Jobs: cgmp

  • Validation Manager

    4 days ago


    Melrose Park, United States cGMP Consulting Full time

    Job DescriptionJob Description Job DescriptioncGMP Consulting is looking for an individual to manage the Validation personnel. This individual will oversee validation activities related to equipment and computerized system qualifications and re-qualifications. The ideal candidate for this job is resourceful, independent, organized, and capable of working in...


  • Los Angeles, United States University of Southern California Full time

    cGMP Microbiological TechnicianApply ( Keck School of Medicine Los Angeles, California The University of Southern California (USC), founded in 1880, is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the...

  • Principal CGMP Compliance Consultant

    Found in: beBee jobs US - 2 days ago


    Southeast Fairbanks, United States Parexel Full time

    Parexel's Strategic CGMP Compliance team is known for our unparalleled breadth and depth of expertise globally. Parexel CGMP Compliance offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific, regulatory, and business expertise. We are the pre-eminent regulatory and GxP...


  • Hildale, United States Premium Production Full time

    Job DescriptionJob DescriptionPremium Production is a manufacturing company building a team to help change the world.Located in Hildale, Hurricane, and St. George, Utah. We are looking for a full-time, in-person cGMP Quality Control SpecialistYou will ensure regulatory compliance by understanding, inspecting, and reporting production and manufacturing...


  • North Chicago, United States cGMP Consulting Full time

    Job DescriptionJob Description Job DescriptionThis position is responsible for designing, creating and modifying CAD drawings for Facility, Utilities and Process related projects. This person will work independently under the guidance of a supervisor or lead with clear and specific objectives. cGMP Consulting is looking for an individual who is efficient,...

  • cGMP Quality Assurance Senior Manager

    Found in: Appcast Linkedin GBL C2 - 46 minutes ago


    Lompoc, United States Life Sciences Recruitment Full time

    As the Senior Manager of Quality Assurance, you will lead a team of quality professionals and direct and coordinate the activities of Quality Control and Quality Assurance. As a Medical Device Manufacturer with a Drug product requiring adherence to cGMP, our client is in need of a passionate quality professional with experience in the pharmaceutical/drug...

  • cGMP Quality Assurance Senior Manager

    Found in: Appcast US C2 - 58 minutes ago


    Lompoc, United States Life Sciences Recruitment Full time

    As the Senior Manager of Quality Assurance, you will lead a team of quality professionals and direct and coordinate the activities of Quality Control and Quality Assurance. As a Medical Device Manufacturer with a Drug product requiring adherence to cGMP, our client is in need of a passionate quality professional with experience in the pharmaceutical/drug...

  • Senior Program/Project Manager

    Found in: Appcast Linkedin GBL C2 - 2 days ago


    Marietta, United States AM Technical Solutions, Inc Full time

    Senior Program/Project Manager (cGMP – Pharmaceutical – Operational Readiness)Marietta, PA areaSummary: We are looking for a proven Project Management resource to join our Life Sciences team in support of the management and coordination of a client-based team consisting of Process Development, Engineering, Manufacturing, Validation, Quality, Supply...

  • Automation Engineer

    4 days ago


    Madison, United States Randstad Life Sciences Full time

    Job DescriptionJob DescriptionImmediate opportunity for an automation engineer, preferably with strong automation, engineering experience, preferably cGMP regulated manufacturing experience.The Automation Engineer is needed to support and maintain the process control system. The Automation Engineer will identify and execute projects related to the process...

  • cgmp Quality Validation pharma

    Found in: Appcast Linkedin GBL C2 - 2 days ago


    Minnetonka, United States MEDVACON TALENT ACQUISITION, LLC Full time

    This is a HYBRID in Minnetonka, MN3 days on-site6+ monthsLocal$75 on W2 maxNo c/cSUMMARY:Lead validation and quality engineering activities for internally manufactured products, including validation plans, protocols and reports, maintenance of DMR, change control and CAPA/Deviation investigations. This position is the owner of the process validation system...


  • Hopkins, United States Medvacon Life Sciences Full time

    Job DescriptionJob DescriptionThis is a HYBRID in Minnetonka, MN3 days on-site6+ monthsLocal$75 on W2 maxNo c/cSUMMARY:Lead validation and quality engineering activities for internally manufactured products, including validation plans, protocols and reports, maintenance of DMR, change control and CAPA/Deviation investigations. This position is the owner of...

  • GMP Facilities Engineer

    Found in: Appcast Linkedin GBL C2 - 2 days ago


    Durham, United States Medasource Full time

    SummaryThis position is responsible for assisting the Business Operations Lead to develop, implement, and oversee equipment and facility maintenance management for cGMP manufacturing facility deliverables. Additionally, this position will develop/deploy/maintain standard work and systems for proactive predictive key performance indicators to prevent...

  • Manufacturing Associate

    Found in: beBee S US - 2 days ago


    Minneapolis, United States Takeda Full time

    Here everyone matters and you will be a vital contributor to our inspiring bold mission. As a Manufacturing Associate II working on the Biologics Manufacturing team you will be empowered to use your GMP experience to improve process operations and a typical day will include The Manufacturing Associate II performs and documents cGMP activities to support...

  • Manufacturing Associate

    Found in: beBee jobs US - 3 days ago


    Minneapolis, Minnesota, United States Takeda Full time

    Here everyone matters and you will be a vital contributor to our inspiring bold mission. As a Manufacturing Associate II working on the Biologics Manufacturing team you will be empowered to use your GMP experience to improve process operations and a typical day will include The Manufacturing Associate II performs and documents cGMP activities to support...

  • Biomanufacturing Associate I, II, III

    Found in: Talent US C2 - 19 hours ago


    College Station, United States MyKelly Full time

    Biomanufacturing Associate I, II, III & IV  (cGMP)Central Texas Direct Hire Relocation AssistanceDay ShiftKelly Science is currently recruiting for several Biomanufacturing Associates working in an FDA regulated environment. This role will provide cleanroom manufacturing support for the Biological Services Biomanufacturing Operations group. This...


  • Manassas, United States Granules Full time

    Job DescriptionJob DescriptionDescription:The Senior QA Associate, Compliance/QA Lead will be responsible for identifying, closing, and implementing corrective actions regarding gaps in current good manufacturing practices (cGMP) related activities to comply with FDA regulations, support Serialization and aggregation process implementation for Granules...


  • Bethlehem, United States Sharp Clinical Services Full time

    The Clinical Supplies Room Leader, acting under direct supervision, executes and oversees all phases of clinical packaging, labeling, manufacturing, and assembly of investigational drug product that includes but is not limited to blistering, bottling, carding, encapsulation, manufacturing, labeling, and assembly. He/She prepares and completes packaging...

  • Packaging Operator III

    Found in: Resume Library US A2 - 3 days ago


    Waco, Texas, United States AbbVie Full time

    Job Description Job Summary Manage production lines to meet the established production schedule in accordance with Standard Operating Procedures (SOP’s) and Good Manufacturing Principles (GMP’s) while monitoring product to ensure quality standards are maintained.   Responsibilities Comply with all safety regulations and conduct all activities in a safe,...

  • Room Leader 2nd shift

    Found in: Talent US C2 - 3 days ago


    Bethlehem, United States Sharp Services Full time

    The Clinical Supplies Room Leader, acting under direct supervision, executes and oversees all phases of clinical packaging, labeling, manufacturing, and assembly of investigational drug product that includes but is not limited to blistering, bottling, carding, encapsulation, manufacturing, labeling, and assembly. He/She prepares and completes packaging...

  • Packaging Technician I, UD Packaging, B1 Shift

    Found in: Resume Library US A2 - 3 days ago


    Waco, Texas, United States AbbVie Full time

    Job Description Job Summary Manage production lines to meet the established production schedule in accordance with Standard Operating Procedures (SOP’s) and Good Manufacturing Principles (GMP’s) while monitoring product to ensure quality standards are maintained. Job Details This position will be responsible for the following: Comply with all safety...