Ophtapharm AG

Quality Projects Specialist, 80-100%

Ophtapharm AGHettlingen CH80–100%EN
Охорона здоров'я та доглядОпубліковано 1 вересня 2026 р.
Відгукнутися

Вакансію розміщено на jobs.ch. Відгук відкриє їхній сайт, далі веде роботодавець.

Про вакансію

Quality Projects Specialist, 80-100% Ophtapharm AG is an FDA/EU-GMP certified manufacturer in the pharmaceutical sector (ophthalmic products). At our production site in Hettlingen near Winterthur, high-quality products such as eye drops, ointments, and gels are aseptically produced, filled, and packaged for international markets. As part of our Quality organization, you will help shape and strengthen key quality initiatives across the site. Working closely with cross-functional teams, you will oversee QC data systems, support digital transformation initiatives, and contribute to a culture of continuous improvement. To strengthen our dedicated team, we are looking for an analytical and execution-driven personality to join us at our site near Winterthur starting as soon as possible or by agreement as Quality Projects Specialist, 80-100%. Quality Projects Specialist, 80-100% Your Role Manage QC instrumentation data and lifecycle activities to ensure GMP compliance. Drive cross-functional quality and compliance projects with measurable business and quality impact. Conduct risk assessments and drive compliance improvement initiatives. Provide expert guidance on QC instrumentation, computerized systems, and GDP requirements. Your Profile Experience in GMP-regulated environments, including QC instrumentation, Data Integrity, and data lifecycle management. Knowledge of GMP requirements, Good Documentation Practices (GDP), computerized systems, and Data Integrity principles. Experience in cross-functional projects and laboratory systems such as OpenLab and Chromeleon. Strong analytical and problem-solving skills with a structured and pragmatic approach. Fluency in German and good working knowledge of English. What you can expect The opportunity to shape quality processes in an evolving GMP environment, both internally and with external partners. A role with real ownership, visibility, and influence across functions and leadership levels. The chance to contribute to a significant transformation journey and help build sustainable quality practices for the future. A collaborative culture with short decision-making paths and openness to new ideas. Flexible working conditions, an attractive pension scheme, and convenient accessibility with public transport and free parking. For recruitment agencies:Thank you for your interest. We are not engaging external support for this role. Arbeitsort Ophtapharm AG Riethofstrasse 1 8442 Hettlingen CH Do you have any questions?Our HR team is happy to assist you. Tel: . Jetzt bewerben jidf272a07cs jit0937cs jiy26cs

Оголошення тією мовою, якою його написав роботодавець.

Оголошення та відгук через jobs.chВідгукнутися
ПартнерScribendiРедагування та вичитка англійською мовоюСертифіковані редактори виправляють дисертацію, заяву на роботу чи супровідний лист, написані іншою мовою. Оцінка ціни за хвилини, а послуга працює з 1997 року.Перевірте ціну

Схожі вакансії

Responsible Person / Fachtechnisch verantwortliche Person

Ophtapharm AGHettlingen CH18 серп.
Охорона здоров'я та доглядjobs.ch

Sachbearbeiterin / Sachbearbeiter Service Desk Fakturierung 100%

Hirslanden AGBern100%9 вер.
Охорона здоров'я та доглядjobs.ch

Spezialist/in medizinische Codierung

KPT Krankenkasse AGBern und Homeoffice9 вер.
Охорона здоров'я та доглядjobs.ch

ASSC mobile à 70%

Fondation Les Perce-NeigeLes Hauts-Geneveys70%9 вер.
Охорона здоров'я та доглядjobup.ch

Medizinische/r Praxisassistent/in

Universitätsspital BaselBasel9 вер.
Охорона здоров'я та доглядjobs.ch

Spezialist/in medizinische Codierung

KPT Krankenkasse AGBern und Homeoffice9 вер.
Охорона здоров'я та доглядjobs.ch
Усі вакансії