Quick Summary
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
The Manufacturing Trainer supports Avid’s GMP manufacturing operations across Upstream, Downstream, and Formulation by delivering high quality training, executing hands on qualification, and reinforcing documentation and compliance standards.
Experience in Upstream, Downstream, or Formulation operations. Understanding of adult learning principles. Position Type/Expected Hours of Work: This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00 a.m.
- Deliver classroom, virtual, and on‑the‑floor training for Upstream, Downstream, and Formulation operations.
- Facilitate OJT qualification sessions and ensure proper documentation.
- Support new hire onboarding and early competency development.
- Conduct refresher and capability‑based training as needed.
- Assist in developing SOP‑based modules, technical process training, e-learning content, and qualification materials.
- Create and update training checklists, assessments, and job aids.
- Ensure training materials reflect current processes and regulatory expectations.
- Maintain accurate training records.
- Support curriculum updates, retraining triggers, and assignment accuracy.
- Reinforce GDP and ALCOA+ principles.
- Conduct and document Training Impact Assessments.
- Provide routine floor support to ensure correct technique and documentation.
- Coach employees on new processes, proper execution, and safety.
- Identify training gaps and escalate to L&D Manager.
- Track training status, qualification progress, and compliance KPIs.
- Support analysis of RFT documentation performance and correction trends.
- Recommend improvements to training methods and onboarding workflows.
- Partner with SMEs to maintain accurate technical content.
- Collaborate with QA to ensure compliance alignment.
- Associate’s or Bachelor’s degree in a scientific or technical discipline.
- 1–3 years of GMP manufacturing or technical training experience.
- Strong understanding of GMP, GDP, and ALCOA+ principles.
- Experience delivering training or coaching.
- Strong attention to detail and documentation accuracy.
- Clear communication and coaching skills.
- Ability to work in a fast‑paced GMP environment.
- Collaborative and cross‑functional mindset.
- Experience in Upstream, Downstream, or Formulation operations.
- Understanding of adult learning principles.
- You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
- Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
- You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
- You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Location & Eligibility
Listing Details
- Posted
- April 10, 2026
- First seen
- May 6, 2026
- Last seen
- May 8, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 42%
- Scored at
- May 6, 2026
Signal breakdown
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