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Director, Microbiology
Director, MicrobiologyKBI Biopharma • Durham, NC, US
Director, Microbiology

Director, Microbiology

KBI Biopharma • Durham, NC, US
[job_card.30_days_ago]
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  • [job_card.full_time]
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Microbiology Director

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.

Position Summary :

This individual will direct microbiology activities at Patriot Park. Responsible for the development, maintenance and harmonization of microbiology procedures and systems related to Quality Control oversight. Provides strategic and technical expertise in all cGMP compliance related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the KBI internal requirements.

Responsibilities :

  • Develop strategy and drive harmonization of microbiology programs.
  • Provide strategic and technical expertise to Patriot Park and Hamlin Rd. KBI sites to ensure microbiology procedures, and decisions meet regulatory and KBI requirements and are based on documented scientific rationales.
  • Lead, assess, coach and develop departmental associates. Manage performance; ensure team meets company, site and personal expectations and meets objectives; guide the professional growth of team.
  • Ensure all personnel at both facilities are trained to appropriately perform expected duties.
  • Encourage a quality culture of inclusion and high standards to ensure a high performing team.
  • Expert understanding of regulations and industry expectations. Support regulatory and client audits.

Requirements :

  • BS and 12+ years' experience or MS and 10+ years' experience in a QA or GMP environment or equivalent.
  • Experience leading and managing microbiology laboratories in an FDA regulated manufacturing environment.
  • Demonstrated expert knowledge of relevant FDA and EU regulations as well as hands on experience in a low bioburden and aseptic processing setting.
  • Language Ability :

    Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedures. Ability to effectively present information and respond to questions from staff, colleagues, managers and clients. Ability to read, analyze and author complex documentation.

    Reasoning Ability :

    Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

    Math Ability :

    Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

    Computer Skills :

    Word processing, Database, Spreadsheets, Power Point, Internet, E-mail, Calendar Management, quality management electronic systems

    Salary Range : $173,000 - $238,700 / yr.

    Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.

    About KBI :

    KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe.

    KBI is a proud EEO / AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.

    I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

    I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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