Process Engineer II; Pharmaceutical Manufacturing

Position: Process Engineer II (Pharmaceutical Manufacturing)
** Process Engineer II (Pharmaceutical Manufacturing)*
* Manufacturing

Wilmington, Ohio, US

+ Added - 23/02/2026

Pay Rate Low: 90000 | Pay Rate High: 115000

_Our client is a global biopharmaceutical company seeking a Process Engineer II to support commercial and clinical pharmaceutical manuacturing, with a focus on oral solid dosage (OSD) products._

*
* Title:

** Process Engineer II **(Pharmaceutical Manufacturing)*
* ** Salary** : $90-115K +Bonus

** Hours** : 1st shift ~8am-5pm M-F

** Location** :
Onsite in Wilmington, OH (Excellent Relocation assistance provided if needed!)

** Summary*
* The Process Engineer supports commercial and clinical pharmaceutical manufacturing, with a focus on oral solid dosage (OSD) products. This role is responsible for process scaleup and transfer, equipment selection and commissioning, and continuous improvement of manufacturing and packaging operations.

** Essential Functions*
* + Troubleshoot and maintain manufacturing systems, processes, and equipment.

+ Support the development or transfer of manufacturing and cleaning processes for the manufacturing area.

+ "Hands-on" ability to install and troubleshoot instrumentation and equipment.

+ Author high-quality technical protocols/reports (engineering studies, summary reports, equipment specifications, change controls, and investigations)

+ Specify and size manufacturing systems, equipment, and process equipment.

*
* Basic Qualifications:

*
* + BS degree in Engineering or technical discipline.

+ 2-5 year of manufacturing experience or technical experience.

** Preferred

Qualification:

*
* + 2-5 years of OSD pharmaceutical experience or 5 years of pharmaceutical engineering experience.

+

Experience with OSD equipment procurement.

+ Thorough knowledge of cGMP, OSHA, EPA and FDA facility requirements and regulations.

+ Thorough knowledge of OSD operations, statistics, equipment design, process control, and process scale-up.

+ Knowledge of OSD pharmaceutical process and equipment validations.

+ Experience in statistical analysis: sample sizing, ANOVA, regression analysis, control charts, etc

+ MUST be authorized to work in the US without sponsorship

** Physical Demands*
* + Ability to properly gown and don PAPR for potent controlled substance formulations for extended periods of time

+ Ability to lift/move 40 lbs. overhead.  Ability to team lift up to 100 lbs.

+ Must be able to be medically cleared for respirator use (PAPR)

+ Ability to operate different types of production equipment.

+ Ability to gown correctly for clean room manufacturing operations.

+ Ability to stand or sit for extended periods (up to 2 hours at a time).

+ Must be able to work in an office and a manufacturing environment.

INDBH

LI-MG1

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.