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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. Execute method validation, process validation, and cleaning validation testing, along with all associated documentation. 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, 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.

Skills

Chemistry, gc, method validation, pharmaceutical, gas chromatography, method development, Hplc, Mass spectrometry, Titration, Wet chemistry

Top Skills Details

Chemistry,gc,method validation,pharmaceutical,gas chromatography,method development

Additional Skills & Qualifications

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. Strong 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. Proven expertise in analytical testing within a cGMP-compliant laboratory environment. 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. Ability to consistently deliver high-quality work in a pharmaceutical environment regulated by agencies such as the FDA and DEA. Demonstrated proficiency in operating advanced laboratory instrumentation and associated software. Capable of working under pressure, following detailed instructions, and managing priorities in a deadline-driven setting. Comfortable working with chemicals, reagents, and solvents, involving physical activity in the laboratory.

Experience Level

Expert Level

Job Type & Location

This is a Contract to Hire position based out of Laurelton, NY.

Pay and Benefits

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

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits 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)

Workplace Type

This is a fully onsite position in Laurelton,NY.

Application Deadline

This position is anticipated to close on Nov 6, 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.