ISO Implementation Specialist at Princeton

Job Description

Job Classification: Contract JOB DESCRIPTION:- Responsible for the project management of the entire ISO 9001 implementation life cycle and ensures that the project is completed on time, within budget and to the satisfaction of internal clients.- Provide support in the documentation, implementation, maintenance and continuous improvement of the companys quality management system and ISO 9001 requirements.- Lead, guide and mentor all members of the project team during the implementation.- Coordinate and support efforts towards the achievement and maintenance of the Companys quality management system to ISO 9001 certification.- Plan and conduct company-wide awareness and training program on ISO 9001 requirements and quality improvement tools.- Plan, lead and conduct internal quality systems audits and report findings and recommendations.- Administer the Corrective and Preventive Action Program (CAPA).- Develop, establish and document needed quality assurance processes into procedures and instructions as necessary; such as Document Control System (DCS) and Document Release Authorization (DRA).- Vendor management skills; such as determining purchase control and developing a supplier score card.- Identify, implement, drive and provide support to continuous quality improvements, internal and external- Provide quality reports, analysis and recommendations.- Set up and perform Internal Quality System Audits.- May be required to travel, do irregular hours of work and work hours in excess of the normal daily work hours in order to meet deadlines and schedules- Project and Change Management leader who continually analyses the company and current business practices with a view to successfully implementing the project.- Ability to work directly with, interact and effectively communicate with all levels of employees, manager and consultants with varying degrees of business and technical experience.- Performing operational and technical assessments and creating detailed roadmaps.JOB QUALIFICATIONS:- B.S. in Engineering or the Technical Sciences.- 8+ years working experience in quality management preferably in a pharmaceutical, biopharmaceutical or medical device environment- Excellent knowledge and experience in implementing and maintaining quality management systems.- Proficiency in implementing ISO 9001 QMS requirements for a small to mid-sized company.- Knowledge of quality improvement tools and techniques.- Project based experience on an ISO 9001 QMS implementation, in a role providing leadership in production or project-oriented activities such as planning, organizing, coordinating, and evaluating.- Related position on Business Process Improvement/Redesign and Operational Efficiency initiatives.- Demonstrated experience in defining business processes, training and change management.- Ability to develop reliable project timelines and deliver against established timelines.

Join Aerotek, one of the leading providers of engineering and engineering support professionals in North America. Due to our growth, were constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across a number of different industries. We know its more than just your day-to-day responsibilities that can make or break a job. Its the support you get. Thats the reason Aerotek offers a variety of benefits including medical, dental, optical, 401k, and many more. Dont put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law.

Job Requirements

• ISO CERTIFICATION

Country: USA, State: New Jersey, City: Princeton, Company: Aerotek.