
Quality Assurance Document Control (QADC)
Welcome to Catalent, a leading global provider of advanced delivery technologies and development solutions for drugs, biologics, and consumer health products. We are currently seeking a meticulous and detail-oriented individual to join our team as a Quality Assurance Document Control (QADC) specialist. As a QADC specialist, you will play a critical role in ensuring the accuracy, completeness, and compliance of all documentation related to our manufacturing processes. Your attention to detail and strong organizational skills will be essential in maintaining our high standards of quality and regulatory compliance. If you have a passion for precision and a desire to make a meaningful impact in the pharmaceutical industry, we encourage you to apply for this exciting opportunity.
- Review and verify all documentation related to manufacturing processes to ensure accuracy, completeness, and compliance with regulatory standards.
- Maintain a thorough understanding of all relevant regulations, guidelines, and company policies related to document control and quality assurance.
- Communicate any discrepancies or issues with documentation to the appropriate departments and work with them to resolve any concerns.
- Collaborate with cross-functional teams to identify areas for improvement in document control processes and implement necessary changes.
- Manage and maintain the document control system, including organizing and categorizing documents, tracking revisions, and ensuring timely approval and distribution.
- Conduct periodic audits of documentation and processes to ensure compliance and identify any potential areas for improvement.
- Train and educate employees on document control procedures and expectations to ensure consistent compliance across the organization.
- Serve as a subject matter expert on document control and quality assurance matters, providing guidance and support to colleagues as needed.
- Maintain confidentiality and security of all sensitive documents and information.
- Contribute to the continuous improvement of the overall quality management system within the organization.
Bachelor's Degree In Quality Assurance, Engineering, Or A Related Field.
Minimum Of 2 Years Of Experience In Document Control In A Pharmaceutical Or Medical Device Industry.
Strong Understanding Of Cgmp Regulations And Fda Guidelines.
Excellent Attention To Detail And Organizational Skills.
Proficient In Document Management Software And Microsoft Office.
Process Improvement
Training
Data Analysis
Communication
Attention to detail
Problem Solving
Auditing
Quality Control
Compliance
Record keeping
Document management
SOP Development
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
flexibility
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Quality Assurance Document Control (QADC) in Philadelphia, PA, USA is $44,000 - $76,000 per year. This salary range may vary depending on factors such as experience, education, and company size. QADCs in larger companies or with more experience may earn higher salaries within this range.
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Catalent, Inc. is a multinational corporation headquartered in Somerset, New Jersey. It is a global provider of delivery technologies, development, drug manufacturing, biologics, gene therapies and consumer health products. It employs more than 14,000 people, including approximately 2,400 scientists and technicians.

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