Quality Assurance Associate II


Premium Job From Real Staffing

Recruiter

Real Staffing

Listed on

2nd September 2021

Location

Zug

Salary/Rate

Upto £124

Type

Contract

This job has now expired please search on the home page to find live IT Jobs.

Quality Assurance Associate II Duration: 1 year initially, with possible extension

Location: Zug, Switzerland DescriptionThe person in this function provides support to the management of the local pharmaceutical quality system. He/she also acts as Quality contact for closure of exceptions, CAPAs and change controls related to Quality systems (including IT Quality systems). He/she supports process improvements related to GxP activities, by providing quality oversight. The role may also participate in projects to support enhancements of IT Quality Systems, which may include testing and roll-out of the enhancements to end-users. The role also supports site compliance activities such as advising other departments on GxP compliance aspects, managing preparation for, and follow-up of audits and inspection. RESPONSIBILITIESSupport maintenance and improving of the local Pharmaceutical Quality System established to ensure compliance to local regulations and in alignment with the global Corporate Quality System. This includes cross-site alignment for common processes and systems. Follow regulation updates and deploy them when deemed applicable.Act as Quality contact for exceptions, CAPAs, and change controls related to Quality Systems (including IT Quality Systems).Provide support in the quality oversight for IT Quality systems enhancements and business processes. Support improvements and roll out for those systems to the end usersParticipate as a GEQ Quality Systems representative on cross-functional teams and projects. Give advice on regulatory and compliance question to stakeholders. Address potential gaps for processes or practices within teams and projects to avoid incomplianceSupport general support in Program Management activities, including collection for data for monthly reports, Management Reviews and follow up of action items. RequirementsMaster Degree / Bachelor Degree in scientific field + 3 years experience in relevant industry or equivalent.Quality experience in the pharmaceutical industryKnowledge of cGMP requirements, EU/FDA regulations and complianceExperience in IT systems qualification & project management QA, Quality Assurance, Quality Assurance Associate II, Biopharma, Pharmaceuticals, Manufacturing, CAPA, Process, GMP, GxP, Project Management, IT, Systems, Qualification, Switzerland, ZugSthree Switzerland is acting as an Employment Business in relation to this vacancy.

You are currently using an outdated browser.

Please consider using a modern browser such as one listed below: