Johnson & Johnson

Quality Operations Manager

Johnson & Johnson$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a Technical or Science field is required.
  • 5-8 years of relevant work experience in Quality Assurance.
  • Two years of management experience with direct supervision and matrix management.
  • Ten years of related experience or equivalent education and experience.
  • Proficiency in statistical and analytical problem solving; certification in PE tools preferred.
  • Knowledge of lean manufacturing and manufacturing processes is preferred.
  • Excellent oral communication and technical writing skills.

Responsibilities

  • Establish and maintain quality assurance programs, procedures, and controls.
  • Ensure product quality meets company and regulatory standards.
  • Analyze significant quality trends and recommend improvements.
  • Review and approve quality system documents, including non-conformances and CAPA.
  • Manage qualification and validation of products and quality control activities.
  • Lead investigations to eliminate root causes of non-conformances.
  • Initiate actions to prevent nonconformities and implement remediation plans.

Benefits

  • Health, dental and vision insurance.
  • 401(k) retirement plan with company match.
  • Paid time off and holidays.
  • Employee assistance programs and wellness initiatives.
  • Opportunities for professional development and growth.
Full Job Description
Job Function:
Quality

Job Sub Function:
Quality Assurance

Job Category:
People Leader

All Job Posting Locations:
Cornelia, Georgia, United States of America

Job Description:

Johnson & Johnson is currently recruiting for a Quality Operations Manager! This position will be located in Cornelia, GA.

Position Summary:

Plans, coordinates, and directs quality assurance programs designed to ensure continuous production of products consistent with established standards by performing the following duties personally or through subordinates. At this level, the position has a greater degree of impact on the business results and typically, responsibility for managing a group of professionals.

Implement and lead the quality operations organization for the Ethicon Cornelia, Georgia site by:
  • Planning, coordinating, and directing quality assurance programs designed to ensure continuous production of products consistent with established standards
  • Serving as the Quality Operations Site Lead and overseeing day-to-day quality operations
  • Verifying that the Quality System in in place and maintained at the required compliance level

Driving Quality System efficient execution and reduced risk of non-conforming product

Key Responsibilities:Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
  • Establishes and maintains quality assurance programs, procedures, and controls.
  • Ensures that performance and quality of products conform to established company and regulatory standards.
  • Analyzes data sources significant quality trends and recommends actions as needed.
  • Reviews and approves non-conformances, CAPA, Audit Observations, Change Controls, Validations and Completion Reports, and other quality system documents or records as required.
  • Manages the qualification and validation for all products and processes and quality control support activities.
  • Supports and in some cases leads investigation, evaluation, and implementation of actions to eliminate root causes of non-conformances
  • The individual has the necessary independence, authority, and responsibility to initiate action to prevent nonconformities, enact remediation plans, identify and document quality issues, initiate, recommend, provide and verify solutions.
  • Ensures effective risk management process is implemented to prevent unanticipated failure.
  • Formulates and maintains quality control objectives and coordinates objectives with preproduction and production procedures in cooperation with other manufacturing managers to maximize product reliability and minimize costs.
  • Participates in auditing of production areas and systems.
  • Reviews reports findings and makes recommendations for corrective action.
  • Submits and administers budget schedules and performance standards.
  • Supports and manages cost improvement projects.
  • Acts as back up to QA Director for signature authority and meeting representation.
  • Responsible for Succession Planning, Goals and Objectives, and Salary planning for direct reports and subordinates.
  • Actively supports other plant functions in the implementation of company programs and projects.
  • Enforces, promotes, and observes all safety, environmental, industrial hygiene rules and regulations established by the Company.
  • Responsible for effectively communicating business related issues or opportunities to next management level.
  • For those who supervise or manage a 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:

Education:

A minimum of a Bachelors or equivalent University degree is required, with a focus in Technical or Science field preferred.

Required:
  • A minimum of 5-8 years relevant work experience.
  • Two (2) years active management experience including direct supervision and matrix management.
  • Ten (10) years related experience and/or training or an equivalent combination of education and experience.
  • Statistical and analytical problem solving. Certified in PE tools (preferred)
  • Preferred knowledge of lean manufacturing and manufacturing processes
  • Excellent oral communication and technical writing skills.

Other:

This position may require up to 10% domestic travel.

Required Skills:

Preferred Skills:

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.

Johnson & Johnson Careers

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Our team at Johnson & Johnson thrives on collaboration and diversity. You will work alongside over 130,000 employees globally who are committed to making a lasting impact. With a culture that values diversity training and leadership, you are supported in both personal and professional growth.

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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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