104 Food Quality jobs in Manama
Production Supervisor - Food Manufacturing
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Production Line Supervisor - Food Manufacturing
Posted today
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Key Responsibilities:
- Supervising and guiding a team of production operators to meet daily production targets.
- Ensuring adherence to all food safety, quality, and sanitation standards (HACCP, GMP).
- Monitoring production line performance, identifying inefficiencies, and implementing corrective actions.
- Training new team members and providing ongoing development for existing staff.
- Managing the scheduling of personnel and production resources.
- Troubleshooting production issues and implementing immediate solutions.
- Maintaining accurate production records and reporting on key performance indicators (KPIs).
- Ensuring a safe working environment for all team members and adherence to safety protocols.
- Collaborating with quality control and maintenance teams to ensure optimal line operation.
- Implementing lean manufacturing principles and driving continuous improvement efforts.
The ideal candidate will have a Bachelor's degree in Food Science, Industrial Engineering, or a related field, or equivalent work experience. A minimum of 5 years of experience in food manufacturing production, with at least 2 years in a supervisory role, is required. Strong understanding of food safety regulations and quality management systems is essential. Excellent leadership, communication, and problem-solving skills are crucial for this remote-based supervisory role. You must be highly organized, self-motivated, and able to effectively manage and motivate a team remotely. Experience with production planning software and a solid understanding of manufacturing processes are required. We are looking for a proactive leader committed to excellence in food production and team performance. This is an excellent opportunity to lead a production team and drive efficiency in a dynamic food manufacturing environment, fully remotely.
Quality Control Manager - Food Production
Posted 2 days ago
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Production Supervisor - Food & Beverage Manufacturing
Posted 2 days ago
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Key Responsibilities:
- Supervise and coordinate the daily activities of the production team, ensuring smooth workflow and adherence to schedules.
- Monitor production processes to ensure optimal efficiency, quality, and adherence to standards.
- Implement and enforce strict safety protocols and hygiene standards in compliance with food safety regulations (e.g., HACCP, GMP).
- Train, coach, and motivate production associates to perform their duties effectively and safely.
- Manage staffing levels, schedule shifts, and ensure adequate coverage on the production floor.
- Conduct regular performance reviews and provide constructive feedback to team members.
- Troubleshoot production issues and implement corrective actions to minimize downtime and waste.
- Maintain accurate production records, including output, waste, and quality control data.
- Collaborate with the Quality Assurance team to ensure all products meet stringent quality specifications.
- Contribute to continuous improvement initiatives aimed at enhancing productivity and reducing costs.
- Ensure proper maintenance and operation of production machinery and equipment.
- Oversee inventory management of raw materials and finished goods within the production area.
- Promote a positive and safe working environment for all employees.
- Proven experience as a Production Supervisor or similar role in a food and beverage manufacturing setting.
- Strong knowledge of manufacturing principles, lean manufacturing, and process optimization.
- Familiarity with food safety standards and quality control procedures (HACCP, GMP preferred).
- Excellent leadership, communication, and interpersonal skills.
- Ability to manage and motivate a diverse team.
- Strong problem-solving and decision-making abilities.
- Proficiency in using production management software and MS Office Suite.
- Understanding of machinery operation and basic maintenance.
- High school diploma or equivalent; Associate's or Bachelor's degree in a relevant field is a plus.
- Ability to work flexible hours and shifts as required.
- Located in or able to commute to **Tubli, Capital, BH**.
Quality Assurance Manager
Posted 2 days ago
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Pharmaceutical Quality Assurance Manager
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Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS) in accordance with cGMP, ICH, and other relevant regulatory guidelines.
- Oversee all quality assurance activities, including batch record review, deviation management, change control, and CAPA (Corrective and Preventive Actions).
- Lead and participate in internal and external audits, including regulatory inspections (e.g., FDA, EMA).
- Ensure all manufacturing, laboratory, and packaging operations comply with approved procedures and regulatory requirements.
- Review and approve validation protocols and reports for equipment, processes, and analytical methods.
- Manage product quality complaints and conduct investigations to determine root causes and implement corrective actions.
- Train personnel on quality systems, GMP principles, and regulatory expectations.
- Monitor quality metrics and key performance indicators (KPIs), identifying areas for improvement.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure seamless product development and commercialization.
- Stay current with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
- Lead and mentor a team of Quality Assurance professionals.
- Approve or reject raw materials, intermediates, and finished products based on quality standards.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. Master's degree is preferred.
- Minimum of 7 years of experience in quality assurance or quality control within the pharmaceutical industry.
- In-depth knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines (e.g., FDA 21 CFR Parts 210/211, ICH Q7).
- Proven experience in leading regulatory audits and inspections.
- Strong understanding of pharmaceutical manufacturing processes, quality systems, and validation principles.
- Excellent analytical, problem-solving, and decision-making skills.
- Exceptional attention to detail and commitment to accuracy.
- Strong leadership, management, and interpersonal skills.
- Effective written and verbal communication skills.
- Experience with Quality Management System (QMS) software.
Lead Quality Assurance Manager
Posted 1 day ago
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Pharmaceutical Quality Assurance Specialist
Posted 2 days ago
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Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and other relevant regulations.
- Conduct internal audits and inspections to assess compliance with established quality standards and identify areas for improvement.
- Review and approve batch records, validation protocols, and other quality-related documentation.
- Investigate deviations, out-of-specification results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Participate in external audits by regulatory agencies and customers.
- Manage change control processes, ensuring all changes are properly evaluated, documented, and implemented.
- Develop and deliver quality training programs to personnel across the organization.
- Monitor key quality metrics and provide regular reports to management.
- Stay up-to-date with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
- Contribute to the continuous improvement of quality processes and systems.
- Support the qualification and validation of equipment, processes, and analytical methods.
- Review and approve raw material and finished product testing results.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related science field.
- Minimum of 4 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry.
- Strong understanding of GMP, ISO, and other relevant regulatory guidelines.
- Experience with QMS implementation and maintenance.
- Proficiency in conducting audits, investigations, and managing CAPA systems.
- Excellent attention to detail, analytical skills, and problem-solving abilities.
- Strong written and verbal communication skills, with the ability to document findings clearly and concisely.
- Ability to work independently and collaboratively in a team environment.
- Familiarity with pharmaceutical manufacturing processes is a plus.
- Proficiency in Microsoft Office Suite and quality management software.
- Relevant professional certifications are an advantage.
Automotive Quality Assurance Engineer
Posted 2 days ago
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Key Responsibilities:
- Develop and execute quality assurance plans and procedures for automotive products.
- Conduct inspections and testing of components, sub-assemblies, and finished products.
- Analyze test data and performance metrics to identify defects and areas for improvement.
- Work closely with R&D, engineering, and production teams to implement corrective and preventive actions (CAPA).
- Manage non-conformance reporting and resolution processes.
- Ensure compliance with automotive quality standards and customer specifications.
- Participate in internal and external audits.
- Develop and maintain quality documentation, including reports, procedures, and work instructions.
- Conduct root cause analysis for quality issues and implement effective solutions.
- Contribute to continuous improvement initiatives within the manufacturing process.
Qualifications: A Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related technical field. Minimum of 3-5 years of experience in quality assurance or quality control within the automotive manufacturing sector. Familiarity with IATF 16949 and other relevant automotive quality standards. Proficiency in using quality tools and methodologies, such as Six Sigma, SPC, FMEA, and Root Cause Analysis. Strong analytical and problem-solving skills. Excellent communication and collaboration abilities. Experience with metrology equipment and testing procedures is a plus. This hybrid role requires the flexibility to work from our office in Seef, Capital, BH for a portion of the week, with remote work options available for other tasks.
Pharmaceutical Quality Assurance Specialist
Posted 2 days ago
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Key Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS) in accordance with regulatory requirements (e.g., GMP, ISO).
- Conduct internal audits and inspections to assess compliance with established quality standards and identify areas for improvement.
- Review and approve batch records, validation reports, and other quality-related documentation.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, determining root causes and implementing corrective and preventive actions (CAPAs).
- Participate in external audits and regulatory inspections, serving as a subject matter expert.
- Develop and deliver quality training programs for relevant personnel.
- Monitor quality metrics and key performance indicators (KPIs), reporting on trends and recommending improvements.
- Ensure that all manufacturing processes and products meet predefined quality standards and regulatory requirements.
- Manage change control processes, evaluating the impact of proposed changes on product quality.
- Stay up-to-date with current pharmaceutical quality regulations and industry best practices.
- Collaborate with various departments, including R&D, manufacturing, and regulatory affairs, to ensure a cohesive approach to quality.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related Life Science field.
- Minimum of 4 years of experience in a Quality Assurance role within the pharmaceutical industry.
- Strong understanding of Good Manufacturing Practices (GMP) and other relevant quality regulations.
- Experience with internal and external audits, regulatory inspections, and QMS implementation.
- Proficiency in deviation investigation, root cause analysis, and CAPA development.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong attention to detail and commitment to accuracy.
- Effective communication and interpersonal skills, with the ability to collaborate cross-functionally.
- Experience with validation processes (e.g., process validation, cleaning validation) is a plus.
- Familiarity with documentation control systems and batch record review.