Associate Manufacturing Process Technician - Thousand Oaks, United States - Quality Consulting Group, LLC

Mark Lane

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Mark Lane

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Description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team.

In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.


Responsibilities:


  • Work in a highly collaborative team environment and be responsible for both moderately complex to complex nGMP and GMP manufacturing activities to support of our early phase clinical pipeline of synthetic drug products.
  • Handson cleaning, sanitization, and setup of processing equipment and process rooms
  • Support in manufacturing process readiness activities
  • Assist in the review of facility and equipment documentation (equipment/room logbooks)
  • Maintenance of Raw Materials & Consumables Inventory
  • Supporting the daytoday operational needs of the facility
  • Collaborate in multidisciplinary teams with Process Development scientists, engineers, EH&S, Quality, F&E, maintenance, and other supporting functions.
  • Identify, recommend, and implement improvements related to routine functions.

Qualifications:

  • Associate's degree in science/pharmaceutical sciencerelated area
  • Experience in pharmaceutical industry
  • Understanding of typical unit operations for the manufacture of synthetics drug product (i.e., granulation, roller compaction, drying, milling, blending, compression, encapsulation and film coating).
  • PPE familiarity and ability to use a PAPR.
  • Ability to work with Microsoft Word, Excel, and PowerPoint
  • Excellent verbal and written communication skills
  • Monday-Friday 8 AM5 PM with 1 hour lunch.
  • Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law._

Job Types:
Contract, Temporary


Pay:
$ $21.00 per hour


Schedule:

  • 8 hour shift
  • Monday to Friday

Education:


  • Associate (preferred)

Experience:

- pharmaceutical industry: 1 year (preferred)

  • GMP: 1 year (preferred)
  • Manufacturing: 1 year (preferred)

Ability to Relocate:

  • Thousand Oaks, CA: Relocate before starting work (required)

Work Location:
In person

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