Manufacturing Technician (FTC) - Night Shift

Dechra Pharmaceuticals PLC

Skipton

Hybrid

GBP 28,000 - 34,000

Full time

3 days ago
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Benefits offered by this job

Onsite parking
Training & development opportunities
Extra holiday option
Pension 8% Employer Contribution

Job summary

Dechra Pharmaceuticals PLC, based at the Skipton site in North Yorkshire, is seeking a Manufacturing Technician for the night shift on a fixed-term 9‑month contract. The role involves manufacturing to GMP standards, SOP compliance, training colleagues, and ensuring safe operation of plant and equipment.

Key responsibilities include maintaining housekeeping, adhering to procedures, and escalating safety or GMP issues promptly.

Qualifications

  • Good knowledge and understanding of Health & Safety compliance.
  • Ability to communicate effectively with both peers and senior staff.
  • Ability to work in a manual role with good dexterity.
  • A positive attitude and teamwork mindset; local to Skipton.

Responsibilities

  • Manufacture product to high standard in line with GMP and SOPs.
  • Ensure compliance with SOPs and complete required training.
  • Capable of training others in the team and supporting operations.
  • Ensure efficient and safe use of plant and equipment.
  • Adhere to documented manufacturing methods and escalate issues to supervisors.
  • Keep equipment clean and maintained; escalate deficiencies.
  • Maintain high standards of housekeeping, cleanliness and personal hygiene.
  • Report any serious GMP or safety issues to management immediately.
  • Identify issues and escalate if unresolved; support Operational Excellence.

Skills

Health & Safety
Communication
Dexterity
Team player
Positive attitude

Job description

Manufacturing Technician - Night Shift

The role is a Fixed Term Contract of 9 months.

2130-0600 Mon to Thurs, then every other Friday 1800-0230. Yes, we work a 9 day fortnight!

Based at our Skipton, North Yorkshire manufacturing site.

We are Dechra 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.

Our Recruitment Process

We understand applying for roles isn’t always a great experience! From this point we want you to have a positive experience with our recruitment process.

We will review your application and CV and notify promptly if you will be progressing to the next stage.

If you are selected, we will arrange a brief informal call to discuss the role.

If after that call both agree the position is a good match, we will arrange a face‑to‑face interview at our Skipton site, at the earliest mutually convenient date and time.

We will provide you with speedy feedback following your interview.

The Role

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

  • Manufacture product to high standard ensuring the quality of those products is in accordance with the set GMP standards and Standard Operating Procedures.
  • Ensure compliance with Standard Operating Procedures (SOPs)
  • Attend and comply with any planned in house training or on the job training.
  • Capable and willing to train others in the team.
  • To ensure the efficient and safe use of plant and equipment.
  • To keep strictly to manufacturing methods as laid down in the documentation and raise any issues or errors with the Manufacturing Supervisors or Manager
  • To ensure all equipment is clean and maintained in good working order and where deficiencies are found, escalating to a supervisor.
  • Maintain the highest standards of housekeeping, cleanliness and personal hygiene within the department.
  • To notify the Manufacturing Manager, Supervisor or Senior Manufacturing Technicians, as a matter of urgency, if there has been any serious failure of safety or GMP which could affect staff safety or product quality or operational efficiency.
  • To identify any issues and attempt to resolve these and escalating if it cannot be resolved.
  • To support Operational Excellence incentives to drive and improve efficiency.
You

A self‑motivated enthusiastic individual who can work well within a team environment performing manufacturing activities including the operation and cleaning of equipment, whilst being able to complete associated documentation accurately and in a timely manner, in line with strict procedures. A person with a positive attitude who can constructively challenge others as well as give and receive feedback in a respectful and professional manner whilst demonstrating the Dechra values.

Essential

  • Good knowledge and understanding of Health & Safety compliance.
  • Ability to communicate effectively with both peers and senior members of staff.
  • Ability to work in manual role with good dexterity
  • A positive attitude
  • Local to our Skipton site

Desirable

  • 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.
  • A working knowledge and practical experience of pharmaceutical manufacture, continuous improvement activities and ability to manage time and workload effectively
Reward
  • £31,087.16 per annum
  • Free and ample onsite parking
  • 36-hour week – Mon – Thurs 2.00pm - 10.30pm Fri - 12.00pm - 8.30pm
  • Tons of great training and development opportunities
  • Option to buy an extra week's holiday each year
  • 8% Employer Pension Contribution

Here at Dechra we pride ourselves on being an inclusive employer and are proud of our diversity and work culture. Take a look at our website to view our truly embedded values.

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