Validation engineer
Amaris Consulting
SINGAPORE
2d ago

Company Description

We are an independent technology and management consulting firm dedicated to driving business transformation & innovation for clients on an international level .

Our expert solutions focus on Strategy & Change, Information System & Digital, Telecoms, Life Sciences and Engineering. We constantly meet and exceed our 850+ worldwide clients ’ expectations this is made possible by an international team of more than 6,000 people, working together from 80 offices in 55 countries.

We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential.

Your Role

  • Responsible for validation projects. Collaborated with other departments. Such as QA, QC, Manufacturing, safety and Bio-technologist department.
  • To ensure processes run smoothly.

  • Aided validation department on the validation of all equipment used for in-house processes and manufacturing
  • Assisted in equipment, facilities, HVAC system, cleaning, process, analytical computation, and computer system validations.
  • Participated in the design, component installation, operation and performance qualification under the guidance of the department supervisor
  • Conducted and gathered results for process related equipment and environment control in areas such as the changing room (air handling unit operation), autoclaves, storage facilities for process and products as well as bio-reactors and other reactors utilized in the process
  • Raise, track and follow up on change control closure.
  • Writing, execution and review of validation protocols (Equipment / Automation).
  • Corresponding with appropriate departments and vendors to address discrepancies in validation protocols.
  • Tracking and resolution of outstanding events from protocols.
  • Any assignment from superior
  • Ideal candidates

  • Bachelor’s degree in Pharmaceuticals / Biotechnology / Pharmaceutical Sciences / Processing technology or relavant courses
  • Should possess a GMP certification
  • Experience in Pharma company is a must
  • The person must understand and have a good command of English.
  • The person should have attention to details.
  • Hands on validation execution.
  • Why us?

  • Be part of an international, multicultural environment of 7,750 talented people over 60 countries and 5 continents
  • Join a fast-growing global group with a turnover of €565M and over 1,000 clients across the world
  • Explore opportunities to grow quickly with a tailor-made career path : 70% of our key senior talent joined the company at entry level
  • Take advantage of over 500 training courses in our ACADEMY catalogue, which includes programs in interpersonal communication, team management, project management, etc.
  • Get the opportunity to support nonprofit organizations thanks to our Foundation initiatives and volunteering platform OneSmallStep
  • Depending on your performance and eligibility criteria, you can benefit from international mobility opportunities and progress your career worldwide, and / or experience other departments and sectors
  • Unlock your full potential, both professionally and personally.
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