QC Raw Material Sampling Scientist

JR United Kingdom; Reading; On-site; GBP 125,000 - 150,000; Full time

Job summary

A global biopharmaceutical company is seeking a QC Raw Material Sampling Scientist for a 6-month contract in Slough. Ideal for graduates in Chemistry, this role involves sampling management, documentation, and collaboration with various teams, ensuring adherence to GMP standards.

Qualifications

• Graduate in Chemistry or a related degree.
• 6 months industrial experience in a GMP setting.
• Desirable practical experience in industrial or academic settings.

Responsibilities

• Generation of sampling labels and documentation of transfer.
• Testing samples and ensuring compliance with GMP procedures.
• Coordinating with various departments to resolve issues.

Skills

GMP procedures

Documentation

Collaboration

Education

BSc/MSc in Chemistry

Job description

Job Title: QC Raw Material Sampling Scientist – Global Biopharmaceutical

Contract: 6 months

Location: Slough

Salary: £19.50 per hour

Hours: 37.5 hours per week

This is a great opportunity for a graduate in Chemistry or a related degree looking for their next role in the industry. Candidates must have at least 6 months of industrial experience in a GMP setting.

Key Responsibilities include:

1. Generation of sampling labels
2. Transfer of raw materials on GMP electronic systems
3. Transfer of raw material containers into sampling clean room environment
4. Opening and sampling of raw material containers following GMP procedures
5. Documentation of transfer and sampling in logbooks and GMP documents
6. Returning raw material containers to original stock location
7. Transferring sampled raw materials to QC laboratory
8. Maintaining ambient raw material retention sample storage area
9. Assisting with disposal of raw material retention samples
10. Coordinating with Warehouse, Supply Chain, and Procurement to resolve issues
11. Ensuring calibration dates for rooms and equipment are maintained
12. Collaborating with engineering and validation for maintenance planning
13. Supervising cleaning and usage logbooks, maintaining high standards
14. Raising EWRP paper/electronic system reports
15. Testing samples and reporting results per GMP procedures
16. Leading or assisting with creation and completion of quality records such as Deviations, Change Controls, OOS/OOT, CAPAs

Candidate Requirements:

1. BSc/MSc Degree in Chemistry or a related field
2. Practical experience in an industrial or academic setting is desirable