QC Chemist II

Perrigo Company plc; New York (NY); On-site; USD 38,572 - 48,216; Full time

Benefits offered by this job

Competitive compensation and benefits

Job summary

Perrigo Company plc in New York, NY, is seeking an analytical testing technician to perform lab analyses on raw materials, finished products, and process samples using HPLC, GC, UV-Vis, FTIR and other instruments. You will work under supervision and ensure regulatory compliance while supporting Perrigo operations.

The role requires a science degree and 1–2 years GMP/FDA experience or an AS with 5+ years in regulated settings; strong documentation, communication, and problem solving are

Qualifications

• Bachelor/AS with lab experience and coursework.

Responsibilities

• Perform analytical testing on lab samples, including raw material, finished product, process equipment, and environmental samples.
• Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations.
• Use analytical laboratory equipment such as HPLC, UPLC, GC, UV, IR, UV‑Vis, FTIR, Malvern, and Empower as applicable.
• Remain informed of regulatory landscape and product portfolio and participate in internal and external quality audits.
• Maintain personal laboratory work area and assist with general laboratory cleaning.
• Perform continuous improvement initiatives, projects, committees, and Mentor Program activities to support laboratory goals.
• Display effective communication skills within the work group and assist other analysts based on department needs.
• Demonstrate independence in daily activities, including decision making, problem solving, and ownership of assigned tasks.

Skills

Effective communication

Documentation

Attention to detail

Independent work

Team collaboration

Problem solving

Education

Bachelor of Science in Chemistry/Food Science/Biology

Associate of Science in scientific discipline with 5+ years in regulated environment

Tools

HPLC

UPLC

GC

UV

IR

UV-Vis

FTIR

Malvern

Empower

Job description

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are a top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over‑the‑counter and infant formula. We are committed to enhancing the wellbeing of our colleagues and consumers alike, fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Description Overview

Perform analytical testing on lab samples including raw material, finished product, process equipment and environmental. Use laboratory equipment such as HPLC, UPLC, GC, UV, IR, UV‑Vis, FTIR, Malvern, Empower and related applications. Work independently and as part of a team under a supervisor while maintaining regulatory compliance and supporting Perrigo operations and manufacturing needs.

Scope of the Role

• Perform analytical testing on lab samples, including raw material, finished product, process equipment, and environmental samples.
• Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations.
• Use analytical laboratory equipment such as HPLC, UPLC, GC, UV, IR, UV‑Vis, FTIR, Malvern, and Empower as applicable.
• Remain informed of regulatory landscape and product portfolio and participate in internal and external quality audits.
• Maintain personal laboratory work area and assist with general laboratory cleaning.
• Perform continuous improvement initiatives, projects, committees, and Mentor Program activities to support laboratory goals.
• Display effective communication skills within the work group and assist other analysts based on department needs.
• Demonstrate independence in daily activities, including decision making, problem solving, and ownership of assigned tasks.

Experience Required

• Bachelor of Science in a scientific discipline (Chemistry, Food Science, or Biology) with academic lab experience.
• 1–2 years experience working in a GMP/FDA regulated manufacturing environment (preferred).
• OR Associate of Science in a scientific discipline with relevant training and 5 or more years of experience in a regulated environment.
• Good written and verbal communication skills, excellent documentation and organizational skills.
• Demonstrated critical thinking, attention to detail, and the ability to work independently and with others.
• Ability to take ownership of assigned tasks and responsibility for results.

Benefits

Competitive compensation and benefits designed to support you and your family, along with opportunities for career development and professional growth.

Pay Rate

$31.05 per hour

EEO Statement

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.