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Supervisor, Cell Therapy Manufacturing

Kite Pharma

This is a Full-time position in Frederick, MD posted October 14, 2021.

Job Description *** We are ramping up for commercial production
– numerous positions available!

If you have been thinking about a new job, now is a great time to apply!

** Both Day Shift and Swing Shift positions are currently available.

Everyone at Kite is grounded by one common goal – curing cancer.

Every single day, we seek to establish a direct line between that purpose and our day-to-day work.

Would you like to join us in this mission?!

We are seeking a highly effective Supervisor, Cell Therapy Manufacturing to be responsible for supervising a team of cell therapy manufacturing specialists in our brand new, state-of-the-art commercial biotechnology facility in Frederick, MD.

In this role, the Supervisor will supervise the on-the-floor operations of our commercial cell therapy manufacturing facility in a cGMP environment including building a team, and providing the necessary training and ongoing coaching, performance management and recognition of direct staff, including performing annual performance reviews.

Responsibilities of the Supervisor, Cell Therapy Manufacturing i nclude: * Supervise the on-the-floor operations of commercial cell therapy manufacturing facility in a cGMP environment * Build a team, Provide leadership, guidance, and necessary training to staff in alignment with cGMP requirements.

* Generate SOPs, MPRs, and SPRs for equipment and procedures used in routine biologics manufacture * Clear communication with outgoing and incoming shift Supervisors to disseminate all relevant information.

* Execute production and resource schedule against operational plan * Ensure performance of all process steps specific to the phase or stage of operation * Process monitoring, including manipulation of databases, documents and/or spreadsheets to support business reporting requirements * Review of completed manufacturing documentation per compliance standards and established timelines * Investigate and resolve problems, identifying root cause, and proposing process improvements through clear communication to senior leadership * Participate in multi-functional project teams, as necessary * Take corrective action to bring about required changes using change control procedures * Other duties as assigned Basic Requirements: MA / MS with 3+ years of cGMP Manufacturing and/or Manufacturing Leadership and/or Operations experience OR BA / BS Degree with 5+ years of cGMP Manufacturing and/or Manufacturing Leadership and/or Operations experience OR High School Degree with 9+ years of cGMP Manufacturing and/or Manufacturing Leadership and/or Operations experience Preferred Qualifications: * 5+ years of experience supervising staff * 9+ years of experience in manufacturing in a biotech/pharma industry * Proven capability to build and lead a team as well as train entry-level personnel * Knowledgeable of the current Code of the Federal Regulations (CFR’s) and Current Good Manufacturing Practices (cGMP’s) * Sufficient understanding of process, systems and equipment to troubleshoot problems and provide solutions to senior management * Sufficient knowledge of electronic batch record, ERP and quality systems * Able to work evening to late mid night hours as well as part of the on-call rotation as needed is required; partial weekend shift * Excellent interpersonal, verbal and written communication skills are important in this collaborative work environment * High energy level and a positive outlook coupled with the requisite “can do” attitude and a willingness to do what it takes to achieve personal and organizational goals and overcome obstacles * Willingness to think outside of the box and adapt standard methodologies to our small, but growing environment * Ability to adapt in a constantly evolving environment * Self-motivated with a strong sense of ownership in areas of responsibility Does this sound like you?

If so, apply today!

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