Pharmaron
Position:
Document Control/Training Specialist
Location:
Germantown, MD (ON-SITE)
Salary:
$60,000 to $75,000 Are you ready to embark on an exhilarating journey with a team that's passionate about making a difference? Pharmaron is thrilled to invite you to join us as our newest
Document Control/Training Specialist ! If you're craving a role that offers challenges, growth, and meaningful impact, then this is the opportunity you've been waiting for. Job Overview:
Document Control/Training Specialist within our Quality department is a pivotal role which requires a dynamic professional with strong hands on experience in document workflows through respective document life cycle and maintaining employee training records utilizing TrackWise Digital. You'll have the opportunity to Collaborate with cross-functional departments to ensure timely implementation of changes to control process and provide GLP training to Pharmaron employees as needed.
Additional tasks:
Maintain a document management system and learning management system compliant with regulatory, quality, and Pharmaron requirements
Ensure completion of improvement projects to enable process efficiencies in document security/archival
Perform day-to-day document control activities in the TrackWise Digital Document Management System (DMS), including formatting, training assignments, and releasing controlled documents
Assists with the creation and maintenance of Documents and On-the-Job training (OJT) items, employee training plans, and administration of quizzes in the TrackWise Digital Training Management System (TMS)
Provide troubleshooting assistance for users regarding the DMS and TMS
Provide training and troubleshooting assistance for users regarding Electronic Document Management System (EDMS).
Provide new hire compliance training for GxP, Data Integrity and TrackWise Digital Workflow navigation.
Conduct quarterly laboratory walkthroughs and support client and regulatory audits.
What We're Looking For:
Bachelor's Degree in Biology, Chemistry or related field is required
2+ years of QA/QC experience related industry experience
Knowledge of FDA regulations, 21 CFR Part 11, 58 and ICH Quality Guidelines
Knowledge of Good Laboratory Practices (GLP) and Good Clinical Practice (GCP)
Prior experience working with electronic quality management systems, such as TrackWise Digital
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture:
You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators.
Comprehensive benefit package : As part of our commitment to your well-being, we offer a comprehensive benefits package:
Insurance including Medical, Dental & Vision with significant employer contributions
Employer-funded Health Reimbursement Account
Healthcare & Dependent Care Flexible Spending Accounts
100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance
401k plan with generous employer match
Access to an Employee Assistance Program
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! #LI-JB1
Document Control/Training Specialist
Location:
Germantown, MD (ON-SITE)
Salary:
$60,000 to $75,000 Are you ready to embark on an exhilarating journey with a team that's passionate about making a difference? Pharmaron is thrilled to invite you to join us as our newest
Document Control/Training Specialist ! If you're craving a role that offers challenges, growth, and meaningful impact, then this is the opportunity you've been waiting for. Job Overview:
Document Control/Training Specialist within our Quality department is a pivotal role which requires a dynamic professional with strong hands on experience in document workflows through respective document life cycle and maintaining employee training records utilizing TrackWise Digital. You'll have the opportunity to Collaborate with cross-functional departments to ensure timely implementation of changes to control process and provide GLP training to Pharmaron employees as needed.
Additional tasks:
Maintain a document management system and learning management system compliant with regulatory, quality, and Pharmaron requirements
Ensure completion of improvement projects to enable process efficiencies in document security/archival
Perform day-to-day document control activities in the TrackWise Digital Document Management System (DMS), including formatting, training assignments, and releasing controlled documents
Assists with the creation and maintenance of Documents and On-the-Job training (OJT) items, employee training plans, and administration of quizzes in the TrackWise Digital Training Management System (TMS)
Provide troubleshooting assistance for users regarding the DMS and TMS
Provide training and troubleshooting assistance for users regarding Electronic Document Management System (EDMS).
Provide new hire compliance training for GxP, Data Integrity and TrackWise Digital Workflow navigation.
Conduct quarterly laboratory walkthroughs and support client and regulatory audits.
What We're Looking For:
Bachelor's Degree in Biology, Chemistry or related field is required
2+ years of QA/QC experience related industry experience
Knowledge of FDA regulations, 21 CFR Part 11, 58 and ICH Quality Guidelines
Knowledge of Good Laboratory Practices (GLP) and Good Clinical Practice (GCP)
Prior experience working with electronic quality management systems, such as TrackWise Digital
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture:
You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators.
Comprehensive benefit package : As part of our commitment to your well-being, we offer a comprehensive benefits package:
Insurance including Medical, Dental & Vision with significant employer contributions
Employer-funded Health Reimbursement Account
Healthcare & Dependent Care Flexible Spending Accounts
100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance
401k plan with generous employer match
Access to an Employee Assistance Program
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! #LI-JB1