Description
Key purpose of the role is to plan and perform validation activities in accordance with site validation master planESSENTIAL DUTIES AND RESPONSIBILITIES
- Must have 5+ years recent experience in validation of product/processes/equipment within the Pharmaceutical industry.
- Must have ability to analyse and interpret data
- Must have good interpersonal and organizational skills
- Must have proficient computer skills ( MS office etc)
- Education - degree qualified - Science / Engineering
DESIRED MINIMUM QUALIFICATIONS / EXPERIENCE
The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
- FDA validation requirements & understanding
- Software validation requirements
- Development of IQ/OQ and PQ protocols
- Performance of qualification activities
- Validation report writing
- Process FMEA
- Risk management
- SOP / specification development
- Document/change control
- CAPA
If you would like to apply for this role please contact Sarah Irvine on or reply with a copy of your current CV. We also offer shopping vouchers for any successful referrals.