Spécialiste, Investigations / Specialist, Investigations at Jubilant DraxImage Inc
Montréal, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

24 Oct, 25

Salary

0.0

Posted On

24 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Technical Writing, Root, French, Investigation Management, Manufacturing, Gmp, Aseptic Processing

Industry

Pharmaceuticals

Description

QUALIFICATIONS :

  • Baccalauréat en sciences
  • 3 à 5 années d’expérience dans l’industrie pharmaceutique
  • Connaissance du traitement aseptique, des processus pharmaceutiques et des BPF
  • Connaissance de la fabrication et capacité de résolution de problèmes
  • Excellente connaissance de la gestion des investigations, de l’identification des causes fondamentales et de la rédaction technique
  • Solides compétences de l’informatique et des logiciels (MS Office)
  • Français (parlé et écrit)

SPECIALIST, INVESTIGATIONS

Join our dynamic team at Jubilant Radiopharma as Specialist, Investigations! We are seeking a driven individual who thrives in a fast-paced environment and is passionate about ensuring the highest standards of quality and compliance in our operations.

QUALIFICATIONS:

  • Bachelor’s degree in sciences
  • Three (3) to five (5) years of experience in the pharmaceuticals industry
  • Knowledge of aseptic processing, pharmaceutical processes, and GMP
  • Understanding of manufacturing and strong problem-solving skills
  • Excellent knowledge of investigation management, root cause identification, and technical writing
  • Strong computer and software skills (MS Office)
  • French (written and spoken)

JOIN US:

If you are looking for a challenging yet rewarding opportunity to make a difference in the healthcare industry, we invite you to apply for the Specialist, Investigations position at Jubilant Radiopharma. Join us in our mission to deliver innovative solutions that enhance patient care and improve lives. Apply now and be part of our success story!
Job Overview

Responsibilities

ROLE OVERVIEW:

Assist in managing incident reports, investigations, and corrective and preventive actions (CAPA) for sterile and non-sterile products. Prepare reports and provide trend analysis on investigations and CAPAs to establish appropriate measures. Additionally, contribute to process improvement.

KEY RESPONSIBILITIES:

  • Participate in incident investigations in collaboration with the manager of the concerned department or their delegate.
  • Draft detailed investigation reports to be submitted for approval by the department head and the Quality Assurance manager. Conduct investigations in a timely manner to meet promised delivery deadlines.
  • Collaborate with the department manager or their delegate to determine appropriate corrective actions. Establish preventive actions based on root cause analysis results to prevent recurrence of similar incidents.
  • Act as a resource person for other investigators and employees involved in the investigation process.
  • Perform any other tasks assigned by management.
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