Jobs for People with MS: National MS Society

JOB REQUIREMENTS: Help us change lives At Exact Sciences, we\'re helpingchange how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you\'re working to help others. Position Overview The Supervisor, Quality Control will supervise, lead, train and assist the QC team in a variety of QC functions including, but not limited to, raw material, in-process material, finished goods and stability testing, process and method development, characterization and validation, and quality document generation. This position will be responsible for equipping, scheduling, and establishing systems for QC functions working closely with other Quality Control management and coordinating efforts. Essential Duties Include, but are not limited to, the following: Supervise the analytical and functional testing of raw materials, intermediates and finished goods in support of R&D, product and process characterization, the validation program, quality control, stability and troubleshooting efforts. Supervise, lead, develop, qualify, troubleshoot and routinely perform analytical and functional techniques associated with oligonucleotides, enzymes, antibodies, standard molecular biology reagents, and complex molecular diagnostics. Provide subject matter expertise for the Quality Control team in Out of Specification and NCMR resolution, Deviation report generation and CAPA efforts. Draft and/or review protocols supporting Process Validation, Test Method Validation, and Stability Studies in accordance with internal procedures, cGMPs, FDA, and ICH guidelines. Write and review quality documents including, but not limited to, Standard Operating Procedures and test and inspection methods that are compliant with cGMP/GLP guidelines. Provide representation or lead support of cross functional teams and process improvements. Lead project activities associated with or supported by QC. Evidence of strong analytical and problem-solving skills, ability to make decisions with limited information and operate with autonomy. Strong documentation, attention-to-detail and procedure writing skills suitable for a GMP environment. Ability to interpret technical data and present findings to management. Demonstrated ability to develop/transfer and thoroughly document... For full info follow application link. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company\'s affirmative action program are available to any applicant or employee for inspection upon request. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/562525B09FEE4D22