Production Operator

Production Operator

At Client'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 Contract Manufacturing Specialist 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. The Specialist, Manufacturing 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 CClient 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.

DE&I Statement

Client embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as, and employment eligibility verification requirements.