• Reviewing and issuing of validation protocols and reports and also the co-ordination of the execution of validation activities (process / cleaning and equipment and computer qualifications) with relevant departments
• Manage the preparation, review and issuing of Validation Protocols and Reports
• To maintain the cleaning validation strategy
• Implementation of Process Validation of new products for regulatory submissions ensuring compliance to proposed registered specifications
• Coordination of the execution of Validation in accordance with protocols by Production, Quality Control and R&D teams
• Establishing, implementing and directing validation and revalidation activities
• Liaise with contract manufacture customers in seeking their approval for protocols and reports where appropriate
• Reviewing and managing Change Control Forms for Validation implications
• Reviewing and managing Non-Conformance's for Validation Implications
• Updating existing quality documentation related to validation activities
• Identifying training requirements in support of validation
• Ensuring completion of validation protocols
• Conduct internal audits and perform in external audits

What will you need?

• Bachelor of Science or Engineering
• 4+ years experience in a pharmaceutical environment
• Good computer skills with Word, Excel and any other statistical programs

Interested? We would love to hear from you! Please submit your CV and we will get back to you.