QC Manager - 166781

Piper Companies; Miami (FL); On-site; USD 95,000 - 110,000; Full time

Benefits offered by this job

Comprehensive Benefits Package

Annual bonus eligibility

Job summary

Piper Companies is seeking a QC Manager for a Pharmaceutical Manufacturing company in Miami, FL. This onsite, permanent role leads QC laboratory operations and champions quality across QA, Manufacturing, and R&D teams.

The ideal candidate holds a Bachelor’s or Master’s in Chemistry or Biology with 7+ years in regulated QC labs, strong cGMP/FDA/data integrity expertise, and proven leadership to mentor staff. Competitive salary plus comprehensive benefits.

Qualifications

• Bachelor’s or Master’s degree in Chemistry, Biology, or related discipline.
• 7+ years of QC laboratory experience in regulated pharma/biotech.
• Strong knowledge of cGMP, FDA requirements, and data integrity.

Responsibilities

• Lead and supervise QC lab operations and staff development.
• Oversee QC systems, SOPs, analytical methods, and testing schedules.
• Support audits and collaborate cross-functionally to drive quality.
• Perform data review and approval of analytical results.
• Manage investigations, CAPA, deviations, and OOS/OOT events.

Skills

QC leadership

cGMP knowledge

FDA regulations familiarity

Data integrity awareness

Project management

Interpersonal communication

Education

Bachelor’s or Master’s degree in Chemistry, Biology, or related field

Job 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