Technical Services Supervisor

Lead Candidate

Fishers (IN)

On-site

USD 100,000 - 190,000

Full time

14 days+

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Benefits offered by this job

Paid time off based on tenure

401(k) plan with company match

Choice of health & wellness plans

Onsite wellness facility

Employee engagement activities

Job summary

A leading biopharma company in Fishers, IN is seeking a Technical Services Supervisor to oversee tech transfer and process validation. The successful candidate will guide a team in optimizing manufacturing processes, ensure compliance with GMP regulations, and lead continuous improvement efforts. Ideal applicants will have a Bachelor's degree in a related field and substantial GMP experience in manufacturing. Competitive benefits offered.

Qualifications

3+ years GMP experience with manufacturing processes and equipment in biologics or pharmaceutical fill and finish.
1-3 years of experience in a leadership or mentorship role.
Experience in regulated GMP manufacturing operations.

Responsibilities

Lead a team of Technical Services Engineers and Technical Writers.
Provide guidance in technical decision-making related to manufacturing operations.
Implement process improvements based on data analysis.
Author and review regulatory information packages.

Skills

GMP manufacturing processes

Leadership in technical decision-making

Process improvement

Regulatory compliance

Education

Bachelor’s degree in science, engineering or related discipline

Master’s degree in science, engineering or related discipline

Job description

4 days ago Be among the first 25 applicants

Direct message the job poster from Lead Candidate

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 regulatory compliance.

The position delivers technical guidance and supervision throughout the production process, with the objective of establishing production processes that are robust, reliable and capable of consistently delivering high-quality products. This entails overseeing production stages, identifying opportunities for improvement, and implementing measures to enhance efficiency and effectiveness of operations.

At INCOG, the team focuses on creating meaningful experiences and a culture that enables everyone to thrive. INCOG is a world-class CDMO for parenteral injectable drugs, shaping a future for patients, for the team, and for clients.

Job Functions

Lead a small team of Technical Services Engineers and Technical Writers with expertise in drug product formulation, single-use system mixing, filtration, filling, and visual inspection.
Provide leadership and guidance in technical decision-making related to manufacturing operations.
Lead 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 groups to support Process Performance Qualification and Continuous Process Verification.
Lead efforts in production excellence to support commercial scalability and compliance.
Author and review regulatory information packages and filings/submissions.
Represent Tech Services in project teams and communicate directly with customers. Recognized as Subject Matter Expert for 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

Note: Don’t meet all the requirements? We’re open to discussing opportunities. Equality and diversity in employment are supported by Lead Candidate and INCOG.

Seniority level