Quality Control Chemist (HPLC & cGMP)

Garonit Pharmaceutical; Mount Olive (IL); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) with company match

PTO and holidays

Job summary

Garonit Pharmaceutical is seeking a Quality Control Chemist to join our Quality team at the Flanders, New Jersey facility. This role supports analytical testing and laboratory operations in a cGMP environment.

The ideal candidate has a Bachelor’s degree in Chemistry and 3–5+ years in a QC laboratory, with hands-on HPLC work and strong documentation practices; position is full-time and onsite.

Competitive compensation and benefits are provided according to company policy.

Qualifications

• Bachelor’s degree in Chemistry or related field.
• 3–5+ years in a QC laboratory preferred.
• Experience with pharmaceutical analytical testing and cGMP.
• Familiarity with USP methods and regulated documentation.

Responsibilities

• Perform sampling and analytical testing of materials and products.
• Follow USP methods and internal analytical procedures.
• Operate and troubleshoot HPLC and other analytical lab instruments.
• Support investigations, deviations, and CAPA activities.
• Assist with method development, transfer, verification, and validation.
• Conduct environmental monitoring of air, water and surfaces.
• Maintain accurate lab records and documentation per cGMP.
• Support audits and follow-up activities.
• Follow safety SOPs and company policies.
• Perform other duties as needed.

Skills

Attention to detail

Organizational skills

Documentation skills

Independent & collaborative work

Education

Bachelor's degree in Chemistry or Life Sciences

Tools

HPLC

Job description

Garonit Pharmaceutical is seeking a Quality Control Chemist to join our Quality team at the Flanders, New Jersey facility. This role supports analytical testing and laboratory operations in a cGMP environment.

The ideal candidate has a Bachelor’s degree in Chemistry and 3–5+ years in a QC laboratory, with hands-on HPLC work and strong documentation practices; position is full-time and onsite.

Competitive compensation and benefits are provided according to company policy.