Julphar UAE Careers – Machine Operator Roles (Sterile, OSD & Packaging) and Team Leader – Sterile Value Stream (QA)
The pharmaceutical industry in the United Arab Emirates continues to expand rapidly, and Julphar (Gulf Pharmaceutical Industries), one of the most reputable and long-standing pharmaceutical manufacturers in the region, is currently recruiting for several specialized roles across sterile manufacturing, oral solid dosage (OSD) manufacturing, packaging operations, and sterile value stream quality assurance.
- Machine Operator – Sterile Manufacturing
- Machine Operator – Packaging Operations
- Machine Operator – OSD Manufacturing (Granulation, Compression, Coating)
- Machine Operator – Manufacturing Operations
- Team Leader – Sterile Value Stream (Quality Assurance)
Each role plays a critical part in maintaining Julphar’s standards of Good Manufacturing Practices (cGMP), sterility assurance, operational excellence, and manufacturing compliance. Whether you are aiming for a technical operator role or a leadership position in sterile value QA, this guide provides a detailed breakdown to help you understand the expectations and growth opportunities associated with each position.
⭐ 1. Machine Operator – Sterile Manufacturing (Aseptic Area)
Apply:
https://careers.julphar.net/job/Ras-Al-khaima-Machine-Operator/732702322/
https://careers.julphar.net/job/Ras-Al-khaima-Machine-Operator/732702122/
The Machine Operator – Sterile Manufacturing position is crucial for ensuring the aseptic production of sterile pharmaceuticals. This role requires deep knowledge of aseptic processing, strict adherence to gowning and behavior inside Class A/B areas, and the ability to execute sterile activities including liquid manufacturing, filtration, filling, and monitoring.
Key Responsibilities
A. Sterile Manufacturing Process (Core Tasks)
Machine Operators in sterile areas perform several highly critical activities:
- Liquid Manufacturing Process including solution preparation, mixing, and controlled handling.
- Aseptic Filtration ensuring microbial removal and product sterility.
- Aseptic Filling operations under strict aseptic guidelines.
- Aseptic Cleaning Activities following validated procedures.
B. Manufacturing-Related Activities
- Receiving raw materials and components for aseptic processing.
- Preparing disinfectants following dilution requirements.
- Executing dispensing activities with precise documentation.
C. Documentation & Compliance
Machine Operators must follow Good Documentation Practices (GDP) and ensure accuracy in:
- In-process logbooks.
- Cleaning logbooks.
- Batch Manufacturing Records (BMR).
- Reconciliation and yield calculations.
D. Incident Reporting
Timely reporting of any event impacting Safety, Quality, or Productivity.
E. Team Collaboration
- Supporting team leaders in process improvement.
- Working with colleagues to meet daily and monthly production targets.
F. Equipment Operation
Operators handle critical equipment such as:
- Filling machines
- Tunnels
- Washers
- CPM systems
- Environmental monitoring equipment
- Dry fog systems
G. Aseptic Qualifications
- Participation in Personal Gown Qualification
- Participation in Aseptic Process Simulations (APS / Media Fill)
Skills & Qualifications
- Technical Diploma with 6+ years experience in aseptic operations
- Experience in lyophilization is strongly preferred
- Deep knowledge of aseptic techniques, aseptic behavior, APS, and cleanroom classifications
- Excellent understanding of GMP, ALCOA+, EHS, and sterile compliance
- Basic microbiology knowledge
- Strong English and computer literacy
- Non-negotiable commitment to GMP and sterility assurance
This is a highly specialized role suited for professionals who have hands-on experience in sterile manufacturing, particularly within injectable, vial, liquid, or lyophilized product environments.
⭐ 2. Machine Operator – Packaging Operations
Apply: https://careers.julphar.net/job/Ras-Al-khaima-Machine-Operator/732268522/
Machine Operators in pharmaceutical packaging ensure efficient and compliant packaging operations, following GMP standards and SOP-driven instructions.
Key Responsibilities
A. Compliance & Hygiene
- Adhere to cGMP principles at all times
- Follow gowning procedures
- Maintain workplace hygiene and order
- Follow safety procedures to avoid accidents
B. Packaging Line Operations
- Prepare packaging machine and line per SOP
- Perform cleaning activities as per MPI and Master Packaging Instructions
- Ensure correct bulk and packaging materials
- Manage line clearance
- Perform packaging operations under the direction of Line Boss
C. Efficiency & Performance
- Track hourly line capacity
- Support maximum operational efficiency
- Maintain cleanliness between batches and at shift end
D. Communication
- Report mistakes or technical faults immediately
- Support line bosses and supervisors with operational insights
Skills & Qualifications
- Bachelor’s / Diploma / High School
- 2–3 years relevant experience
- Basic English skills
- Basic computer proficiency
- Knowledge of cGMP and GDP
- Strong discipline, accountability, and time management
This is an ideal role for candidates who want to grow into supervisory positions within pharmaceutical packaging and manufacturing areas.
⭐ 3. Machine Operator – OSD Manufacturing (Granulation, Compression, Coating)
Apply: https://careers.julphar.net/job/Ras-Al-khaima-Machine-Operator/732607722/
OSD (Oral Solid Dosage) manufacturing requires precision, equipment expertise, and compliance with batch instructions and GMP guidelines.
Key Responsibilities
A. Equipment Cleaning & Preparation
- Clean equipment and areas before use
- Assemble/disassemble machines following procedures
B. Documentation & QA Clearance
- Complete logbooks before QA clearance
- Verify materials (correct, released, within expiry)
- Maintain clean outer containers
C. Manufacturing Operations
- Weigh raw materials accurately
- Record dispensing details
- Perform granulation
- Operate RMG, FBD, Sifter, Compression, Coating machines
- Monitor machine parameters
- Adjust settings, startup, shutdown per plan
D. Documentation
- Complete in-process documentation
- Label containers with product name, lot number, weight
- Record scrap weights
E. Compliance
- Follow gowning procedures
- Report any deviations
Qualifications & Competencies
- Diploma/Bachelor’s degree
- Minimum 2 years experience in OSD manufacturing
- Strong understanding of granulation, compression, coating
- Excellent English skills
- Strong GMP knowledge
This position is perfect for those experienced in tablet/capsule manufacturing and seeking long-term growth in production roles.
⭐ 4. Machine Operator – Manufacturing Operations (General Manufacturing)
Apply: https://careers.julphar.net/job/Ras-Al-khaima-Machine-Operator/732486522/
This Machine Operator role covers broader manufacturing tasks including cleaning, equipment setup, documentation, compression, coating, and material handling.
Key Responsibilities
Manufacturing Preparation
- Clean all areas and equipment
- Assemble/disassemble equipment
- Complete logbooks for QA clearance
Material Verification
- Ensure materials are correct, present, and released
- Check outer container cleanliness
Weighing & Documentation
- Weigh materials and record details
- Prepare coating solutions
- Maintain accurate in-process documentation
Manufacturing Activities
- Perform compression and coating activities
- Label containers and track weights
- Record scrap data in batch loss tracking
- Ensure proper storage after processing
Compliance
- Follow gowning SOP
- Maintain cGMP at all times
Qualifications
- Diploma in Science/Industrial disciplines
- 2–4 years pharmaceutical experience
- Strong knowledge of cleaning chemicals, supply, GMP
- Proficient English communication
This role is suitable for individuals with broad OSD or general manufacturing experience aiming for stable growth in a structured production environment.
⭐ 5. Team Leader – Sterile Value Stream (Quality Assurance)
Apply:
https://careers.julphar.net/job/Ras-Al-khaima-Team-Leader-Sterile-Value-stream-%28QA%29/732616122/
One of the most critical senior QA roles, the Team Leader – Sterile Value Stream, oversees sterility assurance, contamination control strategy, and microbial monitoring programs. This role supports sterile production facilities and ensures compliance with global regulatory expectations.
Core Responsibilities
A. Sterility Assurance Leadership
- Implement sterility assurance programs
- Review gap and risk assessments for sterile operations
- Set product specifications and in-process controls
- Oversee gowning qualification and media fill participation
B. Deviation & CAPA Oversight
- Handle deviations, change controls, market complaints
- Execute CAPA related to sterile operations
- Conduct risk assessments and root cause analysis
C. Contamination Control Strategy
- Develop plant-wide microbial contamination strategies
- Ensure material/personnel flow in sterile areas is compliant
- Govern microbial monitoring controls for utilities, environment, and personnel
D. Regulatory Alignment
- Provide expertise during regulatory inspections
- Ensure compliance with FDA, EU GMP, and other standards
- Review rapid microbiology methods and new technologies
E. Collaboration & Governance
- Work closely with Operations QA Oversight team
- Support sterile manufacturing value stream teams
- Provide QA input for qualification and validation strategies
Qualifications
- Degree in Pharmacy / Life Sciences
- 10+ years pharmaceutical QA experience
- Strong experience in sterile manufacturing
- Expertise in microbiological monitoring, sterility testing, and Annex 1 principles
- Experience with global regulatory bodies (USFDA, EU, MHRA, etc.)
This role is ideal for experienced sterile QA professionals ready for leadership responsibilities in a GMP-regulated multinational environment.
⭐ Your Path to Joining Julphar UAE
Julphar offers several exciting opportunities for skilled Machine Operators across Sterile, OSD, and Packaging operations, as well as a senior leadership role in Sterile Value Stream QA. These jobs provide excellent prospects in one of the most advanced pharmaceutical environments in the Middle East, offering exposure to:
- cGMP
- Aseptic processing
- Sterile manufacturing
- OSD operations
- Packaging line management
- Quality Assurance & compliance
- Microbial monitoring
- Regulatory inspections
With strong technical knowledge, discipline, documentation skills, and a commitment to compliance, candidates can build strong careers within Julphar’s expanding operations.
