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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:
c58ce8b4d433
Job Views:
3
Posted:
24.04.2025
Expiry Date:
08.06.2025
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Job Description:
Summary
Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra!
Dechra is a growing, global specialist in veterinary pharmaceuticals, focusing on development, manufacture, marketing, and sales of high-quality products for veterinarians worldwide.
Our values are embedded within our culture, thriving within our team of nearly 2,500 colleagues globally. Values such as dedication, enjoyment, courage, honesty, relationships, and ambition are central to our operations and business approach.
The Opportunity
You will assist in achieving the daily production targets, ensuring equipment is used properly, including setup, production, strip down, and cleaning, all in line with documentation and GMP procedures.
Additional focus on manufacturing products to the highest quality standards, compliant with GMP guidelines, and ensuring activities adhere to Health and Safety guidelines.
Package
* Competitive salary and benefits
* Average 36-hour workweek with a day off every other Friday
* Working hours: 14:00-22:30
* 22.5 days annual leave plus bank holidays
* Option to buy additional holiday
* Free Headspace App access
* Option to join Sharesave scheme
* Employee Assistance Programme
* On-site parking
Main Responsibilities
The role involves responsibilities such as:
* Manufacturing products to high standards per GMP and SOPs
* Ensuring SOP compliance
* Attending training sessions
* Training others in the team
* Ensuring safe and efficient use of equipment
* Maintaining equipment and escalating issues
* Maintaining cleanliness and hygiene standards
* Reporting safety or GMP issues promptly
* Resolving issues or escalating when necessary
* Supporting operational efficiency initiatives
* Performing other reasonable tasks as assigned
Ideal Candidate
We value inclusivity and welcome candidates from all backgrounds. We are particularly interested in candidates with:
* Knowledge of Health & Safety compliance
* Effective communication skills
* Experience in low to medium volume manufacturing or packaging (beneficial but not essential)
* Experience in GMP manufacturing environments (preferred but not required)
* Knowledge of pharmaceutical manufacturing and continuous improvement activities
* Ability to manage time and workload effectively
* Willingness to undergo DBS checks as required
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