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
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
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