Senior Manufacturing Technician (lates)

at  Dechra Pharmaceuticals PLC

Skipton BD23 2RW, , United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate24 Jan, 2025Not Specified25 Oct, 2024N/ASafety Compliance,Manufacturing ProcessesNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Job Introduction
Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra!
Dechra are 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.
Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2500 colleagues globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business.

THE OPPORTUNITY

You will be responsible to assist and cover the supervisors in the absence of supervision. To take responsibility for the equipment used and ensure all aspects of use (set up, production, strip down and cleaning) are carried out to a high standard, in line with associated documentation and GMP procedures.
Manufacture product to the highest quality standard and compliant to the set GMP guidelines and procedures. To ensure all activities undertaken are within the set Health and Safety guidelines.
Main Responsibilities

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.
  • Support a compliance culture within operations, ensuring all team members adhere to SOPs and other documents, and comply with their individual responsibilities to GMP.
  • 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 and supports with completion of Risk Assessments.
  • To keep strictly to documented manufacturing methods 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 informing the Manufacturing Supervisors or Manager of any faults.
  • Maintain the 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 the Manufacturing Manager, Supervisor, as a matter of urgency, if there has been any serious failure of safety or GMP which could affect staff safety or product quality.
  • To identify any issues and proactively resolve these using prescribed techniques and escalating if it cannot be resolved.
  • Role Model Operational Excellence incentives to drive and improve efficiency and challenge existing processes and behaviours, raising new ideas to improve the current norm.
  • Assists with QMS items including deviations, CAPAs, Change Controls and updating SOPs.

The Ideal Candidate
Here at Dechra we pride ourselves on being an inclusive employer and we encourage applications from a variety of different work backgrounds. We’re keen to learn a little more about you and your career.

Whether you’re already established as a Senior professional within production environments or looking for that next step up, we’d love to hear from you. Additionally, here are some key skills/experiences that will stand you in good stead:

  • 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
  • Good knowledge and understanding of Health & Safety compliance.

About The Company
Dechra are 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.
Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2500 colleagues globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business.
All applications received are reviewed by our internal talent acquisition team and we will get in touch if your skills and experience match what we’re looking for. Should you not hear back from us within 28 days please don’t be too disappointed – we may keep your CV on our database for any future vacancies which may be suitable and we encourage you to keep an eye on our careers site. For any questions or queries, please contact us at recruituk@dechra.com

Package & Benefits

  • 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

Responsibilities:

  • Manufacture product to high standard ensuring the quality of those products is in accordance with the set GMP standards and Standard Operating Procedures.
  • Support a compliance culture within operations, ensuring all team members adhere to SOPs and other documents, and comply with their individual responsibilities to GMP.
  • 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 and supports with completion of Risk Assessments.
  • To keep strictly to documented manufacturing methods 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 informing the Manufacturing Supervisors or Manager of any faults.
  • Maintain the 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 the Manufacturing Manager, Supervisor, as a matter of urgency, if there has been any serious failure of safety or GMP which could affect staff safety or product quality.
  • To identify any issues and proactively resolve these using prescribed techniques and escalating if it cannot be resolved.
  • Role Model Operational Excellence incentives to drive and improve efficiency and challenge existing processes and behaviours, raising new ideas to improve the current norm.
  • Assists with QMS items including deviations, CAPAs, Change Controls and updating SOPs


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Skipton BD23 2RW, United Kingdom