Spécialiste aux Investigations / Specialist, Investigations

at  Jubilant DraxImage Inc

Montréal, QC, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate25 Jan, 2025Not Specified26 Oct, 2024N/APharmaceutical Industry,Root,Technical Writing,Investigation Management,Manufacturing Principles,Aseptic ProcessingNoNo
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Description:

QUALIFICATIONS :

  • Baccalauréat en sciences
  • Trois (3) à cinq (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
  • Connaissance des principes de fabrication sans gaspillage (atout)

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 science
  • Three (3) to five (5) years’ experience in the pharmaceutical industry
  • Knowledge of aseptic processing, pharmaceutical processes and GMPs
  • Manufacturing knowledge and problem-solving skills
  • Excellent knowledge of investigation management, root cause identification and technical writing
  • Knowledge of lean manufacturing principles (asset)

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 the management of incident reports, investigations and corrective and preventive actions (CAPAs) for sterile and non-sterile products. Prepare reports and provide trend analysis on investigations and CAPAs to establish appropriate actions. In addition, contribute to process improvement.

KEY RESPONSIBILITIES:

  • Participate in the investigation of incidents in collaboration with the relevant department manager or delegate.
  • Prepare detailed investigation reports which are then submitted for approval by the Department Manager, Quality Assurance Manager. Carry out investigations on time to meet promised delivery deadlines.
  • Work with department manager or delegate to determine corrective actions. Establish preventive actions based on root cause analysis results and prevent recurrence of similar incidents.
  • Act as a resource person to other investigators and employees involved in the investigation process.
  • Performs any other duties assigned by management.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

IT Software - Other

Clinical Pharmacy

Graduate

Science

Proficient

1

Montréal, QC, Canada