Investigation Specialist 80-100%
Role details
Job location
Tech stack
Job description
- Owns investigations and critical deviations and assists in decision making on production issues.
- Drives process changes, CAPAs, and CAPA efficiency checks related to process within required timelines and through GMP systems (e.g. Trackwise, SAP, MES, training, etc.)
- Performs retraining/awareness sessions as CAPA identified during the investigation/deviation.
Requirements
Do you have experience in Manufacturing?, Do you have a Master's degree?, We're looking for an Investigation Specialist to own critical deviations, drive impactful process changes, and ensure GMP compliance within our sterile manufacturing environment. If you have a scientific degree or equivalent experience, experience in sterile manufacturing, and a knack for thorough investigations, we encourage you to apply!, * Bachelor's or Master's Degree in Pharmaceutical Technology, Chemistry, Pharmacy or equivalent work experience.
- At least one year of experience in Sterile Manufacturing in operations and/or QC/QA.
- Previous experience with investigation/deviation management in TW and CAPA definition.
- Proficient in English, German is an advantage.
- Familiarity with GMP requirements, quality procedures and SOP execution.
- Good interpersonal skills with a variety of interfaces within the organization and within the shopfloor.
- Structured, focused, proactive and well-organized working demeanor.
- High motivation and collaboration focused; oriented towards finding solutions and driven by science.
Benefits & conditions
- An agile career and a dynamic work culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance.
In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.
- Benefits in Visp: https://bit.ly/3wjkoFi