Regulatory Documentation Specialist

hace 2 semanas


Xico, México Thermo Fisher Scientific A tiempo completo
About Thermo Fisher Scientific

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. As a leader in the scientific community, we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies.

Our Mission

We enable our customers to make the world healthier, cleaner, and safer by accelerating research, solving complex scientific challenges, driving technological innovation, and supporting patients in need.

Salary Information

The estimated annual salary for this position is $80,000 - $110,000 depending on experience and qualifications.

About the Role

As a Senior Compliance Specialist within our Quality function, you will execute compliance and quality strategies within the organization as related to document administration. This involves overseeing the creation, periodic review, revision, and retirement of controlled documents. This role will maintain tools and materials, serve as project lead, and provide mentoring and expertise to advance the vision of the department.

Key Responsibilities:
  • System Configuration: Impact assessment (project and system), develop business requirements, test in various environments, prepare for validation
    - Business and account administration for EDMS
    - Researches and addresses issues, tracks metrics, reporting, and documentation related to quality and compliance activities.
    - Communicates to ensure quality and timelines are maintained with respect to compliance activities around documentation procedures.
    - Leads smaller projects and/or some process/quality improvement initiatives.
Requirements:
  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
    - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
Preferred Skills:
  • Strong working knowledge of Part 11, GAMP 5, and other industry standard validation standards
    - Strong working knowledge of document management
    - Experience working with Electronic Data Management Systems (such as VEEVA, Documentum, Master Control, etc)
    - Knowledge of GXP regulations
    - Excellent oral and written communication skills
    - Strong organizational and time-management skills
    - Demonstrated problem-solving skills
    - Excellent attention to detail
    - Strong computer skills: ability to learn and become proficient with appropriate software
    - Demonstrated ability to multitask and prioritize competing demands/workload
    - Proven flexibility and adaptability
Our Values

We share a common set of values - **Integrity, Intensity, Innovation, and Involvement** - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need.



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