Job 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:

• Spend the majority of the day gowned up in the manufacturing plant, supporting formulation/filling activities.
• Wipe in and stage materials and equipment required for production activities.
• Collect in-process samples and log them into the laboratory information management system (LIMS).
• Assist in formulation/filling operations and document task performance in the electronic batch record (EBR).
• Preparation of buffers/media, formulation, and filtration of formulated bulk drug product.
• Operation and occasional troubleshooting of vial and syringe filling/stoppering equipment.
• Vial washing, transfer of vial and syringe tubs into the filling/stoppering line

Qualifications:

• Bachelor’s degree in biology or Life Sciences
• Four (4) years of GMP/ Manufacturing experience
• Ability to work with a diverse group of colleagues in a team setting, while getting along with peers to achieve a common goal.
• Attention to detail.
• Knowledge in LIMS and EBR (Electronic Batch Record)
• Formulation/Filling experience
• Able to carefully follow instructional SOPs to prevent impact to production.
• Great communication skills
• Available to work 7am - 4pm OR 10am - 7pm

Job Types: Full-time, Temporary

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday
• Night shift

Ability to commute/relocate:

• Thousand Oaks, CA: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Preferred)

Experience:

• Manufacturing: 4 years (Required)

Shift availability:

• Day Shift (Preferred)
• Night Shift (Preferred)
• Overnight Shift (Preferred)

Work Location: One location

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