QC Manager

Zp Group Llc

  • Miami, FL
  • 30+ days ago
  • $95,000–$110,000 Per Year
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Skills

  • Administrative Skillsunmatched
  • Analysis Skillsunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Calibrationunmatched
  • Chemistryunmatched
  • Code of Federal Regulationsunmatched
  • Computer Skillsunmatched
  • Continuous Improvementunmatched
  • Corrective and Preventative Action (CAPA) Systemsunmatched
  • Cross-Functionalunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Data Qualityunmatched
  • Drug Manufacturingunmatched
  • FDA Requirementsunmatched
  • Interpersonal Skillsunmatched
  • Laboratoryunmatched
  • Laboratory Managementunmatched
  • Laboratory Operationsunmatched
  • Laboratory Systemsunmatched
  • Leadershipunmatched
  • Lift/Move 50 Poundsunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Materials Testingunmatched
  • Mentoringunmatched
  • Multitaskingunmatched
  • Operations Managementunmatched
  • People Managementunmatched
  • Performance Managementunmatched
  • Presentation/Verbal Skillsunmatched
  • Product Programsunmatched
  • Project/Program Managementunmatched
  • Quality Assuranceunmatched
  • Quality Controlunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Research & Development (R&D)unmatched
  • Staff Developmentunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Systems Administration/Managementunmatched
  • Team Lead/Managerunmatched
  • Test Plan/Scheduleunmatched
  • Writing Skillsunmatched

Description

Piper Companies is seeking a QC Manager to join a Pharmaceutical Manufacturing company located in Miami, FL through on onsite, permanent position.

Responsibilities of the QC Manager include:

  • 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

#LI-TM1 #LI-onsite

Numbers & Facts

LocationMiami, FL
Salary$95,000–$110,000 Per Year

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