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- Tasks: Conduct analysis and develop analytical methods in a fast-paced pharmaceutical environment.
- Company: Join NextPharma, a leading European contract manufacturer in healthcare.
- Benefits: Competitive salary, private medical insurance, pension scheme, and life insurance.
- Other info: Dynamic team environment with opportunities for personal and professional growth.
- Why this job: Make a real impact in drug development while working with cutting-edge technology.
- Qualifications: Relevant science qualification and experience in analytical techniques like HPLC and GC.
The predicted salary is between 30000 - 40000 £ per year.
Are you looking for an exciting professional challenge? We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
Job Purpose
Development analyst: To conduct analysis, technical stability studies, development, validation and transfer of analytical methods. The role will be responsible for providing technical expertise at both a theoretical and practical level. The ideal candidate will therefore have a pharmaceutical analysis background and have gained experience within a cGMP, FDA and MHRA regulated environment.
Key responsibilities and accountabilities:
- Work as part of a team alongside other analytical departments.
- Actively involved in performing analytical activities to determine fitness for purpose of finished products.
- Conduct analysis to support formulation development.
- Perform method development, validation and transfer analysis of analytical methods for Liquid Fill hard capsules.
- Technically competent in analytical activities (e.g., method development and validation, HPLC, GC, Karl Fisher and Dissolution).
- Validation activities performed under current cGMP and ICH Q2.
- Writing of development and validation protocols and reports.
- Checking of analytical data.
- Supporting good internal and external relationships and communication.
- Comply with company health and safety procedures.
Person Profile: Development Analyst
Personality: Results oriented with a positive outlook and clear focus on high quality output; Solid planning and organizational ability; Reliable, tolerant and dependable; Enjoy working in a stimulating environment. Comfortable dealing with peers and customers. Goal-oriented: Able to work under pressure and meet deadlines; Excellent communication/presentation skills. Able to get on with others and be a team player, but is equally comfortable working independently.
Personal Situation: Flexible and able to work extended hours when required.
Specific Job Skills:
Required:
- Relevant qualification, HNC/HND/Science Degree or Equivalent.
- An understanding of drug development and manufacturing processes.
- Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards.
- Must be skilled in analytical techniques e.g., HPLC, Dissolution, Gas Chromatography, and Karl Fisher techniques.
- Experience of the technical and practical skills involved in stability studies, method development, transfer and validation.
- Able to communicate well with others, both laboratory and non-laboratory based.
- Able to work with minimal supervision.
- Good understanding of working within cGMP/GLP environment.
Desired:
- Experience of working within a fast paced pharmaceutical or biotechnology industry.
- Minimum 3 years previous relevant experience in similar environment.
- Ability to work to key regulatory and compliance requirements.
- Experience of Chromeleon software.
- Experience of chemical analysis within a pharmaceutical environment (with formulations of drug products for pre-clinical and clinical trials).
- Experience of data reporting and data checking to GMP standards.
- Able to work with minimal supervision and provide guidance to junior analytical analysts.
- Understand and demonstrate a pragmatic approach to problem solving with GMP constraints.
- Able to communicate well via written media with specific emphasis on report writing.
Computer skills: Must be competent in the use of MS Office, particularly Excel and Word, e-mail and internet.
Literacy and Numeracy: Must be competent in writing reports both for internal use and for customers. Must be competent in the interpretation of analytical data.
Business Presentation Skills: Must be an excellent face-to-face and telephone communicator.
Please note – only applicants with a permanent Right to Work in the UK will be considered.
Remuneration Package:
Basic Salary: £DOE
Private Medical Insurance
Health Cash Plan
Contributory pension scheme
Life Insurance
NextPharma is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
It's time for your next chapter: We look forward to receiving your application.
Specialist Analytical Development in Edinburgh employer: NextPharma
Contact Detail:
NextPharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Specialist Analytical Development in Edinburgh
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical and biotech sectors on LinkedIn. Join relevant groups, participate in discussions, and don’t hesitate to ask 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 NextPharma thoroughly—know their values, recent projects, and industry trends. We want to see your passion for the role shine through, so practice answering common interview questions and think of examples that showcase your analytical skills.
✨Tip Number 3
Showcase your skills! Bring along a portfolio of your work or any relevant projects you've been involved in. This could include reports, presentations, or even case studies. We love seeing tangible evidence of your expertise, especially in analytical methods and compliance with cGMP standards.
✨Tip Number 4
Follow up after your interview! A simple thank-you email can go a long way. It shows your appreciation and keeps you fresh in the interviewer’s mind. Plus, it’s a great opportunity to reiterate your enthusiasm for the role and how you can contribute to NextPharma’s success.
We think you need these skills to ace Specialist Analytical Development in Edinburgh
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the job description. Highlight your analytical skills, especially in HPLC and method validation, to show us you're the right fit for the Specialist Analytical Development role.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about this role and how your background aligns with our needs. Share specific examples of your experience in a cGMP environment to grab our attention!
Showcase Your Communication Skills: Since excellent communication is key, ensure your application is clear and well-structured. We want to see your ability to write reports and communicate effectively, so don’t shy away from demonstrating this in your application.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team!
How to prepare for a job interview at NextPharma
✨Know Your Analytical Techniques
Make sure you brush up on your knowledge of analytical techniques like HPLC, GC, and Karl Fischer. Be ready to discuss how you've applied these methods in previous roles, especially in a cGMP environment. This will show that you're technically competent and understand the practical aspects of the job.
✨Showcase Your Team Spirit
NextPharma values teamwork, so be prepared to share examples of how you've collaborated with others in past projects. Highlight any experiences where you supported good internal and external relationships, as this will demonstrate your ability to work well within a team.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving skills, particularly under GMP constraints. Think of specific challenges you've faced in your previous roles and how you approached them. This will help you illustrate your pragmatic approach to overcoming obstacles.
✨Communicate Clearly and Confidently
Since excellent communication skills are crucial for this role, practice articulating your thoughts clearly. Prepare to discuss your report writing experience and how you've communicated complex data to both laboratory and non-laboratory colleagues. Confidence in your communication can set you apart!