15.08.25

Technical Services Supervisor

  • Permanent
  • USA
  • CDMO

Technical Services Supervisor

INCOG Biopharma Services in Indianapolis, IN is hiring a Technical Services Supervisor, who will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification. This role oversees the optimization and continuous improvement of manufacturing processes and technologies to ensure product quality, efficiency and compliance with regulatory standards.

This position holds the responsibility of delivering substantial technical guidance and supervision throughout the production process. The primary objective is to establish production processes that are not only robust and reliable but also capable of consistently delivering high-quality products. This entails overseeing the various stages of production,
identifying potential areas for improvement, and implementing measures to enhance the overall efficiency and effectiveness of the production operations.

There is a growing need globally for more CDMOs (contract development and manufacturing organization) in the pharmaceutical industry to provide comprehensive services from drug development through drug manufacturing.

At INCOG, they are more than just a CDMO. A better way to create more meaningful experiences. A better way to create a culture that everyone can thrive and succeed in. At their core, that is who they are—a dedicated team that believes they can always be better.

Join the team at INCOG, a world-class CDMO for parenteral injectable drugs, shaping a new future for patients, for yourself, and for INCOG’s clients.

Job Functions:

  • Lead a small team of Tech Services Engineers and Technical Writers with expertise in drug product formulation, single-use system mixing, filtration, filling, visual inspection etc.
  • Provide leadership and guidance in technical decision-making related to manufacturing operations.
  • Leads technical troubleshooting and investigations of manufacturing processes to support root cause analysis, product impact assessment and effective corrective and preventive actions.
  • Implement process improvements based on data analysis and scientific principles.
  • Provide technical guidance and oversight to Operations and Validation group to support Process Performance Qualification and Continuous Process Verification.
  • Lead efforts in production excellence to support commercial scalability and compliance.
  • Author and review of regulatory information packages and filings/submissions.
  • Represents Tech Services in project teams and communicates directly with customers.
  • Recognized as Subject Matter Expert for the INCOG processes.

Candidate Requirements:

  • Bachelor’s degree in science, Engineering or related scientific discipline required.
  • Master’s degree in science, Engineering or related scientific discipline strongly preferred.
  • 3+ years GMP experience with manufacturing processes and equipment in related fields such as biologics, pharmaceutical fill and finish required.
  • 1-3 years of experience in leadership or mentorship
  • Experience in regulated GMP manufacturing operations required.

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

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.

Apply here
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