Reference Standard Scientist - Client - dedicated in Stevenage

Reference Standard Scientist - Client - dedicated in Stevenage

Stevenage Full-Time 35000 - 45000 £ / year (est.) Home office (partial)
T

At a Glance

  • Tasks: Lead the management of Reference Standards for drug substances and ensure compliance with regulations.
  • Company: Join a leading pharmaceutical company dedicated to quality and innovation.
  • Benefits: Enjoy a hybrid working model, competitive salary, and opportunities for professional growth.
  • Other info: Dynamic role with opportunities for travel and continuous improvement in processes.
  • Why this job: Make a real impact on patient safety and product quality in a collaborative environment.
  • Qualifications: Bachelor's degree in a scientific discipline and experience in project teams required.

The predicted salary is between 35000 - 45000 £ per year.

The Reference Standard Scientist will lead the management and oversight of Reference Standards (RS) for small molecule drug substances and products. This role ensures compliance with Good Manufacturing Practices (GMP), regulatory requirements, and internal standards, supporting the quality and integrity of analytical data for clinical and commercial use.

Responsibilities:

  • Co-ordinate and support the testing and documentation of all aspects of characterization, qualification and stability, including retest and shelf-life extensions, of Reference Materials (Primary, Working, and Development Standards) in accordance with client processes and procedures, ensuring compliance with GMP requirements where required.
  • Manage the inventory and coordinate distribution of reference materials.
  • Establish and maintain partnerships with Global Supply Chain, Analytical Project Scientists, Quality and third parties to ensure high quality, efficient service delivery.
  • Coordinate and manage the transfer of information for R&D reference materials to the commercial reference materials group.
  • Actively prepare and support internal quality and external regulatory inspections.
  • Proactively contribute to the resolution of technical and operational problems for reference materials and certificate of analysis generation.
  • Draft Certificates of Analysis in accordance with the relevant regulations, corporate policies and standards to ensure patient safety, product quality and data integrity.
  • Adopt data and digital tools to drive continuous improvement and deliver simplified, efficient business processes.

Qualifications:

  • Bachelor of Science in Chemistry, Biology, or other related scientific discipline or experience in a directly related discipline.
  • Experience in a project team or directly related discipline.
  • Experience in LIMS system for data recording and reporting.
  • Knowledge and/or experience with digital tools for inventory management or data reporting is beneficial.
  • Ability to work with multiple tasks simultaneously to meet client needs is essential.
  • Ability to work in a collaborative work environment with a team.
  • Knowledge of general chemistry and separation science.
  • Proficiency on technical operating systems.
  • Proven ability in technical writing skills.
  • Time management and project management skills.
  • Good written and oral communication skills.

Work Conditions:

  • Ability to travel to the Ware site occasionally.
  • This role is offered on a hybrid working model, combining home-based work with time on site in Stevenage.

Reference Standard Scientist - Client - dedicated in Stevenage employer: Thermofisher Scientific

As a Reference Standard Scientist at our company, you will thrive in a dynamic and collaborative work environment that prioritises employee growth and development. With a hybrid working model based in Stevenage, we offer a supportive culture that values innovation and compliance, alongside competitive benefits and opportunities for professional advancement in the pharmaceutical industry.

T

Contact Details:

Thermofisher Scientific Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Reference Standard Scientist - Client - dedicated in Stevenage

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Thermofisher Scientific. 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 Thermofisher Scientific.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Thermofisher Scientific. 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 Thermofisher Scientific is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Reference Standard Scientist - Client - dedicated in Stevenage

Good Manufacturing Practices (GMP)
Analytical Skills
Project Management
LIMS system experience
Technical Writing Skills
Data Reporting
Inventory Management

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 Thermofisher Scientific!

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 Thermofisher Scientific 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 Thermofisher Scientific!

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 Thermofisher Scientific, 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 Thermofisher Scientific

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 Thermofisher Scientific 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 Thermofisher Scientific’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.