Pharmaceutical Manufacturing Technician

1w1 week ago

Merck Group

Verona, US · Full-time · $50,000 – $82,000

About this role

Join MilliporeSigma and work your magic in pharmaceutical manufacturing. This lab-based role focuses on safe and efficient production of active pharmaceutical ingredients (APIs) under current Good Manufacturing Practice (cGMP) requirements. Adhere to GMP standards in 21 CFR parts 210 & 211, 820, ICH Q7, and safety under ISO 14001 & 45001.

Execute equipment cleaning and setup, verification tasks during GMP manufacturing, and maintain safety and quality in the production environment. Serve as primary or secondary operator for cGMP production of APIs and intermediates. Operate production equipment during production, cleaning, and maintenance activities.

Ensure safety and cleanliness in production areas with focus on potent compound handling techniques. Communicate production status using shift pass-off tools and computer systems. Participate in a collaborative, multi-shift manufacturing environment and address safety and process issues from inspections and audits.

Stand for long periods, lift up to 50 pounds with assistance, and utilize PPE including respiratory protection and full-body suits. Work with highly potent/hazardous materials in Class 1/Div 2 areas near moving parts. Bring curiosity and passion to innovate with science and technology enriching lives in Healthcare, Life Science, and Electronics.

Requirements

High School Diploma or GED
2+ years of pharmaceutical manufacturing, chemical manufacturing, or analytical lab experience
Ability to read and understand written protocols
Basic computer literacy (Microsoft Word, PowerPoint, Email, etc.) and strong problem-solving skills
Effective oral and written communication skills
Basic mathematical skills
High degree of motivation and self-starter attitude
Ability to multi-task

Responsibilities

Ensure safety and cleanliness in production areas, focusing on potent compound handling techniques
Utilize and update various written procedures, including batch records and operating procedures
Serve as a primary or secondary operator for cGMP production of APIs and intermediates
Operate production equipment effectively during production, cleaning, and maintenance
Communicate production status clearly using shift pass-off tools and computer systems
Address safety and process issues identified during inspections and audits promptly
Participate in a collaborative, multi-shift manufacturing environment and support departmental responsibilities