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Supervisor, Quality Control

Company: Catalent
Location: Bloomington
Posted on: January 10, 2019

Job Description:

Job DescriptionPosition Overview:-- Catalent is a leading provider of advanced technologies and outsourced services for the pharmaceutical, biotechnology and consumer health industry. Catalent develops, manufactures, packages and distributes pharmaceutical and other products for customers in nearly 100 countries. https://www.youtube.com/watch?time_continue=1&v=65rz3LwTPX8Position Summary Catalent is looking to recruit a Supervisor, Quality Control to join a growing team in Bloomington, Indiana.A Supervisor, Quality Control primary duty is to plan, organize, direct and evaluate the routine activities and project deliverables of the QC laboratories to ensure the safety and reliability of products produced in compliance with quality and regulatory requirements.--Responsibilities include overseeing the scheduling of daily activities for QC personnel, interpreting applicable quality and regulatory requirements and develop associated policies and procedures for the laboratories operations, interfacing with investigators during both internal and external inspections, evaluating audit observations and developing responses and oversight for related action plans, making critical decisions concerning testing operations, working collaboratively with manufacturing, technical and product development teams to improve quality, increase efficiency, solve problems, generate cost savings, and provide new product support, managing operations for the QC laboratories and supporting the QC documentation and LIMS activities.In concert with Catalent---s Patient First philosophy, the Supervisor, Quality Control position contributes to this philosophy by ensuring quality of data and that all data is consistent with expectations.-- This position is critical to the patient first philosophy because it confirms tests were executed according to defined procedures and results are within the required specifications.-- This positions also manages the scheduling of testing to help meet batch release timelines, which contributes to delivering product to patients in a timely manner.The Role

  • Demonstrated Informal Leadership
  • Typically manages 2-15+ employees
  • Provides direction on daily work, planning for up to 1 month in advanceThe Candidate
    • High School/GED
    • Bachelor---s degree preferred
    • 2 years laboratory experience
    • 2 years GMP experience
    • 0-1 years of management experienceCatalent---s standard leadership competencies that are used to interview and for Performance & Development:
      • Leads with Integrity and Respect
      • Delivers Results
      • Demonstrates Business Acumen
      • Fosters Collaboration and Teamwork
      • Champions Change
      • Engages and Inspires
      • Coaches and DevelopsPosition Benefits
        • Potential for career growth within an expanding team
        • Defined career path and annual performance review & feedback process
        • Cross functional exposure to other areas of Catalent
        • Medical, Dental, Vision, and 401K are all offered from day one of employment
        • 19 days of paid time off annually + 7 paid holidaysCatalent offers rewarding opportunities to further your career!-- Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.-- ---- --Catalent. More products. Better treatments. Reliably supplied. ---Visit www.catalent.com/careers to explore career opportunities.---- --Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.------ --Notice to Agency and Search Firm Representatives:--Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting.-- Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent.-- No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.-- Thank you.

          Keywords: Catalent, Bloomington , Supervisor, Quality Control, Other , Bloomington, Indiana

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