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Job Title: GC ChemistJob 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.

Responsibilities

+ Execute method validation, process validation, and cleaning validation testing, along with all associated 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, including lab notebooks, chromatograms, report forms, Certificates of Analysis (C of A), specification sheets, and glassware labeling.

+ Provide training, guidance, and mentorship to Level 1 and Level 2 chemists.

+ Promote and adhere to all laboratory health, safety, and housekeeping protocols; take a leadership role in lab clean-up efforts and related initiatives.

+ 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, repeats, and analyst-related deviations; follow management directives to meet deadlines and priorities.

+ Actively participate in laboratory and company meetings and training sessions.

Essential Skills

+ Bachelor’s degree in Chemistry or a closely related scientific discipline required.

+ A minimum of 4–5 years of laboratory experience is preferred, ideally within a pharmaceutical setting focused on solid dosage forms.

+ Proven expertise in analytical testing within a cGMP-compliant laboratory environment.

+ Demonstrated proficiency in operating advanced laboratory instrumentation and associated software.

+ Exceptional time management and attention to detail to ensure accurate project completion with minimal errors.

+ Fluent in English with strong command of both verbal and written communication.

Additional Skills & Qualifications

+ Excellent verbal and written communication skills, including proficiency in technical writing for reports and the ability to interpret technical documents, instructions, diagrams, and schedules.

+ Excellent interpersonal skills for effective collaboration with colleagues and supervisors.

+ Ability to consistently deliver high-quality work in a pharmaceutical environment regulated by agencies such as the FDA and DEA.

+ Capable of working under pressure, following detailed instructions, and managing priorities in a deadline-driven setting.

Work Environment

The work environment involves working with chemicals, reagents, and solvents, requiring physical activity in the laboratory. The facility is FDA-approved, employing approximately 200 people, with the QC Lab having about 20 staff members.

Job Type & Location

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

Pay and Benefits

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.

Workplace Type

This is a fully onsite position in Laurelton,NY.

Application Deadline

This position is anticipated to close on Nov 19, 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 [email protected] (%[email protected]) for other accommodation options.