Johnson & Johnson Posted October 16, 2026

Pilot Plant Quality and Compliance Engineer

Geel, Belgium Full time
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Johnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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:

R&D Product Development

Job Sub Function:

R&D Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Beerse, Antwerp, Belgium, Geel, Antwerp, Belgium

Job Description:

Johnson & Johnson Innovative Medicine develops innovative therapies that address unmet medical needs through science and technology.

The Chemical Process Research and Development (CPRD) department is looking for a Pilot Plant Quality and Compliance Engineer to join its team in Belgium.

CPRD operates three chemical pilot plants in Beerse and Geel. These facilities develop and scale up chemical processes and manufacture active pharmaceutical ingredients (APIs) for clinical trials. The Chemical Development Pilot Plant in Geel also supports the launch of new, low-volume commercial products. Our pilot plants continuously invest in technology, automation, and data capabilities to prepare for future products and evolving manufacturing requirements.

The Role

As a Quality and Compliance Engineer, you support day-to-day pilot plant operations in close collaboration with operations personnel, process engineers, maintenance teams, and Quality Assurance.

Deviations may occur during the manufacture of experimental drug substances because of process- or equipment-related issues. You coordinate cross-functional investigations to identify root causes, define corrective and preventive actions, and assess the potential impact on product quality and regulatory compliance. You also ensure that investigations are documented in accordance with established standards and are ready for review by health authorities.

Because the pilot plants use multiproduct equipment, robust cleaning processes are essential to prevent cross-contamination. Your responsibilities therefore also include establishing cleaning limits and supporting the validation and continuous improvement of cleaning methods.

You report to the Pilot Plant Quality and Compliance Lead and apply a phase-appropriate quality approach that reflects the product’s development stage and the available process and product knowledge.

This role is limited to two-year term.

Your Responsibilities

· Support pilot plant operations and the timely release of clinical batches and equipment.

· Coordinate and document deviation investigations.

· Facilitate root-cause analysis and the definition of corrective and preventive actions.

· Assess the impact of deviations on product quality and regulatory compliance.

· Support cleaning-limit calculations, cleaning validation, and the improvement of cleaning methods.

· Implement projects that maintain the compliance of pilot plant systems with evolving regulatory requirements.

· Contribute to lifecycle-management activities for systems including deviation management, equipment qualification, cleaning validation, and contamination control.

· Work closely with operations, engineering, maintenance, and Quality Assurance.

Qualifications and Skills

· A PhD or master’s degree in chemistry, chemical engineering, or a related field, or relevant experience in the pharmaceutical industry.

· Practical knowledge of current Good Manufacturing Practices and ICH Q7 is an asset.

· Understanding of process safety, pilot plant operations, process development, and engineering.

· Strong analytical and problem-solving skills.

· Ability to challenge existing practices and identify improvement opportunities.

· Strong communication and collaboration skills.

· Project-management skills and the ability to manage several priorities simultaneously.

Working in Belgium

Johnson & Johnson’s Belgian campus brings together approximately 5,000 employees and capabilities spanning the full drug-development lifecycle, from discovery through market access. This integrated environment offers broad opportunities to learn, collaborate, and build experience across different areas of drug development.

Our Offer

· A challenging role in an international and dynamic environment.

· Continuous learning and career-development opportunities.

· An attractive remuneration and benefits package, including hospital insurance and healthcare-related benefits.

· An inclusive workplace where different perspectives are respected and valued.

· A work environment that supports a healthy work-life balance.

Interested? Please submit your current CV through the online application system.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is:

€60.000,00 - €96.255,00

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.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Geel, Belgium
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 1523 comparable Quality roles across 149 biopharma companies.

1523Comparable roles tracked
1325Currently active
149Companies hiring similar roles
53Countries represented

Salary context

248 of 1523 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QA - Stat Sort Specialist · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $55,037 – $350,000 (median $128,002)

Where these roles are based

Top locations among the 1523 comparable roles

United States608
Ireland86
France76
Germany76
China67
Belgium51

+ 47 more countries

Seniority mix

690 of 1523 peers have a known seniority level

Manager198
Senior179
Intern/Fellow/Postdoc94
Associate73
Associate Director40
Principal38
Director33
Senior Director28
Executive/VP7

Therapeutic area mix

1 of 1523 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
GlaxoSmithKline Biologicals S.A. Belgium-Wavre, Belgium Intern/Fellow/Postdoc
Same function Same country
40%similar
GlaxoSmithKline Biologicals S.A. Belgium-Wavre, Belgium Intern/Fellow/Postdoc
Same function Same country
40%similar
UCB Braine L'alleud, Walloon Brabant, Belgium
Same function Same country
40%similar
UCB Braine L'alleud, Walloon Brabant, Belgium
Same function Same country
40%similar
UCB Braine L'alleud, Walloon Brabant, Belgium
Same function Same country
40%similar
UCB Braine L'alleud, Walloon Brabant, Belgium Manager
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Quality job in Belgium, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Stage : Optimisation digitale des documents de tests en laboratoire QC, Belgique - 2026
GlaxoSmithKline Biologicals S.A. · Belgium-Wavre, Belgium · Intern/Fellow/Postdoc
Function Therapeutic area Seniority Country
40%
Evidence Quality Lead
UCB · Braine L'alleud, Walloon Brabant, Belgium · Seniority not listed
Function Therapeutic area Seniority Country
40%
Media, Buffer & Logistics (MBL) Bio DS Operations Quality Manager
UCB · Braine L'alleud, Walloon Brabant, Belgium · Manager
Function Therapeutic area Seniority Country
40%
Stage : Pharmacien.ne Assurance Qualité, Belgique - 2026
GlaxoSmithKline Biologicals S.A. · Belgium-Wavre, Belgium · Intern/Fellow/Postdoc
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.