Staff Customer Quality Complaint Lead
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:
Quality
Job Sub Function:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
Warsaw, Indiana, United States of America, West Chester, Pennsylvania, 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.
Depuy Synthes is recruiting for a Staff Customer Quality Complaint Lead, located in Warsaw IN; West Chester, PA; or Palm Beach Gardens, FL.
An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
The Staff Customer Quality Complaint Lead provides leadership and oversight of Business Process Outsourcing (BPO) partners supporting DePuy Synthes Customer Quality complaint handling operations. This role serves as the primary liaison between DePuy Synthes and BPO partners, ensuring outsourced activities are performed in compliance with company procedures, quality standards, regulatory requirements, and business objectives.
The Staff Customer Quality Complaint Lead is accountable for monitoring performance, quality, compliance, and continuous improvement of complaint handling activities internal or outsourced functions, including complaint mailbox management, complaint intake, literature surveillance, litigation support, file processing, activity management, and complaint coding. The role drives operational excellence through effective oversight, performance management, risk mitigation, and process improvement.
Key Responsibilities:
Partners with management to support the development and execution of BPO governance frameworks.
Provides operational oversight of assigned BPO activities.
Supports governance meetings by attending, Weekly Review Boards (WBR), and Monthly Review Board meetings (MRB) to ensure compliance with company procedures, Quality System requirements, contractual obligations, and regulatory expectations.
Partners with stakeholders to identify and address performance gaps, risks, compliance concerns, and operational challenges.
Drives continuous improvement through process standardization, ongoing training, automation, change management, and implementation of operational enhancements.
Monitors BPO performance against established KPIs, SLAs, quality metrics, productivity expectations, backlog, and compliance requirements.
Fosters a culture of accountability, collaboration, compliance, customer focus, and continuous improvement.
Supports audits as the need arises.
Performs other duties as assigned.
Qualifications
Education:
Bachelors or equivalent degree is required. Concentration in Business, Quality, Engineering, Life Sciences, Nursing, Health Sciences, Regulatory Affairs, or related field is preferred.
Experience and Skills:
Required:
Minimum of 5 years of experience in a regulated health care, medical device, pharmaceutical, quality, complaint handling, post-market surveillance, or regulatory environment .
Proven track record to lead through influence, build cross-functional partnerships, and drive operational results.
Knowledge of quality systems and global regulatory requirements, including FDA Quality System Regulations, ISO 13485, ISO 14971, and complaint handling requirements.
Experience with complaint handling required.
Demonstrated ability to analyze operational data and drive process improvements.
Strong project management, organizational, and prioritization skills.
Strong analytical, critical thinking, and problem-solving skills.
Strong verbal and written communication skills.
Ability to effectively influence partners at multiple levels of the organization.
Ability to manage multiple priorities in a fast-paced environment.
Proficiency in Microsoft Office applications, including Word, Excel, PowerPoint, Outlook, and SharePoint.
Preferred:
Experience managing outsourced service providers, vendor relationships, or BPO operations.
Experience leading process improvements and operational excellence initiatives.
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 Savvy, Coaching, Communication, Compliance Management, Continuous Improvement, Fact-Based Decision Making, ISO 9001, Issue Escalation, Problem Solving, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 909 comparable Quality roles across 103 biopharma companies.
Salary context
183 of 909 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.
Where these roles are based
Top locations among the 909 comparable roles
+ 42 more countries
Seniority mix
428 of 909 peers have a known seniority level
Therapeutic area mix
1 of 909 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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.
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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.
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.