KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Officer (Documentation) will be varied however the key duties and responsibilities are as follows:
1.Issue SOPs, Record Sheets and Batch Records ensuring the quality system will be updated accordingly.
2.Update SOPs related to training management and quality documentation management.
3.Ensure the existence and maintenance of the training management system and to provide the resources and skills required in your department to execute staff training.
4.Work with the Assistant Production Managers and Supervisors to create and maintain the training matrix for each role and manage CAPA's related to training and quality documentation systems.
To be successful in your application to this exciting opportunity as the QA Officer (Documentation) we are looking to identify the following on your profile and past history:
1. Good organisation skills.
2. Proven industry experience in a quality documentation role.
3. Good communication and teamwork skills.
Key Words: Pharmaceuticals | GMP | cGMP | Quality Assurance | QA | Sterile | Licensed Medicines | Quality Management System | Change Control | CAPA's | Deviations | Supplier Management | Compliance | Audits | Specialist | Associate | Aseptic | Biologics | Quality | Documentation
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant 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 processionals and scientists. We look forward to helping you with your next career moves.
Bank or payment details should not be provided when applying for a job. reed.co.uk is not responsible for any external website content. All applications should be made via the 'Apply now' button.Report this job