Description
FREELANCE/CONTRACT Pharma Quality Control Data Intergrity Specialist Role / ASAP / Minimum 6 Months / INDIAWe are looking for a expert in 21 CFR Part 11 expert to help out at an API production site in India as soon as possible. Hiring via German Head Office of the client!
For a German client we are currently looking for a data integrity specialist within a GMP environment.
For this pharmaceutical client you will be supporting its active pharmaceutical ingredients production site in India for at least six months.
For this outstanding role you bring extensive knowledge in the treatment of electronic records and signatures within a Good Manufacturing Practice plant as stated in the 21 CFR regulations and broad knowledge of quality control measurements within the API production (ICH Q7).
Experience with Water Empowers software and any Laboratory Information Management System (LIMS) is beneficial. You must be a minimum english speaker, German is a plus.
As we and the client are aware that for some this role and its location might be a great challenge, consideration and compensation will meet your expectations. Accomodation and commuting will be taken care of.
This will be a minimum 6 months assignement with numerous possibilities to travel back home.
If you meet the qualification and are up for such an challenging role, like different cultures and see new places, I´d be happy to provide some more details on this fantastic role and am looking forward to receiving your latest CV stating availability and expected rates. Don´t miss out on this opportunity to add a well-known company and an extraordinary role to your consultant CV!
Start Date: ASAP
Duration: Minimum 6 Months
Location: India
Role: Data Intergrity Specialist with QC expertise / India
!YOU MUST HOLD A VALID EU OR US WORK PERMIT!
Best regards,
Roland Knoefel,
Real Staffing Group, Freelance Division; Quality Pharma, Frankfurt/Germany
Für mehr Informationen über Real, besuchen Sie www.realstaffing.com