Chemistry Laboratory

Maintain Quality Reports

Maintain Quality Reports.

Responsibilities

• Perform chemical analysis on drug products and incoming raw materials.
• Maintain and implement efforts in housekeeping, and safety programs.
• Maintenance of the Calibration program for laboratory equipment.
• Responsible for Chemistry and Life-sciences related disciplines performing basic and applied research to provide innovative solutions for reducing hospital acquired infections and improving the quality of health care
• Has an academic background and hands on laboratory training in the field of Chemistry or Biological Sciences
• Understands and consistently follows multi-step documented procedures while conducting laboratory research
• Has hands on experience with USP/ISO/ASTM based chemical testing and performs all testing with strict adherence to the written laboratory work instructions
• Understands the validation principles for chemical methods, develops and validates new chemical test methods, and prepares study reports
• Maintains accurate and well-organized laboratory records, notebooks and/or worksheets
• Use theoretical knowledge to interpret data and to trouble-shoot experiments
• Maintain assigned aspects of the chemistry laboratory work to provide material and technical support to scientific staff
• With moderate or no supervision, apply comprehensive understanding of defined productivity goals and objectives
• Maintain appropriate training/certification including GLP and GMP
• Knowledge of FDA regulations for drugs and device desirable

Qualifications

• Must have awareness and respect of all company policies and safety rules.

Skills

• Hands on laboratory training in the field of Chemistry or Biological Sciences
• Understanding of multi-step documented procedures
• Hands on experience with USP/ISO/ASTM based chemical testing
• Validation principles for chemical methods
• Theoretical knowledge to interpret data and trouble-shoot experiments
• Comprehensive understanding of defined productivity goals and objectives
• GLP and GMP training/certification
• Knowledge of FDA regulations for drugs and devices

Benefits

• Not specified

Pay

• TBD

Schedule

• 8:00 AM - 5:00 PM