307 Quality Control Specialists jobs in Saudi Arabia

• Ensure products meet qualityand efficiency standards set by the company.
• Ensuring that manufacturing processes comply with standards at both national and international level.
• Direct or coordinatequality assurance programs and formulate quality control policies.
• Specifyingqualityrequirements of raw materials with suppliers.
• Investigating and setting standards forqualityand health and safety.
• Work to improve an organization’s efficiency and profitability by reducing waste.

• Language: Must be fluent in English (read & write)
• Experience: Minimum 6 years Work experience

Job Purpose
: The
Quality Control Specialist
is responsible for ensuring that raw materials and production processes meet defined quality standards throughout the supply chain and manufacturing cycle. This role involves coordinating with international suppliers, inspecting incoming materials, overseeing in-process and final product quality, and managing quality documentation. The specialist conducts sample testing, supports production line readiness, and ensures non-conformities are recorded and addressed. The ideal candidate will demonstrate attention to detail, strong knowledge of inspection procedures, and the ability to maintain a high level of compliance and accuracy in quality operations.

Key Responsibilities:

• Coordinate with international suppliers regarding raw material quality and resolve any related issues.
• Inspect and test raw materials and final products using Oracle or other quality systems.
• Review and update product artwork and technical specifications according to quality standards.
• Collect and analyze material samples upon arrival and during production for compliance.
• Prepare and submit quality reports, including non-conformance and periodic performance reports.
• Conduct inspections during production processes and ensure adherence to acceptance criteria.
• Evaluate new samples and maintain organized storage of reference materials.
• Supervise quality inspectors and escalate any major findings to the Quality Manager.
• Inspect packaging materials before use and manage sorting of tester and product bottles.
• Maintain all quality-related documentation, including inspection records and rework logs.

Qualifications & Requirements

• Bachelor's degree in
  Industrial Engineering
  ,
  Chemistry
  , or a related scientific/technical field.
• Minimum of
  2 years
  of experience in quality control or quality assurance, preferably in a manufacturing.
• Familiarity with international and local quality standards and inspection techniques.
• Experience using ERP systems such as Oracle.
• Strong attention to detail with excellent analytical and reporting skills.
• Good command of English, both written and spoken.
• Ability to work collaboratively with cross-functional teams under tight production timelines.

Job Title: Quality Control Specialist

Location: Saudi Arabia

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary
We are seeking a passionate and talented
Quality Control Specialist
to join our dynamic team in
Saudi Arabia
.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities:

• Perform chemical and physical tests on raw materials, intermediates, and finished products using techniques like HPLC, GC, UV, and FTIR.
• Ensure adherence to cGMP, GLP, and SOPs; accurately record test results, deviations, and observations
• Operate, calibrate, and maintain laboratory instruments per schedule and SOPs
• Handle sample receiving, labeling, and traceability; ensure data integrity and proper documentation practices.
• Assist with method development, audits, training, and inventory/reagent management while contributing to continuous improvement efforts

Requirements

• Bachelor's degree in Science, Biotechnology, or Pharmacy with 0-2 years of relevant lab experience.

• Basic knowledge of GMP/GLP, lab safety, wet chemistry techniques, and use of instruments like HPLC and UV-Vis.

• Strong attention to detail, time management, adaptability, teamwork, and communication.
• Proficiency in Microsoft Office and basic LIMS or digital documentation systems.
• Demonstrated reliability, receptiveness to feedback, problem-solving ability, and focus on regulatory compliance and data accuracy
• Saudi manufacturing experience is a MUST.

Responsibilities

• Perform field inspections, sampling, and verification testing.
• Maintain up-to-date quality records, test reports, and non-conformance logs.
• Support ISO audits and assist in developing corrective action plans.
• Coordinate with construction teams to resolve deficiencies.
• Contribute to training on quality procedures and documentation practices.

Qualifications

• Bachelor's in engineering, Construction Management, or related discipline.
• 5+ years QA/QC or auditing in engineering/construction.
• Understanding of ISO 19011, ISO/IEC 17025.
• Familiarity with KSA codes and project documentation workflows.
• Strong organizational, analytical, and English communication skills.

Required Skills

• Analytical Skills

Job Details

• Location Riyadh - Saudi Arabia
• Industry
  
  Engineering
• Job Type Full-Time
• Degree Bachelor
• Experience 5-10
• Nationality
  
  Unspecified

Location
: (Jeddah)

About Us:

Salehiya started commercial activities in 1964 as a specialized healthcare company. It is one of the leading Saudi Arabian companies in distributing pharmaceuticals, medical and laboratory equipment, diagnostics, medical disposables, and hospital and consumer supplies. The company kept pace with the rapid development of the health sector in Saudi Arabia and gradually evolved to meet the needs and demands of a constantly growing market.

Salehiya is based in three major cities: Riyadh, Jeddah, and Dammam. It also has branches around the kingdom to cover the whole market and provide prompt and efficient client services, with over 1000 workforce.

For more information, you can visit our website:

Why Work with Us:

Salehiya Healthcare is committed to creating a diverse and inclusive workplace where all employees are valued and respected. We believe in fostering a culture that encourages creativity and innovation, particularly in technology. We utilize the latest tools in our field and stay ahead of industry trends. Our comprehensive training programs and mentorship opportunities are designed to support professional growth and development. We prioritize maintaining a welcoming atmosphere for everyone.

Job Purpose:

The core values that guide our people derive from our purpose to elevate the healthcare experience in the kingdom.

To ensure the quality, compliance, and operational excellence of the CHUA (Cold-Chain Healthcare & Urgent Applications) logistics systems, processes, and services in accordance with internal standards, customer expectations, and regulatory requirements. The CHUA Specialist will monitor, verify, and improve quality control procedures related to storage, handling, and distribution of sensitive healthcare products.

Key Accountabilities:

Operational

• Conduct quality checks and inspections of cold-chain logistics processes and CHUA systems.
• Monitor temperature-sensitive shipments and ensure compliance with GDP (Good Distribution Practice) and internal SOPs.
• Perform root cause analysis and corrective action implementation for any quality-related issues.
• Ensure documentation accuracy, including batch records, deviation reports, and inspection logs.
• Collaborate with warehouse, transportation, and customer service teams to resolve quality concerns.
• Ensure that quality control standards are consistently maintained in day-to-day operations.

Strategic

• Support the implementation of continuous improvement initiatives across CHUA operations.
• Analyze quality trends and suggest data-driven strategies to reduce risks and enhance service quality.
• Assist in audits (internal, customer, and regulatory) by providing necessary documentation and leading quality process reviews.
• Contribute to the development and periodic revision of quality manuals, SOPs, and training materials related to CHUA processes.

Qualifications and Experience:

Minimum Qualifications

• Bachelor's degree in pharmacy, Quality Management, Biomedical Engineering, Life Sciences, or a related field.

Minimum Experience

• 2–4 years of experience in a quality control or cold-chain logistics environment within the healthcare or pharmaceutical industry.
• Experience with CHUA systems or temperature-controlled healthcare logistics is preferred.

Skills and Competencies

• Strong knowledge of GDP, GSP, and other relevant quality standards.
• Proficient in documentation, reporting, and data analysis.
• Detail-oriented with strong problem-solving skills.
• Effective communication and interpersonal skills.
• Ability to work independently and in cross-functional teams.
• Familiarity with QMS (Quality Management Systems) and audit procedures.
• Technical understanding of cold-chain equipment and monitoring tools.

Job Title: Quality Control Specialist

Location: Saudi Arabia

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary

We are seeking a passionate and talented Quality Control Specialist to join our dynamic team in Saudi Arabia.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities:

• Perform chemical and physical tests on raw materials, intermediates, and finished products using techniques like HPLC, GC, UV, and FTIR.
• Ensure adherence to cGMP, GLP, and SOPs; accurately record test results, deviations, and observations.
• Operate, calibrate, and maintain laboratory instruments per schedule and SOPs.
• Handle sample receiving, labeling, and traceability; ensure data integrity and proper documentation practices.
• Assist with method development, audits, training, and inventory/reagent management while contributing to continuous improvement efforts.

• Bachelor's degree in Science, Biotechnology, or Pharmacy with 0–2 years of relevant lab experience.

• Basic knowledge of GMP/GLP, lab safety, wet chemistry techniques, and use of instruments like HPLC and UV-Vis.

• Strong attention to detail, time management, adaptability, teamwork, and communication.
• Proficiency in Microsoft Office and basic LIMS or digital documentation systems.
• Demonstrated reliability, receptiveness to feedback, problem-solving ability, and focus on regulatory compliance and data accuracy.
• Saudi manufacturing experience is a MUST.

: Quality control in a food preparation plant to ensure that the food products being manufactured adhere to required health standards and regulations

• Inspect raw materials to ensure their quality before starting production

• Performing periodic checks on production lines to ensure that operations adhere to specified specifications

• Monitoring packaging operations to ensure quality and cleanliness are maintained

• Ensuring the expiration dates of products and raw materials

• Ensuring the validity of health cards for all Production employees-Ensure the availability of sterilizing liquid in all sterilizing devices

• Ensuring the cleanliness of all departments in the factory, in addition to the entire corridors

• Periodically check the validity of the fire extinguisher

• Periodically verify the validity of the safety tools in the factory

• Recording and supervising visits received from government agencies to the factory and placing them in a register related to those visits.

• Attempting to resolve any issues with customers and satisfy them before escalating the problem to the restaurant manager.

• Review and check merchandise and ensure pricing is accurate.

• Inventory and collect payments either by cash or credit cards

• Issuance of receipts, refunds or change.

• Carry out replacement and product retrieval operations in accordance with the work policy.

• Communicate any feedback or suggestions from customers to the supervisor or manager

Job Title: Quality Control Specialist

Location: Saudi Arabia

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary

We are seeking a passionate and talented Quality Control Specialist to join our dynamic team in Saudi Arabia.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities:

• Perform chemical and physical tests on raw materials, intermediates, and finished products using techniques like HPLC, GC, UV, and FTIR.
• Ensure adherence to cGMP, GLP, and SOPs; accurately record test results, deviations, and observations.
• Operate, calibrate, and maintain laboratory instruments per schedule and SOPs.
• Handle sample receiving, labeling, and traceability; ensure data integrity and proper documentation practices.
• Assist with method development, audits, training, and inventory/reagent management while contributing to continuous improvement efforts.

Requirements

• Bachelor's degree in Science, Biotechnology, or Pharmacy with 0–2 years of relevant lab experience.

• Basic knowledge of GMP/GLP, lab safety, wet chemistry techniques, and use of instruments like HPLC and UV-Vis.

• Strong attention to detail, time management, adaptability, teamwork, and communication.
• Proficiency in Microsoft Office and basic LIMS or digital documentation systems.
• Demonstrated reliability, receptiveness to feedback, problem-solving ability, and focus on regulatory compliance and data accuracy.
• Saudi manufacturing experience is a MUST.

As a trusted global transformation partner, Welocalize accelerates the global business journey by enabling brands and companies to reach, engage, and grow international audiences. Welocalize delivers multilingual content transformation services in translation, localization, and adaptation for over 250 languages with a growing network of over 400,000 in-country linguistic resources. Driving innovation in language services, Welocalize delivers high-quality training data transformation solutions for NLP-enabled machine learning by blending technology and human intelligence to collect, annotate, and evaluate all content types. Our team works across locations in North America, Europe, and Asia serving our global clients in the markets that matter to them.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

**Main Purpose of the Role

Welocalize is seeking for an experienced Quality Control (QC) Specialist for Arabic to join our growing team. The selected candidates will be responsible for performing non-linguistic and linguistic quality checks on clinical research documents and other life sciences-related content. This role is crucial to ensuring that our high standards of accuracy and compliance are maintained across all translated materials.

Responsibilities

• Quality Control (QC):
  Perform rigorous quality control checks on translated documents to ensure accuracy, consistency, and adherence to client-specific guidelines
• Non-Linguistic QC:
  Review and verify the formatting, layout, and non-linguistic elements of documents in Arabic
• Content Specialization:
  Handle specialized content areas such as In Vitro Diagnostics, Biology, Chemistry, Medical Devices, Patient-facing materials, Pharmacovigilance, Pharmacy, Scientific Publications, and Investigator-facing documents
• CAT Tools:
  Utilize CAT tools such as XTM/Phrase/Trados/MemoQ to carry out QC tasks. Familiarity with integrated QA checks within these tools is essential
• Client-Specific Applications:
  Adhere to the specific requirements of client-provided applications and tools
• Capacity Management:
  Ensure daily full-time availability and maintain the expected capacity of reviewing 5,000+ weighted words per locale, per week, able to work on Fridays
• Documentation:
  Use Microsoft Office, particularly the Track Changes function in Word, to document and communicate QC findings
• Collaboration:
  Work closely with the project management team to ensure timely delivery of high-quality translations

Requirements

• Minimum of 6 months of experience in localization
  , with a focus on quality assurance and quality control
• Experience with CAT tools
  (XTM, Trados, MemoQ, Phrase, or similar). No OmegaT, as it is considered obsolete
• Experience with QA tools
  like Xbench, Verifika, or integrated QA checks within CAT tools
• Technical Skills:
  Proficiency in Microsoft Office, with a particular focus on the Track Changes function in Word
• Language Skills:
  Advanced level in English (C1 or higher), with native knowledge of Arabic
• Location:
  Remote
• Availability:
  Must be able to commit to daily availability.

This is an ongoing collaboration, which means that we will be happy to involve you in more projects and to grow our collaboration together over time, if you wish so: this is just one of the many interesting projects offered by Welocalize for English into Arabic.

If interested please, feel free to apply to this job posting.**