Quality Assurance Training Specialist/ QA Training Coordinator

We're Hiring: Quality Assurance Training Specialist!

We are seeking a detail-oriented Quality Assurance Training Specialist to develop and deliver comprehensive training programs that ensure our team maintains the highest quality standards. The ideal candidate will have expertise in quality assurance methodologies, training design, and the ability to translate complex QA processes into engaging learning experiences.

Location: Philadelphia, PA

What You'll Do

• Assist in the development and/or review developed training materials.
• Maintain qualification training requirements in eLMS.
• Administer and assign training in eLMS
• Provide eDMS/eLMS End User Support
• Collaborate with Quality Assurance Document Control on training requirements impacting Document Change Control process.
• Supports training implementation in response to quality events
• Deliver training sessions, when applicable, and ensure training documentation is maintained. Ensure training schedules meet company production and quality targets.
• Assists functional groups with the creation or improvement of training content
• Continuously seek and support new approaches, practices and processes to improve the efficiency and efficacy of training.
• Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP).
• Supports documentation needs, which may include drafting and approval of SOPs, Work Instructions, Deviations, CAPAs, etc. Perform basic revisions as needed to accurately reflect current procedures.
• Attends meetings and escalates issues/concerns at that forum to Area Management for further investigation.
• May work on assignments that are moderately complex in nature, where judgment is required to resolve operational issues without negatively impacting manufacturing efforts.
• Ability to work in a team environment and independently as required.
• Contribute to department operations improvement in areas such as SOP revisions and department inspections.
• Other duties as assigned.
  
  

What We're Looking For

• Bachelor’s degree in Life Sciences discipline preferred, not required.
• Minimum of two (2) years of experience training and documentation in pharmaceutical or biopharmaceutical GMP based facility.
• Familiar with document change management and FDA quality systems
• Familiar with an eDMS system (MasterControl is a plus)
• Must possess a high level of attention to detail and proficient in Word and Excel
• Strong computer, organizational, and compliance skills
• Ability to work effectively on multiple projects simultaneously with minimum supervision.
• Strong interpersonal and communication skills
  
  

Ready to make an impact? Apply now and let's grow together!