Document Control Administrator
3 days ago
Key Roles/Responsibilities:
Assist in day to day document control support service for QA at Grangemouth. Overall responsibility for the following:
- Issuing of controlled copies of GMP documents from Ensur.
- Logging and tracking of documents through QA.
- Provide Document Control input including but not limited to mastering of documentation, issuing documentation to operational departments, scanning and archiving of completed documentation.
- If required; participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.
- Supply of controlled documents for use in the audits of, production and support functions as required.
- Be involved in the preparation for customer, MHRA/FDA and other regulatory body audits.
- Provide document control support for the introduction of new products, thus ensuring that all GMP documents are appropriate and all requirements are satisfied.
Assist in the management of document transfer to off-site archive facilities.
**Essential Experience**
A minimum of 3 years’ experience within a cGMP environment manufacturing Active Pharmaceutical Ingredients is required.
The job holder must have excellent organisational skills.
The job holder should be competent in the use of Microsoft Word, Excel and PowerPoint.
Experience in dealing with quality assurance, analytical chemistry, development, and manufacturing groups is beneficial.
The job holder will work in compliance with GMP requirements to assist with the document control activities associated with QA clearance and archiving activities.
**Benefits**:
- Flexitime
- Language training provided
Schedule:
- 10 hour shift
- Flexitime
- Monday to Friday
Supplemental pay types:
- Bonus scheme
Ability to commute/relocate:
- Grangemouth: reliably commute or plan to relocate before starting work (required)
Work Location: One location
Flextime
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