- 经验
- 10–18 yrs
- 薪水
- —
- 职位空缺
- 1
- 发布
- 15 小时前
- 工作模式
- 在办公室
- 学历
- Bachelor's or Master's in Engineering/Quality Management/Manufacturing
- 恢复
- 需要申请
你的工作地点
职位描述
Position Summary
Best NanoTech seeks an experienced QMS Manager to oversee the development, execution, and ongoing refinement of the Quality Management System (QMS) in a high-volume semiconductor assembly and test facility located in Ahmedabad, Gujarat, India. This full-time onsite role requires leadership in quality system governance, audit management, document and change control, CAPA processes, and adherence to semiconductor, automotive, and customer-specific quality standards.
Core Responsibilities
- Create, deploy, and sustain the site’s Quality Management System ensuring compliance with standards like ISO 9001 and IATF 16949 as well as customer expectations.
- Define and enforce quality policies, procedures, and work instructions alongside governance frameworks.
- Lead and manage various audits including internal, external, customer, supplier, and certification audits with full cycle management from planning to closure.
- Oversee CAPA, non-conformance handling, deviation management, and initiatives preventing recurrence.
- Administer document control including approvals, revisions, distribution, retention, and electronic document management systems.
- Drive manufacturing, product, material, and equipment change management processes effectively.
- Conduct management reviews presenting QMS performance indicators, risks, and improvement strategies.
- Define, monitor, and report quality KPIs, compliance dashboards, and early-warning indicators.
- Champion risk management approaches including PFMEA, control plans, process audits, and 8D problem-solving methodologies.
- Collaborate with cross-functional teams including manufacturing, process, equipment, product, quality, and reliability groups.
- Support new product introductions and production ramp-ups from quality and compliance perspectives.
- Manage customer-specific quality requirements and ensure traceability within site procedures.
- Develop supplier quality governance, audit procedures, and corrective action processes.
- Coordinate quality system training programs, competency development, and promote a quality-focused culture emphasizing disciplined execution and continuous improvement.
- Prepare the site for regulatory, certification, and customer assessments ensuring QMS effectiveness in a 24/7 manufacturing environment.
Required Qualifications and Experience
- Bachelor’s or Master’s degree in Engineering, Quality Management, Manufacturing, or related fields.
- 10 to 18 years’ experience in quality systems, manufacturing quality, or compliance roles.
- At least 4 to 6 years in a leadership role managing QMS teams or site-level quality initiatives.
- Background in semiconductor, ATMP, OSAT, electronics, or similarly controlled high-volume manufacturing environments.
- Strong familiarity with ISO 9001 standards and quality system auditing.
- Preferred experience with IATF 16949, VDA 6.3, or automotive quality requirements.
- Proven expertise in managing CAPA, change control, documentation, and management reviews.
- Experience conducting certification, customer, and internal audits.
- In-depth knowledge of risk-based quality management and statistical quality tools.
- Ability to operate effectively across global and cross-functional teams.
Technical Expertise
- QMS development and deployment
- ISO 9001 and IATF 16949 compliance
- Quality audits including internal, supplier, customer, process, product, and certification audits
- Corrective and Preventive Actions (CAPA), 8D problem-solving, and root cause analysis techniques (5 Why, Ishikawa, Fault Tree)
- Risk and process management tools such as PFMEA, control plans, SPC, process capability analyses, and quality gates
- Document lifecycle and change control management including SOPs, training records, revision controls, and traceability systems
Leadership Responsibilities
- Build and lead the site’s QMS and compliance team with clear ownership across audits, CAPA, documentation, and change management.
- Define quality responsibilities across manufacturing functions and develop QMS personnel through structured training and mentoring programs.
- Coordinate cross-departmental responses to audits and critical quality issues.
- Establish governance forums for reviewing QMS performance and risk.
- Drive a prevention-focused culture centered on quality and compliance principles.