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>
<\/span><\/span><\/p>
<\/span><\/span><\/span><\/span><\/span><\/b>
<\/span><\/span><\/p>
Job Duration:<\/span><\/span><\/span><\/span><\/span><\/b> <\/span><\/span>Long term Contract (Possibility Of
Further Extension)<\/span><\/span><\/b><\/span><\/span><\/span>
<\/span><\/span><\/p>
<\/span><\/span><\/span><\/span><\/span><\/b>
<\/span><\/span><\/p>
Company Benefits: Medical, Dental,
Vision, Paid Sick leave, 401K<\/span><\/span><\/span><\/span><\/span><\/b>
<\/span><\/span><\/p>
<\/span><\/span><\/span><\/span><\/span><\/b>
<\/p>
<\/span><\/span><\/span><\/span><\/span>
<\/p>
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.
<\/p>
Key Responsibilities<\/b>
<\/h3>
Perform environmental monitoring and water sampling in compliance with cGMP standards.
<\/p><\/li>
Maintain a constant state of inspection readiness and ensure documentation accuracy.
<\/p><\/li>
Apply scientific theory and technical principles to resolve moderately complex quality issues.
<\/p><\/li>
Troubleshoot and support root -cause investigations through strong cross -functional partnerships.
<\/p><\/li>
Serve as a technical SME for environmental monitoring and quality -related activities.
<\/p><\/li>
Work independently on routine assignments and with guidance on complex tasks.
<\/p><\/li>
Contribute to the design and implementation of process improvements and departmental initiatives.
<\/p><\/li>
Communicate effectively with Supervisors and Managers, including handling sensitive information.
<\/p><\/li>
Support Quality oversight activities and perform additional duties as assigned.
<\/p><\/li><\/ul>
Qualifications<\/b>
<\/h3>
Bachelor’s degree in Life Sciences or related field.
<\/p><\/li>
Minimum 3 years of experience in a cGMP pharmaceutical or biopharmaceutical environment.
<\/p><\/li>
Hands -on laboratory experience with aseptic sampling and testing techniques.
<\/p><\/li><\/ul>
<\/span><\/span><\/span><\/span><\/span>
<\/span><\/span><\/p>
If interested, please send us your updated
resume at<\/span><\/span><\/span><\/span><\/span>
<\/span><\/span><\/p>
hr@dawarconsulting.com<\/span><\/span><\/a>/
