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- Tasks: Conduct solid form screening projects for pharmaceutical ingredients in a dynamic lab environment.
- Company: Join Cambrex, a leading global CDMO with over 40 years of experience.
- Benefits: Full-time role with opportunities for professional growth and development.
- Why this job: Make a real impact in drug development while working with cutting-edge technologies.
- Qualifications: BSc or higher in chemistry, with 2+ years in a pharmaceutical setting.
- Other info: Collaborative team atmosphere with a focus on innovation and quality.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid‑phase peptide synthesis, solid‑state science, material characterization, and highly potent APIs.
As a solid form scientist based in Edinburgh, you will, together with our clients across the pharmaceutical industry, participate in the discovery and selection of the most important solid forms of active pharmaceutical ingredients (APIs) to take into the next stage of development. You will work with small and large molecules to identify optimal solid forms to move the API further along the development pipeline. You will form an important part of our technical team and will work at the cutting‑edge in a fast‑paced and rewarding environment. You will demonstrate the highest technical standards, while maintaining compliance to quality and safety systems.
ResponsibilitiesThe main purpose of the Solid Form Scientist is to carry out solid form screening projects to the highest technical standards, on the Active Pharmaceutical Ingredients (APIs) for clients of Cambrex. Also, to facilitate closure of projects with minimal lead‑time, while maintaining compliance to quality and safety systems, so that clients can progress development of their product/API.
Qualifications / Skills- An enthusiastic team player with excellent communication skills.
- Ability and willingness to learn new skills and techniques.
- Application of knowledge to solve complex problems.
- Demonstrate high levels of motivation and the organisational planning tools to manage workload across multiple projects.
- Be commercially aware of business development needs.
- Knowledgeable of the pharmaceutical development continuum of APIs.
- Knowledge of polymorphism, salt/co‑crystal screening, and peptide crystallization screening (essential).
- Ability to discuss complex technical data clearly and succinctly (essential).
- Ability to work safely in a lab environment, adhering to local SHE policies (essential).
- Experience of working independently and within a team in an R&D environment, within ISO9001 and/or cGMP quality standards (essential).
- BSc (Hons), Masters in chemistry, PhD in chemistry, chemical engineering or related discipline (essential).
- 2+ years industrial experience in a pharmaceutical company / contract research organisation.
- Experience of working with small molecules and/or large molecules (peptide fragments, cyclic and linear peptides) and other complex modalities (essential).
- Practical experience in a laboratory setting using wet chemistry techniques (essential).
- Experience/knowledge of solid‑state analytical techniques (e.g., XRPD, DSC, TGA/DSC, microscopy, DVS, single‑crystal X‑ray diffraction) and more general spectroscopic (e.g., NMR, FT‑IR, Raman) (essential).
- Experience using automated screening platforms (desirable).
- Experience in working independently and within a team in an R&D environment.
- Experience with working safely in a lab environment and adhering to local SHE policies.
- Able to participate in client meetings and discuss technical data clearly and succinctly.
- Possess excellent oral and written communication skills.
- Be well organised and able to manage high workloads.
- Able to meet deadlines and plan one’s own work effectively.
- Possess excellent problem‑solving skills.
- Be commercially aware of business development needs.
- Knowledgeable of the pharmaceutical development continuum of APIs.
Cambrex Edinburgh is unable to offer visa sponsorship for this job role; applicants must be able to provide proof of their right to work in the UK. Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, colour, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
Seniority level: Mid‑Senior level
Employment type: Full‑time
Job function: Research, Analyst, and Information Technology
Industries: Pharmaceutical Manufacturing
Screening Scientist II employer: Cambrex
Contact Detail:
Cambrex Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Screening Scientist II
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that Screening Scientist II role.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and being ready to discuss your experience with solid-state analytical techniques. We want you to shine when it comes to showcasing your skills!
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe showing appreciation goes a long way in making a lasting impression.
✨Tip Number 4
Apply through our website for the best chance of getting noticed. We’re always on the lookout for passionate candidates who fit the bill, so make sure your application stands out!
We think you need these skills to ace Screening Scientist II
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Screening Scientist II role. Highlight your relevant experience in solid form screening and any specific techniques you've used, like XRPD or DSC. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the pharmaceutical industry and how your background makes you a great fit for Cambrex. Keep it concise but impactful – we love a good story!
Show Off Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Use clear and succinct language, especially when discussing your technical experience. We want to see how well you can convey complex information!
Apply Through Our Website: Don't forget to apply through our website! It’s the best way to ensure your application gets into the right hands. Plus, it shows us you're serious about joining our team at Cambrex!
How to prepare for a job interview at Cambrex
✨Know Your Solid Forms
Make sure you brush up on your knowledge of solid forms, polymorphism, and salt/co-crystal screening. Be ready to discuss how these concepts apply to the role and share any relevant experiences you've had in your previous work.
✨Showcase Your Lab Skills
Prepare to talk about your practical experience in a laboratory setting. Highlight specific wet chemistry techniques you've used and any solid-state analytical methods you're familiar with, like XRPD or DSC. This will demonstrate your hands-on expertise.
✨Communicate Clearly
Since excellent communication skills are essential for this role, practice explaining complex technical data in a clear and succinct manner. You might even want to do a mock interview with a friend to refine your delivery.
✨Demonstrate Team Spirit
As an enthusiastic team player, be prepared to share examples of how you've collaborated with others in an R&D environment. Discuss how you manage workloads across multiple projects while maintaining high standards and compliance with quality systems.
