Expert - QA Technical Operations
About The Position
About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. The Expert of QA Technical Operations will be responsible for: Interpreting, building upon, and complying with company quality assurance standards Managing daily supplier quality activities and controls Supporting the Strategic Supplier Management process to meet quality, delivery, and cost objectives Developing and executing strategic plans to improve supplier quality, delivery, and costs Overseeing inbound material release process Champion quality assurance procedures, tools, and techniques
Requirements
- Bachelor's degree in Science, Engineering, Business, Management or related field (Advance degree a plus)
- 3-5+ years of experience in Quality, Manufacturing, Engineering, or related field
- Results oriented, driven individual
- Excellent interpersonal, communication and negotiation skills
- Strong organizational and problem-solving abilities
- High attention to detail and accuracy
- Ability to work collaboratively in a team environment
Responsibilities
- Author/Review SOPs
- Oversee the GMP supplier qualification program and supplier risk management
- Completes the approval requirements to qualify new suppliers including negotiating quality agreements, as well as audit scheduling, conduction of audits, and authoring of audit reports
- Periodic review of suppliers and identification of supplier compliance issues
- Manages vendor complaints
- Participates in or manages quality assessments of internal operations and suppliers to analyze compliance and assess risk
- Liaison between Supplier and QA representatives in addressing the quality concerns from the supply chain
- Monitor supplier non-conformance performance, and drive root-cause analyses, corrective actions & process improvements to reduce the Number of Defects & Cost of Quality
- Ensures effective and timely investigation and closure of all CAPAs, supplier non conformances, complaints, and product issues
- Development and maintenance of measurement systems for quality costs, indicators, trends and supplier rating
- Collects data and compiling supplier scorecards
- Manages audit schedule and executes supplier audits
- Generates specifications for materials and consumables
- Responsible for disposition of materials and consumables
- Approve calibration reports for GMP equipment
- Support QA Validation in review of SOPs
- May interface with auditors during regulatory inspections
- Works closely with Facilities, QA Validation, Manufacturing, and QC teams
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
