GC Chemist

Job Title: GC Chemist

Job Description

Independently perform advanced laboratory testing of raw materials using Gas Chromatography (GC), following approved test methods and in full compliance with QC procedures, company SOPs, and cGMP standards. Operate a range of GC instruments, including those equipped with headspace and direct injection capabilities. Develop GC methods autonomously as needed and execute method validation, process validation, and cleaning validation testing.

Responsibilities

• Carry out method verification, validation, optimization, and transfer activities as required.
• Support lab management in conducting investigations and handling deviations.
• Assist in preparing for and responding to audits and regulatory inspections.
• Perform internal laboratory audits as necessary.
• Maintain accurate, organized, and cGMP-compliant documentation for all testing activities.
• Provide training, guidance, and mentorship to Level 1 and Level 2 chemists.
• Promote and adhere to all laboratory health, safety, and housekeeping protocols.
• Ensure proper handling and documentation of controlled substances in strict accordance with federal and company regulations.
• Complete assigned projects with precision and timeliness, minimizing errors and repeats.
• Actively participate in laboratory and company meetings and training sessions.

Essential Skills

• Expertise in Chemistry, particularly in GC, method validation, and method development.
• Proficiency in GC methods development, validation, and transfer.
• Experience with Gas Chromatography troubleshooting and Quality Control Chemistry.
• Strong knowledge in Pharmaceuticals and experience with Mass spectrometry, Titration, and Wet chemistry.

Additional Skills & Qualifications

• Bachelor’s degree in Chemistry or a closely related scientific discipline required.
• Minimum of 4–5 years of laboratory experience, preferably within a pharmaceutical setting focused on solid dosage forms.
• Excellent verbal and written communication skills.
• Proficiency in technical writing for reports and ability to interpret technical documents.
• Exceptional interpersonal skills for effective collaboration.
• Proven expertise in analytical testing within a cGMP-compliant laboratory environment.
• Exceptional time management and attention to detail.
• Fluent in English with a strong command of both verbal and written communication.
• Ability to deliver high-quality work in a regulated environment by agencies such as the FDA and DEA.
• Proficient in operating advanced laboratory instrumentation and associated software.
• Capable of working under pressure and managing priorities in a deadline-driven setting.
• Comfortable working with chemicals, reagents, and solvents, involving physical activity in the laboratory.

Work Environment

The role is based in an FDA-approved facility employing approximately 200 people, with the QC Lab consisting of about 20 members. The environment is deadline-driven, requiring the ability to handle chemicals and physical activity in the laboratory. The position offers an opportunity to bring immediate value and potentially stay long-term.

This is a Permanent position based out of Laurelton, NY.

The pay range for this position is $80000.00 - $85000.00/yr.

Epic Pharma offers benefits including medical, dental, and vision insurance, a 401k with company match, and various paid time off options. Other benefits can include life insurance, short and long-term disability, tuition reimbursement, and employee activities.

This is a fully onsite position in Laurelton,NY.

This position is anticipated to close on Dec 29, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.