Specialist Quality Assurance

Posted 11 Days Ago
Be an Early Applicant
Leiden, NLD
In-Office
45K-71K Annually
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Support implementation and execution of Quality Systems for biotherapeutic product introduction and manufacture. Review and approve GMP documentation, perform batch record review and release, act as deputy process owner for raw material and product release, represent QA in audits and inspections, and deputize for the QA Manager to oversee key quality processes.
Summary Generated by Built In

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Quality Assurance

Job Category:

Professional

All Job Posting Locations:

Leiden, Netherlands

Job Description:

About Innovative Medicine  

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. 

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. 

Learn more at https://www.jnj.com/innovative-medicine 

Role Overview

The Specialist Quality Assurance acts as a quality expert supporting the implementation and execution of Quality Systems to enable the successful introduction and manufacture of new biotherapeutic products. The role ensures compliance with cGMP, global regulatory requirements, and company policies by working cross‑functionally with Operations, QC, Engineering, Planning, and Development. Through independent judgment and subject‑matter expertise, the Specialist QA contributes to a strong quality culture while enabling the consistent delivery of safe, compliant, and high‑quality products.

Key Responsibilities:

  • Implement and maintain Quality Systems including validation, change control, batch record review, and batch release for new and existing products

  • Review, prepare, and approve GMP documentation such as validation reviews, method transfer protocols, MES master batch records, material master changes, and change controls

  • Perform batch record review and prepare release documentation for raw materials, intermediates, and bulk products

  • Act as deputy process owner and subject matter expert for raw material release and WCB/DS/DPC release processes

  • Ensure quality systems are compliant, effective, and continuously optimized across the organization

  • Serve as a QA representative and subject matter expert during internal and external audits and regulatory inspections

  • Deputize for the QA Manager as required, including approval of QA documentation and oversight of key quality processes

Requirements:

  • Bachelor’s degree or higher in Biochemistry, Biology, Pharmacy, or a related scientific discipline

  • Minimum of 2 years (MSc) or 4 years (BSc) experience in Quality or regulated supply chain operations

  • Strong knowledge of biotechnological or pharmaceutical manufacturing and global regulatory guidelines (cGMP, ICH, FDA, EMA)

  • Proven analytical, problem‑solving, and risk‑based decision‑making skills with high attention to detail

  • Ability to work independently, prioritize effectively, and manage complex or conflicting stakeholder requirements

  • Strong communication, influence, and collaboration skills in cross‑functional environments

  • Fluent in written and spoken English; knowledge of Dutch and experience in vaccines are considered a plus

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time. 

  

Here’s what you can expect: 

  

  • Application review: We’ll carefully review your CV to see how your skills and experience align with the role. 

  • Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.  

  • Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step. 

  • Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.  

   

Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA 

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.

Here’s what you can expect:

  • Application review: We’ll carefully review your CV to see how your skills and experience align with the role.
  • Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
  • Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
  • Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.

                                                                                                                          

Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA



Required Skills:



Preferred Skills:

  


The anticipated base pay range for this position is:

€44.700,00 - €70.840,00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.


*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.



Skills Required

  • Bachelor's degree or higher in Biochemistry, Biology, Pharmacy, or related scientific discipline
  • Minimum of 2 years (MSc) or 4 years (BSc) experience in Quality or regulated supply chain operations
  • Strong knowledge of biotechnological or pharmaceutical manufacturing and global regulatory guidelines (cGMP, ICH, FDA, EMA)
  • Proven analytical, problem-solving, and risk-based decision-making skills with high attention to detail
  • Ability to work independently, prioritize effectively, and manage complex or conflicting stakeholder requirements
  • Strong communication, influence, and collaboration skills in cross-functional environments
  • Fluent in written and spoken English
  • Knowledge of Dutch
  • Experience in vaccines

Johnson & Johnson Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Johnson & Johnson and has not been reviewed or approved by Johnson & Johnson.

  • Healthcare Strength Healthcare coverage is characterized as comprehensive across medical, dental, and vision, with added supports like onsite clinics, fitness centers, and Employee Assistance resources. Mental-health services and wellbeing reimbursements are also described as meaningful components of the overall package.
  • Retirement Support Retirement offerings are portrayed as a major differentiator, combining a 401(k) with employer matching and an employer-funded pension plan. Stock options and other long-term financial supports are also positioned as part of the broader rewards mix.
  • Parental & Family Support Family-related benefits are presented as notably strong, including paid parental leave for all new parents and additional leave types for caregiving and bereavement. Financial assistance for adoption, fertility treatment, and surrogacy is highlighted as a significant support.

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The Company
HQ: New Brunswick, NJ
143,612 Employees
Year Founded: 1886

What We Do

Profound Change Requires Boldness. Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world. Social Media Community Guidelines: http://www.jnj.com/social-media-community-guidelines

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