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JT117 - CELL CULTURE MANUFACTURING ASSOCIATE

qualityconsultinggroup · 14 days ago
Negotiable
Full-time
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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 dynamic production environment at site supporting development, clinical, and launch activities.
  • Under general supervision, employee will perform operations in the Manufacturing area.
  • Operations will be performed according to Standard Operating Procedures (SOPs).
  • Performing in-process sampling of equipment and operating analytical equipment
  • Performing washroom activities: clean small- and large-scale equipment used in production activities.
  • Maintaining an organized and clean workspace
  • Initiating quality reports
  • Drafting and revising documents (SOPs, MPs)
  • Assisting in the review of documentation for assigned functions (equipment logs, batch records)
  • Working around high-pressure systems and occasionally work around heavy equipment.
  • Execute routine validation protocols

Qualifications:

  • Bachelor's Degree in Life Sciences, Chemistry, Biology, Chemical Engineering Biotech, Biochem, etc. Process Development or Manufacturing experience.
  • 4 years of Process Development or Manufacturing experience
  • Experience in Set-up, cleaning, and sanitization of various manufacturing equipment
  • Experience in preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
  • Knowledge of GMP documents (SOPs, MPs) with strict adherence to safety and compliance
  • Ability to work in a manufacturing plant environment wearing steel toe shoes, lab coat, safety glasses and gloves when performing all work.
  • Experience with Delta V
  • Experience with lab equipment/testing
  • Mechanically inclined
  • Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule
  • Will work day shift but should be flexible and able to work swing/ graves as business needs may require

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.

Last updated on Nov 18, 2024

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