14 Chemists jobs in Bahrain
Lead Pharmaceutical Research Chemist
Posted 1 day ago
Job Viewed
Job Description
Responsibilities include:
- Designing and executing multi-step synthetic routes for target molecules, including small molecules and complex organic structures.
- Developing and validating robust synthetic procedures suitable for scale-up.
- Leading the identification and optimization of lead compounds in collaboration with medicinal chemists and biologists.
- Utilizing advanced spectroscopic and analytical techniques (e.g., NMR, MS, HPLC, GC) for compound characterization and purity assessment.
- Mentoring and guiding junior chemists, fostering a collaborative and high-performance laboratory environment.
- Troubleshooting synthetic challenges and implementing innovative solutions.
- Preparing comprehensive documentation, including synthesis reports, laboratory notebooks, and contributions to regulatory filings.
- Staying current with the latest advancements in synthetic organic chemistry, medicinal chemistry, and pharmaceutical sciences.
- Ensuring strict adherence to safety regulations and laboratory best practices.
- Collaborating effectively with internal teams and external partners to achieve project milestones.
Remote Senior Research Chemist
Posted 5 days ago
Job Viewed
Job Description
Responsibilities:
- Design and execute complex multi-step organic synthesis.
- Synthesize and characterize novel chemical compounds.
- Develop and optimize synthetic methodologies.
- Utilize advanced analytical techniques for compound characterization.
- Conduct literature searches and stay current with scientific advancements.
- Troubleshoot synthetic challenges and develop alternative routes.
- Contribute to the preparation of patent applications and research publications.
- Collaborate with cross-functional teams on research projects.
- Present research findings to scientific audiences.
- Maintain detailed laboratory notebooks and research records.
- Mentor and guide junior research chemists.
- Ph.D. in Organic Chemistry or a closely related field.
- Minimum of 5 years of post-doctoral or industry research experience.
- Demonstrated expertise in synthetic organic chemistry.
- Proficiency in various analytical techniques (NMR, MS, HPLC, etc.).
- Proven ability to work independently and manage research projects remotely.
- Excellent problem-solving and critical thinking skills.
- Strong written and oral communication skills.
- Track record of scientific publications and/or patents.
- Experience with catalysis and green chemistry principles is a plus.
Senior Pharmaceutical Research Chemist
Posted 5 days ago
Job Viewed
Job Description
Senior Pharmaceutical Research Chemist
Posted 5 days ago
Job Viewed
Job Description
Key Responsibilities:
- Design and synthesize novel organic molecules for drug discovery.
- Optimize synthetic routes and troubleshoot complex chemical reactions.
- Characterize synthesized compounds using advanced analytical techniques.
- Conduct structure-activity relationship (SAR) studies.
- Collaborate with multidisciplinary research teams.
- Mentor and guide junior research chemists.
- Manage research projects and timelines.
- Contribute to patent applications and regulatory filings.
- Stay updated on the latest advancements in medicinal chemistry.
Qualifications:
- Ph.D. in Organic Chemistry, Medicinal Chemistry, or a related field.
- Minimum of 6 years of relevant post-doctoral or industry experience.
- Extensive experience in synthetic organic chemistry.
- Proficiency in modern analytical techniques (NMR, MS, HPLC).
- Experience with SAR studies and computational chemistry tools is a plus.
- Strong problem-solving and analytical skills.
- Excellent communication and teamwork abilities.
Senior Research Chemist - Materials Science
Posted 1 day ago
Job Viewed
Job Description
Responsibilities:
- Design and conduct research experiments in materials science and chemistry.
- Synthesize and characterize novel materials and chemical compounds.
- Evaluate material properties using advanced analytical techniques (e.g., spectroscopy, microscopy, thermal analysis).
- Develop and optimize chemical processes for material fabrication and modification.
- Collaborate with engineering teams for pilot-scale production and product integration.
- Write detailed research reports, scientific articles, and patent applications.
- Troubleshoot experimental challenges and propose innovative solutions.
- Stay abreast of the latest developments in materials science and chemistry.
- Mentor and guide junior research scientists.
- Ensure laboratory safety protocols are strictly followed.
- Ph.D. in Chemistry (with specialization in Materials Science), Materials Science, Chemical Engineering, or a related field.
- Minimum of 7 years of post-doctoral or industry research experience in materials science.
- Proven expertise in polymer synthesis, inorganic materials, or solid-state chemistry.
- Hands-on experience with advanced analytical instrumentation.
- Strong understanding of structure-property relationships in materials.
- Excellent scientific writing and presentation skills.
- Demonstrated ability to lead research projects and contribute to innovation.
- Proficiency in literature searching and intellectual property landscape analysis.
- Ability to work collaboratively in a multidisciplinary team environment.
Senior Process Chemist - Research & Development
Posted 5 days ago
Job Viewed
Job Description
Responsibilities:
- Develop and optimize chemical processes for new and existing products.
- Conduct laboratory-scale experiments to investigate reaction pathways and kinetics.
- Analyze experimental data using advanced statistical methods.
- Troubleshoot and resolve process-related issues in pilot and production plants.
- Collaborate with cross-functional teams to ensure seamless technology transfer.
- Prepare detailed technical reports, presentations, and documentation.
- Ensure compliance with all safety, environmental, and regulatory standards.
- Evaluate and implement new process technologies and equipment.
- Mentor junior chemists and technicians.
Qualifications:
- Ph.D. or Master's degree in Chemical Engineering or Chemistry.
- Minimum of 7 years of experience in process chemistry or chemical process development.
- Strong knowledge of organic synthesis, reaction mechanisms, and catalysis.
- Proficiency in analytical techniques (e.g., HPLC, GC-MS, NMR).
- Experience with process simulation software (e.g., Aspen Plus) is a plus.
- Excellent problem-solving and analytical skills.
- Strong communication and interpersonal abilities.
- Familiarity with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Ability to manage multiple projects and prioritize effectively.
Clinical Research Associate (Drug Development)
Posted 2 days ago
Job Viewed
Job Description
As a CRA, you will be responsible for monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements (e.g., GCP, FDA regulations), and company policies. This involves conducting site visits (pre-study, initiation, interim monitoring, and close-out), assessing the quality of trial conduct, and verifying the accuracy and completeness of source data and case report forms (CRFs). You will serve as the primary point of contact for study sites, providing training to investigators and site staff on study-related matters, and resolving any site-level issues that may arise. Data management is a key component, ensuring that all data is collected, reviewed, and reported in a timely and accurate manner. You will also be involved in regulatory document review, study budget management, and liaising with various internal departments, including data management, biostatistics, and regulatory affairs. The successful candidate will possess a strong understanding of clinical trial processes, excellent communication and interpersonal skills, and the ability to travel to clinical sites as needed. A meticulous approach to work and a commitment to maintaining the highest standards of research ethics are essential.
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory guidelines.
- Conduct site initiation visits, routine monitoring visits, and close-out visits.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Ensure proper documentation and maintenance of site regulatory files.
- Train and support investigators and site staff on study procedures and requirements.
- Identify and resolve site-level issues and escalate as necessary.
- Liaise with study participants, investigators, and other stakeholders.
- Oversee drug accountability at trial sites.
- Contribute to the development of study protocols and case report forms.
- Ensure timely data entry and query resolution.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Experience in site monitoring and management.
- Strong understanding of clinical trial processes and documentation.
- Excellent written and verbal communication skills.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required.
- Strong organizational skills and attention to detail.
- Ability to work independently and as part of a team.
Be The First To Know
About the latest Chemists Jobs in Bahrain !
Senior Formulation Scientist - Drug Development
Posted 5 days ago
Job Viewed
Job Description
Key Responsibilities:
- Design and execute experiments for the development of oral, injectable, topical, or other dosage forms.
- Investigate and select appropriate excipients and active pharmaceutical ingredients (APIs) for formulation development.
- Develop and optimize formulations to achieve desired drug release profiles, stability, and bioavailability.
- Conduct pre-formulation studies, including solid-state characterization and solubility enhancement techniques.
- Perform compatibility studies between APIs and excipients.
- Develop and validate analytical methods for the characterization of drug products and intermediates.
- Troubleshoot formulation-related issues encountered during development and scale-up.
- Collaborate closely with analytical development, process chemistry, and regulatory affairs teams.
- Prepare comprehensive technical reports, documentation for regulatory submissions (IND, NDA), and patent applications.
- Stay abreast of the latest scientific literature, industry trends, and regulatory guidelines in pharmaceutics.
- Mentor junior scientists and contribute to the scientific growth of the R&D department.
- Manage external collaborations with contract research organizations (CROs) as needed.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a closely related field.
- Minimum of 7 years of hands-on experience in pharmaceutical formulation development, preferably with experience across multiple dosage forms.
- Strong understanding of physical chemistry, materials science, and drug delivery principles.
- Proficiency in laboratory techniques used for formulation development and characterization (e.g., particle size analysis, DSC, TGA, XRPD).
- Experience with common pharmaceutical manufacturing equipment (e.g., blenders, granulators, tablet presses, capsule fillers).
- Familiarity with regulatory requirements for drug development (e.g., FDA, EMA guidelines).
- Excellent problem-solving, critical thinking, and analytical skills.
- Strong written and verbal communication skills, with the ability to present complex scientific information clearly.
- Ability to work independently and collaboratively in a team environment.
- This role requires a hybrid work arrangement, with significant on-site laboratory work in **Nuwaidrat, Southern, BH**.
Remote Senior Formulation Scientist, Drug Development
Posted 5 days ago
Job Viewed
Job Description
Key Responsibilities:
- Design, develop, and optimize novel drug formulations for various therapeutic indications.
- Evaluate physicochemical properties of APIs and select appropriate excipients and formulation strategies.
- Conduct laboratory experiments to prepare and characterize different dosage forms (e.g., tablets, capsules, injectables, topicals).
- Perform stability studies and develop analytical methods for formulation assessment.
- Troubleshoot formulation issues and propose scientifically sound solutions.
- Collaborate with analytical, process development, and regulatory affairs teams to advance drug candidates.
- Prepare detailed technical reports, development protocols, and documentation for regulatory submissions.
- Stay updated on the latest advances in drug delivery technologies and pharmaceutical sciences.
- Mentor and provide technical guidance to junior scientists and research associates.
- Contribute to the strategic planning and decision-making for formulation development projects.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field.
- Minimum of 6 years of progressive experience in pharmaceutical formulation development.
- Proven expertise in the design and development of various dosage forms.
- Strong understanding of drug solubility, stability, bioavailability, and drug delivery principles.
- Experience with analytical techniques used in formulation characterization (e.g., HPLC, dissolution testing, DSC, XRPD).
- Excellent experimental design and data analysis skills.
- Strong written and verbal communication skills, with experience in report writing and technical documentation.
- Ability to work independently and effectively manage multiple projects in a remote setting.
- Familiarity with regulatory guidelines (e.g., FDA, EMA) pertaining to drug product development.
Senior Clinical Research Scientist - Drug Development
Posted 5 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop clinical trial protocols and study designs that align with strategic objectives.
- Oversee the operational execution of clinical trials, ensuring quality and compliance.
- Manage relationships with Contract Research Organizations (CROs) and other vendors.
- Analyze and interpret clinical trial data, preparing study reports and summaries.
- Contribute to the development of regulatory submission documents (e.g., IND, NDA, MAA).
- Provide scientific and clinical expertise to cross-functional teams.
- Stay current with scientific literature, emerging technologies, and regulatory trends in drug development.
- Identify and engage with key opinion leaders (KOLs) in relevant therapeutic areas.
- Ensure ethical conduct of clinical research and patient safety throughout study duration.
- Participate in the evaluation of new drug candidates and therapeutic strategies.
Qualifications:
- Ph.D. or M.D. in a relevant life science discipline (e.g., Pharmacology, Medicine, Biology).
- Minimum of 7 years of experience in clinical research and drug development within the pharmaceutical or biotechnology industry.
- Extensive experience in designing, managing, and reporting on Phase I-IV clinical trials.
- In-depth knowledge of ICH-GCP guidelines and regulatory submission processes.
- Proven ability to analyze complex clinical data and translate findings into actionable insights.
- Excellent scientific writing and communication skills, with experience in preparing publications and regulatory documents.
- Strong project management and organizational abilities.
- Demonstrated success in leading cross-functional teams in a remote environment.
- Ability to work independently, manage multiple priorities, and meet tight deadlines.
- Experience in therapeutic areas such as oncology, immunology, or cardiovascular disease is highly desirable.
This is an outstanding opportunity for a dedicated scientist to make a significant contribution to bringing life-saving therapies to patients globally, all within a flexible, remote work setting.