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
We'll look to you to provide the technical support for executing new product commercialisation/scale up projects (primarily solid dose) from Dechra PD (Product Development) and drive optimisation projects for currently approved products from site or from other internal sites or from CMOs (Contract Manufacturing Organisations) using product lifecycle approach. You'll also troubleshoot current commercialised products; new production equipment selection and significant process change
So, what will you be doing?
This role has a broad and varied remit and the successful candidate will have responsibility for duties including:
- Support the Technical Manager and represent the department on project team level
- Execution of product commercialisation projects for the site (NPI and post approval changes). This will require close collaboration with Product Development, Production and QA groups on NPIs using product lifecycle approach, preparation and approval of GMP documentations to support such projects, scheduling, raw material acquisition, supervising engineering batch manufacture, etc.
- Identifying potential process improvements for existing commercial products including proposals for formulation / process optimisation. Then support implementation of changes after management approval* Provide technical support to all departments to solve problems as they occur
- Lead problem solving and resolution efforts in a timely, well documented manner
- Assist in new equipment evaluation by interfacing with the Engineering group
- Assist in activities for successful transfer of new equipment to production, including training of both supervisors and operators
- Assist in the evaluation and qualifying alternate sources of raw materials and commodities
- Using the Product lifecycle approach and statistics, take project leadership for the technical activities involve in the commercialisation of internal products during Product Development, Registration, Optimisation, Validation / Launch of veterinary drug products as applicable
- Assist in the Technical assessment of products / projects (development and commercialised products for optimisation/site transfer)
- Assist in implementing the product life cycle program for the site to ensure compliance with Dechra's commercialisation standards and compliance with current Global Regulatory expectations
- Proactively identify and troubleshoot formulation and process type issues of products manufactured internally to improve product quality and to minimize product supply interruptions
So, what do I need to bring to the table?
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:
- Degree in life sciences, engineering, pharmaceutics, chemistry, or similar fields.
- Relevant work experience combined with technical knowledge, problem solving skills, sound understanding of process validation and verification, and the ability to plan and co-ordinate multiple activities.
- This individual should be able to make competent scientific recommendations
- Minimum of 4 years of industrial experience in the pharmaceutical or related industry, or an equivalent combination of education and experience with knowledge of pertinent Regulatory and Industry guidance's and regulations.
- Has demonstrated the ability to design, develop and implement effective technical transfer and product lifecycle strategies for the dosage forms manufactured by the site (solids, liquids, gels, terminal sterilisation) and a firm working knowledge of manufacturing platforms and pharmaceutical facility infrastructure.
Desirable skills/experience
- 'Hands-on' knowledge of pharmaceutical manufacturing equipment, and ability to supervise batch manufacture and instruct production operators.
- Manufacture of potent products and associated containment systems.
- Supervisory experience would be beneficial as would step-in technical managers absence.
- Understanding of the dosage form development process, along with some knowledge of process development techniques, cGMP regulations, FDA and EMA regulations, and recent trends in product lifecycle concepts.
- Experience with solid dose formulation/scale up
We've got you covered
- Average 36-hour working week (with a day off every other Friday!!)
- 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
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
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