Full-Time

Process Operator

Medvacon Life Sciences

Medvacon Life Sciences

No salary listed

Malvern, PA, USA

In Person

Category
Operations & Logistics (1)
Requirements
  • A High School Diploma or General Educational Development credential is required.
  • Be dependable, ready and eager to learn, and able to meet the physical requirements of the job.
  • Have oral and written communication skills.
  • Have basic math skills and interpretation ability.
  • Be able to work safely with high-potency active pharmaceutical ingredients and novel compounds of unknown potency and toxicity.
  • Be able to wear required personal protective equipment, including gloves, a respirator hood, safety glasses, and safety shoes, in designated areas.
  • Be able to lift or move items up to 44 pounds individually, or use a two-person lift for items between 45 and 76 pounds; items 77 pounds and over require a lift-assistance device.
  • Be able to perform moderate physical labor, including lifting, climbing, bending, crouching, reaching, and twisting.
  • Be able to stand or walk for up to 8 hours per day.
  • Be able to climb steps and ladders and occasionally work from elevated platforms.
  • Be able to wear a respirator hood and pass the required respiratory medical examination.
  • Be able to work in loud environments and wear various types of hearing protection.
  • Be able to work safely with chemicals and hazardous materials in compliance with the site safety program.
  • Be available to work the stated weekday shift and potential overtime, including weekends.
Responsibilities
  • Perform entry-level micronization and milling of hazardous and non-hazardous pharmaceutical active ingredients and excipients.
  • Set up and operate equipment and monitor production processes.
  • Record production on batch records following good documentation procedures.
  • Work in a regulated environment in adherence to standard operating procedures and policies.
  • Adhere to current good manufacturing practice standards.
  • Identify and promptly communicate non-routine events, deviations, and good manufacturing practice deficiencies to the supervisor.
  • Clean the entire processing area and processing equipment.
  • Produce thorough, clear, and consistent documentation in compliance with quality standards.
  • Participate in shift-change meetings, site and team meetings, email communications, improvement suggestions, and projects.
  • Work at the site-based facility.
  • Strive to achieve First Time Right as a key performance indicator to meet yearly targets.
Desired Qualifications
  • Some good manufacturing practice experience is preferred.
  • Prior manufacturing experience and work in a regulated environment are preferred.
  • Prior production experience is preferred.
  • Ability to work weekday and weekend overtime is a plus.
Medvacon Life Sciences

Medvacon Life Sciences

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