QC Chemist IV

Perrigo Company plc

. Ensure the quality and compliance of raw materials, finished products, and stability samples .

Posted 9/28/2026full-timeBronx • New York • United StatesMid-LevelSenior💰 $36 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in laboratory analytical testing, including HPLC, GC, and UV-Vis, while ensuring compliance with cGMP requirements. Proficient in method validation, troubleshooting analytical instruments, and maintaining quality control standards in a pharmaceutical environment.

Highest-signal resume keywords

HPLC AnalysisGC AnalysisCGMP ComplianceLaboratory Analytical TestingProcess Validation Testing

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Analytical TestingMethod ValidationCleaning Verification TestingPhysical TestingImpurity Analysis

Soft Skills

Excellent CommunicationInterpersonal SkillsAttention to DetailTeam Collaboration

Tools & Technologies

HPLCGCUV-VisFTIRMalvernEmpowerMicrosoft OfficeSAP

Industry Keywords

Pharmaceutical Quality ControlLaboratory PoliciesGMP RequirementsSOPsStability Samples

About the role

Key responsibilities & impact

Ensure the quality and compliance of raw materials, finished products, and stability samples
Perform laboratory analytical testing to support Perrigo operations and manufacturing needs
Prepare solutions and reagents for testing
Use analytical laboratory equipment including HPLC, UPLC, GC, UV, and IR
Communicate with the supervisor to determine needs and expedite work when appropriate
Prioritize tasks to meet company needs
Execute analytical testing for atypical or out-of-specification results
Adhere to laboratory policies, procedures, and GMP requirements
Troubleshoot analytical instruments independently
Establish testing priorities with the supervisor and team
Execute method transfer and validation activities following protocols
Perform process validation testing
Perform cleaning verification testing following protocols
Update departmental SOPs
Cross-train staff on equipment and laboratory techniques

Requirements

What you’ll need

Bachelor’s or Associate Degree in Chemistry or related discipline
6 years of experience in a pharmaceutical quality control laboratory
Advanced application of cGMP requirements for all data generated by the QC laboratory
Laboratory skills including physical testing, HPLC analysis, GC analysis, impurity analysis, UV-Vis, FTIR, Malvern, and Empower
Excellent oral and written communication, interpersonal skills, and computer literacy
Proficiency with Microsoft Office and SAP
Ability to work as a team to achieve desired results
Ability to work overtime as required
Strong attention to detail and ability to follow written procedures
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