Laboratory Technician

Society for Conservation Biology; Totowa (NJ); On-site; USD 40,000 - 65,000; Full time

Job summary

An established industry player is seeking a detail-oriented Laboratory Technician to support the QC and Microbiology departments. This role involves preparing and maintaining reagents, performing environmental monitoring, and ensuring compliance with safety regulations. The ideal candidate will have an Associate Degree in a Life Science discipline and experience in a cGMP environment. Join a dynamic team where your contributions will enhance laboratory operations and support critical quality control initiatives. If you're passionate about science and eager to make a difference, this opportunity is perfect for you.

Qualifications

• 0-3 years in a cGMP environment preferred.
• Knowledge of USP, FDA, and cGMP regulations is a plus.

Responsibilities

• Prepare standards and samples for analytical methods.
• Perform calibration and maintenance of laboratory equipment.
• Assist with environmental sampling and testing.

Skills

Problem-solving skills

Data analysis capabilities

Interpersonal communication skills

Education

Associate Degree in Life Science

Tools

MS Office

Job description

Job Title: Laboratory Technician

Location: NJ5-Totowa, New Jersey

Department: Radiopharmaceutical Contract Manufacturing

Overview: The Laboratory Technician supports the QC and Microbiology departments at the NJ5 site by preparing and maintaining reagents and supplies, performing environmental monitoring, and maintaining equipment.

Essential Duties and Responsibilities

1. Prepare standards, samples, and mobile phase solutions for analytical methods.
2. Perform calibration and maintenance of laboratory equipment.
3. Dispose of waste according to regulations.
4. Maintain cleanliness and manage glassware in labs.
5. Assist with environmental sampling and handling of samples for testing.
6. Support non-complex analytical tests under supervision.
7. Comply with SOPs and regulations, including 21 CFR Part 211 and Eudralex Volume 4.
8. Maintain qualification and validation standards for ISO areas.
9. Ensure a safe working environment and perform radiation safety duties.
10. Perform other duties as assigned.

Qualifications

• Associate Degree in a Life Science discipline; 0-3 years in a cGMP environment preferred.
• Experience with Environmental Monitoring is preferred.
• Knowledge of USP, FDA, and cGMP regulations is a plus.
• Ability to interpret safety rules and manuals.
• Problem-solving skills and data analysis capabilities.
• Proficiency in MS Office.
• Strong interpersonal communication skills.