Validation Engineer

Sector:
Pharmaceutical
Location:
Switzerland
Sub-location:
Any
Currency:
CHF
Job Type:
Any
Salary:
1 per hour
Posted:
09/11/2021
Ref No:
CR/107395

A Pharmaceutical company is searching for:

Validation Engineer (CSV)

Main Responsibilities

● Coordination of computerized system qualification and validation activities within the Quality Control department

● Define the validation strategy

● Perform and/or support the writing of specification documents (URS)

● Review test protocols, plans and reports

● Support test execution

● Support and train team members in CSV methodology

● Supporting the timely and effective completion of investigations, change controls and CAPA’s

Requirements:

● Degree in a LifeSciences/ Biotechnology, Chemistry discipline or comparable work experience

● Several years of experience in computerized system validation (CSV) in a GMP environment and good knowledge of related regulatory requirements in the life sciences industry (GAMP 5, 21 CFR part 11, ...)

● Good understanding of analytical technologies,

● Strong analytical thinking and problem-solving ability

● Ability to simultaneously support multiple projects, duties and assignments and prioritize accordingly

● Excellent writing skills for scientifically sound technical documents, instructions, protocols and reports.

● Self-dependent way of working and taking ownership of assigned task to plan and deliver according to agreed timelines.

● Good verbal and written skills in English, German is a plus

Michael Bailey International is acting as an Employment Business in relation to this vacancy.

< Go back to your projects search results

Latest Job Listings