357 Quality Control Analysts jobs in Bahrain

Quality Control Analyst

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.

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.

We're in search of a proactive Quality Control Analyst 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. The position has responsibility of the Quality Control activities over the Bahrain Factory Production.

• 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.

• 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.

• Commercial Awareness
• Business Partnership
• Collaboration
• Partnership building
• Ability to challenge the status quo
• Propose improvement
• Accountability
• Adaptability
• Collaborator
• R&D
• Product Lifecycle Management

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.

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.

Overview

Reckitt is home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose is 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. In Research & Development, we have scientists, engineers, medical, clinical and regulatory professionals who work to create a cleaner, healthier world. With nine Centres of Excellence, we seek new opportunities by using science, entrepreneurial flair and fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.

We do the right thing, always, by acting with responsibility and integrity, complying with regulatory legislation globally, and ensuring our products are safe and of the highest quality. The size of our organisation provides opportunities to learn and work in different functions within R&D, exposing you to different disciplines, teams and environments. You will also have access to our Research and Development Academy to develop and grow within the organisation.

We are in search of a proactive Quality Control Analyst 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. The position has responsibility for the Quality Control activities over the Bahrain Factory Production.

• 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.

• 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.

• Commercial Awareness
• Business Partnership
• Collaboration
• Partnership building
• Ability to challenge the status quo
• Propose improvement
• Accountability
• Adaptability
• Collaborator
• R&D
• Product Lifecycle Management

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.

About the role:

The Quality Control Analyst plays a crucial role in maintaining the integrity of product quality throughout the development process.

Responsibilities

• Ensure all product designs meet quality standards.
• Identify potential issues before products reach the market.
• Refine product specifications.
• Improve production techniques.
• Contribute to overall product optimization.

Qualifications

• Experience with quality control processes.
• Worked in a consumer goods or FMCG company
• Familiarity with product development cycles.

• Performing analytical testing on pharmaceutical samples using various laboratory techniques, including HPLC, GC, UV-Vis spectroscopy, and titrations.
• Preparing reagents, solutions, and standards required for analytical testing.
• Documenting all testing procedures, results, and observations accurately and thoroughly in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Reviewing and interpreting analytical data, identifying any deviations from specifications, and reporting out-of-specification (OOS) results to supervisors.
• Calibrating and maintaining laboratory equipment, ensuring proper functioning and adherence to maintenance schedules.
• Assisting in the validation of analytical methods and equipment qualification.
• Participating in internal audits and regulatory inspections as needed.
• Staying updated on current pharmacopeial standards (e.g., USP, EP) and regulatory guidelines relevant to pharmaceutical quality control.
• Collaborating with R&D, production, and other departments to resolve quality-related issues.
• Maintaining a clean and safe laboratory environment.

• Perform analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and instruments (e.g., HPLC, GC, UV-Vis, FTIR).
• Ensure all testing is conducted in accordance with established Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and other relevant regulatory guidelines.
• Accurately document all experimental procedures, results, and observations in laboratory notebooks and electronic systems.
• Calibrate and maintain laboratory equipment, ensuring its proper functioning and accuracy.
• Prepare reagents, solutions, and standards required for testing.
• Investigate out-of-specification (OOS) results and deviations, contributing to root cause analysis and corrective actions.
• Participate in method validation and transfer activities as required.
• Maintain a clean and organized laboratory environment, adhering to safety protocols.
• Review and interpret analytical data, preparing reports for management and regulatory submissions.
• Collaborate effectively with other departments, including production, R&D, and regulatory affairs.
• Stay updated on current scientific literature, industry best practices, and regulatory changes impacting pharmaceutical quality control.
• Assist in internal and external audits related to quality control processes.

• Bachelor's degree in Chemistry, Pharmacy, Biochemistry, or a closely related scientific field. Master's degree is a plus.
• Minimum of 3 years of hands-on experience in pharmaceutical quality control or analytical laboratory testing.
• Proficiency with common analytical instrumentation and techniques used in the pharmaceutical industry.
• Thorough understanding of GMP, FDA regulations, and ICH guidelines.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent attention to detail and accuracy in data recording and reporting.
• Good organizational and time management skills, with the ability to prioritize tasks.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a collaborative team.
• Experience with method validation and stability testing is advantageous.

• Perform quantitative and qualitative analysis of raw materials, intermediates, and finished pharmaceutical products.
• Conduct analytical tests using techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Prepare reagents and solutions required for analytical testing.
• Calibrate and maintain laboratory equipment to ensure accurate results.
• Document all testing procedures, results, and observations in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Review and interpret analytical data, identifying any deviations from specifications.
• Investigate out-of-specification (OOS) results and contribute to root cause analysis.
• Prepare certificates of analysis (CoAs) and other quality control reports.
• Collaborate with the R&D and production departments to resolve quality-related issues.
• Ensure compliance with all relevant regulatory guidelines and pharmacopeial standards.
• Participate in method validation and transfer activities.
• Maintain a clean and organized laboratory environment.
• Assist in the training of junior QC personnel.
• Stay updated on current industry trends and regulatory requirements in pharmaceutical quality control.
• Contribute to continuous improvement initiatives within the QC department.

• Bachelor's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum of 3 years of experience in pharmaceutical quality control or analytical testing.
• Hands-on experience with analytical instrumentation such as HPLC, GC, and spectrophotometers.
• Thorough understanding of GMP, GLP, and relevant regulatory guidelines (e.g., FDA, EMA).
• Proficiency in laboratory techniques and procedures.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent attention to detail and accuracy in data recording and reporting.
• Good written and verbal communication skills.
• Ability to work independently and as part of a team in a laboratory setting.
• Proficiency in Microsoft Office Suite, particularly Excel.
• Experience with pharmacopeial methods (USP, BP, EP) is essential.
• Commitment to safety and quality in all laboratory activities.

• Conduct analytical testing of raw materials, intermediates, and finished pharmaceutical products using various techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Perform method validation and verification studies according to regulatory guidelines.
• Prepare and maintain detailed laboratory records, analytical reports, and Certificates of Analysis (CoAs).
• Ensure all laboratory activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory standards (e.g., FDA, EMA).
• Calibrate and maintain laboratory equipment, ensuring accuracy and reliability of test results.
• Investigate out-of-specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
• Participate in internal and external audits as required.
• Stay updated with the latest advancements in analytical techniques and pharmaceutical regulations.
• Collaborate with R&D, production, and regulatory affairs teams to resolve quality-related issues.
• Contribute to the continuous improvement of quality control processes and systems.

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 3 years of experience in pharmaceutical quality control or analytical development.
• Hands-on experience with analytical instrumentation such as HPLC, GC, dissolution apparatus, and Karl Fischer titrators.
• Strong knowledge of GMP/GLP principles and regulatory requirements.
• Proficiency in data analysis and interpretation.
• Excellent documentation and technical writing skills.
• Strong problem-solving abilities and a meticulous approach to work.
• Ability to work independently and as part of a team in a fast-paced environment.
• Good communication skills.