I'm currently looking for a Validation Manager to join a leading Biopharmaceutical business based in the Hertfordshire area. You will be responsible for managing the Qualification & Validation activities, as well as some of the following duties:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Manager will be varied however the key duties and responsibilities are as follows:
Lead Validation activities and assist in the establishment of a new Quality System to ensure compliance to manufacture to GMP requirements.
Work with the Quality Assurance team to support the establishment and maintenance of Validation Systems, including within the PQS.
Approve and oversee the management of external suppliers of qualification and validation activities, ensuring their compliance to GMP.
Manage validation deviations and progress CAPA's relating to Validation processes, including participating in internal and external validation activities.
To be successful in your application to this exciting opportunity as the Validation Manager we are looking to identify the following on your profile and past history:
1. Experienced working within small scale GMP environments, e.g. Clinical Trials
2. Proven industry experience working within a Validation related environment and role
3. A working knowledge and practical experience of Clean Room, Aseptic or Sterile environments
Key Words: Validation, Quality System, PQS, GMP, Aseptic, Sterile, Qualification, Biopharmaceutical
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.