Johnson & Johnson Posted August 24, 2026

LOC Sr Reg Compliance Specialist

Singapore, Singapore Full time
Quality Senior

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:

Singapore, Singapore

Job Description:

Job Description

DePuy Synthes is recruiting for a LOC Sr Reg Compliance Specialist located in Singapore.

Job Overview

The LOC Sr Regulatory Compliance Specialist is responsible for leading and executing regulatory compliance activities for the Local Operating Company (LOC) in Singapore. This role ensures adherence to applicable regulatory requirements, quality system standards, and internal policies across local commercial and distribution activities. The position plays a key role in safeguarding patient safety, maintaining regulatory readiness, and enabling compliant business operations by partnering closely with Quality, Regulatory Affairs, Commercial, and Supply Chain teams within the local market.

Key Responsibilities

Execute and oversee regulatory compliance activities for the local operating company in alignment with global and regional compliance requirements.

Support Schedule development of internal audits in the region, support response development, and track action to point of completion

Ensure adherence to local regulatory requirements, internal policies, and quality system standards across commercial operations.

Partner with Regulatory Affairs, Quality, Commercial, and Supply Chain teams to support compliant product distribution and lifecycle activities.

Interpret regulatory requirements and translate them into practical compliance guidance for local stakeholders.

Support internal audits, external audits, and health authority inspections at the local level.

Monitor compliance risks, trends, and performance metrics; support corrective and preventive actions.

Ensure accurate maintenance of compliance documentation, records, and reports.

Contribute to continuous improvement initiatives to strengthen regulatory compliance maturity within the LOC.

Qualifications

Education:

Bachelor’s degree in Regulatory Affairs, Quality, Engineering, Life Sciences, or a related discipline (required).

Advanced degree in a scientific or regulatory field (preferred).

Experience and Skills:

Required:

Typically 4-6 years of experience in Regulatory Compliance, Quality, or related roles within a regulated industry.

Strong working knowledge of regulatory and compliance requirements applicable to local commercial operations.

Experience supporting audits, inspections, or compliance assessments.

Ability to manage complex compliance topics with strong attention to detail.

Preferred:

Experience in medical devices, healthcare, or other highly regulated industries.

Familiarity with APAC and Singapore regulatory and compliance expectations.

Experience working in a global or matrixed organization.

Exposure to regulatory inspections involving local operating companies.

Quality or Regulatory certifications (e.g., RAC, ASQ).

Other:

Language: English required; additional APAC languages preferred.

Travel: Limited; occasional regional travel within APAC.

Certifications: Quality or Regulatory certifications preferred but not required.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit  www.careers.jnj.com .

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.​

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.

#LI-Hybrid

#DePuySynthesCareers

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
Singapore, Singapore
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 204 comparable Senior Quality roles across 48 biopharma companies.

204Comparable roles tracked
185Currently active
48Companies hiring similar roles
25Countries represented

Salary context

64 of 204 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 – $219,500 (median $142,078)

Where these roles are based

Top locations among the 204 comparable roles

United States107
India17
Ireland12
Singapore9
China9
United Kingdom6

+ 19 more countries

Seniority mix

204 of 204 peers have a known seniority level

Senior139
Associate Director46
Principal19

Therapeutic area mix

0 of 204 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.

60%similar
Tuas, Singapore Senior
Same function Same seniority Same country
60%similar
Amgen Singapore Manufacturing Pte. Ltd Singapore Manufacturing, Singapore Senior
Same function Same seniority Same country
60%similar
Amgen Singapore Manufacturing Pte. Ltd Singapore Manufacturing, Singapore Senior
Same function Same seniority Same country
60%similar
AbbVie Singapore, sg Senior
Same function Same seniority Same country
60%similar
AbbVie Singapore, sg Senior
Same function Same seniority Same country
60%similar
Glaxo Wellcome Manufacturing Pte Ltd Tuas, Singapore Senior
Same function Same seniority 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.

60%
Senior/ QA Executive (Materials)
· Tuas, Singapore · Senior
Function Therapeutic area Seniority Country
60%
Senior Supplier Quality Assurance Specialist
AbbVie · Singapore, sg · Senior
Function Therapeutic area Seniority Country
60%
Senior Quality Partner - Supply Chain Quality (2 years contract)
Roche · Singapore, Central Singapore, Singapore · Senior
Function Therapeutic area Seniority Country
45%
Sr R&D Quality Assurance Engineer F/M
AbbVie · Annecy, Auvergne-Rhône-Alpes · 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.