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Sr Scientist - Steriles Packaging Development & Design (client dedicated)

Thermo Fisher Scientific

Sr Scientist - Steriles Packaging Development & Design (client dedicated)

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies

Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

Thermo Fisher Scientific are currently hiring for a Sr Scientist to provide support for multiple device development work streams for R&D combination product development projects. The role will be based at our client’s site in Ware, Hertfordshire, UK and can offer hybrid working. As a Senior Scientist you will be tasked with:

  • Support packaging and device development work streams for R&D integral drug device combination and/or co-packaged product development projects.

  • Management of Design History File (DHF) documentation

  • Ownership of device work packages, co-ordinate testing activities (e.g. verification, validation, Design of Experiments, robustness studies) to ensure combination product safety and performance

  • Author device development documentation including Design History Files (DHF) and Risk Management Files (RMF).

  • Participate in packaging and device risk assessments (e.g. user, design or process risk assessments) as needed

  • Participate in design reviews at critical stages of development as needed

  • Supplementatry activities to support specific projects as required


Essential Qualifications/Experience:

  • Graduate in Mechanical Engineering, Biomedical Engineering or related degree

  • Experience of medical device or combination product development.

  • Understanding and experience of working within device regulatory requirements and industry processes such as design controls (21 CFR 820.30), EU MDR 2017/745, risk management (ISO 14971), QMS (ISO 13485) and GMP.

  • Experience in Design History File, Risk Management File, and design controls for combination product experience in the pharmaceutical industry

Preferred Qualifications/Experience:

  • Experience in sterile drug primary packaging development for large and small molecules including vial/stopper, pre-filled syringes, and cartridges presentations.

  • Knowledge of device and packaging requirements and regulations (i.e., current applicable FDA/MAA guidelines, USP/Ph Eur, etc, ISO)

  • Knowledge of integral and non-integral parenteral packaging materials (such as vials, stoppers, PFS, syringes, needles), components, vendors, analytical equipment, and technologies.

  • Experience in sterile drug primary packaging development for large and small molecules including vial/stopper, pre-filled syringes, and cartridges presentations.

  • Knowledge of domestic and international device and packaging requirements and regulations (i.e., current applicable FDA/MAA guidelines, USP/Ph Eur, etc, ISO).

  • Knowledge of statistical analysis and Design of Experiments

  • Ability to quickly establish relationships with internal and external stakeholders. 

  • Strong time management / organizational skills. 

  • Evidence of team working skills and flexibility. 

Benefits

We offer competitive remuneration, annual incentive plan bonus, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. 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. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.  

Apply today! http://jobs.thermofisher.com 

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status

Locations

  • Ware, Hertfordshire, United Kingdom

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 GBP / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Packaging developmentintermediate
  • Device developmentintermediate
  • Design controlsintermediate
  • Risk management (ISO 14971)intermediate
  • Design of Experiments (DoE)intermediate
  • Verification and validation testingintermediate

Required Qualifications

  • Graduate in Mechanical Engineering, Biomedical Engineering or related (experience)
  • Experience in medical device or combination product development (experience)
  • Understanding of device regulatory requirements (21 CFR 820.30, EU MDR, ISO 13485, GMP) (experience)

Responsibilities

  • Support packaging and device development work streams
  • Manage Design History File (DHF) documentation
  • Own device work packages and coordinate testing
  • Author DHF and Risk Management Files (RMF)
  • Participate in risk assessments
  • Participate in design reviews

Benefits

  • general: Hybrid working
  • general: Full-time benefits
  • general: Direct experience at pharmaceutical site

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Thermo Fisher Scientific logo

Sr Scientist - Steriles Packaging Development & Design (client dedicated)

Thermo Fisher Scientific

Sr Scientist - Steriles Packaging Development & Design (client dedicated)

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies

Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

Thermo Fisher Scientific are currently hiring for a Sr Scientist to provide support for multiple device development work streams for R&D combination product development projects. The role will be based at our client’s site in Ware, Hertfordshire, UK and can offer hybrid working. As a Senior Scientist you will be tasked with:

  • Support packaging and device development work streams for R&D integral drug device combination and/or co-packaged product development projects.

  • Management of Design History File (DHF) documentation

  • Ownership of device work packages, co-ordinate testing activities (e.g. verification, validation, Design of Experiments, robustness studies) to ensure combination product safety and performance

  • Author device development documentation including Design History Files (DHF) and Risk Management Files (RMF).

  • Participate in packaging and device risk assessments (e.g. user, design or process risk assessments) as needed

  • Participate in design reviews at critical stages of development as needed

  • Supplementatry activities to support specific projects as required


Essential Qualifications/Experience:

  • Graduate in Mechanical Engineering, Biomedical Engineering or related degree

  • Experience of medical device or combination product development.

  • Understanding and experience of working within device regulatory requirements and industry processes such as design controls (21 CFR 820.30), EU MDR 2017/745, risk management (ISO 14971), QMS (ISO 13485) and GMP.

  • Experience in Design History File, Risk Management File, and design controls for combination product experience in the pharmaceutical industry

Preferred Qualifications/Experience:

  • Experience in sterile drug primary packaging development for large and small molecules including vial/stopper, pre-filled syringes, and cartridges presentations.

  • Knowledge of device and packaging requirements and regulations (i.e., current applicable FDA/MAA guidelines, USP/Ph Eur, etc, ISO)

  • Knowledge of integral and non-integral parenteral packaging materials (such as vials, stoppers, PFS, syringes, needles), components, vendors, analytical equipment, and technologies.

  • Experience in sterile drug primary packaging development for large and small molecules including vial/stopper, pre-filled syringes, and cartridges presentations.

  • Knowledge of domestic and international device and packaging requirements and regulations (i.e., current applicable FDA/MAA guidelines, USP/Ph Eur, etc, ISO).

  • Knowledge of statistical analysis and Design of Experiments

  • Ability to quickly establish relationships with internal and external stakeholders. 

  • Strong time management / organizational skills. 

  • Evidence of team working skills and flexibility. 

Benefits

We offer competitive remuneration, annual incentive plan bonus, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. 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. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.  

Apply today! http://jobs.thermofisher.com 

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status

Locations

  • Ware, Hertfordshire, United Kingdom

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 GBP / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Packaging developmentintermediate
  • Device developmentintermediate
  • Design controlsintermediate
  • Risk management (ISO 14971)intermediate
  • Design of Experiments (DoE)intermediate
  • Verification and validation testingintermediate

Required Qualifications

  • Graduate in Mechanical Engineering, Biomedical Engineering or related (experience)
  • Experience in medical device or combination product development (experience)
  • Understanding of device regulatory requirements (21 CFR 820.30, EU MDR, ISO 13485, GMP) (experience)

Responsibilities

  • Support packaging and device development work streams
  • Manage Design History File (DHF) documentation
  • Own device work packages and coordinate testing
  • Author DHF and Risk Management Files (RMF)
  • Participate in risk assessments
  • Participate in design reviews

Benefits

  • general: Hybrid working
  • general: Full-time benefits
  • general: Direct experience at pharmaceutical site

Target Your Resume for "Sr Scientist - Steriles Packaging Development & Design (client dedicated)" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Sr Scientist - Steriles Packaging Development & Design (client dedicated). Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr Scientist - Steriles Packaging Development & Design (client dedicated)" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Sr Scientist - Steriles Packaging Development & Design (client dedicated) @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.