ability to develop and sustain high-performing, diverse, and ... Aerospace Engineering, Automotive Engineering, Biomedical Engineering, Chemical Engineering ...
Kalamazoo, MI · On-site
$53 - $56/hr
... Pharma, Automotive) * 3-5 years supplier facing experience Additional responsibilities include ... Good knowledge of FMEA, validation programs and SPC processes * Good knowledge of manufacturing ...
Kalamazoo, MI · On-site
$53 - $56/hr
... Pharma, Automotive) * 3-5 years supplier facing experience Additional responsibilities include ... Good knowledge of FMEA, validation programs and SPC processes * Good knowledge of manufacturing ...
$19.69 - $24.09
2% of jobs
$24.09 - $28.49
6% of jobs
$28.49 - $32.89
13% of jobs
$34.27 is the 25th percentile. Wages below this are outliers.
$32.89 - $37.29
13% of jobs
$37.29 - $41.69
11% of jobs
The median wage is $43.89 / hr.
$41.69 - $46.09
12% of jobs
$46.09 - $50.49
9% of jobs
$53.89 is the 75th percentile. Wages above this are outliers.
$50.49 - $54.89
13% of jobs
$54.89 - $59.29
13% of jobs
$59.29 - $63.69
6% of jobs
$63.69 - $68.09
3% of jobs
$19
$45
$68
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.
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.
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.
Contractor
This job post has expired today. Applications are no longer accepted.
Hello,
I hope you’re doing well.
My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Mold Validation Engineer based in Grand Rapids, MI / Dexter, MI / Minneapolis, MN with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com
Job Title: Mold Validation Engineer
Locations: Grand Rapids, MI / Dexter, MI / Minneapolis, MN
Role Summary:
Responsible for executing injection mold validations (IQ/OQ/PQ) to ensure compliant, production-ready processes in a regulated (medical device) environment.
Key Responsibilities:
Qualifications:
Thanks & Regards,
Vyshnavi
Recruiter
Intellectt Inc
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999 - Ext: 225
Sourced by ZipRecruiter
51 - 200 Employees
Iselin, NJ, US
2018
