What are the responsibilities and job description for the R&D Associate Scientist position at MMQCI-Maine Molecular Quality Controls Inc.?
We are seeking an eager scientist to provide support to various projects for new product development and validation of quality control products for clinical molecular diagnostic tests. We have found that our most effective collaboration and creative output stem from daily in-person interactions. As such, this role requires a full-time presence at our office in Saco, ME, and remote work is not an option for this position.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Education
MMQCI is conveniently located in beautiful southern coastal Maine, minutes from the Maine Turnpike, Portland International Jetport, and less than 2 hours from Boston. Close by are fabulous Portland restaurants, sandy beaches, and a plentiful supply of Maine lobsters! Many terrific outdoor activities are easily accessible including hiking, biking, kayaking, fishing, skiing and snowshoeing. Our beautiful state-of-the-art facility is conveniently located in Saco, right next to the Eastern Trail. Come join us!
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The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills of personnel so classified.
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PRINCIPAL DUTIES AND RESPONSIBILITIES:
- Conducts general laboratory support activities and procedures using various manual molecular techniques
- Assigned various tasks to support the development, validation and manufacturing of new quality control products for molecular diagnostic tests according to current Good Manufacturing Practice (cGMP)
- May help to organize data, under the guidance of the lead scientist to assist in the interpretation of results.
- Perform accurate and reproducible testing in accordance with Standard Operating Procedures (SOPs) in order to carry out clinical and in-house assays to assess stability of products, in-service training and support regulatory requirements in accordance to current Good Manufacturing Practice (cGMP)
- Supports in the validation of new products under Design Control according to FDA 21CFR820 regulations and to help prepare appropriate reports according to MMQCI’s Quality System.
- May be trained to work with pathogens in a BSL2 environment
Education
- S, B.A. or B.S. in biology, chemistry, or in a relevant discipline
- Familiarity with general laboratory techniques, including pipette handling, amplification, electrophoresis, nucleic acid extractions is preferred
- Basic skills in applicable computer programs and mathematical calculations
- Well-organized
- Ability to perform laboratory procedures accurately and reproducibly
- Works efficiently but with attention to detail
- Strong teamwork and interpersonal skills
- Strong work ethic
- Medical insurance
- Dental insurance
- 401(k)
- Profit sharing plan
- Vacation
- Holidays
- Sick leave
MMQCI is conveniently located in beautiful southern coastal Maine, minutes from the Maine Turnpike, Portland International Jetport, and less than 2 hours from Boston. Close by are fabulous Portland restaurants, sandy beaches, and a plentiful supply of Maine lobsters! Many terrific outdoor activities are easily accessible including hiking, biking, kayaking, fishing, skiing and snowshoeing. Our beautiful state-of-the-art facility is conveniently located in Saco, right next to the Eastern Trail. Come join us!
______________________________________________________________________
The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills of personnel so classified.
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