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About Curia
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. We have a fantastic opportunity to come and join our Formulation team here in Glasgow. If you are looking to develop your experience in pharmaceutical drug manufacturing within a formulation team, this is the perfect opportunity to join Curia as we enter our next stage of Growth and work towards the gold standard in pharmaceuticals. We provide excellent training in a fast-paced environment, offering variety and progression. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.
The Role
We are seeking a high-calibre Formulation Scientist to deliver formulation design, pre-formulation, and process development activities for sterile injectable dosage forms across a diverse range of compound categories, including small molecules, large molecules (biologics), highly potent compounds, and controlled substances.
Operating within a fast-paced CDMO environment, you will act as a technical subject matter expert across multiple client projects, converting bench-scale science into robust, GMP-ready manufacturing processes.
Key Responsibilities
- Technical & Project Execution: Deliver formulation design activities for small molecules, peptides, and biologics. Operate formulation and characterisation equipment, analyse complex laboratory data, and provide clear scientific explanations.
- Technology Transfer: Translate bench-scale variables (e.g., mixing protocols, filtration parameters, etc.) into workable clinical manufacturing processes. Liaise with production to ensure a seamless handoff to GMP manufacture.
- Documentation & Client Relations: Write clear work plans, project reports, and technical transfer documents. Attend and actively contribute to customer calls, act as a technical guide during timeline or data shifts, and support client audits.
- Quality & Safety Compliance: Strictly maintain GLP/GMP quality standards, follow department & site SOPs, and maintain meticulous technical notebooks.
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Role Requirements
Essential Qualifications & Experience
- Education: Degree-level qualification (or equivalent) in Chemistry, Biochemistry, Pharmacy, Biomedical Engineering, or a related science field.
- Experience: Minimum of 3 years of industry laboratory experience focused on pharmaceutical drug product formulation, pre-formulation, and/or process development. Other levels of relevant experience will be considered.
- Core Lab Skills: Hands-on experience utilising wet chemistry techniques, relevant formulation processes, and characterisation methods.
- Autonomy & Drive: Proven ability to take ownership of tasks, design experiments, manage equipment care, and navigate multiple project timelines under pressure.
- Communication: Exceptional oral and written communication skills with strong problem-solving abilities.
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Desirable Attributes
- Sterile Technical Expertise: Knowledge of aseptic processing regulations and parenterally acceptable excipient functionality.
- Advanced Processing: Practical knowledge of lyophilisation cycle optimisation/development, complex formulation processes (i.e., emulsion, liposomal, suspensions, etc.) and tangential flow filtration (TFF).
- Pre-formulation Depth: Experience measuring physical properties (e.g., XRPD, DVS, pH-solubility profiles).
- CDMO Agility: Ability to switch fluidly between diverse client molecules (small molecules, biologics, peptides, highly potent compounds) while maintaining strict scope and timeline discipline.
Benefits
- Up to 9% employer contribution to pension
- Dental
- Private healthcare
- 4x salary life scheme
- gym membership contribution
- cycle to work
- holiday purchase scheme
- sick pay
- 1 day’s extra holiday for every year you work here for up to 5 years
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