Laboratory Technician

Job Overview

Job Title: QC Lab Technician

Duration: 12+ Months

Location:
Belvidere, NJ 07823

Shift:
Monday – Friday; 40 hours per week; 8:00 AM – 5:00 PM

Pay Rate: $25/hr on W2 (all inclusive)

Base pay range: $25.00/hr - $25.00/hr

To analyze and / or test under cGMP, raw materials, intermediates and finished products by applying validated or compendia methods.

• Performs/Applies knowledge and skills to diverse reactions.
• Release testing of products per current compendia, regulatory and corporate quality systems, and principles.
• Performs analysis in the laboratory with minimal supervision.
• Prepares standards, mobile phases, and reagents.
• Calibrates and monitors laboratory equipment (HPLC, GC, ICP, etc.).
• Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods.
• Performs calculations, collects and prepares data for evaluation.
• Keeps supervisor informed of work status.
• Investigates OOS results under guidance of senior staff.
• Maintains good documentation practices.
• Follows SHE duties and responsibilities: displays and promotes positive safety behaviors; uses proper PPE; ensures area and equipment operate at high safety levels; ensures compliance with safety directives; keeps area neat and clean.
• Ensures incidents are investigated, reported, and risks are assessed promptly.
• Demonstrates safety awareness and accident prevention in performing tasks.
• Supports SHEQ standards and encourages colleagues to uphold them.
• Supports plant and corporate initiatives as outlined in the manufacturing plan.
• Ensures correctness of determined results and works according to SOPs and specification sheets.

• Demonstrate the ability to learn and perform lab-specific analytical methods.
• Complete analysis on raw materials and finished products within agreed turnaround times.
• Ensure SOPs and specifications are up to date and compliant with current compendia; update as required.
• Perform and document all work in adherence with cGMP guidelines.

• Bachelor’s degree in a relevant scientific discipline preferred; associate’s degree required.
• Broad knowledge of quality control techniques and methods.
• Broad understanding of safety, laboratory hygiene and GMP rules.
• Overtime eligible; ability to work shifts, weekends, overtime (including coverage) and holidays as required. Overtime may be adjusted based on business needs.

• 0-3 years of lab experience.
• Experience in Microsoft Office (Outlook, Word, Excel).