QA deviation ada

4 settimane fa


Rovigo, Italia Amaris Consulting A tempo pieno

**Who are we?**:
**Amaris Consulting** is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 7,500 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

**Brief Call**: Our process typically begins with a brief virtual/phone conversation to get to know you The objective? Learn about you, understand your motivations, and make sure we have the right job for you

**Interviews** (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities

**Case study**: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.

We look forward to meeting you
**Job description**:
Join the Amaris Consulting talent network as a **QA Deviation Specialist** in the **Pharmaceutical** industry at** Rovigo**

***What will you do?**
- Conduct thorough investigations into deviations from established quality standards within the pharmaceutical sterile sector.
- Collaborate closely with cross-functional teams to identify root causes and implement effective corrective and preventive actions.
- Review and evaluate deviation reports, ensuring accuracy, completeness, and alignment with regulatory requirements.
- Develop and enhance quality systems and processes to proactively prevent deviations in the pharmaceutical sterile manufacturing environment.
- Provide guidance and support to manufacturing and quality teams on best practices for deviation management.
- Interface with regulatory agencies during inspections and audits related to sterile manufacturing processes.
- Maintain accurate and up-to-date documentation of deviation investigations and resolutions.
- Actively participate in continuous improvement initiatives to elevate overall quality and efficiency in the pharmaceutical sterile sector.

**✍️ **What do we request?**
- Bachelor's degree in a relevant scientific or engineering discipline.- Minimum of 2-4 years of hands-on experience in a pharmaceutical sterile manufacturing environment.- In-depth knowledge of regulatory requirements associated with pharmaceutical sterile manufacturing (e.g., FDA, EMA).- Proven expertise in deviation management, root cause analysis, and the implementation of corrective and preventive actions.- Excellent communication skills, both written and verbal, with strong interpersonal abilities.- Detail-oriented with exceptional analytical and problem-solving capabilities.**✨ **What do we offer?**
- Work by objectives with quarterly monitoring.
- Educational and technical growth path.
- Inclusive work climate.
- Lunch vouchers of €8 per working day.
- Free access to Mantu Academy platform with more than 500 courses.
- Psychological counselling.
- **Pioneer Spirit**: desire to explore new technologies, ideas, and skills to build a more sustainable world.
- **Care**:commitment to promoting diversity, meritocracy, and environmental protection for a better future.
- **Performance**:constant ambition to achieve excellence through creativity, innovation, and technology.
- **Trust**:trust is a pillar of progress, driving freedom, creativity, and innovation.
- **Independence**:independence is the basis for realizing a prosperous and agile future.

**Amaris Consulting** is an industry-leading **Top Employer 2023**-certified company that supports its partners in the main areas for Pharma and Biomed Industries in Quality, Laboratories, R&D and Production.


  • QA Deviation Specialist

    4 settimane fa


    Rovigo, Italia amaris A tempo pieno

    Job description Join the Amaris Consulting talent network as a QA Deviation Specialist in the Pharmaceutical industry at Rovigo! What will you do? Conduct thorough investigations into deviations from established quality standards within the pharmaceutical sterile sector. Collaborate closely with cross-functional teams to identify root causes and implement...