Manager, Regulatory Operations Documentation Specialist (Contractor)
Apply NowLocation:
Florham Park, NJ, US
Company:
Shionogi Inc. is dedicated to developing innovative pharmaceuticals to improve patient health and well-being.
Summary:
The Manager, Regulatory Operations Documentation Specialist will oversee documentation processes, ensuring accuracy and compliance. Applicants need a Bachelor's degree and 5+ years of experience in documentation management, including leadership experience.
Requirements:
Credentials: Bachelor's degree preferred
Experience: 5+ years of experience in documentation management or a related role, 1+ years in a supervisory or leadership position, Proven experience with document control systems and compliance standards
Job Description:
Overview
This role will lead the Regulatory Operations - Documentation Specialist team in overseeing the documentation processes within an organization, ensuring that all documents are accurate, compliant, and efficiently managed. This role involves leading a team of documentation specialists, improving documentation workflows, and ensuring regulatory compliance.
The scope of this role includes document formatting, remediation and quality control (QC) of documentation for submissions to Health Authorities. It also includes the archiving of correspondences to and from the health authorities and internal and external GRM archiving.
Responsibilities
This role will lead the Regulatory Operations - Documentation Specialist team in overseeing the documentation processes within an organization, ensuring that all documents are accurate, compliant, and efficiently managed. This role involves leading a team of documentation specialists, improving documentation workflows, and ensuring regulatory compliance.
The scope of this role includes document formatting, remediation and quality control (QC) of documentation for submissions to Health Authorities. It also includes the archiving of correspondences to and from the health authorities and internal and external GRM archiving.
Responsibilities
- Provide direction and support to the documentation team, ensuring high-quality work and adherence to standards.
- Train team on documentation standards, procedures, and tools to ensure consistency and compliance.
- Ensure all documents meet the organization's quality standards and regulatory requirements.
- Continuously enhance documentation processes to improve efficiency and productivity.
- Maintain document control processes for proper classification, indexing, distribution, and archiving.
- Ensure all documentation complies with industry regulations and standards.
- Work closely with other departments to gather information and ensure comprehensive documentation.
- Manage and Support team members that ensure all correspondences to and from the health authorities are archived within the company’s system and comply with regulatory standards and guidelines.
Minimum Job Requirements
Qualifications
- Bachelor’s degree preferred.
- 5+ years of experience in documentation management or a related role
- 1+ years in a supervisory or leadership position
- Proven experience with document control systems and compliance standards
Competencies
- Proficient in MS Office and Acrobat Adobe.
- Experience with ISI Toolbox or equivalent software packages.
- Experience in document management systems; Veeva is a plus.
- Familiarity with regulatory compliance
- High level of attention to detail and accuracy in work.
- Effective time management and organizational skills.
- Strong written and verbal communication skills.
- Proficiency in training and mentoring document specialists
- Able to work within a high-performance, collaborative team environment.
Other Requirements
- This position has significant managerial and decision-making authority.
- No travel is required for this position
- Must live a commutable distance to our US Corporate Headquarters in Florham Park, NJ. Office presence required at least 50% of the time per month
To be considered for this position, you must apply and meet the requirements of this opportunity.
We look forward to reviewing your resume & qualifications.