95 Pharmaceutical Manager jobs in India

Pharmaceutical Sales Manager

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Ahmedabad, Gujarat Kivonyx Healthcare Pvt. Ltd.

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Company Description

Kivonyx Healthcare Pvt. Ltd. is a division of Octavius Pharma Pvt. Ltd., a company dedicated to supplying quality healthcare products. Octavius Pharma designs, manufactures, markets, and packages a wide range of products, including tablets, capsules, dry syrups, liquid orals, ointments, nasal sprays, injectables, softgel capsules, food supplements, nutraceuticals, dietary supplements, herbal/ayurvedic medicines, and cosmetics. Our products are promoted to medical professionals through a trained team of representatives and distributed through a network of distributors and stockists.


We are having strong market presence with very good product range. We are a leading PCD Pharma Franchise Company in India with Presence in more than 400 Districts in India. We are known for our excellent product Quality and Service.


Role Description


As a part of expansion we are having opening for PCD Pharmaceutical Sales Manager for Pharma Company in Ahmedabad. Candidate should have PCD pharma marketing experience.


Candidate should be capable of Handling a team of 4 to 5 people. Should have good communication and convincing skills.


This is a full-time, on-site role for a Pharmaceutical Sales Manager located in Ahmedabad. The Pharmaceutical Sales Manager will be responsible for managing sales operations, building and maintaining relationships with clients, developing and implementing business plans, and achieving sales targets. Daily tasks include overseeing account management, coordinating with the sales team, strategizing sales initiatives, and ensuring customer satisfaction through effective communication and professional conduct.



Salary : 5000 to 6000 depending on experience + Great Incentives


If you are interested kindly send your updated resume on


Build your career with us.


  • Only Ahmedabad Candidates should apply


Qualifications

  • Pharmaceutical Sales and Sales skills
  • Experience in Sales Management
  • Ability in Business Planning and strategizing sales initiatives
  • Excellent written and verbal communication skills
  • Strong leadership and team coordination abilities
  • Bachelor's degree in Pharmaceuticals, Business, or related field
  • Experience in the healthcare or pharmaceutical industry is an advantage
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Pharmaceutical Quality Assurance Manager

160022 Chandigarh, Chandigarh ₹90000 Annually WhatJobs

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full-time
Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Assurance Manager to oversee quality systems and compliance at their facility in **Chandigarh, Chandigarh, IN**. This vital role ensures that all pharmaceutical products meet rigorous quality standards and comply with regulatory requirements set forth by bodies such as the FDA, EMA, and national health authorities. The QA Manager will be instrumental in maintaining and improving the company's overall quality management system (QMS).

Key responsibilities include developing, implementing, and maintaining quality assurance policies and procedures, managing internal and external audits, and ensuring Good Manufacturing Practices (GMP) are strictly adhered to. You will be responsible for batch record review, deviation investigations, change control management, and CAPA (Corrective and Preventive Actions) implementation. This hybrid role requires your presence in the **Chandigarh, Chandigarh, IN** office for critical quality oversight, batch release, and team leadership, with opportunities for remote work on documentation review and system analysis. The ideal candidate will possess strong leadership skills, a thorough understanding of pharmaceutical manufacturing processes, and excellent analytical and problem-solving abilities.

Responsibilities:
  • Develop and implement quality assurance strategies and systems.
  • Ensure compliance with cGMP, ICH, and other regulatory guidelines.
  • Manage and conduct internal and external audits.
  • Review and approve batch records, validation protocols, and reports.
  • Lead deviation investigations and implement CAPA plans.
  • Manage change control processes for manufacturing and quality systems.
  • Oversee the qualification and validation of equipment and processes.
  • Train QA/QC personnel and other relevant staff on quality systems.
  • Monitor and report on key quality performance indicators (KPIs).
  • Stay up-to-date with evolving regulatory requirements.
Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
  • Minimum 6 years of experience in Quality Assurance within the pharmaceutical industry.
  • In-depth knowledge of cGMP and pharmaceutical regulatory requirements.
  • Proven experience in audit management, deviation investigation, and CAPA implementation.
  • Strong understanding of pharmaceutical manufacturing processes.
  • Excellent leadership, communication, and interpersonal skills.
  • Proficiency in quality management software and documentation practices.
  • Strong analytical and problem-solving skills.
  • Ability to work effectively in a fast-paced, regulated environment.
This hybrid role requires regular attendance at the **Chandigarh, Chandigarh, IN** office.
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Pharmaceutical Quality Assurance Manager

751001 Bhubaneswar, Orissa ₹90000 Annually WhatJobs

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full-time
Our client is a leading pharmaceutical company seeking an experienced Pharmaceutical Quality Assurance Manager to oversee quality operations at their facility in Bhubaneswar, Odisha, IN . This critical role ensures that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. The Quality Assurance Manager will be responsible for developing, implementing, and maintaining the Quality Management System (QMS), ensuring compliance with Good Manufacturing Practices (GMP) and other relevant guidelines.

Key responsibilities include leading and managing the QA team, conducting internal audits and inspections, reviewing and approving batch records, validation protocols, and change controls. You will also manage external audits from regulatory agencies and customers, investigate deviations and out-of-specification (OOS) results, and implement corrective and preventive actions (CAPA). The role involves close collaboration with Production, QC, R&D, and Regulatory Affairs departments to ensure seamless integration of quality processes.

The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline. A minimum of 7-10 years of experience in pharmaceutical quality assurance is required, with at least 3 years in a managerial or supervisory capacity. A thorough understanding of GMP, ICH guidelines, and regulatory submission processes is essential. Strong leadership, communication, problem-solving, and decision-making skills are critical for success. Experience with quality risk management and data integrity principles is highly valued. This is a significant opportunity to make a substantial impact on product quality and patient safety within a reputable organization.
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Pharmaceutical Quality Assurance Manager

400601 Thane, Maharashtra ₹1000000 Annually WhatJobs

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full-time
Our client is seeking a highly meticulous and experienced Pharmaceutical Quality Assurance Manager to lead their QA department in Thane . This role is critical for ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory guidelines. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), overseeing compliance activities, and managing audits. The ideal candidate will possess a deep understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant pharmaceutical quality standards. Exceptional leadership, analytical skills, and a keen eye for detail are essential. You will lead a team of QA professionals, drive continuous improvement initiatives, and ensure robust quality control processes throughout the manufacturing and development lifecycle. This is an outstanding opportunity to make a significant impact on product quality and regulatory compliance within a leading pharmaceutical organization. Key responsibilities include:
  • Developing, implementing, and maintaining the company's Quality Management System (QMS).
  • Ensuring compliance with all applicable regulatory requirements, including GMP, ICH guidelines, and local regulations.
  • Overseeing all quality assurance activities, including batch record review, deviation management, and CAPA implementation.
  • Conducting internal audits and facilitating external regulatory audits.
  • Managing the validation of equipment, processes, and analytical methods.
  • Leading and mentoring the Quality Assurance team.
  • Reviewing and approving specifications, test methods, and validation protocols.
  • Monitoring and analyzing quality metrics to identify trends and implement corrective actions.
  • Collaborating with R&D, manufacturing, and regulatory affairs departments to ensure product quality.
  • Managing product release processes.
  • Developing and delivering quality training programs for employees.
  • Staying current with pharmaceutical industry regulations and best practices.
Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
  • Minimum of 6-8 years of experience in Quality Assurance within the pharmaceutical industry.
  • Extensive knowledge of GMP, GLP, and other relevant quality standards.
  • Proven experience in managing QA teams and QMS.
  • Strong understanding of pharmaceutical manufacturing processes.
  • Excellent analytical, problem-solving, and decision-making skills.
  • Exceptional attention to detail and commitment to quality.
  • Strong communication, leadership, and interpersonal skills.
  • Experience with regulatory inspections and submissions.
Join our client and play a pivotal role in upholding the highest quality standards in the pharmaceutical sector in the bustling city of Thane .
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Pharmaceutical Quality Assurance Manager

302001 Jaipur, Rajasthan ₹900000 Annually WhatJobs

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full-time
Our client, a reputable pharmaceutical company, is looking for a dedicated and experienced Pharmaceutical Quality Assurance Manager to oversee quality control and assurance processes at their facility in **Jaipur, Rajasthan, IN**. This role is pivotal in ensuring that all products meet stringent regulatory standards and quality benchmarks throughout the manufacturing lifecycle.

Responsibilities:
  • Develop, implement, and maintain comprehensive quality management systems (QMS) in compliance with cGMP, ICH, and other relevant regulatory guidelines.
  • Lead and manage the QA team, providing training, guidance, and performance evaluations.
  • Oversee the batch release process, ensuring all products meet specifications before distribution.
  • Conduct internal audits and support external audits by regulatory agencies and customers.
  • Manage deviation investigations, CAPA (Corrective and Preventive Actions) implementation, and change control processes.
  • Review and approve manufacturing batch records, validation protocols, and reports.
  • Monitor manufacturing processes and provide guidance on quality-related matters.
  • Stay updated on evolving regulatory requirements and industry best practices.
  • Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality and compliance.
  • Manage supplier qualification and audits to ensure the quality of raw materials and components.
Qualifications:
  • Master's degree in Pharmacy, Chemistry, Microbiology, or a related life science field.
  • A minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry, with at least 2 years in a managerial or supervisory role.
  • In-depth knowledge of cGMP, FDA regulations, and international pharmaceutical guidelines.
  • Proven experience in developing and implementing QMS, conducting audits, and managing deviations.
  • Strong leadership, analytical, and problem-solving skills.
  • Excellent written and verbal communication abilities.
  • Ability to effectively manage multiple projects and prioritize tasks.
  • Experience with validation processes (process, cleaning, analytical method) is essential.
  • Familiarity with sterile manufacturing processes is a plus.
This is an exceptional career opportunity for a quality-focused professional in **Jaipur, Rajasthan, IN**, to make a significant impact on product quality and patient safety. Our client offers a competitive compensation package and benefits.
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Pharmaceutical Quality Assurance Manager

700016 Kolkata, West Bengal ₹1400000 Annually WhatJobs

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full-time
Our client, a renowned pharmaceutical company, is seeking a highly experienced and detail-oriented Pharmaceutical Quality Assurance Manager to lead their QA department in **Kolkata, West Bengal, IN**. This critical role is responsible for ensuring that all pharmaceutical products manufactured by the company meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory requirements and Good Manufacturing Practices (GMP). The QA Manager will oversee the development, implementation, and maintenance of the company's Quality Management System (QMS). Key responsibilities include managing batch record reviews and releases, conducting internal and external audits, investigating deviations and customer complaints, and implementing CAPA (Corrective and Preventive Actions). You will also be responsible for validation activities, change control processes, and ensuring compliance with national and international pharmaceutical regulations (e.g., FDA, EMA, WHO-GMP). The successful candidate will lead and mentor a team of QA professionals, foster a culture of quality excellence, and collaborate with various departments, including R&D, manufacturing, and regulatory affairs. Strong analytical skills, a thorough understanding of pharmaceutical manufacturing processes, and expertise in regulatory compliance are essential. We are looking for a proactive, decisive leader with excellent communication and problem-solving abilities, committed to upholding the company's reputation for quality. This position offers a significant opportunity to influence product quality and patient safety within a leading pharmaceutical organization. The ideal candidate will be adept at managing complex quality systems and ensuring continuous improvement in all QA-related activities.

Responsibilities:
  • Oversee the Quality Assurance department and QMS implementation.
  • Ensure compliance with GMP and relevant pharmaceutical regulations.
  • Manage batch record review and product release processes.
  • Conduct internal and external (vendor) audits.
  • Investigate deviations, OOS/OOT results, and customer complaints.
  • Develop and implement CAPA plans.
  • Oversee validation activities (process, equipment, cleaning).
  • Manage change control processes and documentation.
  • Train QA staff and other personnel on quality systems.
  • Collaborate with R&D, manufacturing, and regulatory affairs teams.

Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
  • Minimum of 7-10 years of experience in Quality Assurance within the pharmaceutical industry.
  • Extensive knowledge of GMP, ICH guidelines, and regulatory requirements.
  • Proven experience in managing QA teams and systems.
  • Experience with audits, validation, and deviation management.
  • Strong analytical, problem-solving, and decision-making skills.
  • Excellent leadership, communication, and interpersonal skills.
  • Proficiency in pharmaceutical quality control processes.
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Pharmaceutical Quality Assurance Manager

390001 Vadodara, Gujarat ₹90000 Annually WhatJobs

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full-time
Our client, a leading pharmaceutical company, is looking for an experienced Pharmaceutical Quality Assurance Manager to oversee their quality management systems. This hybrid role offers a blend of remote work and on-site presence at our Vadodara facility. You will be instrumental in ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy. Your responsibilities will include developing, implementing, and maintaining robust QA policies and procedures in compliance with regulatory requirements such as GMP, ICH, and FDA guidelines. You will manage the QA team, conduct internal audits, review batch records, and handle deviations and CAPA investigations. The role also involves validating manufacturing processes, equipment, and analytical methods. Collaboration with R&D, production, and regulatory affairs departments is crucial for ensuring product lifecycle integrity. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field, with at least 7 years of progressive experience in pharmaceutical quality assurance. A deep understanding of pharmaceutical manufacturing processes, quality control principles, and regulatory landscapes is mandatory. Excellent leadership, communication, and problem-solving skills are required to effectively manage the QA department and interact with regulatory bodies. You must be proficient in risk management techniques and quality metrics reporting. This position requires a meticulous approach to documentation and a commitment to upholding the highest ethical standards in pharmaceutical quality. The ability to balance remote work with occasional site visits for critical activities is essential.
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Pharmaceutical Quality Assurance Manager

226001 Lucknow, Uttar Pradesh ₹80000 month WhatJobs

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full-time
Our client is seeking an experienced and meticulous Pharmaceutical Quality Assurance Manager to lead their Quality Assurance department in Lucknow, Uttar Pradesh, IN . This vital role ensures that all pharmaceutical products meet stringent quality standards and comply with regulatory requirements. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), including GMP (Good Manufacturing Practices) and GDP (Good Distribution Practices). Your duties will encompass overseeing quality control processes, conducting internal audits, managing deviations, CAPAs (Corrective and Preventive Actions), and change control systems. The ideal candidate will possess a deep understanding of pharmaceutical regulations (e.g., ICH guidelines, FDA, WHO-GMP) and a proven ability to drive quality initiatives. You will collaborate with R&D, production, and regulatory affairs teams to ensure product quality throughout the lifecycle. Strong leadership, analytical, and problem-solving skills are essential. This hybrid role requires effective communication and collaboration across departments. You will be responsible for training QA/QC personnel and fostering a culture of quality excellence. Experience in validation processes and documentation review is critical.

Key Responsibilities:
  • Develop, implement, and maintain the Quality Management System (QMS).
  • Ensure compliance with GMP, GDP, and other relevant pharmaceutical regulations.
  • Oversee quality control testing and release of raw materials and finished products.
  • Conduct internal audits and manage external audits.
  • Manage deviations, CAPAs, and change control processes.
  • Review and approve batch manufacturing records and validation protocols.
  • Provide quality training to personnel.
  • Collaborate with cross-functional teams on quality-related matters.

Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific field.
  • Minimum of 6-8 years of experience in Quality Assurance within the pharmaceutical industry.
  • In-depth knowledge of GMP, GDP, and regulatory requirements for pharmaceuticals.
  • Experience with Quality Management Systems, audits, and regulatory submissions.
  • Strong analytical, problem-solving, and decision-making skills.
  • Excellent leadership, communication, and interpersonal abilities.
  • Proficiency in quality documentation and data analysis.
  • Experience with validation (IQ, OQ, PQ) is a must.
This is an excellent opportunity to lead quality assurance in a growing pharmaceutical organization.
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Pharmaceutical Quality Control Manager

800001 Patna, Bihar ₹110000 Annually WhatJobs

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full-time
Our client, a rapidly growing pharmaceutical company, is seeking an experienced and detail-oriented Pharmaceutical Quality Control Manager to oversee their quality operations in Patna, Bihar, IN . This senior role is responsible for ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. The ideal candidate will have a comprehensive understanding of pharmaceutical quality systems, GMP guidelines, and analytical testing methodologies. Responsibilities include managing the day-to-day operations of the QC laboratory, supervising a team of QC analysts, and ensuring the timely and accurate testing of raw materials, in-process samples, and finished products. You will be responsible for developing and validating analytical methods, maintaining laboratory equipment, and ensuring compliance with all relevant regulatory bodies. The QC Manager will play a crucial role in investigating deviations, implementing corrective and preventive actions (CAPA), and managing change control processes. Strong leadership abilities, excellent problem-solving skills, and a commitment to maintaining the highest quality standards are essential. A minimum of 7 years of experience in pharmaceutical quality control, with at least 3 years in a supervisory or managerial capacity, is required. Proficiency in pharmacopoeial methods (IP, USP, BP, EP) and experience with HPLC, GC, and other analytical instrumentation are necessary. If you are a seasoned quality professional looking for a challenging and rewarding opportunity to lead quality initiatives in a dynamic pharmaceutical environment, we encourage you to apply.
Responsibilities:
  • Manage the operations of the Quality Control laboratory, ensuring compliance with GMP and regulatory standards.
  • Supervise and mentor a team of QC analysts and technicians.
  • Oversee the testing of raw materials, intermediates, and finished pharmaceutical products.
  • Develop, validate, and transfer analytical methods.
  • Ensure the proper maintenance, calibration, and qualification of laboratory equipment.
  • Review and approve analytical data, test methods, and specifications.
  • Investigate Out-of-Specification (OOS) results and implement CAPAs.
  • Manage laboratory documentation and ensure data integrity.
  • Liaise with other departments, including Production, R&D, and Regulatory Affairs.
  • Stay updated with current GMP regulations and industry best practices.
Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Microbiology, or a related field.
  • Minimum of 7 years of experience in pharmaceutical quality control.
  • Minimum of 3 years of experience in a supervisory or managerial role within QC.
  • In-depth knowledge of GMP, ICH guidelines, and pharmacopoeias.
  • Proficiency in analytical techniques such as HPLC, GC, UV-Vis, FTIR.
  • Experience with method validation and OOS investigations.
  • Strong leadership, team management, and problem-solving skills.
  • Excellent attention to detail and organizational abilities.
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Pharmaceutical Quality Assurance Manager

452001 Bhopal, Madhya Pradesh ₹1000000 Annually WhatJobs

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full-time
Our client, a prominent pharmaceutical company, is seeking an experienced Pharmaceutical Quality Assurance Manager to oversee all quality control and assurance activities at their facility in Bhopal, Madhya Pradesh, IN . This is a critical on-site role, vital for ensuring compliance with all regulatory standards and maintaining the highest product quality. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), ensuring adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant industry regulations.

Key responsibilities include managing the QA team, conducting internal audits, reviewing batch records, investigating deviations and out-of-specification (OOS) results, and implementing corrective and preventive actions (CAPA). You will also be involved in vendor qualification, change control management, and ensuring that all manufacturing and laboratory processes meet stringent quality requirements. Preparing for and hosting regulatory inspections (e.g., FDA, WHO) will be a significant part of your role. You will also contribute to the development and improvement of quality policies and procedures.

The ideal candidate will possess a Master's or Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field, with a minimum of 7-10 years of progressive experience in Quality Assurance within the pharmaceutical industry. A deep understanding of pharmaceutical manufacturing processes, quality control methodologies, and regulatory affairs (including ICH guidelines) is essential. Strong leadership, problem-solving, and decision-making skills are required. Excellent analytical and documentation skills, along with the ability to communicate effectively with regulatory bodies and internal stakeholders, are crucial. Experience in managing audits and inspections, and a proven track record of implementing successful CAPA systems are highly desirable. Join our client to ensure the integrity and quality of life-saving medicines.
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