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Biotechnology Job USA | Technical Lead position @ Bristol-Myers Squibb

Biotechnology Job USA | Technical Lead position @ Bristol-Myers Squibb

Biotechnology Job USA  |  Technical Lead position @ Bristol-Myers Squibb : Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

The Bristol-Myers Squibb Devens site is a state-of-the-art biologics manufacturing facility located on 89 acres, just 45 minutes west of Boston. It is here that we will be fulfilling our critical mission to help patients prevail over serious diseases. This 400,000 square foot complex represents the single largest capital investment in the nearly 125 year history of BMS, $750 million, and is a key part of our strategic BioPharma transformation.

Biotechnology Job USA  |  Technical Lead position @ Bristol-Myers Squibb

Responsibilities:

  • Works on routine manufacturing assignments as well as assignments that are very complex in nature where independent action and a high degree of initiative are required in resolving problems and making recommendations.
  • Striving for right first time through adherence of GMP activities
  • Support Tech transfer team through active participation in ensuring that new process can fit and executes in sustainable manner
  • Being resource to support routine investigations and CAPAs– author, review, approval, in case of excess investigation beyond planned capacity
  • Assigned area owner – drive facility upkeeps
  • Adheres to Good Manufacturing Practices and standard operating procedures
  • Weighs and checks raw materials. Assembles, cleans and sterilizes process equipment, monitors processes
  • Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements
  • Operates and trains others all production equipment within the assigned functional area (i.e. Upstream: Media formulation equipment, glass washers, dispensary, bioreactors, harvest
  • equipments or Downstream: Buffer equipment, glass washers, chromatography skids, membrane operations, column packing skids, etc.)
  • Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.)
  • Ensures less experienced manufacturing personnel comply with Standard Operating Procedures (SOPs) and electronic work instructions and that training is completed on time
  • Assists with the coordination and implementation of special projects such as validation or complex investigations
  • May provide scheduling and work assignment guidance to peers. Modifies group work plan, schedule or assignments to meet shift/unit priorities, maintains operational efficiency, making
  • corrections as necessary, regularly provides training and operational guidance to other staff
  • Advises Shift Supervisor/Manager on improvements which may optimize work processes and informs of work issues requiring management action

Qualifications:

  • B.S., in science, engineering, biochemistry or related discipline, or its equivalent is highly desired
  • A minimum of 5+ year’s process operations experience in a highly automated biotechnology manufacturing facility subject to Good Manufacturing Practices (GMP) regulations
  • Practical knowledge of regulations such as GMP and company Standard Operating Procedures (SOP) and strong technical and operational knowledge of either upstream and/or downstream unit operation is essential
  • Demonstrated experience in solving complex technical issues in biologics manufacturing
  • Prior evidence of successful participation on work teams where combined contribution, collaboration, and results were expected
  • Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications
  • Previous work experience where attention to detail and personal accountability were critical to success
  • Demonstrates good interpersonal skills, is attentive and approachable
  • Maintains a professional and productive relationship with area management and co-workers
  • Must have ability to work as self-starter and handle multiple priorities in a dynamic cross-functional team based environment

Bristol-Myers Squibb is an equal opportunity employer – Vet/Disability

Job Function : Prod/Process Equipment – Operator
Primary Location : NA-US-MA-Devens
Organization : GMS – Biologics Devens
Job published: 9 Sept ,2016

Biotechnology Job USA  |  Technical Lead position @ Bristol-Myers Squibb

How to Apply and View Original Notification: https://bms.taleo.net/careersection/jobdetail.ftl?job=1603819&lang=en

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