Vendor Quality Control Analyst jobs in Florida

Vendor Quality Control Analyst evaluates vendor operations, products, and services for compliance with government and company quality standards. Conducts audits and testing of products, materials, and processes to measure effectiveness and compliance with company expectations. Being a Vendor Quality Control Analyst analyzes and monitors metrics and KPIs to suggest improvement initiatives. Works with vendors and identifies alternative vendors to mitigate risks and resolve problems. Additionally, Vendor Quality Control Analyst assists with drafting and negotiating service-level agreements to ensure performance/quality metrics, responsibilities, expectations, and penalties are adequately defined. Prepares reports and updates on vendor status and quality. Requires a bachelor's degree. Typically reports to a manager or head of a unit/department. The Vendor Quality Control Analyst occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. To be a Vendor Quality Control Analyst typically requires 2 -4 years of related experience. (Copyright 2024 Salary.com)

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Senior Analyst, Quality Control
  • BioSpace
  • Alachua, FL FULL_TIME
  • A career at Resilience is more than just a job – it’s an opportunity to change the future.

    Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

    For more information, please visit www.resilience.com

    Position Summary

    The Senior QC Analyst will partner and collaborate with the Analytical Development and QC operations teams to ensure that all required method transfers, qualifications and validations are performed, meeting all partner needs in compliance with standard operating procedures and testing methods. Specific activities include authoring/executing/review of study design, protocols and reports associated with qualification/validation/transfer studies.

    This position is a first shift role and reports to the Head of QC, Method Lifecycle and Stability. The position will be in our Alachua, FL facility.

    Position Responsibilities

    • Sr Analyst, Method Lifecycle activities to include, supporting method selection and development to leading method transfer, qualification and validation, monitoring routine use, leading change controls and retirement of the method
      • Transfer/qualification/validationactivities using protein-based assays, molecular methods, and cellular assays
      • Author and/or review method transfer, qualification and validation protocols and reports.
      • Collaborate with Analytical Development personnel to ensure methods are suitable for transfer to QC fortransfer/qualification/validation.
      • Assists in developing, troubleshooting, optimizing complex biological QC procedures according to regulatory requirements.
      • Collaborate with QC Product Testing personnel to ensure analysts are trained on newlytransferred/qualified/validatedprocedures.
      • Analyze, document, and report experimental data in accordance to Resilience requirements
      • Collect/evaluate data trends to ensure qualified/validated methods remain in a state of control.
      • Present/discuss data in client facing meetings

  • May require occasional early morning, late evening, and / or weekend work.
  • Provide support to the QC Operations team as needed
    • Performing immunoassays, cell-based assays, molecular biology assays and virology testing in support of product release, in-process testing and stability
    • Train analysts on analytical techniques
    • Troubleshoot assay failures
    • May require occasional early morning, late evening, and / or weekend work
    • Other activities as assigned


    Minimum Qualifications

    • Experience performing Protein based assays, Cell Assays and/or Ligand binding assays.
    • Knowledge of Analytical Method Lifecycle requirements with previous experience in method transfer, qualification and validation
    • Experience with cGMPs applicable to the pharmaceutical industry.
    • Strong verbal / written and interpersonal communication skills as a team player and willing to work in an environment where individual initiative, collaboration and accountability are valued.
    • Analytical problem-solving and troubleshooting skills.
    • Adaptable and flexible in response to a dynamic operating environment


    Preferred Qualifications

    • BS (MS preferred) in a Biological Science (Biochemistry, Microbiology, Immunology, Molecular Biology, Virology), or related field
    • Familiarity with ELISA type assays (colorimetric, fluorometric, chemiluminescent, etc.) and/or qPCR and ddPCR molecular assays; virology methods such as TCID50, plaque, FFU. Experience with Capillary Electrophoresis and/or HPLC a plus.
    • This level of technical proficiency is typically gained through a degree in a scientific discipline and 5 years of relevant experience.


    Role/Site Specific Requirements

    This position may also include the following:

    Physical work

    • This role is primarily a non-Sedentary role. This can include climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects.


    Visual acuity (such as: working with data & figures, viewing computer terminal, extensive reading, operating machinery, operating motor vehicles, general observations of facilities, etc.)

    Participation in an occupational health program (which can include medical assessment, surveillance, vaccination, and testing)

    Use of personal protective equipment (which can include respirators, Personal Air Purifying Respirators [PAPR], gowns, gloves, face protection, other barrier equipment, etc.)

    Exposure To The Following

    • Use of personal protective equipment (which can include respirators, Personal Air Purifying Respirators (PAPR), gowns, gloves, face protection, other barrier equipment, etc.
    • Handling, managing, disposing hazardous and non-hazardous waste (which can include: chemicals, universal and e-wastes, oil, aqueous wastewater, etc.), inclusive of exposure to bloodborne pathogens
    • Working in BSL-2/3 laboratories & production rooms, waste holding areas, or other facilities where biological hazards and hazardous chemicals may be stored or handled.
    • Packaging, transporting, and shipping of infectious or potentially infectious substances


    The items described here are representative of those that must be met to successfully perform the essential functions of this job.

    Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.

    Resilience offers employees a robust total rewards program including equity, an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $70,000.00 - $107,500.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.
  • 2 Days Ago

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Quality Control Analyst
  • VIVEX Biologics
  • Miami, FL FULL_TIME
  • DescriptionJob purposeThe Quality Control Analyst is responsible for performing and managing results of quality control testing for human tissue donors, recovered tissues, and final processed grafts. ...
  • 8 Days Ago

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Quality Control Laboratory Analyst
  • Treatt USA
  • Lakeland, FL FULL_TIME
  • Job Description: This role is an introductory level position to the Quality Control Department, with potential to becoming a Quality Analyst. The Junior Analyst will gain familiarity in good laborator...
  • Just Posted

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Senior Analyst, Quality Control
  • Resilience
  • Alachua, FL FULL_TIME
  • A career at Resilience is more than just a job – it’s an opportunity to change the future.Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re bu...
  • 1 Day Ago

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Quality Control Analyst
  • VIVEX BIOLOGICS INC
  • Miami, FL FULL_TIME
  • DescriptionJob purposeThe Quality Control Analyst is responsible for performing and managing results of quality control testing for human tissue donors, recovered tissues, and final processed grafts. ...
  • 1 Month Ago

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Quality Control Analyst
  • GBI Bio
  • Fort Lauderdale, FL FULL_TIME
  • DescriptionScope of Function: Work within the Analytical Chemistry area to provide analytical support, test results and qualification of analytical methods and stability studies for clients in pre cli...
  • 12 Days Ago

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Quality Control Analyst
  • Hiring Now!
  • Kansas City, MO
  • Ingredion is hiring for a QC Analyst based out of the North Kansas City site. This role will be responsible for performi...
  • 6/11/2024 12:00:00 AM

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Quality Control Analyst
  • Meet
  • Novato, CA
  • Our esteemed client, a leading pharmaceutical company known for its continuous growth, is seeking a Quality Control (QC)...
  • 6/10/2024 12:00:00 AM

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Quality Control Analyst
  • WuXi AppTec
  • 2108 Couvet, NE
  • This position is responsible to perform all type of analytical testing that is required for release of raw and packaging...
  • 6/9/2024 12:00:00 AM

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Quality Control Analyst
  • BEPC Inc. - Business Excellence Professional Consulting
  • Vacaville, CA
  • BEPC has an open position for a QC Analyst I in Vacaville, CA! Contract W2 Period: 6-month contract with possibilities f...
  • 6/9/2024 12:00:00 AM

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Quality Control Analyst
  • ACL Digital
  • Newark, CA
  • Job Title: QC Analyst/Analyst II, QC Cell and Molecular Biology. Location: Newark, CA Duration: 08 Months This role is f...
  • 6/8/2024 12:00:00 AM

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Quality Control Analyst
  • Randstad Sourceright
  • Glendale, CA
  • At one of our top Pharmaceutical companies, we are transforming the pharmaceutical industry through our R&D-driven marke...
  • 6/8/2024 12:00:00 AM

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Quality Control Analyst
  • EPM Scientific
  • Boston, MA
  • EPM currently working with a reputable pharmaceutical client and they are looking for an QC Analyst contractor to help w...
  • 6/7/2024 12:00:00 AM

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Quality Control Analyst
  • Haleon
  • Dungarvan, WD
  • Hello. We’re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving e...
  • 5/28/2024 12:00:00 AM

Florida (/ˈflɒrɪdə/ (listen); Spanish for "land of flowers") is the southernmost contiguous state in the United States. The state is bordered to the west by the Gulf of Mexico, to the northwest by Alabama, to the north by Georgia, to the east by the Atlantic Ocean, and to the south by the Straits of Florida. Florida is the 22nd-most extensive (65,755 sq mi or 170,300 km2), the 3rd-most populous (21,312,211 inhabitants), and the 8th-most densely populated (384.3/sq mi or 148.4/km2) of the U.S. states. Jacksonville is the most populous municipality in the state and the largest city by area in th...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Vendor Quality Control Analyst jobs
$79,612 to $94,535