QC Analyst (18month FTC) Earlies

Dechra; Skipton; On-site; GBP 30,000 - 40,000; Full time

Job summary

An established industry player is seeking a QC Analyst for an 18-month fixed-term contract. This role involves conducting critical testing and ensuring compliance with quality standards in a dynamic pharmaceutical environment. As a key player in the quality assurance team, you will engage in sample collection, testing, and validation studies, contributing to the production of high-quality veterinary products. The company fosters a culture of dedication and inclusion, offering a supportive work environment with opportunities for training and development. If you're passionate about quality control and looking to make a meaningful impact, this role is an exciting opportunity.

Benefits

36-hour workweek with a day off every other Friday

Training and development opportunities

22.5 days annual leave plus bank holidays

Option to purchase additional holiday

8% Employer Pension Contribution

Free access to Headspace App

Employee Assistance Programme

Free on-site parking

Qualifications

• Minimum 3 years in a GMP pharmaceutical QC laboratory.
• Experience with various analysis techniques and precise work.

Responsibilities

• Conduct testing on raw materials and finished products.
• Manage sample collection and perform stability research.
• Investigate Out-of-Specification results and deviations.

Skills

HPLC

UV-VIS

Titration

Karl Fischer

TOC

Attention to Detail

Analytical Skills

Education

BSc Hons in Chemistry

Tools

Word

Excel

HPLC Data Systems

Job description

Join to apply for the QC Analyst (18month FTC) Earlies role at Dechra

Group Development and Inclusion Director

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

Dechra is a growing, global specialist in veterinary pharmaceuticals, focusing on the development, manufacture, marketing, and sales of high-quality products for veterinarians worldwide.

Our values are embedded in our culture and shared among nearly 2500 colleagues globally. Dedication, Enjoyment, Courage, Honesty, Relationships, and Ambition are core to our daily operations and business ethos.

The Opportunity

As a QC Analyst, you will conduct testing (chemical and administrative) on raw materials, semi-finished and finished products, veterinary medicinal products, and packaging materials.

Your responsibilities will include stability research, calibration of analysis equipment, and performing all QC activities in accordance with established procedures and the Dechra Quality Management System.

Package

• Average 36-hour workweek with a day off every other Friday
• Training and development opportunities
• 22.5 days annual leave plus bank holidays
• Option to purchase additional holiday
• 8% Employer Pension Contribution
• Free access to Headspace App
• Employee Assistance Programme
• Free on-site parking

Main Responsibilities

The role involves:

• Sample collection, archiving, and monitoring of raw materials, packaging, and products
• Efficient work division aligned with production planning
• Maintenance and calibration of equipment and spaces
• Testing raw materials, semi-finished, and packaging materials before production
• Releasing raw materials and finished products for market
• Conducting validation studies and preparing analysis certificates
• Investigating Out-of-Specification results and deviations
• Managing external research samples and reports
• Drafting specifications and analytical regulations
• Ensuring waste disposal compliance

Ideal Candidate

We value diversity and welcome candidates from all backgrounds. The ideal candidate will have:

• Experience in precise, concentrated work
• At least 3 years in a GMP pharmaceutical QC laboratory
• Knowledge of analysis techniques such as HPLC, UV-VIS, titration, Karl Fischer, TOC, etc.
• Proficiency with Word, Excel, and HPLC data systems
• Understanding of environmental, health, safety, GMP, and company regulations
• BSc Hons in Chemistry or related scientific field
• Willingness to travel occasionally

Additional Details

• Seniority level: Entry level
• Employment type: Temporary
• Job function: Quality Assurance
• Industry: Pharmaceutical Manufacturing