Quality Control (QC) Lab Technician I
: Job Details :


Quality Control (QC) Lab Technician I

Elvis Eckardt Recruitment & Sales Solutions Limited

Job Location : Central Islip,NY, USA

Posted on : 2025-08-05T07:13:18Z

Job Description :
Job Title: Quality Control (QC) Lab Technician IIndustry: Pharmaceutical ManufacturingLocation: 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
Apply Now!

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