Manufacturing Supervisor
Gilead
IT
3 gg fa

Job Description

We are seeking a highly effective Supervisor Manufacturing to be responsible for supervising a team of 10-15 manufacturing technicians in a commercial pharmaceutical environment.

Responsibilities (include but are not limited to) :

  • Supervise the on-the-floor operations of our commercial cell therapy manufacturing facility in a cGMP environment
  • Build a team, provide necessary training and ongoing coaching, discipline and recognition of direct staff, including performing annual performance reviews
  • Generate SOPs, MPRs, and SPRs for equipment and procedures used in routine biologics manufacture
  • 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 management
  • Interact with outside vendors and senior management
  • Participate in multi-functional project teams, as necessary
  • Take corrective action to bring about required changes using change control procedures
  • Other duties as assigned
  • Requirements :

  • Bachelor’s degree in biology or related field (or equivalent experience required), relevant hands on cell culture experience and 2+ years of experience supervising staff
  • Excellent people management skills, able 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 quality systems
  • Flexibility to work off-shift and irregular hours as required as well as part of the on-call rotation as needed, weekend shift likely
  • Excellent interpersonal, verbal and written communication skills are essential 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 best practices 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
  • Flexibility / availability for a training in the USA
  • In possession of a valid EU work permit
  • More information? Please contact Heidi Kroon - talent acquisition specialist, via : CareersEU kitepharma.com.

    Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-

    term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors.

    Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow KitePharma on Twitter at www.twitter.com / kitepharma.

    For Current Kite Pharma Employees and Contractors :

    Please log onto your Internal Career Site to apply for this job.

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