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Quality Control Chemist - I-Night Shift

NET2SOURCE INC

  • Frederick, MD
  • 10 days ago
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    Skills

    • Agile Programming Methodologiesunmatched
    • Analysis Skillsunmatched
    • Assaysunmatched
    • Biological Assayunmatched
    • Biotech and Pharmaceuticalunmatched
    • Calibrationunmatched
    • Case Report Form (CRF)unmatched
    • Chemistryunmatched
    • Communication Skillsunmatched
    • Continuous Improvementunmatched
    • Drug Releaseunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • Industry/Trade Analysisunmatched
    • Leadershipunmatched
    • Materials Testingunmatched
    • Metricsunmatched
    • Microsoft Excelunmatched
    • Microsoft PowerPointunmatched
    • Microsoft Wordunmatched
    • Polymerase Chain Reaction (PCR)unmatched
    • Presentation/Verbal Skillsunmatched
    • Quality Controlunmatched
    • Quality System Requirements (QSR)unmatched
    • Real-time PCR (qPCR)unmatched
    • Regulatory Requirementsunmatched
    • Regulatory Submissionsunmatched
    • Root Cause Analysisunmatched
    • Secondary Schoolunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Test Dataunmatched
    • Testingunmatched
    • Validation Planunmatched
    • Writing Skillsunmatched

    Description

    Join a Global Leader in Workforce Solutions - Net2Source Inc.

    Who We Are

    Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision-Right Talent. Right Time. Right Place. Right Price.

    Title-Quality Control Chemist

    Location-Frederick, MD, 21704

    Duration- 12 months contract

    Onsite - Shift flexibility preferred

    • Wed-Saturday
    • Time: Day 3PM - 1:30AM EST

    Responsibilities (include but are not limited to):

    • Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.
    • Work with internal and external resources to maintain lab in an optimal state.
    • Assist with monitoring and trending data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release. Supply information to support generation of CoAs for product release.
    • Maintains laboratory instruments for calibration and routine maintenance
    • Author or revise SOPs, qualification/validation protocols and reports.
    • Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.
    • Provide updates at daily and weekly meetings.
    • Monitor the GMP systems currently in place to ensure compliance with documented policies.
    • Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate.
    • Gather metric information for use in continuous improvement of areas of responsibility.
    • Perform other duties as required.

    Basic Qualifications:

    • Bachelor's Degree OR AA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience OR High School Degree and 3+ years' experience in biotechnology or related field and Quality Control experience

    Preferred Qualifications:

    • Strong knowledge of GMP, SOPs and quality control processes.
    • Identifying, writing, evaluating, and closing OOS's and investigations.
    • Proficient in MS Word, Excel, Power Point and other applications.
    • Strong written and verbal communication skills.
    • Ability to communicate and work independently with scientific/technical personnel.
    • Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals.
    • Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).
    • Preferred: Experience in the biotech and/or pharmaceutical industry.

    Why Work With Us?

    We believe in more than just jobs-we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.

    Our Commitment to Inclusion & Equity

    Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.

    Awards & Recognition

    • America's Most Honored Businesses (Top 10%)
    • Fastest-Growing Staffing Firm by Staffing Industry Analysts
    • INC 5000 List for Eight Consecutive Years
    • Top 100 by Dallas Business Journal
    • Spirit of Alliance Award by Agile1

    Numbers & Facts

    LocationFrederick, MD
    IndustryOther/Not Classified
    Company Size50 to 99 employees
    Websitehttp://www.net2source.com

    About Company

    Net2Source Inc. is a Global Workforce Management Solutions Company, headquartered in New Brunswick, NJ with its local offices in Texas, California, Florida, Illinois, Colorado and Michigan and its global operations in Canada, UK, Europe, UAE, Malaysia, Australia, China, Singapore and India. Net2Source offers a wide gamut of consulting solutions customized to specific client needs including but not limited to Application Development, Workforce Management and Project Consulting. Whether it’s a Fortune client, whether it’s a System Implementer or whether it is a Start -up, our recipe to success – Exceed expectations! Under promise, over deliver.

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