Teams at Bimeda

The Technical Services Specialist manages pharmaceutical manufacturing technical projects, including line transfers, batch scale changes, new product introductions, CMO transfers, investigations, process improvements, and regulatory documentation. The role analyzes manufacturing data, updates SOPs and batch records, leads cross-functional teams, supports equipment qualification, resolves environmental excursions, and advances electronic quality and manufacturing systems across sites.

Leads pharmaceutical quality assurance systems, compliance, audits, inspections, CAPAs, investigations, complaints, product release, and regulatory readiness. Manages QA Associates, customer quality requests, quality metrics, continuous improvement, budgets, and cross-functional resolution of quality events. Requires regulated pharmaceutical QA/QC experience, leadership capability, scientific education, and strong knowledge of cGMP, quality systems, regulatory affairs, and stability protocols. The role is based in-office in a warehouse and production environment with occasional weekend or after-hours work.

Leads environmental, health, and safety programs for a regulated manufacturing site and North American network. Responsibilities include regulatory compliance, audits, inspections, incident investigations, risk assessments, training, emergency preparedness, corrective actions, environmental initiatives, and continuous improvement. The role uses analytics, dashboards, digital workflows, and EHS software to improve reporting and accountability while partnering with operations, quality, engineering, maintenance, HR, leadership, regulators, and auditors.