Quality Assurance Specialist - Complaint Handling
Collabera Technologies
Description
- Home
- Search Jobs
- Job Description
Days Left: 0 days, 3 hours left Apply *]:pointer-events-auto [content-visibility:auto] supports-[content-visibility:auto]:[contain-intrinsic-size:auto_100lvh] R6Vx5W_threadScrollVars scroll-mb-[calc(var(--scroll-root-safe-area-inset-bottom,0px)+var(--thread-response-height))] scroll-mt-[calc(var(--header-height)+min(200px,max(70px,20svh)))]" dir="auto" data-turn-id="request-WEB:750ac9c5-8f2c-42cf-afee-b49086f4e931-10" data-testid="conversation-turn-8" data-scroll-anchor="false" data-turn="assistant"> To Discuss more about this job opportunity, please reach out to Deepak Arya LinkedIn URL email your updated resume at Email View email address on click.appcast.io . Thank you! Pay Range: $20 to $25 an hour Client Industry: Pharmaceutical Job Mode: Onsite Contract Duration: 06 Months (Possibilities of Extension) Job Summary:
The Quality Assurance Specialist is responsible for supporting product quality through complaint investigation, laboratory testing, and documentation in a regulated environment. This role focuses on identifying product issues, analyzing test results, and ensuring compliance with quality and regulatory standards. The individual will contribute to maintaining high quality processes while supporting continuous improvement initiatives. The position requires strong analytical thinking, attention to detail, and the ability to work independently. This role plays a critical part in ensuring product safety and reliability. Key Responsibilities:
- Perform product complaint documentation, investigation, and review of non medical complaint content.
- Conduct laboratory testing and analyze results for routine to moderate complexity products.
- Ensure all documentation meets Good Documentation Practices and regulatory standards including GMP and GLP.
- Initiate and support investigation records and exception documentation as per procedures.
- Review and approve investigation results under guidance from senior team members.
- Troubleshoot laboratory instruments and resolve technical issues during testing.
- Maintain laboratory safety, compliance, and training requirements.
- Support process improvements and contribute to overall team objectives.
- Bachelor degree in Science Engineering or related field.
- Hands on laboratory experience with product testing.
- Knowledge of GMP GLP GxP and Good Documentation Practices.
- Strong analytical and critical thinking skills.
- Effective written and verbal communication skills.
- Ability to manage multiple tasks and prioritize work independently.
- Experience in medical device or regulated industry environment.
- Familiarity with quality management systems and complaint handling systems.
- Experience supporting audits or regulatory inspections.
- Exposure to process improvement initiatives.
- Quality Assurance
- Laboratory Testing
- GMP
- GLP
- GxP
- Complaint Investigation
- Technical Documentation
- Recruiter
- Phone
- Deepak Arya
- View email address on click.appcast.io
Vacancy posted more than 2 months ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Quality Assurance Specialist - Complaint Handling. Be the first to apply!
Related searches
- quality lead North Chicago, IL
- quality distribution North Chicago, IL
- rn quality North Chicago, IL
- quality management nurse North Chicago, IL
- quality tech North Chicago, IL
- water quality North Chicago, IL
- quality equipment North Chicago, IL
- water quality scientist North Chicago, IL
- quality manufacturing North Chicago, IL
- lead qa North Chicago, IL
