Research and Development Scientist

Posted 11 Hours Ago
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Luton, Bedfordshire, England, GBR
In-Office
Senior level
Pharmaceutical • Industrial • Manufacturing
The Role
Perform formulation R&D, plan and execute development and validation activities, author regulatory/technical documents, conduct process optimization and stability studies per ICH, provide technical support and troubleshooting across production and compliance to meet MHRA and cGMP standards.
Summary Generated by Built In
Job Description

About us
Bristol Laboratories Ltd is one of the leading and fastest growing pharmaceutical companies in the United Kingdom engaged in the development, manufacturing, marketing and distribution of generic medicines, as well as formulation brands. We have state-of-the art manufacturing facilities in Luton & Peterlee.
As a result of continued growth and expansion, we have an excellent opportunity to appoint Research and Development Scientist in Luton
About the Role:
We are looking for Research and Development Scientist with varied & extensive experience within the Pharmaceutical or similar Industries. This role will be based on a rolling contract to begin with and potential to become permanent in future. The role will involve meticulous planning and execution of timely maintenance to ensure productivity is not hampered. The role will also involve working with other departments to meet production targets while meeting the MHRA and cGMP compliance standards.
Key Responsibilities
• Must have current scientific literature knowledge, should be able to research on the same and leverage existing knowledge appropriately, being mindful of potential information formulation, analytical and development.
• Should be able to perform daily tasks with minimal guidance, develop and communicate an executable formulation development plan
• Authors and reviews formulation development sections of regulatory and technical documents like manufacturing batch records, process validation protocols, process validation reports, any other study reports and technology transfer documents etc.
• Should be able to conduct Process Optimization and validation with updated knowledge from relevant sources.
• Should be able to involve in preparation and execution of stability study as per ICH norms for Exhibit and developmental batches and close follow-up of stability results.
• Directly or indirectly leads, guides, and works with research scientists in conducting research and developmental work, and investigate to solve development problems and troubleshooting at shop floor and product improvisation
• Technical support to the other related function like Production, Regulatory, Marketing, Costing and Purchase.
• Participates in general lab and instrument maintenance.
About You:
• A minimum Science education with specialising in Engineering/Technology.
• With significant experience in a similar role within a pharmaceutical GMP compliant factory.
• As a person, you have excellent communication and interpersonal skills, have strong integrity, able to liaise with stakeholders at all levels and navigate cultural differences with ease.
• With strong organisation and administration skills, you make good decisions, have a strong eye for detail and can prioritise a busy workload to meet deadlines.
Reward:
• In return, we offer a competitive salary and rewards package.( Holidays, Free Parking, Occasional Opportunity to travel to different locations, attend seminars and meet industry experts)
• A fantastic training & development opportunity for someone seeking to enhance their learning in a challenging and fast-paced environment.
• Opportunity to grow further in your career by interacting and engaging with stakeholders at all levels.

Skills Required

  • Minimum Science education with specialism in Engineering/Technology
  • Significant experience in a similar role within a pharmaceutical GMP-compliant factory
  • Knowledge of current scientific literature and ability to apply research to formulation and development
  • Ability to develop and communicate executable formulation development plans
  • Experience authoring and reviewing regulatory and technical documents (batch records, process validation protocols/reports, technology transfer documents)
  • Experience in process optimization and validation
  • Experience preparing and executing stability studies as per ICH guidelines
  • Experience leading, guiding, or supervising research scientists and troubleshooting development problems
  • Experience working to MHRA and cGMP compliance standards
  • Excellent communication and interpersonal skills; ability to liaise with stakeholders at all levels
  • Strong organisation, administration skills, attention to detail, and ability to prioritise workload
  • Willingness to participate in general lab and instrument maintenance
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The Company
727 Employees
Year Founded: 1997

What We Do

Bristol Laboratories Ltd is a British pharmaceutical company founded in 1997 and based in Berkhamsted, Hertfordshire. The company specializes in the development, manufacture, marketing, and distribution of high-quality generic and over-the-counter medicines. Committed to improving health and wellbeing, Bristol Laboratories focuses on expanding its product pipeline to ensure the increased accessibility and availability of safe and effective pharmaceutical products across the UK and Europe.

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