Direct message the job poster from Warman O'Brien
Consultant at Warman O’Brien | Medical Affairs | UK & Europe
Technical Writer – Quality Assurance (UK – Remote) Warman O’Brien is proud to be partnered with a leading Consulting Firm looking for Technical Writers on behalf of a leading Mid-Size Biotechnology Company. As part of a global transformation project, we’re looking for a team of Technical Writers to support this Biotech’s Quality teams (SMEs) to develop SOPs, quality documents, and procedures for the department. If you have the below experience then please click apply! 3+ years direct experience in the pharmaceutical industry Awareness of GxP regulatory requirements Experience with deviations, inspection commitments, corrective/preventative actions, and other gaps Experience in design/development of SOPs, supporting documents, and forms/templates Contract specifics: 30-40 hours per week Must be a British Citizen or have UK permanent settlement status Seniority level
Associate Employment type
Contract Job function
Writing/Editing and Quality Assurance Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
Technical Writer – Quality Assurance (UK – Remote) Warman O’Brien is proud to be partnered with a leading Consulting Firm looking for Technical Writers on behalf of a leading Mid-Size Biotechnology Company. As part of a global transformation project, we’re looking for a team of Technical Writers to support this Biotech’s Quality teams (SMEs) to develop SOPs, quality documents, and procedures for the department. If you have the below experience then please click apply! 3+ years direct experience in the pharmaceutical industry Awareness of GxP regulatory requirements Experience with deviations, inspection commitments, corrective/preventative actions, and other gaps Experience in design/development of SOPs, supporting documents, and forms/templates Contract specifics: 30-40 hours per week Must be a British Citizen or have UK permanent settlement status Seniority level
Associate Employment type
Contract Job function
Writing/Editing and Quality Assurance Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
