QA Specialist III, Quality on the Floor (12-hour days)

Thermo Fisher Scientific

26d • Onsite

About The Position

In this position, you’ll drive quality execution across the sterile operations including manufacturing, filling, packaging and inspection, and associated non batch specific activities in for both commercial and product development services products. Additionally, this position will provide quality guidance and expertise for implementation of practical process improvements and continuous improvement initiatives. Typical hours are 6a - 6p, on a 2-2-3 rotation.

Requirements

• Bachelor’s degree, preferably in technology, engineering or microbiology related field required.
• 5+ years of experience with previous experience in Quality Assurance or Quality control or Operations/Manufacturing required
• Previous experience in pharmaceutical industry; preferably aseptic or steriles processes strongly preferred, experience in other GMP environments may be considered (i.e. ISO 9001)
• An equivalent combination of education and relevant experience may be considered.
• Ability to capture data, analyze & troubleshoot process issues, equipment problems along with production leadership
• Ability to troubleshoot process and equipment issues
• Hard-working, demonstrated ownership & responsibility;
• Ability to lead, support & empower a team/peers
• Technical Writing experience
• Primary responsibilities require consistent production floor presence which necessitate physical fitness for prolonged standing, walking, and repetitive bending, and aseptic and non-aseptic gowning.

Nice To Haves

• Professional certifications (ex: CQA) and training (Six Sigma) are a plus

Responsibilities

• Perform daily quality assessments of facility, personnel, and documentation both classified and non-classified areas to uncover errors or deficiencies, assure quality, and compliance per site procedures and cGMPs.
• Daily interaction with employees to assist with troubleshooting, documentation corrections/notes, and guidance with aseptic technique
• Champions quality culture by aiding personnel in understanding application of policies and controls
• Participates in RAPID event response and provides quality guidance for deviation events
• Advances deviation events to the appropriate area and quality management
• Performs quality review and approval of procedures, training documents, and forms of moderate to high complexity
• Performs quality review and approval of deviation and change control of moderate to high complexity
• Participates as the quality assurance representative in Root Cause Analysis to support deviation investigations of moderate to high complexity
• Performs quality batch record review
• Aids in identification of continuous improvement opportunities; Participates in practical process improvement initiatives

Benefits

• We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
• Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.
• We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees