Associate Program Manager, Quality Engineering - Merrimack, NH - Merrimack, NH - Getinge

Date de Publication 8/29/2019

Résumé de l'offre

  • Type d'employé :
    Employé à plein temps
  • Expérience :
    Not Specified
  • Date de Publication

Description de l'offre

Job Function Summary:

Manages teams and project timelines addressing quality and compliance issues, including audit findings, CAPAs, improvement projects and new or revised regulations and standards.

Job Functions:

  • Manages the timeline and activities for CAPA and project teams, including escalating late actions, inadequate resources and other issues as needed.
  • Leads cross-functional team meetings by creating agendas and providing meeting minutes.
  • Prepares and provides presentations to various departments.
  • Directly interacts with supporting functional groups (Regulatory, Quality Engineering, Manufacturing, Engineering, Marketing, and Quality Control) to meet project objectives and keep programs on track.
  • Generates project status reports and presents to executive management as needed.
  • Prepares and submits project plans and budgets, which identify milestones and resources, and tracks project timelines and costs.
  • Identifies project and timeline risks and develop risk mitigation strategies.
  • Manage unexpected program delays and direct cross-functional team efforts to re-align with established project timelines.
  • Participate in negotiation of business transactions with outside parties.
  • Contribute to the team effort by accomplishing related tasks as necessary.

Required Knowledge, Skills and Abilities:

  • Experience leading the development and implementation of projects, with ability to handle multiple projects and effectively manage timelines. 
  • Demonstrated analytical and problem solving skills. 
  • Demonstrated strong technical skills, including technical writing experience.
  • Ability to work independently, as well as effectively interact and communicate with all levels of the organization in a team environment. 
  • Working knowledge of medical device industry, FDA regulations, quality systems and design control, preferred.
  • Proficient oral and written communication skills.
  • Strong skills with MS Office applications are required (Word, Excel, Powerpoint and Project). 

Minimum Requirements:

  • Bachelor’s Degree in engineering, science or a related field.
  • Two to four years of relevant experience in a regulated industry preferred.
  • One-year experience managing projects is desirable.
  • Experience in surgical and interventional medical device design is desirable.
  • Agile PLM and Oracle experience preferred.

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.