QC Inspector – cGMP & Quality Control

Sharp Services; Bethlehem (Northampton County); On-site; USD 52,000 - 78,000; Full time

Job summary

Sharp Services is seeking a Quality Control Inspector I to ensure compliance with cGMP standards and oversee quality related to documentation, inspection, and manufacturing/packaging processes. The role involves in-process and finished product inspections, sampling, and daily verification activities to maintain product quality and traceability.

The position requires strong communication, ability to work independently, and a solid understanding of quality control principles in a biotech/pharma

Qualifications

• Requires ability to work independently and manage multiple tasks.
• Excellent oral and written communication is required to coordinate with team and external contacts.
• Strong knowledge of Microsoft Office products and basic data handling.
• Familiarity with cGMPs, FDA regulations and CFRs preferred.

Responsibilities

• Perform quality control inspections of components, in-process items and finished product.
• Determine in-process test standards and ensure compliance with specifications.
• Conduct sampling and inspection of bulk drug and excipients.
• Maintain accurate, detailed records of work performed and communicate issues to supervisor.
• Ensure testing adheres to current procedures and sampling plans.
• Maintain a clean, safe work environment and meet scheduled requirements.

Skills

Independent worker

Oral and written communication

PC proficiency

Time management

Education

High School Diploma or equivalent

Bachelor’s degree preferred

Tools

Microsoft Office

Excel

Word

Project

Job description

Sharp Services is seeking a Quality Control Inspector I to ensure compliance with cGMP standards and oversee quality related to documentation, inspection, and manufacturing/packaging processes. The role involves in-process and finished product inspections, sampling, and daily verification activities to maintain product quality and traceability.

The position requires strong communication, ability to work independently, and a solid understanding of quality control principles in a biotech/pharma