What are the responsibilities and job description for the Product Design Quality Engineer position at Stark Pharma Solutions Inc?
About The Company
Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.
Position: Product Design Quality Engineer
Location: Bothell, WA
Duration: Long Term
Job Overview
We are seeking a Product Design Quality Engineer with experience in design quality, process validation, risk management, CAPA, and product development within a regulated environment.
Key Responsibilities
Support products from concept through commercialization and design transfer.
Develop and execute process validation strategies.
Support IQ/OQ/PQ and process capability activities.
Manage design control activities, including design inputs, reviews, verification, and validation.
Prepare and maintain quality plans and technical documentation.
Support hardware, software, and system quality activities.
Identify and assess product and manufacturing risks.
Support risk management and risk mitigation activities throughout the product lifecycle.
Perform root cause analysis and resolve quality issues.
Manage CAPA activities and verify corrective action effectiveness.
Review product performance and post-market data to identify quality improvements.
Support quality audits and regulatory inspections.
Drive continuous improvement and product quality initiatives.
Work closely with Engineering, R&D, Manufacturing, Quality, and other cross-functional teams.
Required Qualifications
Bachelor's or Master's degree in Mechanical Engineering, Electronics Engineering, Science, or a related field.
4 years of experience with a Bachelor's degree in Quality Engineering, Safety Engineering, R&D Engineering, or a related field.
Master's degree candidates may be considered with limited or no prior experience.
Experience with Design Quality Management and Design Controls.
Experience with design verification and design validation.
Experience with process validation and IQ/OQ/PQ.
Strong knowledge of risk assessment and risk management.
Experience with CAPA and root cause analysis.
Strong data analysis and interpretation skills.
Experience with technical and quality documentation.
Knowledge of regulatory and quality requirements.
Experience with product quality, reliability, and defect management.
Strong problem-solving and continuous improvement skills.
Good communication and cross-functional collaboration skills.
How To Apply
Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.
Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.
Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.
Position: Product Design Quality Engineer
Location: Bothell, WA
Duration: Long Term
Job Overview
We are seeking a Product Design Quality Engineer with experience in design quality, process validation, risk management, CAPA, and product development within a regulated environment.
Key Responsibilities
Support products from concept through commercialization and design transfer.
Develop and execute process validation strategies.
Support IQ/OQ/PQ and process capability activities.
Manage design control activities, including design inputs, reviews, verification, and validation.
Prepare and maintain quality plans and technical documentation.
Support hardware, software, and system quality activities.
Identify and assess product and manufacturing risks.
Support risk management and risk mitigation activities throughout the product lifecycle.
Perform root cause analysis and resolve quality issues.
Manage CAPA activities and verify corrective action effectiveness.
Review product performance and post-market data to identify quality improvements.
Support quality audits and regulatory inspections.
Drive continuous improvement and product quality initiatives.
Work closely with Engineering, R&D, Manufacturing, Quality, and other cross-functional teams.
Required Qualifications
Bachelor's or Master's degree in Mechanical Engineering, Electronics Engineering, Science, or a related field.
4 years of experience with a Bachelor's degree in Quality Engineering, Safety Engineering, R&D Engineering, or a related field.
Master's degree candidates may be considered with limited or no prior experience.
Experience with Design Quality Management and Design Controls.
Experience with design verification and design validation.
Experience with process validation and IQ/OQ/PQ.
Strong knowledge of risk assessment and risk management.
Experience with CAPA and root cause analysis.
Strong data analysis and interpretation skills.
Experience with technical and quality documentation.
Knowledge of regulatory and quality requirements.
Experience with product quality, reliability, and defect management.
Strong problem-solving and continuous improvement skills.
Good communication and cross-functional collaboration skills.
How To Apply
Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.
Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.