230 matching jobs for “Product Specialist”

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Johnson & Johnson

Senior Compliance Specialist

Xi’an, China

Full time
Regular

Senior Compliance Specialist (Xian China) Johnson & Johnson is the world's most comprehensive and broadly-based healthcare Company, …

Added Oct 15, 2026

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Johnson & Johnson

Warehouse & Distribution Specialist

GIMPO-SI, Korea, Republic of +1 location

We are looking for the best talent to join us as a W&D Specialist, initially based in Gimpo and later relocating to the Icheon warehouse. Job Summary Key Responsibilities 1. …

Added Oct 19, 2026

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Johnson & Johnson

… bienestar. Obtén más información en https://www.jnj.com/medtech Buscamos incorporar un/a Clinical Account Specialist (CAS) para sumarse a nuestro equipo de Electrofisiología, con base en la ciudad de Rosario, provincia de …

Added Oct 20, 2026

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Johnson & Johnson

[MedTech] Heart Recovery Therapy & Product Marketing Manager

Chiyoda, Japan

… GS上の”Employee Referral Program”の詳細を理解した上で、コンプライアンスを守って紹介したものとみなします。 Abiomed Japan is seeking a Therapy & Product Marketing Manager based in J-One Tower, Tokyo. Abiomed provides the Impella® heart pump, a percutaneous …

Added Oct 19, 2026

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Johnson & Johnson

Quality Systems Specialist

Wilson, North Carolina, United States

We are currently seeking a highly qualified individual to join our team as a Quality Systems Specialist at our new Biotherapeutics Manufacturing facility in Wilson, North Carolina (BioNC). Our expertise in …

Added Oct 18, 2026

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Johnson & Johnson

Snr Clinical & Sales Specialist

North Ryde, New South Wales, Australia

Full time
Regular

… to wellness. The Opportunity An opportunity has become available for a results driven Senior Clinical Specialist to join our Electrophysiology Team in Sydney . The overall responsibility of this role is to provide expert …

Added Oct 15, 2026

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Johnson & Johnson

Brand Specialist Immunology (IBD)

Prague, Czechia

Brand Specialist Immunology (IBD) location: Prague full time Overall purpose of job: The Brand Specialist is a …

Added Oct 18, 2026

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Johnson & Johnson

Commercial Quality Specialist

Xi’an, China

Full time
Regular

Job Description Perform product quality acceptance management to ensure its effective operation, including related SOP/WIs management, …

Added Oct 15, 2026

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Johnson & Johnson

Medical Affairs Specialist

Brussels, Belgium +19 locations

Full time
Regular

… to effectively supervise products´ clinical performance in close collaboration with all related partners (Product Safety, Marketing, R&D and Commercial) Assist HCPs with post-operative outcomes analysis, providing …

Added Oct 15, 2026

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Johnson & Johnson

Senior Regulatory Affairs Specialist

Warsaw, Indiana, United States of America +2 locations

Full time
Regular

Pay posted by employer$79,000–$127,650

… any necessary consultation processes. We are searching for the best talent for Senior Regulatory Affairs Specialist in Warsaw, IN, West Chester, PA , Raynham, MA. Purpose: The Senior Regulatory Affairs Specialist is …

Added Oct 15, 2026

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Johnson & Johnson

Senior Hospital Operations Specialist

West Chester, Pennsylvania, United States +2 locations

Pay posted by employer$79,000–$127,650

… more at https://www.jnj.com/medtech We are searching for the best talent for Senior Hospital Operations Specialist to be in West Chester, PA. Remote work options may be considered on a case-by-case basis and if approved by …

Added Oct 18, 2026

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Johnson & Johnson

Key Account Specialist Immunology

Prague, Czechia

Key Account Specialist Immunology Location: Across Czechia full-time About Immunology Our expertise in Innovative Medicine is …

Added Oct 20, 2026

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Johnson & Johnson

Regulatory Affairs Specialist

Markham, Canada

Full time
Regular

Pay posted by employer$61,000–$98,900 CAD

… combination products, to achieve and exceed business objectives. Manage all Regulatory aspects of the product lifecycle from pre-market to post-marketing phase including reviewing and approving promotional material in …

Added Oct 15, 2026

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Johnson & Johnson

Executive Account Specialist

Taipei City, Taiwan

… Market Knowledge, Oncology, Pharmaceutical Industry, Pharmaceutical Sales Marketing, Problem Solving, Product Knowledge, Sales, Sales Enablement, Sales Trend Analysis, Strategic Sales Planning

Added Oct 18, 2026

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Johnson & Johnson

Senior Product Development Engineer Surgical Robotics – OTTAVA

Santa Clara, California, United States

Full time
Regular

Pay posted by employer$109,000–$174,800

Johnson & Johnson RAD (Robotics and Digital) is seeking for a Senior Product Development Engineer Surgical Robotics – OTTAVA , for our Santa Clara, Location. At Johnson & Johnson, we …

Added Oct 15, 2026

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Johnson & Johnson

Staff Prod Plan Specialist

Jacksonville, Florida, United States

Full time
Regular

… more at https://www.jnj.com/medtech We are searching for the best talent for a Staff Production Planning Specialist . This position is fully on-site and is located in Jacksonville, FL . Focus day-to-day efforts towards the …

Added Oct 15, 2026

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Johnson & Johnson

Clinical Account Specialist - CAS

Bogotá, Colombia +2 locations

Full time
Regular

… business. Our close partnerships with customers enable deep clinical insights, a strong and differentiated product portfolio, and a robust innovation pipeline focused on shaping the future of cardiac care. Summary and …

Added Oct 15, 2026

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Johnson & Johnson

Clinical Sales Specialist Cardiovascular

Riyadh, Saudi Arabia

Full time
Regular

… to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent for Clinical Specialist - Cardiovascular in Riyadh KSA You will be responsible for: Provide expert clinical product and technical …

Added Oct 15, 2026

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Johnson & Johnson

Senior Clinical Specialist Cardiovascular

Riyadh, Saudi Arabia +1 location

Full time
Regular

… Learn more at https://www.jnj.com/medtech We are searching for the best talent for Senior Clinical Specialist - Cardiovascular in Riyadh/Jeddah, KSA You will be responsible for: Provide expert clinical product and …

Added Oct 15, 2026

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Johnson & Johnson

Manufacturing Operations Support Specialist

Beerse, Belgium

Full time
Regular

… We are searching for the best talent for the Manufacturing Operations Support Specialist to be based in Beerse. Join our Device Assembly & Packaging team to lead technical investigations that …

Added Oct 15, 2026

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Johnson & Johnson

Senior Compliance Specialist

Xi’an, China

Full time
Regular

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REQUIREMENTS · employer excerpt

· Bachelor’s degree in science or related field is required.
· Minimum of five (5) years of experience in GMP-regulated industry and at least one (1) year of regulatory compliance experience is required.
· Strong knowledge of global GMP regulations is required.
· Strong analytical skills. Ability to clearly articulate issues.
· Must have excellent communication skills, able to quickly build credibility within the Quality and Compliance community.

6 more in the full description below.

About this opportunity

Original employer 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 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:

Legal & Compliance

Job Sub Function:

Enterprise Compliance

Job Category:

Professional

All Job Posting Locations:

Xian, Shaanxi, China

Job Description:

Senior Compliance Specialist (Xian China)

Johnson & Johnson is the world's most comprehensive and broadly-based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in pharmaceutical, and medical devices markets and have the skills and resources to tackle the world's most pressing health issues.

The Innovative Medicines Regulatory Compliance organization is recruiting for a Senior Compliance Specialist. This position will be based in the Xian site, China.

DESCRIPTION

The Senior Compliance Specialist reports directly to the Manager, IMRC-SBC (China).

This position will execute the internal audit program at the Xian site, prepare and manage external GMP audits and inspections (e.g. Health Authority, Customer, ERC, etc.), provide compliance subject matter expertise to the manufacturing site and site-based projects, deploy compliance initiatives for the site in alignment with Innovative Medicines Regulatory Compliance.

RESPONSIBILITIES

· Execute internal audits (schedule, issue agenda, prepare, conduct audit, issue report)

• Execute compliance walk-throughs (e.g. GEMBA)

• Evaluate responses to internal audits

• Enter internal audit data into COMET

• Enter GEMBA findings into the appropriate database

· Facilitate and/or support external GMP audits and inspections (Health Authority, Customer). Including:

• Inspection Readiness (audit preparation, schedule and manage mock inspections, SME coaching)

• Partner with Quality to manage inspections (host and/or coordinate front room and back room, daily inspection summaries)

• Review site response and associated CAPA for Health Authority inspections.

• Provide input to daily inspection summaries, as needed.

· Identify changes in regulations that impact compliance procedure, perform gap analysis against current practices. Implement J&J Compliance Standards (e.g. Audit/Inspection Management) and partner with sites on J&J standard implementation.

· Provide Compliance Subject Matter Expertise (SME) for site personnel, Quality Systems and/or projects. As needed, review complaints and field actions.

· Represent Regulatory Compliance at Site Management Reviews, CAPA Review Boards, Escalations, Platform Compliance meetings, etc.

· Partner with site for execution of proactive compliance scans.

· Partner with site and segment personnel (e.g. Regulatory Affairs, Operations, Product Quality Management, etc.) to proactively identify risks and drive compliance improvement across the site.

· As applicable, monitor progress of site compliance remediation plans (e.g. MCAP, SDCAP, etc.)

· Collaborate with other groups in IMRC and JJRC to support execution of independent audits and special investigations. Support site during ERC audits (e.g. document review, front/back-room support). Review and provide input to site response, and associated CAPA, to ERC audits.

· Ensure timely and accurate reporting of compliance metrics.

· Lead the Inspection Readiness Governance meetings.

· Coordinate compliance training for the site.

· Connect with external groups to benchmark industry standards.

· As needed, co-authors, review, and revise compliance procedures.

· As needed, review (not approve) significant manufacturing and laboratory investigations, confirmed complaints and S1/S2 Field Actions.

REQUIREMENTS

· Bachelor’s degree in science or related field is required.

· Minimum of five (5) years of experience in GMP-regulated industry and at least one (1) year of regulatory compliance experience is required.

· Strong knowledge of global GMP regulations is required.

· Strong analytical skills. Ability to clearly articulate issues.

· Must have excellent communication skills, able to quickly build credibility within the Quality and Compliance community.

· Delivers on commitment timelines and has high sense of urgency.

· Experience preparing for inspections, managing inspections and/or supporting inspections.

· QA/RA certification is preferred.

· Experience performing internal or external audits is strongly preferred.

· Experience in change management and project management.

· Ability to communicate in both Chinese and English is strongly preferred.

Required Skills:

Preferred Skills:

Audit and Compliance Trends, Audit Management, Audit Reporting, Business Behavior, Business Writing, Coaching, Communication, Compliance Frameworks, Compliance Management, Compliance Risk, Corporate Investigations, Critical Thinking, Legal Function, Legal Services, People Centricity, Problem Solving, Process Improvements

Why this result? · Employer labels

Keywords also found in description

Full time
Legal & Compliance
Regular

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.