Sr. Specialist EQ Supplier Quality

Sr. Specialist EQ Supplier Quality - ~~~W

Description

Innovative Medicine is recruiting for a Senior Specialist, EQ Supplier Quality , located in Raritan, NJ site. Remote work options may be considered on a case-by-case basis and if approved by the Company.

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 ~~~/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

We are part of the Innovative Mecine Supply Chain (JSC), a global organization responsible for supplying medicines to markets and patients around the world. With Supplier Quality as our primary focus, we strive to provide access and affordability through innovation and collaboration with our Internal Sites, Procurement, R&D, and other Commercial partners to deliver life-changing solutions for patients in need.

As a Senior Specialist within EQ Supplier Quality, you will ensure quality and compliance for suppliers in adhering to policies, enterprise standards and regulatory guidelines. As Innovative Medicine is part of Johnson & Johnson, you will represent the J&J Credo and its Quality Principles.

Key Responsibilities:

• Lead a portfolio of suppliers including performing of supplier qualification activities; primarily for suppliers within North America.

• Be responsible for quality engagements with suppliers to identify and implement improvements regarding their performance, quality, and cost.

• Document risk assessments of a supplier's quality systems by the means of on-site audits, questionnaires, or other tools to assure the quality and conformity of supplied materials.

• Be involved in assessing the impact of supplier change management, non-conformances, compliance issues, and corrective actions.

• Establish and perform periodic review of Quality Agreements.

• Lead and participate in projects and optimization initiatives to improve supplier management processes.

• Collaborate with partners such as Site Quality, Operations, Procurement, R&D, and Regulatory Compliance.

Qualifications

Qualifications

Education:

• A Bachelor's degree or higher is required with a preference focused in Engineering or Science.

Experience and Skills:

Required:

• 3 or more years of demonstrated experience in quality management, production, quality control, or R&D in a pharmaceutical and/or biotechnology environment or similar.

• Knowledge and experience with GMP regulations and ICH guidance.

• Capable of working remotely.

• Must be available for travel for up to 25%, primarily within North America.

Preferred:

• External auditing experience as a lead auditor.

• Experience handling the quality oversight of external suppliers or manufacturers, including selection, qualification, and monitoring.

• Experience using risk management strategies and tools.

• Experience with change control, investigation & complaint handling, corrective actions, and quality agreements.

• Experience collaborating in a highly cross functional environment including interacting with areas such as Site Quality, R&D, Operations, Procurement, and Regulatory Compliance.

• Exposure to regulatory authority inspections.

Other:

• Location: Raritan, NJ. Remote location may be considered within the US.

• Relocation assistance is not available for this role.

The anticipated base pay range for this position is $61,000 to $97, 750. The anticipated base pay range for this position, in the Bay Area, is $71,000 to $112,413

The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis.

• Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.

• Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

• Employees are eligible for the following time off benefits:

• Vacation - up to 120 hours per calendar year

• Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year

• Holiday pay, including Floating Holidays - up to 13 days per calendar year

• Work, Personal and Family Time - up to 40 hours per calendar year

This job posting is anticipated to close on July 16, 2024. The Company may however extend this time-period, in which case the posting will remain available on ~~~ to accept additional applications.

For additional general information on Company benefits, please go to:

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Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

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

Primary Location NA-United States

Other Locations NA-US-Puerto Rico-Gurabo, NA-US-New Jersey-Raritan, NA-US-California

Organization JANSSEN SUPPLY GROUP, LLC (6046)

Job Function Supplier Quality

Req ID: ~~~W