Qc Specialist

A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

**Your role**:
An exciting new opportunity has arisen to join our production site in Aubonne as QC Specialist (M/F). With the management of the QC analytical support & technology manager, you manage the external testing needed in the frame of legacy products release and lifecycle management.

You ensure autonomous execution and documentation of planning, follow-up and results from external analysis with the help of our internal stakeholders. Thus, you address related requirements in terms of cGMP, data integrity, investigation, inspection readiness to ensure compliance and availability of external analysis results required for release, tech transfer or covalidations. Moreover, you ensure related budget compliance, managing purchase order process and related payments.

Being the key contact person for this global scientific and organizational expertise, you foster a strong and positive collaboration within the QC analytical & support team (25 people) and beyond, sharing your expertise and scientific background.

**Who your are**:

- Bachelor or CFC in Biotechnology/Life Sciences/Chemistry or equivalent with one to five years of relevant experience, respectively
- Experience of laboratory analysis in a GMP environment and compendial methods (pharmacopoeia)
- Theoretical knowledge of the different analytical technologies (HPLC, Biochemistry, Chemistry, Microbiology, Virology)
- Knowledge of LIMS and SAP software would be considered as a plus
- Ease and appetite to work in a team and in laboratory environment, with international stakeholders and issue related documentation
- Comfortable with delivering timely commitments, being accountable for them to her/his manager and customers, and communicate on their related status
- Languages : French and English (oral and writing), Italian would be an asset

**What we offer**: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life

Job Requisition ID: 256394

Location: Aubonne

Career Level: C - Professional (1-3 years)

Working time model: full-time

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