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Manufacturing Associate I

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Posted : Tuesday, August 06, 2024 02:43 AM

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) Qualifications: * Bachelor’s Degree in Engineering or IT/IS/Computer Science background * Mechanically inclined (understanding of repairs, etc.
) * GMP (drug substance) worked in biotech manufacturing, bench top production with a engineering, comp sci background.
* Chromatography Experience - At least 1 year experience preferred.
* Large Scale processing, buffer prep or media prep 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 * Able to work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work.
* Must be able to work multiple shifts at 3-month intervals (Day and swing shift) * Swing Shift: 2:30pm - 11:30PM and Day shift: 7:30am - 4:30PM _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 Salary: $28.
00 - $30.
00 per hour Schedule: * 10 hour shift * Day shift * Evening shift * Monday to Friday * Night shift * Rotating shift Education: * Bachelor's (Required) Experience: * Pharmaceutical industry: 1 year (Preferred) * Manufacturing: 1 year (Preferred) * Chromatography: 1 year (Preferred) Ability to Relocate: * Thousand Oaks, CA: Relocate before starting work (Required) Work Location: In person

• Phone : NA

• Location : Thousand Oaks, CA

• Post ID: 9141113763


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