.png){kind=logo}
Sr. Specialist – Quality Assurance | Julphar
Company: Julphar
Position: Sr. Specialist – Quality Assurance
Industry: Pharmaceutical / Life Sciences
Experience: Minimum 5 Years
Qualification: Bachelor’s or Master’s Degree in Science / Pharmacy
Specialization: Quality Assurance / Quality Management Systems
Location: As per the official Julphar vacancy
Sr. Specialist – Quality Assurance Job Opportunity at Julphar
Julphar is inviting applications for the position of Sr. Specialist – Quality Assurance. This opportunity is suitable for experienced pharmaceutical and life-science professionals with a strong background in Quality Management Systems, cGMP, regulatory compliance and eQMS management.
The role will involve supporting and strengthening quality systems across Julphar's plants, with particular responsibility for Change Control, Product Complaints, Product Recall activities, quality performance monitoring and Quality Council reporting.
Job Highlights
| Particular | Details |
|---|---|
| Company | Julphar |
| Job Title | Sr. Specialist – Quality Assurance |
| Department | Quality Assurance |
| Industry | Pharmaceutical / Life Sciences |
| Experience | Minimum 5 Years |
| Qualification | Bachelor’s / Master’s in Science or Pharmacy |
| Key Area | Quality Management Systems |
| Key Skills | cGMP, eQMS, Change Control, Complaints, Product Recall, KPI, Statistical Analysis |
About Julphar
Julphar is focused on transforming its organizational culture while working toward its mission of providing a better quality of life for families through high-quality healthcare solutions.
The organization emphasizes values such as:
Respect
Collaboration
Innovation
Integrity
Compassion
Julphar also highlights diversity, inclusion and equal opportunities as important elements of its workplace culture.
The company's focus is on delivering quality healthcare solutions while creating a supportive environment for employees and encouraging research, innovation and professional development.
Job Responsibilities
The selected candidate will be responsible for supporting and maintaining pharmaceutical quality systems and ensuring compliance with applicable GMP requirements.
1. cGMP Compliance
Adhere to established current Good Manufacturing Practices (cGMP) principles.
Support the effective implementation and maintenance of GMP requirements.
Ensure quality activities are performed in accordance with applicable procedures and regulatory expectations.
2. Change Control Management
The position will be responsible for leading and organizing Change Control activities.
Key responsibilities include:
Coordinating Change Control activities.
Monitoring the progress of Change Controls.
Following up with relevant departments for timely completion.
Supporting effective implementation of approved changes.
Ensuring appropriate documentation and tracking of quality changes.
3. Product Complaints & Recall Management
The role will also involve managing activities related to Product Complaints and Product Recall.
Responsibilities include:
Leading and organizing the Complaints / Product Recall group.
Following up on complaints and product recall activities.
Coordinating activities across Julphar plants.
Ensuring quality-related actions are appropriately tracked and completed.
Supporting compliance with applicable procedures and regulatory requirements.
4. Quality Performance & KPI Reporting
The candidate will be responsible for providing quality data for Key Performance Indicators (KPIs) and Quality Council activities.
This may include:
Collecting relevant quality data.
Monitoring quality-system performance.
Preparing KPI information.
Supporting Quality Council compilation.
Reviewing quality trends and performance indicators.
Identifying areas requiring improvement.
5. System Development & Performance Analysis
The role involves developing and supporting user-friendly quality systems and analyzing their performance.
The selected professional may be involved in:
Improving quality-system processes.
Supporting user-friendly system development.
Monitoring system performance.
Analyzing quality-related data.
Identifying opportunities for continuous improvement.
Educational Qualification
Candidates should possess either:
Bachelor’s Degree or Master’s Degree in:
Science
Pharmacy
Related Life Science discipline
A qualification in Pharmacy or a relevant Science/Life Science field may be particularly suitable for this position.
Experience Required
Minimum 5 years of professional experience in the Life Sciences industry is required.
Experience in Quality Management Systems (QMS) is preferred.
Candidates with proven experience in eQMS management will be particularly relevant for this opportunity.
Technical Knowledge & Skills
The ideal candidate should have strong knowledge of:
cGMP
Pharmaceutical Quality Systems
Quality Management Systems
eQMS
Change Control
Product Complaints
Product Recall
Quality KPIs
Quality Council reporting
Regulatory Guidelines
Statistical Analysis
Data Analysis
Microsoft Office
Strong knowledge of applicable GMP and regulatory guidelines is an important requirement for the position.
Key Competencies
The successful candidate should demonstrate:
Strong quality and compliance mindset.
Good analytical and problem-solving skills.
Ability to manage multiple quality-system activities.
Strong follow-up and coordination skills.
Good communication and teamwork abilities.
Ability to analyze quality data and performance.
Good understanding of pharmaceutical quality systems.
Ability to work collaboratively with cross-functional teams.
Attention to detail and commitment to compliance.
Who Should Apply?
This position may be suitable for experienced professionals working in:
Quality Assurance | Quality Management Systems | Pharmaceutical Quality | eQMS | Change Control | Product Complaints | Product Recall | GMP Compliance
Professionals with 5+ years of experience in the pharmaceutical or life-science industry, particularly those with hands-on experience in QMS and eQMS management, should consider this opportunity.
Why Consider This Opportunity?
The position provides an opportunity to work in a quality-focused pharmaceutical environment with responsibilities covering multiple important areas of the Quality Management System.
Professionals can gain exposure to:
Global quality systems
Change Control management
Product Complaint management
Product Recall processes
eQMS
Quality KPIs
Quality Council activities
cGMP compliance
Regulatory requirements
Quality-system improvement
How to Apply
Interested and eligible candidates should visit the official Julphar website and check the current career opportunities for the Sr. Specialist – Quality Assurance position.
https://careers.julphar.net/job/Ras-Al-khaima-Sr_-Specialist-Quality-Assurance/733376722/
Candidates are advised to verify the current vacancy, eligibility requirements, job location and application procedure through the official Julphar recruitment channel before applying.
⚠️ Disclaimer
This job information is published by Helbert Solutions for educational and career-information purposes. Helbert Solutions is not the employer or recruitment agency for this vacancy and does not guarantee selection or employment.
Job details may be updated or changed by the employer. Candidates should independently verify the latest vacancy information through the official Julphar website before submitting their application or personal information.
