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Lonza

Global life sciences contract manufacturer

QC Chemist

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeTampa, FL, USANo salary listed

About the Job

Requirements

  • Experience performing analytical testing in a GMP-regulated pharmaceutical, biotechnology, or life sciences laboratory environment.
  • Hands-on expertise with analytical techniques including HPLC, UPLC, FTIR, UV-Vis spectroscopy, Dissolution, TOC, titration, and other wet chemistry methods.
  • Working knowledge of cGMP regulations, data integrity principles, and regulatory expectations from agencies such as FDA, EMA, and USP.
  • Experience documenting, reviewing, and interpreting analytical data, laboratory investigations, and technical reports.
  • Ability to work a 12-hour shift schedule, including days, nights, weekends, and holidays, as required.
  • A bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.

Responsibilities

  • Perform analytical testing of raw materials, in-process, stability, environmental monitoring, water, and finished product samples to support manufacturing and product release activities.
  • Operate and maintain laboratory instrumentation including HPLC, UPLC, Dissolution, FTIR, UV-Vis, TOC, and other analytical systems while ensuring data integrity and compliance.
  • Generate accurate laboratory documentation and reports in accordance with cGMP, GDP, ALCOA+, and regulatory requirements.
  • Investigate laboratory deviations, out-of-specification (OOS), out-of-trend (OOT), and other quality events while supporting CAPA activities.
  • Collaborate with Quality, Manufacturing, Validation, and Regulatory teams to ensure timely and compliant testing support.
  • Support method validation, method transfer, equipment qualification, training activities, internal audits, and regulatory inspections.
  • Contribute to continuous improvement initiatives that enhance laboratory efficiency, quality performance, and operational excellence.

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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