Our teams are our strength, and we're proud of the hard work and dedication they put in every day. In June, Tanner, Ella, Chelsea, and Eric stood out for the ways in which they supported our educators and agents. Great work!
#ingoodcompany
Hi David, Congratulations, and well done on this. To any future employers, David covered the following areas during this programme:
- Introduction – to pharmaceutical, (bio)pharmaceutical manufacturing in a GMP (Good Manufacturing Practice) regulated environment, quality systems, regulation and validation
- Industry regulations and guidelines for GMPs – including, FDA GMPs for the United States, EMA GMPs for European Union, ICH, and PICs GMP regulation
- FDA medical device rules – medical device regulations & and guidelines
- GMPs vs ISO 9001:2015 – what’s the difference and why we use both
- Process validation and documentation – design and verification of manufacturing systems
- Key manufacturing technologies – such as organic chemical synthesis, biopharmaceutical manufacturing, tablet manufacturing and aseptic and sterile manufacturing
- Supporting technologies – such as purified water generation, storage and distribution, clean steam, water for injection, storage and distribution
- Introduction to Quality Risk Management (QRM) – and the importance of risk management and the basic steps involved in its application
- Working in a cleanroom environment – layout, classification, gowning and monitoring
- Professional Writing Skills Program – This will guide you through the assignment writing process and equip you with the written communication skills you need for working in the industry
And as part of part of his end-of-module assignment, David completed a 1200-word report on the cGMPs that are required to consistently manufacture safe medicines, vaccines and medical devices for patients.
It included:
- The key requirements of a quality management system
- The cleaning validation sequence and how to determine cleanliness levels
- The documentation of a complete risk management process in terms of identifying risk, analyzing risk, evaluating risk and controlling risk.
- The typical equipment and process stages used in the manufacture of active pharmaceutical ingredients
- The generation, storage and distribution of pharmacopoeia grade Purified Water (PUW).
- The common cleanroom configuration and airflow direction that governs personnel and material flows in a biopharmaceutical manufacturing environment
Well done again.
👏We proudly present this week's Fundamental Champ...Betheny B.!
FUNDAMENTAL #33: INVEST IN RELATIONSHIPS
“Betheny consistently maintains open communication with drivers she hires, extending beyond the initial hiring phase. She not only celebrates their achievements but actively builds lasting relationships with them."
Each week we recognize a team member for living into one of our 34 fundamentals that make up ✨THE VERIHA WAY.✨ 🏆
Say congratulations to Betheny!!
#appreciationpost#Verihatrucking#Truckingindustry#Verihavip#Truckinglife#Thankatrucker#Trucking#Vip#Thankyou#appreciationpost
Wow what a review. Thank you so much Debbie and Randy.
We're thrilled to hear you had a fantastic experience and appreciate your kind words. Your satisfaction means the world to us and makes everything we do totally worthwhile!
See you in 2025 :)
#grateful#HappyClients#thankyouforyoursupport
Certified EQ Coach Multi Health Systems (MHS 2.0),
BAUD Facilitator. Sr. Business Process Analyst, Project Manager, Emotional Intelligence Coach, Trainer | Embracing Life Long Learning.
Veteran Spouse • Clemson University • MHRD Student
1moWoohoo! Go Tanner!