Johnson & Johnson Posted September 9, 2026

Sr Quality Engineer

Grecia, Costa Rica Full time
Quality Senior
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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:

Quality

Job Sub Function:

Quality Assurance

Job Category:

Professional

All Job Posting Locations:

Grecia, Costa Rica

Job Description:

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

About Cardiovascular

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

We are searching for the best talent for.

Purpose:

Provide high performance quality system guidance and support for development, maintenance and enforcement of compliance of the company Quality Management System. The Quality Senior Analyst will collaborate closely with business partners to provide leadership regarding the Quality System Standardization activities ensuring the site is compliant with franchise procedures and external standards & regulations.

You will be responsible for :

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

Will serve as a Quality Systems subject matter expert, track and report action plan status/ completion as relates to quality systems improvement efforts.

As needed, assist with creation, modification and improvement of Quality System procedures, work instructions and related documentation.

Drive robust quality and compliance execution in the business and drive successful Q&C scorecard metrics by working closely with key stakeholders in the business.

Works on complex investigations and coordinates technical teams and leads cross functional teams to ensure sound experimental design, effective data analysis, identification, implementation, verification and validation of CAPA, Non-Conformance, and subsequent closure of investigations.

Oversee all Compliance activity within the facility in conjunction with the Regulatory Compliance and Quality Operations groups. Liaise with management at all levels of the business and produce metrics and present data on site performance at meetings such as the weekly and monthly management meetings

Oversee the Customer Complaints system in conjunction with Complaints and Vigilance Manager, ensuring that timely closure is met whilst fully satisfying all Customer Complaint requirements.

Ensure that the Quality System Review (QSR) continues to develop in terms of inputs and to ensure that any trends noted at this forum are challenged and acted upon

Responsible for conducting training in Quality Systems Management principles to business partners

Facilitates process of product issue assessment, quality review board preparation, and field action execution.

Facilitates technical innovations to enhance Quality Systems and support business goals.

Provides back room support for 3rd Party Inspections and Audits (e.g. Registrar, Notified Body, FDA, or customer audits).

Serves as a SME on the Quality Planning process, assists Quality Plan authors with the process, and files Quality Plans

Responsible for communicating business-related issues or opportunities to next management level

Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.

For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable

Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures

Performs other duties assigned as needed

Qualifications / Requirements:

Experience and education

Required Minimum Education: University Bachelor’s Degree or Equivalent (preferably in Engineering, Math, Science, or Business)

4-6 years’ experience in Quality Systems, Quality Engineering, Quality Assurance, or other technical work experience.

Minimum of 4+ years’ experience in an FDA regulated industry (medical device, pharmaceutical, etc.).

Required knowledge, skills, abilities, certifications/licenses and affiliations

Working knowledge of 21 CFR Part 820, 21 CFR 806, ISO 13485 and familiarity with ISO 14971.

Broad-based technical knowledge and experience to work effectively with others in diverse areas of business (Operations, Quality, R&D, R.A., Engineering).

Ability to effectively prioritize and manage multiple activities and responsibilities.

Must have outstanding business and technical communication skills (verbal, written, presentation)

Project Management Certification (example: PMI Certification, Graduate Certificate in Program Management, etc.) preferred

Proficiency with quality-related statistical applications such as those for Minitab.

American Society for Quality (ASQ) credentials preferred

Experience leading teams and with change management activities

Bilingual (English and Spanish)

#LI-Onsite

Required Skills:

Preferred Skills:

Business Alignment, Business Savvy, Coaching, Communication, Compliance Management, Continuous Improvement, Fact-Based Decision Making, Human-Centered Design, ISO 9001, Issue Escalation, Problem Solving, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)

Job details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
Grecia, Costa Rica
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 195 comparable Senior Quality roles across 49 biopharma companies.

195Comparable roles tracked
172Currently active
49Companies hiring similar roles
26Countries represented

Salary context

59 of 195 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 Not listed on this posting
Lowest disclosed · Quality Assurance Senior Specialist - Statistical Sorting · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Peer group range $55,037 – $208,845 (median $142,155)

Where these roles are based

Top locations among the 195 comparable roles

United States94
India12
China12
Ireland11
Singapore7
Netherlands7

+ 20 more countries

Seniority mix

195 of 195 peers have a known seniority level

Senior129
Associate Director42
Principal24

Therapeutic area mix

0 of 195 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

45%similar
AbbVie Annecy, Auvergne-Rhône-Alpes Senior
Same function Same seniority
45%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same seniority
45%similar
Regeneron Ireland Limerick, Ireland Senior
Same function Same seniority
45%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority
45%similar
Regeneron Ireland Limerick, Ireland Senior
Same function Same seniority
45%similar
Regeneron Ireland Limerick, Ireland Senior
Same function Same seniority

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.

45%
Sr R&D Quality Assurance Engineer F/M
AbbVie · Annecy, Auvergne-Rhône-Alpes · Senior
Function Therapeutic area Seniority Country
45%
Senior Quality Assurance Validation Specialist
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Senior
Function Therapeutic area Seniority Country
45%
Senior Scientist, Drug Product Analytical Science (ASAT), Cell Therapy
JuN - Seattle Dexter · Seattle 400 Dexter, United States · Senior
Function Therapeutic area Seniority Country
45%
Senior Validation Engineer
Amgen Singapore Manufacturing Pte. Ltd · Singapore Manufacturing, Singapore · Senior
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.