QC Manager to join a
Pharmaceutical Manufacturing company located in Miami, FL through on onsite, permanent position.
Responsibilities of the QC Managerinclude:- Lead and supervise QC laboratory operations, including oversight of technical staff, performance management, training, and continuous staff development.
- Manage QC systems, procedures, analytical methods, SOPs, and testing schedules to ensure compliance with cGMP requirements, 21 CFR Parts 210/211, and Part 11 regulations.
- Oversee analytical testing activities for raw materials, in-process materials, bulk products, finished products, and stability programs, including data review and approval.
- Direct laboratory quality initiatives such as method validations, method transfers, equipment qualification/calibration, investigations, deviations, OOS/OOT events, and CAPA implementation.
- Support internal, client, and regulatory audits while collaborating cross-functionally with Quality Assurance, Manufacturing, and R&D to drive product quality and continuous improvement.
- Perform administrative and laboratory responsibilities requiring prolonged computer and laboratory work, adherence to safety protocols/PPE requirements, and occasional lifting of up to 50 pounds.
Qualifications for the QC Manager include: - Bachelor's or Master's degree in Chemistry, Biology, or a related scientific discipline.
- Minimum of 7 years of Quality Control laboratory experience within a regulated pharmaceutical, biotechnology, or related industry environment.
- Strong knowledge of cGMP regulations, FDA requirements, guidance documents, and data integrity standards.
- Proven leadership and team management experience with the ability to mentor staff and drive performance.
- Demonstrated ability to manage multiple projects and priorities effectively in a fast-paced, cross-functional environment.
- Excellent verbal, written, interpersonal, and computer skills, including proficiency with laboratory systems and standard office software.
Compensation for the QC Manager includes: - Salary Range: $95,000-$110,000/annually, plus bonus
- Work Schedule: Monday-Friday, 8:00am-5:00pm
- Comprehensive Benefits Package
This job opens for applications on
05/11/2026. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: quality control, QC, manager, cGMP, laboratory operations, SOPs, product validation, production quality, PPE requirements, safety protocols, quality assurance, QA, R&D, manufacturing
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