QC Analyst II

QC Analyst II

Swindon Full-Time 30000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Conduct quality control testing and prepare technical documentation for products.
  • Company: Join Thermo Fisher Scientific, a leader in making the world healthier and safer.
  • Benefits: Enjoy opportunities for remote work, training, and a collaborative team environment.
  • Why this job: Be part of a mission-driven team that values innovation and diversity.
  • Qualifications: Degree in Chemistry or related field; experience with analytical techniques required.
  • Other info: Opportunity for overseas travel and involvement in continuous improvement activities.

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

Perform quality control analytical testing of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies.

Conduct technical transfer/method development/method validation as required.

Prepare technical documentation including but not limited to analytical write-ups, standard operating procedures, specifications, investigations and reports.

Perform planned preventative maintenance and performance calibrations on equipment.

Provide technical troubleshooting and problem solving related to analytical equipment, analytical methods or unexpected results.

Maintain own training records and support and train other team members as required.

Communicate effectively with others on site and internationally, and participate with them in problem solving activities.

Ensure cGMP is applied and followed in all areas of the business.

Work with HSE, cGMP and 5S in mind at all times including participation in continuous improvement activities looking for further opportunities to progress the team/department.

Carry out any other tasks which may be required from time to time.

Raw Material testing (includes instruments like FTIR, pH, UV-Vis, Density Meter, Karl Fischer).

Testing to Pharmacopeia (USP and Ph. Eur. in particular, which are the American and European Pharmacopeia respectively).

Experience in writing Deviations, Out of Specifications, Change Controls.

Understand emergency procedures and comply with safe systems of work.

Ensure compliance with environment, health and safety and security policies and procedures, rules, signage and instructions at all times.

Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules.

Minimum Requirements/Qualifications:

  • Degree in Chemistry or strongly related scientific discipline.
  • Experience of instrumental and traditional analytical techniques.
  • Ability to work to critical timelines with the ability to commit to overseas travel as part of a project team.
  • A strong ability to build positive working relationships with both internal and external business customers and clients.
  • Highly motivated and detail oriented individual with excellent communication, computer and organisational skills.

About us:

Our Mission is to enable our customers to make the world healthier, cleaner and safer.

As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.

QC Analyst II employer: Thermo Fisher Scientific

At Thermo Fisher Scientific, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our commitment to employee growth is evident through continuous training opportunities and a supportive environment where diverse perspectives are valued. Located in a dynamic setting, our QC Analyst II role offers the chance to contribute to meaningful projects that enhance global health and safety, all while working alongside a dedicated team of over 100,000 colleagues who share a passion for making the world a better place.
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Contact Detail:

Thermo Fisher Scientific Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QC Analyst II

✨Tip Number 1

Familiarise yourself with cGMP regulations and the specific analytical techniques mentioned in the job description, such as FTIR and UV-Vis. This knowledge will not only help you during interviews but also demonstrate your commitment to quality control standards.

✨Tip Number 2

Network with professionals in the pharmaceutical and quality control sectors. Attend industry events or join relevant online forums to connect with people who can provide insights into the role and potentially refer you to opportunities at StudySmarter.

✨Tip Number 3

Prepare to discuss your experience with technical documentation and problem-solving in analytical settings. Be ready to share specific examples of how you've handled deviations or out-of-specification results in past roles.

✨Tip Number 4

Showcase your ability to work under pressure and meet critical timelines. Think of instances where you've successfully managed tight deadlines or complex projects, as this will resonate well with the expectations for the QC Analyst II position.

We think you need these skills to ace QC Analyst II

Quality Control Analytical Testing
cGMP Compliance
Technical Transfer
Method Development
Method Validation
Technical Documentation Preparation
Analytical Write-Ups
Standard Operating Procedures (SOPs)
Specifications and Investigations
Preventative Maintenance
Performance Calibration
Technical Troubleshooting
Problem Solving
Raw Material Testing
Instrumental Techniques (FTIR, pH, UV-Vis, Density Meter, Karl Fischer)
Pharmacopeia Knowledge (USP and Ph. Eur.)
Deviation and Out of Specification Writing
Change Control Documentation
Emergency Procedures Understanding
Health, Safety and Environment (HSE) Compliance
Strong Communication Skills
Organisational Skills
Ability to Work to Critical Timelines
Team Collaboration

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in quality control and analytical testing. Emphasise your familiarity with cGMP conditions and any specific instruments mentioned in the job description, such as FTIR or UV-Vis.

Craft a Strong Cover Letter: In your cover letter, express your passion for quality control and how your background aligns with the company's mission. Mention your ability to work under critical timelines and your experience in writing technical documentation like SOPs and reports.

Showcase Communication Skills: Since effective communication is key for this role, provide examples in your application of how you've successfully collaborated with teams or solved problems in previous positions. This will demonstrate your ability to build positive working relationships.

Highlight Continuous Improvement: Discuss any experiences you have with continuous improvement activities or initiatives. This could include participation in projects that enhanced processes or compliance with health and safety standards, showcasing your proactive approach.

How to prepare for a job interview at Thermo Fisher Scientific

✨Know Your Analytical Techniques

Make sure you brush up on your knowledge of both instrumental and traditional analytical techniques. Be prepared to discuss your experience with specific instruments like FTIR, UV-Vis, and Karl Fischer during the interview.

✨Understand cGMP Regulations

Familiarise yourself with current Good Manufacturing Practices (cGMP) as they are crucial for the role. Be ready to explain how you've applied these regulations in your previous work and how you ensure compliance in all areas.

✨Prepare Technical Documentation Examples

Since the role involves preparing technical documentation, think of examples where you've written analytical write-ups, standard operating procedures, or reports. Highlight your attention to detail and ability to communicate complex information clearly.

✨Showcase Problem-Solving Skills

Be prepared to discuss specific instances where you've encountered unexpected results or equipment issues. Emphasise your troubleshooting skills and how you collaborated with others to resolve these challenges effectively.

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