Johnson & Johnson

Technical Launch Manager

Johnson & Johnson$102K — $177K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree required.
  • 7+ years related professional experience required.
  • Preferred experience in Medical Device or Pharmaceutical sectors.
  • Strong communication and management influence skills needed.
  • Extensive Manufacturing Experience required.

Responsibilities

  • Lead and manage the assigned group effectively.
  • Coach and develop direct reports to enhance their performance.
  • Provide global operations leadership for programs/projects.
  • Develop and execute operations strategy and project plans for successful launches.
  • Collaborate with cross-functional teams to meet business objectives.
  • Ensure compliance with defined processes in new product development.
  • Communicate business-related issues to upper management.

Benefits

  • Participate in the Company's retirement plan and 401(k).
  • Eligible for a long-term incentive program.
  • Vacation time of 120 hours annually.
  • Sick time of 40-56 hours annually, depending on the state.
  • Holidays plus floating holidays amounting to 13 days annually.
  • Up to 40 hours for work, personal, and family time per year.
  • Parental leave of 480 hours within one year of child arrival.
Full Job Description
Job Function:
Supply Chain Manufacturing

Job Sub Function:
Manufacturing Deployment

Job Category:
People Leader

All Job Posting Locations:
Raritan, New Jersey, United States of America, West Chester, Pennsylvania, United States of America

Job Description:

Johnson & Johnson is recruiting for a Technical Launch Manager to be located in Raritan, NJ or West Chester, PA.

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.

Responsibilities include but are not limited to:

- Responsible for leading the assigned group.

- Manages, coaches and develop the direct reports

- Provides global operations leadership to assigned programs or projects.

- Responsible for developing operations strategy, assembling team and development/execution of operations project plan from project charter through the hand-off to the manufacturing/supplier site all the way to global launch.

- Partners with other functions to achieve overall business objectives for a project, including commercial success, profitability, timeliness and quality.

- Partner with R&D, Quality and Supply Chain teams to supply chain manufacturing to achieve business objectives and provide governance through effective prioritization and allocation of resources to achieve strategic goals.

- Ensures that design transfer, pre-DFMA/DFMA, manufacturing process design and development, process characterization/CTQ cascade, process capability analyses, and technology transfer readiness are planned and executed to ensure business success.

- Builds strong cross-functional teams, providing feedback and coaching to team members.

- Follows defined processes & procedures related to new product development to ensure compliance and meet business deliverables.

- Responsible for communicating business-related issues or opportunities to next management level

- Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.

- For those who supervise or manage staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable

- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures

- Performs other duties assigned as needed

Qualifications:
  • Minimum of a Bachelor's Degree is required.
  • Minimum of 7 years professional related experience is required
  • Medical Device/Pharmaceutical experience is preferred.
  • Strong communication and management influence skills are required.
  • Strong Manufacturing Experience is required.


Required Skills:

Preferred Skills:
Compliance Management, Critical Thinking, Developing Others, Financial Competence, Good Manufacturing Practices (GMP), Inclusive Leadership, ISO 9001, Leadership, Manufacturing Engineering, Manufacturing Processes, Performance Measurement, Plant Operations, Production Operations, Profit and Loss Responsibility, Quality Assurance (QA), Risk Assessments, Strategic Supply Chain Management, Sustainability, Team Management, Value Stream Mapping (VSM)

The anticipated base pay range for this position is :
$102,000.00 - $177,100.00

Additional 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)).

This position is eligible to participate in the Company's long-term incentive program.

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

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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