Job Title: Quality Control (QC) Lab Technician I

Industry: Pharmaceutical Manufacturing

Location: Central Islip, NY (Onsite)

Employment Type: Full-Time, Non-Exempt (Hourly)

Shift: General Shift: Monday – Friday, 8:30 AM – 5:00 PM (some flexibility required)

Compensation: $19.00 – $24.00 per hour (Depending on Experience)

Position Overview:

We are seeking a QC Lab Technician I to support quality control functions within a cGMP-compliant pharmaceutical manufacturing environment.

This individual will play a key role in sample management, chemical inventory control, data entry, and lab support tasks. The ideal candidate will be detail-oriented, dependable, and eager to contribute to maintaining high-quality standards in pharmaceutical production.

Key Responsibilities:

• Manage incoming raw material, in-process, finished product, and stability samples (receipt, logging, distribution, destruction).

• Track chemical and reference standard inventory; verify and dispose of expired materials according to procedures.

• Enter and update sample data using SAP.

• Maintain and replenish lab consumables and supplies.

• Monitor temperature and humidity levels in stability chambers.

• Load samples into stability chambers and ensure timely submission per schedule.

• Assist with sample shipments to external contract laboratories.

• Support general housekeeping and lab organisation.

• Perform other related duties as assigned by QC Management.

Qualifications & Experience:

• Required: High School Diploma or GED.

• Preferred: Associate degree or higher in Chemistry, Laboratory Science, or related field.

• Minimum 2 years of laboratory experience (pharmaceutical or related industry preferred).

• Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).

• Experience using SAP or similar ERP systems is a plus.

• Experience working with inhalation (MDI) products is a strong advantage.

• Ability to understand and interpret complex data sets.

• Strong organisational and communication skills.

• Fluent in English (written and verbal).

Work Environment & Physical Demands:

• Work is performed in a cGMP laboratory or manufacturing setting.

• Requires use of PPE: lab coats, gloves, safety glasses, and possibly respiratory protection.

• Regular exposure to chemicals, powders, and solvents.

• Requires extended periods of standing or walking.

• Must be able to lift up to 35 lbs and ascend/descend ladders as needed.

Additional Information:

• No remote work option; this is a fully onsite position.

• Flexibility to work second shift or weekends if required by business needs.

• Must have the right to work in the United States.

Application Process:

To apply, please submit your CV and a cover letter detailing your relevant experience and qualifications for the role. Applications will be reviewed on a rolling basis, so early submissions are encouraged.

Equal Opportunity Employer:

We value diversity and are committed to creating an inclusive work environment. We encourage applicants from all backgrounds to apply.

Contact: Elvis Eckardt