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Sr Production Supervisor Job

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Date: Jan 25, 2019

Location: Quincy, MA, US, 02171

Company: Boston Scientific

Additional Locations:

 

 

Purpose and Passion • Comprehensive Benefits • Life-Work Integration • Community • Career Growth

At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we’re solving some of the most important healthcare industry challenges. Together, we’re one global team committed to making a difference in people’s lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life’s work.

 

Sr Production Supervisor

 

About the role:

The Senior Production Supervisor supervises the production (Including Rework) operations in Quincy.  Responsibilities include managing production build priorities, production processes, and the production personnel.  Provide day-to-day direction to the production personnel concerning work assignments, overtime requirements, quality issues/non-conformances, and site priorities. 

 

You will oversee the production process and production documentation (SOPs, and Work Instructions) to ensure compliance to regulatory requirements and the BSC Quality Policy.  Support continuous improvement projects in Production area, fostering teamwork and maintaining a positive work environment.  Position requires direct involvement with Quality Assurance.  Represent Production (including Rework) Operations during third party audits and internal audits.  Support validation testing and the launch of new products, components, and equipment.

 

Your responsibilities will include:

  • Manage the production build priorities, production processes, and the production personnel.  Provide day-to-day direction to the production personnel to the production personnel concerning work assignments, overtime requirements, quality issues/non-conformances, and site priorities.  Ensure compliance to standard operating procedures and quality regulations.  Drive department performance through various production and quality metrics such as output, yield, production schedule, daily fill rates.  Develop, implement and maintain the production documentation (using BSC’s document control system).  Work closely with supply chain, BSC manufacturing sites, and quality to coordinate production builds and ensure product quality and patient safety.
  • Conduct training related to Production (including Rework) Operations to the production personnel.  Oversee and manage the training records for the production personnel using the electronic training system.  Ensure compliance to the training plans, procedures, and industry regulations.  Represent Production Operations during third party audits and internal audits.  Support validation testing and the launch of new products, components, and equipment.  Support site and corporate Quality initiatives and CAPAs.  Manage various projects, tasks, and site initiatives as assigned.
  • Provide short-range and long planning concerning staffing requirements, OT requirements, production schedules, process improvements, and budgets.  Perform administrative duties, such as regular (i.e. daily or weekly) employee meetings, Kronos timekeeping/attendance/vacation requests, performance appraisals (input with manager.), disciplinary actions, job descriptions, interviewing, rewards, recognition, training and development.  Manage various projects, tasks, and site initiatives as assigned.
  • Support site process improvement projects and initiatives.  Process improvements may include but are not limited to Lean, Six Sigma, 5S, and cost reduction/savings.  Initiate equipment/automated system improvements related to the Production Operations.  Work closely with the Engineering Support and Quality Departments.  Work with other BSC sites to coordinate and support labeling and kitting activities.  Manage various projects, tasks, and site initiatives as assigned.
  • Work with other BSC sites to support rework, labeling, serialization activities as needed.  Oversee the schedules, production personnel, and build plans as needed for the other BSC sites while onsite in Quincy.  Manage various projects, tasks, and site initiatives as assigned.
  • Investigate root cause(s) of non-conformances (i.e. NCEP, CAPA, etc.), identify and execute corrective actions by expected completion date(s).

 

What we’re looking for in you:

Basic Qualifications

  • Bachelor’s degree required
  • Minimum 2 years of professional and highly regulated Manufacturing experience
  • Minimum 3 years Supervisory experience.
  • Demonstrate leadership capabilities and possess the ability to lead a team of product builders
  • Flexible individual with good written and verbal communication skills
  • MS office suite experience

 

Preferred Qualifications

  • Master’s degree preferred
  • SAP experience preferred
  • MES experience preferred
  • Pharmaceutical or Medical Device experience preferred

 

 

 

About us

As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.

 

Boston Scientific is an Equal Opportunity Employer – Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran

 

Requisition ID: 441257

 


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