Start Date
Immediate
Expiry Date
19 Jan, 27
Salary
60000.0
Posted On
21 Oct, 26
Experience
5 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Industry
Pharmaceutical Manufacturing
Aufgabenbeschreibung Description of tasks:
Coordination, review and of processing of events, deviations, nonconformances and complaints, requests for corrective and preventive actions (CAPAs) and the preparation of final reports.
Coordination of change controls, following up on change control actions with respective action owners and ensuring timely completion.
Interdepartmental communication and problem solving in due consideration of the European GMP guidelines.
Draft, rework and review of SOPs, Work Instructions and forms.
Participation in the preparation of risk analyses.
Supports continual improvement processes, validation and qualiciation activities as required.
Supports the creation, review and provision of relevant quality system metrics data to management.
Carrying out administrative work in the quality system, such as maintaining lists, folder structures and logbooks and preparation of monthly metrics.
Supports and assists with customer audits and regulatory inspections and actions as required.