Document Quality, Senior Manager
Welcome to Pfizer, a global leader in the pharmaceutical industry dedicated to improving the lives of people around the world. We are currently seeking a highly skilled and experienced Document Quality Senior Manager to join our dynamic team. As our Senior Manager, you will play a critical role in ensuring the accuracy, completeness, and compliance of our documents, ultimately contributing to the quality and safety of our products. We are looking for an individual with a strong attention to detail, exceptional communication skills, and a passion for maintaining high standards of quality. If you are ready to take on this challenging and rewarding position, we encourage you to apply and become a part of our innovative and driven organization.
- Oversee and manage the document quality processes and procedures for Pfizer, ensuring compliance with company standards and regulations.
- Develop and implement quality control measures to ensure accuracy and completeness of all documents, including but not limited to regulatory submissions, manufacturing documents, and internal policies.
- Collaborate with cross-functional teams to review and approve documents, ensuring alignment with company objectives and regulatory requirements.
- Conduct regular audits and inspections to identify any gaps or deficiencies in document quality and work with relevant teams to address and resolve any issues.
- Stay up-to-date with industry regulations and standards related to document quality and ensure that Pfizer is in compliance with all requirements.
- Train and mentor team members on document quality processes and procedures, ensuring consistency and accuracy across all documents.
- Act as a point of contact for any document quality-related inquiries or issues, providing timely and effective resolution.
- Continuously review and improve document quality processes to enhance efficiency and effectiveness.
- Communicate and report on document quality metrics and performance to senior management and stakeholders.
- Represent Pfizer in external audits and inspections related to document quality.
- Foster a culture of quality and compliance within the organization by promoting and reinforcing the importance of document accuracy and completeness.
- Handle any other tasks or projects related to document quality as assigned by senior management.
Bachelor's Degree In A Relevant Field Such As Life Sciences, Pharmaceuticals, Or Quality Management.
Minimum Of 8 Years Of Experience In Document Quality Management In The Pharmaceutical Industry.
In-Depth Knowledge Of Global Regulatory Requirements And Guidelines, Including Fda, Ema, And Ich.
Experience Implementing And Maintaining Document Control Systems, Including Electronic Document Management Systems.
Strong Leadership And Communication Skills, With The Ability To Effectively Manage A Team And Collaborate With Cross-Functional Teams.
Quality Assurance
Process Improvement
Project Management
Training
Data Analysis
Team Management
Auditing
Risk assessment
DOCUMENT CONTROL
Regulatory compliance
SOP Development
Gmp Standards
Communication
Conflict Resolution
Leadership
Time management
Interpersonal Skills
Critical thinking
Attention to detail
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Document Quality, Senior Manager in Cambridge, MA, USA is $120,000-$150,000 per year. However, this salary range can vary based on factors such as years of experience, education, and specific job duties and responsibilities.
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Pfizer Inc. is an American multinational pharmaceutical corporation headquartered in New York City, with its research headquarters in Groton, Connecticut. It is one of the world's largest pharmaceutical companies.
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