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Senior Technical Editor (Manufacturing)

Berkshire   •  Negotiable  •  Contract/Temporary, Full time

Senior Technical Editor (Manufacturing)


£18.70PH PAYE

12 Month Contract

CPL Life sciences are working alongside a leading Pharmaceutical company who are seeking a Senior Technical Editor contractor to join a busy team. The ideal candidate will have Experience of editing and workflow management of tasks in DMS for batch records, process descriptions and product specifications. They will also be able to independently write batch documentation to support new product campaigns. Identifies, understands and communicates potential impact of changes to other functions in a timely manner.


• Able to manage changes throughout the document / change lifecycle from document submission to effective state with minimal errors

• Good working knowledge of Manufacturing operations to allow independent drafting of documents

• In depth knowledge and awareness of the Manufacturing schedule and understanding of the impact to on time delivery of schedule changes


• Good interpersonal and organizational skills with ability to work within a cross functional team.

• Able to identify and act with own initiative on situations which require escalation, can recognize an abnormal or potentially impacting event and will routinely escalate to appropriate levels of attention

• Proactively offer suggestions to supervisor, manufacturing or technical owners on process improvements or scheduling issues

• Ability to internally communicate documentation updates to other affected departments

Proven ability to deliver to deadlines

Qualities & Attitude

• Has excellent attention to detail, interpersonal qualities, self-motivated and positive with a desire to develop technically in their area of expertise and a positive approach to team work

• Presents facts clearly and logically. Clear concise and accurate presentation. Checks for understanding of different perspectives

• Liaising with MSAT, QC, Manufacturing etc. as well as with customer to ensure changes are incorporated appropriately and all requirements met

• Work with project teams to coordinate customer review and approval (where applicable)

• Good understanding of business impact and responsibilities regarding own role

• Actively promotes a continuous improvement and safety culture, Identifying and remediating potential unsafe behaviour in documents and the workplace


• Ideally HND / HNC within relevant subjects or demonstrated equivalency

For more information please apply within or send your CV to mark.bathe@cpl.com

  • Agency: Cpl Life Sciences
  • Reference: JO-2301-509326
  • Posted: 25th January 2023
  • Expires: 22nd February 2023

Cpl Life Sciences

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