- Use of Personal and Collective Protection Devices in compliance with EHS guidelines.
- Adhere to all safety regulations within the department.
- Maintain a clean and organized work environment (Housekeeping).
- Conduct air, water, and manufacturing sample sampling.
- Conduct microbiological tests on Raw materials, Intermediates, and Cleaning validation samples following official analytical methods under aseptic conditions.
- Utilize the Smarteam system to reference effective analytical methods.
- Document all results in Laboratory Notebooks and/or Analytical Sheets per relevant procedures.
- Verify results in accordance with official procedures.
- Review results verified by colleagues.
- Utilize the StarLims system for results documentation.
- Immediately report any analytical issues or unexpected results to the direct Supervisor.
- When necessary, use the TrackWise system to initiate analytical investigations.
- Collaborate with team members to enhance laboratory productivity.
- Handle all analytical solutions post-activity (including deactivation).
- Conduct periodic internal checks on laboratory instruments.
- Capable of basic troubleshooting on analytical instruments.
- Perform additional supportive activities beneficial for the laboratory (e.g. receiving and labeling reagents).
- Receive, register, and manage analytical samples.
- Ensure compliance with departmental safety regulations.
- Knowledge of common microbiological techniques for various samples, including manufacturing, environment, air, water, surfaces, personnel, etc.
- Work under aseptic conditions.
- Familiarity with computer systems (Windows, Office).
- Strong communication skills.
- Precision and accuracy in all activities.
- Proficiency in English (basic) and fluency in Italian.
- Minimum of 3 years of experience in a Microbiological Laboratory of QC or equivalent.
- On-site Canteen.
- Flexible working arrangements for Caregivers and parents.
- Coffee Key.
- Recognition Program.
- Wellbeing Digital Platform.
- Welfare Platform.
- Health agreement with leading medical centers.
- Diverse and inclusive working environment.
- Continuous learning and development opportunities through programs like Linkedin Learning.
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Microbiological Quality Control Analyst - Santhia, Italia - Teva Pharmaceuticals
Descrizione
Who we are
TAPI is a top international supplier of active pharmaceutical ingredients (APIs), boasting a diverse portfolio of over 350 API products. We are the primary global API supplier for 80% of the leading pharmaceutical companies worldwide. With a rich history of over 80 years in the generic API industry, we are recognized as one of the most dependable API providers, positioning TAPI as an industry leader based on our extensive experience, expertise, cutting-edge technologies, and exceptional customer service.
Main responsibilities and activities
In the Microbiological Quality Control Department, we are seeking a dynamic individual to report to the Quality Control Microbiology Manager with the following tasks:
What we offer?
At TAPI, we value our employees and provide them with a range of benefits, including but not limited to:
Type of contract: long term contract
Location and working schedule
Santhià (VC), full-time position (5 days per week).
Teva's commitment to equal opportunities
Teva is dedicated to providing equal opportunities in the workplace. Our global policy ensures that equal employment opportunities are extended to individuals regardless of various factors like age, race, religion, gender expression, and other legally protected statuses.
