Process Engineer, Biologics and Pharma Facilities
Life sciences design and engineering firm, biologics and pharma clients
About the role
You will design the processes inside new biologics and pharma facilities, from basis of design through startup. Clients are major pharma and biotech companies building drug substance, drug product and cell and gene therapy capacity.
This seat is for an engineer who wants real ownership of process design on large projects, working alongside architects, MEP engineers, construction teams and CQV.
What you will own
- Process flow diagrams, P&IDs and equipment specifications
- Basis of design and process sizing for upstream and downstream operations
- Equipment selection, vendor reviews and FAT/SAT support
- Coordination with architecture, MEP, automation and construction teams
- Support through commissioning, qualification and startup
- Client meetings and design reviews with owner process teams
What we are looking for
- 4+ years in process engineering for biologics, pharma or other GMP manufacturing
- Hands-on PFD and P&ID development
- Understanding of single-use and stainless process systems
- Exposure to GMP, cGMP and FDA requirements
- Has supported at least one project through qualification or startup
- Strong communication with clients and multidisciplinary teams
- Bachelor's in chemical, biochemical or mechanical engineering
Nice to have
- Owner-side manufacturing or scale-up experience
- PE license
- Cell and gene therapy or aseptic processing projects
- Experience at an A/E or process design firm
What working with Satoriq is like on this search
You will talk with a Satoriq recruiter who works life sciences engineering every day. We share the full picture on the first call, prep you for each interview, and you will hear back within two business days either way.
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