BAS Systems Specialist JobotBAS Systems SpecialistWorcester, MA$35–$50 / hourInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. This role will work closely with project managers, engineers, and customers to deliver high-quality HVAC controls and systems integration solutions across a variety of commercial and institutional facilities.
Accounting Specialist Kforce Inc.Accounting SpecialistAttleboro, MA$60,000–$65,000Kforce's client, a growing organization located in the Attleboro, MA area, is seeking a detail-oriented Accounting Specialist to support invoicing, reporting, and account maintenance functions. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs.
Equipment Specialist, Senior - Secret DCS CorporationEquipment Specialist, Senior - SecretBedford, MA$90,220–$130,000 / yearSupport configuration control by processing, tracking, and recommending dispositions for change notices, ecps, deviation/waiver requests, service bulletins, deficiency reports, Airworthiness Directive Notes, and qcps. Provide integrated logistics support, including provisioning, source coding, maintenance data collection, configuration management data, QDR analysis, and identifying alternate sources of supply for DMS/MS issues.
NewPharmacy Specialist K2 Staffing LLCPharmacy SpecialistFoxborough, MASponsor Relations & Study Close-Out: The Pharmacy Specialist interacts with sponsors and clients in regard to potential and on-going studies, explaining K2 Med procedures and responding to sponsor/client requests regarding handling of drug, close-out issues, and other operational matters. This role involves assisting in the development and continued evaluation of a training process for Clinic staff interacting with the pharmacy, to assure compliance with pharmacy procedures (i.e., drug accountability, storage, administration of doses, and proper documentation of the trail of study drug to and from the pharmacy).
Client Services Specialist AxelonClient Services SpecialistJohnston, RIIndependently service both internal and external customers on a wide variety of Commercial Card, ACH & cash management products, services and technical issues through all incoming channels. The candidate must be goal driven with a desire to productivity goals; including meeting day to day business needs, with advanced problem-solving skills/ability to negotiate through difficult situations.
NewPayroll Specialist, LATAM FMPayroll Specialist, LATAMJohnston, RIRemote$75,000–$106,000The Payroll Specialist, LATAM is responsible for the accurate, compliant, and timely execution of payroll activities across multiple Latin American countries, utilizing third-party vendors such as ADP Celergo and Deloitte. This role partners closely with internal stakeholders and external providers to ensure adherence to complex local statutory, tax, and labor regulations, while supporting payroll transformations, process improvements, and ongoing compliance initiatives.
NewDigital Marketing Specialist Acclaro CorporationDigital Marketing SpecialistCenterdale, RICommitted to continuous innovations, Acclaro Corporation aspires to lead the energy-based medical device industry by aligning the latest technologies with market demand to deliver life-changing results for healthier and happier life for all men and women in the world. You will leverage marketing automation, CRM, and analytics tools—particularly HubSpot—to design and manage targeted campaigns for our manufacturing-focused audience, ensuring alignment with sales objectives and broader business goals.
NewFamily Advocacy Intervention Specialist Choctaw GlobalFamily Advocacy Intervention SpecialistHanscom Air Force Base, MAFamily Advocacy Intervention Specialist (FAIS) - Family Advocacy Program (FAP) - POSITION AVAILABLE UPON SUCCESSFULL AWARD OF CONTRACT Location: CONUS - Various Locations Employment Type: Full-Time Company: Choctaw Advantage Solutions (CAS) Position Summary CAS is seeking a Family Advocacy Intervention Specialist (FAIS) to join the installation’s multidisciplinary Family Advocacy Program (FAP) team. Maintain current certification in either the American Heart Association Basic Life Support Course (BLS) (Course C) or the American Red Cross Cardiopulmonary Resuscitation (CPR)/BLS (Heart Saver) Course Preferred Qualifications Experience working within a military Family Advocacy Program (FAP).
Child Life Specialist - FT Days - Pediatrics and PICU - Boylston Lehigh Valley Health NetworkChild Life Specialist - FT Days - Pediatrics and PICU - BoylstonWorcester, MAFinally, Lehigh Valley Hospital - Cedar Crest, Lehigh Valley Hospital - Muhlenberg, Lehigh Valley Hospital- Hazleton, and Lehigh Valley Hospital - Pocono each received an 'A' grade on the Hospital Safety Grade from The Leapfrog Group in 2020, the highest grade in patient safety. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region.
NewBilingual Customer Service Specialist (Spanish or Portuguese) Sherwin-WilliamsBilingual Customer Service Specialist (Spanish or Portuguese)Shrewsbury, MA$20The wage range listed for this role takes into account the wide range of factors considered in making compensation decisions including skill sets; experience and training; licensure and certifications; and other business and organizational needs. The Company therefore has determined that a review of criminal history is necessary to protect the business and its operations and reputation and is necessary to protect the safety of the Company’s customers, staff, employees, vendors, contractors, and the general public.
Senior Supply Chain Sourcing Specialist Michael Page USASenior Supply Chain Sourcing SpecialistChelmsford, MA$90,000–$110,000 / yearFull timeWe are seeking a Senior Supply Chain Sourcing Specialist to lead procurement and sourcing activities that ensure materials are available to support production, customer demand, and revenue objectives. This position combines strategic sourcing with hands-on supply chain execution, including supplier management, inventory optimization, backlog analysis, and supply risk mitigation.
Quality Specialist The Panther GroupQuality SpecialistWest Boylston, MATrainingAssists in the development and maintains associate training curriculum, which consists of documentation, training records, training matrix and materials. Documents any non-conformances and ensures all product non-conformance paperwork is complete and is included in the work order package.
QA Specialist IV Integrated Resources, IncQA Specialist IVLexington, MassachusettsFull timeResponsibilities-This position is responsible for monitoring and supporting batch disposition of bulk drug products (DP) and finished drug products (FDP)The individual may be responsible for, but is not limited to: Conducting record review of executed batch records for finish drug products to support CMO packaging & labeling record reviewPerforming review of bulk drug product executed records, if neededPrepares all paper work for product disposition (bulk and finished product) and performed assessments for impact to disposition from deviations and change controlsReviews and approve deviations and change controls related to DP and FDPMay own CAPAs associated within the QA unitSupports drug product and finish drug product annual review report sectionsUnderstanding of GMP'sSupports departmental projects as neededQualificationsBachelor's degree in chemistry, biology or a related discipline6-8 years Quality Assurance experience supporting the manufacture and/or release of drugs, biologics, or devices at CMOsWorking knowledge of DP and FDP batch record reviewUnderstanding of quality systems and cGMPs. Interpersonal skills and professional skills to interact with customersMust be flexibleMust be able to prioritize and multitask in a stressful environmentFluency in English is requiredSignificant experience in parenteral biotech manufacturing (aseptic or sterile processing)Significant experience working with suppliers and/or contract manufacturing organizationsExperience with TrackWise and LIMS systemsExperience with packaging and labeling operationsEvaluation of batches to ensure completeness, accuracy and complianceEvaluation of manufacturing or operational issues for impact and communication to management.
Quality Systems Specialist The Steely GroupQuality Systems SpecialistProvidence, RIReporting to the Sr Director, Quality Systems, the Quality Systems Specialist will support and provide oversight of quality system-related activities for internal and external operations in areas such as Deviation/CAPA, Change Controls, Quality Management Review and Monthly Metrics, Supplier Notification of Changes, Deviation and CAPA. Demonstrated experience work within Change Control, Deviation and their associated CAPAs, Investigations, Supplier Notification of Changes and Supplier Corrective Actions Requests a plus.
Senior Specialist, Field Quality QA Operations Bristol Myers SquibbSenior Specialist, Field Quality QA OperationsDevens, MA$89,530–$108,490 / yearThe Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs, and supporting timely return-to-service (RTS) walkthroughs to confirm that manufacturing areas and equipment are properly cleaned, calibrated, and ready for production use. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
NewSr. QA Specialist (Fri-Sun 6am-6:30pm) GenezenSr. QA Specialist (Fri-Sun 6am-6:30pm)Lexington, MA$100,000–$115,000 / yearThis role is accountable for all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), excursions, Out of Specifications (OOS), change controls, and upholding data integrity. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
NewQuality Assurance Specialist - Supplier Quality Actalent IncQuality Assurance Specialist - Supplier QualityWestborough, MA$38–$40 / hourThis role will work closely with internal stakeholders and external suppliers to ensure materials, services, and vendors meet established quality, regulatory, and business requirements. The ideal candidate will have experience supporting supplier qualification, audits, CAPA activities, quality systems, and supplier performance management within a GMP-regulated environment.
NewQA Specialist II (M-F 3:00pm-11:30pm) GenezenQA Specialist II (M-F 3:00pm-11:30pm)Lexington, MA$80,000–$95,000 / yearIn support of biologics/gene therapy manufacturing operations, the Quality Assurance Specialist II engages in collaborative day to day floor support and batch record review which ensures timely and compliant batch disposition. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Quality Specialist Hollingsworth & Vose CoQuality SpecialistMAThese efforts will result in improved product quality, reduced variation, less waste, reduced cost, improved reliability, increased efficiency, increased speed, improved employee safety, employee education and training, improved environmental status and greater overall system capability. POSITION SUMMARY: The Quality Specialist will support critical Quality Assurance and Quality Control functions as well as planned process studies/projects/improvements and identify opportunities for continual process improvements for H&V Operations in the MA Mills.
Quality Assurance (QA) Document Control Specialist II Collins Consulting, IncQuality Assurance (QA) Document Control Specialist IIWorcester, MassachusettsFull timeUnder direct supervision, perform day-to-day Document Control activities: Process DCR packages and review for correctness and completeness; monitor and update in-process documents; create, assign and archive QA controlled lab notebooks and logbooks; assist in managing the electronic document management system; assist in managing access to Master Documents in the Document Control Vault; and create reports. Proficient with computers and word processing software (i.e. Microsoft Office products).High school diploma with 2 + years of general document control experience.
Quality Assurance Specialist Nova Biomedical CorpQuality Assurance SpecialistBillerica, MA$77,000–$86,000 / yearThis role works cross-functionally to maintain an inspection-ready QMS, ensure compliance with regulatory and quality requirements, support implementation of external requirements, and drive continuous improvement initiatives that enhance overall quality system performance and operational effectiveness. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, were building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.
Quality Systems Specialist II - Training processes and Learning Management System (LMS) Integrated Resources, IncQuality Systems Specialist II - Training processes and Learning Management System (LMS)Mansfield, MassachusettsContractorQuality Systems Specialist II - Training Processes And Learning Management System (LMS)Implementation of the training process and Learning Management System (LMS)POSITION RESPONSIBILITIES: • Monitor and support consistent execution of Client's training process and quality training programs. • Consults with Client's leaders, process owner, and managers to ensure that the correct training is assigned to Client's employees.
NewQuality Specialist Nesco Resource, LLCQuality SpecialistDevens, MA$25–$26 / hourCommunicates with internal and/or external contacts in- and outside of the quality function on matters that involve obtaining or providing information requiring explanation, such as coordinating corrective actions with manufacturing teams, interpreting compliance guidelines for suppliers, and assisting auditors with documentation reviews during inspections. Refines testing protocols to accommodate new product designs, troubleshoots unexpected deviations in quality metrics, or adjusts compliance procedures in response to regulatory updates.
NewQuality Specialist ARCH Medical Solutions CorpQuality Specialistathol, MALead and support investigations, root cause analyses, and corrective and preventive action (CAPA) activities for internal and customer-related quality issues. Manage quality documentation, including document control, revision management, filing structures, and electronic record retention.
Quality Systems Specialist - Manufacturing - Shirley, MA Michael Page InternationalQuality Systems Specialist - Manufacturing - Shirley, MAAyer, Massachusetts$80,000–$83,000 / yearFull timeLead Iso Audits & Shape Qms Strategy At A Global ManufacturerLead ISO audits & shape QMS strategy at a global manufacturer. They operate across multiple critical industries and are known for investing in employee growth, inclusion, and long-term career development.
NewData Quality Specialist for the Office of Special Education Worcester Public SchoolsData Quality Specialist for the Office of Special EducationWorcester, MA1.) Bachelor''s Degree - Computers/Data Analytics/Mathematics/ Special Education and/or educational field 2.) Recent successful experience managing compliance reporting in a highly regulated environment 3.) Organizational skills with the ability to multitask projects and assignments to meet deadlines 4.) Excellent communication, writing skills, and technical skills given the aptitude to navigate various data reports to meet the needs of the department 5.) Strong interpersonal skills, including the ability to successfully support colleagues of varying skill levels 6.) Ability to manage multiple processes in order to complete projects and reports with accuracy PREFERRED QUALIFICATIONS: 1.) Knowledge of DESE reporting requirements and working knowledge of State Special Education Regulations 2.) College Degree or coursework in Information Technology systems, Special Education, or an education field 3.) Experience working in a public school district with Special Education. Circuit Breaker) 3.) Under the direction of the Director of Special Education, maintain fiscal reports of all tuition accounts and meet with Special Education Administration to review expenditures, and develop contracts of students placed in Out of District programs, as well as maintain the Tuition Accounts Access database 4.) Maintain Tuition Out of District tuition database accounts and monitor fiscal payments for accuracy, given ongoing communication with accounting, Out of District schools, and the Data and Analytic Specialist.
Product Disposition Sr. Specialist, Quality The Steely GroupProduct Disposition Sr. Specialist, QualityBedford, MAThe Senior Specialist, Product Disposition will support the timely and compliant disposition of all the company Gene Therapy products across all stages of manufacturing. The Senior Specialist will bring strong attention to detail, a quality-first mindset, and the ability to work cross-functionally in a fast-paced, regulated environment.
Change Control and Quality System Specialist Integrated Resources, IncChange Control and Quality System SpecialistLexington, MassachusettsContractorPrimary role includes:Provide collaborative support for execution of global change control strategies to US and other regions (EU & International)Quality system support and Tech Ops liaisonProvide support to other HA interactions as requiredEssential FunctionsRepresent CMC regulatory affairs as the change control coordinator for CMC regulatory and key contact (30%)Collaborate and communicate with global CMC leads, EU and international regulatory colleagues to provide consistent, clear and timely assessments into the change control management system (50%)Assist with supporting other quality system events (20%)Education and Experience Requirements:BN B.S / M.S in biochemistry, biology, engineering or related pharmaceutical field2-4 years of drug development experience previous experience in regulatory and/or quality preferredDemonstrated leadership, strong communication and excellent organizational skillsKey Skills and Competencies:Excellent interpersonal, communication, analytical and organizational skills. Change Control And Quality System SpecialistThe incumbent will assist in the management of change controls for the CMC regulatory affairs group for all biological, plasma and/or small molecule products.
NewQuality Specialist ARCHQuality SpecialistAthol, MassachusettsLead and support investigations, root cause analyses, and corrective and preventive action (CAPA) activities for internal and customer-related quality issues. Manage quality documentation, including document control, revision management, filing structures, and electronic record retention.
Senior Specialist, GMP Quality Assurance Kailera TherapeuticsSenior Specialist, GMP Quality AssuranceWaltham, Massachusetts$122,000–$150,000 / yearThe Senior Specialist will help continuously improve Quality System Procedures related to GMP activities related to their function and will collaborate closely with internal cross-functional teams. The Senior Specialist will perform review of drug substance/drug product manufacturing records and associated documents (i.e. deviations) for product that will be released for use in Kailera phase I-III clinical programs.
Data Review Specialist, Quality Control Ocular Therapeutix IncData Review Specialist, Quality ControlBedford, MA$98,000–$113,000 / yearPosition Summary: The Data Review Specialist will apply strong technical knowledge of laboratory operations, analytical data review, data integrity requirements, and quality systems to perform thorough reviews of analytical chemistry, microbiology, stability, and release testing data for accuracy, completeness, scientific soundness, and compliance with cGMP, GLP, and ALCOA+ expectations. In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging patterns, atypical results, potential OOT signals, and opportunities for improved product understanding.
NewSupplier Quality Operations Specialist Danaher CorpSupplier Quality Operations SpecialistMarlborough, MA$57,500–$75,000 / yearThe amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. The Supplier Quality Operations Specialist is responsible for maintaining global documentation, processes and systems activities to drive efficiency and improvement in supplier quality data management.
Sr. Quality Lab Specialist Quanterix CorpSr. Quality Lab SpecialistBedford, MAOur industry-leading precision instruments, digital immunoassay technology and CLIA-certified Accelerator laboratory have supported research that advances disease understanding and management in neurology, oncology, immunology, cardiology, and infectious disease. As part of Quanterix, Akoya complements a leading portfolio of ultra-sensitive biomarker detection technologies, together enabling a more complete view of biology and disease across both tissue and blood.
Quality Assurance Compliance Specialist I ZOLL MedicalQuality Assurance Compliance Specialist IChelmsford, MassachusettsRemote$60,000–$70,000 / yearThe Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Job Summary The Quality Assurance Compliance Specialist I supports the Quality Assurance Compliance team in maintaining compliance with global regulatory requirements and the Quality Management System (QMS).
Principal Clinical Quality Assurance Specialist Boston Scientific CorpPrincipal Clinical Quality Assurance SpecialistMarlborough, MAAs a Principal Clinical Quality Assurance Specialist, you will support the internal clinical quality assurance program for your assigned business area, partnering with cross-functional teams to ensure clinical investigations comply with applicable regulatory requirements, Good Clinical Practice (GCP) and Boston Scientific policies and procedures. The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role.
Senior Quality Assurance Document Specialist Candel TherapeuticsSenior Quality Assurance Document SpecialistNeedham, MA$143,000–$155,000 / yearEssential Areas of Responsibility: Administers Document Management Program and provides support to end users for the creation, revision, and retirement of documents including: Reviews GxP documents and records for completeness and compliance with internal procedures and applicable regulations and ensures ALCOA++ principles are followed to ensure data robustness. Administers the Training Management Program and provides support to end users for the maintenance of training activities including: Maintains user roles, training curricula, and training assignments.
Data Review Specialist, Quality Control Ocular TherapeutixData Review Specialist, Quality ControlBedford, MA$98,000–$113,000 / yearPosition Summary: The Data Review Specialist will apply strong technical knowledge of laboratory operations, analytical data review, data integrity requirements, and quality systems to perform thorough reviews of analytical chemistry, microbiology, stability, and release testing data for accuracy, completeness, scientific soundness, and compliance with cGMP, GLP, and ALCOA+ expectations. In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging patterns, atypical results, potential OOT signals, and opportunities for improved product understanding.
Quality Assurance Specialist Integrated Resources, IncQuality Assurance SpecialistLexington, MassachusettsContractorTrending, support of Quality System data analysis and metrics for QMR, KPIs, and other reportable forums Work Order review Batch Record review of more complex process records. Quality Assurance SpecialistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Supplier Quality Senior Specialist Lantheus Holdings IncSupplier Quality Senior SpecialistBedford, MA$111,000–$185,000 / yearDomestic and international suppliers consist of Contract Manufacturing Organizations (CMO), drug substance precursors, active pharmaceutical ingredient (API) providers, raw material and component suppliers, contractors, 3PL and service providers. The Supplier Quality Senior Specialist is responsible for maintaining Lantheus's Supplier Quality Management (SQM) program, ensuring that systems, processes and procedures between Quality, Supply Chain, Technical Operations and R&D are compliant and aligned with business needs.
Principal Specialist, Quality Assurance Cardinal HealthPrincipal Specialist, Quality AssuranceMansfield, MassachusettsCross-functional Collaboration: Leads complex cross-functional projects to identify root causes of significant quality issues, educates stakeholders on quality requirements, and develops sustainable solutions to minimize future risks. The Principal Specialist, Quality Assurance, is a highly experienced individual contributor who applies advanced knowledge of quality assurance concepts and technical capabilities to drive uncompromised laboratory integrity and minimize risks.
JZ894. Senior QA Specialist Batch Record Raw Material , MAV Nitto Denko Avecia IncJZ894. Senior QA Specialist Batch Record Raw Material , MAVMilford, MASenior QA Specialist Batch Record Raw Material, MAV. Avecia: Milford, MA, Massachusetts, US.
Senior Specialist, Quality Assurance Laboratory Operations Bristol-Myers Squibb CoSenior Specialist, Quality Assurance Laboratory OperationsMA$89,780–$108,789 / yearThe Senior Specialist, Shop Floor QA, is accountable to monitor and track process performance related to key Shop Floor quality assurance quality tasks and other operational tasks through data and analytics; to own, review or approve Floor Quality GxP records including but not limited to procedures, CAPAs, change controls, impact assessments, documentation, or deviations; and represents SFQA at relevant governance forums. Demonstrated experience in GxP electronic systems such as Quality Management Systems (QMS); Manufacturing Execution Systems (MES) for electronic batch records; Enterprise Resource Planning (ERP) such as SAP; laboratory information management systems; or electronic logbooks/forms.
Senior Specialist, QA Shop Floor M-F, Cell Therapy Bristol Myers SquibbSenior Specialist, QA Shop Floor M-F, Cell TherapyDevens, MA$89,780–$108,789 / yearThe Senior Specialist, Shop Floor QA, is accountable to monitor and track process performance related to key Shop Floor quality assurance quality tasks and other operational tasks through data and analytics; to own, review or approve Floor Quality GxP records including but not limited to procedures, CAPAs, change controls, impact assessments, documentation, or deviations; and represents SFQA at relevant governance forums. Demonstrated experience in GxP electronic systems such as Quality Management Systems (QMS); Manufacturing Execution Systems (MES) for electronic batch records; Enterprise Resource Planning (ERP) such as SAP; laboratory information management systems; or electronic logbooks/forms.
Supplier Quality Senior Specialist Lantheus Holdings, Inc.Supplier Quality Senior SpecialistBedford, MA$111,000–$185,000 / yearDomestic and international suppliers consist of Contract Manufacturing Organizations (CMO), drug substance precursors, active pharmaceutical ingredient (API) providers, raw material and component suppliers, contractors, 3PL and service providers. The Supplier Quality Senior Specialist is responsible for maintaining Lantheus's Supplier Quality Management (SQM) program, ensuring that systems, processes and procedures between Quality, Supply Chain, Technical Operations and R&D are compliant and aligned with business needs.
Senior Quality Assurance Document Specialist Candel Therapeutics IncSenior Quality Assurance Document SpecialistNeedham, MA$143,000–$155,000 / yearEssential Areas of Responsibility: Administers Document Management Program and provides support to end users for the creation, revision, and retirement of documents including: Reviews GxP documents and records for completeness and compliance with internal procedures and applicable regulations and ensures ALCOA++ principles are followed to ensure data robustness. Administers the Training Management Program and provides support to end users for the maintenance of training activities including: Maintains user roles, training curricula, and training assignments.
Quality Control Specialist Doyon Properties IncQuality Control SpecialistMA$55,000–$78,000 / yearThe employee is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; viewing a computer terminal; reading; visual inspection involving small defects, small parts and/or operation of machines (including inspection); using measurement devices. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
Post Closing/HMDA Quality Assurance Specialist Dean Co-operative BankPost Closing/HMDA Quality Assurance SpecialistFranklin, MAWorking in conjunction with the VP Loan Servicing Operations Officer in developing an internal quality assurance auditing program and after identifying areas of concern, the Post Closing/HMDA Quality Assurance Specialist will assist in creating a subsequent training program to enhance post-closing and create efficiencies in loan audits, loan funding, post-closing and servicing. Post-Closing: Assist the VP Loan Servicing Operations Officer in developing an internal pre-funding and post-closing Quality Assurance review process identifying adherence to department procedures, bank policies, regulatory compliance and investor guidelines.
Quality Specialist Brown University HealthQuality SpecialistRIBrown University Health employees are expected to successfully role model the organization''s values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another. Location: Brown Health Medical Group Primary Care - 593 Eddy St - Executive Suite Providence, Rhode Island 02903.
Quality Assurance Specialist PGI FoodsQuality Assurance SpecialistLowell, Massachusetts$20–$25 / hourFull timeIf you're passionate about quality, enjoy working as part of a team, and want to build a long-term career in food manufacturing, apply today! Partner with Quality Assurance, R&D, and Production teams to improve product consistency and manufacturing processes.
Senior Quality Assurance Document Specialist Candel Therapeutics Inc.Senior Quality Assurance Document SpecialistNeedham, MA$143,000–$155,000 / yearEssential Areas of Responsibility: Administers Document Management Program and provides support to end users for the creation, revision, and retirement of documents including: Reviews GxP documents and records for completeness and compliance with internal procedures and applicable regulations and ensures ALCOA++ principles are followed to ensure data robustness. Administers the Training Management Program and provides support to end users for the maintenance of training activities including: Maintains user roles, training curricula, and training assignments.