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Job Details

Facilities and Utilities Validation Specialist

Company: Lonza Biologics Plc
Location: Slough
Reference: R2163
Closing Date: 26 Sep 17
Type: Full Time
Salary (£): Negotiable
Benefits:

Job Summary:

At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life. ...

Requirements:

At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. 

Our vision:

We strive to be the leading supplier using science and technology to improve the quality of life.

Our mission:

We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.
 

Do you want to help us as we shape the future of this great organization?

 

Job Description SummaryWe are currently looking for an experienced Facilities and Utilities Validation Specialist to join our Validation team on a permanent basis. This role will be based out of our state of the art Slough facility.

As a Validation Specialist you will be responsible for the generation and execution of validation protocols and reports in line with cGMP, industry best practice and Lonza policy. You will plan your own work and work as part of the validation and wider team supporting GMP manufacturing and supporting functions.

 

Job Description

Key Responsibilities:

  • Responsible for the generation and execution of validation project plans, protocols and reports specifically related to facilities (eg. manufacturing unit, cell banking and warehouse) and utilities (including special gases).
  • Planning and managing delivery of validation projects and procedures to meet current GMP regulations and guidelines, industry best practice and company policy.
  • Formal review of validation protocols, reports and procedures generated by Lonza staff or external vendors.
  • Process and manage quality records including change control, deviation and CAPA
  • Plan all work with and report progress to the validation scheduler, line manager and internal customer to ensure validation activities are aligned.

Interested?

What we need you to have:

  • Experience delivering multiple validation projects within the biopharmaceutical industry
  • Experience of validating GMP facilities (eg. manufacturing, cell banking and warehouse)
  • Experience of utility validation, including special gases, clean water and steam systems
  • Experience with HVAC systems
  • Good understanding of validation principles and practices
  • Experience of Pharmaceutical Quality Systems including change control, deviation, CAPAs
  • Knowledge and understanding of manufacturing operations; fermentation, purification and controlled storage

Responsibilities 

Education

 

Work Experience

Certifications

 

Skills

 

Language(s)

 

 

 

Lonza.  The place to Go, Stay and Grow.

Apply for this job: Facilities and Utilities Validation Specialist

Contact Information:

Address:  Head Office
228 Bath Road Slough Berkshire
SL1 4DX
England
Tel:  +44 1753 777000
Fax:  +44 1753 777001
Website:  Visit Our Web Site

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