Minnnesota Bioscience Jobs

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Atterro Chemist in Plymouth, Minnesota

Cantel in partnership with Pro Staff are in search for a Chemist for a one-year contract. As a Chemist you would support remediation activities in order to improve regulatory compliance position. This chemist will assist in the gap assessment of technical documentation for Medical Device Regulation compliance activities across the product portfolio. You would also be an integral team member on the Technical Documentation Team in order to update or prepare technical documentation to reconcile product technical files. ESSENTIAL DUTIES AND RESPONSIBILITIES: Prepare, author, and edit technical documentation required to meet the EU MDR requirements. Review and understand global regulatory requirements (FDA, EU MDD, MDR, Health Canada, etc.) with emphasis on EU MDR 2017/745. Collaborate with cross-functional teams to prepare related technical documentation for Change Order publication and approval Prepare and/or Author QP s (Qualification Protocols), ECO s (Engineering Change Orders), BOM s (Bills of Material), Component Spec Sheets, and Item masters, for entry into documentation system into order to build technical documentation for the device. Supports in providing information for quotations on custom test applications to support gaps identified in technical documentation. (Including test specifications, drawings, scope, labor hours, equipment costs, lead times, schedules and out-sourcing services) Develop test plans, test strategies and test sequences to collect relevant performance data required for EU MDR technical documentation Interfaces with internal customers, and external vendors to provide a technical support for EU MDR related documentation. QUALIFICATIONS REQUIRED FOR POSITION: Bachelor s degree in chemistry from four-year College. Demonstrated experience in an academic or corporate laboratory environment. Prefer that work experience is in the medical device industry in a RandD position with technical ability. Must be highly organized and have the ability to manage multiple projects concurrently. Must possess good written and verbal communication skills as well as team building skills, basic PC skills, and have working knowledge of Microsoft Word, Excel, and Power Point. One or two years of experience working in a corporate Quality Control laboratory Ability to process data and formulate plan of action to support data analysis Mandatory- Experience with Technical Writing About Pro Staff Pro Staff is committed to providing equal employment opportunity for all persons regardless of race, color, religion (including religious dress and grooming practices), sex, sexual orientation, gender, gender identity, gender expression, age, marital status, national origin, ancestry, citizenship status, pregnancy, medical condition, genetic information, mental and physical disability, political affiliation, union membership, status as a parent, military or veteran status or other non-merit based factors. We will provide reasonable accommodations throughout the application, interviewing and employment process. If you require a reasonable accommodation, contact us. Pro Staff is an E-Verify employer. This policy is applicable to all phases of the employment relationship, including hiring, transfers, promotions, training, terminations, working conditions, compensation, benefits, and other terms and conditions of employment. All employees are directed to familiarize themselves with this policy and to act in accordance with it. All decisions with respect to employment matters and other phases of employer-temporary employee relationships will be in keeping with this policy and in accordance with all applicable laws and regulations. Pro Staff makes all employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, ancestry, medical condition, age, marital status, national origin, citizen status, political affil

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