Manufacturing Supervisor, Solution Prep

FujifilmCollege Station, TX
433d

About The Position

The Manufacturing Supervisor at Fujifilm is responsible for overseeing the Solution Preparation Unit Operations, which includes supervising a team involved in the preparation of media and buffers for biopharmaceutical production. This role involves ensuring compliance with cGMP regulations, managing daily manufacturing activities, and leading continuous improvement initiatives. The supervisor will also engage in training, mentoring, and performance evaluations of staff while collaborating with various teams to support production and development activities.

Requirements

  • Master's degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or related field and 3+ years of experience in a manufacturing environment; OR Bachelor's degree in the same fields with 5+ years of experience; OR Associate's degree with 7+ years of experience; OR High School/GED with 9+ years of experience.
  • 2+ years of experience in a leadership or supervisory role required.
  • 3+ years of experience in a GMP environment required.
  • Demonstrated leadership, coaching, and mentoring skills.
  • Excellent skills with Microsoft Office applications.
  • Advanced math and computer skills.

Nice To Haves

  • Biotechnology Certificate preferred.
  • Green-Belt Certification preferred.
  • Experience with mammalian, insect, yeast, or bacterial cell lines and their cultivation and/or purification of biologics or viral vectors.

Responsibilities

  • Supervise daily manufacturing activities and staff, including hiring, performance evaluations, coaching, mentoring, and disciplinary actions.
  • Implement project safety and quality assurance programs.
  • Execute SAP functionality for batch close out and generate SAP reports as required.
  • Develop, write, and review Standard Operating Procedures, Buffer Formulation Records, and Batch Production Records (BPRs).
  • Ensure proper documentation and execution of BPRs and activity records according to cGMP regulations.
  • Lead deviation resolution and closure with subject matter experts and quality teams.
  • Track CAPAs to closure and provide input to R&D functions during development and scale-up activities.
  • Represent the organization in client meetings as the subject matter expert regarding assigned manufacturing processes.
  • Ensure an adequate supply of materials for production and maintain confidentiality of proprietary information.
  • Drive continuous improvement in areas of responsibility.

Benefits

  • Competitive salary range of $89.2K - $113K per year.
  • Opportunities for professional development and training.
  • Supportive work environment that encourages innovation and collaboration.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Industry

Machinery Manufacturing

Education Level

High school or GED

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