At a Glance
- Tasks: Support drug development by performing analytical testing and method optimisation.
- Company: Join a leading pharmaceutical company focused on innovation and collaboration.
- Benefits: Gain hands-on experience, competitive salary, and opportunities for professional growth.
- Other info: Dynamic lab environment with a focus on teamwork and scientific excellence.
- Why this job: Make a real impact in healthcare by contributing to new drug formulations.
- Qualifications: Bachelor's degree in Chemistry or related field; familiarity with analytical techniques.
The predicted salary is between 30000 - 40000 £ per year.
The Associate Scientist (Analytical) plays a key role in supporting research and development studies by performing analytical testing of pharmaceutical compounds, drug substances, and drug products. This role is integral to the development of new drug formulations, ensuring accurate data generation to guide formulation design and process development. Working under the supervision of team leaders and senior scientists, the associate scientist is responsible for executing analysis through HPLC and GC in compliance with internal protocols and industry standards. The position involves HPLC method development and optimisation to support early and late-stage pharmaceutical development. This role requires strong technical and organisational skills, attention to detail, and a commitment to scientific excellence in a fast-paced, collaborative R&D environment.
Essential Functions
- Responsible for executing a variety of analytical techniques such as HPLC and GC to support the development of pharmaceutical drug products as well as assist in the day-to-day running of the laboratory in compliance with MedPharm’s QMS.
- Performing pre-defined experiments according to internal standard operating procedures (SOP) (e.g. forced degradation of substance and product, saturated solubility, excipient compatibility and formulation stability).
- Support analytical method development and validation in accordance with ICH and FDA guidelines.
- Accurately document all experiments and results and have a good understanding and demonstration of good laboratory practice (GLP), data integrity and quality.
- Analyze data using Empower and interpret results to support formulation development, stability studies and product release.
- Take an active responsibility for your analytical work with respect to quality and compliance, particularly in the support of the analytical team.
- To assist the progression of the study by collaborating with other departments, with oversight from your supervisor where appropriate.
- To attend meetings and contribute when appropriate.
- To aid in the department’s method development and continuous improvement strategies.
- Adhere to Health and Safety and COSHH regulations and read relevant safety data sheets and risk assessments prior to undertaking work.
- To maintain your training file (physical and MasterControl based) and to not use any equipment or handle any chemicals without following the appropriate health and safety guidance.
- To undertake general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment.
- To conduct yourself in concordance with the MedPharm Ethos, professionalism and confidentiality.
Key Relationships
- R&D Laboratory staff
- Analytical Team Leaders
- FD, PD and PT Study Managers
- Project Management team
- QC team
- Quality Assurance team
Education and Experience
- Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline.
- Familiarity with common analytical equipment and instrumentation (e.g. analytical balance, pH meter, HPLC, GC).
Knowledge, Skills, and Abilities
- Computer literate and knowledgeable in Microsoft Office Applications.
- Effective oral and written communication.
- Good observation skills and ability to document accurately.
- Strong ability to work in teams and collaboration.
- Good time management and organisational skills.
- Good knowledge and practical experience in analytical laboratory.
Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position. Example:
- Occasionally required to lift up to 20kg.
- Requires standing for extended periods.
- May be exposed to loud noise levels.
- May be exposed to hot or cold temperatures.
Other Duties
You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.
Limitations and Disclaimer
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.
Associate Scientist, Analytical in Surrey employer: MedPharm
As a Process Technician in our cGMP-compliant biopharmaceutical manufacturing environment, you will be part of a dynamic team that values safety, quality, and continuous improvement. We offer a supportive work culture that encourages professional growth through training and development opportunities, ensuring you can thrive in your role while contributing to meaningful advancements in healthcare. Located in a state-of-the-art facility, we provide a collaborative atmosphere where your skills and expertise will be recognised and rewarded.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Scientist, Analytical in Surrey
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We think you need these skills to ace Associate Scientist, Analytical in Surrey
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at MedPharm!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show MedPharm that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at MedPharm!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At MedPharm, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at MedPharm
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at MedPharm that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with MedPharm’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.