Operations Process Support Specialist
- Midlands (Ireland)
- Contract
- Commissioning, Qualification and Validation
This vacancy has now expired
Do you want to be involved with exciting Pharmaceutical projects?
When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require an Operations Process Support Specialist.
This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.
Role Summary:
- Serve as a technical and operations representative for established manufacturing processes and new product introduction.
- Collaborate within cross-functional teams and partner with colleagues to perform vendor management, communications, training, project work, audit/inspection duties, and ensure department readiness for audits/inspections.
- Design, author, review, approve, and execute process updates in support of ongoing manufacturing support and new product introduction.
- Provide technical input into quality notifications by authoring, reviewing, and approving investigations.
- Drive continuous process improvements using Lean Principles to optimize equipment uptime and target outputs.
- Oversee operations processes to ensure continuous, reliable, and repeatable manufacturing.
- Drive effective writing, revising, and rolling out of accurate operational procedures, training materials, and manufacturing procedures.
- Ensure process reliability and performance by facilitating effective systems for identifying root cause failures, making recommendations, and implementing improvement changes throughout processes.
- Drive continuous improvement by leading and actively participating in system failure investigations, investigation reports, change control execution/development, and Kaizen events.
Qualifications & Education
- Bachelor’s Degree or equivalent, ideally in a Science, Engineering, or other Technical discipline
- Proven track record and established experience in a process engineer role with measurable accomplishments and achievements.
- Relevant experience and a particular skill set in their area of expertise that adds value to the business; ideally in a manufacturing, preferably in a GMP setting.
- Knowledge of regulatory and code requirements to Irish, European, and International Codes, Standards, and Practices.
- Proficiency in report, standards, and policy writing.
- Proficiency in Microsoft Office and job-related computer applications.
- Desired experience in Lean Six Sigma Methodology.
If this role is of interest to you, please apply now!
#LI-CH3
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
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
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
Denmark
Salary
Competitive
Sector
Commissioning, Qualification and Validation
Job type
Contract
Location
Denmark
Description
Packaging CQV - Denmark - 6-12 Months Contract Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Packaging CQV to join their new and exciting large-scale CAPEX
Reference
36927
Expiry Date
01/01/0001
Author
Abigail StierAuthor
Abigail StierSalary
Competitive
Location
Brussels
Salary
Competitive
Sector
Commissioning, Qualification and Validation
Job type
Contract
Location
Belgium
Brussels
Description
Cleaning Validation SME - Brussels, Belgium - 3/6 Months Contract We are looking for an experienced Cleaning Validation SME for a fantastic 3-6 months contract based in Brussels. You will be
Reference
36903
Expiry Date
01/01/0001
Author
Chris BlandAuthor
Chris BlandSalary
Competitive
Location
Carlow
Salary
Competitive
Sector
Commissioning, Qualification and Validation
Job type
Contract
Location
Ireland
West
Description
Validation Engineer - Ireland - 11 Months Contract Do you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our
Reference
36688
Expiry Date
01/01/0001
Author
Christopher HutchinsonAuthor
Christopher HutchinsonInsights
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.
Christopher
I manage this role.