IntePros
Location:
Kankakee, IL (On-site required) Employment Type:
Part-Time Start Date:
Immediate
IntePros is assisting our biopharmaceutical client in hiring a part-time
Process Owner
to support a capital project focused on mechanical Lift Systems at a regulated manufacturing site in Kankakee, IL. This role is ideal for someone with a background in mechanical lifting systems, ergonomics, and GMP compliance within a pharmaceutical or biotech setting.
Key Responsibilities Act as the Process Owner for the implementation of mechanical lift systems used in manufacturing environments Ensure ergonomic safety, regulatory compliance, and operational usability Collaborate with Engineering, Manufacturing, Quality, and EHS to guide system design and operational readiness Participate in URS development, HAZOP/FMEA reviews, and FAT/SAT/CQV activities Support creation of SOPs, work instructions, and training documentation Monitor lift system performance post-deployment and propose improvements as needed Ensure compliance with GMP, GDP, and support audit readiness
Qualifications Bachelors in Mechanical Engineering or a related technical field 4+ years of experience in a GMP-regulated environment, preferably pharma or biotech Strong knowledge of lifting equipment, manual handling ergonomics, and cleanroom standards Familiarity with risk assessments, P&IDs, and equipment validation Excellent collaboration and documentation skills
Kankakee, IL (On-site required) Employment Type:
Part-Time Start Date:
Immediate
IntePros is assisting our biopharmaceutical client in hiring a part-time
Process Owner
to support a capital project focused on mechanical Lift Systems at a regulated manufacturing site in Kankakee, IL. This role is ideal for someone with a background in mechanical lifting systems, ergonomics, and GMP compliance within a pharmaceutical or biotech setting.
Key Responsibilities Act as the Process Owner for the implementation of mechanical lift systems used in manufacturing environments Ensure ergonomic safety, regulatory compliance, and operational usability Collaborate with Engineering, Manufacturing, Quality, and EHS to guide system design and operational readiness Participate in URS development, HAZOP/FMEA reviews, and FAT/SAT/CQV activities Support creation of SOPs, work instructions, and training documentation Monitor lift system performance post-deployment and propose improvements as needed Ensure compliance with GMP, GDP, and support audit readiness
Qualifications Bachelors in Mechanical Engineering or a related technical field 4+ years of experience in a GMP-regulated environment, preferably pharma or biotech Strong knowledge of lifting equipment, manual handling ergonomics, and cleanroom standards Familiarity with risk assessments, P&IDs, and equipment validation Excellent collaboration and documentation skills