Document Control Administrator II

Work Schedule

Environmental Conditions

Job Description

Join Thermo Fisher Scientific to contribute globally making a positive impact daily.

Location/Division Specific Information:

Marietta Manufacturing site is in the Laboratory Products Division providing equipment for pharmaceutical and biotechnology research.

How Will You Make an Impact:

In this role you will play a crucial part in ensuring flawless documentation practices which are essential for maintaining our worldclass standards. Your meticulous attention to detail will help us strictly adhere to regulatory requirements and successfully implement continuous improvement initiatives.

You will ensure that all documents are accurate uptodate and aligned with industry standards and regulations reducing the risk of noncompliance issues.

You will improve communication and collaboration across departments by providing easy access to accurate and consistent documentation.

By implementing efficient document control processes and systems you will help streamline workflows reduce redundancies and improve overall efficiency.

By managing project documentation effectively you will support project managers in meeting deadlines and achieving project goals

A Day in the Life:

• Review DHRs for Good Documentation Practice and Good Manufacturing Practice.
• Inspect measure and report Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP) performance of reviewed records.
• File records (electronic or hard copy) in designated locations retrieve as necessary to support the business.
• Perform and record inspections / acceptance control and release of manuals.
• Identify errorcheck log and file documents critical to GMP compliance.
• Assist in the creation revision and formatting of standard operating procedures (SOPs) work instructions and other controlled documents.
• Lead change control processes ensuring that all document changes are accurately reviewed approved and implemented.
• Handle the retention and archiving of documents in accordance with company policies and regulatory requirements.
• Participate in continuous improvement initiatives to improve document control processes and systems.
• Stay updated with regulatory requirements and industry standards to ensure ongoing compliance.
• Work closely with other departments such as Quality Assurance Manufacturing and Supervisor/Managers to ensure document control processes align with their needs.
• Monitor and report on critical metrics linked to document control activities.

Education:

High school diploma or equivalent experience required.

Experience:

• Required: Minimum of 1 year of work experience in QA or QC or related field
• Preferred: Experience in a cGMP environment

Knowledge Skills Abilities:

• SAP experience desired
• Strong attention to detail
• Written and verbal communication skills
• Experience with Microsoft Office

Physical Requirements / Work Environment

• Ability to lift up to 35 lbs unassisted unpackage / repackage materials

What We Offer

Compensation

• Competitive Hourly Pay Rate
• Annual performancebased bonus
• Annual merit performancebased increase

Excellent Benefits

• Benefits & Total Rewards Thermo Fisher Scientific
• Medical Dental & Vision benefitseffective Day 1
• Paid Time Off & Designated Paid Holidays
• Retirement Savings Plan
• Tuition Reimbursement
• Employee Referral Bonus
• Career Advancement Opportunities

Apply today!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.

Accessibility/Disability Access

Thermo Fisher Scientific provides accessibility services for job seekers needing accommodations during the application process. This includes help for hearing vision mobility or cognitive challenges.

• Dedicated telephone line for job seekers with disabilities needing application process accommodations.