Lonza Group is seeking a QC Specialist III for Raw Materials in Portsmouth, NH, to manage the raw material release process, ensuring compliance with global standards. The role involves coordinating testing, documentation, and project management while offering opportunities for career development in a collaborative environment
Job Summary
This role coordinates the end-to-end raw material release process including receipt, sampling, testing, data authorization, and archival.
The position offers opportunities to lead cross-functional and external projects while ensuring compliance with global compendial and cGMP requirements.
Candidates will work in a supportive and collaborative team environment with access to cutting-edge technology and comprehensive benefits.
Matching Summary
Match Score: 85
Lonza Group is seeking a QC Specialist III for Raw Materials in Portsmouth, NH, to manage the raw material release process, ensuring compliance with global standards. The role involves coordinating testing, documentation, and project management while offering opportunities for career development in a collaborative environment.
Salary
Competitive salary; Comprehensive benefits package; Not specified
Skills & Requirements
Must-have
cGMP regulated environment experience
raw material testing and release coordination
USP EP JP pharmacopeial knowledge
LIMS and SAP system proficiency
SOP management and document control
Nice-to-have
cross-functional project leadership skills
data trending and historical analysis
collaborative team environment
strategic improvement initiatives
advanced Microsoft Office skills
Key Requirements
Bachelor's or Associate's Degree in Microbiology or Biochemistry
2-4 years of GMP industry experience
2+ years supporting raw material testing or quality activities
Working knowledge of USP, EP, and JP pharmacopeial requirements