JOB DESCRIPTION

We are seeking a detail-oriented QC Chemist to perform day-to-day activities in our laboratory. You will work under prescribed procedures, ensuring quality and accuracy in quantitative analysis and environmental monitoring. You will prepare solutions, calibrate and maintain laboratory instruments, and assist with technical writing and administrative tasks. You will also contribute to problem-solving, data review, and training support staff as needed.

ESSENTIAL SKILLS

• 3-5 years of routine testing using HPLC and Dissolution.
• Experience with solid oral dosage and focus on raw materials and finished products.
• Proficiency in GC, FTIR, KF, UV-VIS, and Pharma GMP.
• Experience in a laboratory setting with wet chemistry, titration, and chromatography.

ADDITIONAL SKILLS & QUALIFICATIONS

• Bachelor’s or Master’s degree in Pharmaceutical, Biological, Chemical science or related field.
• 5-6 years of related laboratory work experience; minimum of 5 years as a QC Chemist in a GMP environment.
• Proficiency in computer applications such as MS Word, Excel, and Outlook.
• Ability to work both independently and in a team environment.
• Capability to manage priorities and maintain timelines for multiple projects.
• Ability to perform basic calculations and handle stress from time pressure and customer demands.

RESPONSIBILITIES

• Conduct analysis in compliance with cGMP requirements, compendia standards, and internal procedures.
• Maintain accurate records of analysis and perform documentation to company standards.
• Prepare test solutions, volumetric solutions, and samples used in analysis.
• Perform sampling, physical, and chemical tests on raw materials, active pharmaceutical ingredients, in-process, finished bulk, finished product, and stability products in an FDA-regulated lab environment.
• Utilize analytical instruments such as HPLC, GC, Dissolution, Malvern particle size analyzer, IR, Auto Titrator, UV Spectrophotometer, and Potentiometer.
• Perform laboratory analysis with practical understanding of test procedures and instrument operation.
• Conduct laboratory investigations under supervision.
• Perform maintenance and calibrations of laboratory instruments and equipment.
• Comply with all regulatory and in-house requirements, including safety, housekeeping, laboratory chemical waste, cGMP, cGLP, and documentation.
• Maintain required level of training needed to perform GMP tasks.
• Prepare and review test procedures, SOPs, and protocols as assigned.

available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave