QC Analyst

Atom Recruitment; Hitchin; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player in the pharmaceutical sector is seeking a dedicated QC Analyst to join their team. This full-time permanent role offers the chance to work in a collaborative environment, focusing on quality control of raw materials and finished products using advanced techniques like HPLC and GC. With a 4-day work week, you will enjoy a great work-life balance while contributing to the success of the pharmaceutical development and support team. If you have a keen eye for detail and a passion for quality assurance, this opportunity could be the perfect fit for you.

Benefits

4-day work week

Comprehensive benefits

Competitive salary

Qualifications

• Experience in analytical testing, preferably in a GMP environment.
• Familiarity with HPLC and GC analysis techniques.

Responsibilities

• Conduct quality control of raw materials and finished products using HPLC and GC.
• Perform cleaning verification analysis and maintain laboratory equipment.

Skills

Analytical Testing

Attention to Detail

Organisational Skills

Collaboration

Self-Motivation

Education

Relevant Experience in Analytical Testing

GMP Environment Experience

Tools

HPLC

GC

Chromatography Data Handling Software

LIMS

Excel

Job description

Our Client is a very successful pharmaceutical company. They are now seeking a QC Analyst. This position is a full-time permanent role and will be based near Hitchin, Hertfordshire.

Our Client operates a 4 day week. The hours will be Tuesday to Friday 07.30 to 16.45.

Job Purpose

An opportunity has arisen for an Analyst to join an existing QC team within the Pharmaceutical Development and Support (PDS) department.

Key Areas of Responsibility

1. Carry out the Quality Control of raw materials, bulk and finished products in accordance with relevant authorised documentation using HPLC, GC and wet chemical techniques.
2. Perform swabbing and analysis of samples for cleaning verification of the pilot production facility.
3. Take equal part in the overall running of the laboratory, including equipment maintenance, calibration of apparatus and other general duties such as solvent disposal.
4. Perform manual and automated tests and assays in accordance with GMP to a high level of accuracy and precision and to operate associated analytical equipment.

Qualifications / Experience

1. Some relevant experience in an analytical testing role, preferably in a GMP environment. (This experience could include an industrial placement year).
2. Some experience in the techniques of HPLC and GC analysis.
3. Excellent attention to detail and organisational skills and the ability to self-motivate under your own initiative.
4. Collaborative skills to work closely with colleagues and managers.
5. Use of software packages, such as Chromatography Data Handling, LIMS and Excel, for the collection, processing and reporting of data.

In return, our client is offering a competitive basic salary plus comprehensive benefits for the successful Candidate.

Please send your C.V to Lorraine Roger, Director at Atom Recruitment Ltd.