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Process Validation Engineer

NL976

DPS Engineering is looking for a Process Validation and Improvement Expert.

Category:
Validation
Location:
Netherlands
Years of Experience Req.:
>2 years
Date Posted:
31/07/2019
Days Remaining:
10
Employment Type:
Contract
Education Level Req.:
MSc Degree

DPS

DPS is a leading Project Management and Engineering Company serving industry around the world for 40 years. Our reputation is based on forming successful partnerships with our clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.
We provide Full Service Engineering for our clients including Project and Programme Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification and Start-up on numerous projects across a range of market sectors. Our Main market sectors are; Pharmaceutical and Biotechnology, Medical Technologies, Oil & Gas, Advanced Technology, Science & Education, Food & Beverage, and Energy.

 

Job Description

  • Within the MS&T (Manufacturing Science and Technology) department we are looking for a Process Validation and Improvement Expert.
  • You are a subject matter expert, responsible for planning and execution of process/cleaning validations, media fills, line/operator qualification, as well as process improvement and product robustness initiatives. You will work in dynamic project teams responsible for new project introductions, process improvements and remediations to meet current regulatory requirements, and will ensure that the executions are in line with international and our global guidelines.
  • You will carry out risk assessment, and prepare validation plans, protocols, execution of experiments and reporting of the work.
  • Participate in the execution of the respective validation activities, evaluate the results and prepare reports from them.
  • You are part of operational excellence and product robustness teams, responsible for critical assessment of processes and design of improvement plans, continued process verification.
  • Keep up-to-date with regulatory guidelines on process validation requirements.
  • In addition, you take part in many other activities required for optimal quality of validation activities.

 

Qualifications

  • MSc in bioprocess engineering/technology, pharmacy, chemistry or similar
  • At least 2 years’ experience in a cGMP environment
  • Experience with process improvement/validation or quality assurance
  • Working knowledge of FDA/EU GMP guidelines
  • Good command of the English language
  • Team player with pro-active approach.
  •  This is a dynamic challenging position with possibilities for growth within our company.

 

Function

Manufacturing

Sub Function

Technical Transfer

 

Interested?

If you’re interested in this role and if you want to be part of growing organisation within engineering projects in the pharma industry, please send you application to [email protected] or give us a call +31(0)715730810.

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