Teams at Syner-G

Support reliability, maintenance, and asset management for GMP pharmaceutical/biotech facilities. Improve PM programs, perform criticality assessments and RCAs, analyze failure data, use CMMS, recommend life-extension and spare-parts strategies, and collaborate cross-functionally to reduce downtime and improve asset availability.

Lead regulatory review and risk assessment of US and Canadian promotional materials across channels to ensure compliance with FDA/OPDP, Health Canada, and PAAB. Advise cross-functional teams on claim substantiation, evidence use, launch and lifecycle promotional strategy, support submissions/preclearance, deliver training, and monitor regulatory developments. Role involves stakeholder collaboration and may require extensive client travel.

Provide senior technical leadership for design, optimization, automation, and scale-up of bioprocess and manufacturing systems. Lead process strategy, commissioning, qualification, modeling, automation integration, multi-site transfers, vendor management, and mentor engineering teams to deliver robust, scalable processes across development, clinical, and commercial operations.