Explore numerous pharmaceutical job opportunities within Bahrain's growing healthcare sector. Pharmaceutical roles involve 3 058 Pharmaceutical jobs in Bahrain
Senior Pharmaceutical Quality Assurance Manager
502 Al Seef
BHD105000 Annually
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Our client, a reputable pharmaceutical company dedicated to improving global health outcomes, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager. This vital role ensures that all products meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory requirements. You will lead a dedicated QA team, oversee quality management systems, and drive continuous improvement initiatives across all manufacturing and operational processes. The ideal candidate will possess a deep understanding of GMP, regulatory affairs, and pharmaceutical manufacturing, coupled with exceptional leadership and analytical skills. This position requires hands-on involvement within our state-of-the-art facilities.
Key Responsibilities:
Qualifications:
This role is based in **Salmabad, Northern, BH**, and requires regular on-site presence to effectively manage operations and collaborate with cross-functional teams. The successful candidate will be a key contributor to our commitment to delivering high-quality pharmaceutical products.
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with cGMP, ICH guidelines, and other relevant global regulations.
- Lead and manage the Quality Assurance team, providing guidance, training, and performance evaluations.
- Oversee all QA activities, including batch record review and release, deviation management, CAPA implementation, change control, and complaint handling.
- Conduct internal audits and participate in external audits by regulatory authorities and customers.
- Ensure that all manufacturing processes and procedures are validated and operating within established quality parameters.
- Review and approve validation protocols and reports for equipment, processes, and analytical methods.
- Monitor and analyze quality metrics and key performance indicators (KPIs), identifying trends and implementing corrective and preventive actions.
- Manage vendor qualification and auditing processes to ensure the quality of raw materials and outsourced services.
- Stay up-to-date with evolving regulatory requirements and industry best practices, ensuring the company remains compliant.
- Promote a culture of quality and compliance throughout the organization.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 7 years of progressive experience in Quality Assurance within the pharmaceutical industry.
- Extensive knowledge of Good Manufacturing Practices (GMP) and regulatory requirements (e.g., FDA, EMA).
- Proven experience in managing and leading QA teams.
- Strong understanding of pharmaceutical manufacturing processes, quality control, and validation principles.
- Excellent analytical, problem-solving, and decision-making skills.
- Exceptional attention to detail and organizational abilities.
- Strong written and verbal communication skills, with the ability to effectively interact with regulatory agencies and internal stakeholders.
- Experience with quality management software and electronic systems is highly desirable.
This role is based in **Salmabad, Northern, BH**, and requires regular on-site presence to effectively manage operations and collaborate with cross-functional teams. The successful candidate will be a key contributor to our commitment to delivering high-quality pharmaceutical products.
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Senior Clinical Research Associate (Remote)
25552 Manama, Capital
BHD95000 Annually
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Our client, a leading pharmaceutical innovator, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join our esteemed, fully remote clinical operations team. This role is critical in ensuring the successful execution of clinical trials, adhering strictly to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. As a remote Senior CRA, you will be responsible for monitoring investigational sites, ensuring data accuracy and integrity, managing patient safety, and facilitating timely study progression. You will conduct pre-study visits, site initiation visits, routine monitoring visits, and close-out visits, all while maintaining effective communication with study personnel and investigators. The ability to work autonomously, manage your time effectively, and maintain meticulous records is paramount. You will collaborate closely with internal teams, including data management, regulatory affairs, and project management, to ensure seamless trial execution. This position offers the opportunity to contribute to groundbreaking pharmaceutical research from the comfort of your home office, making a significant impact on global health outcomes. The ideal candidate will possess a strong understanding of drug development processes, therapeutic areas, and the challenges inherent in conducting clinical trials across diverse patient populations. This fully remote role requires a commitment to excellence and a passion for scientific advancement. We are looking for a dedicated professional who can independently manage multiple sites and study activities, ensuring compliance and driving study milestones.
Key Responsibilities:
Key Responsibilities:
- Monitor investigational sites according to study protocols, GCP, and regulatory guidelines.
- Ensure accurate and timely collection, verification, and review of clinical data.
- Assess patient safety and ensure protocol adherence, reporting adverse events and serious adverse events promptly.
- Conduct pre-study, initiation, interim monitoring, and close-out visits virtually or on-site as required.
- Build and maintain strong relationships with investigators, study coordinators, and site staff.
- Oversee study supplies, drug accountability, and regulatory documentation at the site level.
- Identify, assess, and resolve site-specific issues and deviations from protocol.
- Ensure compliance with all ethical and regulatory requirements.
- Prepare and present monitoring reports to internal project teams and management.
- Contribute to the development and review of study-related documents, including protocols and case report forms.
- Bachelor's degree in a life science, nursing, pharmacy, or a related discipline. Advanced degree is a plus.
- Minimum of 5 years of experience as a Clinical Research Associate, with significant experience in remote monitoring.
- Thorough knowledge of ICH-GCP guidelines and relevant regulatory requirements.
- Proven ability to manage multiple clinical sites and study activities independently.
- Excellent communication, interpersonal, and organizational skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel as required (less than 20%).
- Strong analytical and problem-solving abilities.
- Experience in relevant therapeutic areas is highly desirable.
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1
Senior Pharmaceutical Research Scientist
105 Isa Town, Northern
BHD110000 Annually
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Our client, a leading pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Research Scientist to join their innovative R&D department. This is a critical on-site role focused on advancing the discovery and development of novel drug candidates. You will be instrumental in designing and executing complex research projects, leading laboratory experiments, and contributing to the overall scientific strategy. The ideal candidate possesses a strong background in medicinal chemistry, pharmacology, or a related discipline, with a proven track record of successfully bringing drug candidates through preclinical development. Your responsibilities will include hypothesis generation, experimental design, data analysis, interpretation, and the preparation of research reports and regulatory documentation. You will collaborate closely with cross-functional teams, including analytical development, formulation, and toxicology departments, to ensure the seamless progression of projects. This position demands exceptional scientific rigor, advanced problem-solving skills, and effective leadership abilities.
Key Responsibilities:
Key Responsibilities:
- Lead and conduct cutting-edge research projects aimed at discovering and developing new pharmaceutical compounds.
- Design and execute complex in vitro and in vivo experiments to evaluate drug efficacy and safety.
- Analyze and interpret scientific data, utilizing statistical methods and advanced software.
- Develop and optimize synthetic routes for novel drug candidates.
- Contribute to the preparation of research protocols, scientific reports, and regulatory submissions (e.g., IND applications).
- Collaborate with other scientific disciplines, including biology, pharmacology, and toxicology teams.
- Stay abreast of the latest scientific literature, technological advancements, and industry trends in pharmaceutical R&D.
- Mentor and guide junior research scientists and laboratory personnel.
- Ensure compliance with all laboratory safety regulations and Good Laboratory Practices (GLP).
- Present research findings at internal meetings and external scientific conferences.
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2
Senior Pharmaceutical Research Scientist
440 Jbeil
BHD75000 Annually
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Our client, a leading innovator in the pharmaceutical sector, is seeking a highly skilled and experienced Senior Pharmaceutical Research Scientist to join our dynamic team in **Janabiyah, Northern, BH**. This role is crucial for driving forward groundbreaking research and development initiatives, with a focus on novel drug discovery and therapeutic advancement. The ideal candidate will possess a deep understanding of molecular biology, pharmacology, and drug development processes. You will be responsible for designing and executing complex experiments, analyzing data, and interpreting results to guide research strategies. This includes leading projects from conceptualization through to pre-clinical development, ensuring adherence to regulatory guidelines and quality standards.
Key responsibilities include:
Qualifications:
This is an exceptional opportunity to make a significant impact in a company committed to improving global health outcomes. Join us and contribute to the development of life-saving medicines.
Key responsibilities include:
- Conceptualizing, designing, and implementing in-vitro and in-vivo studies to evaluate drug candidates.
- Developing and validating new assays and methodologies for drug screening and characterization.
- Analyzing and interpreting experimental data using advanced statistical methods and bioinformatics tools.
- Preparing comprehensive reports, presentations, and publications for internal stakeholders and external scientific communities.
- Collaborating closely with cross-functional teams, including medicinal chemists, toxicologists, and clinical scientists, to advance drug development programs.
- Mentoring junior scientists and providing technical guidance and training.
- Staying abreast of the latest scientific literature, emerging technologies, and regulatory requirements in the pharmaceutical industry.
- Managing project timelines, resources, and budgets effectively.
- Ensuring all research activities comply with ethical standards and safety protocols.
- Contributing to intellectual property generation through patent applications.
Qualifications:
- Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related field.
- A minimum of 5 years of post-doctoral or industry experience in pharmaceutical research and drug discovery.
- Proven track record of successful project leadership and scientific innovation.
- Expertise in drug discovery techniques, including high-throughput screening, lead optimization, and mechanism of action studies.
- Strong analytical and problem-solving skills with meticulous attention to detail.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly.
- Proficiency in data analysis software (e.g., GraphPad Prism, R) and laboratory information management systems (LIMS).
- Experience with regulatory submissions and Good Laboratory Practice (GLP) is highly desirable.
- Ability to work independently and collaboratively in a fast-paced, team-oriented environment.
This is an exceptional opportunity to make a significant impact in a company committed to improving global health outcomes. Join us and contribute to the development of life-saving medicines.
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3
Lead Pharmaceutical Research Scientist (Oncology)
BH-777 Al Muharraq
BHD130000 Annually
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Our client, a pioneering biopharmaceutical company dedicated to discovering and developing life-changing therapies, is seeking an accomplished Lead Pharmaceutical Research Scientist specializing in Oncology to join their esteemed research division in Sitra, Capital, BH . This critical role will involve spearheading innovative research programs aimed at identifying novel targets and developing groundbreaking treatments for various forms of cancer. You will lead a team of talented scientists, guiding them through the entire research lifecycle, from hypothesis generation and experimental design to data analysis and interpretation. Responsibilities include designing and executing complex in vitro and in vivo studies, managing research projects, and staying at the forefront of oncological research advancements. The ideal candidate will possess a deep understanding of cancer biology, molecular mechanisms of disease, and cutting-edge therapeutic modalities. You will also play a key role in strategic planning, external collaborations with academic institutions, and contributing to regulatory submissions. This position offers an exceptional opportunity to make a significant impact on patient lives and advance the field of oncology.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Lead and manage oncology research projects from conception to preclinical development.
- Design and conduct innovative experiments to identify and validate novel cancer targets and therapeutic strategies.
- Oversee the execution of in vitro assays, cell-based assays, and in vivo animal models to assess drug efficacy and safety.
- Analyze and interpret complex experimental data, drawing sound conclusions and developing actionable plans.
- Mentor and guide junior research scientists, fostering a collaborative and high-performance research environment.
- Collaborate with internal departments (e.g., DMPK, toxicology, clinical development) to advance drug candidates.
- Establish and manage external collaborations with academic researchers and key opinion leaders.
- Prepare scientific reports, manuscripts for publication, and presentations for scientific conferences.
- Contribute to the strategic direction of the oncology pipeline and intellectual property development.
- Ensure adherence to laboratory safety protocols and ethical research standards.
Qualifications:
- Ph.D. in Cancer Biology, Molecular Biology, Immunology, or a closely related field.
- Minimum of 8 years of post-doctoral research experience in oncology drug discovery.
- Proven expertise in cancer biology, signaling pathways, and tumor microenvironment.
- Extensive experience with a range of experimental techniques, including cell culture, molecular biology, immunology, and animal models.
- Demonstrated leadership experience and the ability to manage and mentor a scientific team.
- Strong publication record in high-impact peer-reviewed journals.
- Excellent analytical, problem-solving, and critical thinking skills.
- Exceptional communication and presentation skills, capable of conveying complex scientific information clearly.
- Experience with biologics and small molecule drug development is highly desirable.
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4
Senior Pharmaceutical Research Scientist
45670 Northern, Northern
BHD130000 Annually
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Our client, a leading biopharmaceutical company dedicated to developing life-saving therapies, is seeking a highly motivated and accomplished Senior Pharmaceutical Research Scientist to join their innovative R&D team. This role, based in Shakhura, Northern, BH , offers a hybrid work arrangement, allowing for collaborative lab work and flexible remote analysis and writing. You will play a crucial role in the discovery and development of novel drug candidates, contributing significantly to our pipeline and bringing transformative medicines to patients worldwide.
Responsibilities:
Responsibilities:
- Design and execute complex experiments to identify and validate new drug targets and therapeutic pathways.
- Conduct preclinical research, including in vitro and in vivo studies, to assess the efficacy, safety, and pharmacokinetic properties of potential drug candidates.
- Develop and optimize assay methodologies for drug screening and characterization.
- Analyze experimental data using advanced statistical and computational tools, interpreting results to guide research direction.
- Collaborate closely with cross-functional teams, including medicinal chemists, biologists, toxicologists, and clinicians, to advance projects from discovery to early clinical development.
- Prepare detailed research reports, scientific manuscripts for publication, and regulatory submission documents.
- Present research findings at internal meetings and external scientific conferences.
- Stay abreast of the latest scientific literature, emerging technologies, and advancements in pharmaceutical research and drug development.
- Mentor junior scientists and contribute to the scientific and technical growth of the research team.
- Ensure compliance with all relevant laboratory safety regulations and Good Laboratory Practice (GLP) standards.
- Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline.
- Minimum of 7 years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
- Proven track record of successful drug discovery and development experience, with a focus on specific therapeutic areas (e.g., oncology, immunology, neurology).
- Extensive hands-on experience with a variety of in vitro and in vivo experimental techniques and relevant instrumentation.
- Proficiency in data analysis software and bioinformatics tools.
- Excellent written and verbal communication skills, with a strong publication record.
- Demonstrated ability to lead research projects, manage timelines, and work effectively in a collaborative team environment.
- Strong problem-solving skills and the ability to think critically and creatively.
- Experience with assay development and high-throughput screening is highly desirable.
- A deep commitment to scientific rigor and innovation.
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Senior Pharmaceutical Research Scientist
5050 Isa Town, Northern
BHD95000 Annually
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly skilled and dedicated Senior Pharmaceutical Research Scientist to drive cutting-edge research and development initiatives. This role is crucial for discovering and advancing novel therapeutic compounds. The position offers a hybrid work arrangement, providing flexibility while ensuring access to state-of-the-art laboratory facilities.
Responsibilities:
Responsibilities:
- Design and conduct complex experiments to identify, characterize, and validate potential drug candidates.
- Develop and optimize innovative research methodologies and protocols.
- Analyze experimental data, interpret results, and draw insightful conclusions.
- Prepare detailed research reports, manuscripts for publication, and presentations for scientific conferences.
- Collaborate effectively with interdisciplinary teams, including medicinal chemists, biologists, pharmacologists, and regulatory affairs.
- Manage research projects, ensuring adherence to timelines, budgets, and scientific rigor.
- Oversee laboratory operations, including equipment maintenance, reagent inventory, and safety compliance.
- Mentor and guide junior research staff, fostering scientific growth and development.
- Stay abreast of the latest scientific literature, emerging technologies, and industry trends in pharmaceutical research.
- Contribute to the intellectual property strategy through patent disclosures and applications.
- Ensure all research activities comply with Good Laboratory Practices (GLP) and regulatory guidelines.
- Present research findings to internal stakeholders, including senior management and project teams.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, Chemistry, or a related life science discipline.
- Minimum of 6 years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
- Proven track record of significant contributions to drug discovery and development projects.
- Extensive experience with relevant experimental techniques (e.g., in vitro assays, cell-based assays, small molecule screening).
- Strong understanding of drug metabolism, pharmacokinetics (DMPK), and toxicology principles.
- Proficiency in data analysis software and statistical methods.
- Excellent written and verbal communication skills, with a strong publication record.
- Demonstrated ability to lead research projects and mentor junior scientists.
- Experience with compound libraries and high-throughput screening is highly desirable.
- Familiarity with regulatory submission processes (e.g., IND, NDA) is a plus.
- Ability to work effectively in a collaborative, fast-paced research environment.
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6
Remote Pharmaceutical Sales Representative
555 Al Daih, Northern
BHD60000 annum + com
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Our client, a leading pharmaceutical company, is seeking a motivated and results-oriented Remote Pharmaceutical Sales Representative. This is a fully remote position, offering flexibility and the opportunity to manage your territory effectively from home. You will be responsible for promoting and selling pharmaceutical products to healthcare professionals, including doctors, pharmacists, and hospital administrators. The ideal candidate possesses excellent communication and interpersonal skills, a strong understanding of the pharmaceutical industry, and a proven track record in sales. You will build strong relationships with clients, educate them on product benefits, and drive sales growth. This role requires self-discipline, excellent organizational skills, and the ability to work autonomously.
Responsibilities:
Responsibilities:
- Promote and sell pharmaceutical products to healthcare providers within an assigned territory.
- Develop and maintain strong, long-lasting relationships with physicians, pharmacists, and other key opinion leaders.
- Educate healthcare professionals on the features, benefits, and appropriate use of company products.
- Achieve and exceed sales targets and objectives for your territory.
- Develop and implement effective sales strategies to maximize market share.
- Stay up-to-date with the latest clinical data, competitor information, and industry trends.
- Prepare and deliver compelling sales presentations and product demonstrations.
- Manage a sales pipeline, track customer interactions, and forecast sales accurately using CRM software.
- Attend virtual conferences, webinars, and industry events as required.
- Ensure compliance with all company policies and pharmaceutical industry regulations.
- Provide excellent customer service and support to healthcare professionals.
- Collaborate with internal teams, such as marketing and medical affairs, to support sales efforts.
- Report on sales activities, market feedback, and competitive intelligence.
- Effectively manage your time and schedule to optimize customer engagement.
- Handle objections and address customer concerns professionally.
- Bachelor's degree in Science, Business, Marketing, or a related field.
- Proven experience in pharmaceutical sales or a related healthcare sales role.
- Strong understanding of the pharmaceutical market and clinical practices.
- Excellent communication, negotiation, and presentation skills.
- Ability to build rapport and establish trust with healthcare professionals.
- Self-motivated, disciplined, and capable of working independently in a remote setting.
- Proficiency in CRM software (e.g., Veeva, Salesforce) and Microsoft Office Suite.
- Valid driver's license and ability to travel as needed (though this is a remote role, occasional travel may be required).
- Strong organizational and time-management skills.
- Ability to understand and convey complex scientific and medical information.
- A commitment to ethical sales practices and regulatory compliance.
- Proven track record of meeting or exceeding sales quotas.
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7
Senior Clinical Research Associate
450 Al Muharraq
BHD95000 Annually
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Our client , a leading pharmaceutical innovator, is seeking a dedicated and experienced Senior Clinical Research Associate (CRA) to join their global clinical operations team. This role will be fully remote, allowing you to contribute to groundbreaking research from anywhere. You will be responsible for monitoring clinical trials, ensuring data integrity, and maintaining compliance with regulatory requirements and study protocols. The ideal candidate will possess a strong background in clinical trial management, excellent organizational skills, and a passion for advancing healthcare.
Key Responsibilities:
Key Responsibilities:
- Conduct site visits (remote and potentially on-site as needed) to assess protocol and regulatory compliance, data accuracy, and completeness.
- Initiate, monitor, and close-out clinical trial sites according to GCP guidelines and study protocols.
- Ensure timely collection and accurate documentation of all study-related data.
- Communicate effectively with investigators, site staff, and study sponsors.
- Identify and report adverse events and protocol deviations.
- Manage site issues and facilitate prompt resolution.
- Train site personnel on study procedures and regulatory requirements.
- Contribute to the development of study protocols, case report forms (CRFs), and other trial-related documents.
- Ensure all study documentation is maintained in compliance with regulatory requirements and company SOPs.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate.
- In-depth knowledge of Good Clinical Practice (GCP), FDA regulations, and ICH guidelines.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Excellent communication, interpersonal, and organizational skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently, manage time effectively, and travel as required (though this role is primarily remote).
- Strong problem-solving abilities and attention to detail.
- Experience in the pharmaceutical or biotechnology industry.
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8
Clinical Research Associate (Remote)
3050 Al Muharraq
BHD85000 Annually
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Our client, a leading pharmaceutical company committed to advancing global health, is seeking a dedicated and experienced Clinical Research Associate to join their team. This role offers a hybrid work arrangement, blending the flexibility of remote work with essential on-site collaboration and site visits. As a Clinical Research Associate, you will play a crucial role in ensuring the successful execution of clinical trials, from site initiation to study close-out. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. This includes conducting site visits (remote and on-site), verifying data accuracy and integrity, managing study documentation, and acting as a primary liaison between the investigative sites and the study team. The ideal candidate will possess a strong understanding of clinical trial processes, drug development, and regulatory affairs. Excellent organizational skills, meticulous attention to detail, and the ability to manage multiple priorities are essential. You will be expected to build and maintain strong relationships with investigators, study coordinators, and other site personnel. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is required. This hybrid position requires a balance of independent remote work and travel to assigned clinical sites. We are looking for a self-motivated individual with excellent communication and interpersonal skills who is committed to patient safety and data quality. Experience in therapeutic areas relevant to the company's pipeline is advantageous. The ability to travel as needed is a key requirement for this role.
Responsibilities:
Responsibilities:
- Monitor clinical trial sites according to protocol and GCP guidelines.
- Verify accuracy, completeness, and validity of clinical trial data.
- Ensure regulatory compliance at assigned investigative sites.
- Conduct pre-study, initiation, interim, and close-out visits.
- Manage and maintain essential study documents.
- Serve as the primary point of contact for clinical trial sites.
- Identify, evaluate, and resolve site-level issues.
- Ensure timely reporting of study progress and site performance.
- Train site staff on study procedures and data collection.
- Collaborate with internal study teams to facilitate study milestones.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate (CRA) or similar role.
- Thorough knowledge of ICH GCP guidelines and relevant regulatory requirements.
- Experience with EDC and CTMS systems.
- Strong monitoring and site management skills.
- Excellent organizational and time-management abilities.
- Effective written and verbal communication skills.
- Ability to travel to clinical sites as required.
- Proficiency in Microsoft Office Suite.
- Self-motivated and able to work independently as well as part of a team.
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