Chemence Medical Inc. seeks Sr. Process Validation Engineer in Alpharetta, GA to develop IQ/OQ/PQ ... pharma, medical device, or biotech industry.
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Chemence Medical Inc. seeks Sr. Process Validation Engineer in Alpharetta, GA to develop IQ/OQ/PQ ... pharma, medical device, or biotech industry.
Quick apply
Chemence Medical Inc. seeks Sr. Process Validation Engineer in Alpharetta, GA to develop IQ/OQ/PQ ... pharma, medical device, or biotech industry.
Johns Creek, GA ยท On-site
$60K - $115K/yr
Autoclave Validation Engineer Work Location: Johns Creek, GA 30092 Pay rate: $60K - 115K/annum ... Pharma/MedTech environments
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Johns Creek, GA ยท On-site
$60K - $115K/yr
Autoclave Validation Engineer Work Location: Johns Creek, GA 30092 Pay rate: $60K - 115K/annum ... Pharma/MedTech environments
Atlanta, GA ยท 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 ...
Atlanta, GA ยท 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 ...
Social Circle, GA ยท On-site
CSV Engineer I Location: Social Circle, Georgia, USA Duration: Longterm Job Summary The CSV ... Basic knowledge of CSV, CQV, GMP, and validation lifecycle . * Understanding of pharma regulations ...
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Social Circle, GA ยท On-site
CSV Engineer I Location: Social Circle, Georgia, USA Duration: Longterm Job Summary The CSV ... Basic knowledge of CSV, CQV, GMP, and validation lifecycle . * Understanding of pharma regulations ...
Atlanta, GA ยท 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
Atlanta, GA ยท 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
Atlanta, GA ยท 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
Atlanta, GA ยท 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
Atlanta, GA ยท 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
Atlanta, GA ยท 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
... 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 ...
Duluth, GA ยท On-site
$94K - $124K/yr
Lead Design Engineer - PAS-X MES Location: Duluth, Georgia (Onsite/Hybrid - as per client ... in Pharma, Biotech, or Life Sciences environments * Solid understanding of MES validation ...
Duluth, GA ยท On-site
$94K - $124K/yr
Lead Design Engineer - PAS-X MES Location: Duluth, Georgia (Onsite/Hybrid - as per client ... in Pharma, Biotech, or Life Sciences environments * Solid understanding of MES validation ...
Pharma, Bio Pharma, & Specialty Pharma; Medical Device, Medical Technology & Diagnostics; Generics ... Key experience: (e.g., process engineering, process validation) and strong management consulting ...
Pharma, Bio Pharma, & Specialty Pharma; Medical Device, Medical Technology & Diagnostics; Generics ... Key experience: (e.g., process engineering, process validation) and strong management consulting ...
Peachtree Corners, GA ยท On-site
... Validation. Have responsibilities related to the planning, design, and implementation of ... engineering pharma project interests on collaborative teams for pharmaceutical manufacturing ...
Peachtree Corners, GA ยท On-site
... Validation. Have responsibilities related to the planning, design, and implementation of ... engineering pharma project interests on collaborative teams for pharmaceutical manufacturing ...
... Validation. Have responsibilities related to the planning, design, and implementation of ... engineering pharma project interests on collaborative teams for pharmaceutical manufacturing ...
... Validation. Have responsibilities related to the planning, design, and implementation of ... engineering pharma project interests on collaborative teams for pharmaceutical manufacturing ...
Behind every product sold by Roche is Pharma Global Technical Operations (PT). Starting with Phase ... Drafting and execution of validation documentation (IQ/OQ/PQ) and standard operating procedures ...
Behind every product sold by Roche is Pharma Global Technical Operations (PT). Starting with Phase ... Drafting and execution of validation documentation (IQ/OQ/PQ) and standard operating procedures ...
ITOT supports Pharma Technical Manufacturing (PTM), PTM is responsible for managing all aspects of ... the validated state of systems and processes. Initially, participates in Basic Design, Detailed ...
ITOT supports Pharma Technical Manufacturing (PTM), PTM is responsible for managing all aspects of ... the validated state of systems and processes. Initially, participates in Basic Design, Detailed ...
... validation and any other applicable document. * Promotes continuous improvement within quality ... pharma). * Demonstrated leadership in owning and improving one or more QMS processes. * Strong ...
... validation and any other applicable document. * Promotes continuous improvement within quality ... pharma). * Demonstrated leadership in owning and improving one or more QMS processes. * Strong ...
... validation and any other applicable document. * Promotes continuous improvement within quality ... pharma). * Demonstrated leadership in owning and improving one or more QMS processes. * Strong ...
... validation and any other applicable document. * Promotes continuous improvement within quality ... pharma). * Demonstrated leadership in owning and improving one or more QMS processes. * Strong ...
The Opportunity ITOT supports Pharma Technical Manufacturing (PTM), PTM is responsible for managing ... within its validated safety envelope. * Manage Site Robotics Fleet Management Systems in ...
The Opportunity ITOT supports Pharma Technical Manufacturing (PTM), PTM is responsible for managing ... within its validated safety envelope. * Manage Site Robotics Fleet Management Systems in ...
Ensure compliance with applicable cGMP, GAMP, ASTM E2500, and other industry standards for pharma ... Proficient in reviewing, interpreting, and validating complex engineering documentation including ...
Ensure compliance with applicable cGMP, GAMP, ASTM E2500, and other industry standards for pharma ... Proficient in reviewing, interpreting, and validating complex engineering documentation including ...
Ensure compliance with applicable cGMP, GAMP, ASTM E2500, and other industry standards for pharma ... Proficient in reviewing, interpreting, and validating complex engineering documentation including ...
Ensure compliance with applicable cGMP, GAMP, ASTM E2500, and other industry standards for pharma ... Proficient in reviewing, interpreting, and validating complex engineering documentation including ...
The Opportunity ITOT supports Pharma Technical Manufacturing (PTM), PTM is responsible for managing ... within its validated safety envelope. * Manage Site Robotics Fleet Management Systems in ...
The Opportunity ITOT supports Pharma Technical Manufacturing (PTM), PTM is responsible for managing ... within its validated safety envelope. * Manage Site Robotics Fleet Management Systems in ...
$19.08 - $23.34
2% of jobs
$23.34 - $27.60
6% of jobs
$27.60 - $31.87
13% of jobs
$33.20 is the 25th percentile. Wages below this are outliers.
$31.87 - $36.13
13% of jobs
$36.13 - $40.39
11% of jobs
The median wage is $42.52 / hr.
$40.39 - $44.65
12% of jobs
$44.65 - $48.92
9% of jobs
$52.20 is the 75th percentile. Wages above this are outliers.
$48.92 - $53.18
13% of jobs
$53.18 - $57.44
13% of jobs
$57.44 - $61.70
6% of jobs
$61.70 - $65.97
3% of jobs
$19
$43
$65
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.

Summary:
Key Duties and Responsibilities:
Chemence Medical Inc. seeks Sr. Process Validation Engineer in Alpharetta, GA to develop IQ/OQ/PQ protocols, coordinate and perform equipment qualifications, and ensure that automated process equipment that mass produce medical device consumables and other products, are designed, developed, or changed in compliance with specifications, requirements, safety, and Company and regulatory guidelines. The Sr. Process Validation Engineer will work closely with engineering, operations, and R&D teams to create and document procedures to validate products and processes.
Qualifications, Education and/or Experience Required:
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Chemical manufacturing
501 - 1,000 Employees
Alpharetta, GA, US
1983