- Cipla (Fall River, MA)
- Job Title : QA Document Control Associate FLSA Classification : Full-Time, Professional Work Location : Fall River, MA Work Hours: General Shift: 08:30 AM - 5:00 PM ... based on business needs) Reports To : QA QMS Lead Salary Range : $64,272 - $77,662 PURPOSE The...Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment is responsible for… more
- Insmed Incorporated (NJ)
- …Are:You have a Bachelor's degree along with 2+ years of experience ona document control team using a quality management system , with preference to Veeva.You are ... Are you?About the Role:We're looking for a Quality Management System (QMS) Specialist on the Analytical Development team to...based on trend analysis of CAPAs, deviations and change controls .Serve as a key audit contact point by assisting… more
- GlobalPundits (Aiken, SC)
- …in the use of automated accounting, cost management, scheduling and estimating systems as tools for performing required duties. - Possesses considerable practical ... experience in the use of the Site Business systems . Nice to Have: - Candidates who have possessed...performance against an approved project/program baseline. Experience with Change Control including trends and Baseline Change Proposals (BCPs). -… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent) Our company's Device Product & Process ... device industries to set tactical and strategic direction on programs they lead to ensure high quality products and robust manufacturing processes.-- This position… more
- Digital Installers (Long Beach, CA)
- …to use hand and power tools Develop and maintain proficiency in the following areas: Control Systems : Control4 - High Volume Savant - Low Volume URC Commercial- ... Job Summary: Works with Lead Installers and independently, in the completion of...work on rotating "on-call" service schedule Proficient in all Lead level qualifications Assist in training and evaluation of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Scientist, Device Risk Management Lead , is a crucial member of our team, responsible for spearheading risk management efforts in ... and post-market surveillance. Key Responsibilities and Activities: The Senior Scientist, Device System - Device Risk Management will be responsible for device risk… more
- Merck & Co. (Durham, NC)
- …Molecular Microbiology, Quality Auditing, Quality Control Documentation, Quality Control Management, Quality Management Systems (QMS), Quality Metrics, ... Job DescriptionThe Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the full… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in developing, writing and approving technical documents.Experience with Quality systems (Change control , investigations, LIMs, etc.).Extensive technical writing ... the treatment of multiple myeloma.Legend Biotech is seeking Validation Lifecycle & Technical Lead as part of the Global MSAT team based in Remotely. Role… more
- Insmed Incorporated (San Diego, CA)
- …and security requirements. \tEnsure compliance and operational efficiency of validated systems through participating in release management, change control , ... stakeholders and project teams. Provide operational support in maintaining systems in a validated state including Change Control...etc. This role will participate in on site Change Control CAB meetings as the CSV lead .… more
- Repligen (Waltham, MA)
- …Change Management, System Operations, and IT Governance.Conduct IT application control reviews for key systems (eg, SAP, Tagetik, Workday, ... remediation plans for identified control weaknesses.Serve as SME for system implementations and infrastructure changes to ensure " controls by… more
