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TSMS Engineer, 3rd shift

Job in Fishers, Hamilton County, Indiana, 46085, USA
Listing for: INCOG BioPharma
Full Time position
Listed on 2025-12-14
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer, Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below

The Manufacturing Science and Technology Engineer will be responsible for supporting all facets of tech transfer, process validation, GMP floor support, and continued process verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs. This role will provide strong technical oversight to the business to ensure robust and reliable production processes are established. The MSAT Engineer is responsible for scaling up and transferring processes into full scale manufacturing process based on data generated internally or received from the client.

Third shift position.

Essential

Job Responsibilities:
  • Develop technical documentation such as Process FMEA, Process Flow Diagrams, and Tech Transfer Plans
  • Select appropriate equipment and single-use components for GMP manufacturing
  • Recognized as Subject Matter Expert for manufacturing processes in project teams
  • Author GMP manufacturing documentation including Master Batch Records, BOM, and Processing Forms
  • Monitor process data, identifying trends and proposing actions
  • Lead technical troubleshooting and investigations of process issues to support root‑cause analysis, product impact assessment and effective corrective and preventative actions
  • Provide technical guidance and oversight to Operations and Validation group to support process performance qualification and continuous process verification
  • Assess the impact of changes to the product, process, equipment, procedures, and/or materials
Special

Job Requirements:
  • Bachelor’s degree in science or engineering
  • 2+ years in Technical Transfer for pharmaceutical or similar industry
  • 2+ years GMP experience
  • 1+ year in client‑facing role
  • Master’s degree preferred
Additional info about INCOG Bio Pharma Services:

At INCOG Bio Pharma we have built a world‑class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long‑term value for our customers, we are committed to a service‑culture mindset, technical excellence, and a collaborative and team‑centered approach to doing business.

If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke‑free campus.

INCOG Bio Pharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG Bio Pharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.

We will not tolerate discrimination or harassment based on any of these characteristics.

By submitting your resume and details, you are declaring that the information is correct and accurate.

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