We are seeking a Validation Engineer to support validation activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on equipment utilities and process validation ensuring compliance with regulatory requirements and supporting ongoing manufacturing operations.
The ideal candidate will have strong experience in IQ/OQ/PQ documentation and cross-functional collaboration within pharma or biotech settings.
Key Responsibilities
Execute and support equipment utility and process validation activities (IQ OQ PQ)
Develop and review validation protocols reports and supporting documentation
Ensure compliance with GMP FDA and regulatory requirements
Perform risk assessments and support validation strategies
Collaborate with Engineering Quality and Manufacturing teams
Support deviation investigations CAPA and change control activities
Assist with commissioning and qualification (CQV) activities
Maintain accurate and compliant documentation
Required Qualifications
Bachelors degree in Engineering Science or related field
3 7 years of experience in validation within pharmaceutical or biotech industry
Hands-on experience with IQ/OQ/PQ and validation documentation
Strong understanding of GMP and regulatory compliance
Experience with equipment and/or utility validation
Job Title: Validation Engineer Location: Concord NC (Onsite) Duration: Long Term Job Summary: We are seeking a Validation Engineer to support validation activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on equipment utilities and process validation e...
Job Title: Validation Engineer
Location: Concord NC (Onsite)
Duration: Long Term
Job Summary:
We are seeking a Validation Engineer to support validation activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on equipment utilities and process validation ensuring compliance with regulatory requirements and supporting ongoing manufacturing operations.
The ideal candidate will have strong experience in IQ/OQ/PQ documentation and cross-functional collaboration within pharma or biotech settings.
Key Responsibilities
Execute and support equipment utility and process validation activities (IQ OQ PQ)
Develop and review validation protocols reports and supporting documentation
Ensure compliance with GMP FDA and regulatory requirements
Perform risk assessments and support validation strategies
Collaborate with Engineering Quality and Manufacturing teams
Support deviation investigations CAPA and change control activities
Assist with commissioning and qualification (CQV) activities
Maintain accurate and compliant documentation
Required Qualifications
Bachelors degree in Engineering Science or related field
3 7 years of experience in validation within pharmaceutical or biotech industry
Hands-on experience with IQ/OQ/PQ and validation documentation
Strong understanding of GMP and regulatory compliance
Experience with equipment and/or utility validation