Quality Assurance Specialist

We are actively looking for a full time role for one of our clients located in Brussels:

Quality Assurance Specialist

  • Do you hold a Master Degree in Sciences? 
  • Do you have 3 years experience in a QA function?

Then you might be the right candidate for this role! Read more and apply as soon as you can!

Job Description 

As Quality Assurance Specialist you will be working as part of the Quality Assurance Department, ensuring that the products are manufactured, stored and packaged in accordance with cGMP. You will also support the development of GMP training packages and, if necessary, deliver training. Under the direction of the reporting manager, you will continuously improve QA and Compliance systems, strengthen quality awareness and investigate quality issues using applicable process improvement and problem solving techniques to assure successful outcomes of Company and external Health Authority inspections.

Responsibilities 

Main responsibilities / Major Activities

  • You will provide QA support for:
    • Investigation and closure for the Deviation and the Out Of Specifications 
    • Change Control initiation and implementation 
    • CAPA initiation and implementation 
  • You will have documentation and records review responsibilities:
    • Procedure, Master Batch Record, Specifications…
    • Batch records and associated documents after production 
    • Control Cleaning Records 
    • Maintain the calibration program and the monitoring for the facilities up to date
  • You will have the responsibility of Documentation System Management :
    • Traceability (controlled copy, follow-up approvals,…)
    • Official documents distribution
    • Maintaining the training files and the archives area up to date 

Other activities:

  • You will work with relevant departments to ensure timely closure of quality actions 
  • You will actively contribute to continuous improvement initiatives 
  • You will perform inspections/internal audits 
  • You will collaborate with the different departments to resolve compliance matters / Collabore avec les différents départements pour résoudre les problèmes de conformité

 

Profile 
  • You have a Master degree Sciences
  • You have at least 3 years experience in a QA position 
  • You have good knowledge of cGMP in a regulated environment  
  • You have knowledge of quality systems 
  • You possess excellent accuracy and attention to detail 
  • You have excellent interpersonal skills 
  • You have working knowledge of MS office packages (Word, Excel, Power Point) and TrackWise® System 
  • You possess strong skills of problems solving, issue resolution and root cause analysis 
  • You are highly Flexible and Adaptable, Able to work independently in a fast paced multitasking environment 
  • You speak French (English knowledges is an asset )
Contact Information 

Mihaela Lascar
mihaela.lascar@valesta.com
010/68.53.30

Application form : Quality Assurance Specialist

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.