Regulatory Affairs Specialist III

Thermo Fisher Scientific Oslo, Norway

Company

Thermo Fisher Scientific

Location

Oslo, Norway

Type

Full Time

Job Description

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

We are currently seeking a Regulatory Affairs (RA) Specialist to join Biosciences Division Regulatory Affairs Team. As a member of the RA team, you will be planning, managing, and tracking of regulatory CMC submissions and regulatory documentation, including Drug Master Files for raw, ancillary, and starting materials used in the manufacturing of cell and gene therapies.

Key responsibilities:

  • Support of activities at Thermo Fisher Scientific site(s) located in Norway for the bead-based technology products and processes (part time).
  • Serving as the liaison between Research scientists and key cross-functional partners, including Regulatory Affairs, Quality Control, Manufacturing Sciences, Product Management, and IP Legal.
  • Collecting, consolidating and ensuring accuracy of documentation required for regulatory support in target markets (EU, US, and other global markets).
  • Creating and maintaining up to date product technical documentation - Master Files.
  • Reviewing and approving product labeling and marketing information to assure compliance with the applicable requirements.
  • Providing regulatory support and expertise to new product introduction project teams and different departments.
  • Participating in change control activities by evaluating impact of manufacturing changes on technical documentation and submitting updates to the competent authorities.
  • Developing regulatory affairs internal policies and procedures and providing trainings as and when required.
  • Appropriately handling confidential information.

Want more jobs like this?

Get jobs in Oslo, Norway delivered to your inbox every week.

By signing up, you agree to our Terms of Service & Privacy Policy.

Requirements for qualification / education / experience:

  • University degree in life sciences.
  • Familiar with global Health Authority regulations/guidances eg. FDA regulations, ICH and EMA guidelines/directives. Understanding of QMS standards (e.g. ISO 9001, ISO 13485) and GMP requirements.
  • Experience in the field of regulatory affairs and/or in the pharmaceutical or medical device manufacturing company for over 3 years.
  • Abilities to plan, prioritize and coordinate working process independently and with minimal direction.
  • Proficiency with computer programs/systems (MS office, etc.) with demonstration. Ability to learn new systems quickly.
  • Strong analytical skills and problem-solving skills. Ability to coordinate and work effectively with cross-functional teams.
  • Willingness to travel 2-10% of time.

We offer:

  • The innovative environment of the rapidly growing international company with encouraging working culture and outstanding development possibilities to increase your potential.
  • An opportunity to work in a dynamic global organization and collaborate with expert professionals.

Apply today! http://jobs.thermofisher.com

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

Compensation
The monthly salary range estimated for this position based in Lithuania is €2 625,00-€3 500,00.

Apply Now

Date Posted

12/23/2024

Views

0

Back to Job Listings ❤️Add To Job List Company Info View Company Reviews
Positive
Subjectivity Score: 0.8

Similar Jobs

Mainframe DB2 Infrastructure Specialist for z/OS - Kyndryl

Views in the last 30 days - 0

Kyndryl is seeking a skilled Mainframe DB2 System Programmer with extensive experience The role involves designing building managing and modernizing m...

View Details

Project Quality specialist - Hitachi Energy

Views in the last 30 days - 0

Hitachi Energys Grid Power Quality Solutions and Service global product group is a leading provider of grid connections and power quality solutions a...

View Details

Sales Account Manager Grid Software - Nordics - GE Vernova

Views in the last 30 days - 0

The role involves identifying qualifying and growing sales and customer base in the Transmission and Distribution domain in the Nordics and Baltic reg...

View Details

Program Manager, Logistics Operations Specialist - Google

Views in the last 30 days - 0

Google is seeking a Logistics Operation Specialist for Server Operations Logistics The role involves leading thirdparty logistics team and managing al...

View Details

Order Fulfillment Specialist (OFS) - GE Vernova

Views in the last 30 days - 0

Grid Solutions a global leader in power grid solutions is seeking an OFS for Electricity Substation projects in Norway The role involves delivering co...

View Details

Senior analyst, Risk Management - Mastercard

Views in the last 30 days - 0

Mastercard is seeking a Senior Risk Governance and Framework professional to join their Governance Risk and Control team in MPS RTP The role involves ...

View Details