QA Inspector

QA Inspector Thermo Fisher Scientific - 3.4 Allentown, PA Job Details Full-time 1 day ago Qualifications Laboratory instruments Analytical chemistry Procedural guides Technical documentation Safety standards in production Laboratory information management systems GMP Team management Laboratory quality control Mentoring Technical writing Quality standards in production Cleanroom Technical Proficiency Full Job Description Work Schedule Third Shift (Nights) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP)

Safety Standards, Cleanroom:

no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, 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.

DESCRIPTION

Join our team at Thermo Fisher Scientific as a Lead QC Technician, where you'll help make the world healthier, cleaner and safer. In this important role, you'll ensure quality standards are met through testing and inspection of products in a cGMP environment. You'll coordinate quality control activities, lead a team of QC technicians, and collaborate with cross-functional teams to maintain the highest quality standards. You'll perform analytical testing, document results, and support continuous improvement initiatives while mentoring team members.

REQUIREMENTS

Minimum 4 years of experience in quality control within a regulated environment (pharmaceutical/medical device preferred)

Preferred Fields of Study:

Chemistry, Biology, or related scientific field Demonstrated proficiency with analytical testing equipment and techniques (HPLC, GC, spectrophotometry) Strong understanding of cGMP requirements and quality systems Experience with quality documentation and data review Proven ability to lead and mentor others while maintaining quality standards Excellent attention to detail and organizational skills Strong verbal and written communication abilities Proficiency with standard office software and LIMS systems Ability to work in cleanroom environments and follow gowning procedures Physical ability to stand for extended periods, lift up to 25 lbs occasionally Flexibility to work various shifts as needed Problem-solving skills and ability to troubleshoot technical issues Experience writing and reviewing SOPs and technical documentation