JT734 - MCS SUPPLY CHAIN ASSOCIATE

Thousand Oaks, CA
Temporary
Biopharmaceutical
Mid Level

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:

  • Picking, reviewing, shipping, dispensing, and other tasks in support of Distribution/Dispensing.
  • Consistently follow Standard Operating Procedures (SOP's) and departmental policies with strict adherence to current Good Manufacturing Practices (cGMP's).
  • Material handling associated with the movement of materials within a warehouse setting.
  • Gown to grade 8-9 and work in a classified Dispensary.
  • Material handling/dispensing and all associated cleanings. Staging materials for transport and delivery.
  • Support and identify escalating potential risks associated with shipping/dispensing activities.
  • Collaborates with cross-functional teams in completing operational activities associated with shipping/dispensing.
  • Supports Continuous Improvement initiatives, programs, and projects.
  • Actively participate in Work Center Team efforts as well as Safety programs.
  • Provides support during regulatory inspections and be ready to present information to auditors (as required).
  • Support ATO external warehouse operation teams and all associated tasks.
  • Collaborate with Global Distribution Teams to meet ever evolving needs of the business.
  • Complete all transactions in a prompt and correct/compliant manner.
Qualifications:
  • Bachelor's degree or Associate's degree and 4 years of experience.
  • Polished GMP professional with Shipping, Dispensing, Warehousing, Manufacturing and/or Quality experience.
  • Support documentation revisions in CDOCS.
  • DQMS (Digital Quality Management System) and QMTS (Quality Management Tracking System) knowledge, supporting deviation investigations including initiating and owning minor deviations and CAPAs. 
  • Must be available to work various shifts as needed (day, swing, weekends, holidays) as dictated by the production schedule.

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.

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