Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

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.

How will you make an impact?
Join our collaborative team at Thermo Fisher Scientific, where you'll contribute to our mission of making the world healthier, cleaner, and safer. As a QC Scientist III, you'll perform sophisticated analytical testing and provide quality oversight for biopharmaceutical products. You'll work with advanced technology and collaborate with cross-functional teams to ensure product safety and compliance with regulatory requirements. This role offers significant opportunities to grow your expertise while supporting the development and manufacturing of life-changing therapeutics.

You'll conduct complex analytical testing, lead method validations, perform data review, and troubleshoot technical issues. Key responsibilities include executing and reviewing tests for product release, stability, and in-process samples; authoring and reviewing technical documentation; participating in investigations; and interfacing with clients and regulatory authorities. Your work will directly impact patient safety and product quality while advancing scientific innovation.

How will you get there?

• Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in GMP pharmaceutical/biopharmaceutical quality control
• Preferred Fields of Study: Chemistry, Biology, Biochemistry, or related scientific field
• Expertise in analytical techniques such as HPLC, UPLC, CE-SDS, cIEF/ICE, ELISA, and cell-based assays
• Strong knowledge of FDA, EMA, ICH, and GxP regulations
• Experience with method validation, transfer, and qualification
• Proficiency in data analysis and laboratory information management systems
• Advanced technical writing and documentation skills
• Strong project management and organizational abilities
• Excellent interpersonal and communication skills
• Ability to work independently and lead cross-functional teams
• Experience with quality investigations and CAPAs
• Proficiency with Microsoft Office Suite and relevant analytical software
• Ability to wear PPE and work in laboratory environments
• May require weekend/flexible scheduling based on business needs
• Physical requirements include standing, lifting up to 25 lbs, and manual dexterity
• Strong attention to detail and problem-solving skills
• Experience mentoring team members preferred

Job Tags

Remote job, Full time, Work at office, Flexible hours, Weekend work,

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