QA Documentation Review Specialist - Pharmaceutical
Pharmaceutical manufacturing client have a long term contract assignment for an experienced QA /Data Documentation Specialist.
The Project: The client is currently in the process of building a product database where customers are able to access product specification that includes QA and validation documentation.
You will be working alongside the Data Supervisor and will be required to check, verify and correct information prior to input of the product information specifically focused around QA and Regulatory documents
Skills & Experience:
- Prior experience of biotech/medical device QA Documentation
- Pharmaceutical Industry experience
- Documentation / Data review
- Strong IT skills
- Knowledge regulatory documentation
- Eye for detail
Duration 12 months + (2 year project)
Interviews process: Telephone
Working situation On site induction and then remote working for a majority of the time which will be reviewed Jan 2020
40 hour week
If this role is of interest, please apply now.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta Consultancy Services does not sponsor Visa applications.
Our client, an innovative pharmaceutical organisation responsible for manufacturing unique therapeutic products within the EU and US are currently entering a period of exciting growth. Located within
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