Scientist

Scientist

Deeside Temporary 30000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as a Scientist, executing physical testing and supporting R&D projects.
  • Company: We're a global leader in medical products, focused on chronic condition management.
  • Benefits: Enjoy a competitive pay of £122 per day and gain valuable industry experience.
  • Why this job: Be part of innovative projects that make a real impact on healthcare.
  • Qualifications: Bachelor's degree in a relevant science; lab experience in medical devices preferred.
  • Other info: Work in a compliant lab environment with opportunities for professional growth.

The predicted salary is between 30000 - 42000 £ per year.

Job Description

  • Job Title: Scientist 1 – Physical Testing
  • Contract: 12 months
  • Location: Deeside
  • Pay: £122 per day

SRG are partnered with a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care.

We are seeking a Scientist to join their Deeside team.

Duties

  • Maintain compliance Working within a controlled ISO13485 and ISO9001 Laboratory quality system and in accordance with GLP/GMP procedures.
  • Design, plan and execute Physical testing in support of R&D activities and base business projects in accordance with applicable and procedures and guidelines.
  • Involvement in the development and validation of new physical testing methods.
  • Effective organization of assigned workload; ensures integrity of all data generated and timely/accurate provision of results to GLP standards.
  • Accurate recording and analysis of laboratory data in accordance with good documentation practices
  • Perform detailed laboratory investigations to determine the root cause of atypical and out of specification results, apply corrective and preventative actions and author concise investigation reports.
  • Author validation protocols, reports and technical documents for medical Devices/ Pharmaceutical products
  • Assist in laboratory test method/procedural revisions.
  • Responsible for standard laboratory routines, equipment calibration, maintenance replenishment etc.
  • Ensures lab compliance with applicable cGMP regulations and SOPs/TD’s.
  • Involvement in change control activities and associated actions.

Requirements

  • Bachelor's Degree in a relevant science related discipline.
  • Experience in a working laboratory environment, within Medical Devices/ Pharmaceutical Industry is preferred.
  • Working knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (ISO13485:2016, ISO9001:2000, FDA 21 CFR part 820) and GMP Guidelines and Regulation.
  • Good working knowledge of Microsoft Office, specifically Word and Excel.
  • A detailed understanding of common statistical analysis and experience with MiniTab desirable.
  • Have an understanding of the role of Physical Testing within the product development process for both new product development and existing product development of medical devices / pharmaceuticals
  • Commands good physical testing and problem-solving skills and demonstrates an understanding of the steps involved in initiating and completing a variety of physical testing tasks to support key R&D projects.
  • Statically analyze data for reporting to senior physical testing staff
  • Effectively communicate both oral and written scientific and technical data to peers and managers
  • A thorough knowledge and understanding of the principles and concepts of compliance management, GMP/GLP and good documentation practices.
  • Competent in the production of high quality, accurate R&D technical documentation in a timely manner.
  • A forward-thinking team-player who willingly accepts new challenges and works to tight deadlines.
  • Commands Flexibility – ability to prioritize, manage multiple tasks and react/respond positively to changes in priority and workload.
  • Accurate with excellent attention to detail.
  • Decisive thinker; ability to make decisions and recommendations using own initiative.

Scientist employer: SRG

Joining our Deeside team as a Scientist offers you the chance to work in a dynamic environment focused on innovative medical solutions. We pride ourselves on fostering a collaborative work culture that encourages professional growth and development, providing employees with access to ongoing training and career advancement opportunities. With a commitment to quality and compliance, you will be part of a team that values integrity and excellence, making a meaningful impact in the healthcare industry.
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Contact Detail:

SRG Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Scientist

✨Tip Number 1

Familiarise yourself with ISO13485 and ISO9001 standards, as well as GLP/GMP procedures. Understanding these regulations will not only help you in the interview but also demonstrate your commitment to compliance in a laboratory setting.

✨Tip Number 2

Brush up on your physical testing methods and statistical analysis skills, particularly with tools like MiniTab. Being able to discuss specific testing methods and how you've applied them in past roles can set you apart from other candidates.

✨Tip Number 3

Prepare to discuss your experience with data integrity and documentation practices. Be ready to share examples of how you've maintained accurate records and complied with good documentation practices in previous roles.

✨Tip Number 4

Showcase your problem-solving skills by preparing examples of how you've tackled atypical results or challenges in the lab. Highlighting your ability to conduct thorough investigations and implement corrective actions will demonstrate your value to the team.

We think you need these skills to ace Scientist

Analytical Skills
Attention to Detail
Technical Aptitude
ISO 13485 Compliance
ISO 9001 Compliance
Good Laboratory Practice (GLP)
Good Manufacturing Practice (GMP)
Physical Testing Method Development
Data Analysis
Statistical Analysis
Microsoft Office Proficiency
MiniTab Experience
Problem-Solving Skills
Effective Communication Skills
Technical Documentation Skills
Change Control Management
Team Collaboration
Time Management
Flexibility in Task Management
Decisive Thinking

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in laboratory environments, particularly within the medical devices or pharmaceutical industry. Emphasise your knowledge of compliance with FDA and European regulations, as well as any specific skills related to physical testing.

Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Discuss how your background aligns with the job requirements, particularly your experience with ISO13485 and GMP guidelines, and your problem-solving skills in a laboratory setting.

Highlight Relevant Skills: When detailing your skills, focus on those mentioned in the job description such as statistical analysis, documentation practices, and effective communication. Provide examples of how you've successfully applied these skills in previous roles.

Proofread Your Application: Before submitting your application, thoroughly proofread all documents for spelling and grammatical errors. Ensure that your formatting is consistent and professional, as attention to detail is crucial for this role.

How to prepare for a job interview at SRG

✨Know Your Compliance Standards

Familiarise yourself with ISO13485, ISO9001, and GMP regulations. Be prepared to discuss how you have adhered to these standards in your previous roles, as compliance is crucial in the medical devices industry.

✨Demonstrate Your Problem-Solving Skills

Prepare examples of past experiences where you identified root causes of issues and implemented corrective actions. Highlight your analytical skills and how they contribute to effective physical testing.

✨Showcase Your Technical Documentation Skills

Be ready to talk about your experience in producing high-quality technical documents. Discuss any specific protocols or reports you've authored, and how you ensure accuracy and compliance in documentation.

✨Communicate Effectively

Practice explaining complex scientific concepts in simple terms. During the interview, demonstrate your ability to communicate both orally and in writing, as this is essential for collaborating with peers and reporting to management.

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