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QC Analyst

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Carbon

24d ago

  • Job
    Full-time
    Junior & Mid Level
  • Science
    Healthcare
  • Liverpool

AI generated summary

  • You need a degree in Chemistry or related fields, practical experience, GMP knowledge, raw materials testing skills, and strong communication abilities.
  • You will conduct analytical and biosafety testing, ensure precise lab documentation per regulations, and apply technical skills to troubleshoot assays.

Requirements

  • Degree qualified in Chemistry, Biochemistry, Biomedical Science or a related scientific discipline
  • Demonstrated practical experience
  • Prior industrial experience in a GMP regulated environment is highly desirable
  • Knowledge of pharmacopoeias
  • Skills performing raw materials testing highly desired
  • Strong verbal & written communication skills.

Responsibilities

  • Perform analytical, biosafety & cell science testing on raw materials, intermediates and finished products
  • Complete laboratory documentation accurately and in accordance with industry regulatory standards
  • Utilise technical expertise to troubleshoot various assays as required

FAQs

What is the job title for this position?

The job title is QC Analyst - AMB.

Where is the job located?

The job is located in Speke, Liverpool.

What is the hourly rate for this job?

The hourly rate is £15.25 per hour, inclusive of shift uplift.

What are the working hours for this position?

The working hours are 4 days on, 4 days off from 7am to 7pm.

What is the duration of the contract for this job?

The contract duration is 6 months.

What type of products will the QC Analyst be working with?

The QC Analyst will be working with sterile injectable products for the treatment of the flu.

What are the key responsibilities of the QC Analyst?

Key responsibilities include performing analytical, biosafety, and cell science testing on raw materials, intermediates, and finished products, completing laboratory documentation accurately in accordance with regulatory standards, and troubleshooting various assays.

What qualifications are required for this position?

A degree in Chemistry, Biochemistry, Biomedical Science, or a related scientific discipline is required.

Is prior industrial experience in a GMP regulated environment necessary?

Yes, prior industrial experience in a GMP regulated environment is highly desirable.

What skills are highly desired for this role?

Skills in performing raw materials testing and strong verbal & written communication skills are highly desired.

Are there specific knowledge requirements for this position?

Yes, knowledge of pharmacopoeias is required for this position.

Who is handling the recruitment for this vacancy?

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

It's radically better with the Carbon idea-to-production platform.

Manufacturing & Electronics
Industry
201-500
Employees
2013
Founded Year

Mission & Purpose

The Idea-to-Production Platform Rapidly design, develop and scale production of better products in less time with the Carbon platform. Integrated end-use materials, software, and 3D printers enable teams to accelerate bringing products to market — from idea to production. Create radically better products with Carbon.