Quality Control (QC) Lab Technician I

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The Role

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.

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.

Ideal Profile

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.

What's on Offer?

• Join a well known brand within Pharmaceuticals / Biotechnology
• Attractive Salary & Benefits
• A role that offers a breadth of learning opportunities