Speaker Profile

Joy
Joy McElroy
Owner, McElroy Training and Consultancy, LLC

Joy McElroy Upon earning a degree in Zoology at North Carolina State University, Joy began working in the pharmaceutical and biotech industries in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing. Her work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw the Quality Control Lab.

In 1998 Joy moved to Wyeth Lederle and worked in Quality Assurance, performing GMP Compliance audits, batch record reviews, and holding annual GMP training for new employees. After working in Quality Assurance for a few years, Joy moved into Equipment Qualification and Cleaning Validation at Mallinckrodt.

With 19 years of experience as a consultant, and over 25 years total experience in the pharmaceutical and biotech industries, Joy has gained extensive knowledge of Quality Assurance, Technical Writing, Process and Cleaning Validation, and Equipment Qualification and Computer System Validation and Part 11 Compliance. She has written and executed Equipment Qualifications and Validation Protocols for numerous Companies such as Mallinckrodt, Wyeth Lederle, Merck, BioMerieux, Catalent, and Biotest, Novartis, Imprimis, Cody Laboratories, and Xceilence.

Her knowledge, experience, have made her a highly sought-after engineer, technical writer, and trainer in both the pharmaceutical and biotech industries. Joy specializes in Equipment Qualification, Cleaning Validation, and GMP Compliance Auditing, and technical writing, and GMP, Audit Preparation, and SOP writing training, Computer System Validation and Part Compliance.

In 2019 she opened her own company, McElroy Training and Consultancy, LLC which provides consultants for various projects as well as on and off - site training to pharmaceutical and biotech companies throughout the United States.

Joy also spends her time mentoring and speaking as an Empowerment Speaker. Her goal is to empower people all over the world to live their dreams though implementing 5 simple techniques she has learned and applied through the years.

Upcoming Webinars Recorded Webinars
Joy McElroy

FDA Regulations for Analytical Instrument Qualification and Validation Processes

In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system.

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

Best Practices for an Effective Cleaning Validation Procedures

In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system.

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

FDA Regulations for Environmental Monitoring(EM) Program

Upon completion of this training, you will be able to Describe how Clean room Environmental Monitoring (EM) Program fits into the Regulations. Explain the basis of the Four (4) Phases of Clean room transitional monitoring (Pre-qualification through post-qualification EM) and what each type stands for. List the basic content of a well-designed, effective and compliant EM Program. Explain the relationship between an EM Excursion Program and CAPA

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $190.00 | View Details
Joy McElroy

Writing Validation Master Plans; Best Practices for Writing a Compliant Document

This webinar will discuss the major components of Validation Master Plans. It will discuss how the VMP is different from Validation SOPs.

Speaker: Joy McElroy | View Anytime | Duration: 90 Minutes | Price: $190.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

Good Laboratory Practices (GLPs), CFR part 58 is a set of guidelines for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA.

Speaker: Joy McElroy | View Anytime | Duration: 90 Minutes | Price: $190.00 | View Details
Joy McElroy

FDA Regulations for Environmental Monitoring(EM) Program

Upon completion of this training, you will be able to Describe how Clean room Environmental Monitoring (EM) Program fits into the Regulations. Explain the basis of the Four (4) Phases of Clean room transitional monitoring (Pre-qualification through post-qualification EM) and what each type stands for. List the basic content of a well-designed, effective and compliant EM Program. Explain the relationship between an EM Excursion Program and CAPA

Speaker: Joy McElroy | View Anytime | Price: $390.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $390.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $390.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $390.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $390.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

In this webinar you will learn what GLPs are, why they were created, what is the objective of GLPs, and how they relate and are associated with GMPs.

Speaker: Joy McElroy | View Anytime | Price: $390.00 | View Details
Joy McElroy

Writing Validation Master Plans; Best Practices for Writing a Compliant Document

This webinar will discuss the major components of Validation Master Plans. It will discuss how the VMP is different from Validation SOPs.

Speaker: Joy McElroy | View Anytime | Duration: 90 Minutes | Price: $390.00 | View Details
Joy McElroy

GLPs: How are they Associated with GMPs and SOPs

Good Laboratory Practices (GLPs), CFR part 58 is a set of guidelines for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA.

Speaker: Joy McElroy | View Anytime | Duration: 90 Minutes | Price: $390.00 | View Details