16 Manufacturing jobs in Ras Al Khaimah

he Lean Manufacturing Engineer is responsible for implementing and driving continuous improvement initiatives within the production environment. This role focuses on optimizing processes, reducing waste, and improving efficiency through Lean principles and methodologies. The engineer works closely with cross-functional teams, including production, quality, supply chain, and engineering, to enhance overall operational performance.

Key Responsibilities:

Process Optimization: Analyze current manufacturing processes and identify areas for improvement using Lean tools such as 5S, Kaizen, Value Stream Mapping (VSM), and Kanban.

Waste Reduction: Implement strategies to eliminate waste (TIMWOODS: Transportation, Inventory, Motion, Waiting, Overproduction, Overprocessing, Defects, and Skills) and increase efficiency.

Continuous Improvement: Lead Kaizen events and root cause analysis (RCA) sessions to drive sustainable improvements.

Standard Work & SOPs: Develop and maintain Standard Operating Procedures (SOPs) and work instructions to ensure process consistency.

Production Support: Work closely with operators and production managers to resolve bottlenecks and improve workflow.

Performance Metrics: Define and monitor Key Performance Indicators (KPIs) such as cycle time, Overall Equipment Effectiveness (OEE), First Pass Yield (FPY), and defect rates.

Training & Coaching: Educate and train employees on Lean methodologies and foster a culture of continuous improvement.

Cross-functional Collaboration: Partner with engineering, quality, and supply chain teams to integrate Lean principles into product development and production planning.

Automation & Digitalization: Identify opportunities for Industry 4.0 solutions, such as digital work instructions, IoT-enabled process monitoring, and real-time data analytics.

Required Qualifications & Skills:

Education: Bachelor's degree in industrial engineering, Mechanical Engineering, Manufacturing Engineering, or a related field.

Experience: 2-5 years of experience in a Lean Manufacturing or Continuous Improvement role.

Technical Skills:

Proficiency in Lean Manufacturing, Six Sigma (Green Belt preferred), and Kaizen methodologies.

Familiarity with ERP systems (SAP, Oracle, etc.) and PLM/PDM systems.

Experience with AutoCAD, SolidWorks, or similar design tools (optional).

Knowledge of statistical analysis tools (Minitab, JMP) and data visualization (Power BI, Tableau).

Soft Skills:

Strong problem-solving and analytical abilities.

Excellent communication and leadership skills.

Ability to work in a fast-paced, dynamic environment.

Preferred Qualifications:

Lean Six Sigma Black Belt certification.

Experience in high-mix, low-volume manufacturing environments.

Knowledge of ISO 9001, ISO 14001, or IATF 16949 standards.

Background in automotive, aerospace, or marine manufacturing.

The Planning and Order Management Solutions Analyst plays a pivotal role in leading planning and global order promising initiatives within a fast-paced manufacturing environment. Their primary responsibility is to ensure seamless integration between planning systems and order fulfillment processes, driving digital transformation forward.

This position offers the unique opportunity to work remotely from any country where our company has an established office.

• Implement, configure, and support Oracle Fusion Planning and Global Order Promising modules to optimize business performance.
• Design and optimize planning processes, including demand planning, supply planning, and production scheduling, to meet evolving business needs.
• Configure GOP rules, sourcing strategies, and ATP logic to align with manufacturing constraints and fulfillment goals, ensuring efficient operation.
• Collaborate closely with manufacturing, procurement, and logistics teams to achieve end-to-end visibility and alignment.
• Translate business requirements into functional specifications and system configurations to drive successful outcomes.
• Oversee system upgrades, patching, and performance tuning to maintain optimal system performance.
• Act as a subject matter expert, mentoring colleagues and building knowledge across the organization.
• Develop reports, dashboards, infolets, alerts, OTBI, and visualizations to support business needs and inform strategic decisions.

• Experience with Oracle Fusion Supply Chain modules, specifically Planning (Supply, Demand, S&OP), Production Scheduling, and GOP, is essential for success.
• A minimum of one full end-to-end Oracle Fusion implementation in a manufacturing environment is required.
• Proven track record of delivering Oracle Fusion-driven transformations in complex manufacturing operations is highly valued.
• Deep knowledge of Oracle GOP configurations, sourcing rules, ATP logic, and fulfillment workflows is necessary for this role.
• Experience with Oracle Supply Planning Cloud, Production Scheduling, GOP, Demand Management, and Inventory is desirable.
• Strong analytical, problem-solving, and process improvement skills are essential for this position.

Our team seeks a highly motivated and detail-oriented Quality Assurance Specialist to maintain effective quality control throughout in-process production and packaging activities for biotech and sterile products. The ideal candidate will ensure adherence to cGMP principles, investigate deviations, and support corrective and preventive actions.

• cGMP Principles Enforcement

  Enforce strict compliance with cGMP guidelines in all in-process quality checks and activities, maintaining the highest standards of quality and safety.

• Deviation Investigation and Corrective Action

  Investigate deviations and support corrective and preventive actions, ensuring prompt resolution and minimization of disruption to production.

• Media Fills and Process Compliance

  Participate in media fills and ensure process compliance during production and packaging, guaranteeing the highest level of product quality.

• Process Review and Compliance

  Review processes and procedures to ensure strict compliance, identifying areas for improvement and implementing necessary changes.

• Regulatory Audits

  Participate in internal and external regulatory audits, demonstrating our commitment to quality and compliance.

• In-Process Quality Checks

  Perform in-process quality checks according to SOPs, recording results accurately and in a timely manner.

• Material Inspection and Record Keeping

  Inspect incoming materials, maintaining accurate records and performing necessary tests to ensure product quality.

• Quality Data Entry and Reporting

  Input quality data into the SAP system and assist in preparing Annual Product Quality Review reports, providing valuable insights for continuous improvement.

• Equipment Calibration and Maintenance

  Ensure calibration and proper functioning of in-process check equipment, guaranteeing accurate results and minimizing downtime.

• Line Clearance and Material Verification

  Conduct line clearance checks and verify materials required for manufacturing steps, ensuring seamless production and packaging processes.

• Record Keeping and Testing

  Maintain accurate records and perform necessary tests, providing a clear audit trail and supporting regulatory compliance.

Factory line worker vacancy in Ras-al-Khaimah UAE. Attention This vacancy is temporarily suspended Vacancy opening in our company cross rail construction company.

• Description of work: collection of orders by invoices, packaging and sticking of goods in warm and cold warehouses.
• Additional factory line worker duties in Ras-al-Khaimah and related postings.

• Good physical form
• Documents required: International Passport Copy, Passport Photograph, Resume Copy, Online Application form payment receipt

• Telegram link:
• Telegram number:
• Email: (emailprotected)

• United Kingdom job opening notice: NEW COMPANY OPENING IN UNITED KINGDOM; All nationalities can apply; United Kingdom 18-65; visa paid; etc. (as listed in original)
• Urgent recruiting to Canada serious candidates needed
• Subscribe to our telegram channel @layboard_in
• WAREHOUSE WORKER | CZECH REPUBLIC | Without work experience | for all foreign citizens
• Warehouse - Logistics - Customs
• FOOD warehouses: We DON'T have sponsorship program, DON'T have free services. City of Prague Description of work: collection of orders, packaging and other warehouse duties
• PACKAGING OF SWEETS | POLAND | Without work experience | for all foreign citizens
• PACKAGING OF SWEETS. LINE OPERATOR: address and city of work: Skarbimierz
• We need urgent workers here in our new company opening; all nationalities can apply now, both male and female

This is a vacancy for an entry-level factory worker position in Ras-al-Khaimah, UAE. Please note that this job posting is temporarily suspended.

• The selected candidate will be responsible for collecting orders by invoices, packaging goods in warm and cold warehouses.
• Additional duties may include handling tasks related to factory operations in Ras-al-Khaimah and other locations.

• Candidates must possess good physical health.
• Required documents include an International Passport Copy, Passport Photograph, Resume Copy, and Online Application form payment receipt.

Candidates can apply via the provided Telegram link or email address.

• A job opening notice for the United Kingdom lists requirements and details for applicants.
• There is an urgent recruiting need in Canada for serious candidates.
• Applicants are encouraged to subscribe to our telegram channel for updates.
• Available positions include Warehouse work in the Czech Republic with no prior experience required.
• Other available jobs involve Packaging of Sweets in Poland and Logistics roles.

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.

Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

The Quality Control (QC) Manager at Julphar HQ is a strategic leadership role responsible for managing the overall Quality Control operations, ensuring adherence to regulatory standards (GMP/GLP) and internal quality policies. The role oversees both Chemical and Microbial laboratories , ensuring all materials and products meet approved specifications, regulatory requirements, and internal standards of excellence.

The QC Manager is responsible for managing ongoing commercial stability programs, regulatory compliance, laboratory operations, documentation, and investigations. This role plays a critical part in maintaining product quality, safety, and data integrity , and contributes to the continuous improvement of quality systems and cross-functional collaboration.

• Ensure the quality of raw materials, packaging materials, and finished products is in strict compliance with approved specifications and GMP/GLP standards.
• Lead, manage, and oversee operations in both the Chemical and Microbial QC laboratories, ensuring timely and accurate testing in accordance with protocols, GMP, and safety regulations.
• Oversee and execute commercial stability programs (ongoing/commitment) in compliance with regulatory expectations.
• Review and approve SOPs, protocols, and reports (including method validation, method transfers, process validation, and stability studies).
• Approve chemical and microbiological analysis reports and analytical batch records.
• Ensure timely completion and closure of investigations (OOS, OOT, deviations) in compliance with SOPs and regulatory expectations.
• Lead and manage all laboratory investigations, implementing appropriate CAPAs.
• Ensure data integrity compliance in all QC processes, as per current regulatory and company protocols.
• Update procedures and quality practices to remain aligned with evolving cGMP and regulatory guidelines.
• Provide technical support to internal and external audits and ensure effective closure of audit observations.
• Support cross-functional departments (R&D, Regulatory Affairs, Production, Compliance, etc.) in achieving organizational objectives.
• Manage quality systems within the QC department including Change Controls, Deviations, CAPAs, and Self-Inspections, using the AmpleLogic EQMS system.
• Oversee training and development of QC staff; conduct onboarding and continuous training to ensure competency and compliance.
• Participate in the preparation of department budgets and monitor resource allocation and spending.
• Continuously analyze and improve QC processes to increase operational efficiency, reduce errors, and enhance product quality.
• Ensure full adherence to cGMP practices and promote a strong culture of quality and compliance.

• Leadership & Collaboration Proven leadership skills with the ability to manage multi-disciplinary teams and collaborate with cross-functional departments to align on quality goals.
• Strategic Thinking & Quality Culture Strong analytical and strategic mindset, with the ability to influence and drive transformation of quality culture at the organizational level.
• Decision-Making & Problem-Solving Solution-oriented with the ability to make sound scientific and compliance-based decisions under pressure.
• Project & Performance Management Experienced in managing multiple priorities, delivering results, and driving continuous improvement initiatives.
• Technical & Regulatory Expertise In-depth understanding of regulatory guidelines (e.g., GMP, GLP), data integrity principles, and audit readiness, with strong documentation and reporting skills.
• Communication & Interpersonal Skills Excellent verbal and written communication skills with strong interpersonal abilities to effectively engage with stakeholders at all levels.

• Education: Bachelor's degree in Pharmacy (Master's preferred).
• Experience: Minimum of 10 years in Quality Control within the pharmaceutical industry, with at least 3–5 years in a managerial or leadership role.
• Regulatory Knowledge: Deep understanding of cGMP, GLP, ICH guidelines, and other applicable regulatory requirements.
• Systems & Tools: Experience with EQMS systems (e.g., AmpleLogic), SAP, and data integrity practices.
• Leadership: Proven ability to manage complex, cross-functional teams and resolve operational challenges.
• Audit Experience: Hands-on experience with regulatory inspections and implementing effective post-audit action plans.

• Lean Six Sigma or equivalent quality/process improvement certification (preferred).
• Training in data integrity, regulatory inspection management, and risk-based quality systems.
• Strong business acumen and cost-conscious mindset.

We value people from different backgrounds.

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism. Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents, create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

• Perform testing of sterile samples including Sterility, LBPC (Limulus-Based Pyrogen Test), and BET (Bacterial Endotoxin Test) with proper documentation.
• Conduct testing of non-sterile samples, such as Microbial Limit Test (MLT) and Bioburden, along with accurate record-keeping.
• Perform microbiology assay testing and document results in compliance with GMP.
• Carry out microbiology culture testing including maintenance, sub-culturing, Growth Promotion Testing (GPT), and microbial identification.

• Perform water testing, release analysis, and related documentation.
• Conduct environmental monitoring in classified areas across Julphar production plants and microbiology labs, ensuring accurate and timely documentation.

• Execute various microbiology lab support activities including equipment monitoring, cleaning validations, and media preparation.
• Monitor equipment and area temperatures using Vaisala/SIRIUS systems.
• Ensure real-time documentation and compliance for all assigned tasks.
• Handle sample and result entries, reservation creation, and notification processes in SAP.

• Adhere strictly to Good Laboratory Practices (GLP), Data Integrity, and Good Documentation Practices (GDP).
• Prepare and review Standard Operating Procedures (SOPs) and support microbiology-related qualification/validation documentation.
• Participate in internal and external audits and promptly report any deviations, OOS (Out of Specification), OOL (Out of Limit), or excursions.
• Manage documentation and deviation handling through eQMS (Amplelogic system).

• Follow all safety protocols and ensure a clean and compliant laboratory environment.
• Ensure full compliance with company policies, GMP, and regulatory guidelines.

• Strong sense of accountability and ownership
• Highly disciplined, motivated, and well-organized
• Excellent process compliance and implementation skills
• Effective time and task management
• Proficient English communication skills (verbal and written)

• Bachelor's or Master's Degree in Microbiology or other Biological Sciences
• 4–6 years of relevant experience in a pharmaceutical microbiology lab (preferably in sterile and non-sterile product testing)
• Proficient in computer applications including MS Word, Excel, and PowerPoint
• Familiarity with SAP, eQMS (Amplelogic), and temperature monitoring systems like Vaisala/SIRIUS is a plus

We value people from different backgrounds. Could this be your story? Apply today or visit to read more about us and the journey of Julphar

The Process Lead oversees quality control processes and projects, ensuring products meet standards and regulatory requirements.

• Optimizing processes
• Leading a team of professionals

This role involves developing, implementing, and maintaining QC processes, analyzing current processes to propose improvements, coordinating with cross-functional teams, conducting audits and inspections, leading and mentoring staff, analyzing quality data, preparing reports, and ensuring adherence to industry regulations and standards.

• Quality control management
• Process optimization
• Leadership and teamwork

This role offers a dynamic work environment, opportunities for growth and development, and the chance to make a meaningful impact in the field of quality control.