At a Glance
- Tasks: Assist in executing innovative projects and conduct experiments in a dynamic lab environment.
- Company: Join MedPharm, a leader in process development with a collaborative ethos.
- Benefits: Gain hands-on experience, develop your skills, and work in a supportive team.
- Why this job: Make a real impact in the pharmaceutical industry while learning from experienced professionals.
- Qualifications: BSc in a relevant field and a passion for research and development.
- Other info: Opportunity for career growth in a vibrant and inclusive workplace.
The predicted salary is between 30000 - 50000 £ per year.
General Information:
- Department: Process Development
- Site: Guildford, UK
- Reporting To: Team Leader
Position Summary
To assist the Scientist / Senior Scientist in executing projects within the set timeline. Perform pre-defined experiments according to the study plan and in compliance with GxP regulations and MedPharm's QMS.
Essential Functions
- Adhere to MedPharm ethos and comply with MedPharm's SOPs, policies and QMS systems.
- Maintain confidentiality of information and data.
- Assist more senior team members in executing projects in accordance with the study documentation, experimental designs, and SOPs, in agreed timelines and in compliance with MedPharm's QMS.
- Maintain cross-functional communication with the internal stakeholders of the project(s) being worked on.
- Review literature (including equipment operating procedures) in preparation for studies and regularly update knowledge by reading appropriate literature and/or attending appropriate training courses/webinars.
- Under the guidance of a more senior team member, manufacture and fill formulations as required for the stage of the project, including but not limited to, working on BMRs to provide toxicology batches in Process Development and clinical batches in GMP.
- Characterise formulations during different project phases.
- Communicate the progress of studies to the Team Leader / Scientist / Senior Scientist / Study Manager as appropriate and other internal stakeholders where required.
- Assist Team Leader / Scientist / Senior Scientist / Study Manager with data input for written project updates.
- Attend and contribute to internal project meetings as required.
- Plan and organise the work with a certain degree of autonomy with due consideration to the resources.
- Report any amendments and deviations from SOPs and study plans/testing protocols to Team Leader / Scientist / Senior Scientist / Study Manager as appropriate.
- Ensure that all activities are carried out in line with MedPharm's Health and Safety policy and COSHH regulations to ensure the safety of themselves and others in any procedures or tasks performed.
- Assist other team members as and when required to complete project work.
- Assist in the smooth running of laboratory activities and maintenance of laboratory standards in compliance with MedPharm's QMS.
- Undertake general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment.
- Maintain training records.
- Be sufficiently trained to undertake GMP activities on request.
Supervisory responsibilities: None
Key Relationships:
- Departmental Scientists of all grades
- Study managers
- Head of Department
- Technicians
- Quality assurance
Travel requirements: None
Education And Experience
BSc in a relevant field
Knowledge, Skills, And Abilities
Knowledge:
- Emulsions
- Excipients
- Testing according to a monograph, e.g., USP
- Moving through different scales of manufacture
Skills:
- Solution-focused
- Attention to detail
- Problem solving
- Ability to work independently and within a team
Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.
- Regularly required to walk within production and laboratory areas.
- May be required to stand for extended periods.
- Exposure to cleanroom environments and temperature-controlled zones.
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, Process Development in London employer: MedPharm
Contact Detail:
MedPharm Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Scientist, Process Development in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews! Research the company, understand their projects, and think about how your skills align with their needs. We want you to walk in feeling confident and ready to impress!
✨Tip Number 3
Showcase your passion! During interviews, let your enthusiasm for the role and the field shine through. We love candidates who are genuinely excited about contributing to the team and making an impact.
✨Tip Number 4
Don’t forget to follow up! A quick thank-you email after your interview can go a long way. It shows your appreciation and keeps you fresh in their minds. Plus, we’re all about building those connections!
We think you need these skills to ace Associate Scientist, Process Development in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Associate Scientist role. Highlight your relevant experience in process development and any specific skills that match the job description, like your knowledge of emulsions or GMP activities.
Showcase Your Team Spirit: We love a good team player! In your application, mention any experiences where you collaborated with others or assisted senior team members. This shows you can maintain cross-functional communication, which is key for this role.
Attention to Detail is Key: Since the role involves adhering to SOPs and QMS systems, make sure to demonstrate your attention to detail in your application. You could mention specific projects where you followed strict protocols or contributed to maintaining laboratory standards.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the position. Plus, it makes the whole process smoother for everyone involved.
How to prepare for a job interview at MedPharm
✨Know Your Stuff
Make sure you brush up on your knowledge of emulsions, excipients, and testing protocols. Familiarise yourself with the latest literature and any relevant SOPs. This will not only show your commitment but also help you answer technical questions confidently.
✨Showcase Your Team Spirit
Since this role involves cross-functional communication, be ready to discuss how you've successfully collaborated with others in past projects. Share specific examples that highlight your ability to work independently while also being a supportive team member.
✨Prepare for Practical Scenarios
Expect to be asked about how you would handle specific situations related to project timelines or compliance with GxP regulations. Think through potential challenges and how you would address them, demonstrating your problem-solving skills and attention to detail.
✨Ask Smart Questions
At the end of the interview, have a few insightful questions ready. Inquire about the team's current projects or how they measure success in the role. This shows your genuine interest in the position and helps you gauge if it's the right fit for you.