Quality Specialist Salary at Wellness Pet Co BETA

JD : • Lead the supplier qualification process by assessing manufacturing/technology capabilities. • Conduct comprehensive gap assessments at target suppliers to identify areas for improvement and create individual supplier development plans. • Work with suppliers and run SCN and PPAP activity • Develop and refine comprehensive training materials to effectively deploy problem-solving, process control, and quality tools. • Proactively identify and implement continuous improvement activities to prevent the recurrence of non-conformities, ensuring sustained process enhancements. • Review supplier manufacturing processes and collaborate with suppliers on process improvement and value enhancement opportunities. • Facilitate root cause analysis and corrective actions of supplier quality issues. • Independently work with suppliers for the completion of PPAP, Special Process Validation IQ, OQ and PQ requirements. • Knowledge of International standards relative to QMS, ISO 9001:2015, ISO 13485,

Job Description Job Description Job Title: Senior Staff, Manufacturing Technical Operations Location: Boston MA Pay Rate: $50-58/hr POSITION DESCRIPTION TITLE/ROLE: Senior Staff, Manufacturing Technical Operations JOB DESCRPTION: This senior-level staff member on the MTO is responsible for complete ownership of quality records including, but not limited to Deviations, CAPAs, Change Controls, Risk Assessments and Analytical and Quality Control Investigations supporting cell manufacturing at our Boston site. This includes all aspects of record ownership, triages, investigation, CAPA and change controls. The person in this role will drive cross-functional root cause analysis meetings and promote compliance best-practices to ensure timely and thorough completion. This includes all aspects of MTOs operational compliance support with emphasis on tracking and executing CGT initiatives, implementing MTO best practices and ensuring exceptional internal and external department collaboration and

Job Overview: - Implement and promote use of consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating procedures, and assume accountability for the deliverables - Ensure compliance of operations with governing regulatory requirements - Create, maintain and assume accountability for a culture of high customer service - Nurture and sustain an environment of continuous learning- Take ownership of assigned aspects of quality reviews on projects - Compile metrics and identify quality trends - Assist in addressing periodic client quality reviews and other ad-hoc client quality findings - Prepare initial drafts of Corrective and preventive actions - Take ownership of assigned CAPAs with respect to ensuring that the actions are closed and produce documentary evidence to that effect in coordination with the project managers - Contribute to process reviews, own certain aspects of the reviews and use the results to help identi

Location: Boston, MA/Hybrid Schedule: Standard Office Hours Duration: 24-Month Contract Pay Rate Range: $43.00/ph - $48.00/ph The GMP Operational Quality Specialist operates independently to provide QA Analytical support for commercial product stability programs and performs routine QA Analytical tasks. Key Responsibilities: Conduct QA reviews of GMP data for commercial product stability. Collaborate with internal and external partners to resolve quality issues. Act as a Quality technical resource on cross-functional teams. Oversee Root Cause Analysis (RCA), product impact assessments, and ensure appropriate corrective/preventive actions (CAPAs). Support stability-related change control activities, including assessment, implementation, and closure. Perform GMP document reviews (procedures, work instructions, specifications, methods, etc.). Manage external stability program activities, including protocol and data review and study initiation. Enforce Quality Agreements with external part

Job Title: Lab Assistant Job Description Perform testing procedures in a lab and prepare samples and solutions. Document and run tests for blood gas analyzers. Validate and test equipment. Follow instructions utilizing SAP and Oracle software. Run reliability tests. Assist with R&D projects. Must have medical technologist or hospital setting experience Responsibilities * Perform testing procedures in the lab * Prepare samples and solutions * Document and run tests for blood gas analyzers * Validate and test equipment * Follow instructions utilizing SAP and Oracle software * Run reliability tests * Assist with R&D projects Essential Skills * Experience with reagent and sample preparation * Quality assurance knowledge * Hematology expertise * Medical Technologist certification * Proficiency in Excel * Experience with blood gas analyzers * Familiarity with SAP and Oracle software Additional Skills & Qualifications * Preferably from a medical technologist or med tech experience * 1-2 years

Nice to Have: Audit experience CAPA FDA Readiness Medical Device Manufacturing remediation JOB DESCRIPTION Responsibilities may include the following and other duties may be assigned. Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. May speciali

Job Description Job Description Summary: Flybridge Advisors is seeking a highly motivated and experienced Data Steward / Quality Specialist to join our team and play a critical role in helping our Fortune 1000 clients achieve the highest levels of data quality and Enterprise Data Management. In this role, you will leverage your deep understanding of data quality principles, methodologies, and tools to assess, improve, and maintain our clients' critical data assets' accuracy, completeness, consistency, and reliability. This is an excellent opportunity for a passionate data quality professional to work on challenging projects, make a tangible impact on leading organizations, and contribute to the success of our growing data practice. Responsibilities: Data Quality Assessment: Conduct comprehensive data quality assessments to identify issues, risks, and root causes. Utilize data profiling, discovery, and statistical analysis techniques to analyze data patterns, identify anomalies, and mea

Overview: ABOUT THE POSITION Senior Water Resources Engineer | Hybrid | Open to any New England office location VHBs Water Resources group is growing across New England, and we're looking for a Senior engineer to join its dynamic team of Water Resource and Water Quality specialists. In this position you will assist our clients with developing strategic, cost-effective, and forward-thinking solutions to their water resource, ecological restoration, transportation, and environmental challenges. You will have an opportunity to work on a wide variety of projects, ranging from site to watershed scale. Projects may include stormwater designs, bridge hydraulics and scour, stream restorations, flood mitigation and management, and coastal resiliency. Responsibilities Identify both short-term deadlines, deliverables, and tasks as well as long-term client goals Track budgets, schedules, staff availability, and ensure internal and external intermediate and final deadlines are met Assist with ident