12 Manufacturing Technicians jobs in Bahrain
Quality Control Manager
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Quality Control Manager
Posted today
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The primary duties include developing, implementing, and overseeing the company's quality management system (QMS). You will be responsible for conducting regular quality audits, inspections, and process reviews to identify areas for improvement. This involves analysing quality data, identifying root causes of defects, and implementing corrective and preventive actions (CAPA). You will lead and mentor the quality control team, ensuring they are well-trained and equipped to perform their duties effectively. Collaborating with production, engineering, and R&D departments to resolve quality-related issues and implement process improvements is essential. You will also be responsible for managing supplier quality and ensuring incoming materials meet specified standards. Maintaining accurate quality records and preparing reports for senior management will be a key responsibility.
The ideal candidate will possess a Bachelor's degree in Engineering (Mechanical, Industrial, or a related field) or a related discipline, with a minimum of 7 years of experience in quality control or quality assurance within a manufacturing environment. Proven experience in implementing and managing ISO 9001 or other relevant quality management systems is essential. Strong knowledge of statistical process control (SPC), Six Sigma, and Lean Manufacturing principles is required. Excellent analytical, problem-solving, leadership, and communication skills are paramount. The ability to effectively manage a team, drive continuous improvement initiatives, and foster a culture of quality across the organisation will be key to success in this role. Certification in quality management (e.g., ASQ Certified Quality Manager) is a significant advantage.
Quality Control Inspector
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Key Responsibilities:
- Inspect raw materials, components, and finished products to ensure they meet defined quality standards and specifications.
- Utilize various inspection tools and equipment, such as calipers, micrometers, gauges, and vision systems.
- Identify and document non-conforming products or materials, initiating corrective actions as required.
- Perform in-process quality checks at various stages of the manufacturing process.
- Calibrate and maintain inspection equipment to ensure accuracy and reliability.
- Review production documentation, including work orders and inspection reports, for completeness and accuracy.
- Collaborate with production, engineering, and R&D teams to resolve quality issues and implement improvements.
- Participate in the development and refinement of quality control procedures and standards.
- Conduct audits of production processes to ensure compliance with quality management systems (e.g., ISO standards).
- Maintain accurate records of inspections, test results, and non-conformance reports.
- Provide feedback to production teams on quality performance and areas for improvement.
- Ensure adherence to all safety regulations and maintain a clean and organized work area.
- Contribute to continuous improvement initiatives aimed at enhancing product quality and reducing defects.
Qualifications:
- High school diploma or equivalent; a technical certification or associate's degree in a related field is a plus.
- Minimum of 3 years of experience in quality control inspection within a manufacturing environment.
- Proficiency in using various measuring and inspection tools.
- Understanding of quality control principles, methodologies, and statistical process control (SPC).
- Ability to read and interpret technical drawings, blueprints, and specifications.
- Strong attention to detail and accuracy.
- Good analytical and problem-solving skills.
- Effective communication and documentation skills.
- Ability to work independently and as part of a team.
- Familiarity with ISO 9001 or other quality management systems is desirable.
- Basic computer skills, including experience with MS Office Suite.
Quality Control Manager
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Gulf Biotech Company, we specialize in innovative processes to make difficult-to-manufacture specialty and generic drugs easier to use, less labor intensive, and more streamlined in practice. GBC ensures that its high-quality drugs fulfill a critical unmet medical need and deliver dependable live-saving treatment options when and where they’re needed most.
**Key Job Requirements**
- Should have sound knowledge of all Quality Control processes and applicable guidelines
- Able to manage sampling, RM/PM/FPP testing, validation testing, method validations/verifications, method transfers, cleaning validations testing, hold time studies and stability studies programs
- Manage QC inventory of chemicals, reference/working standards, chromatography columns, testing accessories, instrument calibrations, preventative maintenance, etc.
- Post testing release of materials and FPPs by ensuring a complete testing audit trail
- Rich experience in CAPA management, OOS/OOT management, Data Integrity and Quality Risk Management studies
- Experience of managing (direct/indirect) a microbiology lab of a sterile manufacturing facility
- To coordinate with various cross-functional departments for timely availability of materials, products & documents
- Prepare and evaluate trends in quality system to monitor effectiveness and utilize statistical methods for analysis
- Should be able to manage a multi-role team effectively and ensure technical development of QC resources
- Execute annual Quality Control budget effectively to meet company objectives and set targets
- Rich experience in data analytics using statistical tools, documentation and review of key protocols & reports
- Should have excellent leadership, analytical, problem solving, conflict management and communication skills
**Responsibilities**
- Track and manage inventory
- Manage warehouse staff
- Evaluate performance metrics to ensure quality delivery and cost-efficient work-flow processes
**Qualifications**
- Have a degree in Pharmacy
- Above 10 years of experience in QC Department of pharmaceutical industry (preferably sterile manufacturing)
- Proficient in Microsoft Office products (Excel and Word)
Ability to commute/relocate:
- Hidd: Reliably commute or willing to relocate with an employer-provided relocation package (required)
Quality Control Specialist -PRPO
Posted 7 days ago
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Olgoonik is an Equal Opportunity Employer
Overview
The Quality Control Specialist – QC manages quality program planning, quality program evaluation, identifying and resolved quality issues, and providing technical advisory services.
Primary Responsibilities
- Evaluates systems
- Analyzes data
- Establishes Quality Control procedures
- Use Warehouse Management System (WMS)m Distribution Standard System (DSS), Query Management Facility (QMF), QLIK
- Validates processes
- Ensures work is performed IAW DLA Distribution Standard Operating Procedures (SOPs)
- Adheres to all Audits Readiness Internal Controls
- The Quality Control Specialist manages a team of Quality Control Technicians and Specialists.
- Ensures area of responsibility is operating in agreement with all referenced DLA Distribution SOPs, addendums, FRAGOS, and Process Manuals as required for day-to-day operational processing and preparation for any audit event.
- Responsible for compliance with the Audit Assertion Program reporting and documentation requirements, to include monthly assertion reporting that assigned areas of responsibility are ready for audit and or corrective action plans are documented and being corrected if an assertion cannot be made.
- Responsible for the Audit Assertion Program functional areas of Quality Control and Customer Service.
- Three (3) years-experience in the Quality Control field
- Experience with Corrective Action Plans (CAP)
- Extensive knowledge of WMS, DSS, QLIK and QMF.
- Must be proficient with Microsoft Suite of products including Word, Excel, Access and E-mail business software.
- Must demonstrate a good attitude and ability to work as a member of a Team
- Position requires self-motivation and the ability to work effectively under a minimum of supervision
- Must be able to multi-task efficiently, work in a fast-paced environment on multiple projects, and have a strong attention for detail.
- None
- SECRET Level Required
- Must have a current United States Government SECRET Personnel Security Clearance or be able to successfully complete a U.S. government administered Investigation.
- Must be a U.S. Citizen.
- Must be able to maintain a U.S. Government SECRET clearance.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is required to be able to occasionally stand; walk; sit; use hands and/or fingers to handle, or feel objects, tools or controls; operate office equipment, reach with hands and arms; climb stairs; balance; stoop; kneel; talk or hear; taste or smell. The employee must occasionally lift and or move up to 25 pounds.
Work Environment
The work is performed in an indoor and outdoor warehouses and office setting.
Olgoonik is an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local laws. As an Alaska Native corporation, Olgoonik provides hiring preference to Olgoonik shareholders, descendants, and their spouses to the extent allowed by law.
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#J-18808-LjbffrQuality Control Specialist -PRPO
Posted 7 days ago
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Olgoonik is an Equal Opportunity Employer
Overview
The Quality Control Specialist – QC manages quality program planning, quality program evaluation, identifying and resolved quality issues, and providing technical advisory services.
Primary Responsibilities
- Evaluates systems
- Analyzes data
- Establishes Quality Control procedures
- Use Warehouse Management System (WMS)m Distribution Standard System (DSS), Query Management Facility (QMF), QLIK
- Validates processes
- Ensures work is performed IAW DLA Distribution Standard Operating Procedures (SOPs)
- Adheres to all Audits Readiness Internal Controls
- The Quality Control Specialist manages a team of Quality Control Technicians and Specialists.
- Ensures area of responsibility is operating in agreement with all referenced DLA Distribution SOPs, addendums, FRAGOS, and Process Manuals as required for day-to-day operational processing and preparation for any audit event.
- Responsible for compliance with the Audit Assertion Program reporting and documentation requirements, to include monthly assertion reporting that assigned areas of responsibility are ready for audit and or corrective action plans are documented and being corrected if an assertion cannot be made.
- Responsible for the Audit Assertion Program functional areas of Quality Control and Customer Service.
- Three (3) years-experience in the Quality Control field
- Experience with Corrective Action Plans (CAP)
- Extensive knowledge of WMS, DSS, QLIK and QMF.
- Must be proficient with Microsoft Suite of products including Word, Excel, Access and E-mail business software.
- Must demonstrate a good attitude and ability to work as a member of a Team
- Position requires self-motivation and the ability to work effectively under a minimum of supervision
- Must be able to multi-task efficiently, work in a fast-paced environment on multiple projects, and have a strong attention for detail.
- None
- SECRET Level Required
- Must have a current United States Government SECRET Personnel Security Clearance or be able to successfully complete a U.S. government administered Investigation.
- Must be a U.S. Citizen.
- Must be able to maintain a U.S. Government SECRET clearance.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is required to be able to occasionally stand; walk; sit; use hands and/or fingers to handle, or feel objects, tools or controls; operate office equipment, reach with hands and arms; climb stairs; balance; stoop; kneel; talk or hear; taste or smell. The employee must occasionally lift and or move up to 25 pounds.
Work Environment
The work is performed in an indoor and outdoor warehouses and office setting.
Olgoonik is an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local laws. As an Alaska Native corporation, Olgoonik provides hiring preference to Olgoonik shareholders, descendants, and their spouses to the extent allowed by law. Seniority level
- Seniority level Mid-Senior level
- Employment type Full-time
- Job function Quality Assurance
- Industries Executive Offices
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#J-18808-LjbffrSenior Quality Control Engineer
Posted today
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Key responsibilities include leading a team of quality inspectors and technicians, providing training and guidance to ensure adherence to quality procedures. You will collaborate closely with production, engineering, and R&D teams to identify and address quality issues proactively. The successful candidate will also be involved in supplier quality management, evaluating vendor performance and ensuring the quality of incoming materials. Experience with statistical process control (SPC), Six Sigma methodologies, and Lean Manufacturing principles is essential. You will be responsible for maintaining quality documentation, including inspection records, test results, and calibration certificates. The ability to interpret technical drawings and specifications, and to conduct audits of production processes, will be vital.
Required qualifications include a Bachelor's degree in Engineering (Mechanical, Industrial, or Electrical) or a related technical field. A Master's degree is a plus. A minimum of 7-10 years of progressive experience in quality control or quality assurance within a manufacturing environment is mandatory. Proven experience in implementing and managing ISO 9001 or other relevant quality management systems is essential. Strong analytical and problem-solving skills, with a meticulous attention to detail, are required. Excellent leadership, communication, and interpersonal skills are necessary for effective team management and cross-functional collaboration. If you are a dedicated quality professional with a passion for excellence and driving continuous improvement, we encourage you to apply.
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Lead Quality Control Engineer
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Lead Quality Control Engineer
Posted today
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Job Description
Key Responsibilities:
- Lead and manage the quality control department and team.
- Develop, implement, and maintain the Quality Management System (QMS).
- Ensure products meet all quality standards and customer specifications.
- Conduct regular quality audits of production processes and products.
- Analyze quality data, identify trends, and implement corrective actions.
- Manage the Non-Conformance process and CAPA system.
- Collaborate with production and engineering teams on quality initiatives.
- Oversee supplier quality management and conduct supplier audits.
- Train personnel on quality control procedures and best practices.
- Stay updated on industry standards and regulatory requirements.
- Bachelor's degree in Engineering (Mechanical, Industrial, Materials) or a related field.
- Minimum of 7 years of experience in Quality Control or Quality Assurance in a manufacturing environment.
- Proven experience in implementing and managing QMS (e.g., ISO 9001).
- Strong knowledge of SPC, root cause analysis, and CAPA methodologies.
- Excellent leadership, team management, and communication skills.
- Proficiency in quality control tools and software.
- Ability to analyze data and implement data-driven solutions.
- Experience in auditing and compliance is essential.
- Strong problem-solving and decision-making abilities.
Senior Pharmaceutical Quality Control Analyst
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Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various analytical techniques.
- Develop, validate, and transfer analytical methods according to regulatory guidelines.
- Operate and maintain sophisticated laboratory instrumentation such as HPLC, GC, FTIR, UV-Vis spectrophotometers, and dissolution apparatus.
- Prepare and review analytical test methods, specifications, and validation protocols.
- Investigate out-of-specification (OOS) and out-of-trend (OOT) results, identifying root causes and implementing corrective and preventive actions (CAPA).
- Document all laboratory activities, results, and deviations meticulously in compliance with cGMP and internal SOPs.
- Contribute to regulatory submissions and client audits by providing accurate and comprehensive data.
- Train and mentor junior analysts on analytical techniques, instrumentation, and cGMP principles.
- Participate in stability testing programs for pharmaceutical products.
- Maintain laboratory equipment calibration and qualification.
- Ensure a safe and compliant laboratory working environment.
Qualifications:
- Master's degree or PhD in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related field.
- Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
- Extensive hands-on experience with HPLC, GC, UV-Vis, and other relevant analytical techniques.
- Thorough understanding of cGMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
- Strong knowledge of method development and validation principles.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in laboratory information management systems (LIMS) and data analysis software.
- Strong written and verbal communication skills, with the ability to document scientific information accurately.
- Ability to work independently and as part of a team in a fast-paced environment.