Quality Specialist - Environmental Scientist

Our client, a world leader in diagnostics and life sciences, is looking for a<\/span><\/span> "<\/span><\/span><\/b><\/span><\/span><\/span> <\/span><\/span><\/span><\/span><\/span><\/span>Quality Specialist - Environmental Scientist” based out of Hillsboro, OR.<\/span><\/span><\/span><\/span><\/span><\/b>
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Job Duration:<\/span><\/span><\/span><\/span><\/span><\/b> <\/span><\/span>Long term Contract (Possibility Of Further Extension)<\/span><\/span><\/b><\/span><\/span><\/span>
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Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K<\/span><\/span><\/span><\/span><\/span><\/b>
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We are seeking a skilled Quality Assurance Specialist to support environmental monitoring, aseptic sampling, and quality oversight activities in a cGMP -regulated biopharmaceutical environment. This role is responsible for ensuring inspection readiness, executing monitoring programs, resolving quality issues, and contributing to departmental and cross -functional initiatives. The ideal candidate brings strong technical expertise, sound scientific judgment, and excellent communication skills.
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Key Responsibilities<\/b>
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• Perform environmental monitoring and water sampling in compliance with cGMP standards.
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• Maintain a constant state of inspection readiness and ensure documentation accuracy.
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• Apply scientific theory and technical principles to resolve moderately complex quality issues.
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• Troubleshoot and support root -cause investigations through strong cross -functional partnerships.
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• Serve as a technical SME for environmental monitoring and quality -related activities.
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• Work independently on routine assignments and with guidance on complex tasks.
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• Contribute to the design and implementation of process improvements and departmental initiatives.
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• Communicate effectively with Supervisors and Managers, including handling sensitive information.
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• Support Quality oversight activities and perform additional duties as assigned.
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  Qualifications<\/b>
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  • Bachelor’s degree in Life Sciences or related field.
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  • Minimum 3 years of experience in a cGMP pharmaceutical or biopharmaceutical environment.
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  • Hands -on laboratory experience with aseptic sampling and testing techniques.
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    If interested, please send us your updated resume at<\/span><\/span><\/span><\/span><\/span>
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    hr@dawarconsulting.com<\/span><\/span><\/a>/kavitha@dawarconsulting.com<\/a> <\/span><\/span><\/span><\/span><\/span><\/u><\/b>
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