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Cambrex

Global CDMO for drug substances

Head of Laboratory Instrument and Systems

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

About the Job

Requirements

  • A university-level education in technology or natural sciences.
  • Three to five years of relevant experience maintaining and troubleshooting technical or laboratory equipment and software is preferred.
  • Previous leadership experience is considered an advantage.
  • Interest in instruments, technology, and systems.
  • Ability to communicate effectively both orally and in writing.
  • Service orientation and technical interest.
  • Ability to organize a team and challenge and develop employees based on their strengths.

Responsibilities

  • Allocate and prioritize tasks within the group.
  • Drive cross-functional projects concerning instrument purchases and qualifications.
  • Collaborate and interact with internal and external stakeholders.
  • Ensure the group has the knowledge required to perform relevant tasks and that the operation develops.
  • Hold budget and work-environment responsibility.
  • Ensure compliance with purchasing processes and instrument qualification according to applicable instructions and regulations.
  • Ensure periodic reviews of instruments and laboratory data systems are performed.
  • Participate in the quality organization’s management team and report directly to the company’s Head of Quality.

Desired Qualifications

  • Previous experience working as a leader.

About the Company

Cambrex

Global CDMO for drug substances

Cambrex is a global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, plus analytical and IND enabling services. It uses a range of specialized technologies—such as continuous flow chemistry, handling of controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and production of highly potent APIs—to develop and manufacture drug substances for clients. The company differentiates itself with over 40 years of experience, a staff of about 2,000 experts, and a global footprint in North America and Europe, offering end-to-end capabilities from early development through commercial-scale manufacturing. Its goal is to help clients bring new medicines to market by delivering integrated, reliable drug substance development and manufacturing and related analytical support.

Company size
1,001-5,000
Company stage
IPO
Headquarters
East Rutherford, NJ
Founded
1981

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