Pharma QA Validation Specialist

Job Overview

Bausch Health Companies Inc. is seeking a Pharma QA Validation Specialist in Sharjah, United Arab Emirates. This role is crucial for ensuring the quality assurance and validation processes within their pharmaceutical manufacturing operations, contributing to the delivery of safe and effective healthcare products.

Company Overview

Bausch Health Companies Inc. (NYSE/TSX: BHC) is a global, diversified health care company that develops, manufactures and markets a range of products, primarily in gastroenterology, hepatology, neuroscience, dermatology, dentistry, aesthetics, international pharmaceuticals and eye health, through our controlling interest in Bausch + Lomb Corporation. Their ambition is to be a globally integrated healthcare company, trusted and valued by patients, HCPs, employees, and investors. With a global team of over 7,000 employees, Bausch Health is united by its purpose to enrich people’s lives through a relentless drive to deliver better health outcomes, developing, manufacturing, and marketing healthcare products directly or indirectly in approximately 100 countries.

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Qualifications: None / Open to all applicants
• Experience: 3 Year+

Key Responsibilities

• Develop and execute validation protocols for pharmaceutical equipment, processes, and systems.
• Ensure compliance with GxP regulations (GMP, GLP, GCP) and internal quality standards.
• Conduct risk assessments and root cause analysis for deviations and non-conformances.
• Prepare and review validation reports and documentation for regulatory submissions.
• Collaborate with production, engineering, and quality control teams to implement validation strategies.
• Participate in internal and external audits related to QA and validation activities.

Requirements

• Bachelor’s degree in Pharmacy, Chemistry, Engineering, or a related scientific field.
• Proven experience in QA validation within the pharmaceutical manufacturing industry.
• Strong understanding of GxP guidelines (e.g., FDA, EMA) and industry best practices.
• Proficiency in developing and executing validation master plans and protocols.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work independently and as part of a cross-functional team.

Benefits

• Opportunity to work with a leading global healthcare company.
• Contribute to the development of life-changing pharmaceutical products.
• Professional growth and career advancement opportunities.
• Competitive compensation package and comprehensive benefits.
• Engaging and supportive work environment.
• Exposure to international pharmaceutical standards and practices.