Validation Engineer
Glendale, CA · On-site
JSat Automation is hiring a full time Validation Engineer with Pharma Industry experience. The Validation Engineer will be responsible for the following. * Develop, approve, and execute process ...
Glendale, CA · On-site
JSat Automation is hiring a full time Validation Engineer with Pharma Industry experience. The Validation Engineer will be responsible for the following. * Develop, approve, and execute process ...
Glendale, CA · On-site
JSat Automation is hiring a full time Validation Engineer with Pharma Industry experience. The Validation Engineer will be responsible for the following. * Develop, approve, and execute process ...
Certifications related to GMP compliance, quality systems, or validation preferred. * 1-3+ years of experience in validation engineering or a closely related field in a cGMP-regulated pharma or ...
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Certifications related to GMP compliance, quality systems, or validation preferred. * 1-3+ years of experience in validation engineering or a closely related field in a cGMP-regulated pharma or ...
San Jose, CA · On-site
$144K - $191K/yr
Hi, My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Platform Hardware Validation Engineer right now. Please send me your updated ...
New
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San Jose, CA · On-site
$144K - $191K/yr
Hi, My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Platform Hardware Validation Engineer right now. Please send me your updated ...
New
San Francisco, CA · On-site +1
It provides process engineering, process design, and commissioning - qualification - validation ... Knowledge of the local pharma market * Ability to lead and or assist in project execution Education ...
San Francisco, CA · On-site +1
It provides process engineering, process design, and commissioning - qualification - validation ... Knowledge of the local pharma market * Ability to lead and or assist in project execution Education ...
Los Angeles, CA · On-site +1
It provides process engineering, process design, and commissioning - qualification - validation ... Knowledge of the local pharma market * Ability to lead and or assist in project execution Education ...
Los Angeles, CA · On-site +1
It provides process engineering, process design, and commissioning - qualification - validation ... Knowledge of the local pharma market * Ability to lead and or assist in project execution Education ...
Redwood City, CA · On-site
... regulated pharma environments. Responsibilities : • Validating Veeva platforms within a ... CSV Engineer • Ensuring compliance with validation and regulatory standards Qualifications
Redwood City, CA · On-site
... regulated pharma environments. Responsibilities : • Validating Veeva platforms within a ... CSV Engineer • Ensuring compliance with validation and regulatory standards Qualifications
Minimum of two years' experience in Validation or equipment qualification is desired. * Ability to make sound decisions about scheduling and managing of priorities. * Flexibility in problem solving ...
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Minimum of two years' experience in Validation or equipment qualification is desired. * Ability to make sound decisions about scheduling and managing of priorities. * Flexibility in problem solving ...
Minimum of two years' experience in Validation or equipment qualification is desired. * Ability to make sound decisions about scheduling and managing of priorities. * Flexibility in problem solving ...
Quick apply
Minimum of two years' experience in Validation or equipment qualification is desired. * Ability to make sound decisions about scheduling and managing of priorities. * Flexibility in problem solving ...
Minimum of two years' experience in Validation or equipment qualification is desired. * Ability to make sound decisions about scheduling and managing of priorities. * Flexibility in problem solving ...
Quick apply
Minimum of two years' experience in Validation or equipment qualification is desired. * Ability to make sound decisions about scheduling and managing of priorities. * Flexibility in problem solving ...
They are seeking a Pharma Applications Engineer responsible for leading the development and ... validated systems and FDA 21 CFR Part 11 compliance documentation. • Familiarity with ...
They are seeking a Pharma Applications Engineer responsible for leading the development and ... validated systems and FDA 21 CFR Part 11 compliance documentation. • Familiarity with ...
$140K - $180K/yr
About This Role Varda is seeking a Pharma Applications Engineer to join our team. In this role, you ... Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
$140K - $180K/yr
About This Role Varda is seeking a Pharma Applications Engineer to join our team. In this role, you ... Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable ...
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable ...
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable ...
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable ...
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable ...
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable ...
About This Role Varda is seeking a Pharma Applications Engineer to join our team. In this role, you ... Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
About This Role Varda is seeking a Pharma Applications Engineer to join our team. In this role, you ... Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
About This Role Varda is seeking a Pharma Applications Engineer to join our team. In this role, you ... Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
About This Role Varda is seeking a Pharma Applications Engineer to join our team. In this role, you ... Experience with GxP-validated systems and FDA 21 CFR Part 11 compliance documentation.
* Validate ML-Coprocessor, display SOC, Mixed Signal SOC, and IP. * Define validation strategy and test plans for new IP blocks, aligning with RTL, architecture, FW. * Develop silicon validation ...
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* Validate ML-Coprocessor, display SOC, Mixed Signal SOC, and IP. * Define validation strategy and test plans for new IP blocks, aligning with RTL, architecture, FW. * Develop silicon validation ...
Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in ... pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of ...
Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in ... pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of ...
Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in ... pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of ...
Its services include Engineering, Project Management, and Validation. MMR Consulting has offices in ... pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of ...
Its services include Engineering, Project Management, and Validation. MMRConsulting ... pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of ...
Its services include Engineering, Project Management, and Validation. MMRConsulting ... pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of ...
$22.30 - $27.28
2% of jobs
$27.28 - $32.26
6% of jobs
$32.26 - $37.25
13% of jobs
$38.80 is the 25th percentile. Wages below this are outliers.
$37.25 - $42.23
13% of jobs
$42.23 - $47.21
11% of jobs
The median wage is $49.70 / hr.
$47.21 - $52.19
12% of jobs
$52.19 - $57.17
9% of jobs
$61.01 is the 75th percentile. Wages above this are outliers.
$57.17 - $62.16
13% of jobs
$62.16 - $67.14
13% of jobs
$67.14 - $72.12
6% of jobs
$72.12 - $77.10
3% of jobs
$22
$51
$77
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.

Full-time
Medical, Retirement, PTO
Re-posted 18 days ago
Sourced by ZipRecruiter
Industrial automation equipment manufacturing
51 - 200 Employees
Blue Bell, PA, US