QA Coordinator (2nd Shift)

Pay Rate Low: 23.00 | Pay Rate High: 23.00 Quality Control Technician – 2nd Shift Our client, a Fortune 500 industry leader, is seeking a Quality Assurance Coordinator to join their team. This is an exciting opportunity to contribute to innovative work across the biopharma, healthcare, and advanced technologies industries while supporting critical laboratory and quality operations in a GMP-regulated environment. Position Details Pay Rate: $23.00/hour Shift: 2nd Shift | Monday–Friday | 3:00 PM – 11:30 PM Work Environment: Onsite Position Summary The Quality Assurance Coordinator is responsible for performing analytical testing and supporting quality operations to ensure timely and accurate results for raw materials, intermediates, and finished products. This role supports cGMP, ISO, and quality system compliance while collaborating with cross-functional teams to maintain operational excellence and product quality. Key Responsibilities Perform timely analysis of testing samples and report accurate results Conduct sampling and testing of raw materials, intermediates, and finished goods Support coordination with toll manufacturers regarding quality-related questions and issues Ensure compliance with analytical testing requirements (ATR) Assist with ISO implementation and quality system initiatives Prepare and standardize laboratory solutions, standards, and calibration activities Operate and support analytical instrumentation including HPLC, GC, and wet chemistry testing Enter and maintain analytical results and documentation within SAP Complete and maintain all required GMP and ISO documentation and logbooks Support batch timeline, quality, and production goals Promote safe laboratory operations and maintain zero-incident standards Assist in training and supervising operators within the department Participate as a member of the Emergency Response Team and support emergency preparedness activities Maintain compliance with ISO 9001, ISO/IEC 17025, cGMP, and internal quality systems Minimum Qualifications High school diploma or equivalent 1–2 years of experience in Quality within a regulated manufacturing environment Experience supporting cGMP, ISO, and regulatory audit activities Preferred Qualifications Experience in Quality Control within fine chemical or pharmaceutical manufacturing environments Working knowledge of cGMP regulations and laboratory quality systems Hands-on experience with HPLC, GC, and wet chemistry analysis Skills & Competencies Strong attention to detail and organizational skills Effective communication and teamwork abilities Willingness to learn and adapt in a fast-paced environment Commitment to safety, quality, and continuous improvement This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you. J-18808-Ljbffr