Quality Assurance Senior Associate & QP

For one of our clients located in Brabant Wallon, I’m actively looking for a Quality Assurance Senior Associate & QP.

  • Do you have a Scientific Master Degree in industrial Pharmacy and 5 years of relevant experience?
  • Are you recognized as Qualified Person by FAMHP?
  • Are you fluent in French and English?

Then you might be the candidate we are looking for. Don’t hesitate and apply now!

Responsibilities 
  • You review and update Quality Agreements/Contracts with key Service Providers 
  • You are responsible of the QA to process Change Controls, deviations and CAPA’s related to manufacturing, Quality Control and distribution 
  • You write, review and approve SOPs, validation protocols and reports 
  • You execute risk assessment exercises 
  • You are QA support for Change Controls related to new material/service introduction/change 
  • You perform new material/service QA assessment (quality questionnaire, quality agreement, analysis of certificates etc.) 
  • You support the QC department to create material specifications, maintain existing specifications 
  • You maintain approved supplier and material lists, create audit plans 
  • You create new articles and maintain current articles in electronic resource management system and assure link with QA approved material list 
  • You are subject matter expert on raw materials/ services used for the manufacturing of products 
  • You are responsible for deviations related to material/service provider issues 
  • You regularly meet key suppliers/service providers’ representatives to follow-up on ongoing issues and implement improvements 
  • You are responsible for supplier change notifications 
  • As Deputy QP, you are in charge of the coordination of product release within the operational group 
  • You act as Deputy Qualified Person
Profile 
  • You are recognized as Qualified Person by FAMHP (must). 
  • You hold a Scientific Master degree in Industrial Pharmacy
  • You have minimum 5 years of relevant experience 
  • You have good knowledge of GMP and GDP within the bio-pharmaceuticals environment, preferably in product development or early clinical stages 
  • You have experience with regulatory inspections 
  • You have experience with Advanced Therapy Medicinal Products (ATMPs) (advantage)
  • You are autonomous 
  • You have strong communication skills 
  • You are creative; thinking out of the box 
  • You can take the lead 
  • You demonstrate knowledge of Quality Systems and risk management tools 
  • You have excellent organizational skills and strong attention to details 
  • You work precisely as per procedures, rules and regulations 
  • You have team spirit 
  • You have negotiation skills 
  • You have excellent English and French knowledge (oral and written) 
Contact Information 

Amandine Planche
+32 10 68 53 30
amandine.planche@valesta.com

Application form : Quality Assurance Senior Associate & QP

Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.
Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.

I want to stay informed.

I would like to receive Valesta news, valuable insights into industry trends, career opportunities, trainings, and other helpful tips to find assignments that match my skills and interests. Click here to stay connected with Valesta.

Valesta is an expert in life science recruiting and project staffing.  The information you are submitting is important for us to respond to your assignment and contract needs. In compliance with the General Data Protection Regulation (EU) 2016/679) (“GDPR”), Valesta will process your personal data in accordance with our Privacy Policy. Valesta will safeguard your personal information and not disclose to any person unlawfully. As a staffing company, Valesta receives and processes your personal data for the following purpose: to take appropriate steps to find you an assignment with one of our clients and/or to finalise a contract with you.

Please note that Valesta does not wish to receive any data from you if you are under the age of eighteen (18) or data that is classified as Sensitive Data under the GDPR; this includes personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, trade union membership, genetic/biometric/health-related data or data concerning a person's sex life/sexual orientation.

Please read our disclaimer.