What Jobs are available for Pharmaceuticals in Bahrain?
Showing 2008 Pharmaceuticals jobs in Bahrain
Lead Formulation Scientist, Pharmaceuticals
444 Amwaj Islands
BHD8500 Monthly
WhatJobs
Posted 1 day ago
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Job Description
Our client is seeking a highly skilled and experienced Lead Formulation Scientist to drive innovative pharmaceutical product development, working entirely remotely. This senior position will lead the design, development, and optimization of novel drug formulations, ensuring product efficacy, stability, and manufacturability. You will be responsible for guiding a team of formulation scientists, collaborating with cross-functional R&D teams, and staying at the forefront of pharmaceutical formulation technologies. The ideal candidate will possess a deep understanding of pharmaceutical sciences, excipient selection, drug delivery systems, and regulatory requirements, coupled with exceptional leadership and project management skills for a remote setting.
Key Responsibilities:
Key Responsibilities:
- Lead the formulation development of new pharmaceutical products from concept to clinical trials.
- Design and execute studies to optimize drug product formulations, considering factors like bioavailability, stability, and patient compliance.
- Develop and validate analytical methods for characterizing drug products and their components.
- Investigate and troubleshoot formulation challenges, proposing innovative solutions.
- Select appropriate excipients and materials to achieve desired product performance.
- Collaborate with process development and manufacturing teams to ensure successful scale-up and commercialization.
- Mentor and guide junior formulation scientists, fostering scientific excellence and career development.
- Prepare comprehensive formulation development reports and regulatory submission documents.
- Stay abreast of emerging trends and technologies in pharmaceutical formulation and drug delivery.
- Manage external contract research organizations (CROs) for specific formulation development activities.
- Ensure all activities comply with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
- Present research findings and project updates to internal stakeholders and management.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related discipline.
- Minimum of 8 years of progressive experience in pharmaceutical formulation development.
- Proven track record of successfully developing and advancing drug formulations through various stages of development.
- Expertise in various dosage forms (e.g., oral solid dosage, injectables, topical).
- Strong knowledge of excipient properties, drug delivery systems, and analytical techniques.
- Experience with statistical analysis and design of experiments (DoE).
- Excellent leadership, communication, and project management skills, with the ability to lead a remote team.
- Familiarity with regulatory requirements (FDA, EMA) for drug product development.
- Strong understanding of intellectual property within drug formulation.
- Publications in peer-reviewed journals and/or patents are highly desirable.
- This is a fully remote position, allowing collaboration with a global team.
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0
Senior Process Engineer - Pharmaceuticals
20021 Jaww, Southern
BHD110000 Annually
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Posted 1 day ago
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Job Description
Our client, a global leader in pharmaceutical manufacturing, is seeking an accomplished Senior Process Engineer to optimize and innovate production processes within their state-of-the-art facility. This role is crucial for enhancing efficiency, ensuring product quality, and maintaining compliance with stringent regulatory standards. You will leverage your deep technical expertise to design, implement, and troubleshoot complex manufacturing processes, driving continuous improvement initiatives.
Responsibilities:
Qualifications:
Responsibilities:
- Design, develop, and optimize manufacturing processes for pharmaceutical products, ensuring efficiency, scalability, and cost-effectiveness.
- Conduct detailed process analyses, including mass and energy balances, PFDs (Process Flow Diagrams), and P&IDs (Piping and Instrumentation Diagrams).
- Troubleshoot and resolve process-related issues, identifying root causes and implementing corrective actions.
- Lead process validation activities, ensuring compliance with cGMP, FDA, and other relevant regulatory requirements.
- Develop and execute experimental plans for process development and improvement projects.
- Implement new technologies and automation solutions to enhance process performance.
- Collaborate with R&D, Quality Assurance, and Operations teams to ensure seamless technology transfer and production scale-up.
- Prepare technical reports, documentation, and presentations for management and regulatory bodies.
- Stay current with advancements in pharmaceutical manufacturing technologies and best practices.
- Train and mentor junior engineers and technical staff on process engineering principles and operational procedures.
- Oversee process safety assessments and implement risk mitigation strategies.
Qualifications:
- Bachelor's or Master's degree in Chemical Engineering, Mechanical Engineering, or a related field.
- Minimum of 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
- Proven experience with process design, scale-up, validation, and optimization.
- In-depth knowledge of cGMP regulations and FDA guidelines.
- Proficiency in process simulation software (e.g., Aspen Plus, HYSYS) and CAD tools.
- Strong analytical, problem-solving, and project management skills.
- Excellent communication and teamwork abilities.
- Experience with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Ability to work effectively in a highly regulated and complex manufacturing environment.
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1
Senior Process Engineer - Pharmaceuticals
30303 Zallaq, Southern
BHD90000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical manufacturing company, is seeking a highly skilled and experienced Senior Process Engineer to join their operations team in Zallaq, Southern, BH . This role is crucial for optimizing and ensuring the efficiency, safety, and quality of our manufacturing processes. The ideal candidate will possess a strong background in chemical engineering, process design, optimization, and troubleshooting within the pharmaceutical industry. This hybrid role combines on-site work for critical hands-on operations with remote flexibility for analysis and reporting, fostering a productive and collaborative work environment.
Responsibilities:
Responsibilities:
- Design, develop, and implement innovative and efficient manufacturing processes for pharmaceutical products, ensuring compliance with GMP and regulatory standards.
- Optimize existing production processes to improve yield, reduce costs, enhance safety, and minimize waste.
- Conduct process hazard analyses (PHAs) and implement robust safety protocols to ensure a safe working environment.
- Troubleshoot and resolve complex process-related issues, identifying root causes and implementing effective solutions.
- Develop and maintain detailed process documentation, including P&IDs, SOPs, and batch records.
- Lead process validation activities and ensure successful technology transfer from R&D to manufacturing.
- Collaborate with cross-functional teams, including R&D, Quality Assurance, Operations, and Maintenance, to achieve project objectives.
- Stay abreast of new technologies, process improvements, and industry best practices in pharmaceutical manufacturing.
- Monitor key performance indicators (KPIs) for production processes and implement continuous improvement initiatives.
- Manage and mentor junior process engineers and provide technical guidance.
- Participate in the selection and qualification of new equipment and technologies.
- Contribute to capital expenditure projects related to process improvements and facility upgrades.
- Bachelor's degree in Chemical Engineering, Pharmaceutical Engineering, or a related discipline. Master's degree preferred.
- Minimum of 7 years of experience in process engineering, with a significant focus on pharmaceutical or biopharmaceutical manufacturing.
- Strong understanding of Good Manufacturing Practices (GMP) and other relevant regulatory requirements (e.g., FDA, EMA).
- Proven experience in process design, optimization, scale-up, and validation.
- Proficiency in process simulation software (e.g., Aspen Plus) and statistical analysis tools.
- Excellent analytical and problem-solving skills, with a demonstrated ability to troubleshoot complex technical issues.
- Strong project management skills and experience leading cross-functional teams.
- Effective communication, interpersonal, and presentation skills.
- Knowledge of process safety management (PSM) principles.
- Ability to work effectively in a hybrid work setting, balancing on-site and remote responsibilities.
- Experience with automation and control systems in manufacturing environments.
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2
Clinical Research Associate - Pharmaceuticals
222 Manama, Capital
BHD75000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing global health, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in **Manama, Capital, BH**. This hybrid role offers a balance of on-site responsibilities and remote flexibility. The CRA will be responsible for ensuring the smooth execution of clinical trials in accordance with Good Clinical Practice (GCP) guidelines, protocols, and regulatory requirements. Key responsibilities include site selection and initiation, monitoring clinical trial conduct, and ensuring the accuracy, completeness, and quality of data collected. You will act as a liaison between the investigative sites and the sponsor, managing site staff, and resolving issues that arise during the trial. The CRA will also be responsible for source data verification, regulatory document review, and ensuring compliance with all applicable regulations. Duties include conducting pre-study, interim, and close-out visits to assigned clinical sites. A critical aspect of this role involves subject safety monitoring and reporting adverse events. The successful candidate will have a strong understanding of the drug development process and clinical trial methodologies. Excellent communication, organizational, and interpersonal skills are essential for building strong relationships with investigators and site staff. This position offers a fantastic opportunity to contribute to life-changing pharmaceutical research and development within **Manama, Capital, BH**. A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field is required. A Master's degree is a plus. A minimum of 3-5 years of experience as a CRA or in a similar clinical research role is essential. Thorough knowledge of ICH-GCP guidelines and relevant regulatory requirements is mandatory. Strong monitoring skills, data management experience, and the ability to travel to sites as needed are crucial. Join a passionate team committed to improving patient outcomes through rigorous scientific research.
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3
Senior Formulation Scientist - Pharmaceuticals
31603 Al Seef
BHD105000 Annually
WhatJobs
Posted 10 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking an accomplished Senior Formulation Scientist to join their innovative Research and Development team. This role is integral to the drug development process, focusing on the design, optimization, and scale-up of pharmaceutical formulations. Based in **Hidd, Muharraq, BH**, this position requires a candidate with extensive experience in pharmaceutical science, a strong understanding of regulatory requirements, and a passion for bringing life-changing medicines to market.
Responsibilities:
Responsibilities:
- Lead the formulation development of new drug products, from pre-formulation studies to commercial readiness.
- Design and conduct experiments to optimize drug delivery systems, ensuring bioavailability, stability, and efficacy.
- Develop and validate analytical methods for characterizing drug formulations.
- Troubleshoot formulation challenges and implement effective solutions.
- Collaborate with cross-functional teams, including analytical chemistry, process development, and regulatory affairs.
- Prepare comprehensive documentation for regulatory submissions (e.g., IND, NDA).
- Oversee the scale-up of formulations from laboratory to pilot and commercial manufacturing.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Stay current with scientific literature, industry trends, and new technologies in pharmaceutical formulation.
- Mentor junior scientists and provide technical guidance on formulation development projects.
- Evaluate new excipients and technologies for potential application in drug formulations.
- Contribute to the strategic direction of the formulation development group.
- Present research findings at internal meetings and scientific conferences.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 5-7 years of hands-on experience in pharmaceutical formulation development.
- Proven expertise in developing various dosage forms (e.g., oral solid dosage, injectables, topical).
- Strong understanding of physical chemistry, drug delivery systems, and pharmacokinetics.
- Proficiency in formulation development techniques and analytical instrumentation (e.g., HPLC, dissolution testing).
- Experience with GMP regulations and regulatory submission processes.
- Excellent problem-solving, critical thinking, and experimental design skills.
- Strong written and verbal communication skills, with the ability to present complex data clearly.
- Ability to work independently and collaboratively in a team-oriented environment.
- Project management skills and the ability to manage multiple priorities effectively.
- Experience with biologics formulation is a plus.
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4
Clinical Research Associate - Pharmaceuticals
105 Amwaj Islands
BHD70000 Annually
WhatJobs
Posted 15 days ago
Job Viewed
Job Description
Our client, a dynamic pharmaceutical company, is seeking a dedicated Clinical Research Associate (CRA) to join their expanding clinical operations team. This role is crucial in ensuring the smooth and compliant execution of clinical trials, overseeing multiple study sites. The successful candidate will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring adherence to study protocols, GCP guidelines, and regulatory requirements. You will act as the primary liaison between the sponsor and study sites, fostering strong relationships and facilitating efficient data collection. The ideal candidate possesses excellent organizational skills, a keen eye for detail, and a thorough understanding of clinical trial processes.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, routine monitoring, and close-out visits to assigned clinical sites.
- Ensure compliance with study protocols, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
- Verify the accuracy, completeness, and integrity of clinical data.
- Manage site-level regulatory documentation and essential study documents.
- Serve as the main point of contact for investigators and site staff.
- Identify and resolve site-level issues and deviations promptly.
- Train site personnel on study-specific procedures and requirements.
- Track study progress and report findings to the clinical project manager.
- Contribute to the development of study protocols and case report forms.
- Ensure patient safety and data privacy are maintained at all times.
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5
Quality Assurance Manager, Pharmaceuticals
710 Gudaibiya, Capital
BHD90000 Annually
WhatJobs
Posted 16 days ago
Job Viewed
Job Description
Our client is seeking a highly skilled and experienced Quality Assurance Manager to oversee quality operations within their pharmaceutical manufacturing facility. This is a crucial on-site role responsible for ensuring that all products meet stringent quality standards and comply with regulatory requirements, including GMP (Good Manufacturing Practices). You will lead the QA team, implement and maintain the quality management system (QMS), and drive continuous improvement in all quality-related processes. Key responsibilities include developing and executing quality plans, managing deviations and CAPAs (Corrective and Preventive Actions), conducting internal audits, supporting regulatory inspections, and ensuring the quality of raw materials, in-process materials, and finished products. The ideal candidate will have a strong background in pharmaceutical quality assurance, a deep understanding of regulatory guidelines, and excellent leadership and problem-solving skills. You will collaborate closely with production, R&D, and regulatory affairs departments to uphold the highest standards of product quality and patient safety. This position requires a meticulous attention to detail and a commitment to excellence in a regulated industry.
Responsibilities:
Qualifications:
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with pharmaceutical regulations.
- Oversee and manage all aspects of quality assurance for manufacturing operations.
- Lead the Quality Assurance team, providing guidance, training, and performance management.
- Ensure compliance with cGMP (current Good Manufacturing Practices) and other relevant regulatory standards.
- Manage deviations, investigations, and the CAPA process to address quality issues effectively.
- Conduct internal audits and support external regulatory inspections (e.g., FDA, EMA).
- Review and approve batch records, specifications, and validation protocols.
- Oversee the release of finished products after ensuring they meet all quality requirements.
- Collaborate with Production, R&D, and other departments to ensure product quality throughout the lifecycle.
- Monitor quality metrics and KPIs, implementing continuous improvement initiatives.
- Manage supplier qualification and quality agreements.
- Stay up-to-date with evolving regulatory requirements and industry best practices.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, Engineering, or a related life science field. A Master's degree is preferred.
- Minimum of 7 years of experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry.
- At least 3 years of experience in a management or supervisory role.
- In-depth knowledge of GMP regulations (e.g., FDA 21 CFR Parts 210/211, EudraLex Volume 4).
- Proven experience with QMS implementation and maintenance, deviation management, and CAPA systems.
- Strong understanding of validation processes (process, cleaning, equipment).
- Excellent analytical, problem-solving, and decision-making skills.
- Strong leadership and team management capabilities.
- Exceptional communication and interpersonal skills.
- Experience with regulatory inspections and audits.
- Proficiency in relevant software, including LIMS and QMS software.
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6
Quality Assurance Specialist - Pharmaceuticals
70230 Halat Seltah, Muharraq
BHD80000 Annually
WhatJobs
Posted 16 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a diligent and detail-oriented Quality Assurance Specialist to join their team in Jidhafs, Capital, BH . This role is integral to ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout the manufacturing and development lifecycle. You will be responsible for implementing and maintaining quality management systems, conducting internal audits, reviewing batch records, investigating deviations, and supporting regulatory inspections. The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP) and other relevant pharmaceutical quality guidelines. Excellent analytical skills, meticulous attention to detail, and strong documentation abilities are crucial for success. This position offers a hybrid work model, combining essential on-site responsibilities with the flexibility of remote work. You will play a vital role in upholding our commitment to product quality and patient safety.
Responsibilities:
Responsibilities:
- Implement and maintain the company's Quality Management System (QMS).
- Conduct internal audits of manufacturing processes, documentation, and facilities.
- Review and approve batch production and control records.
- Investigate deviations, non-conformances, and out-of-specification (OOS) results.
- Participate in CAPA (Corrective and Preventive Actions) development and implementation.
- Support regulatory inspections from health authorities.
- Ensure compliance with GMP, GCP, and other applicable regulations.
- Develop and deliver quality assurance training to relevant personnel.
- Manage quality-related documentation and records.
- Contribute to continuous improvement initiatives within the QA department.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and other relevant pharmaceutical regulations.
- Experience with quality systems, including document control, deviation management, and CAPA.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and organizational abilities.
- Proficient in Microsoft Office Suite and quality management software.
- Strong written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
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7
Principal Research Scientist - Pharmaceuticals
2115 Saar, Northern
BHD120000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a pioneering pharmaceutical company, is seeking an exceptional Principal Research Scientist to join their innovative, fully remote research and development team. This critical role, while connected to Saar, Northern, BH , allows for complete remote operation. You will lead groundbreaking research initiatives, contributing to the development of novel therapeutics and driving scientific advancement within the organization. Your responsibilities will encompass designing and executing complex experimental protocols, analyzing and interpreting scientific data, and staying abreast of the latest scientific literature and technological advancements. You will be responsible for developing research hypotheses, leading project teams, and potentially mentoring junior scientists. Effective communication of research findings through presentations, publications, and reports will be paramount. The ideal candidate will possess a Ph.D. in a relevant scientific discipline (e.g., Pharmacology, Biochemistry, Molecular Biology), coupled with a minimum of 8-10 years of post-doctoral research experience in the pharmaceutical industry. A strong publication record, a deep understanding of drug discovery and development processes, and expertise in specific therapeutic areas are highly desirable. Experience in leading research projects and managing scientific collaborations is essential. This position requires a highly motivated, intellectually curious individual with excellent critical thinking and problem-solving skills, capable of independent work and thriving in a remote research environment. A competitive salary, comprehensive benefits, and the opportunity to make a significant impact on global health are offered. Join us in shaping the future of medicine from your remote workspace.
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8
Senior Research Scientist - Pharmaceuticals
2250 Al Seef
BHD120000 Annually
WhatJobs
Posted 21 days ago
Job Viewed
Job Description
Our client, a cutting-edge research and development firm, is seeking a highly skilled and experienced Senior Research Scientist specializing in Pharmaceuticals to join their innovative team in Salmabad, Northern, BH . This pivotal role will involve leading complex research projects, driving scientific discovery, and contributing to the development of novel therapeutic agents. The successful candidate will possess a strong academic background, a proven track record in pharmaceutical research, and exceptional leadership qualities. You will be expected to design and execute experiments, analyze data rigorously, and collaborate with cross-functional teams to advance drug discovery pipelines. This position offers a unique opportunity to work in a state-of-the-art facility and make a significant impact on future healthcare solutions. We are looking for a candidate who is passionate about science, driven by innovation, and committed to scientific excellence.
Responsibilities:
Qualifications:
Responsibilities:
- Design, conduct, and interpret complex experiments related to drug discovery and development.
- Lead and mentor a team of junior scientists and technicians.
- Develop and optimize research methodologies and protocols.
- Analyze and present research findings to internal teams and external collaborators.
- Manage research projects from conception to completion, ensuring timely delivery of results.
- Contribute to the strategic direction of the R&D department.
- Identify and evaluate new scientific technologies and approaches.
- Write research reports, publications, and patent applications.
- Ensure compliance with all laboratory safety regulations and ethical guidelines.
- Collaborate with medicinal chemists, biologists, and pharmacologists to achieve project goals.
- Troubleshoot experimental issues and devise solutions.
- Stay current with the latest advancements in pharmaceutical research and relevant scientific literature.
- Contribute to budget planning and resource allocation for research projects.
Qualifications:
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5-7 years of post-doctoral or industry research experience in pharmaceutical R&D.
- Demonstrated expertise in drug discovery, preclinical development, or a specific therapeutic area.
- Proven experience in leading research projects and managing scientific teams.
- Strong publication record in peer-reviewed journals.
- Excellent understanding of experimental design, data analysis (e.g., statistical analysis), and interpretation.
- Proficiency in various laboratory techniques and instrumentation relevant to drug discovery.
- Exceptional problem-solving and critical thinking skills.
- Strong written and verbal communication skills, including presentation abilities.
- Ability to work effectively in a collaborative, fast-paced environment.
- Experience with regulatory requirements (e.g., FDA, EMA) is a plus.
- Familiarity with bioinformatic tools and techniques is advantageous.
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