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JobsThermo Fisher

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

Thermo Fisher

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

Thermo Fisher

Ware, United Kingdom

·

On-site

·

Full-time

·

1w ago

Required Skills

Medical Device Development

Design Controls

Risk Management

Regulatory Compliance

Documentation

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. #Start Your Story 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

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About Thermo Fisher

Thermo Fisher

Thermo Fisher Scientific Inc. is an American life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.

10,001+

Employees

Waltham

Headquarters

Reviews

3.9

2 reviews

Work Life Balance

3.5

Compensation

2.5

Culture

3.5

Career

4.0

Management

3.0

65%

Recommend to a Friend

Pros

Large company with extensive resources

Structured internship program

Career opportunities in product management

Cons

Low compensation ($22/hour)

High cost of living in location

Expensive housing/rent

Salary Ranges

2,260 data points

Mid/L4

Mid/L4 · Adobe Analytics Launch Developer

1 reports

$137,796

total / year

Base

$105,997

Stock

-

Bonus

-

$137,796

$137,796

Interview Experience

8 interviews

Difficulty

3.0

/ 5

Duration

14-28 weeks

Offer Rate

12%

Experience

Positive 12%

Neutral 63%

Negative 25%

Interview Process

1

Application Review

2

Recruiter Screen

3

Hiring Manager Interview

4

Panel Interview

5

Final Interview

6

Offer

Common Questions

Technical Knowledge

Behavioral/STAR

Past Experience

Culture Fit

Industry Specific