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Quality Control Analyst II/III (2nd Shift)

Company: Catalent
Location: Severn
Posted on: March 14, 2020

Job Description:

Job DescriptionPosition Overview:-- Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent---s advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love.-- Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start hereThe Quality Control Analyst II/III (2nd Shift) is responsible for routine QC testing on cleaning, in-process and release samples.----The QC Analyst must demonstrate technical knowledge,--be familiar with basic scientific/regulatory principles, possess initiative, and maintain a strong commitment to scientific excellence.--This is a second shift position that will reside roughly on a 4pm-12am schedule and will report to the QC Supervisor at our Harmans/BWI site.--Paragon Gene Therapy, now a part of Catalent, hires people with a passion to make a difference. Your expertise, coupled with our advanced technologies and collaboration with innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives.The Role/Job Duties:

  • Perform routine testing such as filter integrity testing, TOC, pH, conductivity and HPLC.----Experience with PCR testing preferred.
  • Generate testing records and report results.
  • Provide instrumentation care, maintenance, troubleshooting, and data interpretation.
  • Work under general supervision to meet project goals.
  • Work closely with Manufacturing and Quality Assurance staff to resolve quality issues with regard to the facility and products manufactured.
  • Document writing (laboratory investigations, out of specifications, deviations, CAPAs), data interpretation/presentation, statistical analysis, and trending.The CandidateExperience & Education:
    • Bachelor in a Life Sciences discipline and 2-5 years of experience working in a QC laboratory (will consider reduced experience with increased levels of education in same field).
    • HPLC knowledge/experience is required along with experience in writing SOPS.
    • Knowledge/expertise relevant to QC analytical methods used for protein chemistry and molecular biology.
    • Experience within the biologic, pharmaceutical, or medical device industry performing direct hands-on work in a Quality Assurance/QC function with a strong familiarity of general GMP practices.
    • Broad experience with biochemistry, as well as generating/reviewing the documentation that supports such work.
    • Possesses the knowledge and ability to apply basic scientific and regulatory principles to solve operational, as well as routine quality tasks.We will identify candidates based on the following:
      • Leads with Integrity and Respect
      • Delivers Results
      • Demonstrates Business Acumen
      • Fosters Collaboration and Teamwork
      • Champions Change
      • Engages and Inspires
      • Coaches and DevelopsPosition Benefits:
        • Join a high growth and fast paced organization with a people focused culture
        • Global exposure, defined career path and annual performance review and feedback process
        • Competitive Medical, Dental, Vision and 401KCatalent 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.-- ---- --personal initiative. dynamic pace. meaningful work.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, Severn , Quality Control Analyst II/III (2nd Shift), Professions , Severn, Maryland

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