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QA Officer - Validation - Pharmaceutical Manufacturer

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

Job Description

Our Client is a very successful pharmaceutical manufacturing company. They are now seeking a QA Officer - Validation. This position is a full-time permanent role and will be based in Great Yarmouth.An opportunity has arisen in the QA department for a QA professional to join the team to provide Validation and QA support to the site.Key Areas of Responsibility

  • Active involvement in the management of the site Validation processes
  • Primarily involved in new equipment qualifications, cleaning validations and other validations i.e. process
  • Preparation of validation protocols, execution, and completion of validation reports
  • Assisting other departments involved in validation activities including validation of equipment, processes, and the preparation of associated documentation
  • Maintenance of the validation register for the site
  • Ownership of Change Controls for validation projects as required
  • The control, preparation, review, and approval of Quality documentation to align with the QMS
  • Participation in specific improvement projects as required
Qualifications / Experience
  • Degree (or equivalent) in an appropriate scientific discipline
  • Solid relevant quality experience in a pharmaceutical environment
  • Experience of writing protocols, reports and executing Equipment & Facilities Validations, Cleaning Validations and Process Validations
  • Clear understanding of; GMP, or any other GxP area, regulatory and accreditation systems, quality management, NC/CAPA, & Change Controls
  • Knowledge of legal framework concerning pharmaceutical manufacture i.e. Eudralex, ICH guidelines, medical device legislation
  • Excellent interpersonal skills to be able to liaise effectively at all levels
  • Excellent attention to detail and documentation skills
  • Ability to plan, organise and manage multiple projects
  • Emotionally resilient with the ability to work under pressure with a can-do attitude
In return our client is offering a competitive salary and benefits package for the successful CandidatePlease send your C.V to Lorraine Roger, Director at Atom Recruitment Ltd.

Keyskills :
GMPPharmaceuticalData Validation

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