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Sr. Manager, Pharmaceutical Technology (Medical Devices)

Company: Allergan
Location: Irvine
Posted on: October 11, 2019

Job Description:

Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma.?Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world.
Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective?therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around the world live longer, healthier lives every day.?Allergan is a company that will inspire you to aim high with your ambition. Where you can build bridges all over the world. Where you can power ideas that drive change. And where you will act fast and drive results for customers and patients. ?Power your future & join our bold team.?Position Overview?Engineering management roll leads, manages and coordinates projectsinvolving new product development, commercial introduction and marketed product support. The role will include product and process engineering design, manufacturing processtransfers, production scale-up,validation, launch support and on market technical support.?Main Areas of Responsibilities?This position will:

  • Coordinate and lead the activities and functions for new product technology transfer to? commercial? manufacturing? sites? providing? product? and? process? design? input, defining? specifications? for equipment,? selecting? equipment? suppliers,? and locking down final commercial manufacturing? process. Coordinate and facilitate transfer of product manufacture to additional site(s).
  • Oversee new product process validation at commercial manufacturing sites and support launch of new products.
  • Technical interface with contract manufacturers, vendors and suppliers.
  • Provide technical support to currently marketed products, including technical interface with contract manufacturers,? vendors and suppliers
  • Support due diligence assessments of potential business development opportunities. Requirements?The following listed requirements need to be met at a minimum level to be considered for the job:
    • A minimum of seven (7) years of engineering work experience, preferably in a medical device development and manufacturing environment, and hands-on or technical training in the field of process engineering.
    • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and otherregulatory and safety compliance requirements and guidelines.
    • Design Control Process(ISO 13485 and FDA QSR 820).
    • Device manufacturing processdesign/DFM and scale-upincluding equipment, testing, assembly operations and support systems.
    • Assembly processes and equipment/fixturing (semi-automation, full automation)
    • Injection molding and plastics extrusion
    • Process Validation (process and equipment) ??Preferred Skills/Qualifications?The below skills are attributes that may not be mandatory but are definitely desired in the ideal candidate.
      • Strong projectmanagement and team leadership skills
      • Implementing goals, objectives and practices for effective, efficientand cost-effective management of allocatedresources.
      • Analyzing, troubleshooting and identifying problems,and recommending and implementing methods, procedures and/or techniques for resolution. Problem solving techniques.
      • Experimental design.
      • Statistical techniques.
      • Quality by Design (QbD).
      • Six Sigma/DMAIC process.
      • Communicating clearlyand concisely, both orally and in writing.
      • Establishing and maintaining cooperative working relationships with those contactedin the course of work.
      • Performing all necessary engineering project functions efficiently and in a timely manner.
      • Handles a diverse workloadof assignments, coveringseveral disciplines of engineering; maintains properpriority of multipleassignments.
      • Complies with all Companypolicies and procedures, including safety rules and regulations.Education??
        • A Bachelor?s Degree in Engineering, Science or other technical discipline or equivalent degree.
          ?#LI-SA2

Keywords: Allergan, Irvine , Sr. Manager, Pharmaceutical Technology (Medical Devices), IT / Software / Systems , Irvine, California

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