1 228 Pharmaceutical Field jobs in Bahrain
Process Chemist - Pharmaceutical Manufacturing
23005 Busaiteen, Muharraq
BHD70000 Annually
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Our client, a dynamic pharmaceutical company, is seeking a talented Process Chemist to join their innovative manufacturing team in A'ali, Northern, BH . This role is integral to optimizing and scaling up chemical processes for the production of active pharmaceutical ingredients (APIs) and drug products. The successful candidate will be responsible for developing, validating, and troubleshooting chemical synthesis routes and manufacturing processes. You will conduct laboratory experiments, pilot-scale trials, and full-scale production support, ensuring compliance with stringent regulatory standards (cGMP) and safety protocols. Key responsibilities include identifying opportunities for process improvement, reducing waste, and increasing yield and efficiency. You will analyze process data, identify critical process parameters (CPPs), and implement control strategies to ensure consistent product quality. The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Chemical Engineering, or a related field, with a minimum of 4 years of experience in pharmaceutical process development or manufacturing. Hands-on experience with analytical techniques such as HPLC, GC, MS, and NMR is essential. Familiarity with process safety evaluations and regulatory requirements is highly desirable. This role requires strong problem-solving skills, excellent analytical abilities, and the capacity to work effectively in a team environment. You will collaborate closely with R&D, Quality Assurance, and Production teams. This position offers a remote work option for specific analytical tasks and data reporting, with some on-site laboratory work required. We are looking for a detail-oriented and results-driven chemist who is passionate about advancing pharmaceutical manufacturing technologies and contributing to the development of life-saving medicines.
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Remote Pharmaceutical Manufacturing Process Engineer
20210 Al Jasra
BHD100000 Annually
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Our client, a progressive pharmaceutical organization at the forefront of drug manufacturing, is seeking a highly skilled Remote Pharmaceutical Manufacturing Process Engineer. This is a fully remote position focused on optimizing and ensuring the efficiency, safety, and compliance of our pharmaceutical manufacturing processes. The successful candidate will leverage their expertise in chemical engineering, process validation, and lean manufacturing principles to drive improvements across our production facilities. You will work remotely to analyze process data, design solutions, and collaborate with site teams to implement enhancements, all from your home office.
Responsibilities:
Responsibilities:
- Analyze existing pharmaceutical manufacturing processes to identify areas for improvement in efficiency, yield, and cost-effectiveness.
- Develop and implement process optimization strategies using principles of chemical engineering and industrial best practices.
- Design, validate, and implement new manufacturing processes or modifications to existing ones, ensuring compliance with regulatory standards (e.g., GMP).
- Troubleshoot manufacturing process issues and lead root cause analysis efforts.
- Prepare and review process validation protocols and reports.
- Develop Standard Operating Procedures (SOPs) and batch records for manufacturing processes.
- Conduct risk assessments for process changes and new equipment.
- Collaborate with R&D, Quality Assurance, and Production teams to ensure seamless technology transfer and scale-up.
- Stay current with industry trends, new technologies, and regulatory updates in pharmaceutical manufacturing.
- Manage projects related to process improvement and new product introductions.
- Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Engineering, or a related field.
- Minimum of 6 years of experience in pharmaceutical manufacturing process engineering or a similar role.
- Strong understanding of GMP regulations and their application to manufacturing processes.
- Proven experience in process design, validation, scale-up, and troubleshooting.
- Familiarity with pharmaceutical dosage forms (e.g., tablets, capsules, injectables).
- Proficiency in process simulation software and data analysis tools.
- Excellent problem-solving, analytical, and project management skills.
- Strong interpersonal and communication skills, with the ability to work effectively in a remote, cross-functional team environment.
- Experience with Lean Manufacturing or Six Sigma methodologies is a plus.
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Senior Process Engineer - Pharmaceutical Manufacturing
101 Manama, Capital
BHD7500 Annually
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Our client, a leading pharmaceutical manufacturer, is seeking an experienced Senior Process Engineer to join their innovative team in Manama, Capital, BH . This critical role will be instrumental in optimizing and scaling up manufacturing processes for a range of pharmaceutical products. The Senior Process Engineer will be responsible for designing, developing, troubleshooting, and improving chemical and physical processes in the manufacturing plant, ensuring efficiency, quality, and compliance with stringent regulatory standards. Key responsibilities include process simulation and modeling, equipment selection and validation, development of Standard Operating Procedures (SOPs), and implementation of continuous improvement initiatives using methodologies like Lean Manufacturing and Six Sigma. You will collaborate closely with R&D, Quality Assurance, and Production teams to ensure smooth technology transfer and scale-up of new products. The ideal candidate will have a minimum of 8 years of experience in process engineering within the pharmaceutical or a closely related highly regulated industry. A strong understanding of GMP (Good Manufacturing Practices) is essential. Excellent analytical, problem-solving, and project management skills are required, along with proficiency in process simulation software and statistical analysis tools. A bachelor's or master's degree in Chemical Engineering or a related discipline is mandatory. This is an exceptional opportunity to contribute to the advancement of pharmaceutical manufacturing and drive operational excellence in a state-of-the-art facility.
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2
Lead Process Engineer (Pharmaceutical Manufacturing)
00711 Bilad Al Qadeem, Capital
BHD95000 Annually
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Our client, a leading pharmaceutical manufacturer, is seeking an experienced Lead Process Engineer to oversee and optimize manufacturing processes at their facility in **Salmabad, Northern, BH**. This critical role will focus on enhancing efficiency, ensuring quality, and driving innovation in pharmaceutical production. The ideal candidate will have a strong background in chemical or process engineering, extensive experience in GMP environments, and excellent problem-solving skills.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Lead the design, development, and optimization of pharmaceutical manufacturing processes, ensuring adherence to GMP and regulatory guidelines.
- Develop process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), and mass and energy balances.
- Identify opportunities for process improvement to increase yield, reduce cycle times, and minimize waste.
- Troubleshoot and resolve complex process-related issues during manufacturing operations.
- Conduct process validation activities, including IQ, OQ, and PQ, and prepare necessary documentation.
- Collaborate with R&D, quality assurance, and production teams to ensure seamless technology transfer and scale-up.
- Develop and implement process control strategies and parameters to maintain optimal operating conditions.
- Train and mentor junior process engineers and manufacturing personnel.
- Stay abreast of new technologies and advancements in pharmaceutical manufacturing processes.
- Ensure compliance with all safety, environmental, and regulatory requirements.
- Manage projects related to process upgrades, new equipment installations, and site expansions.
- Analyze process data and performance metrics to identify trends and areas for improvement.
Qualifications:
- Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Engineering, or a related field.
- Minimum of 8 years of experience in process engineering within the pharmaceutical or biotechnology industry, with at least 2 years in a lead or supervisory capacity.
- In-depth knowledge of Good Manufacturing Practices (GMP) and regulatory requirements (e.g., FDA, EMA).
- Proven experience with process validation, scale-up, and technology transfer in a GMP environment.
- Proficiency in process simulation software (e.g., Aspen Plus, HYSYS) and statistical analysis tools.
- Strong understanding of unit operations commonly used in pharmaceutical manufacturing (e.g., filtration, drying, crystallization, granulation).
- Excellent analytical, problem-solving, and critical thinking skills.
- Effective leadership, communication, and interpersonal skills.
- Ability to manage multiple projects simultaneously and meet strict deadlines.
- Experience with lean manufacturing principles and Six Sigma methodologies is a plus.
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3
Quality Control Analyst, Pharmaceutical Manufacturing
325, Muharraq, BH Muharraq, Muharraq
BHD60000 Annually
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Posted 7 days ago
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Our client is seeking a meticulous Quality Control Analyst to join their state-of-the-art pharmaceutical manufacturing facility in Muharraq, Muharraq, BH . This vital role ensures that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. The Quality Control Analyst will perform a variety of analytical tests on raw materials, in-process samples, and finished products, ensuring the integrity and safety of our medicines.
Key responsibilities include:
This is an excellent opportunity to contribute to the quality and safety of pharmaceutical products in a reputable company. Join our client's dedicated quality team and make a difference. Apply today!
Key responsibilities include:
- Performing chemical and physical analysis of raw materials, intermediates, and finished products using various laboratory techniques.
- Conducting dissolution testing, Karl Fischer titration, HPLC, UV-Vis spectroscopy, and other relevant assays.
- Documenting all test results accurately and in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Maintaining laboratory equipment, performing calibration, and ensuring proper functioning.
- Investigating out-of-specification (OOS) results and participating in deviation investigations.
- Preparing and reviewing quality control documentation, including test methods and reports.
- Ensuring the efficient workflow of the QC laboratory and adherence to testing schedules.
- Collaborating with production and quality assurance teams to resolve quality issues promptly.
- Maintaining a safe working environment and adhering to all laboratory safety protocols.
This is an excellent opportunity to contribute to the quality and safety of pharmaceutical products in a reputable company. Join our client's dedicated quality team and make a difference. Apply today!
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4
Quality Assurance Manager - Pharmaceutical Manufacturing
13031 Hamad Town, Northern
BHD75000 Annually
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Posted 12 days ago
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Our client, a reputable pharmaceutical manufacturing firm, is seeking an experienced Quality Assurance Manager to lead their quality control and assurance operations in Hamad Town, Northern, BH . This senior role is responsible for ensuring that all manufacturing processes and products comply with stringent regulatory standards, including GMP, and company quality policies. The ideal candidate will have a comprehensive understanding of pharmaceutical quality systems, risk management, and validation processes. You will oversee the QA team, manage internal and external audits, handle deviations and CAPAs, and drive continuous improvement initiatives. The Quality Assurance Manager will play a critical role in maintaining product integrity, patient safety, and regulatory compliance. This position requires strong leadership, analytical skills, and a deep commitment to quality excellence within a complex manufacturing environment.
Key responsibilities include:
Qualifications:
Key responsibilities include:
- Developing, implementing, and maintaining the company's Quality Management System (QMS).
- Ensuring compliance with cGMP, ICH guidelines, and other relevant regulatory standards.
- Managing and overseeing all aspects of quality assurance for pharmaceutical manufacturing.
- Leading and mentoring the QA team, providing training and performance management.
- Conducting internal audits and hosting regulatory agency inspections and client audits.
- Managing deviation investigations, root cause analysis, and implementing corrective and preventive actions (CAPAs).
- Reviewing and approving batch records, validation protocols, and reports.
- Overseeing product release process and ensuring products meet all quality specifications.
- Identifying and implementing continuous improvement initiatives in quality processes.
- Managing change control processes and ensuring their effective implementation.
Qualifications:
- Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
- Minimum of 7-10 years of experience in Quality Assurance within the pharmaceutical industry, with at least 3 years in a management role.
- Extensive knowledge of cGMP, FDA regulations, and international pharmaceutical quality standards.
- Proven experience with QMS implementation, audits, deviations, CAPAs, and validation.
- Strong leadership, team management, and communication skills.
- Excellent analytical and problem-solving abilities.
- Ability to work under pressure and manage multiple priorities effectively.
- Proficiency in pharmaceutical manufacturing processes and quality control techniques.
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5
Senior Quality Assurance Manager - Pharmaceutical Manufacturing
701 Southern, Southern
BHD35000 Annually
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Our client, a leading pharmaceutical company, is seeking an accomplished Senior Quality Assurance Manager to lead its quality control and assurance efforts in Nuwaidrat. This role is critical in ensuring that all pharmaceutical products manufactured meet the highest standards of quality, safety, and efficacy, in strict accordance with international regulatory guidelines, including GMP (Good Manufacturing Practices). The ideal candidate will have extensive experience in pharmaceutical quality systems, a deep understanding of regulatory compliance, and a proven ability to manage and develop a high-performing QA team. Responsibilities include developing, implementing, and maintaining the company's Quality Management System (QMS), conducting internal audits and inspections, managing external regulatory audits, and overseeing batch release processes. You will also be responsible for risk management activities, deviation investigations, change control procedures, and CAPA (Corrective and Preventive Actions) implementation. This role demands a meticulous approach, strong analytical skills, and the ability to make critical decisions to uphold product integrity. The Senior Quality Assurance Manager will collaborate with R&D, production, and regulatory affairs departments to ensure seamless integration of quality principles throughout the product lifecycle. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field, coupled with at least 8 years of progressive experience in pharmaceutical quality assurance, is required. Candidates should demonstrate a strong knowledge of relevant pharmaceutical regulations (e.g., FDA, EMA, SFDA). Leadership experience and excellent communication and interpersonal skills are essential for success in this challenging yet rewarding position. This is an excellent opportunity to make a significant impact in a company dedicated to improving global health.
Key Responsibilities:
This exciting opportunity is situated in Nuwaidrat, Southern, BH .
Key Responsibilities:
- Lead and manage the Quality Assurance department, ensuring compliance with regulatory standards.
- Develop, implement, and maintain robust Quality Management Systems (QMS).
- Oversee and conduct internal audits and ensure readiness for external regulatory inspections.
- Manage the batch record review and product release process.
- Investigate deviations, implement CAPAs, and manage the change control system.
- Conduct risk assessments and implement appropriate mitigation strategies.
- Ensure adherence to Good Manufacturing Practices (GMP) and other relevant regulations.
- Train QA personnel and promote a culture of quality throughout the organization.
- Liaise with regulatory agencies and manage responses to regulatory inquiries.
- Drive continuous improvement initiatives within the QA function and manufacturing operations.
This exciting opportunity is situated in Nuwaidrat, Southern, BH .
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6
Pharmaceutical Research Scientist
700 Southern, Southern
BHD60000 Annually
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Our client, a leading pharmaceutical innovator, is seeking a highly skilled Pharmaceutical Research Scientist to join their dedicated research and development team in Nuwaidrat . This role is crucial in driving forward our client's mission to discover and develop life-changing medicines. You will be responsible for conducting complex experiments, analyzing data, and contributing to the progression of drug candidates through the development pipeline. This position requires a meticulous approach, a strong scientific background, and a commitment to excellence.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and execute in vitro and in vivo experiments to evaluate drug efficacy and safety.
- Develop and optimize new analytical methods for drug characterization.
- Analyze experimental data using statistical software and interpret results.
- Prepare detailed reports, presentations, and manuscripts for scientific publications and internal review.
- Collaborate with cross-functional teams, including medicinal chemists, pharmacologists, and toxicologists.
- Maintain accurate and organized laboratory records in compliance with Good Laboratory Practices (GLP).
- Stay updated with the latest scientific literature and advancements in pharmaceutical research.
- Contribute to the identification and validation of new therapeutic targets.
- Operate and maintain laboratory equipment, ensuring calibration and functionality.
- Assist in the preparation of regulatory submissions.
Qualifications:
- Ph.D. or Master's degree in Pharmacology, Pharmaceutical Sciences, Biochemistry, or a related life science field.
- Proven experience in drug discovery and development.
- Expertise in molecular biology techniques, cell-based assays, and data analysis.
- Proficiency with laboratory equipment and scientific instrumentation.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a collaborative team.
- Strong analytical and problem-solving abilities.
- Experience with preclinical study design and execution is highly desirable.
- Knowledge of regulatory guidelines relevant to pharmaceutical development.
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7
Pharmaceutical Research Scientist
00981 Bilad Al Qadeem, Capital
BHD95000 Annually
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Our client, a leading pharmaceutical company, is looking for a dedicated and innovative Pharmaceutical Research Scientist to contribute to cutting-edge drug discovery and development efforts in Salmabad, Northern, BH . This role involves a combination of laboratory work and data analysis, with a hybrid work arrangement offering flexibility.
Responsibilities:
Responsibilities:
- Design and conduct experiments to investigate new drug targets and therapeutic modalities.
- Perform laboratory procedures, including cell culture, molecular biology techniques, and biochemical assays.
- Analyze experimental data, interpret results, and draw scientifically sound conclusions.
- Contribute to the development of novel drug candidates through early-stage research.
- Maintain accurate and detailed laboratory notebooks and research records.
- Collaborate with cross-functional teams, including medicinal chemists, pharmacologists, and clinical scientists.
- Prepare scientific reports, presentations, and publications to disseminate research findings.
- Stay current with the latest scientific literature and advancements in pharmaceutical research.
- Contribute to project planning and strategy discussions.
- Ensure compliance with laboratory safety protocols and regulatory guidelines.
- Operate and maintain laboratory equipment.
- Assist in the evaluation of new technologies and methodologies for research applications.
- Ph.D. or Master's degree in Pharmacology, Biochemistry, Molecular Biology, or a related life science field.
- Minimum of 3 years of post-doctoral or industry research experience in pharmaceutical R&D.
- Proven expertise in relevant experimental techniques and methodologies.
- Strong understanding of drug discovery processes and principles.
- Excellent analytical and problem-solving skills.
- Proficiency in data analysis software and statistical methods.
- Effective written and oral communication skills, with the ability to present complex scientific information.
- Ability to work independently and collaboratively in a team-oriented environment.
- Strong organizational skills and attention to detail.
- Familiarity with Good Laboratory Practices (GLP) is a plus.
- Experience with specific therapeutic areas or target classes relevant to the company's focus is advantageous.
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8
Pharmaceutical Research Scientist
BH29 Busaiteen, Muharraq
BHD95000 Annually
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Our client, a leading pharmaceutical innovator, is seeking a dedicated and skilled Pharmaceutical Research Scientist to join our dynamic R&D team. This role involves hands-on laboratory work as well as data analysis and report generation. You will be instrumental in the discovery and development of novel therapeutic compounds, working on cutting-edge research projects from conception through to pre-clinical stages. Responsibilities include designing and conducting experiments, analyzing complex biological and chemical data, and meticulously documenting findings. You will collaborate with a multidisciplinary team of scientists, chemists, and pharmacologists to advance drug discovery pipelines. Proficiency in molecular biology techniques, cell culture, and various analytical methods is essential. Experience with assay development and validation, as well as understanding of drug metabolism and pharmacokinetic (DMPK) principles, would be highly advantageous. You will also be expected to stay abreast of the latest scientific literature and technological advancements in the pharmaceutical field. Contributing to the preparation of research reports, manuscripts for publication, and presentations for scientific conferences will be a key part of your role. The ideal candidate will possess strong critical thinking skills, a meticulous attention to detail, and the ability to work effectively both independently and as part of a collaborative team. This hybrid position offers a balance between focused laboratory work and the flexibility of remote data analysis and collaboration, fostering an environment of both intense scientific inquiry and innovative teamwork. Your contribution will be vital in bringing life-changing treatments to patients worldwide. We are looking for passionate individuals eager to make a tangible impact in pharmaceutical research.
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