Kinetic has partnered with a leading pharmaceutical company who are hiring a validation manager to be based in Riyadh.
Please note that you must meet all the criteria set out below for your application to be considered. Suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.
The main responsibilities will include but not be limited to:
- Plan the validation and qualification activities and schedule in cooperation with relevant departments.
- Design and approve validation protocols, reports, and related documentation.
- Draft and review GMP documentation including SOPs, validation, and training documentation.
- Contribute to the overall validation strategy for the site as well as act as a technical point of contact for internal and external stakeholders.
- Key contributor in the project team to validate the manufacturing unit, working full-time on design, build, and qualification activities.
- Liaise closely with the contractors, engineers, and vendors to ensure full and appropriate information is provided.
To be successful you will need to meet the following:
- Bachelor's degree in chemistry or pharmacy.
- Minimum 10 years of experience within the pharmaceutical industry.
- Must have experience in sterile area.
- Strong experience in manufacturing.
- Excellent communication and strategic thinking skills.
- High attention to detail and a strong focus on quality and safety.
- Applicants should be available for face-to-face interviews in the location mentioned above.
