Team Lead -Deviation & CAPA

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Last checked: 22 hours agoStatus: Live

Job Summary

Lead and oversee the Quality Assurance Compliance team to ensure company operations meet cGMP, GDP, ISO, and regulatory requirements. Own quality system oversight including QMS implementation and continuous improvement, supervise deviation/market complaint/CAPA review and closure, and manage compliance KPIs and management reviews. Plan and lead internal audits and support regulatory/customer inspections, ensuring CAPAs are implemented effectively. Supervise controlled document governance, train staff on GMP/compliance, and drive risk management and data integrity (ALCOA+) across quality systems, while meeting ISO 14001 and HSE responsibilities.

Location: United Arab Emirates

Workplace: Onsite

Employment Type: Full time

Job Function: Administration & Executive Assistance

Seniority: Manager level

Key Responsibilities

•Lead and manage daily QA compliance operations and ensure adherence to company and regulatory requirements.
•Oversee implementation, maintenance, and continuous improvement of the Quality Management System (QMS).
•Supervise review and closure of deviations, market complaints, and CAPAs; analyze and trend quality system data and report via compliance KPIs and management reviews.
•Plan, coordinate, and lead internal audits/self-inspections; prepare for regulatory and customer audits and coordinate responses to findings.
•Supervise control/review/approval of SOPs and controlled documents, ensure GDP and document lifecycle compliance, and lead staff training on GMP/compliance while supporting risk management and continuous improvement.

Key Requirements

•Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biology, Biotechnology, or a related field.
•Minimum 5–10 years of Quality Assurance/Compliance experience in pharma or biotech, including 2–3 years in a supervisory/team leadership role.
•Comprehensive understanding of GMP, GDP, and ISO 9001 plus ISO 14001 requirements.
•Strong familiarity with regulatory guidelines (FDA, WHO, EU).
•Experience with audits, CAPA, risk management, and QMS systems; plus strong leadership, communication, and analytical/problem-solving skills.

Experience:5-10 yearsPharmaceuticalBiotechnology

Education:Bachelor's in Pharmacy, Chemistry, Biology, Biotechnology (or related field)

Skills:LeadershipTeam managementCommunicationCoordinationAnalytical thinking

Certifications:ISO 14001:2015

Tech Stack:CGMPGDPISOISO 9001ISO 14001ISO 14001:2015ALCOA+FDAWHOEUMS OfficeElectronic QMS platforms

Company Brief

Julphar

Website

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Julphar

2 days ago

Team Lead -Deviation & CAPA

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 22 hours agoStatus: Live

Job Summary

Location: United Arab Emirates

Workplace: Onsite

Employment Type: Full time

Job Function: Administration & Executive Assistance

Seniority: Manager level

Key Responsibilities

•Lead and manage daily QA compliance operations and ensure adherence to company and regulatory requirements.
•Oversee implementation, maintenance, and continuous improvement of the Quality Management System (QMS).
•Supervise review and closure of deviations, market complaints, and CAPAs; analyze and trend quality system data and report via compliance KPIs and management reviews.
•Plan, coordinate, and lead internal audits/self-inspections; prepare for regulatory and customer audits and coordinate responses to findings.
•Supervise control/review/approval of SOPs and controlled documents, ensure GDP and document lifecycle compliance, and lead staff training on GMP/compliance while supporting risk management and continuous improvement.

Key Requirements

•Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biology, Biotechnology, or a related field.
•Minimum 5–10 years of Quality Assurance/Compliance experience in pharma or biotech, including 2–3 years in a supervisory/team leadership role.
•Comprehensive understanding of GMP, GDP, and ISO 9001 plus ISO 14001 requirements.
•Strong familiarity with regulatory guidelines (FDA, WHO, EU).
•Experience with audits, CAPA, risk management, and QMS systems; plus strong leadership, communication, and analytical/problem-solving skills.

Experience:5-10 yearsPharmaceuticalBiotechnology

Education:Bachelor's in Pharmacy, Chemistry, Biology, Biotechnology (or related field)

Skills:LeadershipTeam managementCommunicationCoordinationAnalytical thinking

Certifications:ISO 14001:2015

Tech Stack:CGMPGDPISOISO 9001ISO 14001ISO 14001:2015ALCOA+FDAWHOEUMS OfficeElectronic QMS platforms

Company Brief

Julphar

Website