Integra LifeSciences

Supervisor, Manufacturing Operations

Integra LifeSciences$81K — $112K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Science, Engineering, or related fields, or equivalent experience in a regulated environment.
  • 3+ years of leadership experience in a GMP regulated industry.
  • Knowledge of Non-Conformances (NCs) and Corrective and Preventive Actions (CAPAs).
  • Strong written and verbal communication skills with a team-focused attitude.
  • Experience in batch manufacturing and ability to gown into ISO 7 and ISO 5 Clean Rooms.
  • Familiarity with FDA regulations, ISO 9001, ISO 13485, and international standards.
  • Proficient in Microsoft Office, with strong computer skills; automation and Oracle R12/Agile experience preferred.
  • Understanding of Lean and Six Sigma methodologies is a plus.

Responsibilities

  • Direct the daily production activities in Machining, Packaging, and Boxing areas.
  • Ensure daily production goals are met and report progress during shift and tier meetings.
  • Operate and maintain process equipment, troubleshooting and escalating issues as necessary.
  • Maintain accurate records and logs pertaining to Machining, Packaging, and Boxing activities; manage inventories and place purchase requisitions.
  • Lead operations in a cleanroom environment, ensuring proper environmental controls are followed.
  • Support investigations related to Non-Conformances, CAPAs, and audits.
  • Plan and implement manufacturing process improvements and Lean initiatives.

Benefits

  • Medical, dental, and vision insurance options.
  • Life insurance, short- and long-term disability coverage.
  • Business accident insurance and group legal insurance.
  • 401(k) savings plan with potential company match.
Full Job Description
This Supervisor, Manufacturing Operations will lead and direct all activities in the manufacturing area at Integra's Mansfield, MA manufacturing facility. This site manufactures medical devices primarily used in Neurosurgical applications. The Supervisor, Manufacturing Operations is responsible for supervising production personnel to maximize safety, quality, delivery, cost and engagement metrics in the manufacturing operation. Accountable for achieving production targets while maintaining cost controls.

Summary

This position will lead and direct all activities in the manufacturing area at Integra's Mansfield, MA manufacturing facility. This site manufactures medical devices primarily used in Neurosurgical applications. Responsible for supervising production personnel to maximize safety, quality, delivery, cost and engagement metrics in the manufacturing operation. Accountable for achieving production targets while maintaining cost controls.

Job Description
  • Responsible for directing the daily production activities and staff in the Machining, Packaging, Boxing areas in support of multiple product lines.
  • Ensure daily production goals are met and report production line progress at shift and tier meetings.
  • Ability to operate, maintain, troubleshoot process equipment, and make minor adjustments as needed. Escalate issues that cannot be triaged or resolved.
  • Accurately maintain all entries into all required logs, log books and records pertaining to Machining, Packaging, Boxing and other work-in-progress related (WIP)activities. Responsible for maintaining process and component inventories. Place Purchase Requisitions for general processing supplies.
  • Leads operations in cleanroom environment and assurances proper environmental controls and behaviors of team.
  • Support any Non-Conformance/CAPA/Audit related investigations.
  • Responsible for maintaining legible and accurate records and other procedures to comply with regulatory requirements, Good Manufacturing Practices (Quality Systems Regulations) and Standard Operating Procedures.
  • Plan and lead manufacturing process improvements, and other Lean initiatives to optimize performance and drive short-term and long-term business improvements.
  • Support and participate in cross-functional teams.
  • Coach, counsel, train and motivate staff- provide clear direction and oversight of staff in effectively carrying out their daily responsibilities.
  • Perform administrative duties (e.g. review and approve timecards, overtime, absenteeism reports, place purchase requisitions, maintain training records, etc.)
  • Maintain a clean and orderly work area and perform all work in compliance with Good Manufacturing Practices (Quality Systems Regulations), and Standard Operating Procedures, and Health and Safety requirements.
  • Interface with QA department during normal course of work to coordinate inspections of completed product and to interface with the Materials Management Department to ensure efficient flow of materials through operations.
  • Demonstrate safe behavior and support department/plant Safety goals in a continuous improvement process.
  • Perform other related duties as expected.
  • Works with Manufacturing Engineering and Product Development to improve yield and reduce scrap.


Requirements
  • Bachelor's degree or higher in Science, Engineering, or related fields is desired or equivalent combination of education and relevant leadership experience in a regulated environment will be considered.
  • 3+ years of relevant leadership experience in a GMP regulated industry.
  • Knowledge of NCs and CAPAs.
  • Must have strong written and verbal communication skills. Must possess strong leadership skills with team-focused attitude and approach.
  • Must be able to gown into ISO 7 and ISO 5 Clean Room gowning.
  • Batch manufacturing experience.
  • Demonstrated knowledge of FDA regulations, ISO 9001, ISO 13485, and other National and International regulations and standards.
  • Strong computer skills, including Microsoft Office experience required.
  • Automation experience a preferred.
  • Knowledge of Oracle R12/Agile preferred.
  • Understanding of Lean/six Sigma a plus.


Salary Pay Range:

$81,650.00 - $112,700.00 USD Salary

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or trainingIn addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensationYour recruiter can share more about the specific salary range for your preferred location during the hiring process.

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are 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, and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences

About Integra LifeSciences

Integra LifeSciences is an American company that develops, manufactures, and markets medical devices for use in neurosurgery, extremity reconstruction, orthopedics, and general surgery. The company's products include implants, devices, instruments, and systems used in neurosurgery, neuromonitoring, neurotrauma, and related critical care. Integra LifeSciences has its headquarters in Princeton, New Jersey.
Learn more about Integra LifeSciences
Size
3,800 employees
Market Cap
$4.6 billion
Industry
Net Income
$133.8 million
Founded
1989
5 Year Trend
+9.2%
Revenue
$1.3 billion
NASDAQ

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