Clinical and Scientific - Quality Control Analyst II

Mindlance

  • Fort Worth, TX
  • 21 days ago
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    Skills

    • Analysis Skillsunmatched
    • Biotech and Pharmaceuticalunmatched
    • Communication Skillsunmatched
    • Corrective Actionunmatched
    • Documentationunmatched
    • English Languageunmatched
    • Follow Throughunmatched
    • Identify Issuesunmatched
    • Laboratoryunmatched
    • Laboratory Operationsunmatched
    • Maintain Complianceunmatched
    • Microbiologyunmatched
    • Multitaskingunmatched
    • Problem Solving Skillsunmatched
    • Quality Controlunmatched
    • Regulatory Complianceunmatched
    • Regulatory Requirementsunmatched
    • Reporting Skillsunmatched
    • Schedule Developmentunmatched
    • Secondary Schoolunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Time Managementunmatched
    • Warehousingunmatched

    Description

    The Quality Control Analyst II is responsible for maintaining high standards of laboratory operations and ensuring compliance with regulatory requirements. Key responsibilities include:

    -Performs microbiological validations for raw materials and finished products, including Bioburden, Endotoxin, Sterility, and PET.

    -Provides support to QC Microbiology laboratories.

    -Conducts equipment qualifications.

    -Organizes and assists with Media Fill and Reads.

    -Identifies ongoing quality issues, prevents potential problems, and suggests improvements.

    -Interprets and evaluates analyses for accuracy and precision against established specifications, recommending and implementing corrective actions when necessary.

    -May be responsible for analytical and protocol report writing, as well as standard operating procedures.

    -Strictly adheres to Good Documentation Practices (GDP).

    -Collaborates with and supports coworkers to enhance the organization's overall capabilities.

    -Communicates effectively with production, maintenance, warehouse, and other relevant functions.

    -Participates in problem-solving and troubleshooting.

    -Supports training needs of team members and works cohesively with the team.

    -Coordinates with and supports other departments to ensure smooth workflow execution.

    -Ensures the availability of supplies and equipment to meet schedules and carries out tasks as defined by the schedule.


    Qualifications:

    -Bachelor’s Degree or equivalent years of related experience (or high school + 8 yrs; Assoc. + 4 yrs)

    -The ability to fluently read, write, understand and communicate English


    Desired Competencies:

    -Strong knowledge of pharmaceutical regulatory requirements

    -Excellent Communication skills, in both verbal and written form

    -Highly attentive to details and comfortable speaking up

    -Self-Starter with the ability to follow up on and complete multiple projects simultaneously with little direction

    -Able to work overtime and flexible work hours to meet department goals

    EEO:

    “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

    Numbers & Facts

    LocationFort Worth, TX

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