Julphar

21 hours ago

Sr. Manager - Quality Management System

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 21 hours agoStatus: Live

Job Summary

Establish and lead a compliant Quality Management System for the pharmaceutical business, including Internal & Regulatory Audits, CAPA, documentation/change control, deviations, customer complaints, and recall programs. Manage ISO 9001-aligned QMS development, implementation, and certification, ensuring ongoing regulatory compliance through updated standards knowledge. Lead external regulatory inspections and customer audits, drive QMS process improvements, support digitalization, and oversee QMS and documentation team development.

Location: United Arab Emirates

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Seniority: Sr. Manager level

Key Responsibilities

•Establish and maintain a compliant Quality Management System to ensure timely, accurate, and sustained compliant outcomes.
•Manage QMS activities including Internal & Regulatory Audits, CAPA, documentation/change control, deviations, customer complaints, and recall programs.
•Lead QMS development, implementation, and certification compliant with ISO 9001 and ensure ongoing compliance with applicable regulations and standards.
•Oversee QMS documentation and job descriptions/organogram systems; provide guidance to QMS & Documentation teams for GMP change coverage.
•Lead external regulatory inspections and customer audits; manage recall and complaint functions, change controls, CAPA reviews, escalations, and communicate outcomes to upper management.

Key Requirements

•Bachelor/Master degree in Pharmaceutical, Life Sciences, or Engineering.
•Minimum 10 years of experience in the pharmaceutical industry, including at least 7 years in management roles.
•Minimum 5 years of experience in paper and electronic Data Integrity.
•Proven track record in initiating systems and designing KPIs.
•Strong regulatory knowledge across GCC, EU, USA, and WHO, with experience leading quality improvement and cost-saving projects.

Experience:10+ yearsPharmaceutical industryGMPData integrity

Education:

Skills:Cross-functional collaborationConflict managementQuality solutionsCrisis managementLeadership

Tech Stack:ISO 9001GMPData Integrity

Company Brief

Julphar

Gulf Pharmaceutical Industries, known as Julphar, develops and manufactures a broad range of pharmaceutical products, including generics and healthcare solutions. It serves markets across the Middle East and internationally from its UAE base.

Industry: Pharmaceuticals

Company Size: Enterprise (1,001+ employees)

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Ras Al Khaimah, United Arab Emirates

Founded: 1980

Website LinkedIn

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Julphar

21 hours ago

Sr. Manager - Quality Management System

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 21 hours agoStatus: Live

Job Summary

Location: United Arab Emirates

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Seniority: Sr. Manager level

Key Responsibilities

•Establish and maintain a compliant Quality Management System to ensure timely, accurate, and sustained compliant outcomes.
•Manage QMS activities including Internal & Regulatory Audits, CAPA, documentation/change control, deviations, customer complaints, and recall programs.
•Lead QMS development, implementation, and certification compliant with ISO 9001 and ensure ongoing compliance with applicable regulations and standards.
•Oversee QMS documentation and job descriptions/organogram systems; provide guidance to QMS & Documentation teams for GMP change coverage.
•Lead external regulatory inspections and customer audits; manage recall and complaint functions, change controls, CAPA reviews, escalations, and communicate outcomes to upper management.

Key Requirements

•Bachelor/Master degree in Pharmaceutical, Life Sciences, or Engineering.
•Minimum 10 years of experience in the pharmaceutical industry, including at least 7 years in management roles.
•Minimum 5 years of experience in paper and electronic Data Integrity.
•Proven track record in initiating systems and designing KPIs.
•Strong regulatory knowledge across GCC, EU, USA, and WHO, with experience leading quality improvement and cost-saving projects.

Experience:10+ yearsPharmaceutical industryGMPData integrity

Education:

Skills:Cross-functional collaborationConflict managementQuality solutionsCrisis managementLeadership

Tech Stack:ISO 9001GMPData Integrity

Company Brief

Julphar

Industry: Pharmaceuticals

Company Size: Enterprise (1,001+ employees)

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Ras Al Khaimah, United Arab Emirates

Founded: 1980

Website LinkedIn