77 Audit Processes jobs in Bahrain
Quality Assurance Engineer
Posted 17 days ago
Job Viewed
Job Description
We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation. About the role We're in search of a proactive Quality Associate to join the Reckitt team, where innovation and science converge to make a real-world impact. You'll contribute to the growth of our trusted product portfolio, ensuring the highest standards of quality. Your expertise will drive activities from concept to execution, fostering an environment of continuous improvement. If you thrive in a dynamic atmosphere and are looking for a role where your actions directly contribute to the company's success, we would love to see your application. Your responsibilities - Degree in Chemistry, Biology, Engineering, or another relevant science.
- Familiarity with R & D processes and working within a GMP environment.
- Strong project management experiences with demonstrable problem-solving skills.
- Independent and self-starting with the resilience needed to thrive in a fast-paced environment.
- Ability to lead and motivate others, showing strong interpersonal competence and team commitment.
- Commercially aware, with the ability to propose improvements and challenge the status quo for better results.
- Adaptable and collaborative nature, prepared to take accountability for a broad range of activities. The experience we're looking for - Degree in Chemistry, Biology, Engineering, or another relevant science.
- Familiarity with R & D processes and working within a GMP environment.
- Strong project management experiences with demonstrable problem-solving skills.
- Independent and self-starting with the resilience needed to thrive in a fast-paced environment.
- Ability to lead and motivate others, showing strong interpersonal competence and team commitment.
- Commercially aware, with the ability to propose improvements and challenge the status quo for better results.
- Adaptable and collaborative nature, prepared to take accountability for a broad range of activities. The skills for success Commercial Awareness, Business Partnership, Collaboration, Partnership building, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Collaborator, R&D, Product Lifecycle Management. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.
Quality Assurance Manager
Posted 1 day ago
Job Viewed
Job Description
Lead Quality Assurance Manager
Posted today
Job Viewed
Job Description
Pharmaceutical Quality Assurance Specialist
Posted 1 day ago
Job Viewed
Job Description
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.
Pharmaceutical Quality Assurance Specialist
Posted 1 day ago
Job Viewed
Job Description
Automotive Quality Assurance Engineer
Posted 1 day ago
Job Viewed
Job Description
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 1 day ago
Job Viewed
Job Description
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.
Be The First To Know
About the latest Audit processes Jobs in Bahrain !
Quality Assurance Manager - Manufacturing
Posted 1 day ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, implement, and maintain a comprehensive Quality Management System (QMS) compliant with relevant industry standards (e.g., ISO 9001).
- Establish quality control procedures and standards for raw materials, in-process production, and finished goods.
- Lead and manage the QA team, providing training, guidance, and performance evaluations.
- Oversee all quality inspection and testing activities, ensuring accuracy and adherence to protocols.
- Analyze production data to identify trends, root causes of defects, and areas for improvement.
- Implement corrective and preventive actions (CAPA) to address quality issues and prevent recurrence.
- Conduct internal audits of manufacturing processes and quality systems to ensure compliance.
- Collaborate with production, engineering, and R&D teams to integrate quality considerations into product development and process design.
- Manage customer complaints and returns related to product quality, ensuring timely and effective resolution.
- Ensure compliance with all regulatory requirements and industry-specific standards.
- Develop and deliver quality training programs for all manufacturing personnel.
- Maintain all quality-related documentation, records, and reports.
- Stay current with industry best practices and emerging quality management techniques.
- Manage relationships with external auditors and regulatory bodies.
- Drive a culture of quality excellence throughout the organization.
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Industrial, or Chemical), Quality Management, or a related scientific field.
- A minimum of 6-8 years of progressive experience in Quality Assurance within a manufacturing environment.
- Proven experience in implementing and managing ISO 9001 or similar quality management systems.
- Strong understanding of manufacturing processes, statistical process control (SPC), and quality control methodologies.
- Excellent leadership, team management, and coaching skills.
- Proficiency in data analysis tools and techniques.
- Strong problem-solving abilities and a systematic approach to identifying root causes.
- Excellent written and verbal communication skills, with the ability to present complex information clearly.
- Familiarity with Lean Manufacturing or Six Sigma principles is a significant plus.
- Attention to detail and a commitment to maintaining high-quality standards.
- Ability to work effectively in a demanding manufacturing environment.
Pharmaceutical Quality Assurance Manager
Posted 1 day ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS) in accordance with cGMP and other relevant regulatory guidelines.
- Oversee all quality assurance activities, including batch record review, deviation investigations, change control, and CAPA management.
- Conduct internal audits and host regulatory inspections from bodies such as the FDA, EMA, and local authorities.
- Manage and mentor a team of Quality Assurance professionals, fostering a culture of quality and continuous improvement.
- Ensure that all pharmaceutical products manufactured meet established quality and regulatory standards.
- Review and approve validation protocols and reports for manufacturing processes, equipment, and analytical methods.
- Collaborate with Production, R&D, and other departments to resolve quality issues and implement corrective actions.
- Maintain comprehensive documentation and records, ensuring data integrity and traceability.
- Stay updated on evolving pharmaceutical regulations and industry best practices.
- Lead continuous improvement initiatives to enhance product quality and operational efficiency.
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A minimum of 8 years of progressive experience in Quality Assurance within the pharmaceutical industry is required. Strong knowledge of cGMP, ICH guidelines, and regulatory affairs is essential. Excellent leadership, analytical, problem-solving, and communication skills are crucial for success in this demanding role. Our client offers a competitive salary, comprehensive benefits, and opportunities for professional development within a growing organization. If you are passionate about ensuring the highest standards of pharmaceutical quality, we encourage you to apply.
Senior Quality Assurance Manager
Posted 1 day ago
Job Viewed
Job Description
Responsibilities:
- Develop, implement, and manage the company's overall Quality Management System (QMS).
- Establish and monitor quality control standards and procedures for all stages of the manufacturing process.
- Lead and mentor the Quality Assurance team, fostering a culture of quality and continuous improvement.
- Conduct internal audits and facilitate external audits by regulatory bodies and customers.
- Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA).
- Oversee product testing and validation processes to ensure compliance with specifications.
- Manage supplier quality, including audits and performance evaluation.
- Develop and deliver quality training programs for all employees.
- Stay current with industry best practices, regulatory requirements, and new technologies in quality assurance.
- Collaborate with R&D, production, and other departments to ensure quality is integrated into all aspects of product development and manufacturing.
- Manage documentation control and ensure adherence to ISO standards or other relevant certifications.
Qualifications:
- Bachelor's degree in Engineering, Science, or a related field. A Master's degree is preferred.
- Minimum of 7 years of experience in Quality Assurance or Quality Control within a manufacturing environment.
- Proven experience in developing and implementing QMS (e.g., ISO 9001).
- Strong knowledge of quality tools and methodologies (e.g., Six Sigma, Lean Manufacturing, SPC).
- Excellent leadership, team management, and problem-solving skills.
- Proficiency in data analysis and reporting.
- Strong understanding of manufacturing processes and product development lifecycles.
- Excellent communication, interpersonal, and presentation skills.
- Experience with regulatory compliance and certifications relevant to the manufacturing sector.
- Ability to drive change and foster a quality-focused culture.
This is a vital leadership position where your expertise will directly impact the quality and success of our client's products.