Specialist Analytical Development in Livingston

Specialist Analytical Development in Livingston

Livingston Full-Time 36000 - 60000 £ / year (est.) On-site
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At a Glance

  • Tasks: Conduct analysis and develop analytical methods in a fast-paced pharmaceutical environment.
  • Company: Leading European contract manufacturer in pharmaceuticals and biotech.
  • Benefits: Exciting challenges, collaborative team, and opportunities for professional growth.
  • Other info: Flexible working hours and a dynamic environment await you.
  • Why this job: Join a passionate team making a real impact in healthcare innovation.
  • Qualifications: Relevant science degree and experience in analytical techniques like HPLC and GC.

The predicted salary is between 36000 - 60000 £ 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. 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.

Job Purpose: 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:

  • 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 and presentation skills.
  • Able to get on with others and be a team player, but equally comfortable working independently.

Personal Situation:

  • Flexible and able to work extended hours when required.

Specific Job Skills:

  • 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.
  • 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.

Thank you for your interest. We look forward to receiving your application.

Specialist Analytical Development in Livingston employer: NextPharma

NextPharma is an excellent employer that fosters a collaborative and innovative work culture in Livingston, Scotland. Employees benefit from ongoing professional development opportunities, competitive compensation, and a commitment to regulatory excellence, making it a rewarding place for those passionate about pharmaceutical sciences and formulation development.

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Contact Details:

NextPharma Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Specialist Analytical Development in Livingston

✨Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like NextPharma. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

✨Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like NextPharma.

✨Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like NextPharma. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

✨Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what NextPharma is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Specialist Analytical Development in Livingston

Analytical Techniques
HPLC
Gas Chromatography
Karl Fischer
Dissolution
Method Development
Validation

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 NextPharma!

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 NextPharma 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 NextPharma!

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 NextPharma, 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 NextPharma

✨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 NextPharma that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

✨Showcase Relevant Experience

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 NextPharma’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.

✨Be Ready for Regulatory Scenarios

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.