Quality Control Manager

Piper Companies; Wayne (PA); On-site; USD 100,000 - 120,000; Full time

Job summary

An established industry player is seeking a Quality Control Manager to lead quality initiatives within a reputable Biologics Quality Control Testing company. This pivotal role involves overseeing testing processes, ensuring compliance with regulations, and managing a skilled team. The ideal candidate will possess extensive GMP lab experience and a strong background in molecular biology. If you are passionate about driving quality in a dynamic environment and have the leadership skills to mentor a team, this opportunity is perfect for you. Join a company that values innovation and excellence in the biotechnology field.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401K

PTO

Sick Leave

Holidays

Qualifications

• 6+ years of GMP lab experience in pharmaceuticals or biotechnology.
• Supervisory or management experience is essential.

Responsibilities

• Lead projects and ensure compliance with global regulations.
• Train and manage staff while overseeing lab assignments.

Skills

GMP lab experience

molecular biology

supervisory experience

NGS

CSV

validation

quality management

SOPs

lab operations

QMS (Trackwise)

Education

PhD in biological science

MA/MS in scientific discipline

Job description

Join to apply for the Quality Control Manager role at Piper Companies

Piper Companies is seeking a Quality Control Manager to join a reputable Biologics Quality Control Testing company located in Wayne, PA.

Responsibilities

• Lead projects, collaborate with clients and teams, and ensure expectations are met.
• Oversee testing, manage deviations, and ensure adherence to global regulations.
• Represent the team in audits, address issues, and implement corrective actions.
• Manage assay development, validation, and ongoing compliance.
• Maintain documentation, refine processes, and drive quality initiatives.
• Train, mentor, and manage staff while overseeing lab assignments.
• Ensure compliance with local, state, and federal regulations.
• Monitor business metrics, report progress, and resolve issues.

Qualifications

• 6+ years of GMP lab experience in pharmaceuticals, medical devices, or biotechnology.
• Knowledge of molecular biology and sequencing-based applications.
• Supervisory or management experience is essential.
• Subject Matter Expert in NGS, CSV, validation, quality, GMP, SOPs, lab operations, and QMS (Trackwise).
• PhD in a scientific or technical discipline (e.g., biological science) with 3+ years of relevant experience.
• MA/MS in a scientific or technical discipline with 6+ years of relevant experience.

Compensation

• Salary Range: $100,000 - $120,000, depending on experience.
• Benefits include Medical, Dental, Vision, 401K, PTO, Sick Leave (if required by law), and Holidays.

This job opens for applications on 3/21/2025 and will be accepting applications for at least 30 days from the posting date.