Process Operator I

CatalentMalvern, PA
6dOnsite

About The Position

Process Operator I Position Summary Shift: Monday - Thursday 1PM-11PM 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Process Operator micronize\mills client provided material including both active pharmaceutical ingredients and excipients as per Catalent Malvern procedures and policies, client instructions and cGMP guidelines. Consistently models Catalent values and leadership behaviors in all interactions.

Requirements

  • High School Diploma or GED
  • Organizational Skills
  • Detail Orientation
  • Communication Skills Oral and Written
  • Basic Math Skills, interpretation

Nice To Haves

  • Prior manufacturing experience and work in a regulated environment preferred.
  • Ability to work weekday and weekend OT a plus.

Responsibilities

  • Perform entry-level micronization and milling of both hazardous and non-hazardous pharmaceutical actives and excipients.
  • Set up, operate equipment, and monitor production processes.
  • Report production on batch records following good documentation procedures (GDPs).
  • Work in a regulated environment with adherence to standard operating procedures and policies.
  • Execute tasks accordingly.
  • Adhere to cGMP standards.
  • Identify and communicate non-routine events, deviations, and GMP deficiencies to supervisor promptly.

Benefits

  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

High school or GED

Number of Employees

5,001-10,000 employees

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