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For our client, an international company based in Bern, we are looking for a C&Q Engineer.
General Information:
Start date: ASAP, latest in January 2025
Contract duration: 1 year with possibility of extension
Workplace: Bern
Workload: 100%
Home office: possible up to 2 days per week
Tasks and Responsibilities:
The position will report to the C&Q Manger and is in charge of Commissioning & Qualification (C&Q) activities for Technical Services department in order to ensure that:
(re-) qualification of production/QC equipment including thermal mapping studies are performed according to global and local company policies and procedures as well as legal requirements and requirements set by regulatory authorities.
Commissioning & Qualification Master plans are up to date and established for all ongoing projects.
Write/review Commissioning & Qualification plans and reports.
Execution of RQ, IQ, OQ, PQ, including protocol deviations, investigation, and corrective action activities
Plan and track execution of Commissioning & Qualification activities/documentation versus project(s) timelines
Prepare, review and approve technical and GMP related documentation (URS, FMEA, impact/risk assessment, Master plans, qualification/validation documentation)
Coordinate and execute commissioning & qualification activities in collaboration with internal and external partners
Coordination and oversight of external suppliers
Qualifications and Skills:
Bachelor/Master’s degree in technical or natural sciences
Working experience within pharma/Medical Devices companies
Practical experience in a C&Q role is a must
Know-how of Qualification requirements according to cGMP regulations
Know-how of thermal mapping studies
Know-how of quality assurance principles
Excellent communication skills
Analytical thinking and problem-solving ability
Business fluency in English
German language is a plus
Self time management
For our client, an international company based in Bern, we are looking for a C&Q Engineer.
General Information:
Start date: ASAP, latest in January 2025
Contract duration: 1 year with possibility of extension
Workplace: Bern
Workload: 100%
Home office: possible up to 2 days per week
Tasks and Responsibilities:
The position will report to the C&Q Manger and is in charge of Commissioning & Qualification (C&Q) activities for Technical Services department in order to ensure that:
(re-) qualification of production/QC equipment including thermal mapping studies are performed according to global and local company policies and procedures as well as legal requirements and requirements set by regulatory authorities.
Commissioning & Qualification Master plans are up to date and established for all ongoing projects.
Write/review Commissioning & Qualification plans and reports.
Execution of RQ, IQ, OQ, PQ, including protocol deviations, investigation, and corrective action activities
Plan and track execution of Commissioning & Qualification activities/documentation versus project(s) timelines
Prepare, review and approve technical and GMP related documentation (URS, FMEA, impact/risk assessment, Master plans, qualification/validation documentation)
Coordinate and execute commissioning & qualification activities in collaboration with internal and external partners
Coordination and oversight of external suppliers
Qualifications and Skills:
Bachelor/Master’s degree in technical or natural sciences
Working experience within pharma/Medical Devices companies
Practical experience in a C&Q role is a must
Know-how of Qualification requirements according to cGMP regulations
Know-how of thermal mapping studies
Know-how of quality assurance principles
Excellent communication skills
Analytical thinking and problem-solving ability
Business fluency in English
German language is a plus
Self time management
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