Formulation Scientist, Pharmaceutical

  • Russell Taylor
  • Bolton, Lancashire
  • Dec 01, 2022
Full time Engineering

Job Description

Formulation Scientist, Pharmaceutical

Type: Permanent

Location: Greater Manchester

Salary: £24,000 - £27,000 DOE

Hours: Monday - Friday (days) finishing at either 17:00 or 18.00

Additional: Company pension, 21 days + BH hols, parking onsite

Russell Taylor Group is working exclusively with a leading pharmaceutical manufacturing company who is growing and looking to appoint a Formulation Scientist. Alongside extensive training, the successful candidate will be given the chance to progress in this team and work closely with R&D.

The Role:

To undertake Formulation Development duties to support R & D. Supporting in

documentation and record keeping. Conducting validation, optimization and scale up

studies and support in designing new formulations.

  • Plan and schedule work to meet KPIs.
  • Review customer enquiries to create bespoke formulations
  • Conduct checks on data to ensure Quality and consistency of the data.
  • Perform tasks in a safe manner ensuring all relevant COSHH are read and bring delay.
  • any perceived safety issues to the attention of management (or nominee) without
  • To perform method development, verification/validation of existing and new
  • products.
  • Timely release of all products.
  • Support deviations, CAPA, change control, complaints and recalls.
  • Providing auditing support.
  • Ensuring targets are met and our company's strategy is achieved through
  • consistent development and coaching of staff.
  • Undertaking relevant project work as required, as part of continuous improvement
  • of R&D systems and processes.
  • To develop liquid, solid and semi-solid formulations for oral and topical products
  • and support the development of products from initial design to completion.
  • Help in sourcing of new raw materials and the specification of the analysis required
  • to determine the quality of those materials.
  • Writing technical documentation including batch manufacturing records, stage into manufacturing
  • specifications and technical reports and the transfer of projects from the laboratory
  • Involved in Validation activities such as DQ, IQ, OQ, PQ and PV
  • Generate protocols and reports
  • Review existing process to ensure compliance and streamlining

The Person:

  • Will hold a Degree in a relevant, Scientific discipline
  • Previous formulation experience in a Pharmaceutical setting is highly desirable
  • 3 + years working in a similar role within an GMP accredited organisation
  • Strong IT skills
  • Excellent communicator, able to work with various stakeholders in the business and communicate information verbally and written
  • Motivation, accuracy, discretion and helpfulness are critical to this position
  • Excellent problem solving, risk analysis and negotiation skills
  • Ability to adhere to strict deadlines

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please get in touch on h u s s e l l - t a y l o r . c o . u k