Equipment Operator

Healthcare Businesswomen’s Association; Ivrea; In loco; EUR 26.000 - 48.000; Tempo pieno

Vantaggi offerti da questo lavoro

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Flexible and hybrid working options

14 weeks parental leave

Descrizione del lavoro

Novartis in Italy is seeking a production technician for radiopharmaceutical manufacturing, ensuring cGMP compliance, HSE adherence, and operation of approved SOPs.

You will work in shifts (including nights and weekends), perform batch preparation and production activities, and support maintenance, verification, and material control with the Production Manager and Qualified Person. Fluency in Italian and good English are required.

Competenze

• Scientific/technical background is required.
• Willing to work in shifts, including night shifts and weekends.
• Fluent in Italian. Good knowledge of English.

Mansioni

• Carry out the production of radiopharmaceuticals according to cGMP, HSE rules and approved SOPs.
• Working in shifts, perform activities for preparation and production of batches.
• Perform routine maintenance and cleaning; periodic microbiological verification of pharmaceutical areas and equipment; support external personnel in maintenance/qualification activities.
• Promptly report deviations/out of specification to Production Manager and Qualified Person.
• Perform incoming and outgoing verification of raw materials and materials.
• Collaborate with Production Manager on material stocks and waste materials; assist training of new personnel.

Formazione

Scientific/technical background

Strumenti

GMP Compliance

Descrizione del lavoro

Salary Range: 26.000,00 € - 48.400,00 €

Job Description Summary

Carry out the production of radiopharmaceuticals according to cGMP, HSE rules and approved SOPs.

Job Description

Major accountabilities:

• Working in shifts, perform the necessary activities for the preparation and production of batches.

• Perform routine maintenance and cleaning, periodic microbiological verification of pharmaceutical areas and equipment and support external specialized personnel in carrying out extraordinary maintenance/qualification activities.

• Promptly report to the Production Manager and the Qualified Person any deviation and/ or out of specification detected during the production process.

• Perform incoming and outgoing verification activities of raw materials and materials.

• Collaborate with the Production Manager to the management of material stocks and waste materials.

• Collaborate with the Production Manager to the training of new personnel.

Essential Requirements

• Scientific/technical background.

• Willing to work in shifts, including night shifts and weekends.

• Fluent in Italian. Good knowledge of English.

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read our brochure to learn more about our global total rewards offering:

https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Commitment to Diversity and Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Skills Desired

Forklift Operations, GMP Compliance, Health, Safety, and Environment (HSE) Policy, Inventory Management, Machine Operations, Manufacturing, Operations Management, Process Improvements, Production Management, Quality Control (QC), Regulatory Documents