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QA Documentation Editor
2 weeks ago
QA Documentation Editor - Pharmaceuticals - Contract - Reading
One of the leading suppliers to the life science industry is looking to expand its contractor base and is currently recruiting for QA Documentation Editor engineers for an initial 12 month contract.
Based on the M4 Corridor they have undergone a massive refurbishment and expansion at their facility here and seem to keep growing
As part of the QA Document Control Team, the GMP Documentation Editor will generate and revise documentation ensuring technical accuracy and GMP compliance is met.
**QA Documentation Editor Responsibilities**:
Act as a document editor for updates identified in QA
Accountable for ownership, oversight and active management of technical documentation templates.
Independently manage the creation of new documents and revision of existing GMP documents for highly complex technical changes according to documented procedure to maintain accuracy and compliance with other procedures.
Actively monitor progress of document creation, routinely communicate and liaise with internal customer teams to ensure potential issues are resolved in a timely manner and all changes are incorporated appropriately and all requirements met
Use and maintenance of the Documentation Management System (DMS) according to documented procedure.
Manage and own the continual improvement of technical templates and related documentation as well as actively promoting and encouraging a culture of change within QA.
Perform QA review and approval of all site documents on DMS in line with Lonza quality system and regulatory requirements.
**About you**:
BSc Biological science or equivalent.
Advanced experience in Documentation with expert knowledge in the field and be able to independently make decisions based on that experience.
Advanced experience in Document Control.
**Technical profile requirements**:
IT literate - MS Office (advanced) - Word, Explorer, Excel, Access, Outlook
cGMP Quality Systems knowledge
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