Skip to main content
Sanofi logo
Sanofi

Production Operator - Biologics and Vaccines

Auto-translated from Italian · original: Operatore di Produzione - Biologici e Vaccini

5 day weekGenerous PTOHybrid · Anagni, Italy

Location: Anagni

Production Operator - Biologics and Vaccines

Every year, we provide 4.3 billion healthcare solutions to people, thanks to the impeccable planning and meticulous attention to detail of our production and supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and instill hope in patients and their families.

We are looking for qualified operators to join our Biologics and Vaccines production department, with a focus on high-criticality environments such as Isolators and Sterile areas. The selected candidates will work on state-of-the-art production lines, contributing to the creation of biological drugs and vaccines destined to improve the lives of patients around the world.

Main Responsibilities

Operators will be involved in the following activities throughout the entire production cycle:

Operational activities:

  • Preparation: setup and preparation of materials, components, and equipment necessary for the production process, carrying out main preparation processes (washing, sterilization, assembly)

  • Filling: conducting aseptic filling operations for biological products and vaccines in a controlled environment, using both Isolator technology and Aseptic Area (RABS technology)

  • Capping: closing and sealing containers according to the required quality standards

  • Compounding: preparation of solutions intended for filling and carrying out accessory plant preparation operations (CIP/SIP/FIT)

  • Lyophilization: plant preparation and process control

Process management:

  • Conducting and monitoring production processes in compliance with Standard Operating Procedures (SOPs)

  • Accurate management of production materials, ensuring traceability and integrity

  • Compilation and management of batch records and line documentation, with precision and punctuality

  • Execution of in-process checks and timely reporting of any deviations

Quality and Compliance:

  • Strict adherence to Good Manufacturing Practice (GMP) standards after appropriate training

  • Application of safety, hygiene, and environmental protection procedures

  • Active participation in continuous training and qualification programs

Candidate Profile

Essential requirements:

Education:

  • High school diploma (preferably technical-scientific: chemical, biotechnological, mechanical, electronic technician or equivalent)

Experience:

  • Previous experience in production roles, preferably in an aseptic area / Filling via Isolator or classified environments (cleanroom)

  • Knowledge of pharmaceutical production processes or regulated sectors is a plus

Technical skills:

  • Familiarity with Supervisory Control and Data Acquisition (SCADA) systems

  • Good manual dexterity and motor coordination for precision operations

  • Ability to read and interpret technical procedures and GMP documentation

  • Basic knowledge of quality and safety principles in the pharmaceutical field

  • Knowledge of technical language and HMI communication

  • Knowledge of the English language

  • Familiarity with the Office suite

Soft skills:

  • Precision and attention to detail: fundamental to ensuring product quality and patient safety

  • Reliability and sense of responsibility: awareness of the impact of one's work on patient health

  • Ability to work in a team: effective collaboration with colleagues, supervisors, and support functions

  • Flexibility and adaptability: availability to work on three shifts (morning, afternoon, night) including weekends and holidays according to production needs

  • Respect for roles, rules, and procedures: operational discipline and compliance with regulations

  • Strong motivation: orientation towards achieving production and quality goals

  • Problem solving: ability to identify and report anomalies, contributing to continuous improvement

Preferred requirements:

  • Specific experience in the production of biologics, vaccines, or injectable products

  • Knowledge of quality management systems (ISO, GMP)

  • Previous training in GMP or cleanroom environments.

Pursue progress. Discover extraordinary.

Progress does not happen without people: people from different backgrounds, in different places, with different roles, but all united by one thing: the desire to make miracles happen. You can be one of these people. By chasing change, embracing new ideas, and exploring all the opportunities we have to offer. We pursue progress. And together, we discover the extraordinary.

At Sanofi, we offer equal opportunities to everyone, regardless of ethnic origin, color, ancestry, religion, gender, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

The salary range for this position is :€0,00 - €0,00

Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.