832 Qc Analyst jobs in the United Kingdom

This is an exciting opportunity for an experienced Analytical Chemist to join the team at our pharmaceutical client. As a QC Analyst, you will be responsible for the analysis of samples, working to cGMP standards. This role also involves aspects of method development and validation.

Key Responsibilities of the QC Analyst:

• Undertake ongoing instrument utilisation for analysis
• Assume project ownership and liaise with clients
• Report task/project status to the leadership team
• Record keeping and reporting of results
• Troubleshoot analytical problems and define CAPA actions
• Ensure all work meets the prescribed requirements of the company's Quality System and cGMP standards

Qualifications and Skills:

• Degree in Chemistry or a related field
• Chromatography experience (HPLC/GC)
• Experience with Waters Empower CDS is preferred
• Working knowledge of compendial testing is an advantage
• Strong communication skills, both written and verbal
• Keen interest in new technologies, systems, and methods
• Quick learner and adaptable attitude
• Focus on Quality and attention to detail

What's in it for you?

As a QC Analyst at this company, you will have the opportunity to work in a dynamic and innovative environment, contributing to the development and analysis of pharmaceutical products. The company is committed to providing a supportive and inclusive culture, with opportunities for professional development and growth.

If you are an experienced Analytical Chemist looking for your next challenge, we encourage you to apply for this QC Analyst role.

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

ROLE OVERVIEW

An exciting role has arisen for a QC Analyst to join a leading Pharmaceutical company based in the Hertfordshire area. As the QC Analyst, you will be responsible for contributing to the Pharmaceutical Development and Support (PDS) department.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the QC Analyst will be varied; however, the key duties and responsibilities are as follows:

1. Conduct Quality Control of raw materials, bulk, and finished products using HPLC, GC, and wet chemical techniques in accordance with authorised test procedures.

2. Analyse products to provide stability data for new product development and ongoing stability monitoring of commercial products, ensuring compliance with authorised test procedures.

3. Perform manual and automated tests and assays with a high level of accuracy and precision, adhering to GMP standards, and operate associated analytical equipment.

4. Collect, process, and report data using software packages such as Chromeleon, LIMS, Excel, and Word, and participate in the overall running of the laboratory, including equipment maintenance and calibration.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the QC Analyst we are looking to identify the following on your profile and past history:

1. Relevant degree in a chemistry-based discipline.

2. Proven industry experience in an analytical testing role, preferably in a GMP environment.

3. A working knowledge and practical experience with HPLC and GC analysis, as well as Microsoft Office, particularly Word and Excel.

Key Words:

Laboratory Analyst / Quality Control / HPLC / GC / Wet Chemical Techniques / GMP / Pharmaceutical Development / Stability Data / Chromeleon / LIMS / Analytical Testing

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

• Carry out QC testing on raw and finished products.
• Ensure all testing is GMP compliant.
• Maintain and calibrate analytical instrumentation.

• Degree-level qualification or relevant experience.
• Proven expertise in core analytical skills, including HPLC.
• Ability to work independently and collaboratively.
• Dynamic and flexible attitude to thrive in a fast-paced setting.

We are working with an established pharmaceutical company who are looking to employ a Quality Control Analyst, permanently in the Sandwich area.

Please only apply if you live within a commutable distance of Sandwich, Kent. No relocations please.

This is an exciting full-time permanent position, 37.5 hours per week, 8.30am to 5pm, with an hour's lunch. Competitive salary of 29,000 per annum, plus a host of benefits, to include:

• 31 days annual leave, inclusive of Bank Holidays.
• Auto enrolled pension scheme
• Healthcare, Death in Service, Private Medical insurance including dependants
• Annual bonus scheme
• Free parking
• Great working environment

You must be committed and have HPLC experience. Support the production and QA Departments in ensuring all aspects of the manufacture of products are performed in a controlled manner, meeting commitments to international regulatory bodies, as well as Good Manufacturing Practice. Ensure manufactured products are compliant and fit for purpose by performing physical and analytical testing and report accurate results. Duties to include:

• Being responsible for physical analytical testing.
• Follow internal methodologies.
• Adherence to GMP requirements.
• Accurately record microbiological results within data packages, as received.
• Execution of protocols.
• Ensure laboratory housekeeping standards are maintained and documented accurately.
• Ensure all equipment is suitable for use.

The ideal candidate will have the following:

• A relevant BSc degree, eg Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent.
• Be computer literate, with good working knowledge of MS Office.
• Experienced in QC testing of API, including HPLC and GC. Other wet chemistry techniques desirable.
• Good attention to detail, able to prioritise workload, positive and flexible approach.
• One to two years' experience in a similar role would be ideal, but not necessary.
• GMP experience would be desirable.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975. Committed to diversity, equality and opportunity for all. (url removed)

CY Partners are excited to be supporting a leading CRO/CDMO in Durham who are looking for a Quality Control Analyst to join their QC team. This is a fantastic opportunity to work across pharmaceuticals, biotech and fine chemicals, contributing to GMP manufacture of novel APIs and other specialist materials.

The Role

• Routine and non-routine analysis of raw materials, intermediates & finished products
li>Use of HPLC, GC, UV-Vis, FTIR, NMR & wet chemistry techniques
• Method development, validation & stability studies
• Supporting equipment qualification and GMP compliance
• Clear communication of results to colleagues & management

About You

• Degree in Chemistry (or equivalent experience)
• Prior experience in an analytical/GMP testing environment
• Strong knowledge of analytical techniques & method validation
• Excellent attention to detail, communication, and IT/data integrity skills

If you’d like further information, please contact Graham at CY Partners.

This is an exciting opportunity for an experienced Analytical Chemist to join the team at our pharmaceutical client. As a QC Analyst, you will be responsible for the analysis of samples, working to cGMP standards. This role also involves aspects of method development and validation.

Key Responsibilities of the QC Analyst:

• Undertake ongoing instrument utilisation for analysis
• Assume project ownership and liaise with clients
• Report task/project status to the leadership team
• Record keeping and reporting of results
• Troubleshoot analytical problems and define CAPA actions
• Ensure all work meets the prescribed requirements of the company's Quality System and cGMP standards

Qualifications and Skills:

• Degree in Chemistry or a related field
• Chromatography experience (HPLC/GC)
• Experience with Waters Empower CDS is preferred
• Working knowledge of compendial testing is an advantage
• Strong communication skills, both written and verbal
• Keen interest in new technologies, systems, and methods
• Quick learner and adaptable attitude
• Focus on Quality and attention to detail

What's in it for you?

As a QC Analyst at this company, you will have the opportunity to work in a dynamic and innovative environment, contributing to the development and analysis of pharmaceutical products. The company is committed to providing a supportive and inclusive culture, with opportunities for professional development and growth.

If you are an experienced Analytical Chemist looking for your next challenge, we encourage you to apply for this QC Analyst role.

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

• Carry out QC testing on raw and finished products.
• Ensure all testing is GMP compliant.
• Maintain and calibrate analytical instrumentation.

• Degree-level qualification or relevant experience.
• Proven expertise in core analytical skills, including HPLC.
• Ability to work independently and collaboratively.
• Dynamic and flexible attitude to thrive in a fast-paced setting.