450 Pharmaceutical Development jobs in Bahrain
Senior Formulation Scientist - Pharmaceutical Development
33330 Busaiteen, Muharraq
BHD11000 Annually
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Our client, a cutting-edge pharmaceutical company dedicated to developing innovative therapeutics, is seeking a highly experienced Senior Formulation Scientist to join their R&D team in **Busaiteen, Muharraq, BH**. This senior role is critical for the development and optimization of pharmaceutical formulations, ensuring drug stability, bioavailability, and efficacy. The ideal candidate will possess extensive knowledge of various dosage forms (oral solids, injectables, topical preparations), formulation development techniques, and analytical methods used for characterization. You will lead formulation development projects, troubleshoot formulation challenges, and contribute to the scale-up and technology transfer of processes to manufacturing. This position requires a strong scientific background, excellent problem-solving skills, and a proven ability to work collaboratively in a fast-paced research environment.
Responsibilities include:
Responsibilities include:
- Designing and executing formulation development studies for various dosage forms.
- Developing stable and bioavailable drug product formulations.
- Investigating and troubleshooting formulation-related issues.
- Conducting pre-formulation studies, including solubility, stability, and compatibility.
- Performing characterization of drug substances and drug products using various analytical techniques (e.g., HPLC, GC, DSC, XRD).
- Developing and validating analytical methods for formulation analysis.
- Planning and executing pilot scale batches and supporting technology transfer to manufacturing.
- Preparing comprehensive development reports and regulatory submission documents.
- Staying abreast of the latest advancements in pharmaceutical formulation and drug delivery technologies.
- Collaborating with analytical development, process development, and regulatory affairs teams.
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0
Senior Formulation Scientist - Pharmaceutical Development
BH-223 Al Hidd
BHD105000 Annually
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Posted 4 days ago
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Our client, a leading biopharmaceutical company, is seeking an experienced Senior Formulation Scientist to lead critical drug product development activities in **Budaiya, Northern, BH**. This senior role focuses on designing, developing, and optimizing novel pharmaceutical formulations for both solid and liquid dosage forms, ensuring efficacy, stability, and bioavailability. The successful candidate will be responsible for leading formulation research, developing robust and scalable manufacturing processes, and conducting preclinical and clinical trial material preparations. Key duties include performing pre-formulation studies, selecting appropriate excipients, developing analytical methods for characterization and stability testing, and documenting all development activities in compliance with regulatory guidelines. You will work closely with analytical development, process development, and regulatory affairs teams to ensure seamless project progression. The ideal candidate will possess a Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, or a related field, with a minimum of 6-8 years of progressive experience in pharmaceutical formulation development. Proven expertise in oral solid dosage forms (tablets, capsules) and/or parenteral formulations is required. Strong knowledge of regulatory requirements (FDA, EMA) for drug product development and experience with common pharmaceutical manufacturing equipment and techniques are essential. Excellent analytical, problem-solving, and experimental design skills, coupled with strong communication and leadership abilities, are crucial for this role. This is an exceptional opportunity for a skilled Senior Formulation Scientist to make a significant impact on drug development pipelines in **Budaiya, Northern, BH**, and to contribute to bringing life-changing therapies to patients. You will work in a state-of-the-art facility with a collaborative team of scientists and professionals. The position offers a competitive salary, comprehensive benefits, and opportunities for professional growth.
Responsibilities:
Responsibilities:
- Lead the formulation development of new pharmaceutical products (solid and liquid dosage forms).
- Design and conduct pre-formulation studies to understand drug-excipient compatibility and physical properties.
- Select appropriate excipients and optimize formulations to achieve desired drug release profiles and stability.
- Develop and validate analytical methods for formulation characterization and stability testing.
- Scale-up formulation processes from laboratory to pilot and commercial manufacturing.
- Prepare technical reports, development summaries, and regulatory submission documents.
- Collaborate with analytical and process development teams to ensure seamless project execution.
- Stay updated on the latest advancements in pharmaceutical formulation and delivery technologies.
- Manage project timelines and resources effectively.
- Ensure all development activities comply with GMP and regulatory guidelines.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, or a related field.
- Minimum of 6-8 years of experience in pharmaceutical formulation development.
- Expertise in oral solid dosage forms (tablets, capsules) and/or parenteral formulations.
- Strong understanding of drug delivery systems and biopharmaceutics.
- Proficiency with pharmaceutical analytical techniques (HPLC, dissolution testing, DSC, etc.).
- Knowledge of GMP regulations and regulatory submission processes.
- Excellent experimental design, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills.
- Ability to lead projects and mentor junior scientists.
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1
Senior Formulation Scientist, Pharmaceutical Development
403, Northern, BH Saar, Northern
BHD85000 Annually
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Posted 7 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly skilled Senior Formulation Scientist to join their Research and Development team in Saar, Northern, BH . This role is instrumental in the development of innovative drug delivery systems and the optimization of existing pharmaceutical formulations. The Senior Formulation Scientist will lead formulation studies, design experimental plans, and contribute to the overall drug development process from pre-clinical through to commercialization.
Key responsibilities include:
This is an exceptional career opportunity to contribute to life-changing medicines within a forward-thinking organization. If you are passionate about pharmaceutical innovation, we invite you to apply.
Key responsibilities include:
- Designing and executing formulation development studies for oral solid dosage forms, injectables, or other relevant dosage forms.
- Investigating and optimizing critical formulation parameters to achieve desired drug release profiles, stability, and bioavailability.
- Conducting pre-formulation studies, including solubility, compatibility, and excipient screening.
- Developing and validating analytical methods for characterizing formulations and raw materials.
- Preparing comprehensive technical reports, study protocols, and regulatory submission documents.
- Collaborating effectively with cross-functional teams, including analytical development, quality assurance, and regulatory affairs.
- Troubleshooting formulation challenges and proposing innovative solutions.
- Staying abreast of new technologies and scientific advancements in pharmaceutical formulation and drug delivery.
- Mentoring and guiding junior scientists and technicians in the formulation laboratory.
This is an exceptional career opportunity to contribute to life-changing medicines within a forward-thinking organization. If you are passionate about pharmaceutical innovation, we invite you to apply.
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2
Clinical Research Associate - Pharmaceutical Development
105 Manama, Capital
BHD70000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical company dedicated to advancing healthcare, is looking for a meticulous and motivated Clinical Research Associate (CRA) to join their innovative team in Manama, Capital, BH . This role is instrumental in supporting the execution of clinical trials, ensuring adherence to Good Clinical Practice (GCP) guidelines, and maintaining the integrity of trial data. The CRA will be responsible for site selection, initiation, monitoring, and close-out activities for clinical studies across various therapeutic areas. Key responsibilities include verifying data accuracy by reviewing source documents, ensuring proper investigational product accountability, and addressing any protocol deviations. The successful candidate will build and maintain strong relationships with investigators and site staff, providing essential support and guidance. Excellent organizational skills and a keen eye for detail are paramount, as is the ability to manage multiple tasks and prioritize effectively. You will be responsible for preparing trial-related documentation, tracking progress, and reporting findings to project management. A background in life sciences, nursing, or a related field is required, along with a comprehensive understanding of clinical trial phases and regulatory requirements. Experience as a CRA or in a similar clinical research role is highly preferred. This is a fantastic opportunity to contribute to the development of life-saving medicines and to grow your career in the dynamic pharmaceutical industry. The role offers a blend of office-based and on-site monitoring activities, providing a diverse and engaging work experience. A commitment to patient safety and data quality is fundamental to success in this position.
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3
Clinical Research Associate - Pharmaceutical Development
50506 Diplomatic Area
BHD80000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical company dedicated to advancing healthcare through innovative drug development, is seeking a qualified Clinical Research Associate (CRA) to join their esteemed clinical operations team in Isa Town, Southern, BH . This vital role involves overseeing and managing clinical trial activities to ensure compliance with study protocols, regulatory requirements, and ethical standards. The CRA will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring the quality and integrity of data collected during trials.
Key Responsibilities:
Key Responsibilities:
- Identify, evaluate, and select potential clinical trial sites.
- Initiate clinical trial sites, ensuring all necessary documentation is in place and investigators are adequately trained.
- Conduct regular site visits (remote and in-person) to monitor trial progress, data accuracy, patient safety, and adherence to protocol and GCP guidelines.
- Ensure accurate and timely source data verification (SDV) and query resolution.
- Manage study supplies and investigational product at trial sites.
- Act as the primary liaison between the sponsor and the clinical trial sites, fostering strong working relationships.
- Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH-GCP).
- Prepare and present monitoring visit reports and follow-up actions.
- Oversee the management of essential documents required for clinical trials.
- Assist in the resolution of site-specific issues and escalate critical problems as necessary.
- Participate in study team meetings and contribute to the development of study-related documents.
- Support the close-out of clinical trial sites, ensuring all documentation is complete and archived.
- Train site staff on study procedures and data collection requirements.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field. A Master's degree is an advantage.
- Minimum of 2-3 years of experience as a Clinical Research Associate (CRA) or similar role in clinical trial management.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in monitoring clinical trials and performing site visits.
- Excellent understanding of medical terminology and clinical trial processes.
- Strong organizational, time management, and problem-solving skills.
- Exceptional interpersonal and communication skills, with the ability to build rapport with site personnel.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to trial sites as required.
- Attention to detail and a commitment to data integrity and patient safety.
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4
Clinical Research Associate - Pharmaceutical Development
BH2345 Hamala, Northern
BHD75000 Annually
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Posted 4 days ago
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Our client, a globally recognized pharmaceutical innovator, is expanding its clinical operations team and seeks a dedicated Clinical Research Associate (CRA) to support cutting-edge drug development. This role is crucial in ensuring the efficacy, safety, and ethical conduct of clinical trials across various therapeutic areas. Based in Sanad, Capital, BH , you will play a pivotal role in bringing life-changing therapies to patients.
The ideal candidate will be a highly organized and detail-oriented professional with a solid understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring clinical trial sites, ensuring data accuracy and completeness, and managing all aspects of trial conduct from initiation to close-out. This includes site selection, initiation visits, routine monitoring, and close-out visits. Your expertise will be vital in verifying patient safety and data integrity. You will also serve as a key liaison between the investigative sites and the sponsor company, providing training and support to site staff as needed. Collaboration is key, and you will work closely with project managers, data managers, and other members of the clinical trial team.
Key Responsibilities:
The ideal candidate will be a highly organized and detail-oriented professional with a solid understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring clinical trial sites, ensuring data accuracy and completeness, and managing all aspects of trial conduct from initiation to close-out. This includes site selection, initiation visits, routine monitoring, and close-out visits. Your expertise will be vital in verifying patient safety and data integrity. You will also serve as a key liaison between the investigative sites and the sponsor company, providing training and support to site staff as needed. Collaboration is key, and you will work closely with project managers, data managers, and other members of the clinical trial team.
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits in accordance with study protocols and SOPs.
- Verify the accuracy, completeness, and timeliness of clinical trial data through source document verification.
- Ensure compliance with GCP, FDA regulations, and other applicable regulatory requirements.
- Manage and maintain essential study documents and site files.
- Identify and resolve site-level issues, escalating as necessary.
- Train site personnel on study protocols, procedures, and data collection.
- Build and maintain strong relationships with investigators and site staff.
- Prepare and submit accurate and timely monitoring visit reports.
- Contribute to the development and review of clinical trial documentation.
- Monitor subject safety and report adverse events promptly.
- Participate in investigator meetings and training sessions.
- Ensure adherence to study budgets and timelines at the site level.
- Bachelor's degree in a life science, nursing, or related field. Master's degree preferred.
- Minimum of 2-3 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and clinical trial processes.
- Excellent understanding of medical terminology and clinical trial conduct.
- Strong analytical and problem-solving skills.
- Exceptional organizational and time management abilities.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent written and verbal communication skills.
- Ability to travel to clinical trial sites as required.
- High degree of accuracy and attention to detail.
- Proven ability to work independently and as part of a team.
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5
Clinical Research Associate - Pharmaceutical Development
789 Southern, Southern
BHD80000 Annually
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Posted 8 days ago
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Job Description
A pioneering pharmaceutical company is seeking a dedicated Clinical Research Associate (CRA) to support the development of innovative medicines within their operations in Nuwaidrat, Southern, BH . This role is crucial for ensuring the integrity and accuracy of clinical trial data, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. The CRA will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring compliance with study protocols and investigational plans. You will act as the primary liaison between the sponsor and the clinical trial sites, providing essential support to investigators and site staff.
Key responsibilities include initiating, monitoring, and closing out clinical study sites, performing source data verification, and ensuring timely query resolution. The CRA will also be responsible for assessing site compliance with regulatory requirements, ethical standards, and protocol requirements. You will contribute to the preparation of study-related documents, including Investigator Brochures and Case Report Forms. The ideal candidate will possess a strong understanding of clinical trial phases, study design, and regulatory affairs within the pharmaceutical industry. Excellent organizational skills, meticulous attention to detail, and strong communication and interpersonal abilities are essential. A Bachelor's degree in a life science, nursing, or related field, along with a minimum of 3-5 years of experience as a Clinical Research Associate, is required. Experience with electronic data capture (EDC) systems and familiarity with ICH-GCP guidelines are mandatory. This is an excellent opportunity to contribute to life-saving drug development.
Key responsibilities include initiating, monitoring, and closing out clinical study sites, performing source data verification, and ensuring timely query resolution. The CRA will also be responsible for assessing site compliance with regulatory requirements, ethical standards, and protocol requirements. You will contribute to the preparation of study-related documents, including Investigator Brochures and Case Report Forms. The ideal candidate will possess a strong understanding of clinical trial phases, study design, and regulatory affairs within the pharmaceutical industry. Excellent organizational skills, meticulous attention to detail, and strong communication and interpersonal abilities are essential. A Bachelor's degree in a life science, nursing, or related field, along with a minimum of 3-5 years of experience as a Clinical Research Associate, is required. Experience with electronic data capture (EDC) systems and familiarity with ICH-GCP guidelines are mandatory. This is an excellent opportunity to contribute to life-saving drug development.
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6
Research Scientist - Pharmaceutical Development
N/A Busaiteen, Muharraq
BHD100000 Annually
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Our client is seeking a highly qualified and motivated Remote Research Scientist to join their cutting-edge Scientific Research & Development division. This fully remote role focuses on advancing pharmaceutical development through rigorous experimentation and data analysis. The successful candidate will design, conduct, and interpret experiments related to drug discovery, formulation, and efficacy testing. You will be responsible for meticulously documenting experimental procedures, results, and conclusions, contributing to scientific publications and patent applications. This position requires a deep understanding of pharmacology, molecular biology, and analytical chemistry. Proficiency in laboratory techniques, data analysis software, and a strong background in research methodologies are essential. You will collaborate with a global team of scientists, clinicians, and project managers, contributing to the advancement of novel therapeutic solutions. The ideal candidate will possess excellent problem-solving skills, a strong scientific curiosity, and the ability to work independently and as part of a virtual team. A PhD or Master's degree in Pharmacology, Chemistry, Biology, or a related field, with relevant research experience, is required. Experience with specific therapeutic areas or drug delivery systems is a plus. This is an exciting opportunity to contribute to significant advancements in medicine and work in a dynamic, research-intensive environment, all from your home office.
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7
Research Scientist - Pharmaceutical Development
2015 Al Hidd
BHD90000 Annually
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Job Description
Our client, a progressive pharmaceutical company, is seeking a highly qualified and dedicated Research Scientist to contribute to its groundbreaking drug discovery and development programs in Budaiya, Northern, BH . This role offers a significant opportunity to work on innovative therapeutic agents and make a tangible impact on patient health. The Research Scientist will be responsible for designing and executing in vitro and in vivo studies, analyzing experimental data, contributing to the development of new drug formulations, and collaborating with cross-functional teams, including medicinal chemists, pharmacologists, and clinical researchers. Key responsibilities include planning and conducting preclinical studies to assess drug efficacy and safety, developing and validating assay methodologies, performing data analysis using statistical software, preparing detailed research reports and study protocols, staying current with scientific literature and emerging technologies in pharmaceutical research, and contributing to the preparation of regulatory submission documents. The ideal candidate will hold a Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life sciences discipline, with a minimum of 3-5 years of post-doctoral or industry research experience. Proven expertise in areas such as cell-based assays, drug metabolism and pharmacokinetics (DMPK), or specific therapeutic areas like oncology or immunology is highly desirable. Strong analytical, critical thinking, and problem-solving skills are essential, alongside excellent written and verbal communication abilities. Experience with laboratory automation and data management systems is also advantageous. This position offers a chance to work in a state-of-the-art facility with a team of leading experts in pharmaceutical R&D, driving the development of novel treatments. Our client is committed to fostering a culture of scientific excellence and collaboration, providing ample opportunities for professional growth. You will be involved in critical stages of the drug development pipeline, from early discovery to preclinical evaluation. Successful candidates will demonstrate a passion for scientific discovery and a commitment to advancing human health.
Key Responsibilities:
Key Responsibilities:
- Design, execute, and interpret preclinical drug development studies.
- Develop and validate biochemical and cell-based assays.
- Conduct in vitro and in vivo pharmacology experiments.
- Analyze experimental data and prepare comprehensive research reports.
- Collaborate with cross-functional teams to advance drug candidates.
- Stay updated on relevant scientific literature and industry trends.
- Contribute to manuscript preparation and regulatory filings.
- Maintain accurate and detailed laboratory records.
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8
Lead Pharmaceutical Development Scientist
2345 Tubli, Central
BHD110000 Annually
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Posted 1 day ago
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Our client, a groundbreaking pharmaceutical company focused on developing novel therapies, is searching for a talented Lead Pharmaceutical Development Scientist to join their research and development division. This hybrid role combines the flexibility of remote work with essential on-site collaboration, fostering an innovative and efficient work environment. The successful candidate will spearhead the formulation development of new drug products, from pre-clinical stages through to commercialization. You will be responsible for designing, executing, and optimizing formulation strategies, ensuring product stability, bioavailability, and manufacturability. Key responsibilities include conducting formulation studies, pre-formulation characterization, and stability testing according to ICH guidelines. You will also be involved in selecting appropriate excipients, developing manufacturing processes for various dosage forms (e.g., oral solid dosage, injectables), and preparing technical documentation for regulatory submissions. This position requires a Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field, with a minimum of 5 years of relevant experience in drug product development within the pharmaceutical industry. A strong understanding of solid-state chemistry, physical pharmacy principles, and analytical techniques is crucial. Experience with different dosage forms and delivery systems is highly desirable. You will collaborate closely with analytical development, CMC, and regulatory affairs teams, providing scientific expertise and project leadership. Excellent leadership, communication, and project management skills are essential for success in this role. The ideal candidate is a self-motivated individual with a passion for scientific discovery and a proven track record of bringing innovative pharmaceutical products to market. Join a team dedicated to improving patient lives through cutting-edge pharmaceutical science and contribute to the development of life-changing medicines. Your expertise will be valued in our state-of-the-art facilities, with opportunities for professional growth and development.
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