Johnson & Johnson Posted September 30, 2026

Process Quality Leader

Cornelia, United States 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:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Process Improvement

Job Category:

People Leader

All Job Posting Locations:

Athens, Georgia, United States of America, Cornelia, Georgia, United States of America

Job Description:

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./

 

Job Summary

The Process Quality Leader (PQL) provides quality and technical leadership to support manufacturing operations and drive continuous process improvement. This role partners closely with Manufacturing, Engineering, and Quality teams to identify process failures, investigate non-conformances, implement corrective and preventive actions (CAPAs), and ensure compliance with Quality System Regulations (QSR), GMP, ISO standards, and company requirements.

The PQL leads quality improvement initiatives, analyzes performance trends, supports operational excellence efforts, and develops teams while fostering a culture of quality, compliance, and continuous improvement.

 

Key Responsibilities

Quality & Compliance Leadership

Lead investigations of non-conformances, process failures, complaints, and quality trends.

Drive root cause analysis and implementation of effective corrective and preventive actions (CAPAs).

Ensure compliance with QSR, GMP, ISO, and internal quality requirements.

Support audits, inspections, and quality system assessments.

Review quality data and trends to identify opportunities for process improvement.

 

Process Improvement

Partner with Manufacturing and Engineering to improve process capability, product quality, and operational efficiency.

Lead continuous improvement initiatives using tools such as Lean, Six Sigma, FMEA, and statistical analysis.

Develop and maintain procedures, protocols, and training materials that support process enhancements.

Recommend improvements to manufacturing systems, equipment, and processes based on data analysis.

 

Leadership & Team Development

Lead and develop quality and technical professionals while supporting performance management and career development.

Provide coaching and guidance to manufacturing supervisors and cross-functional teams.

Drive accountability for safety, quality, delivery, and continuous improvement performance.

Foster collaboration across Quality, Manufacturing, Engineering, Supply Chain, and other functional areas.

 

Leadership Expectations

Demonstrates strong people leadership and coaching capabilities.

Builds a culture of quality, compliance, accountability, and continuous improvement.

Influences stakeholders across multiple organizational levels.

Drives execution while balancing business, quality, and customer needs.

Supervises supervisors and/or larger technical teams.

Serves as the primary quality partner to Business Unit leadership and may act on behalf of the Manufacturing or Business Unit Manager.

 

Business & Operational Support

Support business unit objectives related to quality, cost, productivity, and customer satisfaction.

Participate in strategic planning and operational reviews.

Present quality metrics, trend analyses, and investigation results to leadership teams.

Support new product introductions, process validation activities, and equipment qualifications.

 

Qualifications

Education

A minimum of a bachelor’s degree and/or University degree in Engineering, Life Sciences, or a related technical field  required

Experience and Skills

Required

Experience in a regulated manufacturing environment (medical device preferred).

Strong knowledge of FDA Quality System Regulations (QSR), GMP, and ISO requirements.

Experience with quality investigations, CAPA, root cause analysis, and process improvement methodologies.

Strong analytical, communication, and problem-solving skills.

Proficiency with Microsoft Office and data analysis tools.

 

Preferred

Master's degree in Engineering, Science, or related field.

Lean Six Sigma certification or equivalent continuous improvement experience.

Experience leading cross-functional teams and driving organizational change.

Experience supporting audits, regulatory inspections, and validation activities.

 

Other:

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

J

ohnson & 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:

Agile Manufacturing, Chemistry, Manufacturing, and Control (CMC), Coaching, Controls Compliance, Data Gathering and Analysis, Detail-Oriented, Developing Others, Document Management, Financial Competence, Goal Attainment, Good Manufacturing Practices (GMP), Inclusive Leadership, Leadership, Operational Excellence, Plant Operations, Process Control, Quality Management Systems (QMS), Quality Standards, Quality Systems Documentation, Time Management

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Cornelia, United States
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 1008 comparable Quality roles across 131 biopharma companies.

1008Comparable roles tracked
957Currently active
131Companies hiring similar roles
48Countries represented

Salary context

193 of 1008 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 · Quality Control Stability Technician · Regeneron Pharmaceuticals, Inc (USA) $19/hr – $30/hr (≈ $39,395–$61,610/yr)
Highest disclosed · Quality Assurance Specialist · Merck KGaA $65,100/yr – $976,000/yr
Peer group range $50,502 – $520,550 (median $136,700)

Where these roles are based

Top locations among the 1008 comparable roles

United States349
Germany54
Ireland53
China53
Switzerland39
France38

+ 42 more countries

Seniority mix

498 of 1008 peers have a known seniority level

Manager160
Senior116
Intern/Fellow/Postdoc60
Associate Director40
Associate39
Director32
Principal23
Senior Director20
Executive/VP8

Therapeutic area mix

2 of 1008 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1
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
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same country
40%similar
AbbVie North Chicago, IL Director
Same function Same country
40%similar
AbbVie North Chicago, IL Manager
Same function Same country
40%similar
Novartis Cambridge (USA), United States Director
Same function Same country
40%similar
Novartis Cambridge (USA), United States Principal
Same function Same country
40%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
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.

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%
Advisor, Physicochemical Properties and Compound Quality
Lilly · Indianapolis, Indiana, United States of America · Associate
Function Therapeutic area Seniority Country
40%
Director, Study Quality and Compliance - Nonclinical Safety/Toxicology
Novartis · Cambridge (USA), United States · Director
Function Therapeutic area Seniority Country
40%
QA Specialist III
Gilead Sciences, Inc. · La Verne, United States · Seniority not listed
Function Therapeutic area Seniority Country
40%
QA Operations Specialist - Shift Based
Novartis · Carlsbad, United States · Seniority not listed
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.