Sr. Quality Documentation Specialist (Contract) 25737

The Senior Document Control Specialist is responsible for overseeing the management, organization, and maintenance of all controlled documents within the company’s quality management system (QMS). This role ensures compliance with regulatory requirements, company policies, and industry standards, supporting the efficient operation of the pharmaceutical development and manufacturing processes.

*** Hours: Wednesday-Saturday 7:30am - $5:00pm ***

Key Responsibilities:

Document Management:

• Manage the lifecycle of controlled documents, including creation, revision, review, approval, distribution, and archiva
• Ensure documents are accessible, accurate, and up-to-date within the electronic document management system (EDMS).
• Coordinate with cross-functional teams to ensure timely review and approval of documents.

Compliance:

• Ensure all document control activities comply with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and per Vertex Procedures.
• Maintain audit readiness by ensuring documents are in a state of compliance and available for internal and external audits.

Process Improvement:

• Identify and implement process improvements to enhance the efficiency and effectiveness of the document control system.
• Develop and maintain document control procedures, work instructions, and training materials.

Training & Support:

• Provide training and support to employees on document control processes.
          •       Act as a subject matter expert for document control during audits and inspections.

Reporting & Metrics:

• Generate and analyze document control metrics and reports to monitor performance and identify areas for improvement.
• Present findings to management and recommend corrective actions as needed.
  
  

Qualifications:

• Bachelor’s degree in a related field (e.g., Life Sciences, Quality Assurance, or Regulatory Affairs).
• Minimum of 5-7 years of experience in document control within the pharmaceutical, biotechnology, or medical device industry.
• Strong knowledge of cGMP, GDP, and regulatory requirements (e.g., FDA, EMA).
• Proficiency in using electronic document management systems and other relevant software.
• Excellent organizational, communication, and interpersonal skills.
• Ability to work independently and as part of a team in a fast-paced, dynamic environment.
• Detail-oriented with a commitment to quality and accuracy.

Preferred Qualifications:
 

• Certification in Document Control or Quality Management
• Experience with lean or continuous improvement methodologies.

Familiarity with global regulatory requirements and international document control standards

$38-$40/hr

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice.   Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners

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If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.

No C2C or Third-Party Vendors