QC Chemist II

Perrigo Company plc

. Ensure the quality and compliance of raw materials, finished products, and stability samples through laboratory analytical testing .

Posted 9/28/2026full-timeBronx • New York • United StatesMid-LevelSenior💰 $31 per hourWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in laboratory analytical testing, including HPLC, UPLC, and GC, while ensuring compliance with cGMP regulations. Possesses strong communication and organizational skills to effectively support laboratory operations and continuous improvement initiatives.

Highest-signal resume keywords

HPLC AnalysisGMP/FDA Regulatory ExperienceAnalytical TestingLaboratory RegulationsDocumentation Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Analytical TestingHPLCUPLCGCUV-VisFTIRMalvernEmpowerPhysical TestingImpurity Analysis

Soft Skills

Communication SkillsOrganizational SkillsCritical ThinkingAttention to DetailProblem-Solving

Tools & Technologies

SAPMicrosoft OfficeLES

Industry Keywords

CGMPLaboratory ComplianceQuality AuditsRegulated EnvironmentContinuous Improvement

About the role

Key responsibilities & impact

Ensure the quality and compliance of raw materials, finished products, and stability samples through laboratory analytical testing
Prepare solutions and reagents for testing
Perform analytical testing on raw material, finished product, process equipment, and environmental samples
Test purchased materials and Perrigo-manufactured products per cGMP requirements
Participate in laboratory investigations
Use analytical laboratory equipment including HPLC, UPLC, GC, UV, and IR
Remain informed of the regulatory landscape and product portfolio
Participate in internal and external quality audits
Maintain the personal laboratory work area and assist with general laboratory cleaning
Perform daily activities, decision-making, and problem-solving with increasing independence
Participate in continuous improvement projects, committees, and the Mentor Program
Communicate effectively within the work group and support other analysts based on department needs

Requirements

What you’ll need

Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) required, including academic lab experience; OR Associate of Science degree in a scientific discipline and relevant training with 5 or more years of experience in a regulated environment
1–2 years of experience working in a GMP/FDA-regulated manufacturing environment preferred
Intermediate laboratory/computer skills, including physical testing, HPLC analysis, impurity analysis, SAP, Microsoft Office, LES, UV-Vis, FTIR, Malvern, and Empower as applicable
Advanced understanding of laboratory regulations and requirements
Good written and verbal communication skills
Excellent documentation and organizational skills
Demonstrated critical thinking, attention to detail, and ability to work independently and with others
Ability to take ownership of assigned tasks and responsibility for results
All application materials, including resumes and CVs, must be submitted in English

Benefits

Comp & perks

Competitive compensation
Benefits tailored to supporting you and your family
Career development opportunities
Inclusive, collaborative culture
Equal opportunity employment