Senior Manufacturing Technician
4 weeks ago
Job Introduction
We are seeking a highly skilled and experienced Manufacturing Technician to join our team at Dechra. As a key member of our production team, you will be responsible for assisting and covering supervisors in their absence, ensuring the efficient and safe use of plant and equipment, and supporting a compliance culture within operations.
The Opportunity
This is an exciting opportunity to work in a fast-paced and dynamic environment, where you will have the chance to develop your skills and experience in a highly regulated GMP manufacturing facility. You will be responsible for manufacturing products to the highest quality standard, ensuring compliance with GMP guidelines and procedures, and maintaining the highest standards of housekeeping, cleanliness, and personal hygiene within the department.
Key Responsibilities
- Manufacture product to high standard, ensuring quality in accordance with GMP standards and SOPs.
- Support a compliance culture, ensuring team members adhere to SOPs and comply with individual responsibilities to GMP.
- Attend and comply with planned in-house training or on-the-job training.
- Capable and willing to train others in the team.
- Ensure efficient and safe use of plant and equipment, and support completion of Risk Assessments.
- Keep strictly to documented manufacturing methods, raising any issues or errors with Manufacturing Supervisors or Manager.
- Maintain equipment in good working order, informing Manufacturing Supervisors or Manager of any faults.
- Maintain highest standards of housekeeping, cleanliness, and personal hygiene within the department.
- Support and guide the team, making routine decisions regarding safety and GMP, and notify Manufacturing Manager, Supervisor, as a matter of urgency, if there has been any serious failure of safety or GMP.
- Identify and proactively resolve issues using prescribed techniques, escalating if it cannot be resolved.
- Role Model Operational Excellence, driving and improving efficiency, challenging existing processes and behaviours, and raising new ideas to improve the current norm.
- Assist with QMS items, including deviations, CAPAs, Change Controls, and updating SOPs.
Requirements
- Experience of low to medium volume manufacturing/packaging, manual/semi-automated manufacturing processes.
- Proven industry experience from a highly regulated GMP manufacturing/packing facility, either from the Pharmaceutical or similarly regulated industry/environment.
- Working knowledge and practical experience of pharmaceutical manufacture, continuous improvement activities, and ability to manage time and workload effectively.
- Good knowledge and understanding of Health & Safety compliance.
Package Description
- Competitive salary and Benefits.
- Average 36 hour working week (with a day off every other Friday).
- Working hours: 1400-2230 hrs.
- 22.5 days annual leave + Bank holidays.
- Option to buy a week's holiday each year.
- 8% Employer Pension Contribution.
- Free access to Headspace App.
- Option to join Sharesave scheme.
- Employee Assistance Programme.
- On-site parking.
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