Overview
Join to apply for the QC Analyst role at Thermo Fisher Scientific
The Binding Site Group, a part of Thermo Fisher Scientific, is a global leader in specialty diagnostics, provides diagnostic assays and instruments to improve the diagnosis and management of blood cancers and immune system disorders. The Binding Site’s Freelite offering is widely recommended for multiple myeloma diagnosis and monitoring across all stages of the disease by major clinical guideline publications. In addition, The Binding Site is an active and influential contributor to the broader scientific community. To find out more visit www.bindingsite.com
Day in the Life / Responsibilities
* Ensure regulatory and quality system compliance for components by adhering to the Quality Management System.
* Conduct inspections of raw materials and finished goods, perform raw materials testing, and archive inspection document records.
* Investigate quality and technical issues, propose corrective actions, and collaborate with other departments for resolution.
* Maintain and calibrate equipment, respond to product changes and new product development, and manage change orders.
* Complete daily work activities promptly, including control plan setup/amendments and undertake QC process improvement projects.
* Raise and manage minor changes.
Environmental Conditions & Work Schedule
* Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22 degrees F/-6 degrees C, Laboratory Setting, Office, Some degree of PPE (safety glasses, gowning, gloves, lab coat, ear plugs, etc.), Warehouse, Will work with hazardous/toxic materials.
* Working hours: 8:00 to 16:30 - Monday to Friday
* Location: UK - Birmingham - 27 Sovereign Rd
* Direct Report To: Supervisor, QC
* Group/ Division: Protein Diagnostics (PDX) / Specialty Diagnostics Group (SDG)
* Career Band: 3
Education
* GCSE Maths and English (Grade A – C) or equivalent
Experience
* Required: Minimum of 2 years of work experience in QA or QC or related field
* Preferred: Experience in a cGMP environment or other highly regulated environment
Knowledge, Skills, Abilities
* Experience of QC checking processes – either raw material, in process or finished product
* Excellent communication skills (both written and verbal)
* Excellent attention to detail
* Ability to plan and prioritize own workload to meet the objectives of the department
* Confident in basic use of Microsoft Office applications, especially Word
Physical Requirements / Work Environment
* Willingness to work in various environments such as Office, Warehouse, Laboratory and Assembly area; may involve manual handling and operating Hand Pallet Truck; wear PPE as required in Warehouse and Laboratory areas
* Willingness to travel off-site to establishments within a 20 mile radius (infrequent)
Employment type
* Full-time
Job function
* Quality Assurance, Product Management, and Engineering
* Industries: Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Thermo Fisher Scientific by 2x
Get notified about new Quality Control Analyst jobs in Birmingham, England, United Kingdom.
#J-18808-Ljbffr