9 compliance representative jobs found

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Cytel. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Cytel is seeking a visionary Vice President, Quality Assurance (QA) to lead our global QA function. This executive role ensures the highest standards of compliance with Good Clinical Practice (GCP) and international regulations, while driving innovation in quality oversight. The Vice President will provide strategic direction, oversee quality systems and audits, lead global inspection readiness, and build a high-performing QA team that partners with the business to deliver excellence....

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Cytel. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Cytel is seeking a visionary Vice President, Quality Assurance (QA) to lead our global QA function. This executive role ensures the highest standards of compliance with Good Clinical Practice (GCP) and international regulations, while driving innovation in quality oversight. The Vice President will provide strategic direction, oversee quality systems and audits, lead global inspection readiness, and build a high-performing QA team that partners with the business to deliver excellence....

Position Admission Counselor/Quality Assurance Support Specialist Reports To OA Supervisor/Project Director Department OA/CTS Department FLSA STATUS Exempt Primary Position Objectives Conduct outreach, recruitment, eligibility determination, and admissions functions and processes and provide support services to admission counselors and CTS in compliance with government and management directives. Position Responsibilities Key Responsibilities Brief Description of Duties Administration Procedures Conduct innovative outreach activities with public service agencies, community organizations, schools and individuals who might refer eligible candidates to the Job Corps program Interview interested candidates and obtain pertinent information on each one Prepare documentation on potential students and review with the center as applicable or necessary Provide...

Associate Director, Quality Assurance Position Summary: Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. This is a full-time salaried position, onsite out of Philadelphia, PA. The Associate...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . PRINCIPAL OBJECTIVE OF THE POSITION: Provide Quality assistance and...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . PRINCIPAL OBJECTIVE OF THE POSITION: Provide Quality assistance...

Job Title: Lead Quality Assurance Technician Book Immediate Interests: https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxl Job Description As a Lead Quality Assurance Technician, you will perform in-process and finished product inspections across manufacturing lines to ensure compliance with cGMP, SOPs, WIs, and product specifications. You will verify line clearance and readiness of production areas prior to use, monitor, sample, and test materials and finished goods, determine their disposition, and ensure appropriate documentation and labeling. Responsibilities Execute rework protocols and support disposition activities as required. Initiate and manage LIMS samples and documentation, and identify, document, and communicate non-conforming material in accordance with hold procedures. Collect required product, reserve, and customer samples per manufacturing specifications. Provide day-to-day coordination and guidance to QA...

This Individual Position is Exempt from the Hiring Freeze. Qualified Applicants are Encouraged To Apply. Welcome to the Department of Health! We’d be delighted to have you join our team. If you envision yourself in this role and are ready to start an exciting career with us, apply today! This position is open to Alaskan Residents only. Please check out the residency definition to determine if you qualify. What You Will Be Doing Functions as the Education & Training Coordinator: Designs and delivers in-house and statewide training on cancer reporting, abstracting, coding (ICD-O, staging, treatment), and case finding according to national standard setters’ requirements, while providing opportunities for Alaskan ODS to earn NCRA-approved continuing education credits. Serves as the Quality Assurance Coordinator: Ensures statewide accuracy, completeness, and timeliness of cancer data through audits, edit analysis, and compliance monitoring aligned with...

HIRING NOW: Quality Assurance Documentation Associate Interested in this role? Reach out directly to apply TODAY to Grace Williams at grawilliams@actalentservices .com (grawilliams@actalentservices.com) | Call/Text 317-567 6610 Summary As a QA Associate, you will play a crucial role in ensuring the quality and compliance of our products and packaging. You will be responsible for reviewing and analyzing data, supporting quality systems, and ensuring adherence to applicable procedures and standards. Responsibilities Provide support to Quality systems. Organize, critically review, and present information in accordance with written procedures. Provide support for the production area. Apply and obtain statistical analysis. Write, review, and revise GMP standard operating procedures. Track, maintain, and critically review manufacturing records. Maintain communication with QC lab regarding test results pertinent to batch release....