What Jobs are available for Pharmaceuticals in Bahrain?
Showing 2008 Pharmaceuticals jobs in Bahrain
Lead Formulation Scientist, Pharmaceuticals
Posted 1 day ago
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Job Description
Key Responsibilities:
- Lead the formulation development of new pharmaceutical products from concept to clinical trials.
- Design and execute studies to optimize drug product formulations, considering factors like bioavailability, stability, and patient compliance.
- Develop and validate analytical methods for characterizing drug products and their components.
- Investigate and troubleshoot formulation challenges, proposing innovative solutions.
- Select appropriate excipients and materials to achieve desired product performance.
- Collaborate with process development and manufacturing teams to ensure successful scale-up and commercialization.
- Mentor and guide junior formulation scientists, fostering scientific excellence and career development.
- Prepare comprehensive formulation development reports and regulatory submission documents.
- Stay abreast of emerging trends and technologies in pharmaceutical formulation and drug delivery.
- Manage external contract research organizations (CROs) for specific formulation development activities.
- Ensure all activities comply with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
- Present research findings and project updates to internal stakeholders and management.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related discipline.
- Minimum of 8 years of progressive experience in pharmaceutical formulation development.
- Proven track record of successfully developing and advancing drug formulations through various stages of development.
- Expertise in various dosage forms (e.g., oral solid dosage, injectables, topical).
- Strong knowledge of excipient properties, drug delivery systems, and analytical techniques.
- Experience with statistical analysis and design of experiments (DoE).
- Excellent leadership, communication, and project management skills, with the ability to lead a remote team.
- Familiarity with regulatory requirements (FDA, EMA) for drug product development.
- Strong understanding of intellectual property within drug formulation.
- Publications in peer-reviewed journals and/or patents are highly desirable.
- This is a fully remote position, allowing collaboration with a global team.
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Senior Process Engineer - Pharmaceuticals
Posted 1 day ago
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Job Description
Responsibilities:
- Design, develop, and optimize manufacturing processes for pharmaceutical products, ensuring efficiency, scalability, and cost-effectiveness.
- Conduct detailed process analyses, including mass and energy balances, PFDs (Process Flow Diagrams), and P&IDs (Piping and Instrumentation Diagrams).
- Troubleshoot and resolve process-related issues, identifying root causes and implementing corrective actions.
- Lead process validation activities, ensuring compliance with cGMP, FDA, and other relevant regulatory requirements.
- Develop and execute experimental plans for process development and improvement projects.
- Implement new technologies and automation solutions to enhance process performance.
- Collaborate with R&D, Quality Assurance, and Operations teams to ensure seamless technology transfer and production scale-up.
- Prepare technical reports, documentation, and presentations for management and regulatory bodies.
- Stay current with advancements in pharmaceutical manufacturing technologies and best practices.
- Train and mentor junior engineers and technical staff on process engineering principles and operational procedures.
- Oversee process safety assessments and implement risk mitigation strategies.
Qualifications:
- Bachelor's or Master's degree in Chemical Engineering, Mechanical Engineering, or a related field.
- Minimum of 7 years of experience in process engineering within the pharmaceutical or biopharmaceutical industry.
- Proven experience with process design, scale-up, validation, and optimization.
- In-depth knowledge of cGMP regulations and FDA guidelines.
- Proficiency in process simulation software (e.g., Aspen Plus, HYSYS) and CAD tools.
- Strong analytical, problem-solving, and project management skills.
- Excellent communication and teamwork abilities.
- Experience with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Ability to work effectively in a highly regulated and complex manufacturing environment.
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Senior Process Engineer - Pharmaceuticals
Posted 2 days ago
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Job Description
Responsibilities:
- Design, develop, and implement innovative and efficient manufacturing processes for pharmaceutical products, ensuring compliance with GMP and regulatory standards.
- Optimize existing production processes to improve yield, reduce costs, enhance safety, and minimize waste.
- Conduct process hazard analyses (PHAs) and implement robust safety protocols to ensure a safe working environment.
- Troubleshoot and resolve complex process-related issues, identifying root causes and implementing effective solutions.
- Develop and maintain detailed process documentation, including P&IDs, SOPs, and batch records.
- Lead process validation activities and ensure successful technology transfer from R&D to manufacturing.
- Collaborate with cross-functional teams, including R&D, Quality Assurance, Operations, and Maintenance, to achieve project objectives.
- Stay abreast of new technologies, process improvements, and industry best practices in pharmaceutical manufacturing.
- Monitor key performance indicators (KPIs) for production processes and implement continuous improvement initiatives.
- Manage and mentor junior process engineers and provide technical guidance.
- Participate in the selection and qualification of new equipment and technologies.
- Contribute to capital expenditure projects related to process improvements and facility upgrades.
- Bachelor's degree in Chemical Engineering, Pharmaceutical Engineering, or a related discipline. Master's degree preferred.
- Minimum of 7 years of experience in process engineering, with a significant focus on pharmaceutical or biopharmaceutical manufacturing.
- Strong understanding of Good Manufacturing Practices (GMP) and other relevant regulatory requirements (e.g., FDA, EMA).
- Proven experience in process design, optimization, scale-up, and validation.
- Proficiency in process simulation software (e.g., Aspen Plus) and statistical analysis tools.
- Excellent analytical and problem-solving skills, with a demonstrated ability to troubleshoot complex technical issues.
- Strong project management skills and experience leading cross-functional teams.
- Effective communication, interpersonal, and presentation skills.
- Knowledge of process safety management (PSM) principles.
- Ability to work effectively in a hybrid work setting, balancing on-site and remote responsibilities.
- Experience with automation and control systems in manufacturing environments.
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Clinical Research Associate - Pharmaceuticals
Posted 4 days ago
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Senior Formulation Scientist - Pharmaceuticals
Posted 10 days ago
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Job Description
Responsibilities:
- Lead the formulation development of new drug products, from pre-formulation studies to commercial readiness.
- Design and conduct experiments to optimize drug delivery systems, ensuring bioavailability, stability, and efficacy.
- Develop and validate analytical methods for characterizing drug formulations.
- Troubleshoot formulation challenges and implement effective solutions.
- Collaborate with cross-functional teams, including analytical chemistry, process development, and regulatory affairs.
- Prepare comprehensive documentation for regulatory submissions (e.g., IND, NDA).
- Oversee the scale-up of formulations from laboratory to pilot and commercial manufacturing.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Stay current with scientific literature, industry trends, and new technologies in pharmaceutical formulation.
- Mentor junior scientists and provide technical guidance on formulation development projects.
- Evaluate new excipients and technologies for potential application in drug formulations.
- Contribute to the strategic direction of the formulation development group.
- Present research findings at internal meetings and scientific conferences.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 5-7 years of hands-on experience in pharmaceutical formulation development.
- Proven expertise in developing various dosage forms (e.g., oral solid dosage, injectables, topical).
- Strong understanding of physical chemistry, drug delivery systems, and pharmacokinetics.
- Proficiency in formulation development techniques and analytical instrumentation (e.g., HPLC, dissolution testing).
- Experience with GMP regulations and regulatory submission processes.
- Excellent problem-solving, critical thinking, and experimental design skills.
- Strong written and verbal communication skills, with the ability to present complex data clearly.
- Ability to work independently and collaboratively in a team-oriented environment.
- Project management skills and the ability to manage multiple priorities effectively.
- Experience with biologics formulation is a plus.
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Clinical Research Associate - Pharmaceuticals
Posted 15 days ago
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Job Description
Responsibilities:
- Conduct pre-study, initiation, routine monitoring, and close-out visits to assigned clinical sites.
- Ensure compliance with study protocols, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
- Verify the accuracy, completeness, and integrity of clinical data.
- Manage site-level regulatory documentation and essential study documents.
- Serve as the main point of contact for investigators and site staff.
- Identify and resolve site-level issues and deviations promptly.
- Train site personnel on study-specific procedures and requirements.
- Track study progress and report findings to the clinical project manager.
- Contribute to the development of study protocols and case report forms.
- Ensure patient safety and data privacy are maintained at all times.
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Quality Assurance Manager, Pharmaceuticals
Posted 16 days ago
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Job Description
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with pharmaceutical regulations.
- Oversee and manage all aspects of quality assurance for manufacturing operations.
- Lead the Quality Assurance team, providing guidance, training, and performance management.
- Ensure compliance with cGMP (current Good Manufacturing Practices) and other relevant regulatory standards.
- Manage deviations, investigations, and the CAPA process to address quality issues effectively.
- Conduct internal audits and support external regulatory inspections (e.g., FDA, EMA).
- Review and approve batch records, specifications, and validation protocols.
- Oversee the release of finished products after ensuring they meet all quality requirements.
- Collaborate with Production, R&D, and other departments to ensure product quality throughout the lifecycle.
- Monitor quality metrics and KPIs, implementing continuous improvement initiatives.
- Manage supplier qualification and quality agreements.
- Stay up-to-date with evolving regulatory requirements and industry best practices.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, Engineering, or a related life science field. A Master's degree is preferred.
- Minimum of 7 years of experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry.
- At least 3 years of experience in a management or supervisory role.
- In-depth knowledge of GMP regulations (e.g., FDA 21 CFR Parts 210/211, EudraLex Volume 4).
- Proven experience with QMS implementation and maintenance, deviation management, and CAPA systems.
- Strong understanding of validation processes (process, cleaning, equipment).
- Excellent analytical, problem-solving, and decision-making skills.
- Strong leadership and team management capabilities.
- Exceptional communication and interpersonal skills.
- Experience with regulatory inspections and audits.
- Proficiency in relevant software, including LIMS and QMS software.
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Quality Assurance Specialist - Pharmaceuticals
Posted 16 days ago
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Job Description
Responsibilities:
- Implement and maintain the company's Quality Management System (QMS).
- Conduct internal audits of manufacturing processes, documentation, and facilities.
- Review and approve batch production and control records.
- Investigate deviations, non-conformances, and out-of-specification (OOS) results.
- Participate in CAPA (Corrective and Preventive Actions) development and implementation.
- Support regulatory inspections from health authorities.
- Ensure compliance with GMP, GCP, and other applicable regulations.
- Develop and deliver quality assurance training to relevant personnel.
- Manage quality-related documentation and records.
- Contribute to continuous improvement initiatives within the QA department.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and other relevant pharmaceutical regulations.
- Experience with quality systems, including document control, deviation management, and CAPA.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and organizational abilities.
- Proficient in Microsoft Office Suite and quality management software.
- Strong written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
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Principal Research Scientist - Pharmaceuticals
Posted 20 days ago
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Senior Research Scientist - Pharmaceuticals
Posted 21 days ago
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Job Description
Responsibilities:
- Design, conduct, and interpret complex experiments related to drug discovery and development.
- Lead and mentor a team of junior scientists and technicians.
- Develop and optimize research methodologies and protocols.
- Analyze and present research findings to internal teams and external collaborators.
- Manage research projects from conception to completion, ensuring timely delivery of results.
- Contribute to the strategic direction of the R&D department.
- Identify and evaluate new scientific technologies and approaches.
- Write research reports, publications, and patent applications.
- Ensure compliance with all laboratory safety regulations and ethical guidelines.
- Collaborate with medicinal chemists, biologists, and pharmacologists to achieve project goals.
- Troubleshoot experimental issues and devise solutions.
- Stay current with the latest advancements in pharmaceutical research and relevant scientific literature.
- Contribute to budget planning and resource allocation for research projects.
Qualifications:
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5-7 years of post-doctoral or industry research experience in pharmaceutical R&D.
- Demonstrated expertise in drug discovery, preclinical development, or a specific therapeutic area.
- Proven experience in leading research projects and managing scientific teams.
- Strong publication record in peer-reviewed journals.
- Excellent understanding of experimental design, data analysis (e.g., statistical analysis), and interpretation.
- Proficiency in various laboratory techniques and instrumentation relevant to drug discovery.
- Exceptional problem-solving and critical thinking skills.
- Strong written and verbal communication skills, including presentation abilities.
- Ability to work effectively in a collaborative, fast-paced environment.
- Experience with regulatory requirements (e.g., FDA, EMA) is a plus.
- Familiarity with bioinformatic tools and techniques is advantageous.
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