Lead Auditor CRS
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Mô tả công việc
Conduct UL GMP certification audits for manufacturing suppliers across Southeast Asia (SEA), ensuring compliance with program standards. Achieve KPI and productivity targets while assessing suppliers in the Medical Devices, Food, Supplements, and Pharmaceuticals industries.
Job Responsibilities:
• Conduct audits independently and collaboratively, ensuring compliance with cGMP and quality management standards (FDA CFR 820, CFR 210/211, ISO 22716).
• Manage and execute assigned audit programs without direct supervision.
• Work with Field Manager to expand technical expertise and audit scope over time.
• Meet process KPIs and monthly productivity targets.
• Represent ULS professionally, upholding impartiality and ethical standards.
• Prepare and distribute audit agendas to clients 14 days in advance (excluding unannounced audits).
• Submit audit results within four calendar days and review CAPA responses for acceptance or rejection.
• Lead and represent the audit team in management discussions, making final decisions on audit conduct and observations.
• Serves as a Competent Evaluator for field evaluations, supervising and assessing auditors during audits.
• Conduct field observations, witness audits, and issue competency reports on auditors' technical performance.
• Maintain specialized qualifications for advanced auditing skills and methodologies.
• Adhere to company policies on administration, confidentiality, business ethics, conflict of interest, and safety.
• Perform additional duties as assigned.
Yêu cầu công việc
• Bachelor's degree in Electrical & Electronic Engineering with 4+ years of experience in manufacturing or quality assurance within the Medical Devices, Cosmetics or Pharmaceutical industries.
• 2 - 3 years’ GMP audit experience in the same industries.
• Strong knowledge of FDA CFR 820, CFR 210/211, ISO22716 regulations is a must.
• Willing to travel across Southeast Asia regions (up to 80% annually).
• Fluent in English (proficiency in a second language is a plus).
• Excellent written and verbal communication skills; able to engage high-level executives and lead opening/closing conferences.
• Strong problem-solving skills with a creative and innovative approach to process improvements.
• Ability to lead audits teams for specialized projects.
Phân tích mức độ cạnh tranh
VietnamWorks AI
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Giá
29.000đ / lượt
Các phúc lợi dành cho bạn
Thưởng
Thông tin việc làm
13/02/2025
Nhân viên
Khoa Học & Kỹ Thuật > Kỹ Thuật Điện/Điện Tử
Electronics & Electrical, Fda Cfr Regulations, Gmp Audit Experience, ISO Knowledge, Problem-solving
Điện/Điện tử
Tiếng Anh
4
Người Việt Nam
Địa điểm làm việc
Lot 5, Conurbation 2, Street K1, Cat Lai Industrial Zone, Thanh My Loi Ward, District 2 Ho Chi Minh City Ho Chi Minh Cit
Hồ Chí Minh
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