QC analyst

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

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

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.

Location/Division Specific Information:
Tilburg, The Netherlands

How Will You Make an Impact?:
Join our team at Thermo Fisher Scientific as a QC Analyst, where you'll help make the world healthier, cleaner, and safer. In this important role, you'll ensure quality standards are met through product testing and inspection in a cGMP environment. You'll perform quality control activities and collaborate with cross-functional teams to maintain the highest quality standards. You'll perform analytical tests, document results, and support continuous improvement initiatives.

A Day in the Life:
Perform Finished product testing on gelatin based softgel capsules
Perform testing on Raw materials to start production


Education: (NA or APAC)
High school diploma or equivalent required.
Education: (EMEA)
Completed degree in Chemistry, Biology, or a related scientific field

Experience:
Required: No previous work experience required
Preferred: Experience in Quality Assurance or Quality Control
Preferred: Experience in a cGMP environment

Knowledge, Skills, Abilities:
2-3 years of experience in quality control within a regulated environment (preferably pharmaceutical/medical device)
Basic knowledge of analytical testing equipment and techniques (HPLC, GC, spectrophotometry)
Understanding of cGMP requirements and quality systems
Experience with quality documentation and data control
Good attention to detail and organizational skills
Good verbal and written communication skills
Basic knowledge of standard office software and LIMS systems
Ability to work in cleanroom environments and follow garment procedures
Physical ability to stand for extended periods, occasionally lifting up to 25 kg
Flexibility to work different shifts as needed
Problem-solving skills and ability to resolve technical issues
Basic experience following SOPs and technical documentation

What We Offer:

Compensation
Competitive Pay
Performance Related Bonus where eligible
Annual merit performance-based increase

Excellent Benefits
Medical benefits
Paid Time Off/Annual Leave
Employee Referral Bonus
Career Advancement Opportunities