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Job Function:
QualityJob Sub Function:
Quality AssuranceJob Category:
ProfessionalAll Job Posting Locations:
Horsham, Pennsylvania, United States of America, Malvern, Pennsylvania, United States of America, Raritan, New Jersey, United States of AmericaJob Description:
We are searching for the best talent for a Manager, External Quality, External Contract Laboratories (ECL) Americas located in either Horsham, PA, Malvern, PA or Raritan, NJ.
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Purpose:
- Drives Quality Assurance, Compliance and Technical Support for External Quality contract laboratories (ECLs) within the Pharma R&D organization and Janssen Supply Chain, primarily in North America and Latin America regions.
- This position serves in teams or major cross-functional project initiatives at the Divisional and the J&J companywide level with regard to management of the external contract labs used globally. Closely works together with other J&J sectors leads for external contract labs, Internal JSC-QC Lab representatives, DPDS, Site Quality leads, Product Quality management, Global Quality Lab Systems, Global Procurement and other stakeholders.
- Supports the EQ-ECL function Leader in the selection, development and management of External Contract Labs globally.
- Responsible for the end-to-end Quality and Compliance oversight of external contract laboratories (ECLs).
- Supports and implements the strategy for continuous improvement of the external contract lab management processes.
- Supports the Pharma consolidation plan of external contract labs within DPDS and JSC-QC labs including increased usage of Preferred Partner networks.
- Active role in the support of new company acquisitions’ onboarding of new ECLs, and associated Q&C remediation efforts, where the Manager will work closely with the various EQ, PQM, DPDS and JSC-QC/QA groups towards effective and timely qualification, and resolution of issues that may surface.
- Lead qualification activities of ECLs, by performing on-site and remote audits, develop corrective action plans to remediate deficiencies.
- May be involved in quality oversight for day-to-day ECL activities, primarily deviation and CPA management (e.g. Vaccines). Will support escalations, as required.
- Manage all utilized systems to ensure deviations are closed in time for release and stability.
- Independently solve issues as well as solving issues with key stakeholders like Subject matter experts from Analytical development or other EQ Account owners.
- May partake in the Vaccines or other platform programs’ Q&C initiatives at the ECLs.
- Apply cGMP regulations, FDA and international requirements to all aspects of the position.
- Ensure timely and proper reporting to partners and stakeholders.
- Position may require flexibility in working schedule on occasion, in order to provide cGMP assistance and quality oversight.
- Responsible for development, negotiations, execution and maintenance of Quality Agreements with the different External Contract Laboratories.
- Pro-actively identify risks at the external contract labs, escalate critical to quality issues in a timely manner and lead resolutions. Monitors compliance of external contract labs through tracking and trending metrics resulting in up-to-date Risk Register.
- Drive periodical Business Review meetings with preferred external contract labs in order to review strategy; metrics; expectations; share best practices; business acumen; further integration with Janssen Quality Systems. Implement the yearly external contract lab audit schedule and receive approval of site auditors to participate within the audit program.
- Travel to External Contract Lab sites to conduct audits, provide cGMP assistance and quality oversight.
Qualifications / Requirements:
- A minimum of a Bachelor’s or equivalent University degree is required; a focus in Engineering, Science or an equivalent technical discipline preferred
- A minimum of 6 years of experience in Pharmaceutical, Medical Device or Biotech regulated environment (e.g. FDA)
- A minimum of 2 years of experience in Pharma Quality Control or Analytical Development laboratories or closely related experience
- Extensive experience in Quality Assurance, Quality Control and/or Compliance.
- Ability to develop Quality Systems and provide cGMP compliance support to ECLs
- Knowledge of FDA/EMA regulatory requirements applicable to biologics and/or pharmaceuticals’ testing
- Ability to independently manage work to meet project objectives and timelines
- Ability to work within multiple cross functional teams with global composition
- Strong interpersonal and written/oral communication skills
- Experience in using Pharmaceutical QMS systems
- Auditing experience
- Ability to build and nurture strong, positive relationships with business leadership and partners in Global Quality, Procurement, DPDS and across the enterprise.
- Strong negotiation skills.
- Ability to build relationships and confidence with suppliers who support J&J.
Preferred:
- Quality Assurance and Quality Control experience
Other:
- Proficiency in spoken, reading and written English is required.
- Up to 20% global travel is required
- Candidates must already have authorization to work in the country of employment. Immigration sponsorship and relocation support are 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:
Business Alignment, Coaching, Collaboration, Compliance Management, Continuous Improvement, Fact-Based Decision Making, Good Manufacturing Practices (GMP), ISO 9001, Process Improvements, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Quality Validation, Regulatory Environment, Standard Operating Procedure (SOP), Tactical Thinking, Technical CredibilityThe anticipated base pay range for this position is :
$102,000.00 - $177,100.00Additional 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
Skills Required
- Bachelor's degree or equivalent university degree, preferably in engineering, science, or an equivalent technical discipline
- At least 6 years of experience in a pharmaceutical, medical device, or biotech regulated environment
- At least 2 years of experience in pharmaceutical quality control or analytical development laboratories, or closely related experience
- Extensive experience in quality assurance, quality control, and/or compliance
- Ability to develop quality systems and provide cGMP compliance support to external contract laboratories
- Knowledge of FDA and EMA regulatory requirements applicable to biologics and/or pharmaceutical testing
- Ability to independently manage work to meet project objectives and timelines
- Ability to work within multiple globally composed cross-functional teams
- Strong interpersonal and written and oral communication skills
- Experience using pharmaceutical quality management systems
- Auditing experience
- Ability to build and maintain relationships with business leadership, Global Quality, Procurement, DPDS, enterprise partners, and suppliers
- Strong negotiation skills
- Proficiency in spoken, reading, and written English
- Quality assurance and quality control experience
- Authorization to work in the country of employment without immigration sponsorship
Johnson & Johnson Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Johnson & Johnson and has not been reviewed or approved by Johnson & Johnson.
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Healthcare Strength — Healthcare coverage is characterized as comprehensive across medical, dental, and vision, with added supports like onsite clinics, fitness centers, and Employee Assistance resources. Mental-health services and wellbeing reimbursements are also described as meaningful components of the overall package.
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Retirement Support — Retirement offerings are portrayed as a major differentiator, combining a 401(k) with employer matching and an employer-funded pension plan. Stock options and other long-term financial supports are also positioned as part of the broader rewards mix.
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Parental & Family Support — Family-related benefits are presented as notably strong, including paid parental leave for all new parents and additional leave types for caregiving and bereavement. Financial assistance for adoption, fertility treatment, and surrogacy is highlighted as a significant support.
Johnson & Johnson Insights
What We Do
Profound Change Requires Boldness. Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world. Social Media Community Guidelines: http://www.jnj.com/social-media-community-guidelines
