Quality Control I
Responsible for all activities involving quality inspections and compliance with applicable regulatory requirements;
Initiate non-conformance reports (NCR).
Responsible for the label printing and labeling maintenance.
Performs all aspects of testing related to manufacturing.
First article inspections
In-process release inspection.
Final QC release of finished goods.
Ensures that all inspections and procedures are properly completed and documented.
Perform environmental monitoring of cleanrooms and warehouses.
Pre and Post-Inspection of product gamma irradiation process.
Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820.
Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices.
Minimum of 2-4 years’ experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment.
Ability to communicate effectively, verbally and in writing, and demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors.
General knowledge and use of measuring devices as calipers, micrometer, rulers, etc.
Knowledge of label printing software (i.e. EasyLabel, Bartender, LabelView, NiceLabel, etc.).
Please apply at:
OnDemand Employment Group
2011 Auto Center Drive #116
Please bring with you two forms of valid identification and updated resume.