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    GMP Technical Writer

    Latitude, Inc.
    North Potomac, MD 20878
    Full-time, Part-time
    Refer friends, get paid!

    Job Description

    Job Description

    GMP Technical Writer

    Location: North Potomac, MD

    Competitive Pay DOE

     

    Your expertise, coupled with our advanced technologies and collaboration with innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Position Summary The Manufacturing Specialist will provide support for Manufacturing Management and Associates to meet batch record review/disposition schedule to adhere to lot release dates. The Specialist will be responsible for, executing root cause investigations, owning/authoring deviations, driving continuous improvement efforts and other quality report types, and revising GMP documents such as SOPs and Manufacturing batch records.

    In concert with our Patient First philosophy, this position is key in our efforts toward continuous improvement of our processes & information which will allow quality drug products to reach patients safely and efficiently. The Role (daily responsibilities)

    • Initiates Quality Records and conducts deviation investigations that meeting both Industry and Paragon expectations

    • Leads or manage investigations including root cause analysis and assesses product impact using input from various departments

    • Develops, executes and oversees CAPAs

    • Technical leadership will be required to ensure that product and process understanding is sufficient to investigate deviations, that investigations are technically sound, meet quality expectations, and that corrective actions are effective.

    • Supports Tech transfer and process monitoring support as needed

    • Works with the team to monitor critical process parameters

    • Revision and management of manufacturing documents such as Batch Records and SOPs

    • Leads or supports Continuous Improvement projects

    • Conducts data gathering, trending, and data presentation as needed to support investigations

    • Responsible for real-time, on the floor response in support of operational deviations by gathering information and completing an initial event report. The Candidate (requirements)

    • Bachelor’s degree in a science or engineering field and 4+ years of demonstrated technical competency in biopharmaceutical manufacturing processing in a GMP compliance environment (e.g. Production, Development, Process Engineering, Technical Services or related field)

    • Previous experience operating equipment such as incubators, single-use bioreactors, depth filtration skids, TFF skids, chromatography skids, single-use mixers and in-process testing equipment

    • Previous experience in process deviation investigations and remediation

    • Previous experience authoring and/or revising technical documents

    • Demonstrated ability to work effectively cross-functionally, lead teams and implement project plans on time and on budget

    • Excellent communication and technical writing skills

    • Ability to support and/or lead system troubleshooting efforts

    • Familiar with Lean Six Sigma Methodologies and proven analytical/problem-solving capabilities

    Performance & Development:

    • Leads with Integrity and Respect

    • Delivers Results

    • Demonstrates Business Acumen

    • Fosters Collaboration and Teamwork

    • Champions Change

    • Engages and Inspires

    • Coaches and Develops

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    Dte08M44Dy

    Posting ID: 593992455Posted: 2021-01-23