Quality Floor Shop Specialist

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 Quality Shop Floor Associate to provide real-time quality oversight and support within a regulated manufacturing environment. This individual will work directly with Manufacturing Engineering and Quality teams to ensure production activities comply with approved procedures Good Manufacturing Practices (GMP) and applicable quality requirements.

• Quality Floor Shop Specialist

Description:

• Provide quality oversight and support on the manufacturing floor
• Verify that manufacturing activities follow approved procedures specifications and GMP requirements.
• Review production documentation for accuracy completeness and compliance.
• Support line clearance material verification equipment readiness and production start-up activities.
• Identify document and escalate quality issues and potential compliance concerns.
• Support investigations involving deviations nonconformances manufacturing events and product-quality issues.
• Participate in root-cause analysis and corrective and preventive action activities.
• Assist with the inspection review and disposition of materials and products.
• Collaborate with Manufacturing and other departments to resolve quality issues promptly.
• Maintain accurate and timely records in accordance with data-integrity requirements.
• Support audits inspections and continuous-improvement initiatives.
• Perform other quality-related responsibilities as assigned.

Minimum Qualifications

• High school diploma or GED required.
• Previous GMP experience is required.
• Experience in quality manufacturing inspection or production within a regulated environment.
• Understanding of good documentation practices and data-integrity principles.
• Ability to read understand and follow written procedures and specifications.
• Strong attention to detail communication and problem-solving skills.
• Ability to work effectively in a fast-paced team-oriented manufacturing environment.
• Availability to work assigned shifts and provide on-site shop-floor support.

Preferred Qualifications

• Bachelors degree in Science Engineering Quality or a related field is a plus but not required.
• Experience in the medical-device pharmaceutical biotechnology or other FDA-regulated industry.
• Experience supporting deviations nonconformances investigations CAPAs and change controls.
• Familiarity with electronic quality and manufacturing documentation systems.
• Bilingual English and Spanish is preferred.

At Validation & Engineering Group people always come first. We believe that when youre empowered to do your best work bold ideas thrive and real progress happens. This isnt just a job - its an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven supportive team.

Excited to build something meaningful together We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race color religion sex sexual orientation gender identity national origin veteran status or disability status.