150 Scientific Research & Development jobs in Bahrain
Administrator/Specialist - Quality Assurance and Accreditation Department
Arab Open University
Posted 17 days ago
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Administrator/Specialist - Quality Assurance and Accreditation Department
12 Jan 2025
The Arab Open University - Kingdom of Bahrain announces a vacancy for the following position:
Administrator/Specialist - Quality Assurance and Accreditation Department
Job requirements
Candidates must have
- A bachelor's degree in (Business Administration, IT, or Statistics)
- 3 years of experience in the QA field, and academic work experience is preferred.
- Proficiency in both Arabic and English, writing and speaking.
- Grand knowledge in data analysis reports & makes statistics.
- Technical Skill in using programs, electronic systems and related applications.
Those who meet the above conditions must submit a copy of the following documents by e-mail:
- A copy of academic and professional certificates (if any).
- A Copy of experience certificates.
- CPR and passport copy
SIGNIFICANT NOTE: Academic certificates not recognized by the Higher Education Council in the Kingdom of Bahrain will not be considered.
Contact Us
- Arab Open University - Bahrain
Street 3220, Building 890, Block 732, A'ali
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Principal Research Scientist (Biotechnology)
505 Amwaj Islands
BHD95000 Annually
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Our client, a pioneering research organization, is seeking a highly accomplished Principal Research Scientist to lead groundbreaking projects in the field of Biotechnology at our advanced research facility in Hidd, Muharraq, BH . This senior position requires a visionary scientist with a Ph.D. in Biotechnology, Molecular Biology, Genetics, or a closely related discipline, and a substantial publication record demonstrating expertise in innovative research methodologies. You will be responsible for conceptualizing, designing, and executing complex research studies, securing research funding through grant writing, and mentoring junior scientists and research staff. Key responsibilities include developing novel therapeutic targets, optimizing existing biotechnological processes, and collaborating with interdisciplinary teams to translate research findings into practical applications. The ideal candidate will possess a deep understanding of current advancements in biotechnology, including gene editing, protein engineering, and bioprocessing. Strong analytical and critical thinking skills are essential, as is the ability to interpret complex data sets and draw meaningful conclusions. Experience in managing research projects, leading laboratory operations, and ensuring adherence to stringent ethical and safety standards is paramount. This role offers an exceptional opportunity to contribute to cutting-edge scientific discovery, publish in high-impact journals, and shape the future direction of our biotechnology research initiatives. A proven ability to secure competitive research grants and a network of scientific collaborators are highly advantageous. Join us and make a significant contribution to advancing human health through innovative biotechnology.
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1
Principal AI Research Scientist
81020 Jidd Haffs, Northern
BHD120000 Annually
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Our client, a cutting-edge technology firm at the forefront of artificial intelligence innovation, is seeking a highly influential Principal AI Research Scientist to drive groundbreaking research and development in **Sanad, Capital, BH**. This senior position requires a visionary leader with a deep passion for exploring the frontiers of AI, machine learning, and data science. The ideal candidate will possess a Ph.D. in a relevant field, a strong publication record, and a history of successfully translating complex research into practical applications.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Lead and conduct advanced research in areas such as deep learning, natural language processing, computer vision, reinforcement learning, or other emerging AI fields.
- Develop novel algorithms, models, and techniques to solve complex problems and advance the state-of-the-art in artificial intelligence.
- Design and execute rigorous experiments to validate research hypotheses and measure the performance of AI models.
- Collaborate with engineering teams to integrate research findings and prototypes into production-ready AI solutions.
- Mentor and guide junior researchers and data scientists, fostering a collaborative and innovative research environment.
- Publish research findings in top-tier conferences and journals, and present work to internal and external stakeholders.
- Identify new research opportunities and develop strategic roadmaps for AI initiatives.
- Evaluate and adopt new technologies and methodologies to enhance research capabilities.
- Contribute to the company's intellectual property portfolio through patents and publications.
- Engage with the broader AI community through conferences, workshops, and open-source contributions.
Qualifications:
- Ph.D. in Computer Science, Artificial Intelligence, Machine Learning, Statistics, or a closely related quantitative field.
- A minimum of 10 years of relevant research experience post-Ph.D., with a significant portion in a lead or principal capacity.
- Demonstrated track record of impactful research, evidenced by publications in top AI conferences (e.g., NeurIPS, ICML, ICLR, CVPR, ACL) and/or highly cited papers.
- Expertise in one or more core AI areas (e.g., deep learning, NLP, computer vision, reinforcement learning).
- Proficiency in programming languages such as Python and relevant AI frameworks (e.g., TensorFlow, PyTorch).
- Strong understanding of machine learning theory, algorithms, and statistical modeling.
- Experience with large-scale data processing and distributed computing environments.
- Exceptional analytical, problem-solving, and critical-thinking skills.
- Excellent communication, presentation, and interpersonal skills.
- Proven ability to lead research projects from conception to completion.
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2
Principal Research Scientist - Biomaterials
23302 Seef, Capital
BHD120000 Annually
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Our client, a leading innovator in biomedical technology, is seeking a highly accomplished Principal Research Scientist specializing in Biomaterials for their cutting-edge research facility located in Seef, Capital, BH . This senior research position will spearhead the discovery, development, and characterization of novel biomaterials for next-generation medical devices and therapeutic applications. The ideal candidate will possess a Ph.D. in Materials Science, Biomedical Engineering, Chemical Engineering, or a closely related field, with a strong publication record and demonstrated success in bringing new materials from concept to application.
Key responsibilities include leading research projects, designing and executing experiments, analyzing complex data sets, and publishing findings in high-impact peer-reviewed journals. You will be responsible for developing and validating advanced characterization techniques for biomaterials, understanding their performance in biological systems. This role requires a deep understanding of polymer chemistry, surface science, and cell-material interactions. Experience with biocompatibility testing, degradation studies, and relevant regulatory pathways (e.g., FDA) is highly desirable.
The Principal Research Scientist will also be involved in intellectual property generation, grant writing, and collaborating with cross-functional teams, including product development, clinical affairs, and manufacturing. Excellent leadership, project management, and communication skills are essential to guide research efforts and effectively communicate complex scientific concepts to diverse audiences. We are looking for an individual with a minimum of 8 years of post-doctoral research experience in a relevant industrial or academic setting. Proven ability to secure research funding and manage budgets is a significant advantage. This is a unique opportunity to shape the future of healthcare through groundbreaking scientific innovation.
Key responsibilities include leading research projects, designing and executing experiments, analyzing complex data sets, and publishing findings in high-impact peer-reviewed journals. You will be responsible for developing and validating advanced characterization techniques for biomaterials, understanding their performance in biological systems. This role requires a deep understanding of polymer chemistry, surface science, and cell-material interactions. Experience with biocompatibility testing, degradation studies, and relevant regulatory pathways (e.g., FDA) is highly desirable.
The Principal Research Scientist will also be involved in intellectual property generation, grant writing, and collaborating with cross-functional teams, including product development, clinical affairs, and manufacturing. Excellent leadership, project management, and communication skills are essential to guide research efforts and effectively communicate complex scientific concepts to diverse audiences. We are looking for an individual with a minimum of 8 years of post-doctoral research experience in a relevant industrial or academic setting. Proven ability to secure research funding and manage budgets is a significant advantage. This is a unique opportunity to shape the future of healthcare through groundbreaking scientific innovation.
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3
Senior Research Scientist - Biotechnology
205 Muharraq, Muharraq
BHD90000 Annually
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Our client, a cutting-edge biotechnology research firm, is seeking a highly skilled and innovative Senior Research Scientist to lead impactful projects in **Muharraq, Muharraq, BH**. This role is crucial for driving forward scientific discovery, developing novel therapeutics, and contributing to the company's mission of advancing human health. The ideal candidate will possess a Ph.D. in a relevant scientific discipline, extensive experience in laboratory research, and a strong publication record.
Responsibilities:
Responsibilities:
- Design, execute, and analyze complex experiments in molecular biology, cell biology, or biochemistry.
- Develop and validate new experimental methodologies and protocols.
- Lead research projects from conception through to completion, including data interpretation and reporting.
- Analyze large datasets using advanced bioinformatics tools and statistical methods.
- Contribute to the writing of research papers for publication in peer-reviewed journals.
- Prepare and present research findings at scientific conferences and internal meetings.
- Manage laboratory operations, including equipment maintenance, inventory control, and safety compliance.
- Supervise and mentor junior researchers, postdoctoral fellows, and technicians.
- Collaborate with internal teams and external partners on research initiatives.
- Seek and apply for grant funding to support research projects.
- Stay current with scientific literature and emerging technologies in the field.
- Contribute to intellectual property development through patent filings.
- Ensure all research activities comply with ethical guidelines and regulatory requirements.
- Troubleshoot experimental challenges and develop creative solutions.
- Participate in the strategic planning of research programs and the identification of new research opportunities.
- Ph.D. in Biotechnology, Molecular Biology, Cell Biology, Biochemistry, or a closely related field.
- Minimum of 5 years of post-doctoral or industry research experience in a relevant area.
- Demonstrated expertise in a specific area of biotechnology relevant to the company's focus (e.g., gene editing, protein expression, immunology).
- Proven track record of successful research project management and execution.
- Strong publication record in high-impact scientific journals.
- Proficiency in relevant laboratory techniques and instrumentation.
- Experience with bioinformatics tools and data analysis software.
- Excellent analytical, critical thinking, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to clearly articulate complex scientific concepts.
- Experience supervising and mentoring junior staff is highly desirable.
- Ability to work collaboratively in a team-oriented environment.
- Fluency in English is required.
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4
Senior Clinical Research Scientist - Oncology
23456 Southern, Southern
BHD110000 Annually
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Our client, a globally recognized pharmaceutical leader, is seeking an exceptional Senior Clinical Research Scientist specializing in Oncology to join their innovative research and development division in Nuwaidrat, Southern, BH . This pivotal role will involve the design, execution, and interpretation of clinical trials for novel oncology therapeutics. You will be at the forefront of advancing cancer treatment, working with cutting-edge investigational drugs and contributing to the development of life-saving therapies. The ideal candidate will possess a profound understanding of cancer biology, clinical trial methodologies, and regulatory requirements within the pharmaceutical industry. Responsibilities will include developing clinical trial protocols, overseeing patient recruitment and monitoring, analyzing clinical data, and preparing comprehensive study reports. You will collaborate closely with a multidisciplinary team of clinicians, statisticians, regulatory affairs specialists, and other scientists to ensure the successful progression of clinical programs. A strong scientific acumen, coupled with excellent analytical and problem-solving skills, is essential. The successful applicant will have a proven ability to interpret complex scientific data, translate research findings into actionable strategies, and contribute to the scientific literature through publications and presentations. We are looking for a motivated and results-oriented individual with a passion for improving patient outcomes in oncology. The ability to thrive in a fast-paced, collaborative environment and a commitment to scientific rigor are crucial. This position offers a unique opportunity to make a significant impact on cancer research and development within a highly respected organization. Embrace the challenge of transforming scientific discovery into tangible patient benefits.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols for oncology drugs.
- Oversee the conduct of clinical trials, ensuring patient safety and data integrity.
- Analyze and interpret clinical trial data, including efficacy and safety endpoints.
- Prepare clinical study reports and regulatory submission documents.
- Collaborate with internal and external stakeholders, including investigators and regulatory agencies.
- Contribute to the scientific strategy for oncology drug development.
- Stay abreast of the latest advancements in oncology research and clinical practice.
- Mentor junior research staff and contribute to knowledge sharing.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biology).
- Minimum of 5 years of experience in clinical research within the pharmaceutical industry, with a focus on oncology.
- In-depth knowledge of cancer biology and therapeutic strategies.
- Strong understanding of clinical trial design, GCP, and regulatory guidelines.
- Excellent analytical, statistical interpretation, and written communication skills.
- Experience in data analysis software and statistical methods.
- Proven ability to manage multiple projects and timelines effectively.
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5
Senior Pharmaceutical Research Scientist
621 Seef, Capital
BHD85000 Annually
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Our client, a leading innovator in the pharmaceutical sector, is seeking a highly skilled and motivated Senior Pharmaceutical Research Scientist to join their dynamic team in **Seef, Capital, BH**. This is an exceptional opportunity for a dedicated scientist to contribute to groundbreaking drug discovery and development initiatives. The ideal candidate will possess a strong academic background in pharmacology, chemistry, or a related life science field, coupled with extensive hands-on experience in preclinical research and development.
Responsibilities:
Responsibilities:
- Design, conduct, and analyze complex experiments related to drug discovery and development.
- Develop and optimize new analytical methods and assays for evaluating drug efficacy and safety.
- Oversee laboratory operations, ensuring adherence to Good Laboratory Practices (GLP) and regulatory guidelines.
- Manage and mentor junior research staff, providing technical guidance and scientific direction.
- Collaborate with cross-functional teams, including medicinal chemistry, biology, and regulatory affairs, to advance projects from discovery through to clinical trials.
- Prepare comprehensive research reports, scientific publications, and presentations for internal and external stakeholders.
- Stay abreast of the latest scientific advancements and emerging technologies in pharmaceutical research.
- Manage project timelines and resources effectively to ensure successful project completion.
- Contribute to the strategic planning and direction of research programs.
- Ensure the safe handling and disposal of chemicals and biological materials.
- Ph.D. in Pharmacology, Pharmaceutical Sciences, Biochemistry, or a closely related field.
- Minimum of 5-7 years of post-doctoral research experience in the pharmaceutical industry.
- Proven track record of successful drug discovery and development, with a deep understanding of the drug development process.
- Expertise in molecular biology, cell biology, in vitro assays, and preclinical models.
- Proficiency in data analysis software and statistical methods.
- Excellent communication, interpersonal, and problem-solving skills.
- Demonstrated leadership capabilities and experience in managing research projects and teams.
- Ability to work independently and collaboratively in a fast-paced, team-oriented environment.
- Strong commitment to scientific integrity and ethical research practices.
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6
Senior Pharmaceutical Quality Assurance Specialist
507 Seef, Capital
BHD90000 Annually
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Our client, a prominent pharmaceutical company, is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist for their facility in Seef, Capital, BH . This crucial role will be responsible for ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy, in compliance with regulatory requirements and Good Manufacturing Practices (GMP). You will play a key role in developing, implementing, and maintaining the company's quality management system. The ideal candidate possesses a strong background in pharmaceutical quality assurance, excellent analytical skills, and a deep understanding of regulatory affairs. Your expertise will be vital in upholding the integrity of our client's product pipeline and ensuring patient safety.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS) in accordance with GMP and regulatory guidelines.
- Conduct internal audits and host regulatory inspections (e.g., FDA, EMA, SFDA).
- Review and approve batch records, validation protocols, and reports.
- Investigate deviations, OOS (Out of Specification) results, and customer complaints; implement CAPAs (Corrective and Preventive Actions).
- Perform supplier qualification and ongoing monitoring.
- Ensure all manufacturing and testing processes comply with approved procedures.
- Participate in change control management and risk assessment activities.
- Develop and deliver quality training to personnel.
- Monitor and analyze quality metrics to identify trends and areas for improvement.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality.
- Stay updated on current pharmaceutical regulations and industry best practices.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 5 years of experience in pharmaceutical Quality Assurance or Quality Control.
- In-depth knowledge of GMP, ICH guidelines, and regulatory submission processes.
- Experience with pharmaceutical manufacturing processes and analytical testing.
- Strong understanding of quality risk management principles.
- Excellent documentation, auditing, and problem-solving skills.
- Proficiency in using quality management software and MS Office.
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7
Senior AI Research Scientist - Generative Models
21052 Hoora, Capital
BHD130000 Annually
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Our client is seeking a highly skilled and motivated Senior AI Research Scientist specializing in Generative Models to join their cutting-edge research team in Jidhafs, Capital, BH . This role will involve pushing the boundaries of artificial intelligence, focusing on the development and implementation of advanced generative algorithms. The ideal candidate will have a strong theoretical foundation in machine learning, deep learning, and statistical modeling, coupled with practical experience in building and deploying complex AI systems. Responsibilities will include conducting independent research, contributing to publication in top-tier AI conferences and journals, mentoring junior researchers, and collaborating with cross-functional teams to translate research findings into tangible product features. You will be instrumental in exploring novel architectures, optimizing model performance, and ensuring the ethical and responsible deployment of AI technologies. The successful applicant will possess a PhD or equivalent research experience in Computer Science, Artificial Intelligence, Machine Learning, or a related field, with a proven track record of innovation in areas such as GANs, VAEs, diffusion models, or large language models. Essential qualifications include proficiency in Python and deep learning frameworks like TensorFlow or PyTorch, excellent problem-solving skills, and the ability to communicate complex technical concepts effectively to both technical and non-technical audiences. Experience with cloud platforms (AWS, Azure, GCP) and distributed training systems is highly desirable. This is an exceptional opportunity to work on groundbreaking AI projects in a dynamic and collaborative environment.
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8
Senior Pharmaceutical Quality Assurance Specialist
801 Bilad Al Qadeem, Capital
BHD6800 Annually
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Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist to join their Quality Unit in A'ali, Northern, BH . This vital role ensures that all manufacturing processes, products, and systems comply with stringent regulatory standards, Good Manufacturing Practices (GMP), and internal quality policies. The successful candidate will play a key role in maintaining and enhancing the company's commitment to quality and compliance. Key responsibilities include:
The ideal candidate will hold a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field; a Master's degree is preferred. A minimum of 6 years of progressive experience in Quality Assurance within the pharmaceutical industry is mandatory. Comprehensive knowledge of GMP, ICH guidelines, and regulatory submission processes is essential. Proven experience in conducting audits, managing deviations, and implementing CAPAs is required. Strong analytical, problem-solving, and critical thinking skills are crucial. Excellent written and verbal communication skills, with the ability to effectively present information to regulatory bodies and internal stakeholders, are necessary. Experience with electronic QMS and LIMS systems is highly desirable. This is an excellent opportunity to contribute to the quality and integrity of life-saving medicines.
- Developing, implementing, and maintaining the company's Quality Management System (QMS) in accordance with global regulatory requirements (e.g., FDA, EMA, local health authorities).
- Conducting internal audits and supporting external regulatory inspections, ensuring readiness and compliance.
- Reviewing and approving batch manufacturing records, validation protocols, and reports.
- Investigating deviations, out-of-specification (OOS) results, and customer complaints, determining root causes and implementing corrective and preventive actions (CAPAs).
- Participating in change control processes, assessing the impact of changes on product quality and regulatory compliance.
- Developing and delivering training programs on GMP and quality assurance principles for manufacturing and other relevant personnel.
- Monitoring and analyzing quality metrics, identifying trends, and recommending improvements to quality systems.
- Collaborating with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to ensure a unified approach to quality.
- Staying current with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
The ideal candidate will hold a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field; a Master's degree is preferred. A minimum of 6 years of progressive experience in Quality Assurance within the pharmaceutical industry is mandatory. Comprehensive knowledge of GMP, ICH guidelines, and regulatory submission processes is essential. Proven experience in conducting audits, managing deviations, and implementing CAPAs is required. Strong analytical, problem-solving, and critical thinking skills are crucial. Excellent written and verbal communication skills, with the ability to effectively present information to regulatory bodies and internal stakeholders, are necessary. Experience with electronic QMS and LIMS systems is highly desirable. This is an excellent opportunity to contribute to the quality and integrity of life-saving medicines.
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