Team Leader, QC Stability & Finished product

Thermo Fisher Scientific; Ferentino; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical sector is seeking a Team Leader for QC Stability & Finished Product in Ferentino, Italy. The role involves supervising laboratory activities, ensuring compliance with GMP regulations, and enhancing customer satisfaction. The ideal candidate will hold a relevant degree and have significant experience in quality control and team management.

Competenze

• Experience in QC chemical laboratory (min 2 years).
• Multi-year experience in people management (min 1 year).
• Experience in development and validation of analytical methods (min 2 years).

Mansioni

• Supervise and coordinate analytical activities ensuring timely delivery.
• Support scientists in drafting specifications and methods.
• Ensure compliance with GMP and company quality standards.

Conoscenze

Leadership

Problem-Solving

Knowledge of GMP regulations

Proficiency in Microsoft Office

Statistical software proficiency

Formazione

Degree in CTF, Chemistry, Biology or similar

Diploma Chemical/Laboratory technician certificate

Strumenti

Empower

MiniTab

Sample Manager

Descrizione del lavoro

Team Leader, QC Stability & Finished product

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Team Leader, QC Stability & Finished product

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Environmental Conditions

Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

When you’re part of Thermo Fisher Scientific, you’ll have the chance to actively performs significant and important work, like helping customers in finding innovative life-saving treatments for severe diseases, protecting the environment or making sure our food is safe. Your work will have real-world implication and impact, and you’ll be supported in achieving your career goals. You will join a team with wide-ranging strengths!

Location/Division Specific Information:

Ferentino, Italy

How will you make an impact?

You will supervise and coordinate analytical activities through effective/efficient planning and progress control, to meet OTD/RFT (timely delivery / right first time) and support client in achieving their requests.

What will you do?

• Ensures both the coordination, execution and constant supervision of analytical laboratory activities for projects assigned in accordance with GMP requirements, supporting analysts in problems solving.
• Supports scientists in drafting analytical specifications, study protocols/reports and analytical methods. Writes and review SOPs in compliance with current regulations (current EU GMP, US GMP) and company quality standards.
• Coordinates along with the Supervisor and Manager the customer's management with the aim of maintaining a high level of customer happiness and completing the required activities on schedule.
• Participates in calls/meetings with customers to support the discussion on technical topics for their area of expertise.
• Collaborates with the Supervisor to identify the requirements for analytical technology transfer from customers, then ensuring the accurate and effective transfer to the laboratories.
• Collaborates with the Supervisor in handling laboratory investigations (Out of Specification and Deviation Reports).
• Ensure the execution of Method Development and/or Method Validation for assigned projects.
• Ensure effective management of the Team and resources assigned.
  
  

How will you get here?

Education:

• Degree in CTF, Chemistry, Biology or other similar fields.
• Diploma Chemical/Laboratory technician certificate.
  
  

Experience:

• Experience in QC chemical laboratory within pharmaceutical industries (min 2 years).
• Multi-year experience in people management (min 1 year).
• Experience in development/validation/transfer of analytical methods (min 2 years).
  
  

Knowledge, Skills, Abilities:

• Knowledge of GMP and national/international regulations.
• Good problem-solving abilities and Leadership experience.
• Proficiency in Microsoft Office suite and both analytical and statistical software (Empower, MiniTab, Sample Manager).
• Be prepared to work with conflicting priorities, under time constraints and in a multifaceted environment.
  
  

At Thermo Fisher Scientific, each one of our 70,000 outstanding minds has a unique story to tell. Join us and give yourself the opportunity to collaborate with us in our important mission—enabling our customers to make the world healthier, cleaner and safer.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance, Product Management, and Engineering

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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