198 Pharmaceutical Manager jobs in Bahrain
Senior Pharmaceutical Product Manager
45001 Southern, Southern
BHD115000 Annually
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Our client, a leading pharmaceutical company committed to improving global health, is seeking a highly experienced Senior Pharmaceutical Product Manager to drive the success of key therapeutic products in Nuwaidrat, Southern, BH . This strategic role demands a deep understanding of the pharmaceutical market, product lifecycle management, and go-to-market strategies. The ideal candidate will hold a Bachelor's degree in Pharmacy, Life Sciences, Business, or a related field, with a minimum of 8 years of experience in pharmaceutical marketing, product management, or a related function. You will be responsible for developing and executing comprehensive marketing plans, leading cross-functional teams, analyzing market trends, identifying opportunities for growth, and managing product positioning and messaging to healthcare professionals and patients. This is a critical position offering the opportunity to shape the future of important therapies.
Key Responsibilities:
Qualifications:
Advance your career by making a difference in healthcare.
Key Responsibilities:
- Develop and implement strategic marketing plans for assigned pharmaceutical products to achieve sales and market share objectives.
- Conduct thorough market analysis, including competitive intelligence, market sizing, and forecasting.
- Define product positioning, messaging, and value proposition for target audiences, including healthcare professionals and patient communities.
- Lead the development and execution of integrated marketing and promotional campaigns across various channels (e.g., medical conferences, digital marketing, sales force materials).
- Collaborate closely with sales, medical affairs, regulatory, market access, and R&D teams to ensure cohesive product strategy and execution.
- Manage product launch activities, from pre-launch planning through post-launch evaluation.
- Monitor and analyze product performance, sales data, and market feedback to identify areas for improvement and adaptation.
- Identify opportunities for brand growth, lifecycle management, and new indication development.
- Manage external agencies and vendors involved in marketing activities.
- Ensure all marketing activities are compliant with pharmaceutical industry regulations and company policies.
- Prepare and present strategic recommendations and business cases to senior leadership.
Qualifications:
- Bachelor's degree in Pharmacy, Life Sciences, Business Administration, Marketing, or a related field. An MBA or advanced degree is a plus.
- Minimum of 8 years of experience in the pharmaceutical industry, with a significant focus on product management, marketing, or commercial strategy.
- Proven success in developing and executing marketing plans for pharmaceutical products, ideally within specific therapeutic areas.
- Strong understanding of the pharmaceutical market, including drug development, regulatory affairs, and market access.
- Excellent analytical, strategic thinking, and problem-solving skills.
- Demonstrated ability to lead and influence cross-functional teams without direct authority.
- Exceptional communication, presentation, and interpersonal skills.
- Proficiency in market analysis and forecasting techniques.
- Experience with digital marketing strategies in the pharmaceutical sector is highly desirable.
- Commitment to ethical practices and compliance with industry standards.
Advance your career by making a difference in healthcare.
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Pharmaceutical Quality Assurance Manager
2372 Busaiteen, Muharraq
BHD110000 Annually
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Our client, a prominent pharmaceutical company, is seeking a highly experienced Pharmaceutical Quality Assurance Manager to join their team in **Busaiteen, Muharraq, BH**. This hybrid role combines essential on-site responsibilities with the flexibility of remote work. You will be instrumental in establishing and maintaining robust quality management systems, ensuring compliance with regulatory standards, and overseeing all QA activities within the manufacturing and development processes. The ideal candidate will possess a deep understanding of Good Manufacturing Practices (GMP), regulatory affairs, and quality control within the pharmaceutical industry. Your role will be critical in upholding the integrity and safety of our client's pharmaceutical products.
Key Responsibilities:
Required Qualifications:
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with international regulations (e.g., FDA, EMA, GMP).
- Oversee all Quality Assurance activities, including batch record review, release, deviation management, CAPA, and change control.
- Conduct internal audits and support external audits by regulatory agencies and customers.
- Ensure that all manufacturing processes and product development activities adhere to strict quality standards.
- Manage and train the Quality Assurance team, fostering a culture of quality and compliance.
- Review and approve validation protocols and reports for equipment, processes, and analytical methods.
- Monitor and analyze quality metrics, identify trends, and implement corrective and preventive actions (CAPA).
- Stay updated on evolving regulatory requirements and guidelines in the pharmaceutical industry.
- Collaborate with other departments, including R&D, Manufacturing, and Regulatory Affairs, to ensure seamless quality integration.
- Manage supplier quality agreements and perform supplier audits.
- Investigate customer complaints and product quality issues, implementing appropriate resolutions.
- Promote a proactive quality culture throughout the organization.
Required Qualifications:
- Master's degree or Ph.D. in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
- Proven experience in managing QMS, audits, validation, and regulatory submissions.
- Strong leadership, management, and team-building skills.
- Excellent analytical, problem-solving, and decision-making abilities.
- Exceptional attention to detail and commitment to accuracy.
- Strong written and verbal communication skills, with the ability to communicate effectively with regulatory bodies and senior management.
- Proficiency in quality management software and tools.
- Ability to work effectively in a hybrid environment.
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Pharmaceutical Quality Assurance Manager
10401 Al Hidd
BHD110000 Annually
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Our client, a leading pharmaceutical company, is looking for an experienced Pharmaceutical Quality Assurance Manager to lead their QA team. This role offers a hybrid work model, requiring a balance of in-office and remote work, allowing for focused strategic planning and team collaboration. The QA Manager will be responsible for ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy. This includes developing and implementing robust quality management systems, overseeing compliance with regulatory requirements (e.g., GMP, FDA), and managing all quality-related activities, from raw material inspection to finished product release. The ideal candidate will possess a strong background in pharmaceutical quality assurance, excellent leadership skills, and a meticulous attention to detail.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Oversee quality control processes, including testing and release of raw materials, intermediates, and finished products.
- Manage and conduct internal and external audits.
- Review and approve batch records, validation protocols, and reports.
- Investigate deviations, CAPAs (Corrective and Preventive Actions), and customer complaints.
- Lead and mentor the Quality Assurance team.
- Collaborate with R&D, manufacturing, and regulatory affairs departments.
- Contribute to the continuous improvement of quality processes and systems.
- Stay updated on regulatory changes and industry best practices.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- 7+ years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and regulatory affairs.
- Proven experience in managing QMS and conducting audits.
- Strong leadership, team management, and interpersonal skills.
- Excellent analytical, problem-solving, and decision-making abilities.
- Proficiency in quality management software and documentation practices.
- Strong communication and report-writing skills.
- Ability to balance onsite and remote work effectively.
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2
Pharmaceutical Quality Control Manager
BH-009 Tubli, Central
BHD100000 Annually
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Our client, a leading pharmaceutical company, is seeking an experienced Pharmaceutical Quality Control Manager to oversee their critical quality assurance operations. This position offers a hybrid work arrangement, combining essential on-site laboratory and facility management with remote strategic oversight. You will be responsible for developing, implementing, and maintaining the company's quality control systems and procedures, ensuring compliance with all regulatory standards (e.g., GMP, FDA). Key duties include managing laboratory testing, validating analytical methods, investigating deviations, and approving raw materials and finished products. You will lead and mentor a team of QC analysts, foster a culture of quality excellence, and collaborate with R&D, production, and regulatory affairs departments. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field, coupled with a minimum of seven years of experience in pharmaceutical quality control and assurance. A strong understanding of analytical chemistry, microbiology, and regulatory compliance is essential. Excellent leadership, problem-solving, and communication skills are required to manage the team and interface with regulatory bodies. This is a pivotal role for a quality-focused professional looking to make a significant impact in the pharmaceutical industry.
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3
Pharmaceutical Quality Assurance Manager
10052 Seef, Capital
BHD125000 Annually
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Our client, a leading biopharmaceutical innovator with a commitment to excellence in patient care, is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager. This vital role will be based in Seef, Capital, BH , and will be responsible for establishing, implementing, and maintaining the company's comprehensive Quality Management System (QMS) in accordance with international pharmaceutical standards, including cGMP, ICH guidelines, and relevant regulatory requirements. You will lead and manage a team of QA professionals, overseeing all aspects of quality assurance, including batch record review, deviation management, change control, CAPA (Corrective and Preventive Actions), internal and external audits, validation activities, and supplier qualification. The QA Manager will play a critical role in ensuring product quality, regulatory compliance, and the overall integrity of the pharmaceutical manufacturing processes. This position demands a profound understanding of pharmaceutical manufacturing, quality control principles, and regulatory affairs. The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline, with a minimum of 8-10 years of progressive experience in pharmaceutical quality assurance, including at least 3 years in a managerial or supervisory capacity. Proven experience in developing and implementing QMS, conducting internal audits, and managing regulatory inspections (e.g., FDA, EMA) is essential. Strong knowledge of aseptic processing, sterile manufacturing, and lyophilization is highly advantageous. Excellent leadership, team management, analytical, and problem-solving skills are required, along with outstanding communication and interpersonal abilities. You must be adept at building relationships with cross-functional teams, including manufacturing, R&D, regulatory affairs, and quality control, to foster a culture of quality throughout the organization. A proactive approach to identifying and mitigating quality risks, and a commitment to continuous improvement, are key attributes for success in this role.
Responsibilities:
Qualifications:
Responsibilities:
- Develop and maintain the company's Quality Management System (QMS).
- Oversee batch record review and release processes.
- Manage deviations, CAPA, and change control systems.
- Conduct internal audits and host regulatory inspections.
- Qualify and monitor third-party suppliers and contract manufacturers.
- Ensure compliance with cGMP, ICH, and other regulatory standards.
- Lead and mentor the QA team.
- Review and approve validation protocols and reports.
- Manage product quality complaints and investigations.
- Contribute to continuous improvement initiatives.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, or related science.
- Minimum of 8 years in pharmaceutical QA, with 3+ years in management.
- Extensive knowledge of cGMP, ICH guidelines, and pharmaceutical regulations.
- Proven experience with QMS implementation and maintenance.
- Experience in conducting audits and managing regulatory inspections.
- Strong understanding of pharmaceutical manufacturing processes.
- Excellent leadership, communication, and analytical skills.
- Ability to effectively manage cross-functional teams.
- Detail-oriented with strong problem-solving capabilities.
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4
Pharmaceutical Quality Control Manager
107 Seef, Capital
BHD90000 Annually
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Our client, a leading pharmaceutical company, is looking for a highly qualified Pharmaceutical Quality Control Manager to oversee quality assurance and control processes at their facility in **Seef, Capital, BH**. This role is critical for ensuring that all pharmaceutical products meet stringent regulatory standards and company quality objectives. The ideal candidate will have extensive experience in pharmaceutical quality systems, regulatory compliance, and laboratory management.
Responsibilities:
Qualifications:
This is a key leadership position for a dedicated professional looking to contribute to the advancement of healthcare through high-quality pharmaceutical products in **Seef, Capital, BH**.
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with cGMP and other relevant regulatory guidelines.
- Oversee all aspects of quality control, including raw material testing, in-process testing, and finished product release.
- Manage the QC laboratory operations, including equipment calibration, maintenance, and validation.
- Develop and validate analytical methods for testing pharmaceutical products.
- Review and approve batch records, analytical data, and quality control reports.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Ensure compliance with national and international pharmaceutical regulations (e.g., FDA, EMA).
- Conduct internal audits and participate in external audits by regulatory agencies and customers.
- Manage and train QC laboratory personnel, fostering a culture of quality and compliance.
- Stay updated with the latest advancements in pharmaceutical quality control and regulatory requirements.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality throughout the lifecycle.
- Prepare and manage the QC budget.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
- Minimum of 8 years of experience in pharmaceutical quality control and assurance.
- Proven experience in managing a QC laboratory and a team of scientists.
- In-depth knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and ICH guidelines.
- Experience with analytical techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
- Strong understanding of regulatory requirements and audit processes.
- Excellent analytical, problem-solving, and decision-making skills.
- Exceptional leadership, communication, and interpersonal skills.
- Proficiency in LIMS and other quality management software.
- Ability to interpret and apply complex regulatory documentation.
This is a key leadership position for a dedicated professional looking to contribute to the advancement of healthcare through high-quality pharmaceutical products in **Seef, Capital, BH**.
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5
Pharmaceutical Quality Assurance Manager
2000 Al Hidd
BHD90000 Annually
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Our client, a reputable pharmaceutical company dedicated to producing high-quality medicines, is seeking an experienced and meticulous Pharmaceutical Quality Assurance Manager to lead their QA department in Budaiya, Northern, BH . This critical role will ensure that all pharmaceutical products meet stringent regulatory standards and company quality objectives. The QA Manager will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS) in accordance with cGMP, GDP, and other relevant international guidelines. You will oversee quality control operations, manage batch record reviews and product release processes, and conduct internal audits and supplier audits. Key responsibilities include investigating deviations and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPAs), and managing change control processes. You will also be responsible for training QA personnel and ensuring overall compliance with regulatory requirements, including submissions to health authorities. The role involves close collaboration with production, R&D, and regulatory affairs departments.
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline. A minimum of 8 years of progressive experience in Quality Assurance or Quality Control within the pharmaceutical industry is required. Thorough knowledge of cGMP regulations, ICH guidelines, and other relevant pharmaceutical quality standards is essential. Demonstrated experience in implementing and managing a QMS, conducting audits, and managing investigations is mandatory. Strong leadership, decision-making, and problem-solving skills are crucial for effectively managing the QA function. Excellent written and verbal communication skills, with the ability to interact effectively with regulatory agencies and internal stakeholders, are vital. This is an outstanding opportunity to take on a leadership role in a growing pharmaceutical organization and contribute to the delivery of safe and effective medications.
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline. A minimum of 8 years of progressive experience in Quality Assurance or Quality Control within the pharmaceutical industry is required. Thorough knowledge of cGMP regulations, ICH guidelines, and other relevant pharmaceutical quality standards is essential. Demonstrated experience in implementing and managing a QMS, conducting audits, and managing investigations is mandatory. Strong leadership, decision-making, and problem-solving skills are crucial for effectively managing the QA function. Excellent written and verbal communication skills, with the ability to interact effectively with regulatory agencies and internal stakeholders, are vital. This is an outstanding opportunity to take on a leadership role in a growing pharmaceutical organization and contribute to the delivery of safe and effective medications.
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6
Pharmaceutical Quality Assurance Manager
22737 Zallaq, Southern
BHD80000 Annually
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Our client, a leading pharmaceutical company, is looking for an experienced Pharmaceutical Quality Assurance Manager to oversee and maintain the highest standards of quality across all operations in Zallaq, Southern, BH . This role is critical for ensuring compliance with regulatory requirements and maintaining product integrity. The ideal candidate will possess a strong understanding of GMP, regulatory affairs, and quality management systems within the pharmaceutical industry.
Responsibilities:
Qualifications:
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines (e.g., FDA, EMA).
- Oversee quality control processes and product release procedures.
- Conduct internal audits and support external audits by regulatory agencies and customers.
- Manage deviation investigations, CAPA (Corrective and Preventive Actions), and change control processes.
- Review and approve batch records, validation protocols, and reports.
- Develop and deliver quality training programs for relevant personnel.
- Monitor and analyze quality metrics and key performance indicators (KPIs).
- Manage and mentor the Quality Assurance team.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality throughout the lifecycle.
- Stay up-to-date with evolving regulatory landscapes and industry best practices.
- Lead efforts for continuous improvement in quality processes.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 6 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and pharmaceutical regulatory requirements.
- Proven experience in implementing and managing QMS, audits, and regulatory submissions.
- Strong leadership, analytical, and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects and prioritize effectively.
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7
Pharmaceutical Quality Control Manager
20110 Seef, Capital
BHD120000 Annually
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Our client, a leading pharmaceutical company, is seeking a highly qualified Pharmaceutical Quality Control Manager to oversee their operations in **Seef, Capital, BH**. This senior management role is responsible for ensuring that all manufactured pharmaceutical products meet stringent quality standards and comply with regulatory requirements, including GMP (Good Manufacturing Practices). You will lead and manage the Quality Control department, including laboratory personnel, analytical testing, and documentation. Key responsibilities include developing and implementing quality control strategies, validating analytical methods, and overseeing the testing of raw materials, in-process samples, and finished products. You will also be responsible for maintaining the laboratory's compliance with regulatory standards, managing deviations and investigations, and contributing to the continuous improvement of quality systems. Collaboration with R&D, Production, and Regulatory Affairs departments is crucial for seamless operations. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field, with significant experience (minimum 7 years) in pharmaceutical quality control and at least 3 years in a management or supervisory role. Thorough knowledge of pharmacopoeial standards (e.g., USP, EP, BP) and regulatory guidelines (e.g., FDA, EMA) is essential. Excellent leadership, analytical, problem-solving, and communication skills are required. This is a critical role for individuals passionate about ensuring the safety and efficacy of pharmaceutical products in **Seef, Capital, BH**. We are looking for a detail-oriented and results-driven professional committed to upholding the highest standards of quality in the pharmaceutical industry. Join our client and contribute to making a difference in healthcare.
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8
Pharmaceutical Quality Assurance Manager
131 Muharraq, Muharraq
BHD95000 Annually
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Our client is seeking a highly competent and experienced Pharmaceutical Quality Assurance Manager to oversee quality systems in Muharraq, Muharraq, BH . This leadership role is critical for ensuring that all pharmaceutical products meet rigorous quality standards and regulatory compliance requirements. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS). This includes overseeing all aspects of quality assurance, such as batch record review, deviation management, CAPA implementation, internal audits, and change control. The ideal candidate will possess a deep understanding of cGMP (current Good Manufacturing Practices), regulatory guidelines (FDA, EMA, etc.), and quality risk management principles. You will lead and mentor a team of QA professionals, fostering a strong quality culture throughout the organization. Key responsibilities include collaborating with manufacturing, R&D, and regulatory affairs departments to ensure seamless quality integration. You will also manage external audits and inspections, ensuring the company's readiness. This position demands exceptional analytical, problem-solving, and leadership skills, along with outstanding communication abilities. A commitment to continuous improvement and maintaining the highest standards of product quality is essential.
Responsibilities:
Qualifications:
Responsibilities:
- Develop, implement, and maintain the Pharmaceutical Quality Management System (QMS).
- Oversee batch record review and release processes.
- Manage deviation investigations, root cause analysis, and corrective/preventive action (CAPA) plans.
- Conduct internal audits and support external regulatory inspections and client audits.
- Manage the change control process to ensure product integrity.
- Ensure compliance with cGMP, ICH guidelines, and other relevant regulations.
- Lead and develop the Quality Assurance team, providing guidance and training.
- Collaborate with cross-functional departments to resolve quality issues.
- Monitor and report on key quality metrics and trends.
- Participate in product lifecycle management from a quality perspective.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Master's degree or equivalent experience is preferred.
- Minimum of 7 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of cGMP, ISO standards, and regulatory requirements.
- Proven experience in managing QMS, audits, and regulatory inspections.
- Strong leadership, team management, and decision-making skills.
- Excellent analytical, problem-solving, and critical thinking abilities.
- Proficiency in quality management software.
- Outstanding written and verbal communication skills.
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