107 Pharmaceutical Manufacturing jobs in Saudi Arabia

KEY ACCOUNTABILITIES

• Food Safety and Quality Culture
• Health, Safety, and Environmental Culture
• Collaboration and Continuous Improvement
• Product samples collection
• Product samples analysis
• Raw and Packaging materials monitoring
• Reports preparation
• Ensure following of Food Safety, Quality, Safety & Environment set standards
• Process monitoring
• Use of laboratory equipment / Good Laboratory Practices (GLP)
• Ensure good laboratory practices are followed and labs maintained in hygienic / adequate condition
• Handling of non-conforming product
• GMP,GHK, Safety Standards Implementation

QUALIFICATIONS, EXPERIENCE, & SKILLS:

MINIMUM QUALIFICATIONS: Diploma / Bachelor of Science – Food Process Engineering / Chemistry / Biochemistry / chemical from a reputed university.

MINIMUM EXPERIENCE:3-5 years of relevant work with prior lab experience (2+ years) in Food/ Beverage industries.

JOB-SPECIFIC SKILLS:

• Understanding of Quality, Safety and Environment Management Systems
• Familiarity with Lean (OE – Operational Excellence), GMP, GLP & GHK standards and policies
• Basic knowledge of packaging and process machinery, instrumentation and bottling / canning/Aseptic lines
• Lab Analytical testing
• Basic food hygiene.
• Use and management of laboratory testing equipment
• Basic computer skills

COMPETENCIES:

• Ability to work under pressure.
• Ability to work in diverse workforce.
• Effective team player.
• Willing to work in shift and long hours if required.

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. You will play a crucial role in improving patients' lives by ensuring the highest standards of quality and safety in our products. Your leadership will be instrumental in driving innovation and excellence, ultimately making a global impact on patient health.

What You Will Achieve

In this role, you will:

• Lead people, technology, and financial resources in QC finished products and Microbiology sections.
• Identify and develop innovative concepts for process or product improvements, taking calculated risks to achieve results.
• Solve complex problems, leveraging experience from various areas as needed.
• Recognize and address development needs, creating growth opportunities for colleagues.
• Lead , oversee and/or manage multiple projects and ongoing work activities, ensuring compliance with approved methodologies and cGMP documentation.
• Provide technical expertise and support for laboratory and core applications, collaborating with business partners to identify and implement improvement areas.
• Utilize IMEx methodology and tool “Lean &sigma” to lead continuous improvement activities in QC laboratory
• Conduct , oversee and/or review/approve investigations, CAPA (Corrective Action and Preventive Action) and change controls.
• Review laboratory data to ensure compliance with approved methodologies.
  Build capabilities of the Process-Centric Team according to skills needs assessments.
• Provide technical expertise and support to the QC laboratory for laboratory and core applications.
• Manage review and approval of Good Manufacturing Practices ‘’ cGMP’’ documentation, such as procedures, analysis data and reports.
• Manage work streams Quality Control Finished Good, Stability, cleaning/process validation, Microbiology and Methodology sections.
• Responsible for developing Quality control Finished Good, Stability and Methodology sections colleagues and prepare Succession plan for the Finished Good, Stability and Methodology sections.
• Responsible for QC analyst qualification program
• Act as site SME for Stability and microbiology.

Here Is What You Need (Minimum Requirements)

• Bachelor’s degree in a relevant scientific discipline with 5+ years’ experience

• Laboratory supervisory experience in FP, Stability and/ or Microbiology
• Proven experience in leading colleagues and managing projects
• A deep understanding of Good Manufacturing Practices (cGMP) compliance requirements for Quality Control Laboratories
• Proficiency with Quality Control instruments and methodologies Microbiology and/ or Finished products analytical
• Experience in lean manufacturing and sigma concepts and tools
• Knowledge of cGMP /Saudi FDA compliance requirements for Quality Control Laboratories
• Proficiency in Laboratory Information Management Systems like Empower and SAP quality module
• Solid understanding of method qualification and testing of components and finished products
• Solid understanding of Data integrity requirements
• Experience in microbiological risk assessments
• Strong problem-solving skills and the ability to think outside the box.

Bonus Points If You Have (Preferred Requirements)

• Master’s degree or higher in a relevant scientific discipline
• Lean six sigma certifications.
• 2+ years of experience in leading people

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

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

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. You will play a crucial role in improving patients' lives by ensuring the highest standards of quality and safety in our products. Your leadership will be instrumental in driving innovation and excellence, ultimately making a global impact on patient health.

What You Will Achieve

In this role, you will:

• Lead people, technology, and financial resources in QC finished products and Microbiology sections.
• Identify and develop innovative concepts for process or product improvements, taking calculated risks to achieve results.
• Solve complex problems, leveraging experience from various areas as needed.
• Recognize and address development needs, creating growth opportunities for colleagues.
• Lead , oversee and/or manage multiple projects and ongoing work activities, ensuring compliance with approved methodologies and cGMP documentation.
• Provide technical expertise and support for laboratory and core applications, collaborating with business partners to identify and implement improvement areas.
• Utilize IMEx methodology and tool “Lean &sigma” to lead continuous improvement activities in QC laboratory
• Conduct , oversee and/or review/approve investigations, CAPA (Corrective Action and Preventive Action) and change controls.
• Review laboratory data to ensure compliance with approved methodologies.
  Build capabilities of the Process-Centric Team according to skills needs assessments.
• Provide technical expertise and support to the QC laboratory for laboratory and core applications.
• Manage review and approval of Good Manufacturing Practices ‘’ cGMP’’ documentation, such as procedures, analysis data and reports.
• Manage work streams Quality Control Finished Good, Stability, cleaning/process validation, Microbiology and Methodology sections.
• Responsible for developing Quality control Finished Good, Stability and Methodology sections colleagues and prepare Succession plan for the Finished Good, Stability and Methodology sections.
• Act as site SME for Stability and microbiology.

Here Is What You Need (Minimum Requirements)

• Bachelor’s degree in a relevant scientific discipline with 5+ years’ experience
• Laboratory supervisory experience in FP, Stability and/ or Microbiology
• Proven experience in leading colleagues and managing projects
• A deep understanding of Good Manufacturing Practices (cGMP) compliance requirements for Quality Control Laboratories
• Proficiency with Quality Control instruments and methodologies Microbiology and/ or Finished products analytical
• Experience in lean manufacturing and sigma concepts and tools
• Knowledge of cGMP /Saudi FDA compliance requirements for Quality Control Laboratories
• Proficiency in Laboratory Information Management Systems like Empower and SAP quality module
• Solid understanding of method qualification and testing of components and finished products
• Solid understanding of Data integrity requirements
• Experience in microbiological risk assessments
• Strong problem-solving skills and the ability to think outside the box.

Bonus Points If You Have (Preferred Requirements)

• Master’s degree or higher in a relevant scientific discipline
• Lean six sigma certifications.
• 2+ years of experience in leading people

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

Join the Team at ABYAT - Your Gateway to Retail Excellence!

About us

Are you ready to be part of the largest retail store in the Middle East? ABYAT , spanning an impressive 22,000 square meters and offering over 22,000 products, is your one-stop destination for all things home improvement and more. From elegant tiles and captivating wallpapers to state-of-the-art lighting solutions and stylish kitchen fixtures, we pride ourselves on offering a diverse array of top-quality products under one roof.

Established locally with a vision for excellence, ABYAT has been setting benchmarks since its inception in September 2005. With an unwavering focus on our customers, we've crafted an experience that revolves around their needs, from our meticulously designed store layouts to our unparalleled service offerings.

Expanding beyond our roots in Kuwait, ABYAT is now making waves in Saudi Arabia and setting our sights on Qatar and the UAE. As we continue to grow, we're seeking passionate individuals to join our dynamic team and contribute to our journey of success.

Position : Manufacturing Quality Controller

Location : Saudi Arabia – Dammam

Type : Full-time

Job Summary:

We are seeking a highly skilled Manufacturing Quality Controller with experience in aluminum and wood manufacturing or a related industry. The ideal candidate will be responsible for ensuring all products and raw materials meet the company’s quality standards through inspection, testing, and documentation. This role is crucial in maintaining our commitment to delivering high-quality products to our clients.

Key Responsibilities:

• Inspect and monitor incoming raw materials to ensure they comply with specifications and quality standards.
• Conduct in-process and final product inspections in alignment with established quality control procedures.
• Utilize various measuring tools and inspection equipment to verify product dimensions, finishes, and tolerances.
• Document inspection results and prepare detailed quality reports for management review.
• Identify and report any non-conformities or quality issues and follow up on corrective actions.
• Collaborate with production and warehouse teams to ensure quality awareness and compliance across all stages.
• Support the implementation of quality control policies and procedures.
• Participate in internal audits and contribute to continuous improvement initiatives.
• Use Microsoft Office programs (Excel, Word, PowerPoint) to track data, prepare presentations, and maintain records.

Requirements:

• Proven experience as a Quality Controller or in a similar role within a manufacturing environment.
• Background in aluminum and wood manufacturing or a closely related industry.
• Strong knowledge of quality control standards, testing procedures, and relevant ISO or industry certifications.
• Proficient in using measurement tools such as calipers, gauges, and micrometers.
• Excellent documentation and report-writing skills.
• Strong analytical, communication, and problem-solving abilities.
• Good command of Microsoft Office applications (Excel, Word, PowerPoint).
• Ability to work under pressure and maintain attention to detail.

Preferred Qualifications:

• Diploma or bachelor’s degree in industrial engineering, manufacturing technology, or a related field.
• Experience working in a lean manufacturing environment or with Six Sigma practices.

Apply now and take the first step towards an exciting career with ABYAT !

Manpower is seeking to recruit a Quality Control Specialist to join our client's team.

Overview

The position entails a rigorous quality assurance process, where the incumbent will report directly to Senior Management. The primary focus is to maintain the highest standards of product integrity by conducting thorough inspections and analyses at various production stages. Additionally, the role requires proactive site management, ensuring ongoing operational excellence and adherence to compliance protocols through regular site evaluations, addressing non-conformities, and maintaining systematic process.

Key Accountabilities

Production process

• Conduct comprehensive testing of products to ensure adherence to quality standards and legal requirements, documenting all quality tests, procedures, and standards.
• Monitor product development and manufacturing processes to detect deviations from desired quality benchmarks.
• Propose modifications in manufacturing processes, methods, or materials to enhance product quality and increase production yield.
• Raw Material and Finished Good
• Perform thorough reviews of records and data from incoming materials and production processes to verify compliance with specifications.
• Approve products that meet quality specifications and reject those that are defective.

Risk Evaluation

• Spearhead the development of material risk assessments and process improvement initiatives, aiming to elevate quality control standards for subsequent production cycles.
• Implement and maintain regular audits to ensure compliance with food safety regulations.
• People Management
• Develop comprehensive training programs for personnel on quality procedures and food safety standards. Lead by example to instil a culture of safety and quality in all work operations.
• Provide continuous training and updates on the latest industry standards and best practices.
• Foster a collaborative environment where employees are encouraged to voice concerns and suggestions regarding food safety and quality.

Ideal Candidate Profile

Education

• Bachelors degree in food science/food technology, Engineering, or related field (Microbiology, Chemistry, Food Biotechnology).

Experience

• Minimum of 6 years of quality assurance/quality control experience within food manufacturing operations, of which 2 + years in leadership role.

Technical Skills

• Performance Management
• Regulatory
• Training & Development
• Supervisory Skills
• Knowledge of and experience with ISO 9001, GFSI Quality Systems
• Business Process Re-engineering
• Root Cause Analysis (e.g., FMEA, SWOT, Ishikawa, Fish Bone)
• Technical / Food Processing automation/ Validations
• Statistical Data evaluation
• Auditing (internal, external)
• ERP system knowledge
• Physical / chemical Analysis & IPC control
• Competencies
• Motivation /Modelling (Leading by Example)
• Developing People
• Monitoring & Measuring
• Programme and Project Management*
• Influencing and Impact, including Conflict Management
• Assertiveness
• Strategic Thinking & Change Management
• Relationship Building
• Customer Service Orientation
• Judgement & Decision Making
• Presentation and Facilitation
• Analytical Thinking & Problem Solving
• Attention to Detail
• Drive for Results
• Quality & Rule Orientation
• Teamwork

We are looking for a detail-oriented Quality Control Inspector-I to join our team. The ideal candidate will hold an industry-recognized trade certificate and have at least 3 years of hands-on experience in quality control inspection activities.

Key Responsibilities:

• Conduct routine QC inspections as per established standards and procedures
• Ensure compliance with applicable specifications and drawings
• Prepare inspection reports and documentation
• Coordinate with production and QA teams to address quality issues
• Participate in internal audits and support continuous improvement initiatives

Qualifications:

• Industry trade certificate (mandatory)
• Minimum 3 years of experience in QC inspection activities
• Strong attention to detail and quality standards
• Knowledge of relevant inspection tools and documentation practices

The Quality Control Supervisor is an essential role within the retail and wholesale industry, focusing on maintaining and enhancing product quality through rigorous testing and inspection processes. This position is particularly suited for individuals with a major in Chemistry or Biochemistry, as it requires a deep understanding of chemical properties and processes that affect product quality. The supervisor will lead a team of quality inspectors, ensuring that all products meet the required specifications and regulatory standards. This role involves not only overseeing quality control operations but also collaborating with various departments to foster a culture of quality and continuous improvement within the organization.

Responsibilities:

1. Manage and oversee the daily operations of the quality control department.
2. Develop and implement quality assurance protocols based on industry standards.
3. Conduct thorough inspections and testing of raw materials and finished products.
4. Train and mentor quality control staff to enhance their skills and knowledge.
5. Analyze quality data to identify trends and recommend improvements.
6. Collaborate with production teams to address quality issues and implement corrective actions.
7. Ensure compliance with safety regulations and quality standards.
8. Maintain accurate records of inspections, tests, and quality control processes.
9. Lead quality improvement initiatives and promote best practices across the organization.
10. Serve as the primary point of contact for quality-related inquiries and issues.

Preferred Candidate:

1. Strong background in Chemistry or Biochemistry with a focus on quality control.
2. Excellent analytical and problem-solving skills.
3. Outstanding communication and interpersonal skills.
4. Detail-oriented with a strong commitment to quality assurance.
5. Proven leadership experience in a quality control environment.
6. Ability to work effectively under pressure and manage multiple tasks.
7. Familiarity with quality management software and tools.
8. Knowledge of industry regulations and compliance standards.
9. Adaptability to evolving processes and technologies.
10. Strong organizational skills with a focus on continuous improvement.

Skills

• Proficient in laboratory techniques and quality testing methods.
• Strong understanding of chemical analysis and quality assurance principles.
• Experience with statistical process control (SPC) methodologies.
• Excellent documentation and report writing skills.
• Ability to use quality inspection tools effectively.
• Strong leadership and team management capabilities.
• Effective time management and prioritization skills.
• Knowledge of regulatory compliance and industry standards.

One of our clients is in the Metal Industry, in Saudi Arabia, and is hiring for the position of Quality Control Inspector.

Industry: Aluminum and Steel Manufacturing and Installation

Years of Experience: 2- 3

Education: Relevant Bachelors or a Masters Degree

Notice Period: Immediate joiners or a maximum one-month notice period.

We are seeking a meticulous and experienced Quality Control Inspector with strong knowledge in HVAC and ducting systems to ensure that all project installations comply with relevant codes, standards, and specifications. The ideal candidate will have a deep understanding of HVAC systems, duct fabrication and installation, and applicable quality standards.

1. Inspect HVAC and ducting installations on-site to ensure compliance with project specifications, drawings, and applicable standards (SMACNA, ASHRAE, etc.).
2. Conduct routine inspections and tests of duct materials, insulation, supports, air leakage, and alignment.
3. Monitor and verify duct fabrication processes to ensure quality workmanship and materials.
4. Collaborate with project engineers and contractors to resolve quality-related issues in a timely manner.
5. Maintain accurate documentation of inspections, test reports, non-conformance reports (NCRs), and corrective actions.
6. Verify and ensure proper installation of HVAC equipment (AHUs, FCUs, exhaust fans, etc.) and alignment with duct systems.
7. Perform quality checks during pressure testing, air balancing, and commissioning stages.
8. Assist in developing and updating the quality control procedures and checklists for HVAC and ducting work.
9. Ensure all work complies with safety standards and company policies.

1. Diploma or Degree in Mechanical Engineering or a related technical field.
2. Minimum of 3 years of experience in HVAC and ducting inspection or quality control.
3. Familiarity with relevant standards (SMACNA, ASHRAE, ISO, etc.).
4. Strong knowledge of HVAC drawings, layouts, and schematic diagrams.
5. Good communication and reporting skills.
6. Attention to detail and strong analytical skills.
7. Certification in QA/QC or HVAC (preferred but not mandatory).

1. Experience working in large-scale MEP or construction projects.
2. Proficiency in MS Office, AutoCAD, and report preparation tools.
3. Knowledge of duct fabrication techniques and materials.

Note: We thank all applicants for their interest however, only those candidates who are shortlisted will be contacted.

5 days ago Be among the first 25 applicants

Direct message the job poster from LanceSoft Middle East

We have a new opportunity for "Inspection - QC II_MB30" with our client. Interested candidates should send their CV to .

Title: Inspection - QC II_MB30

Duration: 6 months contract

Job Description:

Essential Requirements of the role (Experience / Skills / Competencies):

Years of experience: +5 years

Field of experience: +5 years

Technical Skills:

• Certified welding inspector.
• Certified painting inspector (preferred).
• Experience with rotating equipment assembly and packaging (Compressor & Gas turbine).
• Knowledge of safety standards and willingness to use protective gear such as gloves and safety glasses.

Tools or Software (Required / Preferred):

Education Qualifications: Diploma or equivalent

Industry Background or Experience (Required / Preferred): Oil and Gas

Interested candidates should send their CV along with the following details:

• Notice Period
• Current Location
• Nationality
• Visa Status

• Associate

• Contract

• Quality Assurance, General Business, and Administrative

• Oil and Gas, Mining

Referrals can increase your chances of interviewing at LanceSoft Middle East by 2x.

• QC Inspector: Dimensional Inspection Experience in Dammam, Saudi Arabia
• Early Career Trainee – Quality Project Manager Support (Saudi Nationals) in Dammam, Saudi Arabia

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