- Cipla (Fall River, MA)
- …Practices (GDP), USP monograph requirements. Technical Knowledge and Computer Systems Skills Understanding of laboratory equipment operation, qualification ... product analytical documents. Monitoring and ensuring of current Good Laboratory Practices (cGLP) followed by laboratory personnel...to focus on details. Work Schedule and Other Position Information : General shift but must be willing and… more
- Cipla (Fall River, MA)
- …(GMP)/Good Documentation Practices (GDP), etc. Technical Knowledge and Computer Systems Skills: Understanding of laboratory equipment operation, qualification ... product analytical documents. Monitoring and ensuring of current Good Laboratory Practices (cGLP) followed by laboratory personnel...to focus on details. Work Schedule and Other Position Information : General shift but must be willing and… more
- Cipla (Fall River, MA)
- …position is to accurately review the chronological record of Laboratory Instrument/Equipment electronic data related activities that provides documented evidence ... as SME for IT related activities of QMS platforms and other electronic systems including digital platforms which need compliance to 21CFR, Part 11 requirements.… more
- Cipla (Fall River, MA)
- …of quality assurance (QA). Strong knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug ... products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good Distribution Practices (GDP), etc.… more
- Cipla (Fall River, MA)
- …FDA, ). Maintain and ensure the proper documentation of all quality systems and records. Oversee document control processes, ensuring that SOPs (Standard Operating ... This role works in a current Good Manufacturing Practice (cGMP) office, laboratory and manufacturing environment, where personal protective equipment (PPE) may be… more
- Cipla (Fall River, MA)
- …of samples of various types using various techniques or equipment in the QC laboratory . The job itself may be further modified with respect to the department, group, ... preferred. Must have current Good Manufacturing Practices (cGMP) Good Laboratory Practice (GLP) knowledge Professional and Behavioral Competencies Proficiently… more
- Syner-G BioPharma Group (Boston, MA)
- …electronic formats required to perform the respective job at a client.Knowledge of laboratory and manufacturing systems such as LIMS, MES, etc.Experience with ... strategic guidance and hands-on expertise to streamline operations, enhance quality systems , and ensure regulatory compliance, empowering our clients to navigate… more
- Cipla (Fall River, MA)
- …formulation manufacturing with understanding of manufacturing procedures, cGMP and systems related documentation in a cGMP pharmaceutical operation environment. ... Technical Knowledge and Computer Systems Skills Understanding of machines used in pharmaceutical manufacturing....to focus on details. Work Schedule and Other Position Information : Must be willing to work in a… more
- MIT Lincoln Laboratory (Lexington, MA)
- …Conduct security compliance audits and perform security vulnerability assessments on Laboratory information systems * Establish and maintain configuration ... accidental destruction, and sabotage; and safeguards personnel, classified and unclassified information systems , personal identifiable information , property,… more
- Lawrence General Hospital (Methuen, MA)
- …and accreditation compliance (eg, CAP, CLIA, Joint Commission). + Proficiency with laboratory information systems (LIS) and instrument middleware; experience ... of the range to support future salary growth. Job Summary: The Core Laboratory Supervisor oversees operations across two hospital campuses, including a main facility… more
