Quality Control (QC) Lab Technician I
Quality Control (QC) Lab Technician I
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
$ 19 - 24
1 Vacancy
Job Description
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
Required Experience:
IC
Employment Type
Full-Time
