QC Analyst
QC Analyst
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cold Room/Freezers -22degreesF/-6degrees C Laboratory Setting Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Warehouse Will work with hazardous/toxic materialsJob Description
Working hours: 8:00 to 16:30 - Monday to Friday
Direct Report To: Supervisor QC
Group/ Division: Protein Diagnostics (PDX) / Specialty Diagnostics Group (SDG)
Career Band:3
Position Location: UK - Birmingham - 27 Sovereign Rd
Location/Division Specific Information:
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 Sites Freelite offering is widely recommended for multiple myeloma diagnosis and monitoring across all stages of the disease by major clinical guideline addition The Binding Site is an active and influential contributor to the broader scientific community. To find out more visit
A Day in the Life:
In this role you will:
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.
Keys To Success
Success in this role includes excellent communication attention to detail problem-solving abilities knowledge of regulatory requirements strong organizational skills and a dedication to continuous learning.
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. This may involve manual handling and operating Hand Pallet Truck. This also involves wearing appropriate PPE (in the Warehouse and in the Laboratory area).
Willingness to travel off-site to establishments within a 20 mile radius (infrequent).
Required Experience:
IC
Employment Type
Full-Time
