54 Pharmaceutical Manager jobs in Vietnam
Pharmaceutical Quality Assurance Manager
080000 Bien Hoa, Dong Nai
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and experienced Pharmaceutical Quality Assurance Manager to oversee quality systems and ensure compliance with regulatory standards at our **Bien Hoa, Dong Nai, VN** facility. This role involves a hybrid work arrangement, allowing for a balance between on-site quality oversight and remote strategic planning. You will be responsible for developing, implementing, and maintaining the company's quality assurance program, including GMP, GDP, and other relevant regulatory guidelines. The ideal candidate will possess extensive experience in the pharmaceutical industry with a deep understanding of quality control processes, regulatory affairs, and validation. Key responsibilities include conducting internal audits, managing deviations and CAPAs, overseeing change control processes, and ensuring product quality throughout the manufacturing lifecycle. You will also lead and mentor the QA team, foster a culture of quality excellence, and collaborate with other departments, including R&D, production, and regulatory affairs. Strong analytical, problem-solving, and leadership skills are essential. Experience with pharmaceutical manufacturing processes and a thorough knowledge of relevant regulatory bodies are required. This is a critical role that ensures the safety and efficacy of our pharmaceutical products manufactured in **Bien Hoa, Dong Nai, VN**.
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0
Pharmaceutical Quality Assurance Manager
530000 Thuy Van
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager to oversee all quality-related operations at their **Hue, Thua Thien–Hue** facility. This critical role ensures that all products meet stringent regulatory standards and company quality policies throughout the manufacturing lifecycle. The Quality Assurance Manager will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations. Key duties include managing QA personnel, conducting internal and external audits, overseeing documentation control, handling deviations and CAPAs, and participating in regulatory inspections. The ideal candidate will possess a strong background in pharmaceutical quality assurance, excellent leadership skills, and a thorough understanding of regulatory requirements. You must be adept at problem-solving, possess strong analytical skills, and have excellent communication and interpersonal abilities to foster a culture of quality throughout the organization. This is a key leadership position offering the opportunity to make a significant impact on product safety and efficacy.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS).
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant pharmaceutical regulations.
- Manage and mentor the Quality Assurance team.
- Conduct internal audits and support external regulatory inspections.
- Oversee documentation control, batch record review, and release processes.
- Manage deviation investigations, root cause analysis, and Corrective and Preventive Actions (CAPA).
- Review and approve validation protocols and reports.
- Monitor and analyze quality metrics to identify trends and areas for improvement.
- Collaborate with other departments to ensure product quality and compliance.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
- Proven experience in managing QMS and ensuring GMP compliance.
- In-depth knowledge of regulatory requirements (e.g., FDA, EMA, local health authorities).
- Experience with audits, deviation management, and CAPA systems.
- Strong leadership, management, and team-building skills.
- Excellent analytical, problem-solving, and decision-making abilities.
- Outstanding written and verbal communication skills.
- Attention to detail and a commitment to quality.
This advertiser has chosen not to accept applicants from your region.
1
Pharmaceutical Quality Assurance Manager
51000 Hoa Sơn
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client is seeking an experienced Pharmaceutical Quality Assurance Manager to lead their QA operations in **Da Nang, Da Nang, VN**. This pivotal role ensures that all pharmaceutical products manufactured and distributed meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory guidelines such as GMP (Good Manufacturing Practices). The QA Manager will be responsible for developing, implementing, and maintaining the company's quality management system, overseeing all QA activities, and ensuring regulatory compliance.
Key responsibilities include conducting internal audits, reviewing batch records, managing deviations and CAPAs (Corrective and Preventive Actions), and overseeing validation processes. You will also be responsible for training personnel on quality standards and procedures, managing vendor quality agreements, and acting as a key point of contact for regulatory inspections and audits. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline, with a minimum of 7 years of experience in quality assurance within the pharmaceutical industry. Demonstrated knowledge of GMP, ICH guidelines, and regulatory submission processes is essential. Strong leadership, analytical, and problem-solving skills are required, along with excellent communication and interpersonal abilities.
This is an office-based position located in **Da Nang, Da Nang, VN**, requiring the candidate to be on-site to effectively manage operations and interact with manufacturing and laboratory teams. We are looking for a detail-oriented, highly organized, and proactive professional with a commitment to upholding the highest quality standards. If you are a seasoned QA professional passionate about ensuring product integrity and compliance in the pharmaceutical sector, we encourage you to apply.
Key responsibilities include conducting internal audits, reviewing batch records, managing deviations and CAPAs (Corrective and Preventive Actions), and overseeing validation processes. You will also be responsible for training personnel on quality standards and procedures, managing vendor quality agreements, and acting as a key point of contact for regulatory inspections and audits. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline, with a minimum of 7 years of experience in quality assurance within the pharmaceutical industry. Demonstrated knowledge of GMP, ICH guidelines, and regulatory submission processes is essential. Strong leadership, analytical, and problem-solving skills are required, along with excellent communication and interpersonal abilities.
This is an office-based position located in **Da Nang, Da Nang, VN**, requiring the candidate to be on-site to effectively manage operations and interact with manufacturing and laboratory teams. We are looking for a detail-oriented, highly organized, and proactive professional with a commitment to upholding the highest quality standards. If you are a seasoned QA professional passionate about ensuring product integrity and compliance in the pharmaceutical sector, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
2
Sr. Product Manager Pharmaceutical
Ho Chi Minh City
NavigosSearch
Posted today
Job Viewed
Job Description
**What We Can Offer**:
Responsible for directing sale team & MKT team
Develop and communicate vision and expectation levels to unit members, tasked to empower, select, coach and retain qualified staff that contributes to unit and company goals
Building up sale organization and evaluating sale performance and promoting them to meet their ambition and company objectives
Managing recruiting, objectives setting, coaching and performance monitoring of sales team
Ensure compliance with current healthcare regulations, medical laws and ethics
Build up tender’s quota, hospital service, find out project in university.
Build product to all channel such as hospital, clinic, Modern trade
Build up marketing strategy and guide marketing team to follow
Keep track of equipment and devices and manage inventory
Liaise with vendors regarding equipment and supplies
Coordinating with other managers and directors, you report and integrate policies and objectives.
Building up sale strategy
Building up & Implementing sale plan in order to achieve revenues of business
Present sales, revenue and expenses reports and realistic forecasts to the management team
Working with suppliers to build brand awareness and develop business, to identify new market in order to launch new products for business development
**Job Requirements**:
Bachelor degree in related major
Experienced in Marketing or business management related.
Experience and have thorough knowledge of Pharmaceutical market or medical devices market, and good understanding on product positioning, key benefits, and targeting customer.
Competencies: Be creative, a good motivator, ability to work independently & multi-task.
Good at leadership skills
Working time: Monday - Saturday morning
**Job Locations**:
- Ho Chi Minh
Responsible for directing sale team & MKT team
Develop and communicate vision and expectation levels to unit members, tasked to empower, select, coach and retain qualified staff that contributes to unit and company goals
Building up sale organization and evaluating sale performance and promoting them to meet their ambition and company objectives
Managing recruiting, objectives setting, coaching and performance monitoring of sales team
Ensure compliance with current healthcare regulations, medical laws and ethics
Build up tender’s quota, hospital service, find out project in university.
Build product to all channel such as hospital, clinic, Modern trade
Build up marketing strategy and guide marketing team to follow
Keep track of equipment and devices and manage inventory
Liaise with vendors regarding equipment and supplies
Coordinating with other managers and directors, you report and integrate policies and objectives.
Building up sale strategy
Building up & Implementing sale plan in order to achieve revenues of business
Present sales, revenue and expenses reports and realistic forecasts to the management team
Working with suppliers to build brand awareness and develop business, to identify new market in order to launch new products for business development
**Job Requirements**:
Bachelor degree in related major
Experienced in Marketing or business management related.
Experience and have thorough knowledge of Pharmaceutical market or medical devices market, and good understanding on product positioning, key benefits, and targeting customer.
Competencies: Be creative, a good motivator, ability to work independently & multi-task.
Good at leadership skills
Working time: Monday - Saturday morning
**Job Locations**:
- Ho Chi Minh
This advertiser has chosen not to accept applicants from your region.
3
Senior Pharmaceutical Quality Assurance Manager
81000 Bien Hoa, Dong Nai
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company committed to advancing healthcare through innovative drug development and manufacturing, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager for their operations in Bien Hoa, Dong Nai, VN . This pivotal role is responsible for ensuring that all pharmaceutical products manufactured by our client meet stringent global quality standards and regulatory requirements. You will oversee the Quality Assurance (QA) department, developing and implementing robust quality management systems (QMS) in compliance with GMP (Good Manufacturing Practices), ICH guidelines, and other relevant pharmaceutical regulations. Key responsibilities include managing batch record reviews, conducting internal and external audits, handling deviations and CAPA (Corrective and Preventive Actions), and overseeing validation activities. You will also lead the continuous improvement of quality processes, risk management initiatives, and ensure the overall compliance of manufacturing operations. The ideal candidate will possess extensive experience in the pharmaceutical industry, with a strong background in QA, regulatory affairs, and quality control. Excellent leadership, analytical, and problem-solving skills are essential, as is a thorough understanding of pharmaceutical manufacturing processes. You must be adept at interpreting complex regulations and translating them into actionable quality strategies. This role offers a hybrid work model, providing flexibility while maintaining close collaboration with manufacturing and laboratory teams. A strong commitment to patient safety and product quality is paramount.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with cGMP, FDA, EMA, and other relevant regulatory guidelines.
- Oversee batch release process and ensure product quality.
- Conduct internal and external audits of suppliers and manufacturing processes.
- Manage deviations, investigations, and implement CAPAs.
- Lead validation activities for equipment, processes, and analytical methods.
- Monitor and improve key quality indicators (KQIs).
- Provide training and guidance to QA and other personnel on quality standards.
- Manage regulatory inspections and responses.
- Drive continuous improvement initiatives in quality operations.
This advertiser has chosen not to accept applicants from your region.
4
Lead Pharmaceutical Quality Assurance Manager
44000 Hoang Hoa
WhatJobs
Posted today
Job Viewed
Job Description
WhatJobs is seeking an experienced and meticulous Lead Pharmaceutical Quality Assurance Manager to spearhead our quality control initiatives within a fully remote capacity. This role is critical in ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements, contributing to patient safety and product efficacy.
As a fully remote team member, you will oversee the development, implementation, and maintenance of our Quality Management System (QMS). Your responsibilities will encompass a broad range of QA activities, including ensuring Good Manufacturing Practices (GMP) compliance, managing deviation investigations, change control processes, and conducting internal audits. You will lead a team of QA professionals, providing guidance, mentorship, and performance feedback, all managed through virtual collaboration tools.
The ideal candidate will possess a comprehensive understanding of pharmaceutical regulations (e.g., FDA, EMA, WHO) and a proven track record in pharmaceutical quality assurance. You will be responsible for the review and approval of batch records, validation protocols, and product release documentation. Strong leadership skills, excellent problem-solving abilities, and exceptional attention to detail are essential for success in this role. You will work closely with R&D, manufacturing, and regulatory affairs departments to ensure quality is embedded throughout the product lifecycle.
Qualifications: A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 8 years of progressive experience in pharmaceutical Quality Assurance. Demonstrable experience in leading QA teams and managing QMS. In-depth knowledge of cGMP, ICH guidelines, and other relevant regulatory standards. Experience with quality risk management principles. Excellent analytical, critical thinking, and decision-making skills. Superior written and verbal communication abilities, with proficiency in virtual communication platforms. Ability to drive continuous improvement initiatives in a remote setting. Join our mission to deliver high-quality pharmaceuticals globally.
Responsibilities:
As a fully remote team member, you will oversee the development, implementation, and maintenance of our Quality Management System (QMS). Your responsibilities will encompass a broad range of QA activities, including ensuring Good Manufacturing Practices (GMP) compliance, managing deviation investigations, change control processes, and conducting internal audits. You will lead a team of QA professionals, providing guidance, mentorship, and performance feedback, all managed through virtual collaboration tools.
The ideal candidate will possess a comprehensive understanding of pharmaceutical regulations (e.g., FDA, EMA, WHO) and a proven track record in pharmaceutical quality assurance. You will be responsible for the review and approval of batch records, validation protocols, and product release documentation. Strong leadership skills, excellent problem-solving abilities, and exceptional attention to detail are essential for success in this role. You will work closely with R&D, manufacturing, and regulatory affairs departments to ensure quality is embedded throughout the product lifecycle.
Qualifications: A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 8 years of progressive experience in pharmaceutical Quality Assurance. Demonstrable experience in leading QA teams and managing QMS. In-depth knowledge of cGMP, ICH guidelines, and other relevant regulatory standards. Experience with quality risk management principles. Excellent analytical, critical thinking, and decision-making skills. Superior written and verbal communication abilities, with proficiency in virtual communication platforms. Ability to drive continuous improvement initiatives in a remote setting. Join our mission to deliver high-quality pharmaceuticals globally.
Responsibilities:
- Lead and manage the Pharmaceutical Quality Assurance department.
- Develop and maintain the Quality Management System (QMS).
- Ensure compliance with cGMP, ICH, and other regulatory guidelines.
- Oversee batch record review and product release processes.
- Manage deviation investigations and CAPA implementation.
- Conduct internal audits and support external regulatory inspections.
- Lead change control processes for products and processes.
- Mentor and guide QA team members remotely.
- Collaborate with cross-functional teams on quality-related matters.
- Drive continuous improvement in quality systems.
This advertiser has chosen not to accept applicants from your region.
5
Senior Pharmaceutical Quality Assurance Manager
490000 Thuy Van
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager to oversee quality systems and ensure compliance with regulatory standards at their facility in **Hue, Thua Thien–Hue, VN**. This role is vital for maintaining the integrity and safety of our pharmaceutical products. The ideal candidate will have extensive experience in pharmaceutical quality assurance, a deep understanding of GMP regulations, and strong leadership capabilities. This position offers a hybrid work arrangement, combining remote work flexibility with essential on-site responsibilities.
Key Responsibilities:
The successful candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Master's degree or advanced degree is preferred. A minimum of 8 years of progressive experience in Quality Assurance within the pharmaceutical industry is required, with at least 3-5 years in a management or supervisory role. Proven experience with GMP regulations (FDA, EMA, etc.) and quality system implementation is mandatory. Strong knowledge of validation principles, analytical testing, and pharmaceutical manufacturing processes is essential. Excellent leadership, communication, problem-solving, and decision-making skills are required. The ability to analyze complex data, manage multiple priorities, and ensure strict adherence to quality standards is critical. Experience with audit preparation and hosting regulatory inspections is highly valued.
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with cGMP, ICH guidelines, and other relevant regulatory requirements.
- Oversee all QA activities, including batch record review and release, deviation management, CAPA (Corrective and Preventive Actions), change control, and complaint handling.
- Conduct internal audits and participate in external audits by regulatory agencies and customers.
- Develop and manage validation protocols for equipment, processes, and computer systems.
- Ensure that all manufacturing and testing activities are performed in compliance with approved procedures and regulatory standards.
- Review and approve manufacturing process documentation, specifications, and analytical methods.
- Manage and mentor the QA team, fostering a culture of quality and continuous improvement.
- Provide training on quality systems and regulatory compliance to relevant personnel.
- Investigate deviations and out-of-specification (OOS) results, implementing appropriate CAPAs.
- Monitor key quality indicators and report on the performance of the QMS to senior management.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality and compliance.
- Stay updated on evolving regulatory requirements and industry best practices in the pharmaceutical sector.
- Manage supplier qualification and audit programs.
- Lead quality risk management activities.
- Ensure data integrity across all quality-related processes.
The successful candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Master's degree or advanced degree is preferred. A minimum of 8 years of progressive experience in Quality Assurance within the pharmaceutical industry is required, with at least 3-5 years in a management or supervisory role. Proven experience with GMP regulations (FDA, EMA, etc.) and quality system implementation is mandatory. Strong knowledge of validation principles, analytical testing, and pharmaceutical manufacturing processes is essential. Excellent leadership, communication, problem-solving, and decision-making skills are required. The ability to analyze complex data, manage multiple priorities, and ensure strict adherence to quality standards is critical. Experience with audit preparation and hosting regulatory inspections is highly valued.
This advertiser has chosen not to accept applicants from your region.
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Senior Pharmaceutical Quality Assurance Manager
94000 Bien Hoa, Dong Nai
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a dynamic pharmaceutical company, is seeking an experienced Senior Pharmaceutical Quality Assurance Manager to oversee and enhance their quality management systems. This hybrid role requires a strategic thinker with a strong understanding of cGMP regulations and pharmaceutical manufacturing processes, based in Bien Hoa. You will lead a team of QA professionals, ensuring compliance with regulatory standards, driving continuous improvement initiatives, and upholding the highest quality benchmarks for all products. This position involves a balance of remote work and on-site presence for critical quality-related activities.
Key Responsibilities:
Qualifications:
This is a key leadership role offering a challenging and rewarding career path within a growing pharmaceutical company. Take the lead in ensuring product excellence and regulatory compliance.
Key Responsibilities:
- Develop, implement, and maintain robust Quality Assurance (QA) systems in accordance with cGMP, ICH, and other relevant regulatory guidelines.
- Lead and manage the QA team, providing guidance, training, and performance management.
- Oversee batch record review and release processes to ensure product quality and compliance.
- Manage internal and external audits, including preparation, execution, and follow-up on corrective actions.
- Investigate deviations, CAPAs (Corrective and Preventive Actions), and out-of-specification (OOS) results, ensuring timely and effective resolution.
- Review and approve validation protocols and reports for manufacturing processes, equipment, and analytical methods.
- Ensure all quality-related documentation is accurate, complete, and compliant.
- Monitor and analyze quality metrics to identify trends and areas for improvement.
- Collaborate with other departments (Manufacturing, R&D, Regulatory Affairs) to ensure quality integration across all functions.
- Provide QA support during regulatory inspections and submissions.
- Stay current with evolving regulatory requirements and industry best practices.
- Champion a culture of quality and continuous improvement throughout the organization.
Qualifications:
- Master's or Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- A minimum of 7-10 years of progressive experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of cGMP regulations (e.g., FDA 21 CFR Parts 210/211, EU GMP).
- Experience with pharmaceutical manufacturing processes, sterile operations, and analytical testing.
- Proven experience in managing QA teams and overseeing quality systems.
- Strong understanding of validation principles and practices.
- Excellent leadership, problem-solving, and decision-making skills.
- Proficiency in audit management, deviation investigations, and CAPA implementation.
- Strong analytical and report-writing skills.
- Excellent verbal and written communication skills in English.
- Ability to work effectively in a hybrid environment, balancing remote responsibilities with essential on-site duties.
- Experience with regulatory agency inspections is highly desirable.
This is a key leadership role offering a challenging and rewarding career path within a growing pharmaceutical company. Take the lead in ensuring product excellence and regulatory compliance.
This advertiser has chosen not to accept applicants from your region.
7
Senior Pharmaceutical Quality Assurance Manager
81000 Bien Hoa, Dong Nai
WhatJobs
Posted today
Job Viewed
Job Description
Our client is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager to lead their QA operations in **Bien Hoa, Dong Nai, VN**. This is a crucial on-site role, responsible for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements. You will oversee the development, implementation, and maintenance of the Quality Management System (QMS), ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant guidelines. Key responsibilities include conducting internal and external audits, managing deviations and CAPAs, overseeing batch record reviews, and participating in regulatory inspections. You will also be involved in supplier qualification, change control management, and the training of QA personnel. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, with at least 10 years of progressive experience in pharmaceutical quality assurance. A deep understanding of regulatory affairs, quality systems, and risk management principles is essential. Proven leadership skills, excellent analytical abilities, and strong attention to detail are required. You will work closely with production, R&D, and regulatory affairs departments to ensure product quality and compliance throughout the entire product lifecycle. This is a leadership position offering the opportunity to make a significant impact on product quality and patient safety.
**Responsibilities:*** Develop, implement, and maintain the company's Quality Management System (QMS).
* Ensure compliance with GMP, GLP, and other relevant pharmaceutical regulations.
* Conduct internal audits, process validation, and qualification activities.
* Manage deviations, out-of-specifications (OOS), and corrective and preventive actions (CAPA).
* Review and approve batch records, validation protocols, and reports.
* Lead and participate in regulatory inspections and customer audits.
* Oversee supplier qualification and management programs.
* Drive continuous improvement initiatives within the Quality Unit.
* Train and mentor QA staff.
**Qualifications:*** Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
* Minimum of 10 years of experience in pharmaceutical Quality Assurance/Quality Control.
* Extensive knowledge of GMP, GLP, and other relevant regulatory guidelines.
* Strong experience with QMS implementation and maintenance.
* Excellent auditing, problem-solving, and decision-making skills.
* Proven leadership and team management capabilities.
* Strong understanding of pharmaceutical manufacturing processes.
**Responsibilities:*** Develop, implement, and maintain the company's Quality Management System (QMS).
* Ensure compliance with GMP, GLP, and other relevant pharmaceutical regulations.
* Conduct internal audits, process validation, and qualification activities.
* Manage deviations, out-of-specifications (OOS), and corrective and preventive actions (CAPA).
* Review and approve batch records, validation protocols, and reports.
* Lead and participate in regulatory inspections and customer audits.
* Oversee supplier qualification and management programs.
* Drive continuous improvement initiatives within the Quality Unit.
* Train and mentor QA staff.
**Qualifications:*** Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
* Minimum of 10 years of experience in pharmaceutical Quality Assurance/Quality Control.
* Extensive knowledge of GMP, GLP, and other relevant regulatory guidelines.
* Strong experience with QMS implementation and maintenance.
* Excellent auditing, problem-solving, and decision-making skills.
* Proven leadership and team management capabilities.
* Strong understanding of pharmaceutical manufacturing processes.
This advertiser has chosen not to accept applicants from your region.
8
Senior Pharmaceutical Quality Assurance Manager
60000 Hoi An
WhatJobs
Posted today
Job Viewed
Job Description
Our client is a leading pharmaceutical company seeking an experienced and highly motivated Senior Pharmaceutical Quality Assurance Manager for their operations in Buon Ma Thuot, Dak Lak. This role involves overseeing and ensuring compliance with all relevant quality standards, regulations, and guidelines throughout the pharmaceutical manufacturing process. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS). This includes managing internal and external audits, CAPA (Corrective and Preventive Actions) systems, deviation investigations, and change control processes. The ideal candidate will have a strong background in pharmaceutical quality assurance, with a deep understanding of GMP (Good Manufacturing Practices), ICH guidelines, and other regulatory requirements. You will lead and mentor a team of QA professionals, fostering a culture of quality and continuous improvement. Responsibilities also include reviewing and approving batch records, validation protocols, and other critical quality documentation. You will work closely with production, R&D, and regulatory affairs departments to ensure product quality and safety. The ability to identify potential risks, develop mitigation strategies, and implement effective quality controls is crucial. This position requires excellent analytical, problem-solving, and decision-making skills. Strong leadership and communication abilities are essential for collaborating with diverse teams and presenting findings to senior management. If you are passionate about ensuring the highest standards in pharmaceutical production and are looking for a challenging yet rewarding career opportunity, we encourage you to apply.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Manage and enhance the company's Quality Management System (QMS).
- Oversee GMP compliance across all pharmaceutical operations.
- Lead and mentor the Quality Assurance team.
- Conduct and manage internal and external audits.
- Investigate deviations and implement CAPA plans.
- Review and approve critical quality documentation, including batch records and validation protocols.
- Collaborate with cross-functional teams to ensure product quality and safety.
- Identify and mitigate quality-related risks.
- Stay updated on regulatory changes and ensure company compliance.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 8 years of experience in pharmaceutical quality assurance/quality control.
- Extensive knowledge of GMP, ICH guidelines, and regulatory requirements.
- Proven experience in managing a QMS, audits, and CAPA systems.
- Strong leadership, communication, and interpersonal skills.
- Excellent analytical and problem-solving abilities.
- Experience in pharmaceutical manufacturing processes.
This advertiser has chosen not to accept applicants from your region.
9