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
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