Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Technical Operations Process Engineer

Posted Jan 13, 2021
Job ID: JJJP00005483
Location
Cork
Duration
1 year, 11 months
(Feb 1, 2021 - Dec 31, 2022)
Hours/week
39 hrs/week
Payrate range
Unknown

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging and contracting talent for the Johnson & Johnson contingent workforce.


We have an exciting opportunity for a Technical Operations Process Engineer to join our team in Cork. The Technical Operations Process Engineer is a key contributor to process improvement initiatives on the site. In addition, they should have a keen aptitude for implementing and maintaining standards and driving efficiency within the business. This contract would suit a PhD graduate in Chemistry or a related field who has gained industry experience throughout their education. This will be a 23 month contract initially.


As a Technical Operations Process Engineer, your typical day may include:

General

  • Manage / execute the validation program related to LCM for existing products
  • Issue / review validation plan, protocols and reports
  • Be the site TO representative in LCM/NPI project teams as process / validation SME
  • As required coordination of LCM projects on site, under responsibility of global TO organization
  • Own / participate in the CPV program by issuing plans, protocols and reports and oversee execution.
  • Lead complex investigations on the site by providing facilitation / technical expertise
  • Provides process / technology input to SOP s, Master Batch Records and change controls
  • Partner with Engineering & Maintenance and contribute to equipment changes / introduction projects on the site
  • Lead / support process improvement projects, including new technology / analytics introduction (e.g. MVA, PAT)
  • Contribute to Standardization initiatives for Technical Operations
  • Technical support / direct participation in partnership with Quality / Operations on any regulatory audits and inspection
  • requirements.


Be vital:

To be part of this high performing team you will have great attention to detail and have the following:

  • Strong analytical and Problem-Solving skills
  • Excellent communication skills - both written and oral
  • Acute attention to detail
  • Excellent team player with strong customer focus
  • Focus on patients and customers at all times
  • Self-driven and keeps up to date with regulatory, technical developments within the industry.


Qualification Requirements:

  • PhD in Chemistry or equivalent with 5-8 years  experience in a pharmaceutical environment desirable
  • Excellent social and communication skills is desirable 
  • Self-driven and keeps up to date with regulatory, technical developments within the industry.
  • Acute attention to detail
  • Focus on patients and customers at all times.


What you’re great at:

  • Strong analytical skills
  • Excellent communication skills - both written and oral
  • Working on own initiative to achieve both individual and team based targets
  • Excellent team player with strong customer focus
  • Strong Business Acumen
  • Excellent time management skills with good multi-tasking ability


Similar jobs

+ View all jobs