B

Bachem

Develops and manufactures peptides and oligonucleotides

Lead Quality Control Site Development

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeStein, SwitzerlandNo salary listedIn-person

About the Job

Requirements

  • A PhD or MSc in a scientific discipline such as Chemistry or Pharmacy, or a related field.
  • At least 7 years of professional experience in the relevant field, including at least 5 years of leadership experience managing a team.
  • Experience interacting with Swissmedic and international regulatory authorities during audits and inspections.
  • In-depth knowledge of regulatory requirements, including EU GMP Guidelines, the Swiss Therapeutic Products Act (HMG), the Ordinance on Establishment Licences (AMBV), PIC/S Guidelines, ICH Guidelines, FDA requirements, and related regulations.
  • Strong written and spoken German and English language skills.
  • Ability to prioritize tasks and manage multiple responsibilities during the project phase.
  • Ability to identify issues, think analytically, and develop pragmatic, compliant solutions.
  • Flexibility and adaptability as priorities and responsibilities change across project phases.

Responsibilities

  • Build, lead, and continuously develop the Quality Control organization for the Sisslerfeld Site, including establishing Microbiology (MIBI) and In-Process Control (IPC) laboratories.
  • Ensure implementation of regulatory and compliance requirements and support alignment with internal and external stakeholders throughout project execution.
  • Establish, implement, and continuously improve QC systems, processes, and the quality framework.
  • Drive qualification, validation, and implementation of analytical methods, technologies, equipment, and laboratory systems, including support of commissioning and qualification (C&Q) activities: DQ, IQ, OQ, and PQ.
  • Develop and maintain the site's documentation landscape within the areas of responsibility, including QC procedures, applicable regulations, roles, responsibilities, and documentation governance across applicable areas.
  • Define and coordinate operational-readiness activities, milestones, and business processes to ensure a successful transition from project to commercial operations.
  • Oversee and continuously improve ramp-up laboratory operations, QC processes, resource planning, and quality investigations, including out-of-specification (OOS), out-of-trend (OOT), deviations, corrective and preventive actions (CAPAs), and change controls during the operational phase.
  • Ensure inspection readiness, represent Quality Control during audits and inspections, and collaborate with Global Quality and site stakeholders on continuous-improvement initiatives.

About the Company

Bachem

Develops and manufactures peptides and oligonucleotides

Bachem provides development and manufacturing of peptides and oligonucleotides for research, clinical development, and commercial products. Its offerings include custom synthesis and scale-up production, analytical testing, and related services across the drug development spectrum. Customers work with Bachem by specifying desired sequences and specifications, after which Bachem designs, synthesizes, and quality-controls the peptides or oligonucleotides and delivers them in appropriate scales and formats. The company differentiates itself through more than five decades of experience, a global footprint with sites in Europe, the US, and Asia, and an integrated set of services spanning discovery support to commercial manufacturing. Its goal is to help pharmaceutical and biotechnology companies advance peptide- and oligonucleotide-based therapies by providing reliable, scalable, and well-supported manufacturing and development capabilities.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Bubendorf, Switzerland
Founded
1971

Recently Posted Jobs

Explore more opportunities at Bachem

See more jobs