Description

Based in Vouvry (Chablais Valaisan)Specialist in Vouvry (Chablais Valaisan)A pharmaceutical company active in the fields of pharmacy and biotechnology is recruiting for the Metrology Department, a Specialist at 100%, for an indefinite period.The pharmaceutical group, active in more than 60 countries, has been a major player for 40 years in the production and distribution of reference therapies for the treatment of ophthalmological and neurological conditions. A company of human scale, it develops a culture where autonomy, trust, and commitment constitute a true foundation for professional fulfillment. Working in project mode allows talents to develop transversal skills, thus favoring versatility and promotion.The Vouvry site specializes in the production of injectables and a neurological active ingredient. It meets the highest requirements, notably through its compliance with GMP and ISO standards.Specialist contribution to the company:In the context of this function, you report to the Metrology Manager and will be in charge of the following activities related to the qualification and validation of equipment, utilities, systems, and cleaning or sterilization processes:- Define qualification strategies based on risks and document them.- Write, coordinate, and execute qualification/validation tests.- Ensure the maintenance of a qualified and validated state of systems.- Manage documentation related to activities: procedures, instructions, protocols, reports.- Manage external partners: on-site support and reviews of deliverables.- Act as an expert for deviations and CAPA.- Participate in the definition of needs during the acquisition of new equipment, and in impact analyses during changes.- Work in close collaboration with engineering, maintenance, production, QA, and QC teams.- Participate actively in audits and inspections.Your rigor and writing ability allow you to manage all documentation related to your activities. Thanks to your analytical sense and critical spirit, you propose improvements and accompany their implementation.Your aptitudes and talents:- You are ideally in possession of a higher university degree or equivalent in engineering, with experience in the pharmaceutical and/or medical device field.- You master the principles of qualification/validation and life cycle in the context of sterile injectable product manufacturing.- You have solid knowledge of GMP requirements for these activities and good knowledge of ISO requirements. Mastery of standards/referentials specific to the pharmaceutical industry is a plus (ISO series, GAMP 5, ICH).- You master the French language with good knowledge of English and IT tools.- Your ability to communicate concisely and effectively, your sense of organization, your autonomy, as well as your team spirit are qualities that complete your profile.Start date: Immediately or to be agreed.Our proposal:Joining the company is the assurance of benefiting from:- The warm welcome of a competent and dynamic team, committed to fostering professional development.- First-rate social benefits (Pension fund, sickness and accident loss of earnings insurance).- A 13th-month salary, a minimum of 25 days of vacation per year, as well as days offered in addition to the official public holidays of the canton of Valais.- Parking, preferential rates for meals.- Benefits offered by partners in the region.We invite you to send us your complete application file (CV, cover letter, work certificates, and diplomas).Find our vacancies on our website: jid208d374aen jit0625aen jpiy26aen