Johnson & Johnson Posted November 10, 2026

Package Development Manager

Raynham, United States Full time
Notify me about similar jobs

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:

People Leader

All Job Posting Locations:

Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America

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.

The Package Development Manager is responsible for leading a team of package development professionals who develop, qualify and commercialize package solutions for DePuy Synthes.

Key Responsibilities:

Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and DePuy Synthes procedures and guidelines, the Package Development Manager:

Is accountable for all activities associated with the end-to-end delivery of new and updated package designs including request intake, concept development, testing, validations, approvals and commercialization.

Manages a portfolio of multiple projects of different complexities and at various stages, using appropriate project management tools and methodologies to deliver objectives, balance priorities, mitigate risks, and manage stakeholder communications with all levels of the organization.

Interact with senior leadership and major internal and external partners to establish strategic plans and objectives for programs or projects.

Partners with Regulatory Affairs, Product Stewardship, and Label Development to ensure all global regulations are anticipated, understood, and adhered to on a timely basis.

Ensures quality output from each phase of the Package Development process from supplier and design inputs, through execution, and output.

Continuously monitor and adjust business processes to better meet the needs of our evolving business.

Ensures that responses to quality findings are consistent, robust, appropriate, and timely.

Develops talent and ensures the team’s skills are continuously advancing.

Operates within a budget, and may provide input on budget allocation and prioritization

Ensures that team members follow all Company guidelines related to Health, Safety and Environmental practices.

Ensures compliance with all Federal, State, local and Company regulations, policies, and procedures

Performs other duties assigned as needed

Qualifications

Education:

Bachelor’s degree in engineering, business management, or equivalent is required

Advanced degree in engineering, business management is preferred.

6 - 8+ years of relevant work experience is required

Experience and Skills:

Required:

Organization and Talent Development is required.

Medical Device knowledge is required.

Experience partnering across geographies and organizations is required.

Experience within New Product Development, Manufacturing Processes and Quality is required.

Excellent communication, coping and interpersonal skills to motivate and persuade team members, is required.

Understanding of sterile barrier packaging system design verification is required.

Preferred:

Operations and Supply Chain experience is preferred.

Supplier Management experience preferred.

Understanding Regulations and Standards for packaging is preferred.

Six Sigma Green Belt / Black Belt preferred

Project Management Professional Certification (PMP), Flawless Project Execution Training (FPX), or equivalent is preferred

Other:

10% travel may be required.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource. If you are under 18 years of age you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :

$105,000.00 - $181,700.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation –120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year

Holiday pay, including Floating Holidays –13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave – 80 hours in a 52-week rolling period10 days

Volunteer Leave – 32 hours per calendar year

Military Spouse Time-Off – 80 hours per calendar year

For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits

Job details

Seniority
Manager
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Raynham, United States
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 612 comparable Manager Manufacturing & CMC roles across 99 biopharma companies.

612Comparable roles tracked
559Currently active
99Companies hiring similar roles
41Countries represented

Salary context

187 of 612 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 $105,000/yr – $181,700/yr
Lowest disclosed · Warehouse Associate I (M-F 11am-7:30pm) · AbbVie $16/hr – $29/hr (≈ $33,280–$60,320/yr)
Highest disclosed · Advisor, Bioanalytical Chemistry · Lilly $168,000/yr – $268,400/yr
Peer group range $46,800 – $218,200 (median $163,000)

Where these roles are based

Top locations among the 612 comparable roles

United States346
India51
Ireland24
Japan23
Netherlands19
United Kingdom18

+ 35 more countries

Seniority mix

612 of 612 peers have a known seniority level

Manager358
Associate149
Associate Director105

Therapeutic area mix

6 of 612 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease3
Vaccines & Infectious Disease2
Immunology1

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
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority Same country
60%similar
RayzeBio, Inc Indianapolis, United States Manager
Same function Same seniority Same country
60%similar
Celgene - Summit (Corp) Summit West, United States Manager
Same function Same seniority Same country
60%similar
Celgene - Summit (Corp) Summit West, United States Manager
Same function Same seniority Same country
60%similar
E.R. Squibb & Sons,L.L.C. Princeton Pike, United States Manager
Same function Same seniority Same country
60%similar
Amgen Inc. Holly Springs, United States Manager
Same function Same 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.

Or follow a whole field: get every new Manufacturing & CMC job in the United States, 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.

60%
Senior Manager, Site SAP Business Lead
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
60%
Manager, Computer System Validation (CSV) – Cell Therapy
Celgene - Summit (Corp) · Summit West, United States · Manager
Function Therapeutic area Seniority Country
60%
Front Line Manufacturing Manager (Bulk Drug Substance - Downstream) - Night Shift
Amgen Inc. · Holly Springs, United States · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager Instrumentation and Maintenance
Amgen Inc. · Holly Springs, United States · Manager
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.