Equipment Validation Engineer (Secondary packing line)

Adecco

Posted on Aug 13, 2024 by Adecco
Crawley, Sussex, United Kingdom
Research
Immediate Start
Annual Salary
Contract/Project

Are you a Validation Engineer looking for an exciting contract role inside IR35? Our client, an industry-leading organisation, is seeking a talented Validation Engineer to support their existing team in generating and executing life cycle documentation. If you have a passion for quality and a strong attention to detail, this could be the perfect role for you!

Responsibilities:

  • Generate and execute life cycle documentation from SAT to OQ on a secondary packing line, specifically for Auto-injectors.
  • Manage Non Conformances and Change Controls to ensure compliance with industry standards.
  • Provide technical authoring support for Standard Operating Procedures (SOPs).
  • Work within an established validation programme to uphold quality standards and deliver on project objectives.

Requirements:

  • Proven experience as a Validation Engineer, preferably in a pharmaceutical or medical device manufacturing environment.
  • Experience in packaging validation.
  • Strong knowledge of validation processes and procedures, including SAT, IQ, OQ, RTM, and VSR.
  • Ability to assess component criticality and ensure compliance with Master Configuration Specifications.
  • Excellent problem-solving skills and attention to detail.
  • Effective communication and interpersonal skills, with the ability to work collaboratively within a team.

This is initially for a 3 weeks contract, inside IR35.


Reference: 2808454832

https://jobs.careeraddict.com/post/93840501

This Job Vacancy has Expired!

Adecco

Equipment Validation Engineer (Secondary packing line)

Adecco

Posted on Aug 13, 2024 by Adecco

Crawley, Sussex, United Kingdom
Research
Immediate Start
Annual Salary
Contract/Project

Are you a Validation Engineer looking for an exciting contract role inside IR35? Our client, an industry-leading organisation, is seeking a talented Validation Engineer to support their existing team in generating and executing life cycle documentation. If you have a passion for quality and a strong attention to detail, this could be the perfect role for you!

Responsibilities:

  • Generate and execute life cycle documentation from SAT to OQ on a secondary packing line, specifically for Auto-injectors.
  • Manage Non Conformances and Change Controls to ensure compliance with industry standards.
  • Provide technical authoring support for Standard Operating Procedures (SOPs).
  • Work within an established validation programme to uphold quality standards and deliver on project objectives.

Requirements:

  • Proven experience as a Validation Engineer, preferably in a pharmaceutical or medical device manufacturing environment.
  • Experience in packaging validation.
  • Strong knowledge of validation processes and procedures, including SAT, IQ, OQ, RTM, and VSR.
  • Ability to assess component criticality and ensure compliance with Master Configuration Specifications.
  • Excellent problem-solving skills and attention to detail.
  • Effective communication and interpersonal skills, with the ability to work collaboratively within a team.

This is initially for a 3 weeks contract, inside IR35.

Reference: 2808454832

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