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Job Title: Quality ProductionJob Description

Join a dynamic team dedicated to expanding access to high-quality, affordable medicines. This position involves handling a variety of tasks essential to the production process, ensuring compliance with industry standards and company policies.

Responsibilities

+ Weigh finished products to detect missing components.

+ Clear line culls and document all components discarded.

+ Prepare shippers, inspect finished products, and package them into shippers. Seal, label, and stack shippers.

+ Fill cartons, carriers, or shippers by hand with products, labels, literature, or applicators.

+ Perform cleaning tasks on machines during or after machine operation.

+ Maintain compliance with SOPs, good documentation practices (GDP), training requirements, company and safety policies, and current Good Manufacturing Practices (cGMPs).

+ Verify correct lot code/expiration date on all packaging components/finished goods.

Essential Skills

+ Experience in pharmaceutical production.

+ Proficiency in machine operating and packaging.

+ Strong knowledge of Quality Assurance processes.

+ Familiarity with GMP and SOP standards.

+ Ability to operate machinery and perform packaging tasks.

Additional Skills & Qualifications

+ High school diploma or GED.

+ Minimum of 1 year experience working in production for a pharmaceutical company.

+ Experience in bottling, batching, packing, compounding, blending, inspection, mixing, and general production.

Work Environment

The work environment consists of a structured shift schedule. Initial training will be on the 1st shift (6:45 a.m. – 3:30 p.m.) for four weeks. Post-training, assignments may be on the 2nd shift (3 p.m. – 11:45 p.m.) or the 3rd shift (10:30 p.m. - 7:15 p.m.) based on availability. The work environment supports rotating holidays, a 45-minute lunch, and two 15-minute breaks. Emphasis is placed on a respectful, inclusive, and collaborative culture that fosters professional growth and community involvement.

Job Type & Location

This is a Contract position based out of Hicksville, NY.

Pay and Benefits

The pay range for this position is $62.70 - $66.00/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 Hicksville,NY.

Application Deadline

This position is anticipated to close on Dec 8, 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.