QC Analyst

TieTalent; Stockport; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading contract pharmaceutical manufacturing organization is seeking two QC Analysts to join their Quality Control Department in Stockport. The role involves executing hands-on analytical testing and supporting the setup of laboratories and compliance with GMP standards. If you have a degree in a relevant scientific field and experience with HPLC, we want to hear from you.

Qualifications

• Minimum 2 years' experience in pharmaceutical sciences.
• Experience in an analytical laboratory environment with regulatory understanding.

Responsibilities

• Execute hands-on U/HPLC testing on a range of products.
• Conduct dissolution testing and perform pharmacopeial methods.
• Contribute to the setup of the facility and laboratory.

Skills

HPLC analysis

Good Manufacturing Practice (GMP)

analytical testing

Education

Degree in relevant scientific discipline

Job description

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About

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

About

Are you a 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

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 2 QC Analysts to support the QC department with analytical testing.

Typical Responsibilities/accountabilities

Execute hands-on U/HPLC testing on a range of products. Conduct dissolution testing Perform pharmacopeial methods such as IR, Appearance, pH, CU, and water content. Adherence to Good Manufacturing Practice (GMP) standards using a new electronic Quality System. Contribute to the setup of the facility and laboratory, and actively participate in building the LIMS system. 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. Contribution to the creation and review of Plans, Methodologies, Work Instructions, and Standard Operating Procedures (SOPs). Hands-on contribution to building a LIMS system to transition to a paper-free lab.Essential Requirements:

Educated to Degree level in a relevant scientific discipline along with a minimum of 2 years' experience in pharmaceutical sciences within GMP development. Proven experience with HPLC analysis. Experience in an analytical laboratory environment with a sound understanding of regulatory requirements.Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy

• Stockport, England
  
  

Languages

• English

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Technology, Information and Internet

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