Production Technician

Jubilant Life Sciences

Caen

On-site

EUR 38,000 - 46,000

Full time

11 days ago

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Jubilant Radiopharma in Caen, France, is seeking a Production Technician to support the manufacturing of radiopharmaceutical products under strict regulatory controls. You will ensure aseptic processing, quality compliance, and radiation safety while performing daily production tasks.

Responsibilities include executing batch records, cleaning and calibrating equipment, and handling radioactive materials in Grade C/D cleanrooms.

Qualifications

  • Bachelor’s degree or equivalent in a relevant field and GMP exposure.
  • Experience in a pharmaceutical/biotech/GMP environment is an asset.
  • Aseptic environment experience and cleanroom compliance are assets.

Responsibilities

  • Manufacture injectable and oral radiopharmaceutical products per procedures.
  • Work in classified environments with aseptic gowning.
  • Maintain real-time ALCOA+ compliant documentation.
  • Handle radioactive materials safely and in accordance with procedures.
  • Perform environmental monitoring and waste management.
  • Review and execute batch records and work orders accurately.
  • Collaborate with team members and support onboarding/training of new staff.

Skills

GMP compliance
Aseptic processing
Quality & regulatory
MS Word/Excel
Attention to detail
Team collaboration
French communication

Education

AEC/DEC/Bachelor's degree or equivalent

Tools

SAP
Electronic batch records

Job description

At Jubilant Radiopharma, we help support patient care through the manufacturing of radiopharmaceutical products used in healthcare. Our success is built on dedicated people who value quality, safety, teamwork, and continuous improvement.

Role Overview

As a Production Technician, you will play an important role in the manufacturing of radiopharmaceutical products within a highly regulated environment. You will help ensure compliance with quality, aseptic processing, and radiation safety standards while supporting daily production activities.

Key Responsibilities
  • Perform manufacturing operations for injectable and oral radiopharmaceutical products in accordance with established procedures.
  • Carry out production activities in classified environments while complying with current aseptic requirements.
  • Perform aseptic gowning according to procedures and maintain proper cleanroom practices.
  • Follow gowning procedures for classified areas (Grade C and Grade D).
  • Prepare solutions, raw materials, and equipment required for production activities.
  • Review and execute batch records and production work orders accurately.
  • Complete production documentation in real time in compliance with ALCOA+ principles.
  • Conduct in-process tests, measurements, and verification activities.
  • Handle radioactive sources, including iodine and strontium, in strict compliance with radiation safety procedures.
  • Perform environmental monitoring activities, including swipe testing and contamination monitoring.
  • Perform cleaning, disinfection, verification, maintenance, and calibration activities as required.
  • Ensure the safe management and disposal of radioactive waste according to internal procedures.
  • Complete required transactions in computerized systems, including SAP.
  • Participate in inventory activities and material management.
  • Identify, document, and report deviations, incidents, and out-of-specification conditions.
  • Contribute to continuous improvement initiatives and documentation updates.
  • Collaborate with team members and support the onboarding and training of new employees.
Qualifications
  • Completed AEC, DEC, Bachelor's degree, or equivalent education in a relevant field.
  • Experience in a pharmaceutical, biotechnology, or GMP-regulated environment is an asset.
  • Ability to work in an aseptic environment (classified areas, sterile gowning) and follow strict cleanroom requirements is an asset.
  • Demonstrated ability to learn and apply detailed procedures while complying with strict quality and regulatory requirements.
  • Basic proficiency in Microsoft Word and Excel.
  • Excellent French communication skills, both written and verbal.
  • Strong manual dexterity and ability to maintain sustained concentration.
  • Strong communication skills and attention to detail.
  • Ability to work effectively in a fast-paced team environment.
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Production Documentalist
Production Documentalist

Jubilant Life Sciences • Caen

On-site
EUR 32,000 - 42,000
Maintenance Supervisor
Maintenance Supervisor

Jubilant Life Sciences • Caen

On-site
EUR 48,000 - 64,000
Radiopharmaceutical Production Tech: Aseptic & Compliance
Radiopharmaceutical Production Tech: Aseptic & Compliance

Jubilant Pharma, LLC • Caen

On-site
EUR 38,000 - 46,000
Maintenance Technical Specialist, Equipment and Documentation
Maintenance Technical Specialist, Equipment and Documentation

Jubilant Life Sciences • Caen

On-site
EUR 45,000 - 65,000
Specialist, Compliance
Specialist, Compliance

Jubilant Life Sciences • Caen

On-site
EUR 65,000 - 90,000
Supervisor, Microbiology
Supervisor, Microbiology

Jubilant Life Sciences • Caen

On-site
EUR 115,000 - 153,000
Pharma Maintenance Supervisor — GMP/CMMS Leader
Pharma Maintenance Supervisor — GMP/CMMS Leader

Jubilant Pharma, LLC • Caen

On-site
EUR 48,000 - 64,000
Production Maintenance Technician – Injectable Products
Production Maintenance Technician – Injectable Products

Planet Pharma • Auvergne-Rhône-Alpes

On-site
EUR 30,000 - 47,000
Technicien de Production & Contrôle Qualité - Marseille (h/f/nb)
Technicien de Production & Contrôle Qualité - Marseille (h/f/nb)

Siemens Healthineers AG • Marseille

On-site
EUR 26,000 - 34,000
Technicien de Production & Contrôle Qualité - Paris - CDD
Technicien de Production & Contrôle Qualité - Paris - CDD

Curium Pharmaceuticals • Paris

On-site
EUR 32,000 - 35,000
Régime Frais de santé 100%
6e semaine de congés payés
Avantages CSE et CET
+1