LOC Quality Manager
Stiefel Laboratories, Inc
10d ago

Your Responsibilities : LOC Quality Manager

LOC Quality Manager

  • You will be responsible for ensuring overall quality standards are met for products. Responsible for programmes to establish and maintain quality standards of existing products and services, as well as developing programmes to focus employees on quality improvement.
  • Approval of batch release to the market

  • You will develop and implement programs to establish and maintain quality standards of existing products, and internal systems and processes.
  • Develops policies, procedures and methods to check product, material, components and / or operational quality and improve same.

    Key Responsibilities :

  • As an Operational Quality Manager / Lead, you will be responsible for ensuring effective Regional oversight of the Quality Management System (QMS) in your local region to meet both regulatory and customer expectations.
  • This includes harmonizing the quality standards and simplifying processes while driving both compliance and efficiency.

  • You will lead projects and drive quality initiatives across the LOCs in the region to improve quality compliance and efficiency.
  • You will own and implement Regional LOC Quality System and Processes.
  • You will oversight of LOC QMS implementation in use through a program of quality standard harmonization.
  • You will serve as the Regional LOC QMS point of contact.
  • You will manage Regional management monitoring program to assure risks are identified and properly mitigated.
  • You will conduct audits to provide quality assurance and identify areas for improvement.
  • You will harmonize the LOC Quality ways of working with key distributors to drive standardization and efficiency.
  • You need to partner with Supply Chain, CS&L, Regulatory and LOC Quality to ensure significant 3rd party related risks are appropriately escalated and mitigated in a consistent manner.
  • You shall collaborate with other Regional LOC Quality, Regional Regulatory, Regional Supply Chain to promote sharing and learning.
  • Basic Qualifications :

  • You need to have a Bachelor’s Degree in Pharmacy, Science, or an engineering discipline, OR equivalent level of knowledge, understanding and hand on experience of Good Manufacturing Practices in the pharmaceutical environment
  • You have 5 - 10 years of Manufacturing / Quality experience in the Pharmaceutical industry.
  • You must have experience with the application of Quality Systems in manufacturing, warehousing and distribution.
  • Basic qualifications :

    Recruiter required to update

    Preferred qualifications :

    Why GSK? :

    GlaxoSmithKline is science-led global healthcare company with a special purpose : to help people do more, feel better, live longer.

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