QA C&Q Specialist
Validation & Engineering Group, Inc
Job Description
Job Description
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
- QA C&Q Specialist
Position Summary
We are seeking a QA C&Q Specialist to support Quality Assurance activities within Commissioning & Qualification (C&Q) projects. This role will primarily focus on the review of C&Q documentation , ensuring that documents are accurate, complete, properly executed, and compliant with established procedures, quality standards, and project requirements.
The ideal candidate will have experience working in a regulated pharmaceutical or life sciences environment, with a strong understanding of GxP documentation practices and C&Q processes .
Key Responsibilities
- Review C&Q documentation for compliance with approved procedures, standards, and project requirements.
- Verify that documents are complete, accurate, and properly formatted and executed.
- Ensure C&Q activities and documentation follow applicable SOPs, protocols, procedures, and quality requirements .
- Review qualification and commissioning documents, including protocols, reports, forms, and supporting documentation.
- Identify documentation gaps, inconsistencies, or deviations and work with project teams to resolve them.
- Provide QA feedback and recommendations to C&Q and project personnel.
- Ensure appropriate documentation practices are followed throughout the project lifecycle.
- Support document approval and review workflows in accordance with established procedures.
- Maintain a strong focus on data integrity, traceability, and Good Documentation Practices (GDP).
- Participate in meetings and discussions with C&Q, Engineering, Validation, and Quality teams as needed.
- Support the resolution and closure of documentation-related observations or findings.
Qualifications
- Bachelor's degree in Engineering, Science, Pharmacy, Quality, or a related field preferred.
- 2+ years of experience in Quality Assurance, Validation, Commissioning & Qualification, or a related role within the pharmaceutical, biotechnology, or medical device industry.
- Experience reviewing technical and/or validation documentation in a regulated environment.
- Knowledge of GMP/GxP, Good Documentation Practices (GDP), and quality systems .
- Ability to interpret and apply SOPs and established procedures.
- Strong attention to detail and organizational skills.
- Excellent written and verbal communication skills.
- Ability to work independently while collaborating effectively with cross-functional teams.
Preferred Experience
- Experience supporting C&Q documentation and qualification activities .
- Familiarity with equipment, utilities, facilities, or process qualification documentation.
- Experience working with electronic document management or quality systems.
- Knowledge of FDA and/or other applicable regulatory requirements.
Key Competencies
- Document review and quality control
- Procedural compliance
- Good Documentation Practices (GDP)
- Attention to detail
- Quality mindset
- Technical documentation
- Problem solving
- Cross-functional collaboration
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
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