About the role

Aplyr's Quick Take

This role is about ensuring that equipment and processes in pharmaceutical manufacturing meet quality and compliance standards. You'll be writing and reviewing validation protocols, managing projects, and possibly supervising technicians. It's primarily an individual contributor role focused on technical validation tasks.

Good fit

Ideal candidates have at least 2 years of experience in validation within a regulated environment, preferably with an engineering or life sciences background. A detail-oriented, self-motivated person who can work independently and has strong technical writing skills will thrive here.

Worth noting

The job involves supervising external contractors, which may not be typical for all validation roles. The salary range is competitive for the region, but the specific responsibilities and team dynamics are not fully detailed.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our collaborative team as a Validation Engineer at Thermo Fisher Scientific, where you'll contribute to global healthcare and scientific advancement. In this role, you'll be responsible for ensuring compliance, quality, and operational excellence across our facilities through comprehensive validation activities. Working with advanced technologies and diverse teams, you'll help maintain high standards in pharmaceutical manufacturing, laboratory operations, and quality control.

What will you do?

• Assess and define assigned validation projects, maintain the validation schedule, and ensure all equipment remains in a qualified state to support ISO and/or GMP requirements.
• Write, review, and implement procedures and qualification protocols for standard and customized equipment, systems, and facilities.
• Raise discrepancies and ensure timely closure of test documentation.
• Prepare validation summary reports for completed protocols.
• Conduct deviation investigations, identifying and implementing appropriate corrective actions.
• Act as the primary point of contact for qualification activities with internal (site-based) clients.
• Supervise technicians, fitters, and contractors as required when external support is used for qualification activities.

REQUIREMENTS:
• Advanced degree or a Bachelor's degree with at least 2 years of validation experience in a GMP or regulated environment.
• Preferred Fields of Study: Engineering, Life Sciences, Chemistry, or related technical field
• Comprehensive knowledge of cGMP, FDA regulations, and industry standards (ISO, GAMP5)
• Strong technical writing skills for validation documentation
• Experience with IQ/OQ/PQ protocols and execution
• Proficiency in risk assessment and gap analysis
• Experience managing validation projects independently
• Strong data analysis and problem-solving capabilities
• Strong communication skills in both English and Lithuanian, written and spoken
• Proficient in Microsoft Office applications
• Ability to work in cleanroom environments when required
• Effective interpersonal skills for team collaboration
• Ability to manage multiple projects
• Experience with quality management systems and documentation
• Consistent record of completing projects on schedule in a deadline-oriented environment

WE OFFER:

• An innovative environment within a rapidly growing international company.

• A hard-working, supportive team and leadership committed to your professional development.

• The opportunity to be part of a dynamic organization and work alongside experienced professionals.

• A competitive salary range of €2183–€3270 gross, depending on experience and competencies.

At Thermo Fisher Scientific, each one of our 120,000 extraordinary colleagues has a unique story to tell.

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 €2 183,33–€3 270,83.

Aplyr's read

Thermo Fisher Scientific is a powerhouse in biotechnology, attracting professionals passionate about advancing scientific research and innovation across diverse roles and regions.
Synthesized from recent postings & public sources

What's promising

•Thermo Fisher is a leader in the biotech industry, offering stability and growth potential.
•The company invests heavily in R&D, fostering innovation and cutting-edge solutions.
•Global presence provides diverse career opportunities across multiple regions and disciplines.

What to watch

•High pressure and fast-paced environment may not suit everyone.
•Complex organizational structure can lead to communication challenges.
•Frequent acquisitions may result in uncertainty and change for employees.

Why Thermo Fisher

•Thermo Fisher's broad product portfolio spans laboratory equipment to clinical diagnostics.
•The company plays a crucial role in global scientific advancements and healthcare solutions.
•Strong focus on sustainability and corporate responsibility sets it apart in the industry.

Aplyr’s read is generated by AI from public sources. Was it useful?

About Thermo Fisher

Thermo Fisher

thermofisher.com

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Thermo Fisher Scientific is a global leader in serving science, providing a range of products and services to help researchers and scientists in laboratories and clinical settings.