Associate Scientist

NL1836

DPS Group Global is currently looking for an Associate Scientist. Would you like to be directly involved in the fight against the global "Coronavirus" (COVID-19) pandemic? Then keep reading!

Category:
Engineer Manufacturing
Location:
Netherlands
Years of Experience Req.:
>3 years
Date Posted:
07/09/2020
Days Remaining:
6
Employment Type:
Contract
Education Level Req.:
HBO or BSc 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.

 

Department

To strengthen the department we are looking for an Associate Scientist / Senior manufacturing operator (PPIP - production person in plant), to help us realiz628044.816336e the upcoming COVID-19 vaccine manufacturing campaign.

The department DSO is an international team of about 40 people working on the manufacturing of cell banks, virus seeds and clinical batches (phase I to III) to support the development of new vaccine candidates. Manufacturing activities are performed under strict cGMP regulations and the process is established together with development departments, engineering & maintenance, QC, QA and warehouse. Our passion is to deliver high-quality results to our customers and to seek opportunities for improvement: never a dull moment!

Within the department four teams operate, each with specific responsibilities: Preparations, Cell culture/ Upstream processing, Downstream processing and the Operations Support Team. The teams are responsible for their cGMP status by maintaining the documentation system, reporting quality issues and performing the resulting corrective actions, masterbatch documentation, training and inspection readiness.

 

Job Description

In this role you are primary responsible for acute problem solving of issues that manifest during operations to ensure the continuation of the production processes for cGMP clinical trial material. Analysing the issues and following up on the solution is your main task. For this, you will need to connect with specialists and partners inside and outside the department.

Apart from production operations you will be updating documentation to resolve the issues that you found. To improve the operations, small improvements and innovative projects will be a stable part of your daily work package. You will also be tasked in other small and divers tasks as well as reviewing batch documentation. As the job entails team work within a diverse and global organiz628044.816336ation, we require good communication skills in English.

 

The Candidate...

  • has quality always as the main goal, efficiency second
  • is clear in communication, also under pressure
  • aims for full customer satisfaction. What is asked you to deliver with the required quality within the agreed timeframe?
  • has a high degree of accuracy, initiative, and independence
  • is flexible and stress-resistant and remains positive when priorities change
  • helps team members by giving advice and sharing feedback on technical and personal level
  • has great social and trainer skills, is able to provide and receive feedback in a constructive way. You make yourself part of discussions and help transform these into positive actions.

 

Qualifications

  • HBO/BSc with 3 years of proven experience in pharmaceutical/biotechnology
  • Expert in cell culture (USP), virus propagation and/or downstream processing (DSP)
  • Experience with change controls, non-conformances and CAPA records
  • Experience with cGMP and EHSS standards is required
  • Lean green belt certification is preferred

 

Available and 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 or if you would like to discuss this vacancy further and to discuss your career options in confidence, please telephone Ralf Huisman on +31 6 11408791 or send your CV to ralf.huisman@dpsgroupglobal.com

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DPS Group addresses the COVID-19 pandemic:
A message from Frank Keogh, CEO

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