Enter a job title or keyword
Visual Inspection Subject Matter Expert, Visp everyone
Job Location:
Job Location:
Visp - Switzerland
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
19 September 2026 (16 hours ago)
Posted:
Application Deadline:
17 December 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
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
Full-time Visp (5days Onsite)
Start Date : 01 October 2026
End Date : 31 March 2027
We are looking for an experienced Visual Inspection Subject Matter Expert (SME) who can hit the ground running from day one to join our team onsite in Visp for 5 days a week over a 6-month duration with a possibility of extension.
In this critical role your mission is to ensure that the visual inspection of parenteral medicinal products is performed in a regulatory-compliant robust and efficient manner and continuously improved. You will act as the true owner of VI processes to drive deviation and trend analyses standardize workflows and increase inspection robustness. By joining us you will play a key role in inspecting CAPAs deviations and batch releases while also ensuring we remain compliant with internal quality regulations.
Your responsibilities will include
Start Date : 01 October 2026
End Date : 31 March 2027
We are looking for an experienced Visual Inspection Subject Matter Expert (SME) who can hit the ground running from day one to join our team onsite in Visp for 5 days a week over a 6-month duration with a possibility of extension.
In this critical role your mission is to ensure that the visual inspection of parenteral medicinal products is performed in a regulatory-compliant robust and efficient manner and continuously improved. You will act as the true owner of VI processes to drive deviation and trend analyses standardize workflows and increase inspection robustness. By joining us you will play a key role in inspecting CAPAs deviations and batch releases while also ensuring we remain compliant with internal quality regulations.
Your responsibilities will include
- Acting as the owner of VI processes driving deviation and trend analyses standardizing workflows and increasing inspection robustness.
- Driving capacity building through the training of operators as well as the creation and maintenance of testsets and defect libraries.
- Handling document management deviation and change management.
- Supporting New Product Introductions (NPI).
- Acting as the deputy to release preparation of batches.
Your profile
We are looking for someone with:
- Degree in technical sciences (e.g. Pharmacy Chemistry Biotechnology Medical Technology Mechanical Engineering) or equivalent professional experience.
- Experience in a GMP environment (EU GMP Annex 1 Data Integrity GDocP health authority inspections) ideally in sterile pharmaceutical manufacturing visual inspection (manual and/or automated) Quality Assurance or MSAT.
- Methodological expertise in root cause analysis CAPA risk assessments (FMEA) and statistics/SPC; experience with Minitab/JMP is required.
- System knowledge: MES/ERP (e.g. SAP/BC) eQMS (Deviations/CR/CAPA) and VI systems (lighting/optical technology).
- Excellent German and English language skills (spoken & written).
- Knowledge of container/closure systems (vials RTU cartridges/syringes stoppers crimp caps) material-induced artefacts packaging materials and aseptic processing.
- Analytical data-driven mindset and strong problem solving skills under time pressure.
- Strong communication and moderation skills capable of bridging the shopfloor to management.
- Ownership mentality structured working style and high results orientation.
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
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.
