Johnson & Johnson

Sr. Manager, Cryopreservation Operations

Johnson & Johnson • $122K — $208K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required; advanced degree in Science or Engineering preferred
  • Minimum eight years of relevant work experience
  • Experience in a GMP production environment
  • Proven track record in team leadership and talent development
  • Excellent communication and interpersonal skills
  • Strong analytical and problem-solving skills

Responsibilities

  • Lead Cryopreservation/MOI/QCCB operations for personalized cell therapy
  • Foster an innovative environment focusing on quality and performance
  • Oversee hiring and development of operations personnel
  • Collaborate with functions like Quality and Maintenance for seamless operations
  • Drive vision for continuous improvement and cost competitiveness
  • Ensure regulatory compliance and promote health and safety standards
  • Mentor employees and build highly capable teams

Benefits

  • Generous sick time up to 40 hours per year
  • Holiday pay including 13 days of holidays annually
  • Parental leave of 480 hours within the first year of a child's arrival
  • Condolence leave of up to 30 days for immediate family
  • Caregiver leave of 10 days
  • Volunteer leave of 4 days
  • Military spouse time-off of 80 hours
Full Job Description

Job Function:

Supply Chain Manufacturing

Job Sub Function:

Plant Management

Job Category:

Professional

All Job Posting Locations:

Raritan, New Jersey, United States of America

Job Description:

We are searching for the best talent for a Senior Operations Manager to join our Team in Raritan, NJ.

Our Raritan, NJ Cell Therapy facility is scaling up operational flows to serve more patients and meet the highest quality standards without compromising manufacturing efficiency. The Senior Manager is responsible for leading and driving long-term strategy and regulatory compliance, while striving for world-class excellence and performance. This role will also maintain excellent communication with business partners to manage expectations effectively and will help build the organization in alignment with operational ramp-up.


Key Responsibilities:
  • Lead all aspects of Cryopreservation/MOI/QCCB operations for a personalized cell therapy, supporting both clinical and commercial requirements.
  • Build and maintain an environment of innovative continuous improvement, focusing on quality, value creation, performance management, and capacity.
  • Lead managers and operations personnel working in the Value Stream, including hiring and developing people at all levels to grow within and beyond their current roles.
  • Partner effectively with all functions including Quality, Maintenance, Planning, and Operations Support to ensure seamless execution of planned activities.
  • Develop, coordinate, and drive a vision for operations; be passionate about continuously improving performance, technology utilization, and cost competitiveness.
  • Accountable for and foster a culture of regulatory compliance and strong environmental, health, and safety performance.
  • Coach, mentor, and provide development opportunities for all employees in the manufacturing function, building highly capable teams, and developing skills and expertise.

Education:
  • A minimum of a Bachelor’s /University degree is required; advanced degree or focused degree in Science or Engineering is preferred


Experience and Skills:

Required:

  • Minimum eight (8) years of relevant professional work experience
  • Experience working in a Good Manufacturing Practices (GMP) production environment
  • Experience leading teams, developing talent, and championing diversity and inclusion
  • Resilience to address challenges, changes, and unexpected setbacks in a positive way
  • Excellent verbal and written communication skills and strong interpersonal skills to effectively influence in all directions
  • Good analytical and problem-solving abilities, thriving in a fast-paced work environment


Preferred:
  • Experience working in a sterile biological/pharmaceutical manufacturing environment
  • Knowledge of Lean Methodologies, preferably certified Green or Black Belt
  • Experience with electronic batch records and/or ERP systems


Other:
  • May require up to 10% domestic or international travel

Required Skills:

 

Preferred Skills:

Agile Manufacturing, Good Manufacturing Practices (GMP), Innovation, Manufacturing Compliance, Manufacturing Safety, Market Research, Mentorship, Organizational Project Management, Organizing, Plant Operations, Process Improvements, Product Development Lifecycle, Tactical Planning, Technical Credibility

 

 

The anticipated base pay range for this position is :

122,000-208,250

Additional Description for Pay Transparency:

Sick time - 40 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 Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave – 10 days Volunteer Leave – 4 days Military Spouse Time-Off – 80 hours  Additional information can be found through the link below.  https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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