Description Reporting to the Director of Compliance Training with oversight from the Director of Quality Management Systems, the Training Coordinator/Document Management Specialist is an integral member of the Quality and Compliance team. The Training Coordinator/Document Management Specialist is responsible for supporting the day-to-day activities of both the Learning and Document Management systems. This person will also act as an SME for ensuring employees have accurate training to meet compliance requirements and maintaining accuracy of training records. Additionally, this role will be responsible for supporting broader document management within the organization. Responsibilities will include: Training Responsibilities: • Provide management/support of the Learning Management System (LMS) • Facilitate new hire training on the ZenQMS system, as required • Manage the training mailbox • Along with the Director, Compliance Training, gather information from employees and management on previous training to identify knowledge gaps and areas that need additional training • Create and disseminate training communications • Assist with the set-up of company-wide training events • Create and maintain reports on the outcomes of all training • Maintain accuracy of training records for the company within the Learning Management system • Review vendor training to include external and internal SCORM courses • Other related duties, as assigned Document Management Responsibilities: • Support the Document Management System by tracking documents in the review and approval stage • Assist with updating metadata such as categories, document IDs. and effective dates • Manage the document mailbox • Create, prepare, and maintain functional, configuration, and user interface documentation • Create online instructional materials, release notes, user documentation, and basic manuals • Ensure that documentation and corporate records adhere to all applicable legal, clinical, financial, and regulatory requirements • Store, record, recover, archive, scan, and maintain documents in the QMS/LMS • Other related duties, as assigned Additional Skills & Qualifications • 5-7 years of experience managing a Learning Management System (LMS) within pharma/biopharma or other highly regulated industry • 5-7 years of experience working within a Document Management System • Knowledge of instructional design and adult learning principles; experience designing and developing training content • High proficiency in Microsoft PowerPoint, Excel, Word and Visio applications • Understanding of current training trends • High proficiency in navigating and managing Learning Management Systems (LMS) and E-Learning Platforms. • Strong knowledge of SCORM (creating SCORM packages/reviewing/testing courses in sandbox and production environments) • High proficiency in navigating and managing document management systems, managing metadata, and developing/modifying templates • Strong organizational and time management skill; able to handle multiple assignments and/or projects simultaneously. • Strong troubleshooting and problem solving skills • Excellent verbal and written communication skills, including presentation skills. • Strong interpersonal and leadership skills • Ability to work within a team environment • High attention to detail • Experience assessing and analyzing training data. Pay and Benefits The pay range for this position is $30.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Philadelphia,PA. Application Deadline This position is anticipated to close on Mar 12, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.