QC Raw Material Sampling Scientist

SRG; Slough; On-site; GBP 100,000 - 125,000; Full time

Job summary

A leading company in the biopharmaceutical industry is seeking a QC Raw Material Sampling Scientist for a 6-month contract in Slough. This entry-level position is ideal for graduates with a Chemistry background and involves critical GMP processes, including sampling and documentation. The role requires good technical laboratory skills and a strong GMP background, offering a chance to gain valuable experience in a dynamic environment.

Qualifications

• At least 6 months industrial experience in a GMP setting.
• Practical experience within an industrial/academic setting is desirable.

Responsibilities

• Generation of sampling labels and transfer of raw materials.
• GMP documentation of transfer and sampling.
• Testing of samples and reporting results.

Skills

GMP

Technical laboratory skills

Education

BSc/MSc Degree in Chemistry

Job description

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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 a Chemistry or related degree looking for their next role in the industry. You must have at least 6 months industrial experience in a GMP setting.

Key Responsibilities will include:

• Generation of sampling labels
• Transfer of raw materials on GMP electronic systems
• Transfer of raw material containers into sampling clean room environment
• Opening and Sampling of Raw Material containers following appropriate GMP procedures
• GMP documentation of transfer and sampling in logbooks and GMP documents
• Returning of raw material containers to original stock location
• Transfer of sampled raw materials to QC laboratory
• Maintaining ambient raw material retention sample storage area
• Assist with the disposal of Raw Material retention samples
• Coordinates with Warehouse, Supply Chain and Procurement to solve problems and raise issues.
• Be aware and ensure calibration dates for the room and equipment are maintained
• Work with engineering and validation to plan and schedule maintenance activities
• Be the responsible supervisor for cleaning and usage logbooks, ensuring they are maintained to a high standard and are routinely signed
• Raise EWRP paper bases / electronic system
• Testing of samples and reporting of all results according to the relevant procedures in accordance with the expectations of GMP
• Lead or assist with creation and completion of quality records including; Deviations, Change Controls, OOS / OOT, CAPA’s Tasks

Candidate Requirements:

• BSc/MSc Degree in Chemistry or related field.
• Practical experience within in an industrial/academic setting is desirable.
• Strong GMP background.
• Good Technical laboratory skills.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Pharmaceutical Manufacturing

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