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Related keywords
- Validation Engineer
- Commissioning Engineer
- Qualification Documentation Specialist
- Project Qualification Specialist
- Patient Qualification Specialist
- Commissioning Electrical Field Engineer
- Engineer Validation
- Commissioning Mechanical Engineer
- Mechanical Commissioning Engineer
- Commissioning Qualification Validation Engineer
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Recruited by AstraZeneca 11 months ago
Address , Gaithersburg, 20878, Md
Commissioning Qualification Validation Engineer
Company | Hyde Engineering + Consulting |
Address | Frederick, MD, United States |
Employment type | FULL_TIME |
Salary | |
Category | Pharmaceutical Manufacturing |
Expires | 2023-09-23 |
Posted at | 8 months ago |
The CQV Engineer shall perform commissioning and qualification of bio/pharmaceutical equipment, including any or all of systems for medical/buffer preparation, fermentation, cell harvest, ultra-filtration, chromatography, CIP, SIP, TFF, Chromatography, Centrifuge Systems.
- Hands on Experience with Biopharma Process Equipments.
- Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
- Develop risk assessment, system impact assessments, validation plans, protocols and reports that support the qualification and validation of systems.
- Preparation of System Boundaries, SLIA, CLIA, QRA, Facility Risk Assessments
- Develop and execute Commissioning and validation Protocols for Bioprocess Equipment’s
- Review, analyze and interpret system performance data for completed validation and prepare final report packages by summarizing the data.
- Investigate deviations, write investigation reports and create summary reports.
- Promote cGMP and regulatory compliance into assigned projects.
- BS degree or higher in chemical engineering or a related engineering or scientific discipline, or significant related experience
- Knowledge of Validation Lifecycle approach (URS, FRS, FAT/SAT, Commissioning IQ,OQ,& PQ Protocols, etc.) guidelines, international regulatory requirements and standards and other in.
- Experience in multiple GMP validation disciplines with advanced technical knowledge.
- Experience interacting with or creating material for representatives of regulatory agencies and executive level staff.
- Experience working with Documentum or Maximo a plus.
- Ability to work independently and within project teams.
- Validation experience using , traditional, risk based, Hybrid approach.
- 4-10 years in validation, quality systems, operations, engineering or any combination thereof.
- Experience with investigations into manufacturing deviations and determination of product impact potential, root cause and corrective actions.
- Strong verbal and written communication skills; excellent organizational and time utilization skills
- Industry experience related to cGMP drug manufacturing, validation, and chemical process design
- Strong computer knowledge including Microsoft Office products
- Wisdom
- Family
- Integrity
- Respect
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