Quality Manager. Cambridge, MA. $135,000 - £145,000. Medical Device. The ideal candidate is a critical thinker who will proactively improve the quality systems of our implantable medical device client through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive feedback. Responsibilities. Develop standardized production, quality, and customer-service standards. Identify potential...
Job Title: Quality Engineer - Medical Devices. Cambridge, MA. $120,000. Job Summary. The ideal candidate will play a critical role in ensuring that our medical devices meet all quality standards and regulatory requirements. This position involves working closely with cross-functional teams to develop, implement, and maintain quality assurance protocols, as well as identifying areas for improvement within our manufacturing processes. Key Responsib...
Seeking an Experienced Statistical Programming Analyst Consultant. Key Responsibilities. Annotation of Case Report Form (CRF) in compliance with FDA/CDISC or sponsor guidelines. Development of SDTM specifications and creation of SDTM datasets using SAS. Creation of ADaM specifications and generation of ADaM datasets using SAS based on Statistical Analysis Plan. Production of Tables, Listings, Graphs, and Patient Profiles to support Clinical Study...
Opportunity with Clinical Research Organization for Regulatory Medical Writers. Are you a skilled medical writer looking to make an impact in the Clinical Research field. Join Connect Life Sciences' partnered Clinical Research organization as a Regulatory Medical Writer and contribute to essential document preparation for clinical development. Responsibilities. Evaluate and analyze medical literature to select appropriate resources for study desi...
Job Title: Real-World Evidence (RWE) / Data Scientist Consultant. Location. Remote. Type. Contract. We are seeking a highly motivated and experienced Real-World Evidence (RWE) / Data Scientist to join our team. The ideal candidate will have a strong background in data science, statistics, and epidemiology, with a passion for applying these skills to generate actionable insights from real-world data. This role involves working with large datasets,...
Scientist III. The successful candidate will contribute to drug discovery efforts through analysis of multiple disease-relevant data sets, as well as development of core informatics pipelines and data organization. Duties and responsibilities. Strong scientific understanding and experience in bioinformatics analysis of and their implications in disease biology. Apply and develop innovative analysis approaches when standard methods are not adequat...
Senior Complaints Handling Specialist - Quality. Full-time Permanent Position. On-site role with flexible working hours. Salary $75-80K. Overview. Our client, a small-medium sized Medical Device company in St Paul, MN are looking to hire a Senior Complaints Handling Specialist for their Quality department. This is a full time position with an interesting business boasting a strong portfolio of medical devices across several specialisms and classe...
Quality Manager. Pinebluff, NC. Medical Device. $110,000 - $130,000. Job Responsibilities. Champions a quality culture within the organization and communicate objectives across interorganizational levels. Responsibility for the ISO-13485 certified quality system to maintain awareness and audit readiness including internal audits, CAPA, and document control. Collaborate with department managers and team members to ensure shared vision and goals in...
