Morris Plains, New jersey
Quality Control Technician Job Opening in Morris Plains, New jersey - To perform this job successfully, a qualified individual must be able to perform each essential duty satisfactorily either with or without reasonable accommodation. The requirements listed in this job description document are representative of the knowledge, skill, and/or ability required.
Plans and organizes priorities utilizing the Daily Priorities form.
Responsible for timely achievement of assigned tasks and efficient time management.
Performs and reports daily testing of product according to established methods and requirements related to raw materials , final release processes. Supports the in-process testing.
Manages the testing schedule to support timely deliveries of customer orders.
Actively participates in the Quality Control Daily Targets related to safety, quality, delivery, and cost.
Evaluates test data to support production and engineering.
Monitor and report test status of various production runs to QC Manager, Manufacturing Manager, QC Supervisor, Technology, or Process Engineer.
Identifies materials, including placing product on hold, proper identification and segregation of nonconforming materials, initiating non-conforming material report (NCR) and participating in investigations.
Provides support to Engineering, IT and R&D including participation in product/process development trials, carrying out new types of raw material and product testing and use of experimental materials.
Maintains and performs necessary calibrations and re-qualification processes for lab instruments and equipment (ex: densitometers, thermocouples, thermometers, F200s, F100s, PRTs, probes, baths)
Performs trend analysis of data and makes recommendations for improvements.
Supports data collection activities by entering information into various databases and spreadsheets.
Supports/leads calibration program activities to ensure overall Quality Management Process (QMP) compliance.
Verifies completeness of quality related documentation.
Assists/performs internal and external audits.
Maintains and adheres to all company safety policies and procedures.
Maintains work area organization and documentation to satisfy ISO and GMP standards.
Maintains good communication and working relationships with all departments and effectively functions within a team environment.
Exhibits professional etiquette that exemplifies the values of the organization.
Applies risk-based thinking when evaluating processes performance results for improvement opportunities.
Drafts/executes change controls, CAPAs, CIs, validation test protocols and prepares required reports.
Assigned technicians act as a contingency approver for the QC managerial functions such as raw material and interim material (ie manufactured ink) approval and release.
Qualifications & Competencies
Excellent organizational skills.
Ability to work independently with little supervision.
Good communication skills, written and oral.
Ability to read and interpret data, including graphs, as they relate to test results.
Ability to collect pertinent data, establishes facts, draw conclusions and identify problems.
Education and Experience
Must have a High School Diploma or GED and two to four years related experience and/or training or a combination of equivalent education and experience.
About Temptime Corporation Temptime is the world?s leading provider of scientifically based, time-temperature indicators that alert patients, doctors, healthcare professionals, manufacturers and distributors that a medical product has been exposed to potentially damaging heat and/or freeze events.
In addition to pioneering the first heat indicator to monitor temperature sensitive vaccines used by global health organizations including WHO, UNICEF and several countries? Ministries of Health, our technologies are helping to shape the future of medical product storage and management. We continue to use our expertise to find ever more innovative ways to support global manufacturers, distributors and health care providers to protect patients and reduce risk.
Temptime is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, creed, religion, age, sex, sexual preference, national origin, marital status, veteran status, handicap or disability.
Job Type: Full-time
Required education:
High school or equivalent
Required experience:
incoming raw material testing, inspection, approval, release and final release: 2 years
GMP: 2 years
Quality Control: 2 years
Medical Devices: 2 years
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