Chemical Process Operator I – GMP Manufacturing

Piramal Pharma Solutions; Ann Arbor (MI); On-site; USD 46,000 - 60,000; Full time

Job summary

Piramal Pharma Solutions is hiring a Chemical Operator 1 for our on-site facility in Ann Arbor, MI. The role focuses on operating chemical processing equipment according to GMP and safety standards to support production and quality objectives.

You will handle raw materials, monitor processes, and document data while coordinating with QA and engineering to resolve issues. A strong emphasis on safety, attention to detail, and teamwork is essential.

Qualifications

• High school diploma or equivalent (required).
• Experience in chemical manufacturing or pharmaceutical environments preferred.
• Ability to follow SOPs and document process data accurately.
• Ability to operate production equipment safely and with basic mechanical aptitude.
• Strong attention to detail and commitment to safety and compliance.
• Ability to work on-site in rotating shifts, stand for extended periods, and lift moderate weights as required.

Responsibilities

• Operate chemical processing equipment (reactors, mixers, distillation units) per procedures and safety standards.
• Monitor process parameters, record production data, and perform routine adjustments to maintain quality and efficiency.
• Handle raw materials and chemicals; perform basic equipment inspections; support cleaning and changeover activities.
• Collaborate with quality and engineering teams to resolve issues and ensure GMP compliance.

Skills

Chemical Handling

Chemical Processing

Distillation operations

Quality Control

SOPs

Safety compliance

Team collaboration

Shift work

On-site work

Physical stamina

Communication skills

Education

High school diploma or equivalent

Job description

Piramal Pharma Solutions is hiring a Chemical Operator 1 for our on-site facility in Ann Arbor, MI. The role focuses on operating chemical processing equipment according to GMP and safety standards to support production and quality objectives.

You will handle raw materials, monitor processes, and document data while coordinating with QA and engineering to resolve issues. A strong emphasis on safety, attention to detail, and teamwork is essential.