Supervisor, Quality Systems

HaemoneticsSalt Lake City, UT
1d$66,464 - $113,159

About The Position

We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice. Job Details Manage the daily activities of the Quality System for the distribution site. QA functions include but are not limited to: Non Conforming Product (NCE), Customer Complaint Review (PIR), Corrective and Preventative Actions (CAPA), Quality System Metrics, and Trending (Global Key Performance Indicators (KPIs), Training, Document Control and Management Controls including Quality Planning. Provide support in the management of product and process improvement initiatives that directly benefit the customer. The individual shall operate to meet the requirements of International and European Standards and regulations in compliance with company policy and procedures and the requirements of the Quality Management System. Act as a key Quality Systems representative and assume responsibility for the management of the QS department as required for the distribution site. Assume other responsibilities as required to support distribution warehouse departments, projects, and/ or production schedules. Oversee the quality system compliance through Global Key Performance Indicators to monitor the performance of key elements of the quality system. Work to achieve the overall objectives of the company and ensure the quality strategies are aligned for the areas of responsibility. Liaise with manufacturing/ engineering and material groups on process/product-related issues affecting the distribution site. Work with management to ensure the effective maintenance of quality systems requirements and procedures, to domestic and international standards. Perform QS MRB, NCE, CAPA, and PIR functions as applicable. Support Internal and External audits as required. SUPERVISORY RESPONSIBILITIES Carries out supervisory responsibilities in accordance with the organization’s policies and applicable laws. Responsibilities include interviewing, hiring, training and developing employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.

Requirements

  • 1 year experience post qualification Required
  • Effective leadership skills
  • Excellent collaboration and team building skills
  • Seeks to acquire knowledge in area of specialty
  • Demonstrated time management and priority setting skills
  • Ability to work within tight timeframes and meet strict deadlines
  • Ability to drive multiple projects to successful completion
  • Demonstrated written communication skills
  • Effective interpersonal skills
  • Maintains composure under pressure
  • Excellent collaboration and team building skills
  • Performs work independently with minimal supervision
  • Assumes personal responsibility for actions
  • Possesses flexibility to work in a fast paced, dynamic environment
  • Demonstrated analytical skills
  • Demonstrates a high commitment to quality
  • Experience conducting QS audits
  • Intermediary knowledge of Word, Excel, and Outlook

Nice To Haves

  • Bachelor Degree- Preferred
  • Professional Certifications Example: CQA, CQE, ISO Certified Preferred
  • 1 year experience in the medical device/pharmaceutical industry Preferred
  • NB: Qualification requirements can be negated by sufficient experience Required

Responsibilities

  • Manage the daily activities of the Quality System for the distribution site.
  • Provide support in the management of product and process improvement initiatives that directly benefit the customer.
  • Act as a key Quality Systems representative and assume responsibility for the management of the QS department as required for the distribution site.
  • Assume other responsibilities as required to support distribution warehouse departments, projects, and/ or production schedules.
  • Oversee the quality system compliance through Global Key Performance Indicators to monitor the performance of key elements of the quality system.
  • Work to achieve the overall objectives of the company and ensure the quality strategies are aligned for the areas of responsibility.
  • Liaise with manufacturing/ engineering and material groups on process/product-related issues affecting the distribution site.
  • Work with management to ensure the effective maintenance of quality systems requirements and procedures, to domestic and international standards.
  • Perform QS MRB, NCE, CAPA, and PIR functions as applicable.
  • Support Internal and External audits as required.
  • Carries out supervisory responsibilities in accordance with the organization’s policies and applicable laws.
  • Responsibilities include interviewing, hiring, training and developing employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.

Benefits

  • a 401(k) with up to a 6% employer match and no vesting period
  • an employee stock purchase plan
  • “flexible time off” for salaried employees and, for hourly employees, accrual of three to five weeks’ vacation annually (based on tenure), accrual of up to 64 hours (annually) of paid sick time, paid and/or floating holidays, parental leave, short- and long-term disability insurance, tuition reimbursement, and/or health and welfare benefits
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