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Production engineer

Req #: 180002C4_en
Location: Lund, M SE
Job Category: Manufacturing
Date Posted: 2/9/2018 9:01:27 AM
Baxter International

Description

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.
 
 
A Career That Matters
Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.
 
 

The production Support team in Lund Sweden gives support to all production lines in Lund including GWS, Disposables (former DryCart), AK and PrismaFlex. One of our Production engineers shall go on maternity leave and we need to replace her during her absence. The temporary position will be available from February 2018 to 31st of January 2019. We work according to GMP, FDA CFDRs  and applicable ISO standards for ex ISO 13485. The work includes verification and validation of changes in production, development of instruction for production, responsible change owner.

Essentials duties and responsibilities:

  • Development and review of new/updated technical equipment to production /processes /instructions /re-work instructions

  • Develop and maintain VMP for all production lines in Lund

  • Verification of production and process changes including assessment/evaluation of indirect material for the clean room

  • Responsible change owner

  • Validation responsible for changes in production, manufacturing stakeholder for changes

  • Responsible for assigned indirect production equipment, improve and maintain

     

     

Qualifications

We expect you to have minimum a BSc in the chemical/mechanical engineering discipline or corresponding engineering, minimum 3-4 years engineering experience in Medical Device and/or Pharmaceutical industry.  To be able to perform the job you must be self-motivated, have good interpersonal skills, be capable of analyzing and solving complex problems through innovative thought and experience and a continuous improvement mind-set.

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For more information about the position, please contact Talent Acquisition Partner, Mikael Blomberg, Mikael_blomberg@baxter.com or 0046 (0) 701684825.
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