QA TECHNICIAN
DEPARTMENT: QUALITY
REPORTING TO: SITE QUALITY HEAD
HOURS
- 40 hours per week
- Monday to Friday
- Rotating day and evening shift (07:45 16:15 and 15:45 12:15)
MAIN DUTIES AND RESPONSIBILITIES:
The post holder will perform QA activities in support of manufacturing to ensure the Larne Site operates in compliance with regulatory requirements and Millicent business objectives..
JOB PURPOSE:
The purpose of this job is to ensure manufacturing at the Larne site is carried out in compliance with regulatory authorisations.
GENERAL DUTIES
- Provide QA cover for manufacturing shifts as required.
- Carry out spot checks on ongoing manufacturing/packaging operations
- Ensure that all planned changes or deviations have been notified and documented in accordance with written procedures.
- Ensure any additional sampling, inspection, tests and checks have been initiated and performed as appropriate to cover planned changes or deviations.
- Review completed batch records and ensure all deviations /issues are addressed satisfactorily.
- Ensure all necessary quality records have been completed and endorsed appropriately by trained personnel.
- Assist in the maintenance of QA documentation for commercial manufacture
- Assist in the development and maintenance of the Millicent Quality Management System
- Assist in the preparation of validation protocols and reports for manufacturing and test equipment and processes.
- Collate Quality metrics in line with Larne site requirements.
- Perform Quality review of Larne Site SOPs relating to commercial production, site qualification and operational activities.
- Undertake any other duties, which may be assigned by Senior Management.
ESSENTIAL CRITERIA:
- Minimum 3rd level qualification in related scientific discipline (Biology, Chemistry, Laboratory Science
- Experience of working in a recognised quality system
- Strong attention to detail and accuracy.
- Ability to work individually and as part of a team.
- Good communication skills
- Proficiency in Microsoft Office, particularly?Word and Excel
- Right to work in the UK
DESIRABLE CRITERIA:
- Experience of working in the Pharmaceutical industry
- GMP knowledge.
- Experience of document control and report writing
- Ability to work under pressure.
BENEFITS:
- Company sick pay
- Length of service awards
- Discretionary bonus scheme
- Health care plan
- On site parking
- Cycle to work scheme
- 34 day leave per year inclusive of public holidays (FTE)
- Wedding leave
- Competitive salary
Applicants must have the right to work in the UK
WHJS1_NI
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