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Sterile Specialist

Job LocationRuncorn
EducationNot Mentioned
SalarySalary negotiable
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Company InfoTeva 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 number of Sterile Specialists to join the team in Runcorn on a full time, permanent basis.Please note - this role will require you to work shifts which includes nights and weekends.Key Responsibilities:

  • Set-up, operate, maintain, monitor, and improve packing equipment;
  • Plan, dispense, manufacture and fill sterile products in accordance with Standard Operating Procedures (SOPs) and Current Good Manufacturing Practise (cGMP) requirements;
  • To trouble shoot and resolve process issues in a quick and effective manner, and to contribute to the achievement of site performance targets.
  • Plan, dispense, wash and autoclave filling machine parts
  • Trouble shoot and resolve process issues in a quick and effective manner, and to contribute to the achievement of the departments performance targets.
  • Communicate any instances of non-conformances to the CTL/ Operations Manager or QA representative to ensure they are investigated and rectified in real-time.
  • Complete batch & associated manufacturing documentation right first time in accordance with SOPs and ensure compliance with cGMP
  • Support filling machine set-up/ start up activities, changeovers, testing and cleaning activities in accordance with cleanroom SOPs and cGMP
  • Qualifications, Knowledge and Skills
  • Degree qualified - preferably Bioscience
  • Experience working in the Pharmaceutical or related industry - preferably sterile manufacturing
  • Strong technical and problem solving skills that can be applied to the sterile manufacturing environment
  • Team work - must be able to operate as part of an operations team
  • Good communicator
  • High attention to detail and able to deliver high performance standards
  • 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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