MSAT Direct Materials Owner everyone
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Job Location:
Visp - Switzerland
Monthly Salary:
Not Disclosed
Posted on:
14 hours ago
Vacancies:
1 Vacancy
Job Summary
About Us
ten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development manufacture and testing of tomorrows medicines. We support our clients in developing differentiated stable usable and safe injectable treatments for patients.
Your mission
As MSAT Direct Material Lead is responsible for the quality and riskbased assessment and continuous monitoring of all materials used in pharmaceutical manufacturing. This includes raw materials packaging materials components and productspecific materials whose suitability and quality are essential for sterile dosage forms. The role located within the MSAT department ensures that materials with their critical attributes are linked to process performance all materials comply with regulatory requirements are correctly maintained in the ERP system and that appropriate actions are initiated in the event of quality issues including communication with suppliers and customers.
- Spearhead the complete lifecycle management of materials by defining stringent quality requirements in close collaboration with QC and Development. You will evaluate new materials for aseptic processes resolve complex quality deviations and directly link critical material attributes (like purity and composition) to overall process performance yield and robustness.
- Act as a key partner to our suppliers by leading the resolution of deviations and complaints. You will actively participate in rigorous supplier qualifications annual reviews and audits ensuring all quality-related communications are clear and that resulting CAPAs are successfully implemented.
- Serve as the central Subject Matter Expert (SME) bridging internal teamsincluding Production QC QA SCM and Engineeringwith external customers. You will provide critical support on material-related inquiries and ensure that all decisions and deviations are backed by transparent compliant documentation.
- Take absolute ownership of material-related data within our ERP system (Microsoft Dynamics). You will ensure impeccable data quality maintain accurate material master records and expertly coordinate the system onboarding of new materials to guarantee compliant real-time representation.
- Safeguard our operations by executing thorough root cause analyses and driving CAPA processes to resolution. You will proactively create and maintain comprehensive risk-analytical documents (such as FMEAs) and expertly guide material-related updates through the change-control process.
- Continuously elevate our material management standards by initiating strategic improvement measures. You will develop robust material specification frameworks contribute to cross-site standardization projects and drive ongoing enhancements in material quality supplier performance and production safety.
Your profile
We are looking for a dedicated professional who combines scientific expertise with rigorous quality standards to drive excellence in a dynamic pharmaceutical landscape. Here is what you will be bringing to our team:
- Degree in a scientific technical or pharmaceutical field (e.g. Pharmacy Chemistry Biotechnology Quality Management Packaging Technology).
- Solid background in a GMP environment ideally within Quality Control Quality Assurance Supply Chain or Material Management.
- Deep knowledge of material or supplier qualification and regulatory requirements (EU GMP FDA ICH) coupled with a strong inherent awareness of quality and risk.
- Experienced with ERP systems (specifically Microsoft Dynamics) and master data processes as well as proficient use of core quality tools (Deviation Management CAPA Change Control).
- Highly structured and analytical working style with the resilience and competence to solve complex problems in a dynamic environment.
- Confident communicator with internal and external stakeholders bringing a strong team orientation assertiveness and a deep sense of responsibility to the role.
Why us
We offer a dynamic environment where you can contribute meaningfully collaborate with exceptional minds and unlock your full potential.
Heres what sets ten23 apart:
Heres what sets ten23 apart:
- A valuable and impactful career development opportunity in an inspiring environment
- Flexible working arrangements and environment with an open culture and diverse workforce
- The opportunity to work with and learn from highly qualified and experienced employees
- Our learning and self-developing culture offers a wide range of training options
- Competitive pension fund plan annual bonus and other financial and non-financial benefit
Contact
Click on Apply Now!
For more information and clarification please connect Amrith () from our Talent team!
For more information and clarification please connect Amrith () from our Talent team!
About us
While most applicants fall short of 100% qualifications we embrace diverse perspectives and encourage applications from all qualified candidates regardless of background. Women & underrepresented groups we see you!
Join Us & Make a Difference! ten23 champions equal opportunity and is committed to diversity and inclusion.
Learn about ten23
Join Us & Make a Difference! ten23 champions equal opportunity and is committed to diversity and inclusion.
Learn about ten23
About Company
The partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow’s medicines.
