Johnson & Johnson Posted August 17, 2026

Manufacturing Maintenance & Calibration Lead

Raritan, United States Full time
Manufacturing & CMC

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:

Repair & Maintenance Engineering

Job Category:

People Leader

All Job Posting Locations:

Raritan, New Jersey, United States of America

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 .

We are searching for the best talent for a Manufacturing Maintenance & Calibration Lead to join our Team in Raritan, NJ.

Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR-T platform and investigational treatment.

Are you interested in joining a team that is on the front lines supporting the CAR-T Patient Journey? Apply today for this exciting opportunity!

SUMMARY

The Manufacturing Maintenance & Calibration leader is responsible for the maintenance and calibration activities within the manufacturing team, ensuring all equipment and instruments meet regulatory standards, quality requirements, and operational efficiency. This role involves developing and implementing calibration and maintenance procedures, managing a team, and driving continuous improvement initiatives to optimize equipment reliability and compliance across manufacturing, and QC operations. This role applies extensive knowledge of maintenance and calibration processes, industry standards, and regulatory guidelines to establish, streamline workflows, and minimize equipment downtime. Additionally, this role involves analyzing trend data, coordinating with cross-functional teams, and ensuring adherence to safety, quality, and environmental standards to support manufacturing excellence.

KEY RESPONSIBILITIES

Develops and communicates calibration strategies, policies, and procedures aligned with industry standards (e.g., ISO, ASTM, FDA) and organizational goals.

Leads planning and execution of calibration schedules, ensuring timely and accurate calibration of all equipment and instruments.

Implements best practices for calibration, preventive maintenance, and equipment validation to support manufacturing excellence.

Supervises calibration technicians and maintenance personnel, providing coaching, training, and performance evaluations.

Promotes a culture of safety, quality, and continuous improvement within the calibration and maintenance team.

Ensures team compliance with regulatory requirements and internal standards.

Fosters a team environment that encourages innovation, proactive problem-solving, and professional development.

Oversees maintenance and calibration activities, troubleshooting, and root cause analysis to resolve issues promptly.

Develops and monitors key performance indicators (KPIs) such as calibration accuracy, turnaround times, and compliance metrics.

Coordinates with production, quality, and engineering teams to prioritize maintenance and calibration activities and minimize operational disruptions.

Conducts trend analysis of calibration and maintenance data to identify areas for process improvement and risk mitigation.

Presents performance metrics and improvement initiatives to senior management and cross-functional stakeholders.

Leverages advanced analytics and digital tools to enhance predictive maintenance and process optimization.

Participates in regulatory audits and inspections, supporting compliance efforts.

Uphold Johnson & Johnson’s Credo and Leadership Imperatives in daily interactions, exemplifying the company’s core values.

QUALIFICATIONS

Education:

Minimum of a Bachelor’s degree is required - Focused degree in Engineering, engineering technology, or a related technical field is preferred.

Advanced certifications in calibration or maintenance are a plus.

Experience & Skills:

Required:

Minimum 6 years of experience in calibration or maintenance, or manufacturing operations; biopharma or cell therapy experience is preferred

Minimum 3 years of leadership experience within regulated industries

Working knowledge of regulatory standards (FDA, ISO, Anvisa, EMA) and quality systems

Experience supporting audits and maintaining audit-ready documentation

Deep understanding of calibration principles and maintenance practices

Familiarity with calibration management systems and data analysis tools

Proven leadership skills with the ability to motivate and develop teams

Strong analytical, and decision-making capabilities

Excellent communication skills, both written and verbal, with the ability to convey technical information clearly

Skilled in managing multiple projects, prioritizing tasks, and managing schedules

Preferred:

Project management skills, emphasizing safety, quality, and operational efficiency

Operation Excellence Certification (Green Belt, Black Belt, or Problem Solving)

Other

May require standing, walking, and manual handling for extended periods

Occasional lifting of equipment or tools up to a specified weight

Adherence to safety protocols and use of PPE as requires

May require up to 10% domestic and/or international travel

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.

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.

Required Skills:

Preferred Skills:

Audit Management, Business Alignment, Developing Others, EHS Compliance, Equipment Maintenance, Inclusive Leadership, Leadership, Lean Supply Chain Management, Manufacturing Standards, Performance Measurement, Process Improvements, Project Engineering, Quality Control Testing, Quality Validation, Repair Management, Science, Technology, Engineering, and Math (STEM) Application, Standard Operating Procedure (SOP), Team Management

The anticipated base pay range for this position is :

$102,000.00 - $177,100.00

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
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Raritan, 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 2091 comparable Manufacturing & CMC roles across 134 biopharma companies.

2091Comparable roles tracked
1899Currently active
134Companies hiring similar roles
52Countries represented

Salary context

597 of 2091 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 $102,000/yr – $177,100/yr
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Technical Operator, Packaging - 2nd Shift · Mylan Technologies, Inc. $37,000/yr – $800,000/yr
Peer group range $0 – $418,500 (median $128,400)

Where these roles are based

Top locations among the 2091 comparable roles

United States1064
India125
Germany111
Ireland80
Singapore78
France77

+ 46 more countries

Seniority mix

917 of 2091 peers have a known seniority level

Senior298
Manager233
Associate107
Principal93
Director70
Associate Director69
Senior Director26
Intern/Fellow/Postdoc16
Executive/VP5

Therapeutic area mix

6 of 2091 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease4
Oncology1
Respiratory1

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
AstraZeneca New Haven, Connecticut, United States of America
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40%similar
AstraZeneca Cambridge, Massachusetts, United States of America Director
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40%similar
AstraZeneca New Haven, Connecticut, United States of America
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40%similar
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Lilly Boston, Massachusetts, United States of America Associate
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
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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.

40%
Scientist II, LC Development, Biologics Analytical Development
AstraZeneca · New Haven, Connecticut, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
40%
Director, Global Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC), Platform Innovation – Synthetic Peptides and Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
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Lilly · Indianapolis, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
40%
Senior Principal Scientist - Bioanalytical Research
Lilly · Louisville, Colorado, United States of America · Principal
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.