Job Description

Document Control Specialist

We are seeking a meticulous Document Control Specialist who will play a crucial role in managing and maintaining vital production and quality documents. This position involves ensuring accurate storage, organization, and quick retrieval of documents to support audits, investigations, and compliance with quality standards.

Responsibilities:

• File and maintain production and quality documents, ensuring accurate storage and organization.
• Manage and maintain the document room to ensure quick access during audits or investigations.
• Digitize paper records through scanning and upload them into the document management system.
• Retrieve documentation as requested by internal teams or external partners.
• Coordinate with a third-party storage provider to request or send overflow documents.
• Uphold good documentation practices (GDP) and support compliance with quality standards.

Essential Skills:

• Document control
• Quality assurance
• Data entry
• Document review
• Scanning
• Filing
• Archiving
• GMP
• Batch record review

Additional Skills & Qualifications:

• High School Diploma or GED with 1-3 years of experience.
• Strong attention to detail and exceptional organizational skills.
• Technically savvy and comfortable with scanning software and document systems.
• Familiarity with Good Documentation Practices (GDP); quality assurance knowledge is a plus.
• Previous experience in biotech or pharma preferred, but open to diverse backgrounds.

Work Environment:

The position requires working 100% onsite from 7:00am to 3:30pm, Monday through Friday. The specialist will be part of a quality team consisting of 7-10 people. Strong organizational and communication skills are essential, as the role involves interaction and driving communication across various groups.

Job Type & Location:

This is a Contract position based out of Winslow, Maine.

Pay and Benefits:

The pay range for this position is $20.00 - $25.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type:

This is a fully onsite position in Winslow, ME.

Application Deadline:

This position is anticipated to close on Nov 13, 2025.

About Actalent:

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email acta Lentaccommodation@actalentservices.com for other accommodation options.

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