49 Pharmaceutical Manager jobs in Bahrain
Pharmaceutical Regulatory Affairs Manager
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Pharmaceutical Quality Assurance Manager
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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.
Pharmaceutical Quality Assurance Manager
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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.
Pharmaceutical Quality Assurance Manager
Posted 1 day ago
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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.
Pharmaceutical Quality Assurance Manager
Posted 5 days ago
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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.
Pharmaceutical Quality Control Manager
Posted 5 days ago
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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.
Pharmaceutical Quality Control Manager
Posted 5 days ago
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Clinical Trial Manager (Pharmaceutical)
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Pharmaceutical Quality Assurance Manager
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Senior Pharmaceutical Quality Assurance Manager
Posted today
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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.