Quality Operations Manager [Sweden]


 

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Now we are looking for a Quality Operations Manager in Luleå, Sweden.

This is a great opportunity for you with a couple of years within QA wishing to grow into new responsibilities.

This is where you as a Quality Operations Manager provides leadership to the Quality Operations Team to enable the organization to achieve Quality goals. You will work cross functional to identify and resolve production and quality system issues and to drive continuous improvement in compliance and product quality.

Essential Duties and Responsibilities

  • Management and further development of the Quality Assurance Operations Team

  • Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective

  • Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality

  • Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results

  • Implementation of the company-specific quality policy and quality goals

  • Ensuring product conformity, reducing production deviations

  • Ensuring compliance with design and development activities

  • Communication of the quality principles to promote quality awareness in the company

  • Ensuring compliance with production and process controls

  • Ensuring product conformity, reducing production deviations

  • Ensuring compliance with acceptance and validation activities

  • Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes.

  • Serve as primary point of contact for quality and regulatory issues related to manufacturing processes

  • Lead efforts to identify and execute initiatives to improve manufacturing process and product quality

EDUCATION, EXPERIENCE AND QUALIFICATIONS:

  • Proficient with Quality System Regulations, IS013485, Medical device Directive and Regulation and ISO Quality System Standards.

  • Demonstrated ability to succeed in team environments and possesses effective interpersonal skills.

  • Demonstrated attention to detail, analytical decision-making, and problem-solving skills.

  • Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities.

  • Strong customer orientation and excellent written and verbal communication skills.

  • Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change.

  • Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering.

  • 2+ years of experience in the Medical Device or Pharmaceutical industry.

  • 2+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry.

  • Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

100406


 

.

Post a Comment

Previous Post Next Post

Sponsored Ads

نموذج الاتصال