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Siegfried

Contract development and manufacture of APIs

Lab Supervisor Stability

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeEvionnaz, SwitzerlandNo salary listedIn-person

About the Job

Requirements

  • A chemical-engineering education, ideally with a specialization in analytical chemistry.
  • Expertise in stability studies and reference substances, with good command of applicable GMP and regulatory requirements.
  • Ability to supervise a team and coordinate activities involving several departments.
  • Rigor, organizational skills, and ability to manage priorities in a demanding environment.
  • Team spirit, interpersonal ease, and ability to persuade in a matrix organization.
  • Autonomy, judgment, and sense of responsibility in the area of expertise.
  • Proficiency in English.

Responsibilities

  • Coordinate the quality and regulatory compliance of the assigned activities in accordance with GMP requirements and health, safety, and environmental rules.
  • Supervise a team of 5–7 employees and support their development.
  • Serve as a key contact for internal and external clients, collaborating closely with Quality Control, Analytical Development, Quality Assurance, Regulatory Affairs, and Project Management teams.
  • Lead stability studies, including estimating and quoting, drafting protocols, scheduling, organizing sampling, managing samples, reviewing results, conducting trend studies, preparing reports, and communicating with clients.
  • Ensure regulatory follow-up by placing site follow-up studies on stability, updating retest dates and storage conditions, contributing to Product Quality Reviews, and participating in audits and inspections.
  • Coordinate analytical activities related to stability studies and characterization of reference substances with the relevant teams.
  • Ensure equipment reliability and resource availability by monitoring temperature- and humidity-controlled areas and equipment, organizing maintenance, overseeing IT solutions, procuring materials and consumables, and making valid reference substances available.
  • Organize the team's activities, support employees, monitor performance indicators, and keep procedures and work instructions up to date.

About the Company

Siegfried

Contract development and manufacture of APIs

Siegfried is a contract development and manufacturing organization (CDMO) with 16 production sites across four continents. It manufactures pharmaceutical APIs and their intermediates, and also produces finished drug products such as tablets, capsules, sterile vials, ampoules, cartridges, and ointments. In addition, Siegfried offers development services to support customers from early-stage formulation and process development through to large-scale production. The company combines long-standing experience in pharmaceuticals and chemicals to move customers’ innovations from development into industrial-scale manufacturing. Its broad footprint and full-service offering differentiate it from competitors by providing end-to-end support, multiple dosage forms, and global supply capabilities. The goal is to help customers bring their pharmaceutical products to market efficiently by delivering scalable production and comprehensive development services across a global network.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Zofingen, Switzerland
Founded
1873

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