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Validation Engineer
Validation EngineerMarmon Holdings • Angola, New York, USA
Validation Engineer

Validation Engineer

Marmon Holdings • Angola, New York, USA
[job_card.variable_days_ago]
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  • [job_card.full_time]
[job_card.job_description]

Precision Edge Surgical Products Company LLC

As a part of the global industrial organization Marmon Holdingswhich is backed by Berkshire Hathaway youll be doing things that matter leading at every level and winning a better way. Were committed to making a positive impact on the world providing you with diverse learning and working opportunities and fostering a culture where everyones empowered to be their best.

Welcome to Precision Edge Surgical Products!

Precision Edge is a world-renowned contract manufacturer of fine surgical components cutting tools and accessories. As a surgical cutting tool manufacturer we pride ourselves in our technical versatility and ability to assist our customers. We understand the fundamental requirement of superior performance from a surgical instrument and our team takes extreme pride in building quality products which provide a competitive edge for our customers.

We are currently hiring for a Validation Engineer working out of Angola IN supporting locations in Indiana and Michigan. If you meet the requirements below we welcome you to apply.

Education / Experience Required :

  • BS in Mechanical or Bio-Medical Engineering Required
  • Relevant qualifications in science technology or engineering
  • Experience / knowledge preference in Medical Device manufacturing Contract manufacturing and / or Pharmaceutical / Bio-Pharmaceutical

Preferred :

  • Experience in CNC machining processes
  • Experience in any of the following : six sigma lean manufacturing process capability and statistics
  • Essential Functions Knowledge and Competencies

  • Excellent interpersonal skills
  • Ability to lift 50 pounds
  • Excellent communication skills both written and verbal
  • Self-starter / team player / minimal supervision
  • Excellent analytical and reporting capabilities
  • Must be able to plan organize and implement multiple concurrent tasks
  • Blueprint / Engineering schematic reading and interpretation
  • Intermediate PC skills
  • Medical Device experience with a high volume-manufacturing environment desirable
  • Must be willing to work as part of a multi-site team and be able to travel as part of the job
  • Responsibility / Authority

  • Conduct validation activities in compliance with Regulatory standards and requirements and Precision Edge Surgical procedures
  • Develop validation documentation as required (e.g. plans protocols reports procedures)
  • Execute validation protocols as required (e.g. Equipment IQ / OQ Process OQ Process PQ etc.)
  • Prioritize qualification activities in line with the project schedule
  • Coordination implementation and active participation in the site validation program for product process equipment software methods utilities / facilities and cleaning
  • Provide input into all project phases (i.e. from design through to the commissioning and qualification execution phases of the project)
  • Assist in the evaluation of the validation statues of contract manufacturers and provide guidance where needed. Review and approval of documents prepared by the validation team other departments and contractor organizations (e.g. commissioning test plans impact assessments change controls)
  • Resolve and assist in the closure of deviations initiated during qualification / validation execution
  • Initiate and implement change control activities in accordance with Precision Edge Surgical procedures
  • Co-ordinate re-validation activities
  • Generate procedures / other documentation as applicable
  • Conduct training in validation methodologies and related procedures as required
  • Following receipt of a conditional offer of employment candidates will be required to complete additional job-related screening processes as permitted or required by applicable law .

    We are an equal opportunity employer and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process please email your request to and please be sure to include the title and the location of the position for which you are applying.

    Required Experience :

    IC

    Key Skills

    Python,SOC,Debugging,C / C++,FDA Regulations,Minitab,Technical Writing,GAMP,OS Kernels,Perl,cGMP,Manufacturing

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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    Validation Engineer • Angola, New York, USA

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