Quality Control Chemist New Flanders, New Jersey

Garonit Pharma; Northern (KY); Hybrid; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) with Company match

PTO and paid holidays

Job summary

Garonit Pharmaceutical seeks a Quality Control Chemist to join our Quality team at our Flanders, NJ facility. The role supports analytical testing and laboratory operations to ensure compliance with cGMP and regulatory requirements.

The ideal candidate will have a Bachelor's degree in Chemistry or Life Sciences and 3–5+ years in a regulated QC lab, with experience in HPLC and USP methods, ensuring detailed documentation and adherence to SOPs.

Qualifications

• Bachelor’s degree in Chemistry, Life Sciences, or a related scientific discipline.
• 3–5+ years of experience in a Quality Control laboratory.
• Experience with pharmaceutical analytical testing and cGMP requirements.
• Experience operating HPLC and other analytical laboratory instrumentation.

Responsibilities

• Perform sampling and analytical testing of raw materials, in-process materials, finished products, and packaging components.
• Operate, maintain, and troubleshoot laboratory instrumentation, including HPLC and other analytical equipment.
• Support laboratory investigations, deviations, OOS results, and CAPA activities.
• Assist with analytical method development, transfer, verification, and validation activities.
• Maintain accurate and complete laboratory documentation per cGMP requirements and Company procedures.

Skills

Quality Control

Regulatory compliance

Documentation

Education

Bachelor’s degree in Chemistry/Life Sciences

Tools

HPLC

Analytical instrumentation

Job description

Garonit Pharmaceutical is seeking a Quality Control Chemist to join our growing Quality team at our Flanders, New Jersey facility. This role will support analytical testing and laboratory operations for pharmaceutical manufacturing while ensuring compliance with current Good Manufacturing Practices (cGMP), applicable regulatory requirements, and Company procedures.

Key Responsibilities

• Perform sampling and analytical testing of raw materials, in-process materials, finished products, and packaging components.
• Conduct testing in accordance with USP compendial methods, approved internal analytical methods, specifications, and procedures.
• Operate, maintain, and troubleshoot laboratory instrumentation, including HPLC and other analytical equipment.
• Support laboratory investigations, deviations, Out-of-Specification (OOS) results, and Corrective and Preventive Action (CAPA) activities.
• Assist with analytical method development, transfer, verification, and validation activities, as applicable.
• Perform environmental monitoring and testing of air, water, and surfaces, as required.
• Maintain accurate and complete laboratory documentation, records, logs, and related documentation in accordance with cGMP requirements and Company procedures.
• Support regulatory, customer, and internal audits, including preparation and follow-up activities.
• Follow applicable laboratory safety requirements, Standard Operating Procedures (SOPs), and Company policies.
• Perform other related duties as assigned based on business and laboratory needs.

Qualifications

• Bachelor’s degree in Chemistry, Life Sciences, or a related scientific discipline.
• 3-5+ years of experience working in a Quality Control laboratory preferred.
• Pharmaceutical, biotechnology, or other regulated-industry laboratory experience preferred.
• Experience with pharmaceutical analytical testing and cGMP requirements preferred.
• Experience operating HPLC and other analytical laboratory instrumentation preferred.
• Familiarity with USP methods, laboratory documentation practices, SOPs, and applicable regulatory requirements.
• Strong attention to detail, organizational skills, and ability to maintain accurate documentation.
• Ability to work effectively both independently and collaboratively in a regulated laboratory environment.

The anticipated salary range for this position is $60,000-$90,000 per year. Actual compensation will be determined based on factors such as experience, qualifications, skills, and other job-related considerations.

This position is also eligible for consideration for a discretionary year-end bonus, based on Company and individual performance. Any bonus is discretionary and is not guaranteed.

Garonit Pharmaceutical offers eligible employees a benefits package that includes medical, dental, and vision insurance; a 401(k) retirement plan with Company match; paid time off (PTO); paid holidays; and other benefits in accordance with applicable Company plans and policies.

About the Role

This is a full-time, onsite position based in our Quality Control laboratory in Flanders, New Jersey. The position involves routine use of analytical instrumentation and laboratory equipment and requires adherence to applicable safety, quality, and cGMP requirements.

Garonit Pharmaceutical is an equal opportunity employer. We consider qualified applicants for employment without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.