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Lonza

Global life sciences contract manufacturer

Associate Manager - Development Services, Purification

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeTuas, SingaporeNo salary listed

About the Job

Requirements

  • A degree or PhD in a relevant science field, or equivalent experience.
  • Adequate experience in downstream process development, process characterization, or viral clearance, and familiarity with laboratory-scale execution of techniques including affinity and ion exchange chromatography using the AKTA system, ultrafiltration/diafiltration, and viral reduction strategies.
  • Two to five years of experience leading a team in a people-manager role.
  • Strong problem-solving and analytical skills.
  • A good understanding of current Good Manufacturing Practice (cGMP) regulations.

Responsibilities

  • Ensure strict adherence to environmental, health, and safety (EHS) and cGMP standards while maintaining high-quality, compliant laboratory operations.
  • Lead a team of scientists and analysts performing downstream purification activities, including process development and process characterization.
  • Manage and schedule team, equipment, and systems resources to deliver projects aligned with department sales plans.
  • Act as a subject matter expert in key technical areas while developing knowledge of regulatory and intellectual property landscapes.
  • Oversee documentation, review, and approval of reports and protocols to meet quality and compliance standards.
  • Present data to customers and support business development activities, including proposals, presentations, and laboratory tours.
  • Ensure cGMP compliance, participate in internal and external audits, and build cross-functional relationships to support project delivery and business objectives.

Desired Qualifications

  • Experience in process characterization and viral clearance studies.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

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