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Bachem

Develops and manufactures peptides and oligonucleotides

Responsible Person - Rp / Fvp, A

Regulatory & Quality (Life Sciences)Posted on Nov 12
Full-timeBubendorf, SwitzerlandNo salary listed

About the Job

Requirements

  • A university degree in pharmacy, chemistry, or another relevant scientific discipline, together with education, technical knowledge, relevant professional experience, and suitability for the authorised activities.
  • Substantial experience in pharmaceutical, biotechnology, or active pharmaceutical ingredient manufacturing, with strong knowledge of good manufacturing practice, good distribution practice, Swiss pharmaceutical legislation, relevant European Union good manufacturing practice, and International Council for Harmonisation expectations.
  • Demonstrated experience in batch disposition, deviations, investigations, corrective and preventive actions, change control, complaints, product-quality defects, and recalls.
  • Strong scientific judgement, integrity, trustworthiness, and the ability to make independent, well-founded decisions.
  • Ability to ensure direct technical supervision through appropriate availability, on-site presence, and workload for the approved scope.
  • Clear communication and confidence in interactions with authorities, customers, and senior stakeholders.
  • Trustworthiness and independence in exercising the Responsible Person function.
  • Strong German and English language skills.

Responsibilities

  • Act as the designated Responsible Person/Fachtechnisch verantwortliche Person for assigned activities under the Swiss establishment licence and ensure effective technical supervision.
  • Provide independent oversight of applicable manufacturing, testing, batch disposition, storage, and distribution activities in accordance with Swiss good manufacturing and distribution practice requirements and the Pharmaceutical Quality System.
  • Make or support independent quality and regulatory decisions concerning significant deviations, investigations, corrective and preventive actions, changes, product-quality defects, and other critical quality events.
  • Ensure appropriate escalation and measures when product quality, patient safety, or regulatory compliance may be affected, including quarantine, supply restrictions, withdrawal, or recall where required.
  • Support inspections, establishment-licence activities, and required communication with stakeholders and health authorities.
  • Represent Quality in customer audits, quality meetings, and critical product or supply discussions while maintaining the independence of the Responsible Person function.
  • Contribute to key quality governance processes and promote a risk-based quality culture.

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

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