Production Operator
Production Operator
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Job Description
We are a global researchbased biopharmaceutical company that combines the focus and passion of leadingedge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work.
We are now recruiting a Production Operator 12 months FTC) to join our diverse team in Cork. To carry out the range of process operations linked to operating process equipment ie. supply startup sampling running checks first level troubleshooting dismantling and cleaning. Manufacture to GMP standard.
Are you intrigued Do you want to learn more
Responsibilities:
Respect the rules of Quality Assessment
- Know GMP
- Know and apply the Standard Operating Procedures (SOPs) for the equipment and the plant.
Production operations
- Know which operation to carry out from the Production Schedule:
Manufacture Order
Instructions
- Prepare the work area:
Check the coherence of the production schedule.
Carry out or check the work place readiness
Check the supplies (codes lots expiry date FIFO)
- Carry out Preparatory operations:
Preproduction handling: supplying Batch paperwork
The process operation
Identification
Postproduction handling
Sealing the containers
Operate the process machine:
Nano Mill
Niro Granulation
Sifting & Blending
Tabletting
Coating
Sorting/Metal Detection
Inspection 100
Dispensing Equipment
Gral/Niro
Fitzmill and Sweco Sieve
Glatt Coating
Encapsulation
- Adhere to OEE targets for cycle times and changeover times for all processes
- Fill in the Master Batch Paperwork in step with Production:
Complete process operation steps in the paperwork and ensure checks completed prior to continuing.
- Carry out inprocess testing during Processing
Take Samples
Compare to quality standard
Complete inprocess tests
Analyse any deviations
Notify a Team Leader/Supervisor
Carry out necessary corrections
Fill in the quality control documents
- Take samples as instructed by the Quality Control Lab
Fill in the documents
Identify the samples
Remove the samples
- Contribute to the safety of persons and goods
Abide by safety regulations
Notify superiors in event of accidents.
Highlight any concerns on safety to Team Leader/Supervisor.
- Continually improve the activities and systems of production and be attentive to good brand image.
- Survey personal behaviour
Guarantee hygiene in each operation
Report any dysfunction
Pass on useful instructions to others
Keep the work place clean and tidy at all times
Be neatly dressed and behave responsibly.
Qualifications :
Minimum requirement is Leaving Certificate.
Knowledge/Interest in process Equipment and manufacturing.
MS Word MS Excel Mail
Interest in Process Equipment.
Good communication skills and good problemsolving skills
English Fluent written & oral.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
