QA/QC Supervisor - Weekend AM

QA/QC Supervisor - Weekend AM

WHO?

INCOG are looking for a QA/QC Supervisor to join their rapidly growing CDMO. We are looking for a Quality Supervisor who thrives at the intersection of QA and QC — someone who brings hands-on laboratory knowledge and a strong manufacturing floor presence to drive quality outcomes across the full product lifecycle.

This position is on the Weekend AM Shift (Friday, Saturday, Sunday) (7:00 AM to 7:30PM).

WHAT?

Working closely with the Director of Quality, the Quality Supervisor will serve as an integrated quality leader with accountability spanning both Quality Assurance Operations and Quality Control activities.

The role responsibilities are as follows, but are not limited to:

Quality Assurance: Manufacturing Operations Support

• Build, lead, and develop a high-performing QA Operations team supporting aseptic drug product manufacturing.
• Train and maintain a workforce proficient in quality systems, both in theory and practice.
• Provide on-the-floor leadership through coaching and mentoring to uphold quality standards.
• Allocate QA resources to balance production timelines with product quality.
• Lead development of room and line clearance processes across formulation, filling, and packaging.
• Ensure QA team competency in gowning, contamination control, aseptic processes, and equipment verification.
• Partner with Operations on batch record review, correction, and real-time quality oversight.
• Maintain inspection readiness through rapid assessment of deviations, product impact, and initial corrective actions.
• Collaborate with EH&S and Operations to reinforce safety standards and compliance with SOPs and site goals.

Quality Control: Laboratory Operations Support

• Provide leadership and technical oversight across QC Chemistry, Microbiology, and Technical Services.
• Oversee daily QC activities, ensuring timely completion of testing and data review.
• Assign and manage daily priorities for QC staff, providing hands-on support as needed.
• Mentor and develop QC team members, partnering with leadership on performance management.
• Support deviation investigations, laboratory investigations, and CAPA implementation.
• Drive continuous improvement of QC processes and laboratory operations.
• Ensure full compliance with cGMP requirements.
• Conduct routine lab walk-throughs to maintain inspection readiness.

Cross-Functional Quality Responsibilities

• Continuously assess and improve QA and QC processes to enhance efficiency and quality.
• Influence team and organizational goals while modeling ALP values.
• Ensure compliance with regulatory requirements, cGMP, and SOPs.
• Support deviation and CAPA management across both manufacturing and laboratory functions.

YOU!

Ideally, candidates will have a Bachelor’s degree in a scientific discipline, along with 5 years of cGMP experience in Biopharma. Of that experience, a minimum of 3 years should come from Quality Assurance or Quality Control functions. It is preferrable that this candidate will also possess 2 years of experience as a people leader or supervisor.

Why INCOG?

• Paid time off, based on tenure
• 11 paid holidays
• 401(k) plan with company match up, vested immediately
• Choice of health & wellness plans
• FSA and HSA options
• Onsite wellness facility
• Employee engagement activities; food trucks, monthly luncheons, fundraising events, team building competitions, offsite celebrations

Curious? Send us your resume at apply@leadcandidate.com or you can find more information on our website.

Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself…

Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.