CQV Engineer
- Oss
- Contract
- Commissioning, Qualification and Validation
Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for a CQV Engineer for their new Capex investment project. As a scientific and technology innovator, this is a superb opportunity to onboard as our client continues to make strides towards a healthier world for all.
Responsibilities:
- Prepare validation documents including URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
- Execution of IQ/OQ and PQ for equipment, systems and utilities.
- Write reports of completed CQV activities
- Stay informed of industry regulatory changes as it applies to equipment / facility validation.
- Support in writing and/or revising procedures applicable to the Engineering activities.
- Support the Engineering group to prepare the validation, requalification and maintenance program.
Required experience:
- Bachelor degree or equivalent in a relevant subject area.
- Flexibility and adaptability, able to perform in an ever-changing environment.
- Demonstrable (3-6 years) experience within a validation role.
- Experience in GMP environment or similar, familiar with GDocP, Data Integrity and ALCOA++
- Strong planning skills and self-motivated, able to work autonomously.
- Business-level fluency in English; other languages are nice to have but not required.
If this role is of interest to you, please apply now!
#LI-CB1
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Save as job alert
Similar Jobs
Salary
Competitive
Location
Wiltshire
Salary
Competitive
Sector
Commissioning, Qualification and Validation
Job type
Contract
Location
South Coast
Description
CQV Engineer - Pharma - Wiltshire - 6-Month Contract Our client, a global biotechnology organisation, is recruiting for a CQV Engineer to join their capital project in Wiltshire. This new build
Reference
35240
Expiry Date
01/01/0001
Author
Caroline O’SullivanAuthor
Caroline O’SullivanSalary
Competitive
Location
Seattle
Salary
Competitive
Sector
Commissioning, Qualification and Validation
Job type
Contract
Location
United States
Description
Shipping Validation Engineer - Pharma - Seattle - 6-Month Contract Our client, a global biotechnology organisation, is recruiting for a Shipping Validation Engineer to join their capital project
Reference
34852
Expiry Date
01/01/0001
Author
Caroline O’SullivanAuthor
Caroline O’SullivanSalary
Competitive
Location
Seattle
Salary
Competitive
Sector
Commissioning, Qualification and Validation
Job type
Contract
Location
United States
Description
Cleaning Validation Engineer - Pharmaceuticals - Seattle - 12-Month Contract Our client, a global biotechnology organisation, is recruiting for a cleaning validation engineer to join their
Reference
34851
Expiry Date
01/01/0001
Author
Caroline O’SullivanAuthor
Caroline O’SullivanInsights
Send us your CV
Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.
Chris
I manage this role.