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GLP Quality Assurance Manager, Bioanalytical Lab - Growth Driven New Role, Always Hiring!

Company: NorthEast BioLab
Location: Hamden
Posted on: August 7, 2022

Job Description:

NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION.Overview

  • Collaborate with an interdisciplinary team to support high-quality bioanalysis activities while enabling life-changing, life-saving therapeutics
  • Maintain regulator/sponsor trust for excellent bioanalytical study data on Pharmacokinetic (PK), Toxicology (Tox), Biomarker, Bioavailability (BA), Bioequivalence (BE), and other bioanalysis
  • Champion quality and compliance with Good Laboratory Practices (GLP), Company Standard Operating Procedures (SOPs), and Sponsor Study protocolsRole
    • Ensure high-quality, compliant GLP and non-GLP data for LC-MS/MS and HPLC-UV OR ELISA, MSD, Luminex, and qPCR, bioanalysis projects
    • Host Regulators, Sponsors, Potential Clients, and Lead Audit/Inspection Response Team
    • Review all study documentation covering method development, validation, and sample analysis for drug and biomarker bioanalysis of customized Chromatographic and Ligand Binding Assay
    • Perform/document QA audits and facility inspections, in-life and otherwise, plus monitor lab activities plus against SOPs, method validation plans, study protocols, and FDA/ICH/EMA guidelines
    • Maintain controlled, indexed regulated documents (e.g., Study and Method Registers, GLP Master Schedule, etc), archive onsite (including electronic), and send to (and retrieve from) off-site archive
    • Author, review, and maintain SOPs, report templates, training plans, annual regulatory refresher training, data trending reports, etc
    • Track, trend, and ensure quality and compliance of Corrective Action/Preventative Action (CAPA), Investigations, Deviations, and Change Controls
    • Review computerized system validations, equipment maintenance, and calibration records
    • Conduct assessments and handle information requests for clients, potential clients, suppliers and vendors, test facilities, clinical sites, etc
    • Assist with maintaining current facility certificates and registrations, controlled substances, and safety program documentation
    • Support management and business development or marketing activities, foster client relationships, and onboard new clientsQualification
      • QA Candidates with small or large molecule bioanalytical experience in a deadline-driven and regulated GxP setting
      • Knowledgeable in US FDA 21 CFR Part 58 (GLP), Part 11 Regulations and 2003 Guidance, FDA 2018 BMV Guidance, OECD GLP, US FDA & ICH GCP, EMA requirements, etc
      • BS (3+ years experience) or MS (2+ years) degree in analytical chemistry, biochemistry, pharmacology, biotechnology, biomedical sciences, or related areas
      • Hands-on experience with Sciex Mass Spectrometers and Analyst software, or ELISA, MSD, Luminex, and qPCR Assay platforms is a huge plus
      • Excellent interpersonal communication and relationship building where all feel heard and respected
      • Fast and continuous learner, flexible thinker, self-motivated doer who can independently manage responsibilities, take on new challenges, mentor and train others, and with demonstrated ability to thrive in a fast-paced environment.
      • Familiarity with Thermofisher's Watson LIMS, Non-compartmental Analysis (NCA) on Certara's WinNonlin, GMP, and CAP/CLIA regulations is desirable
      • Proficient in Microsoft Office, Adobe Programs plus scientific and technical reading and writingCompensation and Benefits
        • Competitive compensation and commensurate with industry experience
        • Discretionary performance bonus and equity participation at year-end
        • Two weeks paid annual vacation
        • 401k match and healthcare coverage to eligible employees
        • Accelerated career progression with flexibility to expand role and grow into the next levelOther Job DetailsSeniority Level
          • Manager and Individual ContributorIndustry
            • BiotechnologyEmployment Type
              • Full-timeJob Functions
                • Quality
                • ManagementWork Remotely
                  • NoJob Type: Full-time

Keywords: NorthEast BioLab, Hamden , GLP Quality Assurance Manager, Bioanalytical Lab - Growth Driven New Role, Always Hiring!, Executive , Hamden, Connecticut

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