Training Specialist

Integrated Resources Inc.; Wayne (PA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading staffing firm is seeking a QS Training Specialist for a three-month project in Wayne, PA. In this role, you will develop training materials and collaborate with subject matter experts to enhance IT functions through training programs. Suitable candidates should have experience in document management and a background in the biotech or pharmaceutical industry.

Qualifications

• 2+ years of experience in document management and IT training.
• Experience in a GMP role within biotech/pharmaceutical industry preferred.

Responsibilities

• Support the development of procedural documents and training materials.
• Implement on-the-job training and e-learning for IT functions.
• Process procedural documents to meet timelines.

Skills

Communication

Collaboration

Self-motivation

Adaptability

Tools

Microsoft Office

MasterControl

Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.

Job Description

Title: QS Training Specialist

Location: Wayne, PA 19087

Duration: 3 months+

Responsibilities

• This role will primarily support the development of procedural documents and the establishment of training.
• Partner with functional area subject matter experts to implement on-the-job training (OJT), E-Learning (CBT), and Instructor-Led Training (ILT) materials for use in IT functions within specified timelines and according to procedures and standards.
• Partner with functional area subject matter experts to process procedural documents through effective date setting for use in IT functions within specified timelines and according to procedures and standards.

Qualifications

Experience & Knowledge (Essential)

• Demonstrate high-level professional and business judgment when communicating with cross-functional teams and others at all organizational levels.
• Proficient with MasterControl and Microsoft Office applications, including Word, Excel, and PowerPoint.
• Collaborative, customer-focused, and service-oriented.
• Effective verbal and written communication skills across all organizational levels.
• Ability to prioritize and multitask effectively.
• Capable of working under challenging deadlines and accountable for completing tasks within specified timeframes.
• Self-motivated, assertive, energetic team player.
• Adaptable to a diverse, dynamic, and team-oriented environment (Preferred).

Skills/Behaviors

• 2+ years of experience in document management.
• 2+ years of experience in a GMP role within the biotech/pharmaceutical industry (Preferred).