QC Specialist
Biopharmaceutical
ExtonPennsylvania Contract Nov 10, 2025

Job Title: QC Specialist

Job Overview:
Contemporary Staffing Solutions is seeking a QC Specialist to join our client to support quality control operations within a 503B sterile compounding pharmacy located in Exton, PA. This individual will play a key role in ensuring all compounded sterile preparations meet regulatory and quality standards through careful testing, documentation, and collaboration with cross-functional teams. The ideal candidate will have a strong understanding of cGMP compliance, environmental monitoring, and laboratory best practices to uphold the highest standards of product safety and integrity. This is a full-time, contract-to-hire, onsite position.

Compensation:
$28–$35/hour

Work Schedule:
Monday–Friday, onsite

Key Responsibilities of the QC Specialist:

  • Perform Quality Testing & Validation: Conduct testing on raw materials, in-process samples, and finished products to verify sterility, potency, and stability. Support validation of manufacturing processes, equipment, and computerized systems.

  • Ensure Documentation Accuracy & Compliance: Maintain controlled documents, calibration logs, and QC records in alignment with cGMP, FDA 21 CFR Parts 11/210/211/503B, and USP <797>/<800> requirements. Support internal audits and inspection readiness.

  • Collaborate with Quality Assurance: Partner with QA to investigate deviations, review batch records, and implement corrective and preventive actions (CAPAs) to ensure compliance and continuous improvement.

  • Monitor Environmental Conditions: Oversee cleanroom environmental monitoring programs, analyze data trends, identify potential risks, and conduct risk assessments to protect product integrity.

  • Support Training & Process Improvements: Participate in the development and revision of SOPs, and provide training on QC procedures and regulatory standards to promote consistency and accuracy across operations.

Qualifications and Skills for the QC Specialist:

  • Proven experience in a Quality Control or similar laboratory environment within a cGMP-regulated setting.

  • Strong attention to detail and accuracy in testing, documentation, and process execution.

  • Excellent written and verbal communication skills with the ability to train and support colleagues.

  • Familiarity with validation, environmental monitoring, and regulatory standards (USP <797>/<800>, FDA 21 CFR).

  • Highly organized with strong time management and problem-solving abilities.

  • Bachelor’s degree in a scientific discipline preferred; equivalent relevant experience considered.

Why Join Us?
This is a great opportunity to contribute to the quality and safety of life-saving sterile products while developing expertise within a growing, compliant 503B facility. You’ll work alongside a supportive team that values precision, collaboration, and continuous learning—making an impact that truly matters.

About Us:
Contemporary Staffing Solutions (CSS) is a trusted leader in providing contract, temporary, temp-to-hire, and direct hire staffing solutions. With decades of experience, we’ve grown from a staffing agency to a nationwide provider of workforce management solutions. Our niche recruitment expertise spans Accounting & Finance, Call Center & Office Support, Human Resources, Sales & Marketing, and Information Technology. Explore more about CSS and how we connect great talent with exceptional opportunities by visiting www.ContemporaryStaffing.com.