QA Documentation Review Specialist - Pharmaceutical

QA Documentation - 12 months - Portsmouth

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.

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