QC Supervisor

☞ Takeda

View: 124

Update day: 26-03-2024

Location: Neuchâtel Neuchâtel NE

Category: Quality Assurance / Quality Control

Industry: Pharmaceuticals

Position: Mid-Senior level

Job type: Full-time

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Job content

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Job Description

Takeda Neuchâtel

Site de Production Biotech | Biotech Manufacturing Site

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine.

Here, everyone matters, and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own

QC Supervisor

Takeda’s Neuchatel Quality Control department team is looking for a highly motivated QC Supervisor in Analytical group.

Your mission

As QC Supervisor you will report directly to the QC Analytical Manager and be responsible for Supervising the laboratory to ensure reliable and timely availability of test results under cGMP. This position manages a group of around 10 analysts, in collaboration with two other Supervisors (around 35 people in total).

This position will be a back up to the Manager in his function of management and documents approval.

Essential Duties & Responsibilities
  • Supervise the Analytical laboratory activities to assure timely availability and accuracy of results
  • Ensure that all in-process samples, raw material and final products are analyzed in accordance with SOPs and regulatory requirements to applicable GMP’s and standards
  • Enforce all laboratory policies and practices
  • Enforce all safety and security policies and practices
  • Monitor the testing techniques and the accuracy and completeness of all records and documentation
  • Solve problems concerning lab equipment and methods
  • Ensure the calibration and maintenance of the lab instruments
  • Drives continuous improvement in the lab (5S)
  • CAPA owner, investigator
  • Change assessor
  • Ensure audit readiness in laboratory, subjects preparation and presentation during audit
  • Ensure the training of the lab analysts
  • Supervise and participate to the validation activities of the laboratory
  • Ensure that the status of equipment and procedures are compliant.
  • Assure implementation and validation of new methods
  • Conduct adequate laboratory investigations when issues arise. Participate or lead a team when appropriate for the investigation process. If necessary and in accordance with the lab manager, initiate and support Corrective and Preventive actions in the laboratory

Required Skills
  • Master degree (or equivalent) or 10 years in pharmaceutical company
  • Experience within cGMP manufacturing
  • Good experience in people management
  • Strong verbal and written communication with ability to effectively communicate at multiple levels in the organization
  • Strong organizational and follow-up skills, as well as attention to detail.
  • French and English level B2 or higher are a must
  • Very good knowledges of analytical techniques including chromatography, ELISA, electrophoresis, spectroscopy
  • Experience in project management
  • Good knowledges of usuals software (Word, Excel..) and specific (Lims, trackwise, MS-project, Smartsheet)
  • Dynamic, flexible

Takeda’s Outstanding Values

To help us achieve our mission, we believe in focusing on the needs of patients through empowering our teams. Together, we are united by our four priorities (Patients, Trust, Reputation, and Business) and our shared values of Takeda-ism Integrity, Fairness, Honesty, and Perseverance. Takeda-ism is more than just a word. It’s a belief and a mindset which guides our decisions, behaviors, and interactions. It’s how we strive to work and live, every day.

Locations

CHE - Neuchatel

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
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Deadline: 10-05-2024

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