Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Senior Validation Engineer

Posted Nov 4, 2026
Job ID: JJJP00027215
Location
Sassenheim
Hours/week
40 hrs/week
Timeline
1 year
Payrate range
Unknown

Senior Validation Engineer


Location: Sassenheim

Duration: End of 2027 (starting beginning of 2027)

Hours: 40 hours per week

Work style: Hybrid (3 days on-site, 2 days at home.)


Imagine your next project as Senior Validation Engineer, working at the forefront of cutting edge work and technology with one of the leading Pharmaceutical companies in the world!


roles and responsibilities

The Sr. Engineer Validation MSAT Advanced Therapies is responsible for supporting Validation of supporting processes (e.g.  Mixing, Sterilization, Bio-decontamination, Aseptic Process simulation, airflow visualization pattern), process improvements and  standardization and/or technology implementation projects. The Engineer Validation MSAT Advanced Therapies acts as Subject  Matter Expert in one or more validation categories.


GENERAL RESPONSIBILITIES: 

  • Lead the execution of validation activities such as Bio-decontamination qualification, Aseptic process  simulation, mixing validation, bio-decontamination, aseptic process simulation, and airflow visualization  pattern. 

  • Write and review validation plans, protocols and reports.  

  • Communicate with stakeholders to coordinate timing of execution, provide status updates, and escalate  issues.  

  • Act as Project Core Team Member for medium sized projects and as such: 

o Define validation strategy. 

o Represent MSAT in multidisciplinary team and align with extended team members. o Plan and deliver team/project Goals and Objectives. Manage timelines and communicate  project status. 

o Provide direct input to resource planning. 

  • Act as SME for one or more validation categories. Leverage global MSAT network to identify and  implement industry best practices. 

  • Participate in preparation and represent MSAT in audits/inspections 

  • Perform Change Control assessments and execute against assigned actions. 

  • Act as coach for more junior engineers. 

  • Maintain compliance with all company policies and procedures (e.g., Quality, EH&S, Business, Credo  etc.)


how to succeed

[insert summary]  You will also bring:

  • Bachelor’s degree in a Science, Engineering or Technical subject 

  • Minimum 4 years of relevant  experience in the (bio)pharmaceutical industry or related post graduate academic  experience/education is required. 

  • Strong, proven experience leading Validation processes (ie. Write and review validation plans, protocols and reports. 

  • Experience with Aseptic processes, simulations and fill finish is beneficial 

  • Experience / knowledge with Annex 1 

  • Knowledge of and experience in a scientific or technical core area and building knowledge and  experience in other technical and business disciplines. 

  • Proven experience with GMP and Quality Compliance. 

  • Precise, accurate, structured, flexible and customer focused. 

  • Capable of delivering local small projects, regional project work streams or departmental programs successfully under strong supervision. 


details

  • This contract will run until the end of 2027, with a start date of January 2027. 

  • This is a hybrid role (3 days on-site)

  • May require some work over weekends or evenings during peak periods  


you are welcome here

is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.


about Johnson & Johnson Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.


Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.



application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. 


questions

If you would like some additional information about the role please contact: simone.strong@randstadsourceright.co.uk

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.