Johnson & Johnson Posted August 10, 2026

Associate Packaging Development Engineer

Zuchwil, Switzerland Full time
Manufacturing & CMC Associate

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:

Supply Chain Engineering

Job Sub Function:

Packaging Design Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Zuchwil, Switzerland

Job Description:

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Johnson & Johnson is currently seeking “Associate Package Development Engineer join our TEAM.The role is based in” Zuchwil” CH

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 https://www.jnj.com/.

About J&J MedTech

At Johnson & Johnson MedTech, we unleash diverse healthcare expertise, purposeful technology, and a passion for people to transform the future of medical intervention and empower everyone to live their best life possible. For more than a century, we have driven breakthrough scientific innovation to address unmet needs and reimagine health. In surgery, orthopedics, vision, and interventional solutions, we continue to help save lives and create a future where healthcare solutions are smarter, less invasive, and more personalized.

Overview

The Associate Package Development Engineer provides technical expertise/ support in the areas of design, development, testing and production scale-up of new packaging components and systems. They work with guidance of Staff/ Senior Packaging Development leadership.

Position Duties and Responsibilities

Develops packaging for medical devices with mentor oversight.

Enhances and validates package components and packaging processes.

Develops package testing plans and interprets results as required for various projects.

Participates in process improvement, cost improvement, quality improvement, change control or task teams.

Participates and advises in decisions involving equipment, package design, cost saving and source reduction.

Builds technical competencies in packaging materials and processes used in all manufacturing processes.

Participates and provides technical expertise for risk assessment and compliance assurance programs.

Assure delivery of robust, cost effective, fully compliant packaging solutions that meet current and evolving customers need.

Knows and follows all laws and policies that apply to one's job, and maintains the highest levels of professionalism, ethics and compliance at all times.

Extended duties are assigned depending on the packaging business area the employee is supporting :

Packaging representative for special project execution

Designs packaging for medical devices with mentor oversight

Support validation of package systems

Coordinates and executes physical testing to ensure product and package integrity for manufacturing through end users.

Creates package distribution and shelf-life testing plans, interprets results as required for various projects and communicates those to appropriate groups

Reviews and updates technical reports, procedures, policies, and other sources of information to ensure that validations and procedures are consistent with current industry, regulatory requirements and current technology

Support test method validation to assure a successful and on-time implementation of the equipment in our test laboratory

Interprets all test method validation results and creates related documentation

Support and lead small frontend Package Development projects, involvement in design & concept development

Understanding of production processes as well as manufacturability of new design concepts

Support and preparation of VOCs

Lead small potential design problems related to material characteristics, dimensional tolerances, manufacturing procedures (trouble shooting)

Support statistical methods and process/design excellence tools

Support design/process failure mode effects and analysis

Requirements

Education Requirements

Bachelor's Degree in Engineering or equivalent Technical Degree or extensive relevant experience required.

Experience

Basic knowledge of common packaging materials and packaging technologies for medical devices

Technical writing skills is preferred

Knowledge of design and manufacturing FMEA preferred

Polymer knowledge preferred

Interpersonal skills/ characteristics

Team player

Problem Solving Skills

Creative thinker

Able to work independently

Willingness to learn

good communicator

Proficiency in Microsoft Office applications

Proficiency in Microsoft Office applications

Professional-level English

20 % of travel

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Don't miss this exceptional opportunity to join a world-class company and make a lasting impact. Apply now and be part of our ambitious team!

Required Skills:

Preferred Skills:

Analytical Reasoning, Brand Research, Controls Compliance, Detail-Oriented, Execution Focus, Good Manufacturing Practices (GMP), Industrial Hygiene, Lean Supply Chain Management, Package and Labeling Regulations, Process Control, Product Packaging Design, Project Schedule, Proof Reading Software, Quality Assurance (QA), Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Technologically Savvy

Job details

Seniority
Associate
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Zuchwil, Switzerland
Employment type
Full time

How this role compares

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

We currently track 355 comparable Associate Manufacturing & CMC roles across 66 biopharma companies.

355Comparable roles tracked
323Currently active
66Companies hiring similar roles
32Countries represented

Salary context

92 of 355 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Operator - 2nd Shift · Mylan Technologies, Inc. $30,000/yr – $49,000/yr
Peer group range $39,500 – $186,200 (median $146,435)

Where these roles are based

Top locations among the 355 comparable roles

United States199
India48
Ireland20
Netherlands11
Switzerland10
Singapore7

+ 26 more countries

Seniority mix

355 of 355 peers have a known seniority level

Manager233
Associate106
Intern/Fellow/Postdoc16

Therapeutic area mix

1 of 355 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.

60%similar
Celgene International SaRL Boudry, Switzerland Associate
Same function Same seniority Same country
50%similar
Roche Basel, Basel-City, Switzerland Manager
Same function Adjacent seniority Same country
50%similar
Roche Basel, Basel-City, Switzerland Manager
Same function Adjacent seniority Same country
50%similar
Roche Kaiseraugst, Aargau, Switzerland Manager
Same function Adjacent seniority Same country
50%similar
Celgene International SaRL Boudry, Switzerland Manager
Same function Adjacent seniority Same country
50%similar
Roche Kaiseraugst, Aargau, Switzerland Manager
Same function Adjacent seniority 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.

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.

60%
Associate Operator Bulk Operations
Celgene International SaRL · Boudry, Switzerland · Associate
Function Therapeutic area Seniority Country
50%
GMP-Manager (m/w/d) im Manufacturing Support Assembly & Packaging
Roche · Kaiseraugst, Aargau, Switzerland · Manager
Function Therapeutic area Adjacent seniority Country
50%
Senior Technical Sub-Project Manager - Packaging & Device Assembly Equipment (EU)
Roche · Kaiseraugst, Aargau, Switzerland · Manager
Function Therapeutic area Adjacent seniority Country
50%
Manager, Global Regulatory Affairs, CMC
Johnson & Johnson · Allschwil, Switzerland · Manager
Function Therapeutic area Adjacent 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.