JT593 - MANUFACTURING 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:

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.
Daily sampling and cleaning up around the area and performing maintenance tasks.

Qualifications:

Bachelor's Degree in related area
Background in science or engineering
Hands-on experience in manufacturing or laboratory environments, preferably within the biopharma or pharmaceutical industries.
Demonstrate proficiency in process sampling, operating bench analytical equipment, and using tools such as Solo VPE for protein concentration measurements.
Familiarity with document management software like C-Docs and a logical understanding of the scientific method are essential.
Proactive, detail-oriented, and possess strong teamwork and communication skills, with a willingness to learn beyond their immediate responsibilities and contribute to the team’s overall success.
While GMP/GLP experience is a plus, the ability to work in a structured, process-driven environment is critical.
Expectation of Rotating shift 7:30am-4pm /3pm-10:30pm change to occur every four months,
Candidate would expect to begin on the day shift.

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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