Job Id: 259242
Shift: Mon- Fri 7:00am- 3:30pm
Pay rate: $20-$23
Job Description:
In this onsite role you will be a vital part of the calibration documentation program and compliance to regulatory standards. You will be working closely with the Engineering Metrology and Manufacturing Maintenance departments reporting into the Manager of Manufacturing Engineering. You will have the responsibility supporting the calibration documentation system for scheduled calibrations and preventative maintenance. The results of your work may be requested during an audit. This position will need familiarity with working in an FDA regulated environment and will uphold the highest integrity toward data accuracy for ISO 9001 compliance.
Essential Functions:
Updates and maintains accurate and detailed calibration records and maintenance documentation using EAM (Enterprise Asset Management) preventative maintenance system. ? Communicates verbally and in writing project status updates and requests for information. ? Performs duties in compliance with established business policies.
WORK ENVIRONMENT:
The work environment characteristics are representative of both an office and laboratory environment. Some time spent in production areas and warehouse. Flexible work hours to meet product demand deadlines.
PHYSICAL DEMANDS: Position requires ability to lift up to 20 lbs. on occasion. Up to 80% of time at the desk on computer/doing paperwork/ on phone doing analytical work (10% of time in meetings). Some walking in manufacturing areas required. Position may require use of Personal Protective Equipment as posted.
EDUCATION SKILLS:
AA/AS in Life Sciences Laboratory Manufacturing or a related equipment field or 3 to 5 years of relevant experience. ? Experience in FDA regulated environment is strongly preferred. Knowledge/Skills: ? Ability to work seated for approximately 80% of a typical working day. Ability to work standing for approximately 20% of a typical working day. ? Proficient using Microsoft technology including Excel. ? Detail-oriented with excellent documentation skills. ? Ability to learn and follow routine procedures independently as well as part of a team. ? Exhibit effective time management skills to achieve goals in a timely manner. ? Ability to work collaboratively in a team environment and successfully work independently. ? Knowledge of cGMP manufacturing ? Understanding of ISO 9001. ? Must be able to work in a team environment including inter-departmental teams. ? Ability to maintain regular and reliable attendance.