NPI Analyst 12 month FTC

Summary

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 2000 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

Responsible for carrying out analytical and documentational activities relating to Quality Control, including but not limited to: new products introduction analysis of raw materials and finished products, transfer, validation and verification analysis, ensuring all tasks are executed in a timely manner. To perform all operations in accordance with written procedures and the Skipton quality management system.

Package

• Average 36-hour working week (with a day off every other Friday!!)
• 8am - 4:30pm working day
• Plenty of training and development opportunities
• 22.5 days annual leave + Bank holidays
• Option to buy a week's holiday each year
• 8% Employer Pension Contribution
• Free access to the Headspace App
• Employee Assistance Programme
• Free on-site parking

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:

• Propose and implement laboratory improvements with relation to set procedures and analytical test methods and promote a culture of continuous improvement.
• Enhance practices and promote a culture which is consistent with cGMP, cGLP and Health & Safety within a pharmaceutical laboratory environment.
• Actively support QC Analytical and Technical Specialists with preparing and reviewing validation/verification or transfer documents.
• Perform test method transfers, verification and validation.
• Support Technology Transfer for methods / processes being transferred to and from the department.
• Record, report, check and review analytical data, ensuring maintenance of all analytical documentation in an organised and accessible manner for future reference by colleagues and/or inspectors/auditors.
• Take an active role in and be accountable for laboratory investigations, ensuring these are followed through to completion within a timely manner as outlines in set laboratory procedures.
• Take an active role in the completion of change control, CAPA, deviations and other quality related documentation.
• Ensure the maintenance of relevant inventory, including chemicals, reference materials, consumable items etc. required for assigned activities.
• Collaborate with team colleagues to ensure that the workplace environment and workstations remain at a high level or cleanliness and housekeeping that comply with company and legislative standards at all times.
• Promote health and safety, ensuring that all company safety and quality systems and relevant legislations are adhered to, reporting any incidents or suggestions to the manager.
• Ensure all waste is correctly disposed of in accordance with site policy.
• Stay abreast of developments in the field through training and reading of literature.
• Observe and abide by the company's values (Dedication, Enjoyment, Courage, Honesty, Ambition) in all aspects of carrying out the job role, including interaction with co-workers and third parties.
• All other tasks that can reasonably be requested and approved by management.

Ideal Candidate

Here at Dechra we pride ourselves on being an inclusive employer and we embrace candidates from all walks of life. We're particularly keen to hear from those who have/are:

• Due to the nature of our business, all successful candidates will be required to complete a basic DBS check (Disclosure and Barring Service check) before employment can commence, and at regular intervals during employment. This check will be paid for by Dechra.'
• Knowledge of chemical and physical analysis techniques
• Experience of the applicable procedures and their application
• A background in transfer, validation and verification processes within pharmaceutical industry
• Understanding of GMP regulations for products produced, tested and marketed within the UK, EU and US
• Computer literate, with an attention to detail (inc. formatting) and clarity
• Familiar with environmental, health & safety, regulatory and company standards
• Can work in a team
• Good communicative skills
• Good problem-solving ability and investigational skills
• Strong attention to detail

ADZN1_UKTJ

Location: Overdale Park, GB

Posted Date: 9/20/2024