Validation Engineer (Biotech)

Company
Clintec
Salary
Competitive
Posted
26 Oct 2018
Closes
12 Feb 2019
Ref
SWI VE 240418 AD

Main Responsibilities:

Management of Equipment Qualification Projects and Computer System Validation Projects for laboratory equipment as well as manufacturing equipment.

Develop, review and approve Validation Plans, Specifications, Test Scripts, Installations Qualification Protocols, Operational Qualification Protocols, Performance Qualifications Protocols, Traceability Matrices and Summary Reports

Perform Equipment Qualification/ Computer System Validation tests

Generate/review Standard Operating Procedures related to Equipment Qualification

Administration of Equipment Change Controls in TrackWise System

Qualifications:

Bachelors/Master’s degree in Engineering, Life Sciences or another closely related discipline

3-5 years of work experience in pharmaceutical environment

Significant practical experience with Equipment Qualification and Computer System Validation

Strong project management skills with the ability to prioritize assignments

High level of accuracy and quality of work

Demonstrated problem-solving skills with the ability to prioritize, align and simplify, used to manage multiple projects with changing priorities

Strong collaboration skills with the ability to work across boundaries and to develop sustainable professional relationships on all levels of the organization

Strong customer focus and solution orientation; proven ability to deliver practical solutions and to drive results

Excellent communication and interpersonal skills

Fluent in English and German, both verbal and written

Company Information:

Clintec is a dynamic, UK headquartered, privately owned, full service Contract Research Organisation with a presence in over 40 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assisting in their key product development efforts for over two decades. At Clintec we have experience in managing clinical trials in all major therapeutic areas including oncology, rare disease, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.

Clintec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. Clintec offers a competitive salary and rewards package.

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