PDS Analytical Development & GMP Scientist
Italy - FerentinoUpdate time: October 13,2020
Job Description

When you are part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
 
Location/Division Specific Information
The pharmaceutical manufacturing plant in Ferentino (80km from Rome), with more than 850 employees, is specialized in commercial contract manufacturing of injectable drugs, both liquid and lyophilized, with an increasing focus on biologics.
 
How will you make an impact?
You will be part of a dynamic, multinational and result-driven environment. As Analytical Development & GMP Scientist, working with the Team Leader/Supervisor/Manager, you will supervise and execute (if needed) all the chemical testing related to the API/DS, bulk and final product.
The Analytical Development & GMP Scientist is part of the Quality Department and you will ensure an efficacy communication with the clients for what concern the analytical activities.
 
What will you do?           
 

  • Responsible for method validation and related development work;
  • Support all the formulation development activities;
  • Evaluate and run analytical trend (if needed), design and run stability study and ensure the compliance of all the analysis run to the policy in force;
  • As SME (Subject Matter Expert), is responsible to support the investigations to run as part of the deviation department specific.
  • Working with the Team Leader/ Supervisor/Manager, the PDS AD & GMP Scientist has the responsibility to:
  • Manage the assigned resources in the team;
  • Schedule the analytical activities foreseen for the project in line with the fixed project plan to get OE/RFT/OTD (operational excellence, right first time, on time delivery).
 
How will you get here?

Education
Scientific Degree (pharmacy, CTF, Biology, Biotechnology, chemistry)
 
Experience
  • 1-3 years of experience in Analytical/Quality Control labs
  • Knowledge of GMP, ISP
  • Previous experience in manufacturing of sterile injectable drugs will be considered a plus
 
Knowledge, Skills, Abilities
  • Fluent in Italian and English
  • Problem solving skills
  • Team working and excellent communication skills with both internal and external stakeholders

 
At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
 
Apply today! http://jobs.thermofisher.com
 
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.
 

Get email alerts for the latest"PDS Analytical Development & GMP Scientist jobs in "