QC Analyst (6 Month FTC) Earlies

TN United Kingdom; Skipton; On-site; GBP 30,000 - 50,000; Full time

Job summary

An established industry player in veterinary pharmaceuticals is seeking a QC Analyst for a 6-month FTC in Skipton. This role involves performing critical analytical tests on raw materials and products to ensure compliance with Good Manufacturing Practices (GMP). The successful candidate will utilize a range of advanced analysis techniques and equipment, contributing to the quality assurance of veterinary medicines. With a strong commitment to employee development, the company offers extensive training opportunities and a supportive work environment. Ideal for those with a keen eye for detail and a passion for quality control in the pharmaceutical sector.

Benefits

36-hour working week

22.5 days annual leave

Option to buy a week's holiday

Free access to Headspace App

Employee Assistance Programme

Free on-site parking

Qualifications

• 3+ years experience in a pharmaceutical GMP quality control laboratory.
• Knowledge of chemical and physical analysis techniques including HPLC and UV-VIS.

Responsibilities

• Perform analytical tests to ensure quality of raw materials and products.
• Conduct analysis for stability studies and method transfers.

Skills

Analytical Skills

Attention to Detail

Knowledge of GMP

Chemical Analysis Techniques

Physical Analysis Techniques

Education

BSc Hons in Chemistry

Equivalent in Scientific Field

Tools

HPLC

UV-VIS Spectroscopy

Word

Excel

Job description

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QC Analyst (6 Month FTC) Earlies, Skipton

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Client:

Location:

Skipton, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

accdfc1971bb

Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

Summary

Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra!

Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.

Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2500 colleagues globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business.

The Opportunity

As an Analytical Analyst you are involved in carrying out testing (chemical and administrative) on raw materials, semi-finished products, veterinary medicinal products and packaging materials. Stability research and calibration of analysis equipment is also part of your work.

All QC activities are performed according to established procedures and according to the Dechra Quality Management System.

Package

• Average 36-hour working week (with a day off every other Friday!!)
• Plenty of training and development opportunities
• 22.5 days annual leave + Bank holidays
• Option to buy a week's holiday each year
• Free access to the Headspace App
• Employee Assistance Programme
• Free on-site parking

Main Responsibilities

So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including:

Performing analytical and physical tests and evaluating the results obtained in order to guarantee the quality of packaging materials, semi-finished products, raw materials and end products, ie all Good Manufacturing Practice (GMP) requirements are met and all results are met.

• Collection, receipt and archiving of samples of raw materials, packaging, wage products, labels, semi-finished products, end products and water samples. Taking swab samples for monitoring and cleaning validations.
• Ensure an efficient division of the work, taking into account the production planning and agreed lead times.
• Performing regular maintenance and minor repairs, keeping clean and calibrating equipment, materials and spaces.
• Perform tests on raw materials, semi-finished products and packaging materials before use in production, using a wide range of analysis equipment.
• The release of raw materials, semi-finished products and packaging materials for use in production.
• Performing tests on end products for the release of products for the market, using a wide range of analysis equipment.
• Perform analysis for process, product, cleaning and equipment validation studies.
• Conducting analysis for stability studies.
• Carry out analysis for method transfers to or from other laboratories.
• Checking and checking analysis data, documents, methods and procedures.
• Correct interpretation, processing and reporting of analysis data in electronic data systems and validation protocols.
• Preparing analysis certificates for customers.
• Conducting examinations as a result of Out-of-Specification results, deviations and other quality-related investigations.
• Keeping inventory and orders of chemicals, consumer goods and parts of equipment.
• Arranging the execution of external research, sending samples, processing reports and checking the progress of the work to be carried out.
• Drafting of specifications incl. Analytical regulations for raw materials, wage products, semi-finished products, packaging, labels and end products.
• Ensure that all waste is safely removed and is in line with business processes.

Ideal Candidate

Here at Dechra we pride ourselves on being an inclusive employer and we embrace candidates from all walks of life. We're particularly keen to hear from those who have/are:

• Experience in very precise and concentrated work.
• At least 3 years of relevant experience in a pharmaceutical GMP quality control laboratory.
• Knowledge of chemical and physical analysis techniques; HPLC, UV-VIS, DLC, MID-IR, (auto) titration, water determination Karl Fischer, TOC, physicochemical tests as density, melting point determination, color measurement, viscosity measurement, pH measurement.
• Working in Word and Excel and with HPLC data system (CDS).
• Knowledge of environmental, health and safety, GMP and company regulations.
• Global knowledge of production method.
• Knowledge of the applicable procedures and their application.
• BSc Hons in Chemistry or equivalent in scientific field.
• Occasional global travel is required with this role.