Technical Transfer Engineer- 3rd Shift

Talent Partner | Fuelling growth for CDMOs, CROs, and Pharma Services 🌱 | Pragmatic Solution Finder | MSc Psychology

The Technical Services & Manufacturing Science 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 TSMS Engineer is responsible for scaling up and transferring processes into full scale manufacturing process based on data generated internally or received from the client.

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.

• 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

• 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

• 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.

Associate

Full-time

Manufacturing, Science, and Engineering

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing