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 critical role in ensuring all compounded sterile preparations meet regulatory and quality standards through thorough testing, documentation, and cross-functional collaboration. The ideal candidate will have a solid understanding of cGMP compliance, regulatory requirements, and laboratory best practices to maintain 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:

• Develop, review, and update Standard Operating Procedures (SOPs) to ensure alignment with regulatory and quality standards. Maintain accurate documentation for deviations, investigations, and CAPA activities.
• Conduct testing on raw materials, in-process samples, and finished products to verify sterility, potency, and stability. Review batch records to ensure compliance with procedures and specifications.
• Assist in the execution and documentation of validation protocols for processes, equipment, and systems to ensure regulatory compliance and product quality.
• Prepare and maintain regulatory and compliance documentation, supporting internal and external audits and inspections. Ensure all activities align with cGMP, FDA 21 CFR Parts 11/210/211/503B, and USP <797>/<800> requirements.
• Work closely with Quality Assurance and other teams to investigate deviations, implement corrective and preventive actions (CAPAs), and drive process improvements.

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, including the ability to create and maintain quality documentation.
• Familiarity with validation protocols, environmental monitoring, and regulatory standards (USP <797>/<800>, FDA 21 CFR).
• Highly organized with strong time management, problem-solving, and analytical 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 gaining experience in a regulated 503B facility. You’ll work alongside a supportive team that values precision, compliance, and continuous improvement—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.