Before we get further into January, we want to take a moment to announce December's Safe Miles award recipients! CONGRATUALTIONS and thank you for your professionalism and dedication to safety 🏆 🎉 #bestofbarrnunn
Having a group of peers in your corner can be transformative for your career–especially when you’re an emerging professional. That’s why joining TSCPA and other professional organizations can be critical for boosting your network and career. But don’t just take our word for it! Members like Zachary Plattner, CPA, Senior Accountant, Compass East have seen first-hand how joining TSCPA can make a difference.
Congratulations Abdirahman. To receive this Certificate of Award, Abdirahman had to populate a 130-page plus IQ OQ PQ protocol to qualify a Clean-in-Place System in a pharmaceutical manufacturing plant.
The protocol detailed the following elements:
- Product characteristics – showing what your system is looking to achieve/produce
- Production equipment – detailing the equipment necessary
- Test scripts and methods – telling you the steps involved in conducting a test
- Test parameters and acceptance criteria – defining acceptable test results
- Test checksheets – documenting and recording the test results
- Final approval – documenting that the validation process has been successfully carried out.
And to complete this assignment, Abdirahman had to learn the following:
- How to prioritise which parts of the equipment system are critical to qualify and which parts are not etc, using component impact assessments and risk management tools.
- How to read/interpret the engineering documentation such as P&IDs, Piping Isometrics and Electrical Loop Drawings used to define the equipment system.
- How the intent of a process (like maintaining the product at the required temperature) is linked to the equipment that will be used to do this.
- The tests along with the functional test scripts necessary to confirm that the installed equipment is fit-for-purpose, i.e. that it will do what it states that it will do based on the User Requirement Specifications).
- How to use a traceability matrix tool to ensure that all requirements defined within the User Requirement Specifications (URS) are tested in the protocol.
- How to qualify equipment, instruments and piping systems, and automation controls.
Well done again on your hard work!
I’m delighted to receive my Certificate of Award in ‘Commissioning Qualification of Equipment Systems’ from GetReskilled. Thanks to Geraldine Creaner and the team for their guidance throughout the learning process. Donagh Fitzgerald.
Really grateful to reach this milestone once again this year. However, I am even more grateful for the journey and the people I’ve met, know and work with along the way.
This is a reminder to myself to never take any achievements for granted! -each one is a reminder of the hard work and lessons along the way.
#staygrounded#keepgrowing#selfsevelopment#inspiretoinspire#prudentialsingapore#prudentialsg#prudential
🎉Congratulations to Gary Giam for achieving Qualifier Club Elite! 🍾
This recognition is a testament to your unwavering commitment and passion. We are lucky to have you on our team!
Can't wait to see you in GuangZhou to celebrate your success!🎉
#qce#qualityclubelite
Today we'll be assessing the SAQ (speed, agility, quickness) with the modified Shark Skill test.
How many times can you cross the lines in 30 seconds? Harder than you think!
#30daysofmovement
Brand Ambassador | Content Creator| Influencer| Social Media Manager | Owner of TrueBlueNation Media | Entrepreneur | Sports Enthusiast| Alumni of Whiskey University.
Did you know only 3% of care providers achieve an "Outstanding" CQC rating? This accolade is more than just a badge of honour—it's a symbol of delivering exceptional care, boosting team morale, and standing out as an industry leader.
But how can your care home join this elite group?
Key areas to focus on:
✔️ Strong leadership that sets the tone for excellence
✔️ Effective planning for inspections
✔️ Regular mock inspections to identify improvement areas
✔️ Leveraging research and learning from top-rated services
✔️ Focusing on your strengths while maintaining "Good" in all Key Lines of Enquiry
Achieving "Outstanding" is a challenge, but it's absolutely within reach with the right strategies.
🚀 Discover the step-by-step guide here: https://lnkd.in/eBsHnCWr
Let's make your care home a benchmark of excellence 🏆
#HealthcareLeadership#CQC#OutstandingRating#CareHomeManagement
My purpose is to empower and transform people's lives by passionately comprehending the deep aspects of human behavior so they can be the best version of themselves.
LAST DAY TO ORDER! ⏳ 🌾
Today is the last day to take advantage of our Early Order Program!
🌟 What’s in it for you?
✔️ Exclusive Incentives on high-quality BTT products
✔️ FREE Freight on your order
Ensure your equipment is ready for the season ahead while saving big! 💰
Contact your local BTT dealer today to lock in your order and reap the rewards.
#BourgaultTillageTools#FarmSavings#EarlyOrderProgram
Congratulations Thomas Moran. To receive this Certificate of Award, Thomas had to populate a 130-page plus IQ OQ PQ protocol to qualify a Clean-in-Place System in a pharmaceutical manufacturing plant.
The protocol detailed the following elements:
- Product characteristics – showing what your system is looking to achieve/produce
- Production equipment – detailing the equipment necessary
- Test scripts and methods – telling you the steps involved in conducting a test
- Test parameters and acceptance criteria – defining acceptable test results
- Test checksheets – documenting and recording the test results
- Final approval – documenting that the validation process has been successfully carried out.
And to complete this assignment, Thomas had to learn the following:
- How to prioritise which parts of the equipment system are critical to qualify and which parts are not etc, using component impact assessments and risk management tools.
- How to read/interpret the engineering documentation such as P&IDs, Piping Isometrics and Electrical Loop Drawings used to define the equipment system.
- How the intent of a process (like maintaining the product at the required temperature) is linked to the equipment that will be used to do this.
- The tests along with the functional test scripts necessary to confirm that the installed equipment is fit-for-purpose, i.e. that it will do what it states that it will do based on the User Requirement Specifications).
- How to use a traceability matrix tool to ensure that all requirements defined within the User Requirement Specifications (URS) are tested in the protocol.
- How to qualify equipment, instruments and piping systems, and automation controls.
Well done again on your hard work!
Orientation Coordinator
2moCongrats!