Sr Document Control Administrator

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our collaborative team at Thermo Fisher Scientific as a Sr Document Control Administrator where youll contribute to maintaining documentation excellence across our operations. Youll be responsible for managing and optimizing document control processes that support our mission of enabling customers to make the world healthier cleaner and safer. Working with cross-functional teams youll ensure compliance with GMP standards while coordinating change control procedures for critical documentation. This position offers opportunities to enhance documentation processes and contribute to the quality assurance of our products and services.

REQUIREMENTS:
Minimum 2 years experience in document control or quality systems in a regulated environment
Preferred Fields of Study: science business administration or related field
Relevant technical certifications in GMP/GxP documentation practices a plus
Proficiency in document management systems and quality control software (e.g. Agile SAP OCPLM TrackWise E1)
Strong working knowledge of GMP requirements and documentation practices
Advanced Microsoft Office skills particularly in Excel and Word
Excellent attention to detail and organizational abilities
Strong written and verbal communication skills
Ability to manage multiple priorities and meet deadlines
Experience with change control procedures and quality management systems
Additional language skills beneficial
Demonstrated ability to work independently and collaborate effectively with cross-functional teams
Experience with batch record review and documentation preferred

Compensation and Benefits

The hourly pay range estimated for this position based in New York is $19.83$29.74.

This position may also be eligible to receive a variable annual bonus based on company team and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on which includes:

• A choice of national medical and dental plans and a national vision plan including health incentive programs

• Employee assistance and family support programs including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO) 10 paid holidays annually paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave) accident and life insurance and short- and long-term disability in accordance with company policy

• Retirement and savings programs such as our competitive 401(k) U.S. retirement savings plan

• Employees Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits please visit: Experience:

Senior IC