Production Operator

KellyOCG; Los Angeles (CA); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Access to Wellness program

Direct Deposit and Weekly pay

Free skills enhancement and training

Employee Discounts with popular retailers

Job summary

A leading staffing partner is seeking a Contractor for a dynamic Manufacturing team in Tarzana, CA. This role involves supporting cell therapy production operations in compliance with cGMP regulations. The ideal candidate requires at least five years of relevant experience and will be responsible for manufacturing readiness and creating operational documents. This is a contingent assignment of 90 days with possible extension based on project needs and performance. Competitive compensation may apply based on budget availability.

Qualifications

• Minimum of five years of experience in relevant field.
• Understanding of cGMP process and CMC regulatory framework.
• Knowledge of GMP manufacturing and tech transfer.

Responsibilities

• Support GMP readiness for clinical manufacturing.
• Perform operational tasks in a cleanroom environment.
• Assist in developing Standard Operating Procedures (SOPs).
• Maintain appropriate inventories within cleanroom areas.
• Ensure all materials are available for manufacturing activities.

Skills

Understanding of cGMP process

Knowledge of aseptic techniques

Cell therapy manufacturing experience

Problem-solving skills

Education

High School Diploma or a BS/BA in relevant science or engineering

Tools

NC-200 Nucleocounter

Dynasellect

Cue

ISO 5 aseptic operations

Job description

Overview

Working Hours: M-F 8 Hours; subject to change to 4x10's shift on either Sun.-Wed. or Wed.-Sat.

Typically 9am-5pm but subject to change

Interview Process:

At AstraZeneca's Oncology R&D division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.

Position Summary:

We are seeking a Contractor to support our dynamic Manufacturing team in the production of TCR-T, CAR-T, and allogeneic cell therapy investigational products. This contract role is based in Tarzana, CA, with occasional travel to Santa Monica, CA as needed. The contractor will report to the Associate Director of Manufacturing, NGF70.

This role will ensure successful manufacture and release of cell therapy products by following established processes in full compliance with cGMP. This role also supports manufacturing operational readiness and the successful technology transfer of pipeline products using knowledge of cGMP regulations.

This is a 90 day contingent assignment, with the possibility of extension based on project needs, performance, and budget availability.

Compensation and employment terms will be managed through an approved staffing partner. This role is not eligible for company-sponsored benefits unless provided by the staffing agency.

Responsibilities

• Using general application of principles, support activities to ensure GMP readiness for clinical manufacturing, including but not limited to equipment procurement, installation and qualification, facility qualification, and technology transfer.
• Perform operational tasks within a cleanroom environment in a manner consistent with safety policies, quality systems, and cGMP requirements.
• Assist in developing Standard Operating Procedures (SOPs) and other documents for manufacturing processes.
• Set up manufacturing areas and equipment, including complex automated cell processing equipment.
• Follow all cleaning and gowning procedures for the facility.
• Maintain appropriate inventories of material and supplies within the cleanroom areas to support manufacturing activities.
• Ensure all materials and equipment are identified and available in time for manufacturing activities.
• Support Process Development (PD) and Manufacturing Sciences & Technology (MSAT) to align manufacturing plans with product development plans.
• Ensure that all production operations are controlled and performed within cGMP regulatory guidelines.
• Provide verbal and written updates to Manufacturing leadership.
• Perform other responsibilities and project-based assignments as needed to support manufacturing operations.

Experience and Education

• Minimum of five (5) years of experience with a High School Diploma or a BS/BA in a relevant science or engineering discipline.
• Understanding of cGMP process and knowledge of CMC regulatory framework for biologics.
• Knowledge of aseptic techniques for primary human cell cultures and GMP manufacturing and supporting tech transfer and GMP clinical/commercial manufacturing operations.

Additional Requirements

• Knowledge of industry practices, cell therapy manufacturing experience preferred.
• Develop solutions to complex problems independently.
• Refer to established precedents and policies or use original thinking.
• Help determine goals of assignment.
• Plan schedules and arranges own activities.
• Work is reviewed upon completion for adequacy in meeting goals.
• CAR-T immunotherapy production operator/verifier/runner
• Deviation support
• Experience with operating cell therapy equipment such as NC-200 Nucleocounter Automated Cell Counter, Dynasellect, Cue, Welder, Sealer, Microscope, Sefia, Finia, Sepax, and ISO 5 aseptic operations

When we put unexpected teams in the same room, we fuel bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

When it comes to working, we want to help take some of life’s pressures off - where we can. So, Kelly employees get access to great benefits, perks, and discounts.

EnrollVB Program

• Access 2 Wellness - lower medication costs
• Kelly’s Life Advisor Wellness Program - access to counselors to assist with a wide range of issues, including Life Coaching sessions
• Retirement Savings
• Direct Deposit. Weekly pay
• Free skills enhancement and training with More than 6,000 courses and 55,000 eBooks and publications are available
• Employee Discounts/Perk Spot - Thousands of popular retailers and service providers, you can obtain discounts for almost anything you can buy
• Holiday and Service plans where applicable