Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Document Management Specialist – 12 Month contract – Bio-Tec

Company: i-Pharm Consulting
Location: Cambridgeshire
Reference: DAFE2341
Closing Date: 22 Aug 18
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

GCP Document Management Specialist required for a leading Biotech. This opportunity will see you responsible for supporting the development of controlled documentation for R&D processes. Candidate must be eligible to work in the UK.

Requirements:

GCP Document Management Specialist – 12 Month contract – top Biotech

GCP Document Management Specialist required for a leading Biotech. This opportunity will see you responsible for supporting the development of controlled documentation for R&D processes. Candidate must be eligible to work in the UK.

JOB TITLE

Document Management Specialist

LOCATION

UK / England / Cambridge

Duration

12 months



ROLE/DESCRIPTION

* Management of R&D process documentation per required process in accordance with agreed timelines and in adherence with format, content and templates, giving consideration to usability and ensuring accuracy, consistency and quality.
* Development of the creation and/or revision of materials such as SOPs, manuals, and related business process documentation in conjunction with Subject Matter Experts.
* Liaison with other members of the business (e.g. Business Process Owner, Document Owner, Authors, Subject Matter Experts).
* Management of documents via the established R&D Document Review process using the electronic document repository (EDM Quality).
* Track and provide regular updates to process project inventory tool and to key Points of Contact


REQUIREMENTS

* Experience in developing regulated or process documents with the ability to deliver high quality documentation including technical writing.
* Excellent verbal and written communication skills/writing skills; active listening skills; attention to detail. Strong process writing skills
* Prior experience leading cross‐functional team/subject matter experts.
* Experience reviewing / amending GCP SOPs and other controlled documents for the highly regulated bio/pharma/medical industry



ABOUT i-PHARM CONSULTING


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.



www.i-pharmconsulting.com





TO APPLY


If you would like to discuss this vacancy further, please call David Fearnley on +44 (0)20 3189 0497, or email dfearnley@i-pharmconsulting.com. If this role is not suitable, David is also available to discuss other possible positions or answer any general questions regarding your career and the current market.



KEY WORDS



GCP Process Documentation and Technical Writer / GCP Technical Writer / Cambridge / Cambridgeshire / Bio / GCP / Quality / Author / SOP / Document Management Specialist

Apply for this job: Document Management Specialist – 12 Month contract – Bio-Tec

Contact Information:

Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.