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Equal Opportunity Employer
Remington Medical OEM is an equal opportunity employer. We pledge to provide equal employment opportunities to all persons regardless of age, race, color, sex, sexual orientation, religion, national origin, physical or mental disability, or status with regard to public assistance; and to disabled veterans, and veterans of the Vietnam era, and many other status or condition protected by state or federal law. Remington will provide reasonable accommodation to qualified persons with a disability that substantially limits a major life activity, but who are otherwise able to perform the essential functions of the job.
Job Opportunities at Remington Medical OEM
Remington Medical OEM offers competitive salaries and an excellent benefits package along with the opportunity for personal recognition in a safe and clean environment where creativity, initiative and problem solving skills are strongly encouraged.
Job Openings
PRODUCTION ASSOCIATES
Remington Medical, Inc., a growing medical device manufacturing company has immediate openings for experience production employees on 1st and 2nd shifts. Previous soldering and/or assembly experience in a production environment required.
The production environment is clean, climate controlled and we are looking to hire employees with a good work ethic, strong commitment to quality, and ability to be successful in a team environment.
Remington provides a great small company work environment and opportunity to be part of a growth oriented company.
Remington Medical is an Equal Opportunity Employer and a Drug Free Workplace
PROJECT ENGINEER
Remington Medical, Inc., a growing medical device design and manufacturing company based in Alpharetta has an immediate opening for an entry level Project Engineer. Great small company environment with the opportunity to launch your career in the medical device industry!
Responsibilities:
- Coordinate the planning and production of products for contract manufacturing customers
- Analyze existing equipment/processes and develop/implement/sustain continuous improvement plans
- Troubleshoot existing production requests and assist with the R&D efforts of new products
- Function as project manager to make sure product delivery schedule is met or exceeded by following up with appropriate individuals within Remington in a proactive and timely manner
- Update and maintain engineering drawings and documentation
- Writes, reviews and approves protocols, reports and data
- Adhere to and ensure compliance with Quality System SOPs, work instructions, drawings, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), ISO, and FDA requirements
Requirements:
- BS degree in Engineering (or technical discipline)
- Basic knowledge of injection molding products/equipment/processes, electrical systems, mechanical and hydraulic application, and lean manufacturing
- Knowledge of product development practices
- Knowledge of engineering principles, practices, and theories
- Working knowledge of SolidWorks or similar 3D CAD application software and advanced level skill with MS Word, MS Excel, MS PowerPoint, and MS Access
- Working knowledge of FDA and ISO 13485 requirements preferred
- Demonstrated ability to drive initiatives to desired results by getting cooperation from individuals in other departments
- Excellent communication, prioritization, and organizational skills
Remington is an Equal Opportunity Employer
PROJECT MANAGER
Remington Medical, Inc., a growing medical device design and manufacturing company based in Alpharetta has an immediate opening for a Project Manager. Great small company environment with the opportunity to play a key role in Remington’s continued growth and success!
Responsibilities:
- Manage OEM projects by interfacing and coordinating between customer, purchasing, materials, production, quality, and engineering
- Manage multiple projects concurrent projects with competing resources and timelines
- Analyze existing equipment/processes and develop/implement/sustain continuous improvement plans
- Troubleshoot existing production requests and assist with the R&D efforts of new products
- Write technical reports and documentation (i.e., Design History, Risk Management, Product Realization Files, Mold Verifications, Product/Process Validations)
- Update and maintain engineering drawings and documentation
- Implement new technologies and processes to expand manufacturing capabilities
- Perform engineering analysis on Remington and OEM products
- Adhere to and ensure compliance with Quality System SOPs, work instructions, drawings, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), ISO, and FDA requirements
Requirements:
- 5+ years related project engineering experience preferably in medical device or other FDA regulated industry
- Demonstrated ability to manage multiple concurrent projects with competing resources and timelines
- Strong knowledge of injection molding products/equipment/processes, electrical systems, mechanical and hydraulic application, and lean manufacturing
- Strong knowledge of product development practices
- Strong knowledge of engineering principles, practices, and theories
- Working knowledge of SolidWorks or similar 3D CAD application software and advanced level skill with MS Word, MS Excel, MS PowerPoint, and MS Access
- Working knowledge of FDA and ISO 13485 requirements preferred
- Demonstrated ability to drive initiatives to desired results by getting cooperation from individuals in other departments
- Excellent communication, prioritization, and organizational skills
Remington is an Equal Opportunity Employer and a Drug Free Workplace!
QUALITY ENGINEER
Remington Medical, Inc., a growing medical device design and manufacturing company based in Alpharetta has an immediate need for an experienced Quality Engineer.
Responsibilities:
- Provide technical guidance to Quality Technicians and Inspectors.
- Development of Test Protocols and Final Reports.
- Development of the design risk assessment, coordinating input from other design team members.
- Development of the Final Design Verification Protocol and the subsequent Final Design Verification Report including an analysis of all data and a decision on design acceptability.
- Provide input into the project design input requirements and product development quality plan.
- Determination the degree of Biocompatibility testing required on a project. Coordinate the testing at an outside lab and document results.
- Develop or assist in developing test methods for the specifications listed in the DID.
- Develop test protocols and release a final report on Shelf Life Studies in support of expiration dating.
- Utilize statistical methods to ensure processes are capable/repeatable and sample plans are statistically valid (i.e., scientific sample size selection, statistical process capability data analysis, statistical process capability software such as Minitab, StatGraphics).
- Develop and document the monitoring and control program for the manufacture of new products including Inspection Plans for the inspection of components, sub-assemblies and final product.
- Development of the process risk assessment, coordinating input from the Manufacturing Engineer.
- Perform Process Validation Studies to determine the acceptability of new processes or equipment.
- Design and qualify inspection and test equipment.
- Investigation and recommend disposition of nonconforming components and products.
- Organize and generate detailed quality information reports to show trends and the impact of process improvements.
- Support Process Transfers of both OEM customers and RMI products from design to manufacturing.
- Conduct other Quality Control Projects as assigned.
- Perform DOE's and other statistical tests to support product and process optimization or determine causes of quality nonconformance. Initiate corrective actions as required.
- Provide technical support to resolve quality problems in development, pilot, manufacturing or with suppliers as warranted.
- Support goals of the Quality Assurance Department.
- Minimal travel is required (less than 10%).
Requirements:
- Bachelor's Degree in Engineering or Technical Sciences.
- A high level of competence in Quality Engineering including statistical techniques, control charts, sampling plans, Quality costs, design of experiments, correlation and regression, analysis of variance, probability etc.
- 5+ years experience in quality engineering including product/process validation and technical problem solving in medical device or FDA regulated industry.
- Intermediate to advanced level of proficiency with Minitab or StatGraphics software.
- Good oral and written communication skills.
- Knowledge of FDA QSR's, ISO13485, and ISO 14971
- Knowledge and Application of Six Sigma/Process Excellence Tools.
Remington Medical is an Equal Opportunity Employer and Drug Free Workplace!
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