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 processesExperience in any of the following : six sigma lean manufacturing process capability and statisticsEssential Functions Knowledge and Competencies
Excellent interpersonal skillsAbility to lift 50 poundsExcellent communication skills both written and verbalSelf-starter / team player / minimal supervisionExcellent analytical and reporting capabilitiesMust be able to plan organize and implement multiple concurrent tasksBlueprint / Engineering schematic reading and interpretationIntermediate PC skillsMedical Device experience with a high volume-manufacturing environment desirableMust be willing to work as part of a multi-site team and be able to travel as part of the jobResponsibility / Authority
Conduct validation activities in compliance with Regulatory standards and requirements and Precision Edge Surgical proceduresDevelop 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 scheduleCoordination implementation and active participation in the site validation program for product process equipment software methods utilities / facilities and cleaningProvide 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 executionInitiate and implement change control activities in accordance with Precision Edge Surgical proceduresCo-ordinate re-validation activitiesGenerate procedures / other documentation as applicableConduct training in validation methodologies and related procedures as requiredFollowing 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