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Lonza

Global life sciences contract manufacturer

Quality Control Manager - Electrophoresis

Regulatory & Quality (Life Sciences)Updated on Nov 10
Full-timePortsmouth, NH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a science-related field is required.
  • Experience working within a cGMP-regulated pharmaceutical, biotechnology, or life sciences environment is required.
  • Experience leading or mentoring laboratory teams is required.
  • Knowledge of electrophoresis testing and quality control laboratory operations is required.
  • Experience with quality systems such as LIMS, TrackWise, DMS, or electronic laboratory systems is required.
  • Strong troubleshooting, data review, and problem-solving skills are required.
  • Excellent written and verbal communication skills are required.
  • Ability to manage multiple priorities and deliver results in a fast-paced environment is required.
  • Commitment to safety, quality, compliance, and continuous improvement is required.

Responsibilities

  • Lead and support a team of QC analysts to deliver testing activities safely, accurately, and on schedule.
  • Plan and coordinate laboratory testing to meet manufacturing and customer timelines.
  • Review and approve quality control documentation and laboratory records.
  • Drive continuous improvement initiatives that enhance quality, efficiency, and compliance.
  • Support regulatory inspections, customer audits, investigations, and CAPA activities.
  • Resolve technical, operational, and team-related challenges in a timely manner.
  • Monitor compliance with cGMP requirements, quality systems, and data integrity standards.

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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