What Jobs are available for Pharmaceutical Development in Bahrain?
Showing 612 Pharmaceutical Development jobs in Bahrain
Lead Formulation Scientist - Pharmaceutical Development
2145 Jurdab
BHD85000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client is a leading pharmaceutical company seeking an experienced Lead Formulation Scientist to join their innovative Research and Development department based in Janabiyah, Northern, BH . This senior role will be responsible for the design, development, and optimization of novel drug formulations across various therapeutic areas. You will lead a team of scientists in pre-formulation studies, excipient selection, formulation development, and scale-up activities, ensuring the stability, efficacy, and bioavailability of new drug candidates. Your expertise will guide the transition of drug substances from early-stage research to clinical development.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and execute pre-formulation studies, including physicochemical characterization of Active Pharmaceutical Ingredients (APIs).
- Develop and optimize various dosage forms (e.g., oral solids, injectables, topical preparations).
- Select appropriate excipients and investigate their compatibility with APIs.
- Conduct stability studies to assess product shelf-life and degradation pathways.
- Perform method development and validation for analytical testing of formulations.
- Lead formulation scale-up activities from laboratory to pilot plant and manufacturing.
- Troubleshoot formulation-related issues encountered during development and manufacturing.
- Collaborate closely with analytical, process chemistry, and regulatory affairs teams.
- Prepare comprehensive formulation development reports and regulatory submission documents.
- Mentor and guide junior scientists, fostering a collaborative and scientifically rigorous environment.
- Stay current with scientific literature, industry trends, and new formulation technologies.
- Ensure all activities are conducted in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
Qualifications:
- PhD or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related discipline.
- Minimum of 7 years of experience in pharmaceutical formulation development, with a significant portion in a lead or supervisory role.
- Proven track record in developing various dosage forms, including solid dosage forms and parenteral products.
- Strong understanding of drug delivery principles, pharmacokinetics, and biopharmaceutics.
- Hands-on experience with analytical techniques such as HPLC, dissolution testing, and DSC.
- Familiarity with GMP regulations and requirements for drug development.
- Excellent problem-solving, critical thinking, and decision-making abilities.
- Strong leadership, project management, and communication skills.
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0
Senior Formulation Scientist, Pharmaceutical Development
20001 Jbeil
BHD120000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a highly regarded pharmaceutical company at the forefront of therapeutic innovation, is actively seeking a Senior Formulation Scientist to join their dedicated Drug Product Development team. This is a critical fully remote role, enabling you to contribute your extensive expertise without geographical constraints. You will be responsible for the development and optimization of novel drug formulations for a wide range of pharmaceutical products, ensuring product efficacy, stability, and patient compliance.
Key Responsibilities:
Key Responsibilities:
- Lead the formulation development of new drug products, including solid dosage forms, injectables, and topical preparations.
- Design and execute pre-formulation studies, including API characterization and compatibility studies.
- Develop and optimize formulation processes, such as granulation, blending, tablet compression, encapsulation, and sterile filling.
- Conduct stability studies according to ICH guidelines and analyze data to determine product shelf-life.
- Prepare detailed technical reports, formulation development protocols, and batch records.
- Collaborate closely with analytical development, manufacturing, and regulatory affairs teams to ensure seamless product development and lifecycle management.
- Troubleshoot formulation and manufacturing process issues, identifying root causes and implementing corrective actions.
- Evaluate new excipients, technologies, and analytical techniques to enhance formulation performance.
- Stay current with industry trends, regulatory guidelines, and scientific literature related to pharmaceutical formulation.
- Mentor junior scientists and contribute to the scientific advancement of the formulation department.
- PhD or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline.
- Minimum of 6-10 years of hands-on experience in pharmaceutical formulation development, with a strong emphasis on solid oral dosage forms and/or sterile products.
- In-depth knowledge of GMP requirements and regulatory guidelines relevant to drug product development.
- Proven experience with various drug delivery systems and technologies.
- Proficiency in using laboratory equipment for formulation development and characterization (e.g., tablet presses, dissolution apparatus, particle sizers).
- Excellent problem-solving, analytical, and critical thinking abilities.
- Strong project management skills and the ability to manage multiple projects concurrently.
- Exceptional written and verbal communication skills, including the ability to present scientific data effectively.
- Demonstrated ability to work independently and collaboratively in a remote setting.
- Familiarity with the pharmaceutical landscape in Janabiyah, Northern, BH is a plus.
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1
Senior Formulation Scientist (Pharmaceutical Development)
920 Al Seef
BHD155000 Annually
WhatJobs
Posted 26 days ago
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company, is seeking a highly skilled and experienced Senior Formulation Scientist to join their innovative, fully remote drug development team. This critical role focuses on designing, developing, and optimizing novel drug formulations to enhance efficacy, patient compliance, and drug delivery. You will leverage your deep expertise in pharmaceutics and excipient science to bring life-changing medications from concept to clinical stages.
Key Responsibilities:
Key Responsibilities:
- Lead the formulation development of various dosage forms, including oral solids, injectables, and topical preparations.
- Design and execute experiments to identify suitable excipients and optimize formulation parameters for stability, bioavailability, and manufacturability.
- Utilize advanced analytical techniques to characterize formulations and drug products.
- Develop and validate formulation processes, ensuring scalability and reproducibility.
- Conduct pre-formulation studies to understand the physicochemical properties of active pharmaceutical ingredients (APIs).
- Collaborate closely with analytical, regulatory, and manufacturing teams to support drug development milestones.
- Prepare comprehensive formulation development reports, CMC documentation, and regulatory submissions.
- Troubleshoot formulation-related challenges and propose innovative solutions.
- Stay current with advancements in formulation science, drug delivery technologies, and regulatory guidelines.
- Mentor junior scientists and contribute to the overall scientific knowledge within the team.
- Ph.D. or Master's degree in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related field.
- Minimum of 7 years of experience in pharmaceutical formulation development.
- Proven track record in developing various dosage forms and successfully advancing candidates through preclinical and early clinical stages.
- In-depth knowledge of excipient science, drug delivery systems, and manufacturing processes.
- Proficiency in analytical techniques such as HPLC, GC, dissolution testing, and stability studies.
- Experience with Good Manufacturing Practices (GMP) and regulatory requirements (e.g., ICH guidelines).
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong communication and interpersonal skills, with the ability to work effectively in a remote team environment.
- Experience with specialized drug delivery technologies (e.g., nanoparticles, liposomes) is a plus.
- Commitment to scientific rigor and the development of high-quality pharmaceutical products.
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2
Senior Formulation Scientist - Pharmaceutical Development
211 Muharraq, Muharraq
BHD110000 Annually
WhatJobs
Posted 26 days ago
Job Viewed
Job Description
Our client is seeking a highly skilled Senior Formulation Scientist to join their innovative pharmaceutical development team. This is a fully remote position, enabling you to contribute from anywhere. You will play a critical role in the research, design, and development of novel drug formulations, focusing on oral solid dosage forms, but also encompassing other delivery systems. Your expertise will guide the optimization of drug product performance, stability, and manufacturability. Responsibilities include conducting pre-formulation studies, selecting appropriate excipients, developing prototype formulations, and performing detailed characterization and stability testing. You will collaborate closely with analytical chemists, process engineers, and regulatory affairs specialists to ensure that formulations meet stringent quality and regulatory standards. This role requires a deep understanding of pharmaceutical sciences, materials science, and drug delivery technologies. The ideal candidate will have a proven track record of successfully advancing drug candidates from early-stage development through to clinical trial supply. We encourage a proactive, problem-solving approach and a passion for innovation in drug product development.
Responsibilities:
Responsibilities:
- Lead the formulation development of new pharmaceutical products.
- Conduct pre-formulation studies, including solubility, stability, and compatibility assessments.
- Design and optimize formulations for various dosage forms (e.g., tablets, capsules, powders).
- Select appropriate excipients and materials for drug product development.
- Perform characterization and physical property testing of formulations.
- Design and execute stability studies according to ICH guidelines.
- Collaborate with analytical teams for method development and validation.
- Troubleshoot formulation and process-related issues.
- Prepare technical reports, protocols, and documentation for regulatory submissions.
- Stay abreast of new technologies and trends in pharmaceutical formulation.
- Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline.
- 5-8 years of relevant experience in pharmaceutical formulation development.
- In-depth knowledge of drug delivery systems, solid dosage forms, and excipient science.
- Hands-on experience with laboratory equipment for formulation development and characterization.
- Proficiency in designing and executing stability studies.
- Understanding of GMP, ICH guidelines, and regulatory requirements.
- Excellent problem-solving, analytical, and organizational skills.
- Strong written and verbal communication abilities.
- Experience with project management and cross-functional team collaboration is essential for this remote role.
- Ability to work independently and manage multiple projects concurrently.
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3
Clinical Research Associate - Pharmaceutical Development
101 Arad
BHD70000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client is seeking a motivated and detail-oriented Clinical Research Associate (CRA) to support their pharmaceutical development initiatives in Hidd, Muharraq, BH . This role is crucial for ensuring the successful execution of clinical trials in compliance with regulatory standards and company protocols. The CRA will be responsible for monitoring clinical trial sites, ensuring the quality and integrity of data collected, and verifying that trials are conducted, recorded, and reported in accordance with the protocol and Good Clinical Practice (GCP) guidelines.
The ideal candidate will possess a strong understanding of clinical research processes, medical terminology, and regulatory requirements within the pharmaceutical industry. Responsibilities include site initiation, routine monitoring, close-out visits, and providing ongoing support to investigators and study staff. You will be required to review essential documents, track study progress, manage patient safety, and ensure compliance with all ethical and regulatory guidelines. This role requires excellent organizational skills, strong analytical abilities, and exceptional communication and interpersonal skills. The hybrid nature of this role will involve both on-site visits to clinical trial locations and remote data review and administrative tasks. Travel to various sites within the region will be necessary.
Key Responsibilities:
The ideal candidate will possess a strong understanding of clinical research processes, medical terminology, and regulatory requirements within the pharmaceutical industry. Responsibilities include site initiation, routine monitoring, close-out visits, and providing ongoing support to investigators and study staff. You will be required to review essential documents, track study progress, manage patient safety, and ensure compliance with all ethical and regulatory guidelines. This role requires excellent organizational skills, strong analytical abilities, and exceptional communication and interpersonal skills. The hybrid nature of this role will involve both on-site visits to clinical trial locations and remote data review and administrative tasks. Travel to various sites within the region will be necessary.
Key Responsibilities:
- Perform site initiation, routine monitoring, and close-out visits for clinical trials.
- Ensure compliance with protocols, GCP, and relevant regulatory requirements.
- Verify the accuracy and completeness of clinical trial data and source documentation.
- Train and support site staff on study procedures and regulatory requirements.
- Identify, document, and track deviations and issues at clinical trial sites.
- Oversee the management of investigational product and study supplies at sites.
- Liaise between clinical trial sites, sponsors, and regulatory authorities.
- Prepare and present monitoring visit reports.
- Assist in the resolution of site-level issues and risks.
- Contribute to the development and review of study-related documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- Thorough knowledge of GCP guidelines and clinical trial monitoring processes.
- Familiarity with pharmaceutical development and regulatory affairs.
- Strong understanding of medical terminology and clinical data management.
- Excellent attention to detail and organizational skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong written and verbal communication skills.
- Ability to travel to clinical trial sites as required.
- Problem-solving skills and the ability to work independently.
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4
Clinical Research Associate - Pharmaceutical Development
889 Isa Town, Northern
BHD95000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their fully remote clinical operations team. This critical role will support the development and execution of clinical trials, ensuring compliance with regulatory standards and company protocols. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines, clinical trial monitoring, and drug development processes. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as ensuring accurate and timely data collection and reporting. The CRA will serve as the primary liaison between the investigative sites and the sponsor, addressing protocol deviations, and managing site-related issues. A proven ability to manage multiple studies and sites simultaneously, while maintaining high standards of quality and efficiency, is essential. This remote position offers the flexibility to work from anywhere, allowing for effective travel to sites as required by the study protocols. You will play a vital role in bringing innovative therapies to patients by ensuring the integrity and reliability of clinical trial data. Strong organizational, communication, and problem-solving skills are paramount.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, interim, and close-out visits at clinical trial sites.
- Monitor clinical trials to ensure adherence to protocols, SOPs, and regulatory requirements (GCP, FDA, EMA).
- Verify the accuracy, completeness, and integrity of clinical data.
- Manage and resolve site-specific issues, including protocol deviations and data queries.
- Train site staff on study procedures and regulatory compliance.
- Build and maintain strong relationships with investigators and site personnel.
- Prepare and submit monitoring reports and follow-up actions.
- Ensure timely submission of essential documents and regulatory filings.
- Oversee drug accountability and study supplies at investigative sites.
- Participate in investigator meetings and site audits as needed.
- Bachelor's degree in life sciences, nursing, pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proven experience in clinical trial monitoring and site management.
- Excellent understanding of clinical trial processes and documentation.
- Strong analytical, organizational, and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to travel frequently to clinical sites (estimated % travel required).
- Proficiency in clinical data management systems and EDC platforms.
- Ability to work independently and manage time effectively in a remote setting.
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5
Clinical Research Associate - Pharmaceutical Development
7780 Southern, Southern
BHD95000 Annually
WhatJobs
Posted 22 days ago
Job Viewed
Job Description
Our client is a rapidly growing pharmaceutical company dedicated to advancing healthcare through innovative drug development. We are seeking a dedicated and meticulous Clinical Research Associate (CRA) to join our team. This hybrid role offers a blend of remote work flexibility and essential on-site collaboration, contributing significantly to the success of our clinical trials. As a CRA, you will be instrumental in ensuring the smooth execution and integrity of clinical studies, adhering strictly to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. Your primary responsibilities will include site selection, initiation, monitoring, and close-out visits to ensure data accuracy, patient safety, and protocol compliance. You will manage relationships with investigators and site staff, providing essential training and ongoing support. This role demands a proactive approach to identifying and resolving issues that may arise during the trial process, including protocol deviations and data discrepancies. You will be responsible for reviewing and verifying source documentation, querying data, and ensuring the timely submission of trial-related materials. Travel to clinical sites within the region will be required periodically. The ideal candidate will possess strong analytical skills, a keen eye for detail, and a thorough understanding of clinical trial processes and pharmaceutical regulations. A commitment to ethical research practices and patient well-being is paramount. You will work closely with internal project teams, including project managers, data managers, and medical monitors, to ensure successful trial progression.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, routine, and close-out monitoring visits at clinical trial sites.
- Ensure compliance with study protocols, SOPs, GCP, and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data through source data verification.
- Train and mentor site personnel on study procedures and regulatory compliance.
- Build and maintain strong working relationships with investigators and site staff.
- Identify, resolve, and document study-related issues and deviations.
- Manage study supplies and equipment at clinical sites.
- Prepare and submit monitoring reports in a timely manner.
- Ensure all trial-related documentation is maintained accurately in the Trial Master File (TMF).
- Collaborate with internal teams to facilitate timely drug and biologic release.
- Participate in investigator meetings and other relevant forums.
- Contribute to the development of study protocols and other study documents.
- Uphold the highest standards of ethical conduct and patient safety.
- Bachelor's degree in a life science, nursing, or a related field. Advanced degree preferred.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA).
- Thorough understanding of ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA).
- Proven experience in site monitoring, data verification, and regulatory compliance.
- Excellent interpersonal, communication, and organizational skills.
- Ability to travel to clinical sites as required (estimated 30-50% travel).
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong problem-solving abilities and attention to detail.
- Ability to work independently and as part of a remote and on-site team.
- Commitment to patient safety and data integrity.
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6
Clinical Research Associate - Pharmaceutical Development
20202 Al Muharraq
BHD75000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and experienced Clinical Research Associate (CRA) to join their innovative drug development team. This role is pivotal in ensuring the successful execution of clinical trials, from initiation to close-out, adhering to strict regulatory guidelines and ethical standards. The successful candidate will be responsible for monitoring clinical trial sites to ensure data accuracy, patient safety, and protocol compliance. This involves conducting site visits, training site staff, resolving data queries, and ensuring all study-related documentation is maintained meticulously. You will act as a key liaison between the investigative sites, the study team, and regulatory authorities. The position offers a hybrid work model, combining essential on-site responsibilities at our facilities in **Sitra, Capital, BH** with opportunities for remote work. Essential on-site duties include patient interaction coordination, hands-on regulatory document review, and direct collaboration with research teams. Qualifications include a Bachelor's or Master's degree in a life science or related field, a minimum of 3 years of experience as a CRA, a thorough understanding of ICH-GCP guidelines and local regulatory requirements, and excellent communication and interpersonal skills. Strong analytical and problem-solving abilities are crucial. The ideal candidate is highly organized, detail-oriented, and possesses the ability to manage multiple priorities effectively. This role provides an excellent opportunity to contribute to groundbreaking medical advancements and grow within a supportive and progressive organization. You will be instrumental in bringing life-changing therapies to patients, making a tangible difference in healthcare.
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7
Principal Pharmaceutical Development Scientist
2102 Bilad Al Qadeem, Capital
BHD110000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical innovator, is seeking a highly accomplished Principal Pharmaceutical Development Scientist to lead critical aspects of drug product development. This hybrid position, located in **Budaiya, Northern, BH**, requires a blend of hands-on laboratory work and strategic remote leadership. You will be at the forefront of developing and optimizing formulation and manufacturing processes for new drug candidates, ensuring product stability, efficacy, and safety. Responsibilities include designing and executing pre-formulation studies, developing robust formulations, and overseeing scale-up activities. You will lead a team of scientists and technicians, providing expert guidance and mentorship throughout the development lifecycle. A deep understanding of pharmaceutics, solid-state chemistry, analytical development, and GMP (Good Manufacturing Practice) regulations is essential. Experience with various dosage forms, including oral solids, injectables, and topical formulations, will be highly valued. The Principal Pharmaceutical Development Scientist will also be responsible for troubleshooting formulation and manufacturing challenges, preparing regulatory submission documents, and staying current with industry best practices. Collaboration with internal departments such as regulatory affairs, quality assurance, and manufacturing operations is critical for success. The ideal candidate will possess a Ph.D. in Pharmaceutical Sciences, Chemistry, or a related field, with a minimum of 8 years of relevant industry experience in pharmaceutical product development. Exceptional leadership, scientific acumen, problem-solving skills, and a proven ability to innovate are mandatory. This is a premier opportunity to significantly impact the pipeline of life-changing medicines and advance your career in pharmaceutical development.
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8
Senior Pharmaceutical Development Scientist
779 Hamad Town, Northern
BHD100000 Annually
WhatJobs
Posted 9 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing human health, is seeking an experienced Senior Pharmaceutical Development Scientist to join their research and development team. This role is crucial for the formulation and development of novel drug products, from early-stage research through to clinical trial material manufacturing. You will be responsible for designing formulations, optimizing manufacturing processes, and conducting rigorous analytical testing to ensure product quality, efficacy, and safety. The ideal candidate will possess a deep understanding of pharmaceutical sciences, excipient compatibility, drug delivery systems, and regulatory requirements. This position requires a hands-on approach and the ability to work collaboratively in a state-of-the-art laboratory environment.
Responsibilities:
Qualifications:
Responsibilities:
- Design and develop innovative formulations for various dosage forms (e.g., oral solids, injectables, topical).
- Optimize formulation composition and manufacturing processes to achieve desired drug product characteristics and performance.
- Conduct pre-formulation studies, including API characterization, solubility, and stability assessments.
- Perform compatibility studies between the active pharmaceutical ingredient (API) and excipients.
- Develop and validate analytical methods for drug product characterization and quality control.
- Prepare and review technical reports, development protocols, and batch records.
- Support the scale-up of manufacturing processes from laboratory to pilot and commercial scales.
- Collaborate closely with analytical development, manufacturing, and regulatory affairs teams.
- Ensure all development activities comply with Good Manufacturing Practices (GMP) and relevant regulatory guidelines (e.g., FDA, EMA).
- Stay current with advancements in pharmaceutical technology, drug delivery systems, and regulatory science.
Qualifications:
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 7 years of experience in pharmaceutical product development, with a focus on formulation and process development.
- Proven expertise in developing various dosage forms and understanding formulation science principles.
- Strong knowledge of excipient functionality, drug delivery technologies, and drug product stability.
- Experience with analytical techniques such as HPLC, GC, dissolution testing, and spectroscopy.
- Familiarity with GMP regulations and ICH guidelines.
- Excellent problem-solving, critical thinking, and experimental design skills.
- Strong documentation and technical writing abilities.
- Effective communication and interpersonal skills for cross-functional team collaboration.
- Experience with sterile product development is a plus.
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