In this position, you will be responsible for the acquisition, onboarding qualification and requalification of pharmaceutical equipment to ensure optimal performance. You will join a collaborative and innovative work environment, where you can guarantee the quality and efficiency of pharmaceutical production and enjoy opportunities for professional development and growth. Your responsibilities include: Development and execution of qualification protocols (IQ, OQ, PQ) for new and existing equipment, writing of qualification reports as well as ensuring that all equipment and processes comply with GMP, FDA, EMA and other relevant regulatory bodies Scheduling of internal and external equipment service activities on time From small equipment to clean rooms of InnoMedica’s production, you ensure their qualification is always up-to-date Close collaboration with Quality Assurance and Engineering teams to ensure seamless equipment operations As prerequisites for this exciting role, you should hold a Bachelor’s (HES/Fachhochschule) or Master’s degree in Engineering, Pharmaceutical Sciences, or a related field, along with at least 2 years of experience in a regulated environment (pharmaceutical or medical device) or a similar role. Ambitious applicants with a CFC/EFZ in Chemical or Pharmaceutical Production Technology and 3-5 years of experience in regulated environments are also encouraged to apply. Key qualifications include experience with equipment qualification or commissioning, strong attention to detail, excellent problem-solving, organizational and project management skills as well as strong communication and interpersonal abilities. Fluency in English is required; knowledge of German or French is a plus. Interested candidates are kindly requested to submit a complete application (cover letter, CV and reference letters) to Ms. Noëlle Haas, who can also be contacted for additional information by phone (058 521 35 01) or e-mail (hrinnomedica.com). jid21b55f2a jit0313a jiy25a