Quality System Lead - Bulle, Schweiz - UCB

UCB
UCB
Geprüftes Unternehmen
Bulle, Schweiz

vor 2 Wochen

Lena Schneider

Geschrieben von:

Lena Schneider

beBee Recruiter


Beschreibung

Make your mark for patients


We are looking for a
QA System Lead at
80% working time, who is
autonomous, proactive, team player and who has a well-developed sense of discretion and commitment to join us in our
HSE & Quality Culture &Compliance department, based in our
site in
Bulle, Switzerland.



About the role


As a QA System Lead you will provide strategic and operational Quality systems support to senior management, line management and internal customers in order to deliver site expected performances.


You will work closely with partners at local and global levels to proactively support operations and ensure high quality standards are promoted and embedded.


Who you'll work with


Reporting to the Head of HSE & Quality Culture & Compliance, you will work in tandem with a colleague in a very collaborative environment.


What you'll do

  • You will lead as auditor and participate in periodic internal GMP audits.
  • You will work as local process owner of GMP system processes such as deviations, CAPA, RCA, Management review, Quality Risk Management.
  • You will be the main contact for the equivalent corporate process owner
  • You will actively contribute to simplification and streamlining of processes and support continuous Quality improvement initiatives.
  • You will represent the Quality System team internally and you will participate in projects relating to Quality strategies.
  • You will write / approve / authorize Quality documentation and maintain / improve quality system procedures.
  • You will organize and participate in Quality committees.
  • You will lead & organize the quality & HSE management review on a quarterly basis and write the report.

Interested? For this role we're looking for the following
education, experience
and skills

  • Minimum 5 years professional experience in GMPregulated industry, preferably within Quality Assurance or operational department.
  • Very good knowledge of GMPs and pharmaceutical industry
  • Ability to coordinate multifaceted projects and to meet/respect critical deadlines.
  • Very Good oral and written communication skills, in French (C1) and English (B2).
  • Very good negotiation and convincing skills.
  • Demonstrated ability to write up scientific / technical documents.
Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you


About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.


Why work for us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients.

We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work.

We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees or our planet.

Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.


Learn more about sustainability at UCB and how it is integrated into our business approach.

UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.

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