265 Quality Control Analyst jobs in Saudi Arabia

Quality Control Analyst

SAR120000 - SAR180000 Y ITT Inc.

Posted today

Job Viewed

Tap Again To Close

Job Description

About ITT::

At ITT, we have a clear purpose as an organization – to provide our customers with cutting-edge solutions to help solve their most critical needs across key global end markets. Our continuous improvement mindset drives our commitment to evolving our capabilities as a multi-industrial technology, manufacturing and engineering leader. With a strong global footprint of more than 100 facilities, we are well positioned to solve critical challenges for our customers around the world. Our locations include manufacturing facilities and global service capabilities in 35 countries. Through these worldwide operations and building on our heritage of innovation, our approximately ~11,000 team members partner with our customers to deliver enduring solutions that make a lasting difference and help the world move forward. ITT is headquartered in Stamford, CT, with sales in approximately 125 countries. The company generated 2024 revenues of $3.6 billion.

  • Motion Technologies: (Revenue of $.4B; headcount of ~ 4,000; operates in 13 countries) manufactures brake components and specialized sealing solutions, shock absorbers and damping technologies primarily for the global automotive, truck and trailer, public bus and rail transportation markets.
  • Industrial Process: (Revenue of 1.4B; headcount of ~3,400; operates in 30 countries) manufactures engineered fluid process equipment serving a diversified mix of customers in global industries such as chemical, energy, mining, and other industrial process markets and is a provider of plant optimization and efficiency solutions and aftermarket services and parts.
  • Connect and Control Technologies: (Revenue of 0.8B; headcount of ~ 3,800; operates in 10 countries) manufactures harsh-environment connector solutions, critical energy absorption, flow control components, and composite materials for the aerospace and defense, general industrial, medical, and energy markets.

Essential Responsibilities:

  • Manage vendor quality documents & review as per international standard (ASTM, ASME, ISO, API.).
  • Prepare quality documents (ITP, Test Procedure) as per customer specification Requirements.
  • Handling Customer's representative (TPI) and perform witness inspection.
  • Handling IMS– Internal & External Audit and Customer audit.
  • Participate pre-inspection meeting with customer & vendor facilities.
  • Review of supplier ITP & Test procedure as per project needs
  • Monitoring & Handling Instrument / Gauges calibration.
  • Involves in supplier audit program.
  • Finalize the Quality dossier as per approved Inspection and Test plan and submit to customer as per scheduled time.
  • Follows company safety policies and procedures while ensuring quality work.
  • Reconcile and review all final inspection documentation for shipments.
  • Review customer & internal purchase orders for quality requirement flow downs

Position Requirements:

Education: BSME minimum

Experience: Minimum Seven years dealing with QA for pumps and other related rotating equipment

Other Skills/Knowledge/Experience:

  • Technical Capacity (Read and understand drawing/specification)
  • Organizational Skills (Stay organized in a high pace work environment)
  • Problem Solving/Analytical (Work with engineering teams to solve non-conformances as well as participate in continuous improvement and kaizen events)
  • Time Management (Manage time well to ensure productivity goals are achieved)
  • Teamwork (Willing to work with production and fellow inspectors to ensure good workflow)
This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst

SAR60000 - SAR120000 Y Pfizer

Posted today

Job Viewed

Tap Again To Close

Job Description

Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

What You Will Achieve
In this role, you will:

  • Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles.
  • Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials.
  • Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies.
  • Ensure training records are updated and correctly filed to reflect current testing capabilities.
  • Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.
  • Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
  • Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
  • Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
  • Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.
  • Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.

Here Is What You Need (Minimum Requirements)

  • Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
  • Demonstrated technical skills in method validation and testing
  • Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
  • Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
  • Excellent organizational skills and strong ability to multi-task
  • Strong written and verbal communication skills
  • Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation

Bonus Points If You Have (Preferred Requirements)

  • Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques
  • Proven track record in leading continuous improvement projects
  • Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
  • Strong problem-solving skills and attention to detail
  • Ability to manage multiple priorities and meet deadlines.
  • Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
  • Adaptability and willingness to learn new techniques and procedures

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Quality Assurance and Control

This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst - Contract

Pfizer

Posted today

Job Viewed

Tap Again To Close

Job Description

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

What You Will Achieve

  • Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles.
  • Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials.
  • Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies.
  • Ensure training records are updated and correctly filed to reflect current testing capabilities.
  • Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.
  • Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
  • Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
  • Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
  • Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.
  • Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.

Here Is What You Need (Minimum Requirements)

  • Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
  • Demonstrated technical skills in method validation and testing
  • Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
  • Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
  • Excellent organizational skills and strong ability to multi-task
  • Strong written and verbal communication skills
  • Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation

Bonus Points If You Have (Preferred Requirements)

  • Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques
  • Proven track record in leading continuous improvement projects
  • Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
  • Strong problem-solving skills and attention to detail
  • Ability to manage multiple priorities and meet deadlines.
  • Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
  • Adaptability and willingness to learn new techniques and procedures

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

#J-18808-Ljbffr
This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst - Contract

Pfizer

Posted 11 days ago

Job Viewed

Tap Again To Close

Job Description

Quality Control Analyst - Contract page is loaded# Quality Control Analyst - Contractlocations: Saudi Arabia - KAEC PGS Planttime type: Vollzeitposted on: Heute ausgeschriebenjob requisition id: **Use Your Power for Purpose**Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.**What You Will Achieve**In this role, you will:* Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles.* Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials.* Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies.* Ensure training records are updated and correctly filed to reflect current testing capabilities.* Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.* Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.* Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.* Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.* Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.* Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.**Here Is What You Need (Minimum Requirements)*** Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience* Demonstrated technical skills in method validation and testing* Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations* Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.* Excellent organizational skills and strong ability to multi-task* Strong written and verbal communication skills* Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation**Bonus Points If You Have (Preferred Requirements)*** Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques* Proven track record in leading continuous improvement projects* Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis* Strong problem-solving skills and attention to detail* Ability to manage multiple priorities and meet deadlines.* Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels* Adaptability and willingness to learn new techniques and proceduresWork Location Assignment: On Premise#LI-PFEPfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Quality Assurance and ControlKarrieren bei Pfizer sind einzigartig. In unserer Kultur der individuellen Verantwortung glauben wir an unsere Fähigkeit, die Zukunft der Gesundheitsversorgung zu verbessern und an unser Potenzial, viele Millionen Leben zum Besseren zu wandeln. Wir suchen stets nach neuen Talenten für unsere globale Gemeinschaft, um gemeinsam neue innovative Therapien zu entwickeln, die die Welt zu einem gesünderen Ort machen.
#J-18808-Ljbffr
This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst - Contract

Pfizer

Posted today

Job Viewed

Tap Again To Close

Job Description

Quality Control Analyst - Contract page is loaded# Quality Control Analyst - Contractlocations: Saudi Arabia - KAEC PGS Planttime type: Vollzeitposted on: Heute ausgeschriebenjob requisition id: **Use Your Power for Purpose**Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.**What You Will Achieve**In this role, you will:* Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles.* Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials.* Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies.* Ensure training records are updated and correctly filed to reflect current testing capabilities.* Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.* Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.* Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.* Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.* Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.* Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.**Here Is What You Need (Minimum Requirements)*** Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience* Demonstrated technical skills in method validation and testing* Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations* Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.* Excellent organizational skills and strong ability to multi-task* Strong written and verbal communication skills* Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation**Bonus Points If You Have (Preferred Requirements)*** Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques* Proven track record in leading continuous improvement projects* Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis* Strong problem-solving skills and attention to detail* Ability to manage multiple priorities and meet deadlines.* Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels* Adaptability and willingness to learn new techniques and proceduresWork Location Assignment: On Premise#LI-PFEPfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Quality Assurance and ControlKarrieren bei Pfizer sind einzigartig. In unserer Kultur der individuellen Verantwortung glauben wir an unsere Fähigkeit, die Zukunft der Gesundheitsversorgung zu verbessern und an unser Potenzial, viele Millionen Leben zum Besseren zu wandeln. Wir suchen stets nach neuen Talenten für unsere globale Gemeinschaft, um gemeinsam neue innovative Therapien zu entwickeln, die die Welt zu einem gesünderen Ort machen. #J-18808-Ljbffr
This advertiser has chosen not to accept applicants from your region.

Regulatory Compliance Officer

SAR40000 - SAR120000 Y confidential

Posted today

Job Viewed

Tap Again To Close

Job Description

Main Duties and Responsibilities:


• Solving and advising on issues related to the day-to-day tasks of compliance.


• To raise the awareness of the employees of companies and financial institutions in relation to the regulations.


• To clarify the received circulars/regulations from SAMA or CMA etc.


• To review policies/procedures/change requests from compliance point of view.


• Assist the business to obtain regulatory approvals where required by evaluating or initiating investigation procedures as required.


• Maintain a regulatory inventory of all compliance breaches.


• Investigate and establish effective corrective actions.


• Prepare/develop action/corrective plans and ensure that all requirements received are included.


• Ensure that all requirements in the action/corrective plans are delivered before/within the target date.


• Develop and implement a system/process for managing compliance within the Corporate Business and Financial Institution.


• Acts as an independent review and assessment body to ensure that compliance issues and concerns within the business and financial institution are appropriately assessed, investigated and resolved.


• Monitor changes (external & internal) and adapt the compliance program and processes accordingly.


• Timely implementation of corrective action plans by following up with stakeholders within/outside the business and financial institution and maintaining a compliance tracker without missing any deadlines to proactively identify risks and impacts due to changes in regulatory requirements/environment.


• Develops and implements corrective action plans to resolve problematic issues.


• Provides general guidance on how to avoid or deal with similar situations in the future.


• Monitor the compliance risk register related to the business of the company and the financial institution.


• Timely and high-quality reporting of compliance issues to the Manager of Regulatory Compliance.


• Provide Corporate Business and Financial Institution and Compliance Division with a report as required showing the progress in products and services.


• Provide Compliance Division with a weekly and monthly report showing the issues in Corporate Business and Financial Institution Divisions.


• Ensure proper reporting of breaches or potential breaches to the Compliance Team for reporting to management and regulatory reporting.


• Provide guidance and assistance in responding to SAMA.


• Regulatory inquiries related to issues.


• Maintains an effective compliance communication program for the business and the financial institution, including promotion of the organization:


• Awareness of applicable laws and regulations


• Increased awareness of new policies and procedures.


• Understanding of emerging and existing compliance issues and related policies and procedures.


• Ensuring that the compliance program is up to date and addresses the compliance risks associated with the corporate business and financial institution.

This advertiser has chosen not to accept applicants from your region.

Senior Regulatory Compliance Manager

Riyadh, Riyadh Arthur Lawrence

Posted 7 days ago

Job Viewed

Tap Again To Close

Job Description

Arthur Lawrence is urgently looking for a Senior Regulatory Compliance Manager for a client in Riyadh, KSA.

  • Kindly review the Job requirements below.

Your immediate application will enable us to place you successfully.

Must-Have : 10+ years of experience in a regulatory compliance, legal, or risk management role within financial services or fintech.

Strong knowledge of Saudi financial regulatory frameworks (SAMA), particularly Consumer Protection regulations.

Experience working closely with product, engineering, and legal teams in a fast-paced, agile environment.

Proven ability to interpret regulatory requirements and design practical compliance solutions.

Excellent communication and stakeholder management skills, including experience interfacing with regulators or banking partners.

Ability to work independently, make sound decisions, and manage competing priorities.

Nice to have : Bachelors degree in Business Administration, Law, Finance, or Accounting Certifications in CRCM, CAMS, CRCMP, or PMP preferred About Us : Arthur Lawrence is a management and technology consulting firm providing enterprise-wide business transformation and business applications implementation services.

Our in-depth technical knowledge and broad experience of working with world-class companies enables organizations to leverage our capabilities in developing winning strategies and cost-effective solutions.

We are an UN Women Empowerment Principal Signatory and are certified from National Minority Supplier Development Council.

Acknowledgements from Industry Peers : Winner of Entrepreneur 360 Award (2019).

IAOP Award; Ranked in top 100 internationally.

Arthur Lawrence ranked within the Inc 5000 twice in 2016 and 2017 as one of the fastest.

Growing companies of America.

Named one of the top ten fastest growing businesses in Houston in 2016.

Ranked 25th in the HBJ s Fast 100 Private Companies Award in 2017.

Our Seven Pillars : We rely on the seven core values that we believe enable us to deliver quality for our consultants and clients : Education, Integrity, Value Creation, Collaboration, Best Client, Best People and Stewardship Through strict adherence to these core values, we have achieved success beyond all documented forecasts and anticipation.

#J-18808-Ljbffr
This advertiser has chosen not to accept applicants from your region.
Be The First To Know

About the latest Quality control analyst Jobs in Saudi Arabia !

Senior Regulatory Compliance Manager

Riyadh, Riyadh Arthur Lawrence

Posted today

Job Viewed

Tap Again To Close

Job Description

Arthur Lawrence is urgently looking for a Senior Regulatory Compliance Manager for a client in Riyadh, KSA.

  • Kindly review the Job requirements below.

Your immediate application will enable us to place you successfully.

Must-Have : 10+ years of experience in a regulatory compliance, legal, or risk management role within financial services or fintech.

Strong knowledge of Saudi financial regulatory frameworks (SAMA), particularly Consumer Protection regulations.

Experience working closely with product, engineering, and legal teams in a fast-paced, agile environment.

Proven ability to interpret regulatory requirements and design practical compliance solutions.

Excellent communication and stakeholder management skills, including experience interfacing with regulators or banking partners.

Ability to work independently, make sound decisions, and manage competing priorities.

Nice to have : Bachelors degree in Business Administration, Law, Finance, or Accounting Certifications in CRCM, CAMS, CRCMP, or PMP preferred About Us : Arthur Lawrence is a management and technology consulting firm providing enterprise-wide business transformation and business applications implementation services.

Our in-depth technical knowledge and broad experience of working with world-class companies enables organizations to leverage our capabilities in developing winning strategies and cost-effective solutions.

We are an UN Women Empowerment Principal Signatory and are certified from National Minority Supplier Development Council.

Acknowledgements from Industry Peers : Winner of Entrepreneur 360 Award (2019).

IAOP Award; Ranked in top 100 internationally.

Arthur Lawrence ranked within the Inc 5000 twice in 2016 and 2017 as one of the fastest.

Growing companies of America.

Named one of the top ten fastest growing businesses in Houston in 2016.

Ranked 25th in the HBJ s Fast 100 Private Companies Award in 2017.

Our Seven Pillars : We rely on the seven core values that we believe enable us to deliver quality for our consultants and clients : Education, Integrity, Value Creation, Collaboration, Best Client, Best People and Stewardship Through strict adherence to these core values, we have achieved success beyond all documented forecasts and anticipation.

#J-18808-Ljbffr
This advertiser has chosen not to accept applicants from your region.

Senior Manager Regulatory Compliance Retail

SAR120000 - SAR240000 Y BSF

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description & Accountabilities:

  • Senior Manager Regulatory Compliance leads a small group of compliance professionals for Retail Banking Group Compliance areas. This role plans, implements and follows up on Compliance issues is typically the content expert for his area of responsibility.
  • This role is responsible for all testing and monitoring mandated under the Compliance control. He/she will also suggest appropriate areas (identified through their testing and monitoring process) to address in order to prevent further breaches of SAMA rules, policies and external regulations and to ensure implementing the controls in the right methods.
  • This role is a senior professional with significant compliance and people management capabilities. This position reports directly to the Head of Regulatory Compliance.
  • Enhances the effectiveness of the compliance risk by arranging risk assessments and identifies controls in place to mitigate identified risks.
  • Works closely with the Businesses on new, existing services, products to analyze the risk elements and advise them on any actions needed.
  • Promptly reports any suspicious activity and issues in due diligence standards to the Head of Compliance.
  • Supports the Manager in any ad-hoc projects to promote the compliance culture within the BSF, during inspection visits (internal and external) to the bank or to fulfil any compliance reporting requirement from the senior management.
  • Responsible to entertain the Internal and External Auditors and the regulator's Inspectors professionally and tactfully during their inspection visits.
  • Provides direction, guidance to his team on delivering the department's responsibilities and arranges appropriate control self-assessment meetings and trainings for Compliance team.
  • Ensures that all testing and monitoring are undertaken effectively and ensures all reports are submitted complete, accurately and on time.
  • Develops and maintains comprehensive procedures to avoid any misunderstanding for the staff members involved.
  • Responsible for keeping detailed records of all compliance testing and reviews, and provides timely and professional responses to all requests.
  • Supervises Compliance officers work closely with the Businesses on new and existing services and products to analyze the risk elements and advises them on any actions needed.
  • Ensures that all BSF standards and requirements are met by each member of the department.
  • Reviewing related policies and procedures, documents, agreements, forms, terms and conditions, marketing materials and contracts.
  • Provide advice to business line from regulatory prospective.
  • Validating implementation of related SAMA circulars and collected evidences as per compliance procedure manual.
This advertiser has chosen not to accept applicants from your region.

Regulatory Compliance and Licensing Manager

Menasa & Partners

Posted 16 days ago

Job Viewed

Tap Again To Close

Job Description

The Role
Package: SAR 45-50K + Benefits We are looking to speak to all Regulatory Compliance and Licensing Professionals - Land Transport for roles based in Saudi Arabia. Candidates applying for these roles must have a minimum of 10 years' professional experience in land transport sector, with at least 5 years experience at a senior-level function. Candidates must have relevant experience in policy/regulatory/legislative environment of the land transport sector.

Requirements
Requirements: - Bachelor's degree, Master's Degree in Public Administration or Business is preferred. - Must have a minimum of 10 years' experience in transportation related roles. - Experienced in the formulation of policy related to land transport logistics, budget, licensing, etc. - Experienced in the analysis, development and implementation of land transport regulations, procedures and policies.

About the company
The name MENASA originates from both the geographical region of Middle East, North Africa & South Asia as well as the Arabic word for platform or stage. We provide the platform for employers to approach the best global talent available. Menasa & Partners is a privately owned, fully licensed, Executive Search company head-quartered in Dubai, UAE. From our head office in Dubai we are ideally placed to assist organizations in the global search for talent. We specialize in providing companies not only with suitable individuals to work in their organizations but also offer unparalleled knowledge of the global markets. Our staff all have in depth knowledge of their vertical markets therefore offering tailored strategic advice.
This advertiser has chosen not to accept applicants from your region.
 

Nearby Locations

Other Jobs Near Me

Industry

  1. request_quote Accounting
  2. work Administrative
  3. eco Agriculture Forestry
  4. smart_toy AI & Emerging Technologies
  5. school Apprenticeships & Trainee
  6. apartment Architecture
  7. palette Arts & Entertainment
  8. directions_car Automotive
  9. flight_takeoff Aviation
  10. account_balance Banking & Finance
  11. local_florist Beauty & Wellness
  12. restaurant Catering
  13. volunteer_activism Charity & Voluntary
  14. science Chemical Engineering
  15. child_friendly Childcare
  16. foundation Civil Engineering
  17. clean_hands Cleaning & Sanitation
  18. diversity_3 Community & Social Care
  19. construction Construction
  20. brush Creative & Digital
  21. currency_bitcoin Crypto & Blockchain
  22. support_agent Customer Service & Helpdesk
  23. medical_services Dental
  24. medical_services Driving & Transport
  25. medical_services E Commerce & Social Media
  26. school Education & Teaching
  27. electrical_services Electrical Engineering
  28. bolt Energy
  29. local_mall Fmcg
  30. gavel Government & Non Profit
  31. emoji_events Graduate
  32. health_and_safety Healthcare
  33. beach_access Hospitality & Tourism
  34. groups Human Resources
  35. precision_manufacturing Industrial Engineering
  36. security Information Security
  37. handyman Installation & Maintenance
  38. policy Insurance
  39. code IT & Software
  40. gavel Legal
  41. sports_soccer Leisure & Sports
  42. inventory_2 Logistics & Warehousing
  43. supervisor_account Management
  44. supervisor_account Management Consultancy
  45. supervisor_account Manufacturing & Production
  46. campaign Marketing
  47. build Mechanical Engineering
  48. perm_media Media & PR
  49. local_hospital Medical
  50. local_hospital Military & Public Safety
  51. local_hospital Mining
  52. medical_services Nursing
  53. local_gas_station Oil & Gas
  54. biotech Pharmaceutical
  55. checklist_rtl Project Management
  56. shopping_bag Purchasing
  57. home_work Real Estate
  58. person_search Recruitment Consultancy
  59. store Retail
  60. point_of_sale Sales
  61. science Scientific Research & Development
  62. wifi Telecoms
  63. psychology Therapy
  64. pets Veterinary
View All Quality Control Analyst Jobs