Laboratory Technician

Compunnel Inc.; Belvidere (NJ); On-site; USD 34,440; Full time

Job summary

A leading quality control company in Belvidere, NJ is looking for a QC Lab Technician to analyze and test raw materials and finished products. The role requires knowledge of GMP guidelines, quality control techniques, and analytical methods. Candidates should hold at least an associate's degree and have some lab experience. Overtime eligibility and the ability to work flexible hours are necessary for this position.

Qualifications

• Bachelor's degree in a relevant scientific discipline preferred; associate's degree required.
• Broad knowledge of quality control techniques and methods.
• 0-3 years of lab experience.

Responsibilities

• Perform and document all work in adherence with cGMP guidelines.
• Analyze raw materials and finished products for required tests.
• Calibrate and monitor laboratory equipment.

Skills

Quality control techniques

Laboratory hygiene

Analytical methods

Education

Bachelor's degree in a relevant scientific discipline

Associate's degree

Tools

Microsoft Office

HPLC

GC

Job description

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

Job Summary

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

Responsibilities

• 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.

Complexity and Scope

• 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.

Qualifications

• 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.

Experience

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