49 Pharmaceutical Manager jobs in Bahrain
Pharmaceutical Regulatory Affairs Manager
123 Riffa, Southern
BHD4800 month
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Our client, a leading pharmaceutical company, is seeking a highly qualified and experienced Pharmaceutical Regulatory Affairs Manager to oversee regulatory compliance and submissions for their product portfolio in Riffa, Southern, BH . This critical role ensures that all products meet the stringent requirements of local and international health authorities. The ideal candidate will possess a deep understanding of pharmaceutical regulations, excellent analytical skills, and a meticulous approach to documentation and compliance. Key responsibilities include developing and implementing regulatory strategies, preparing and submitting regulatory dossiers (e.g., CTD, ANDA, NDA) to health authorities, and managing post-approval regulatory activities. You will also stay abreast of evolving regulatory landscapes, provide regulatory guidance to internal teams (R&D, manufacturing, marketing), and liaise with regulatory agencies. Experience in managing regulatory affairs for generic and/or innovator pharmaceuticals is essential. A proven track record in successfully navigating regulatory approval processes is required. A minimum of 6 years of experience in pharmaceutical regulatory affairs is mandatory. A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field is required; a Master's or PhD is advantageous. Fluency in English and excellent written and verbal communication skills are essential. Familiarity with GMP, GLP, and GCP is also important. This role offers a significant opportunity to contribute to bringing vital pharmaceutical products to market in compliance with all necessary regulations.
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Pharmaceutical Quality Assurance Manager
121 Seef, Capital
BHD4000 Annually
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Our client, a leading pharmaceutical company located in Seef, Capital, BH , is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager. This critical role will oversee all quality assurance activities, ensuring compliance with regulatory standards, GMP (Good Manufacturing Practices), and internal quality policies. The QA Manager will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), conducting internal audits, and managing external audits. You will lead a team of QA professionals, providing guidance and support to ensure product quality and safety. The ideal candidate possesses a strong background in the pharmaceutical industry, a deep understanding of quality control principles, and exceptional leadership abilities. This position offers a challenging and rewarding opportunity to contribute to the development and delivery of high-quality pharmaceutical products. If you are passionate about ensuring excellence in pharmaceutical manufacturing and possess the required expertise, we encourage you to apply.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS).
- Ensure compliance with relevant pharmaceutical regulations (e.g., GMP, GDP).
- Conduct internal audits and manage external regulatory inspections.
- Oversee batch record review and product release processes.
- Investigate deviations, OOS (Out of Specification) results, and customer complaints.
- Manage change control procedures and risk assessments.
- Train and mentor QA staff.
- Participate in validation activities for equipment, processes, and analytical methods.
- Review and approve quality-related documents, including SOPs and validation protocols.
- Collaborate with R&D, manufacturing, and regulatory affairs departments.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Proven experience as a Quality Assurance Manager in the pharmaceutical industry.
- Extensive knowledge of GMP, GDP, and other relevant regulatory guidelines.
- Strong leadership, team management, and communication skills.
- Experience with audit procedures and QMS implementation.
- Excellent analytical and problem-solving abilities.
- Proficiency in regulatory compliance and quality systems.
- Detail-oriented with a commitment to accuracy and quality.
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1
Pharmaceutical Quality Assurance Manager
108 Al Hajar
BHD110000 Annually
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Our client, a leading pharmaceutical manufacturer, is seeking a highly qualified and experienced Pharmaceutical Quality Assurance Manager to lead their Quality Assurance department. This strategic role, situated in A'ali, Northern, BH , will be responsible for establishing, implementing, and maintaining the company's Quality Management System (QMS) to ensure compliance with all relevant regulatory standards, including GMP, ISO, and other applicable guidelines. The QA Manager will play a critical role in safeguarding product quality and patient safety.
Key responsibilities include developing and overseeing quality assurance programs, policies, and procedures. You will manage the internal and external audit programs, ensuring that suppliers and contract manufacturers meet quality standards. The QA Manager will lead the review and approval of batch records, validation protocols, and other critical quality documentation. You will also be responsible for investigating deviations, out-of-specification (OOS) results, and customer complaints, implementing effective corrective and preventive actions (CAPAs). This role involves managing change control processes and ensuring that all changes to processes, equipment, and materials are properly assessed for their impact on product quality.
The Pharmaceutical QA Manager will supervise and mentor the QA team, providing guidance and fostering a culture of quality excellence. You will represent the company during regulatory inspections and audits by health authorities. Collaborating with R&D, manufacturing, and regulatory affairs departments to ensure seamless integration of quality principles throughout the product lifecycle is crucial. Staying current with evolving regulatory requirements and industry best practices is a continuous requirement of this position. Driving continuous improvement initiatives within the QMS to enhance overall product quality and operational efficiency is a key objective.
Candidates must possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Master's degree or equivalent advanced degree is highly preferred. A minimum of 8-10 years of progressive experience in pharmaceutical quality assurance and quality control, with at least 3-5 years in a management or supervisory role, is required. Extensive knowledge of Good Manufacturing Practices (GMP), quality risk management (QRM), and regulatory submission processes is essential. Proven experience in managing audits, deviations, CAPAs, and change control is mandatory. Excellent leadership, analytical, problem-solving, and communication skills are necessary. The ability to effectively lead and motivate a team, coupled with strong interpersonal skills, is critical.
Key responsibilities include developing and overseeing quality assurance programs, policies, and procedures. You will manage the internal and external audit programs, ensuring that suppliers and contract manufacturers meet quality standards. The QA Manager will lead the review and approval of batch records, validation protocols, and other critical quality documentation. You will also be responsible for investigating deviations, out-of-specification (OOS) results, and customer complaints, implementing effective corrective and preventive actions (CAPAs). This role involves managing change control processes and ensuring that all changes to processes, equipment, and materials are properly assessed for their impact on product quality.
The Pharmaceutical QA Manager will supervise and mentor the QA team, providing guidance and fostering a culture of quality excellence. You will represent the company during regulatory inspections and audits by health authorities. Collaborating with R&D, manufacturing, and regulatory affairs departments to ensure seamless integration of quality principles throughout the product lifecycle is crucial. Staying current with evolving regulatory requirements and industry best practices is a continuous requirement of this position. Driving continuous improvement initiatives within the QMS to enhance overall product quality and operational efficiency is a key objective.
Candidates must possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Master's degree or equivalent advanced degree is highly preferred. A minimum of 8-10 years of progressive experience in pharmaceutical quality assurance and quality control, with at least 3-5 years in a management or supervisory role, is required. Extensive knowledge of Good Manufacturing Practices (GMP), quality risk management (QRM), and regulatory submission processes is essential. Proven experience in managing audits, deviations, CAPAs, and change control is mandatory. Excellent leadership, analytical, problem-solving, and communication skills are necessary. The ability to effectively lead and motivate a team, coupled with strong interpersonal skills, is critical.
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2
Pharmaceutical Quality Assurance Manager
4001 Muharraq, Muharraq
BHD7500 Annually
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Our client, a prominent pharmaceutical company, is actively seeking an experienced and meticulous Pharmaceutical Quality Assurance Manager to oversee quality control and compliance in their **Muharraq, Muharraq, BH** facility. This critical role ensures adherence to international quality standards and regulatory requirements throughout the pharmaceutical product lifecycle, from development to manufacturing and distribution.
Key Responsibilities:
This is an exceptional opportunity to take on a leadership role in ensuring the highest standards of quality within the pharmaceutical sector and contribute to the company's reputation for excellence.
Key Responsibilities:
- Developing, implementing, and maintaining robust Quality Management Systems (QMS) in line with GMP, GDP, and other relevant pharmaceutical guidelines.
- Overseeing all quality assurance activities, including batch record review, deviation management, CAPA implementation, and change control processes.
- Conducting internal audits and participating in external audits by regulatory authorities and customers.
- Ensuring compliance with regulatory requirements, including pharmacopoeial standards and local health authority regulations.
- Managing and mentoring a team of Quality Assurance professionals.
- Approving or rejecting raw materials, intermediate products, and finished products based on quality standards.
- Developing and delivering quality-related training programs to employees.
- Investigating product quality complaints and implementing corrective and preventive actions.
- Monitoring and analyzing quality metrics to identify trends and areas for continuous improvement.
Qualifications:- A Bachelor's or Master's degree in Pharmacy, Chemistry, Life Sciences, or a related field.
- A minimum of 8 years of progressive experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, GDP, and other relevant pharmaceutical quality standards and regulations.
- Proven experience in managing QMS, conducting audits, and handling regulatory inspections.
- Strong analytical, problem-solving, and decision-making skills.
- Excellent leadership, communication, and interpersonal skills.
- Proficiency in quality control laboratory techniques and equipment.
- Experience with electronic quality management systems (eQMS) is preferred.
- Ability to work effectively under pressure and manage multiple priorities.
This is an exceptional opportunity to take on a leadership role in ensuring the highest standards of quality within the pharmaceutical sector and contribute to the company's reputation for excellence.
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3
Pharmaceutical Quality Assurance Manager
60606 Al Malikiyah, Northern
BHD110000 Annually
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Our client, a reputable pharmaceutical company, is seeking a highly qualified and meticulous Pharmaceutical Quality Assurance Manager to join their esteemed team in Salmabad, Northern, BH . This critical role will oversee all aspects of the company's Quality Management System (QMS) to ensure compliance with regulatory requirements and adherence to the highest industry standards for drug manufacturing and product quality.
The QA Manager will be responsible for developing, implementing, and maintaining robust quality assurance procedures and protocols. Key responsibilities include conducting internal audits, managing external audits by regulatory agencies (e.g., FDA, EMA), reviewing and approving batch records, investigating deviations and out-of-specification (OOS) results, and implementing corrective and preventive actions (CAPA). You will also manage the change control process, oversee validation activities, and ensure that all pharmaceutical products meet the required quality and safety specifications. The ideal candidate will lead and mentor the QA team, fostering a strong quality culture throughout the organization.
We are looking for an individual with a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline. A minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry is mandatory, with at least 3 years in a management or supervisory role. In-depth knowledge of cGMP (current Good Manufacturing Practices), ICH guidelines, and pharmaceutical regulatory affairs is essential. Strong analytical, problem-solving, and decision-making skills, coupled with excellent leadership and communication abilities, are required. Join our dedicated team in Salmabad, Northern, BH and play a crucial role in ensuring the quality and safety of life-saving medicines.
The QA Manager will be responsible for developing, implementing, and maintaining robust quality assurance procedures and protocols. Key responsibilities include conducting internal audits, managing external audits by regulatory agencies (e.g., FDA, EMA), reviewing and approving batch records, investigating deviations and out-of-specification (OOS) results, and implementing corrective and preventive actions (CAPA). You will also manage the change control process, oversee validation activities, and ensure that all pharmaceutical products meet the required quality and safety specifications. The ideal candidate will lead and mentor the QA team, fostering a strong quality culture throughout the organization.
We are looking for an individual with a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline. A minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry is mandatory, with at least 3 years in a management or supervisory role. In-depth knowledge of cGMP (current Good Manufacturing Practices), ICH guidelines, and pharmaceutical regulatory affairs is essential. Strong analytical, problem-solving, and decision-making skills, coupled with excellent leadership and communication abilities, are required. Join our dedicated team in Salmabad, Northern, BH and play a crucial role in ensuring the quality and safety of life-saving medicines.
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4
Pharmaceutical Quality Control Manager
400 Tubli, Central
BHD110000 Annually
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Our client, a rapidly expanding pharmaceutical company, is searching for a dedicated and detail-oriented Pharmaceutical Quality Control Manager to oversee operations in Nuwaidrat, Southern, BH . This pivotal role ensures that all manufactured pharmaceutical products meet the highest standards of quality, safety, and efficacy. You will be responsible for developing, implementing, and maintaining robust quality control systems and procedures throughout the entire production lifecycle.
The primary duties include supervising a team of QC analysts, managing laboratory operations, and ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements. You will conduct regular audits, investigate deviations and out-of-specification results, and implement corrective and preventive actions (CAPA). This position requires a strong understanding of analytical testing methods, stability studies, and validation protocols for raw materials, in-process samples, and finished products.
We require a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific discipline, with at least 8 years of progressive experience in pharmaceutical quality control, including a minimum of 3 years in a supervisory or managerial capacity. Demonstrated experience with regulatory inspections and a thorough knowledge of international pharmaceutical regulations (e.g., FDA, EMA) are essential. Strong leadership abilities, excellent analytical and problem-solving skills, and outstanding communication capabilities are necessary to succeed in this role. The successful candidate will be instrumental in upholding our commitment to pharmaceutical excellence and patient safety.
The primary duties include supervising a team of QC analysts, managing laboratory operations, and ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements. You will conduct regular audits, investigate deviations and out-of-specification results, and implement corrective and preventive actions (CAPA). This position requires a strong understanding of analytical testing methods, stability studies, and validation protocols for raw materials, in-process samples, and finished products.
We require a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific discipline, with at least 8 years of progressive experience in pharmaceutical quality control, including a minimum of 3 years in a supervisory or managerial capacity. Demonstrated experience with regulatory inspections and a thorough knowledge of international pharmaceutical regulations (e.g., FDA, EMA) are essential. Strong leadership abilities, excellent analytical and problem-solving skills, and outstanding communication capabilities are necessary to succeed in this role. The successful candidate will be instrumental in upholding our commitment to pharmaceutical excellence and patient safety.
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5
Pharmaceutical Quality Control Manager
241 Al Hidd
BHD95000 Annually
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Our client, a leading pharmaceutical manufacturer, is seeking a meticulous and experienced Pharmaceutical Quality Control Manager for their state-of-the-art facility in Sitra, Capital, BH . This crucial role ensures that all manufactured pharmaceutical products meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory guidelines. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, complemented by at least 5-7 years of progressive experience in pharmaceutical quality control and quality assurance. You will be responsible for overseeing the daily operations of the QC laboratory, managing a team of QC analysts, and implementing robust quality control procedures and systems. Key responsibilities include developing and validating analytical methods, performing stability testing, and ensuring the accurate and timely release of raw materials, in-process samples, and finished products. Experience with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory affairs (e.g., FDA, EMA) is essential. The successful candidate will demonstrate exceptional attention to detail, strong analytical and problem-solving skills, and excellent leadership and communication abilities. You will be instrumental in ensuring compliance with all relevant pharmacopoeial standards and regulatory requirements. The ability to manage budgets, optimize laboratory workflows, and drive continuous improvement in quality processes is critical. This is an exciting opportunity to play a vital role in ensuring patient safety and product integrity within a reputable organization. You will be responsible for maintaining laboratory equipment, managing quality documentation, and conducting internal audits. The candidate must be adept at risk assessment and possess a thorough understanding of pharmaceutical manufacturing processes. A proactive approach to identifying and resolving quality issues is essential. This role offers significant responsibility and the chance to make a tangible impact on public health.
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6
Clinical Trial Manager (Pharmaceutical)
10710 Busaiteen, Muharraq
BHD110000 Annually
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Our client is recruiting for a dedicated and experienced Clinical Trial Manager to oversee the execution of pharmaceutical clinical trials in **Busaiteen, Muharraq, BH**. This critical role involves managing all aspects of clinical trial conduct, from initiation to close-out, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The successful candidate will be responsible for site selection and initiation, monitoring trial progress, data collection and management, and ensuring patient safety. You will liaise with investigators, study coordinators, pharmaceutical sponsors, and regulatory authorities. A strong understanding of clinical trial phases, study design, and medical terminology is essential. The ideal candidate will possess excellent project management skills, including budget management, timeline adherence, and risk assessment. A bachelor's degree in a life science or healthcare-related field is required, along with significant experience in clinical research management. Master's degree or relevant certifications (e.g., CCRP, CCRA) are highly desirable. Strong communication, leadership, and problem-solving abilities are crucial. This position offers the chance to be part of groundbreaking research aimed at improving patient outcomes and advancing medical treatments. We are committed to providing a supportive and growth-oriented work environment for our team members.
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7
Pharmaceutical Quality Assurance Manager
101, BH Riffa, Southern
BHD110000 Annually
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Our client, a rapidly growing pharmaceutical company based in Riffa, Southern, BH , is seeking a seasoned Pharmaceutical Quality Assurance Manager to lead their Quality Assurance department. This critical role will ensure that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. The successful candidate will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), including GMP (Good Manufacturing Practices), GCP (Good Clinical Practices), and GLP (Good Laboratory Practices) compliance. Key responsibilities include overseeing quality control processes, conducting internal and external audits, managing deviations and CAPAs (Corrective and Preventive Actions), and ensuring regulatory compliance with health authorities such as the FDA and EMA. You will also be involved in batch record review, validation activities, and risk management. This position requires a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, with a minimum of 8 years of experience in pharmaceutical quality assurance or quality control, including at least 3 years in a management role. Extensive knowledge of pharmaceutical manufacturing processes, regulatory guidelines, and quality systems is essential. Excellent analytical, problem-solving, and decision-making skills are required. Strong leadership and communication abilities are crucial for managing the QA team and collaborating with other departments. A proven track record of successful regulatory inspections is highly desirable. This is an excellent opportunity to join a dynamic pharmaceutical organization and play a key role in ensuring the safety and efficacy of life-saving medicines.
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8
Senior Pharmaceutical Quality Assurance Manager
90030 Amwaj Islands
BHD7500 Annually
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Our client, a leading pharmaceutical company dedicated to advancing healthcare solutions, is seeking an accomplished Senior Pharmaceutical Quality Assurance Manager for their state-of-the-art facility in **Isa Town, Southern, BH**. This crucial role will be responsible for overseeing and implementing the company's Quality Management System (QMS), ensuring compliance with global regulatory standards (e.g., GMP, GDP), and driving continuous improvement in all quality-related processes.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and maintain a robust Quality Management System (QMS) in compliance with cGMP, GDP, and other relevant regulatory standards.
- Oversee all quality assurance activities, including batch record review, product release, deviation management, CAPA implementation, and change control.
- Lead and manage the QA team, providing guidance, training, and performance evaluations.
- Conduct internal audits and host regulatory agency inspections (e.g., FDA, EMA) and customer audits.
- Review and approve validation protocols and reports for equipment, processes, and analytical methods.
- Ensure that all manufacturing and laboratory operations comply with established quality standards and procedures.
- Manage the qualification and supplier quality assurance program.
- Investigate product complaints and deviations, implementing corrective and preventive actions.
- Stay current with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
- Prepare and present quality metrics and reports to senior management.
- Promote a strong quality culture throughout the organization.
- Manage the document control system and ensure compliance with archival requirements.
- Master's degree or Ph.D. in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 10 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- Demonstrated experience in managing and implementing pharmaceutical QMS.
- In-depth knowledge of GMP, GDP, ICH guidelines, and other relevant regulatory frameworks.
- Proven experience in successfully managing regulatory inspections and audits.
- Strong leadership, team management, and interpersonal skills.
- Excellent analytical, problem-solving, and decision-making abilities.
- Exceptional written and verbal communication skills, with the ability to communicate effectively with regulatory bodies and senior management.
- Proficiency in pharmaceutical quality systems and software.
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