The Process Engineer provides technical input on sterile processes from a facility and operational standpoint, manufacturing project management oversight, and GMP expertise to ensure timely availability of clinical supplies and development batches
Job Summary
The Process Engineer provides technical input on sterile processes from a facility and operational standpoint, manufacturing project management oversight, and GMP expertise to ensure timely availability of clinical supplies and development batches.
Responsibilities include authoring batch records, coordinating batch inputs, providing shopfloor support, sample and batch delivery, and owning change control and leading deviations.
The role offers a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits, paid holidays, vacation, and compassionate and sick days.
Matching Summary
The Process Engineer provides technical input on sterile processes from a facility and operational standpoint, manufacturing project management oversight, and GMP expertise to ensure timely availability of clinical supplies and development batches.
Salary
Base: $87,300.00 - $137,400.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days
Skills & Requirements
Must-have
Sterile process manufacturing
Formulation development
Process Engineering
cGMP Guidelines
Technical writing
Troubleshooting
Nice-to-have
Cross functional leadership
Teamwork
Adaptability
Personal Initiative
Ability to work collaboratively
Key Requirements
Bachelors of Science in Chemical Engineering, Chemistry, Biology or related Scientific Field
Minimum of 1.5 years in a technical or operations support role