Senior Research Associate - Formulation

Talent Works; London; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading biotechnology company is seeking a Formulation Research Associate to advance drug candidates in a collaborative lab environment. The role involves developing solid dosage forms, interpreting experimental data, and ensuring compliance with safety procedures. Ideal candidates are detail-oriented with technical expertise in pharmaceutical sciences and experience in formulation techniques.

Qualifications

• Experience with solid dosage form development for clinical and commercial use.
• Knowledge of QbD and regulatory filings is a plus.
• Experience working with CMOs is a plus.

Responsibilities

• Develop solid dosage forms and conduct optimization studies.
• Maintain accurate laboratory notebooks and document outcomes.
• Assist in technical transfer for clinical trial manufacture.

Skills

Technical knowledge of pharmaceutical principles

Formulation techniques

Statistical analysis

Technical writing

Communication skills

Multitasking

Detail-oriented

Education

Bachelor’s degree in pharmaceutical sciences, chemistry, or related field

Master's degree in pharmaceutical sciences or related field

Job description

View more categories View less categories Discipline R & D ,Chemistry Hours Full Time Contract Type Contract Experience Level Experienced (non-manager)

Looking for opportunities with purpose, impact and possibilities? Our client, Vertex, is a global biotechnology company that invests in scientific innovation. As they grow their pipeline at pace, they are strengthening their reputation for creating transformative medicines for people with serious diseases.

The Formulation Research Associate will perform an array of activities working with other scientists to advance drug candidates from exploratory development through commercial line extension in a Quality by Design (QbD) environment using lab based and computational tools.


Key Duties and Responsibilities:

• Contribute to the development of solid dosage forms for clinical and commercial use, generate data for project progression and regulatory filings, conduct a range of activities for optimization and scale up studies

• Help execute, and interpret laboratory experiments, with minimal supervision, to meet established project timelines

• Maintain accurate and complete laboratory notebook capturing protocols, results and observations

• Interpret data to form sound conclusions

• Timely document integrated experimental outcomes in presentations and research reports

• Perform basic statistical analysis of experimental data

• Assist in technical transfer to CMO partners for clinical trial manufacture

• Initiate experimental troubleshooting on routine problems, with minimal supervision

• Contribute to drafting regulatory filing documentation

• Comply with all relevant Safety and GMP procedures

Knowledge and Skills:

• Sound technical knowledge of pharmaceutical and engineering principles in the solid dosage form development for both clinical and commercial scales

• Hands on experience with formulation techniques, processing equipment, and unit operations at both the laboratory and clinical manufacturing scales

• Strong math skills particularly as applied to material/energy balances, and intermediate applied statistical analysis

• Strong technical writing skills

• Strong verbal and written communication skills

• Successful and efficient multitasking and ability to work on a few projects concurrently

• Detail-oriented

• Direct experience working with CMOs is a plus

• Understanding of QbD and experience with Regulatory filings is a plus

• Strong background in oral solid form development and good understanding of material properties

Education and Experience:

• Bachelor’s degree in pharmaceutical, material science or chemical engineering field

• Typically requires a Master's Degree in pharmaceutical sciences, chemistry, chemical engineering, materials sciences or related field and 0-2 years experience in life sciences, engineering or academia, or

• Typically requires a Bachelor's Degree in pharmaceutical sciences, chemistry, chemical engineering, materials sciences or related field and 4 years experience in life sciences, engineering or academia

Vertex is partnering with Talent Works to manage their international temporary job openings. If you are successful in your application, you will be employed by Talent Works to work on a temporary assignment at Vertex.

Company

At Talent Works, we're changing the way that RPO & MSP programs are accessed, delivered and deployed - delivering smarter, scalable talent solutions to help you build your future workforce.

Braver, bolder and brighter, we are leading the rethink around how companies attract, hire and manage talent.

Website https://www.talent-works.com/ Location Century House
1 The Lakes
Northampton
NN4 7HD
United Kingdom

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