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QA Officer

TEVA
Job LocationRuncorn
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Who Are WeTeva is a global pharmaceutical leader and the worlds largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!Job DescriptionWe are currently recruiting a Quality Assurance Officer to develop, implement and maintain quality standards and systems to ensure that our products comply with Marketing Authorisations, specifications and cGMP.Please note - this role will require you to work shifts (6am - 6pm and 6pm - 6am), including weekends.Key Responsibilities:

  • You will support manufacturing and other operations in the development, implementation and maintenance of cGMP standards
  • You will review and approve batch manufacturing and packaging documentation within agreed timelines
  • You will review and approve quality documentation to ensure compliance with cGMP
  • You will prepare and complete product quality reviews to ensure compliance with regulatory requirements
  • You will close out failure investigations and preventative actions to reduce repeat failures and to monitor actions to prevent overdue actions
  • You will identify, design and deliver cGMP training to support improved application of cGMP standards
  • You will carry out audits to support the identification, actioning and close out of non-compliance issues
    • Who We Are Looking ForDo you have:
  • A degree in a Science based discipline and experience working in the Pharmaceutical industry
  • Sterile and Biologics Manufacturing experience
  • A good understanding of GMP requirements in relation to sterile product manufacture and packaging
  • Understanding of the principles of sterilisation and aseptic processing
  • Understanding of lean manufacturing techniques and Quality Management Systems
    • Are you:
  • IT Literate
  • A self starter and results driven
  • Experienced in auditing and have good problem solving skills
  • Able to work effectively with peers and on your own initiative
    • If so - we would love to hear from you!What We Offer
  • 24 days paid holiday per year
  • Company pension
  • Excellent training and development
  • A number of health benefits including: Life Assurance, Critical Illness Insurance, Income protection
  • Plus many other flexible benefits: Buy and sell annual leave, cycle to work scheme, online and in store discounts and much more
    • Tevas Equal Employment Opportunity CommitmentTeva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

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