QC Supervisor; 3rd Shift

If you’re an experienced QC Chemist or Microbiologist looking to further your leadership experience, this could be a great opportunity for you!

This exciting chance to join the team is offered by INCOG Biopharmaceutical Services, who are continuing to build their state of the art sterile injectable CDMO. Having won the Best Places to Work in Indiana 4 years in a row, INCOG is the perfect place to continue building your career!

INCOG Biopharma Services in Indianapolis, IN is hiring a QC Supervisor to join their 2nd shift (3pm to 11:30pm) who will be working closely with QC lab management (Chem/Micro). They will be will be involved in QC & lab investigations and resulting CAPA implementations. This role offers the opportunity to work at INCOG’s state‑of‑art sterile injectable CDMO during an exciting time of growth, contributing towards a better path to market for life‑saving drugs.

This role will be responsible for overseeing daily QC activities, including ensuring that all testing and data review is completed, delivering daily assignments, providing in‑lab support and oversight, and coaching the QC team.

The role responsibilities are, but are not limited to:

• Provide technical support, oversite and team leadership for Quality Control Chemistry, Microbiology and Quality Control Technical Services.
• Assist in the development of individual team members by providing mentorship to analysts/data reviewers and communicating with Quality Control Leadership on team performance.
• Develop and improve current processes to maintain and control the general functions of INCOG Quality Control.
• Assure compliance with cGMP requirements (current good manufacturing practices).
• Perform laboratory walk‑throughs and ensure laboratory spaces maintain inspection readiness and control.

Ideally, candidates will have 3-5 years working knowledge of GMP laboratory operations (Chemistry or Microbiology), as well as a relevant Bachelor’s degree. They will also have:

• Experience with using laboratory instrumentation from pH/conductivity meters, osmometers, and density meters to more complicated systems used for UHPLC/HPLC, GC, CE, icIEF, endotoxin, and bioburden analysis.
• 1-2 years of people leadership experience
• Knowledge of Quality Control Microbiology and Chemistry, GxP principles, CAPA/Investigation management, and data/document review
• Knowledge of Aseptic techniques and processing

Curious? Send us your resume at  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.