Randstad - India, Quality Control, On-site work

Seeking an experienced **Quality Head** in **Ahmedabad, India** to lead the **QMS** (IATF 16949, ISO 9001). You will manage **VSA, LPA, and Product Audits**, handle **Customer & IATF Audits** with **CAPA**, and ensure **EU Regulation 2018/858** compliance with bodies like **KBA** and **TUV**. Dri...

Seeking a Sr. Executive - Quality for Gears in Chakan, India. This role demands 5-7 years of metallurgy experience in the auto component industry, focusing on heat treatment, material analysis, and supplier audits. A Bachelor's in Mechanical Engineering is required, with Six Sigma Black Belt, IAT...

Dorf Ketal seeks a Manager Corporate HSE Audit in Thane, Mumbai. You will strengthen the HSE audit framework across specialty chemical sites, ensuring compliance with ISO 45001, ISO 14001, and Responsible Care. Ideal candidates hold a B.E Chemical with a safety diploma and 12-18 years of experien...

Seeking an experienced **QA Head** in **Pune, India** to lead quality management for auto component machining. Requires 20+ years in quality, with 7+ in leadership and a mechanical engineering degree. Key duties include driving IATF/ISO compliance, managing audits, and improving defect rates. Ide...

Seeking a **Quality Head** in **Rudrapur, India** to lead QA/QC for a consumer appliance manufacturer. Requires 12-15+ years in manufacturing quality, expertise in **sheet metal, injection moulding, and refrigeration**. Drive ISO 9001 systems, **CAPA, PFMEA**, and supplier quality. Ideal for a le...

Seeking an experienced **Quality Manager** in **Viramgam, India** to lead QA/QC in a manufacturing environment. Requires a Bachelor’s in Engineering and 13+ years of experience with quality systems, audits (IATF, ISO), and CAPA. Drive reduction in customer complaints, cost of poor quality, and co...

Seeking an experienced Quality Regulatory Manager in Bengaluru. This role requires a Master's/Ph.D. in Life Sciences and 6-10 years in IVD/medical device regulatory affairs. You will lead global submissions (EU IVDR, US FDA) and ensure compliance with ISO 13485. Drive successful product registrat...