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

Quality Consulting Group, LLC
Quality Consulting Group, LLC
Verified Company
Thousand Oaks, United States

2 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
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 dynamic production environment at site supporting development, clinical, and launch activities.
  • Under general supervision, employee will perform operations in the Manufacturing area.
  • Equipment set up, operating process equipment, buffer/media prep, equipment cleaning, sampling of inprocess product pools and sample management in electronic sample management system.
  • Analytical testing to support production, including pH, cell counting, protein concentration, etc.
Identify and recommend improvements to operations, and implement after approval

  • Basic troubleshooting
  • Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
  • Performing and monitoring critical processes with the ability to perform basic troubleshooting.
  • Performing inprocess sampling of equipment and operating analytical equipment

Qualifications:

  • Bachelor's degree in Life Science or Biology
  • Mechanically inclined
  • Four (4) years of relevant experience in manufacturing.


  • Chromatography Experience

  • At least 1 year experience preferred
  • Biotech Process Development or Manufacturing experience.
  • Large Scale processing, buffer prep or media prep experience.
  • Must be able to work multiple shifts at 3month intervals (Day and swing shift)
  • Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) 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._

Job Types:
Full-time, Temporary


Pay:
$ $30.00 per hour


Schedule:

  • 12 hour shift
  • 8 hour shift
  • Day shift
  • Monday to Friday
  • Overtime
  • Weekends as needed

Education:


  • Associate (preferred)

Experience:


  • Manufacturing: 2 years (preferred)
- pharmaceutical: 2 years (preferred)


Shift availability:

  • Day Shift (preferred)
  • Night Shift (preferred)
  • Overnight Shift (preferred)

Work Location:
In person
More jobs from Quality Consulting Group, LLC
See all jobs of Quality Consulting Group, LLC