5 дней назад
QC Project Leader (Analytical Chemistry)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
QC Project Leader (Analytical Chemistry): Managing QC projects and coordinating chemical and physical testing of raw materials, in-process samples, and finished products with an accent on analytical method development, validation, GMP compliance, and cross-functional execution. Focus on troubleshooting chromatographic methods and instruments, leading investigations and CAPA activities, coordinating external laboratories, and guiding junior chemists.
Location: Visp, Switzerland; relocation is available for the successful candidate and family if needed.
Company
is a global life sciences company providing products and services across three continents.
What you will do
- Lead QC projects from initiation through completion, including scope, timelines, resources, deliverables, reporting, and issue escalation.
- Coordinate chemical and physical testing of raw materials, in-process samples, and finished products using HPLC, GC, UV/Vis, KF, and FTIR.
- Develop, validate, transfer, and troubleshoot chromatographic analytical methods in line with ICH, GMP, regulatory, and quality requirements.
- Manage change controls, deviations, OOS/OOT/OOE events, laboratory investigations, root cause analysis, impact assessments, CAPA, and documentation.
- Act as the QC contact for customer projects and coordinate activities with external contract laboratories.
- Collaborate with R&D, Production, Quality Assurance, and external partners while coaching junior chemists and supporting audits and continuous improvement.
Requirements
- PhD in Chemistry, Analytical Chemistry, Biochemistry, Chemical Engineering, or a related field; alternatively, a Master's or Bachelor's degree with significant relevant industry experience.
- Strong practical and theoretical knowledge of analytical chemistry, including hands-on HPLC and GC experience.
- Experience with analytical method development, validation, and transfer, plus knowledge of GMP and regulatory standards.
- Strong problem-solving, troubleshooting, organizational, project management, communication, and leadership skills.
- Fluent German and English with excellent written and verbal communication skills.
Nice to have
- Familiarity with ISO 9001.
Culture & Benefits
- Full-time employment at 80–100% workload.
- Relocation support is available for the successful candidate and their family.
- Work in a cross-functional life sciences environment focused on ethical and compliant operations.
- Opportunities to solve complex scientific problems and contribute to products that improve lives.
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