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Responsible for in-house GLP/GCLP infrastructure, hands on troubleshooting, systems and procedures to ensure adequate rigorous laboratory practices & regulatory requirements for bioanalytical activities assuring phase appropriate approach.
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Lead a team to ensure timely assay development, regulatory-compliant qualification or validation of assays, and troubleshooting of any internal or external CRO partner issues. Strong understanding of GLP requirements and current industry trends and regulatory expectations associated with bioanalytical science.
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Transamerica is organized by lines of business (Life Insurance, Annuities, Mutual Funds, Retirement Plans, and Employee Benefits), which are supported by Transamerica Corporate (Corporate Development; Finance; Internal Audit; Legislative, Regulatory & Policy; Office of the CEO; People and Places; Brand; Corporate Affairs; Risk; and Technology.
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Works with the Manager of Regulatory Compliance to ensure all settings that are on the DPH license comply with TJC standards and the CMS COPs Supports Medical Staff credentialing as requested Supports the SMG Quality Department with Culture of Safety implementation and continuing education.
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Works closely with the Chair of Psychiatry, Chief Nursing Officer and other executives, and collaborates with the respective service line Chiefs and fellow service line directors to ensure successful excellent care at the facility, through management of regulatory and accreditation bodies, organizational structure, clinical protocols, and hiring and onboarding of the staff.
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Become the Facilities Management Director you've always aspired to beEnsuring that the rehabilitation hospital, satellite clinics, and all related building systems adhere to Joint Commission standards, as well as local, state, and federal regulatory requirements.
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To accurately, consistently, and efficiently perform pre-analytical, analytical, and post-analytical activities required for laboratory testing in Coagulation, Chemistry, Hematology, Microbiology, and/or the Transfusion Service per standard operating procedures for pediatric/adolescent, adult, and geriatric patients in compliance with laboratory, hospital, state, federal, and regulatory agency policies, procedures, and standards.
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The successful candidate will:have oversight of all day-to-day operations for all food operationseffectively lead the team through all managers and front line staffensure delivery of high quality food services including cafeteria retail, patient meal, and catering operationsachieve company and client financial targets and goalsensure HACCP, regulatory and Sodexo standards complianceIs this opportunity right for you.
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The QA Specialist performs a wide variety of activities to ensure compliance with applicable regulatory. The position has a great deal of interaction with many internal departments, including Production, Cell Culture, Facilities, Validation, Calibration, Materials, Quality Control, and Materials Management.
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Complete all documentation in accordance with agency and regulatory requirements, including but not limited to completion of BRC Approval Requests, referral packets and case filing. DCF works toward establishing the safety, permanency and well-being of the Commonwealth's children by: stabilizing and preserving families; providing quality temporary alternative care when necessary, safely reunifying families; and when necessary and appropriate, creating new families through kinship, guardianship or adoption.
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5-10 years of related management experience with a food or beverage company in Regulatory compliance. Strong knowledge of SQF Certification process, focusing on regulatory compliance. Bachelor’s Degree in Regulatory Science, Nutrition, Food Science, Biology or related field.
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As a Medical Audit Claim Reviewer, you will play a crucial role in our organization by reviewing and auditing medical claims to ensure compliance with policies, procedures, and regulatory requirements.
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As a Clinic Manager you will oversee the clinical, regulatory, and operational functions of our outpatient facility. This is accomplished by hiring, developing, and inspiring a multi-disciplinary team, collaborating with physicians, tracking and delivering superior patient outcomes and monitoring regulatory and safety requirements.
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Design and deliver customized seminars and training sessions, focusing on topics such as product safety, and regulatory compliance, to educate and empower clients and colleagues. Track and analyze regulatory and legislative developments in the US and Canadian markets.
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Offer robust support to North American clients and internal colleagues, addressing technical and regulatory queries with clarity and precision. Proven experience in collaborating with industry standards organizations and technical committees such as ASTM, AATCC, AAFA, and JPMA. Demonstrated proficiency in chemical, regulatory, and performance testing for textiles, toys, and hardlines products, with strict adherence to U.S. and Canadian regulations.
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regulatory cmc jobs in Canton, MA
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