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Lonza

Global life sciences contract manufacturer

Associate Principal Scientist - Quality Control

Regulatory & Quality (Life Sciences)Posted on Nov 12
Full-timeGreenwood, SC, USANo salary listed

About the Job

Requirements

  • A Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline is required.
  • Significant experience in analytical method development, method validation, product development, or quality control within pharmaceutical, nutraceutical, life sciences, or related regulated industries is required.
  • Demonstrated leadership experience managing technical teams, projects, or complex scientific programs is required.
  • At least 5 years of experience with cGMP, cGLP, CFR requirements, laboratory compliance, and regulatory expectations is required.
  • Hands-on experience with analytical techniques such as high-performance liquid chromatography (HPLC), gas chromatography (GC), mass spectrometry, high-performance thin-layer chromatography (HPTLC), photodiode array (PDA), wet chemistry, and other advanced laboratory instrumentation is required.
  • Ability to conduct investigations, perform data analysis, apply statistical tools, and drive technical problem solving in a manufacturing or research and development environment is required.
  • Experience communicating, collaborating, managing projects, and engaging stakeholders across multiple functions and global teams is required.

Responsibilities

  • Lead scientists, analysts, and technicians supporting product development, method development, and global stability programs.
  • Drive color development and reformulation projects for hard capsule products to meet customer and regulatory requirements.
  • Develop, validate, and implement analytical methods that support new product introductions, process improvements, and material characterization.
  • Serve as the technical lead for global stability programs, generating scientific data used to establish product shelf life and support customer studies.
  • Partner with Quality, Regulatory Affairs, Manufacturing, Safety, and Research and Development teams to solve technical challenges and support business growth.
  • Lead complex investigations, root cause analyses, and forensic evaluations of product and process issues using scientific and Six Sigma methodologies.
  • Mentor and develop team members while fostering a culture of scientific excellence, compliance, and continuous improvement.

Desired Qualifications

  • Prior experience with dietary supplements is a plus.

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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