Team Leader, QC Chemical & GMP

Experteer Italy; Ferentino; In loco; EUR 40.000 - 80.000; Tempo pieno

Descrizione del lavoro

An established industry player seeks a dedicated professional to supervise analytical activities in a dynamic environment. This role involves ensuring compliance with GMP standards, managing a team, and supporting clients with their analytical needs. You will collaborate with scientists to draft specifications and lead laboratory investigations, making a significant impact on the quality of life-saving treatments. Join a mission-driven team where your contributions will help shape a healthier and safer world.

Competenze

• Minimum 2 years in QC chemical laboratory within the pharmaceutical industry.
• At least 1 year in people management.

Mansioni

• Supervise and coordinate analytical laboratory activities ensuring compliance with GMP.
• Support scientists in drafting specifications and review SOPs.

Conoscenze

Analytical Techniques

Problem-Solving

Leadership

GMP Knowledge

Microsoft Office

Formazione

Degree in Chemistry

Diploma in Chemical/Laboratory Technician

Strumenti

Empower

MiniTab

Sample Manager

Descrizione del lavoro

Work Schedule
Other
Environmental Conditions
Office

Job Description

When you're part of Thermo Fisher Scientific, you'll have the chance to actively perform significant work, such as helping customers find innovative life-saving treatments for severe diseases, protecting the environment, or ensuring food safety. Your work will have real-world impact, and you'll be supported in achieving your career goals. Join a team with diverse strengths!

Location/Division Specific Information

Ferentino, Italy

How will you make an impact?

You will supervise and coordinate analytical activities through effective planning and progress control to meet OTD/RFT (On-Time Delivery / Right First Time) and support clients in achieving their requests.

What will you do?

• Ensure coordination, execution, and supervision of analytical laboratory activities for assigned projects in accordance with GMP requirements, supporting analysts in problem-solving.
• Support scientists in drafting analytical specifications, study protocols/reports, and analytical methods. Write and review SOPs compliant with current EU GMP, US GMP, and company standards.
• Coordinate with the Supervisor and Manager to manage customer relations, maintaining high customer satisfaction and completing activities on schedule.
• Participate in calls and meetings with customers to support technical discussions.
• Collaborate with the Supervisor to identify requirements for analytical technology transfer from customers and ensure effective transfer to laboratories.
• Assist in handling laboratory investigations such as Out of Specification and Deviation Reports.
• Ensure the execution of Method Development and Validation for assigned projects.
• Manage the team and resources effectively.

How will you get here?

Education:

• Degree in Chemistry, Biology, or related fields.
• Diploma in Chemical/Laboratory technician certification.

Experience:

• Minimum 2 years in QC chemical laboratory within the pharmaceutical industry.
• At least 1 year in people management.
• Minimum 2 years in development, validation, or transfer of analytical methods.

Knowledge, Skills, Abilities:

• Knowledge of chemical-physical and biochemical analysis techniques and validation of analytical methods.
• Understanding of GMP and relevant regulations.
• Strong problem-solving skills and leadership experience.
• Proficiency in Microsoft Office, Empower, MiniTab, Sample Manager.
• Ability to work under conflicting priorities and in a dynamic environment.

At Thermo Fisher Scientific, each of our 70,000 team members has a unique story. Join us to collaborate in our mission to make the world healthier, cleaner, and safer.