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Quality Control Analyst

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Manchester

On-site

GBP 60,000 - 80,000

Full time

11 days ago

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Job summary

An established industry player is seeking a QC Scientist to enhance their Quality Control Department. This role involves hands-on analytical testing, including U/HPLC and dissolution testing, in a GMP environment. The successful candidate will contribute to setting up a new facility and implementing a Laboratory Information Management System (LIMS) for a paper-free lab. This is a fantastic opportunity for a motivated individual to join a rapidly expanding organization that values expertise and innovation in pharmaceutical manufacturing. If you have a passion for quality control and a strong scientific background, this position is perfect for you.

Qualifications

  • Degree level education with hands-on HPLC experience in a GMP environment.
  • Extensive experience in an analytical lab with knowledge of regulatory requirements.

Responsibilities

  • Execute U/HPLC testing and conduct dissolution testing on various products.
  • Support QC department with validation and setup of the new facility.

Skills

HPLC Testing
Analytical Chemistry
Dissolution Testing
Good Manufacturing Practice (GMP)
Laboratory Information Management System (LIMS)

Education

Degree in a relevant scientific discipline

Tools

U/HPLC

Job description

Job Description

Are you an experienced QC Analyst looking for an exciting new challenge to help shape the Quality Control Department of a contract pharmaceutical manufacturing organisation?

Job Title: QC Scientist – Analytical Chemistry

Type: Permanent

Salary: Highly attractive with great benefits

Location: Northwest, England

SRG is currently working exclusively with a highly successful, award winning, contract development and manufacturing organisation, focused on providing expert intelligence and support to their partners, driven by their capabilities.

As a result of rapid expansion, we are looking for a QC Analyst to support the QC department with analytical testing, QC validation and helping set up their new facility.

Typical responsibilities/accountabilities:

  1. Execute hands-on U/HPLC testing on a range of products.
  2. Conduct dissolution testing.
  3. Perform pharmacopeial methods such as IR, Appearance, pH, CU, and water content.
  4. Adhere to Good Manufacturing Practice (GMP) standards using a new electronic Quality System.
  5. Contribute to the setup of the facility and laboratory, and actively participate in building the LIMS system.
  6. Support activities to qualify equipment required for QC testing, ensuring compliance with current European Pharmacopoeia and ICH requirements, and participate in the calibration of analytical equipment as needed.
  7. Contribute to the creation and review of Plans, Methodologies, Work Instructions, and Standard Operating Procedures (SOPs).
  8. Hands-on contribution to building a LIMS system to transition to a paper-free lab.

Essential Requirements:

  1. Educated to Degree level in a relevant scientific discipline along with significant, recent hands-on experience of using HPLC and carrying out dissolutions within a GMP environment.
  2. Extensive experience in an analytical laboratory environment with a sound understanding of regulatory requirements.
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