- Tufts Medicine (Burlington, MA)
- …guidance of the VP of Quality , Compliance and Risk, the Home Health Coder- QA Specialist provides guidance to other members of the clinical team on overall ... quality and completeness of clinical documentation . + The Home Health Coder- QA Specialist is responsible for assigning ICD 10 diagnoses codes to ensure… more
- System One (Devens, MA)
- Job Title: Field QA Specialist Location: Devens, MA Hours/Schedule: 5AM - 5PM, 12 hour shift Type: Contract Join the global biopharmaceutical company committed ... preferred. + Minimum 4 years relevant work experience, with experience in a Quality Assurance role. QUALIFICATIONS REQUIRED + Equivalent combination of education… more
- Bristol Myers Squibb (Devens, MA)
- …readiness walkthroughs per procedures as needed. + Assures all electronic and paper documentation , which requires QA review is in compliance with corporate and ... in a regulated environment with 2 years focus on quality preferred. + Knowledge of Biotech bulk and finished...support release of incoming or manufactured products. + Routine QA Floor Support Activities, including alarm review, logbook review,… more
- Atrius Health (Newton, MA)
- …they are practicing in accordance with department clinical guidelines for accuracy and documentation . Responsible for the quality assurance process by ... appropriately captured on the patient's medical record problem list. Reviews medical record documentation to be sure all chronic conditions on the problem list are… more
- Veterans Inc. (Shrewsbury, MA)
- …date and coordinate admission times to ensure a smooth intake process + Quality Assurance and Compliance: Adhere to regulatory requirements, and compliance with ... programming. Under the general supervision of the Business Manager, the Referral Specialist will work with the admissions team to gather pertinent information from… more
- Olympus Corporation of the Americas (Westborough, MA)
- …by applicable federal, state or local law. Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs ( QA /RA) ... staying **True to Life.** **Job Description** The Sr. L&D Specialist , Global QMS Training will serve as a senior...Training will serve as a senior individual contributor within Quality . This individual will support the management of the… more
- Actalent (Bedford, MA)
- **Language fluency required: English & Chinese essential** Position Summary: The Regulatory Specialist will be responsible for China NMPA and Japan PMDA registration ... regulatory plans for both new products and significant product modifications, documentation of regulatory impact from device modifications, assistance in creating… more
- Tufts Medicine (Framingham, MA)
- …expiration dates, and supply orders. Maintains equipment. 10. Leads and participates in Quality Improvement and Quality Assurance projects. 11. Assists with ... be most commonly applied to patient care and/or scientific/laboratory jobs. A specialist level role requiring advanced knowledge of operational procedures and tools… more
- AbbVie (Worcester, MA)
- …you will lead and inspire a team of operating personnel to produce high- quality clinical or commercial products. Collaboration and teamwork are essential to our ... for ensuring the accurate and timely completion of production-related cGMP documentation . Your attention to detail and commitment to maintaining the highest… more
- AbbVie (Worcester, MA)
- …for the accurate and timely completion of production related cGMP documentation . Responsible for implementation of manufacturing procedures. Ensures the effective ... use of material, equipment, and personnel in producing quality products. Responsibilities + Develops weekly goals and schedules...+ Monitors operator training files and work with compliance specialist to keep files up to date. + Works… more
- AbbVie (Worcester, MA)
- …for the accurate and timely completion of production related cGMP documentation . Responsible for implementation of manufacturing procedures. Ensures the effective ... use of material, equipment, and personnel in producing quality products. Responsibilities + Reviews daily production schedule and...+ Monitors operator training files and works with compliance specialist to keep files up to date. + Works… more
- ConvaTec (Lexington, MA)
- …Join us on our journey to #ForeverCaring as a Clinical Study Management Specialist , and you'll do the same. **About the Role:** Provide operational expertise to ... and report progress. + Coordinate production of key clinical study documentation including Clinical Investigation Plan (CIP), Investigator Brochure (IB), Informed… more