Seattle, WA · On-site
... Engineering, and Regulatory teams * Support internal/external audits and regulatory inspections Required Qualifications: * 15+ years of validation experience in Pharma, Biotech, or Medical Device ...
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Seattle, WA · On-site
... Engineering, and Regulatory teams * Support internal/external audits and regulatory inspections Required Qualifications: * 15+ years of validation experience in Pharma, Biotech, or Medical Device ...
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Columbus, OH · On-site
Your Role The Validation Engineer supports system validation activities within regulated ... e. pharma, biotech). * Well-versed in manufacturing systems, including automation platforms ...
Columbus, OH · On-site
Your Role The Validation Engineer supports system validation activities within regulated ... e. pharma, biotech). * Well-versed in manufacturing systems, including automation platforms ...
Validation Engineer - (JP9979) Location: Thousand Oaks, CA. 91320 Employment Type: Contract ... Client is a special pharma company * Working on drug device and methods * Gain valuable experience ...
Validation Engineer - (JP9979) Location: Thousand Oaks, CA. 91320 Employment Type: Contract ... Client is a special pharma company * Working on drug device and methods * Gain valuable experience ...
$100K - $160K/yr
Your Role The Validation Engineer supports system validation activities within regulated ... e. pharma, biotech). * Well-versed in manufacturing systems, including automation platforms ...
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$100K - $160K/yr
Your Role The Validation Engineer supports system validation activities within regulated ... e. pharma, biotech). * Well-versed in manufacturing systems, including automation platforms ...
Your Role The Validation Engineer supports system validation activities within regulated ... pharma, biotech) Well-versed in manufacturing systems, including automation platforms, control ...
Your Role The Validation Engineer supports system validation activities within regulated ... pharma, biotech) Well-versed in manufacturing systems, including automation platforms, control ...
Position: Hybrid * The CSV Engineer will, as an individual contributor, identify and implement ... Prior experience leading projects in a Biotech/Pharma or biologics industry. * Strong attention to ...
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Position: Hybrid * The CSV Engineer will, as an individual contributor, identify and implement ... Prior experience leading projects in a Biotech/Pharma or biologics industry. * Strong attention to ...
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Boulder, CO · On-site
$110K - $131K/yr
SUMMARY The Sr. Cleaning Validation Engineer role supports all aspects of product changeover ... Represents Corden Pharma Colorado on Corden Corporate Cleaning Team and implements best practices ...
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Boulder, CO · On-site
$110K - $131K/yr
SUMMARY The Sr. Cleaning Validation Engineer role supports all aspects of product changeover ... Represents Corden Pharma Colorado on Corden Corporate Cleaning Team and implements best practices ...
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Irvine, CA · On-site
... or engineering within pharma, biopharma, medical device, or related industries Experience with equipment and process validation (DQ, IQ, OQ, PQ) Familiarity with cGMP, FDA, and ICH guidelines ...
Irvine, CA · On-site
... or engineering within pharma, biopharma, medical device, or related industries Experience with equipment and process validation (DQ, IQ, OQ, PQ) Familiarity with cGMP, FDA, and ICH guidelines ...
Validation Engineer II Location: Portsmouth, New Hampshire(Hybrid) The CSV Engineer will, as an ... Biotech/Pharma or biologics industry. 3) Strong attention to detail and ability to work ...
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Validation Engineer II Location: Portsmouth, New Hampshire(Hybrid) The CSV Engineer will, as an ... Biotech/Pharma or biologics industry. 3) Strong attention to detail and ability to work ...
Validation Engineer Responsibilities: * Support CSV activities for ELLA and Synergy Neo2 instrument ... Experience in biotech, pharma, plasma, or manufacturing laboratory environments * Prior experience ...
Validation Engineer Responsibilities: * Support CSV activities for ELLA and Synergy Neo2 instrument ... Experience in biotech, pharma, plasma, or manufacturing laboratory environments * Prior experience ...
Raleigh, NC · On-site
... Engineering, QC, and Regulatory teams to ensure all validation activities meet GMP, FDA, and internal quality standards. Key Responsibilities * Lead end-to-end validation activities for pharma ...
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Raleigh, NC · On-site
... Engineering, QC, and Regulatory teams to ensure all validation activities meet GMP, FDA, and internal quality standards. Key Responsibilities * Lead end-to-end validation activities for pharma ...
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Principal BioPharma Manufacturing Validation Engineer About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide ...
Principal BioPharma Manufacturing Validation Engineer About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide ...
Holbrook, MA · On-site
$33 - $43/hr
The CQV/Validation Engineer is responsible for supporting the activities required to implement the Holbrook site's validation plan in compliance with current industry and regulatory expectations.
Holbrook, MA · On-site
$33 - $43/hr
The CQV/Validation Engineer is responsible for supporting the activities required to implement the Holbrook site's validation plan in compliance with current industry and regulatory expectations.
PA · On-site
... pharma products to serve our patients. This is an exciting opportunity for anyone who excels at ... Reporting to the Senior Manager, Facilities, Engineering and Validation, the Senior Validation ...
PA · On-site
... pharma products to serve our patients. This is an exciting opportunity for anyone who excels at ... Reporting to the Senior Manager, Facilities, Engineering and Validation, the Senior Validation ...
... pharma products to serve our patients. This is an exciting opportunity for anyone who excels at ... engineering discipline or equivalent work experience. 5+ years of experience in validation in the ...
... pharma products to serve our patients. This is an exciting opportunity for anyone who excels at ... engineering discipline or equivalent work experience. 5+ years of experience in validation in the ...
Bedford, NH · On-site
The Validation Engineer IV performs an array of well-defined validation activities in support of ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...
Bedford, NH · On-site
The Validation Engineer IV performs an array of well-defined validation activities in support of ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...
The Validation Engineer IV performs an array of well-defined validation activities in support of ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...
The Validation Engineer IV performs an array of well-defined validation activities in support of ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...
Validation Engineer Location: Indianapolis / Bloomington, IN (100% Onsite) Duration: Long term Contract Interview Mode: Onsite (Local candidates preferred) Job Summary: We are seeking a Validation ...
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Validation Engineer Location: Indianapolis / Bloomington, IN (100% Onsite) Duration: Long term Contract Interview Mode: Onsite (Local candidates preferred) Job Summary: We are seeking a Validation ...
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Computer Systems Validation Engineer Location: Portsmouth, NH. Relocation assistance is available ... Biotech/Pharma/Medical Device/Medical or biologics industry experience required. * Ability to work ...
Computer Systems Validation Engineer Location: Portsmouth, NH. Relocation assistance is available ... Biotech/Pharma/Medical Device/Medical or biologics industry experience required. * Ability to work ...
Computer Systems Validation Engineer Location: Portsmouth, NH. Relocation assistance is available ... Biotech/Pharma/Medical Device/Medical or biologics industry experience required. * Ability to work ...
Computer Systems Validation Engineer Location: Portsmouth, NH. Relocation assistance is available ... Biotech/Pharma/Medical Device/Medical or biologics industry experience required. * Ability to work ...
$22.60 - $27.64
2% of jobs
$27.64 - $32.69
6% of jobs
$32.69 - $37.74
13% of jobs
$39.32 is the 25th percentile. Wages below this are outliers.
$37.74 - $42.79
13% of jobs
$42.79 - $47.84
11% of jobs
The median wage is $50.36 / hr.
$47.84 - $52.88
12% of jobs
$52.88 - $57.93
9% of jobs
$61.82 is the 75th percentile. Wages above this are outliers.
$57.93 - $62.98
13% of jobs
$62.98 - $68.03
13% of jobs
$68.03 - $73.08
6% of jobs
$73.08 - $78.13
3% of jobs
$22
$51
$78
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
Posted 13 days ago
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Job Title: Senior Validation Engineer / Validation Manager
Location: Near Seattle, WA (100% Onsite)
Duration: 6 Months Contract (High likelihood of extension or full-time conversion)
Job Summary:
We are seeking an experienced Senior Validation Engineer / Manager to serve as the Site Validation Subject Matter Expert (SME). This is a hands-on leadership role requiring both strategic oversight and execution across multiple validation disciplines. The ideal candidate will be capable of independently driving validation activities, ensuring regulatory compliance, and leading a small team in a fast-paced environment.
Key Responsibilities:
Required Qualifications:
Sourced by ZipRecruiter
51 - 200 Employees
Iselin, NJ, US
2018
