Job Title: QC Specialist

Job Overview:

Contemporary Staffing Solutions is seeking a QC Specialist to join our client to support quality operations within a regulated manufacturing environment. This role ensures that incoming materials, in process components, and finished products meet stringent quality standards to protect patient safety. The QC Specialist will play a key role in maintaining compliance, supporting validations, and partnering with Quality Assurance to drive continuous improvement. This is an onsite, contract to hire position based in Exton PA.

Compensation:

$30 to $32 per hour

Work Schedule:

Monday through Friday, onsite between 7 AM and 6 PM

Key Responsibilities of the QC Specialist:

• Oversee quality checks of incoming materials and product samples, ensuring testing, validation, and vendor documentation meet internal specifications and regulatory expectations.

• Support analytical testing activities, outsourced laboratory coordination, environmental monitoring programs, and validation efforts that impact equipment, processes, and computerized systems.

• Maintain accurate documentation aligned with company quality systems, contribute to deviation investigations, and ensure all equipment, logs, and controlled documents remain compliant.

• Partner closely with Quality Assurance to assess results, assist with CAPAs, review batch records, support change controls, and communicate quality trends through KPIs.

• Guide staff through training on quality practices and assist in creating or updating procedures to strengthen compliance.

Qualifications and Skills for the QC Specialist:

• Experience in a regulated manufacturing or laboratory environment with strong attention to detail and commitment to data integrity.

• Ability to manage priorities with urgency, communicate clearly, stay organized, and deliver internal customer support.

• Knowledge of cGMP standards and FDA regulations including 21 CFR Parts 11, 210, 211, and 503B, as well as related USP guidance.

• Capability to train colleagues, troubleshoot issues, and contribute meaningfully to investigations and continuous improvement activities.

• Familiarity with environmental monitoring, validation processes, and quality control testing is strongly preferred.

Why Join Us?

This role offers hands on experience in a highly regulated environment, providing strong exposure to quality systems, validation, and compliance. You will collaborate with experienced quality professionals while contributing to meaningful products that directly impact patient safety. It is an excellent opportunity to grow your skills and advance within a quality driven organization.