Pharma Quality Control Lead – Inspection & Compliance

Sharp Clinical Services, Inc.; Town of Bethlehem (NY); On-site; USD 60,000 - 80,000; Full time

Job summary

Sharp Packaging Services is seeking a detail-oriented Quality Control professional to perform inspections across components, in-process products, and finished goods. You will establish test standards, maintain reserve samples, and mentor QC staff on GDP and quality practices.

The role requires strong cGMP knowledge, documentation rigor, and the ability to work independently within a team. Join a global packaging provider committed to quality and regulatory excellence.

Qualifications

• High School Diploma or equivalent required; Bachelor’s degree preferred.
• 5+ years in pharmaceutical/biotech manufacturing/packaging or related QC/QA roles.
• Strong knowledge of cGMPs, FDA/DEA regulations, and CFRs.
• Proficient in documentation practices and data integrity.

Responsibilities

• Perform quality control inspections on components, in-process items, and finished products.
• Set in-process test standards and assure compliance to established standards.
• Inspect bulk drug and excipients; maintain reserve samples.
• Provide guidance on inspection techniques and GDP to QC staff.
• Perform physical testing using basic inspection instrumentation.
• Verify environmental conditions and change statuses per GMP.
• Ensure testing aligns with current procedures and sampling plans.
• Document work thoroughly and maintain detailed records.
• Maintain clean, safe work environment and adhere to safety standards.

Skills

Quality control

Attention to detail

Communication skills

Independent worker

Team collaboration

Education

High School Diploma or equivalent

Bachelor’s Degree preferred

Tools

Microsoft Office

Job description

Sharp Packaging Services is seeking a detail-oriented Quality Control professional to perform inspections across components, in-process products, and finished goods. You will establish test standards, maintain reserve samples, and mentor QC staff on GDP and quality practices.

The role requires strong cGMP knowledge, documentation rigor, and the ability to work independently within a team. Join a global packaging provider committed to quality and regulatory excellence.