Inactive
B

Bachem

Develops and manufactures peptides and oligonucleotides

Senior Documentation Manager - Engineering Services

Office Clerical & RecordsPosted on Nov 9
Full-timeBubendorf, SwitzerlandNo salary listed

About the Job

Requirements

  • Technical or natural-science education or an equivalent professional background.
  • At least 5 years of professional experience in the chemical, pharmaceutical, or life-sciences industry.
  • Good knowledge of Good Manufacturing Practice (GMP) and Health, Safety and Environment (HSE) requirements, as well as relevant technical regulations and standards.
  • Experience with technical and GMP-compliant documentation and document and filing structures.
  • Confident use of Microsoft Office.
  • Good spoken and written German and English.

Responsibilities

  • Manage the structured handling, filing, and archiving of technical documentation in electronic and physical form.
  • Ensure compliance with GMP, HSE, and internal documentation standards, including audit-proof document filing.
  • Provide technical leadership to document-management teams in engineering and capital expenditure (CAPEX) projects.
  • Create and implement document-management concepts, review processes, and training concepts.
  • Coordinate document deliveries and manage review, approval, and change processes.
  • Create and maintain documentation plans, document registers, and reporting dashboards.
  • Create, revise, and implement standard operating procedures (SOPs), policies, and standards for document management.
  • Advise project teams and support audits, inspections, and inquiries from authorities.
  • Serve as the central contact for documentation matters and as the interface to Engineering, HSE, Quality Assurance, Commissioning, Qualification and Validation (CQV), Maintenance, and Operations.

Desired Qualifications

  • Experience with document-management systems and SAP.

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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