QA Operations Specialist
Location: Visp
Sektoren Andere
Anstellungsart Temporär
Gehalt Negotiable
Reference: BBBH608266
Internal Description
Description:
As a QA Operations Specialist for the Drug Product Services (DPS) in Visp, you will represent Quality Assurance in cross-functional teams, including but not limited to Manufacturing, MSAT, QC, Engineering, Supply, Qualification/Validation, and others to effectively execute tasks related to Drug Product processes.
This is an excellent opportunity for a candidate with previous QA experience who is keen on being involved in QA operational topics related to daily manufacturing operations
Key responsibilities:
Act as point of contact for Drug Product QA-related questions and issues related to the manufacturing operations
Ensure shop floor QA oversight (regular presence in the cleanroom)
Assess, review, and approve GMP documents and quality records e.g. SOPs, risk assessments, deviations, investigation, CAPAs, change controls, rotocols, executed MBRs
Act as QA representative during the conduction of internal / customer / regulatory inspections and audits
Provide GMP-related training to Operations personnel
Support continuous improvement programs to establish an effective Quality Management System for DPS Visp
Key requirements:
Master of Science in biotechnology or a related field
Significant work experience (3-5 years) in the GMP-regulated environment, about aseptic manufacturing activities and preferably within a Quality Unit
Experience working with stakeholders from different departments and management levels
Fluent in English (written and spoken), German language is an advantage
End Date to be confirmed
Hours per week 41
As a QA Operations Specialist for the Drug Product Services (DPS) in Visp, you will represent Quality Assurance in cross-functional teams, including but not limited to Manufacturing, MSAT, QC, Engineering, Supply, Qualification/Validation, and others to effectively execute tasks related to Drug Product processes.
This is an excellent opportunity for a candidate with previous QA experience who is keen on being involved in QA operational topics related to daily manufacturing operations
Key responsibilities:
Act as point of contact for Drug Product QA-related questions and issues related to the manufacturing operations
Ensure shop floor QA oversight (regular presence in the cleanroom)
Assess, review, and approve GMP documents and quality records e.g. SOPs, risk assessments, deviations, investigation, CAPAs, change controls, rotocols, executed MBRs
Act as QA representative during the conduction of internal / customer / regulatory inspections and audits
Provide GMP-related training to Operations personnel
Support continuous improvement programs to establish an effective Quality Management System for DPS Visp
Key requirements:
Master of Science in biotechnology or a related field
Significant work experience (3-5 years) in the GMP-regulated environment, about aseptic manufacturing activities and preferably within a Quality Unit
Experience working with stakeholders from different departments and management levels
Fluent in English (written and spoken), German language is an advantage
End Date to be confirmed
Hours per week 41
Contact: alba.jansa(at)experis.ch
