Johnson & Johnson Posted October 9, 2026

Quality Control Lead - Swing Shift

Santa Clara, United States Full time
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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:

Quality Control

Job Category:

Business Enablement/Support

All Job Posting Locations:

Santa Clara, California, United States of America

Job Description:

We are searching for the best talent for Quality Control Lead - Swing Shift, located in Santa Clara, CA.

 

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

Purpose:

The Quality Control Lead – Swing Shift supports daily IQC operations during the 2:00 p.m. to 10:30 p.m. PST shift and serves as the primary operational point of contact for the shift. This role coordinates incoming inspection and material-release priorities, provides technical guidance to inspectors, reinforces quality and EHS requirements, supports issue escalation, and maintains continuity between shifts. The Lead works cross-functionally to promote safe, compliant, timely, and audit-ready IQC operations.

This role is critical to maintaining safe and compliant swing shift IQC operations, timely material release, inspection readiness, accurate quality records, and effective coordination across shifts and functional teams.

You will be responsible for:

Serve as the primary operational point of contact for swing shift IQC activities and communicate priorities, status, risks, and resource needs.

Coordinate daily inspection assignments, adjust priorities, monitor progress, and support coverage based on material and production needs.

Provide day-to-day technical guidance and coaching to inspectors on drawings, specifications, inspection plans, sampling requirements, supplier documentation, metrology methods, and IQC procedures.

Reinforce Environmental, Health, and Safety requirements, including PPE, safe equipment use, ergonomics, housekeeping, emergency procedures, and prompt escalation of hazards, incidents, near misses, or unsafe conditions.

Support timely material release by confirming inspection completion, required approvals, revision alignment, and electronic record readiness.

Support nonconformance, supplier-blocker, and rework workflows; coordinate issue resolution with cross-functional partners and escalate unresolved quality or release risks.

Use applicable electronic systems, including SAP and EtQ, to support inspection status, quality records, nonconformance activities, and release readiness.

Maintain clear shift handoffs by communicating completed work, open priorities, inspection blockers, and material, facility, or equipment concerns.

Support inspector training and qualification, standardized work, 5S, controlled-document availability, material segregation, and overall area readiness.

Support inspection equipment readiness, including calibration, maintenance, qualification or validation activities, and equipment-related issue escalation.

Participate in tier meetings, audits, safety walkthroughs, investigations, risk assessments, CAPA activities, KPI reviews, and continuous-improvement initiatives as needed.

Collaborate with Quality, Engineering, Manufacturing, Warehouse, Planning, Supplier Quality, and other partners to resolve inspection constraints and support business needs.

Support updates to IQC procedures, work instructions, job aids, and training materials, and promote a culture of quality, compliance, ownership, and customer focus.

Qualifications/Requirements:

High school diploma or equivalent required; Associate degree or technical certification preferred.

At least 2 years of relevant Quality, Inspection, or Regulated Manufacturing experience.

Working knowledge of quality systems and applicable regulatory requirements.

Ability to assign work, manage priorities, communicate clearly, and escalate issues.

 Preferred:

Knowledge of incoming inspection, nonconformance, documentation, and product release processes.

Ability to interpret engineering drawings, specifications, inspection plans, and supplier documentation.

Experience using common inspection and metrology tools.

Experience with systems such as SAP, EtQ, Agile, Windchill, or Microsoft Office.

Prior experience training, mentoring, or providing work direction.

Other:

Availability to work the required swing shift from 2:00 p.m. to 10:30 p.m. PST. This shift may include a 10% differential.

This role is eligible for immigration sponsorship, if required. Relocation support is not available for this position.

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:

Administrative Support, Communication, Compliance Management, Controls Compliance, Execution Focus, ISO 9001, Persistence and Tenacity, Problem Solving, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Report Writing, Standard Operating Procedure (SOP), Teamwork, Technologically Savvy

The anticipated base pay range for this position is :

$69,000.00 - $111,090.00

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
Quality
Therapeutic area
Not listed
Location
Santa Clara, 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 1523 comparable Quality roles across 149 biopharma companies.

1523Comparable roles tracked
1326Currently active
149Companies hiring similar roles
53Countries represented

Salary context

247 of 1523 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 $69,000/yr – $111,090/yr
Lowest disclosed · QA - Stat Sort Specialist · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $55,037 – $350,000 (median $128,003)

Where these roles are based

Top locations among the 1523 comparable roles

United States607
Ireland86
France76
Germany76
China67
Belgium52

+ 47 more countries

Seniority mix

690 of 1523 peers have a known seniority level

Manager198
Senior179
Intern/Fellow/Postdoc94
Associate73
Associate Director40
Principal38
Director33
Senior Director28
Executive/VP7

Therapeutic area mix

1 of 1523 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

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Notify me about similar jobs

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Or follow a whole field: get every new Quality 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.

40%
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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.