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Sr. Quality Engineer, Validation
Sr. Quality Engineer, ValidationCardinal Health • Indianapolis, Indiana, USA
Sr. Quality Engineer, Validation

Sr. Quality Engineer, Validation

Cardinal Health • Indianapolis, Indiana, USA
[job_card.variable_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

Anticipated salary range : $68500 - $97800

Bonus eligible : No

Benefits : Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

  • Medical dental and vision coverage
  • Paid time off plan
  • Health savings account (HSA)
  • 401k savings plan
  • Access to wages before pay day with myFlexPay
  • Flexible spending accounts (FSAs)
  • Short- and long-term disability coverage
  • Work-Life resources
  • Paid parental leave
  • Healthy lifestyle programs

Application window anticipated to close : 12 / 30 / 2025

  • if interested in opportunity please submit application as soon as possible.
  • The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including but not limited to a candidates geographical location relevant education experience and skills and an evaluation of internal pay equity.

    What Quality Engineering contributes to Cardinal Health

    Quality develops and implements quality policies procedures and processes to ensure products and services comply with regulatory standards and specifications.

    Quality Engineering manages product and service quality planning evaluation and control. This job family works cross-functionally in the development and implementation of prevention-based methodologies used in designing manufacturing testing and correction of products and services.

    Job Summary

    The Senior Engineer Quality Engineer leads quality assurance processes at the assigned facility. This position will be responsible for developing key suppliers to improve their processes and process capability to provide enhanced raw material supply resulting in plant cost reductions through improved raw material quality reduced waste and inventory reductions.

    Responsibilities

  • Conducts & develops validation and qualification protocols projects and studies supporting manufacturing facility start-up and operation. Validation documentation to ensure products are manufactured in accordance with cGMP pharmaceutical regulatory agencies manufacturer and Cardinal Health specifications / requirements.
  • Maintains close contact with various functions to assure effective communication on challenges and opportunities related to validation.
  • Provides technical support as needed.
  • Develop policies programs SOPs and Quality standards to meet current industry corporate Quality and external Regulatory requirements regarding validation.
  • Supports the facility in internal and external regulatory inspections.
  • Works directly with management contract customers and / or contract engineers.
  • Maintain effectiveness of the Quality System components relevant to this position.
  • Works autonomously with minimal supervision.
  • Develops maintains and enforces Cardinal Health compliance standards.
  • Learns and carries out laboratory procedures or operating equipment as needed to perform qualification testing.
  • Performs other job duties as assigned.
  • Qualifications

  • 2-4 years of experience preferred
  • Bachelors degree in related field or equivalent work experience preferred
  • 2 or more years of relevant work experience as a Validation Engineer Quality Assurance Engineering or Quality Validation Consultant working with 21 CFR 210 211 in the FDA regulated industry (Pharmaceutical or Medical Device).
  • Experience with equipment qualification software validation test method validation and / or process validation.
  • Validation and Technology Transfer process and experience with writing procedures / reports and execution of laboratory test.
  • Must be detail oriented organized able to multi-task a self-starter and self-motivated.
  • Must be proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills.
  • Preferred : Experience working with radiopharmaceuticals
  • What is expected of you and others at this level

  • Applies working knowledge in the application of concepts principles and technical capabilities to perform varied tasks
  • Works on projects of moderate scope and complexity
  • Identifies possible solutions to a variety of technical problems and takes action to resolve
  • Applies judgment within defined parameters
  • Receives general guidance and may receive more detailed instruction on new projects
  • Work reviewed for sound reasoning and accuracy
  • Candidates who are back-to-work people with disabilities without a college degree and Veterans are encouraged to apply.

    Cardinal Health supports an inclusive workplace that values diversity of thought experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race religion color national origin ancestry age physical or mental disability sex sexual orientation gender identity / expression pregnancy veteran status marital status creed status with regard to public assistance genetic status or any other status protected by federal state or local law.

    To read and review this privacy notice click here

    Required Experience :

    Senior IC

    Key Skills

    Python,SOC,Debugging,C / C++,FDA Regulations,Minitab,Technical Writing,GAMP,OS Kernels,Perl,cGMP,Manufacturing

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

    Monthly Salary Salary : 68500 - 97800

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