QA Specialist 
CordenPharma Peptisyntha

 

The Quality Assurance Specialist will be working as part of the Quality Assurance team on site ensuring products are manufactured, stored and packaged in accordance with cGMP. 

He / she will also support the development of GMP training packages and delivery of training. Under the direction of the reporting manager, 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.

The QA Specialist is reporting to Quality Affairs Director

Principle Responsibilities of the Job Holder: / Responsabilités principales du titulaire du poste:

  • Document approval (procedures, Master Batch Record, specifications, …)
  • Review and approval of batch records and associated documentation
  • Product release
  • Approval of deviation and support to related investigations
  • Provide Quality support for investigation of OOS , approve disposition decision
  • Operate the change control system
  • Operate the CAPA system
  • Review / approval of validation protocol / report
  • Work with relevant departments to ensure timely closure of quality actions / findings
  • Actively contribute to continuous improvement initiatives.
  • Perform inspections/internal audits and provide quality oversight for the inspection/ audit program
  • Collaborate to supplier qualification
  • Collaborate with operations to resolve compliance matters

External and Internal Contacts of the Job Holder / Contacts internes et externes du titulaire du poste

  • Internal Contacts / Contacts internes: All functions
  • External Contacts / Contacts externes: External auditors, Customers, Suppliers

Key Competencies Necessary to Effectively Perform this Job Role / Compétences Clés Nécessaires pour Réaliser Efficacement cette position

  • Minimum qualifications / Qualifications minimum: Master degree Sciences
  • Minimum experience required / Expérience minimum requise: 8 years with 3 years in a QA role

Specific skills required / Compétences spécifiques requises:

  • Very good knowledge of cGMP in a regulated environment
  • Knowledge of quality systems
  • Excellent accuracy and attention to detail
  • Excellent interpersonal skills
  • Working knowledge of computer packages
  • Strong problems solving skills, issue resolution and root cause analysis
  • Auditing experience, auditor certification is an asset
  • Highly Flexible and Adaptable. Able to work independently in a fast paced multitasking environment.
  • Able to work autonomously
  • Language: English, French
To apply please send an application and your resume to:
E-Mail: pepti_HR@cordenpharma.com