Jobs at Bimeda

Manage the Leinster/East Coast territory and designated key accounts for veterinary pharmaceuticals and animal health products. Build relationships with veterinary and agricultural trade customers, achieve sales and financial targets, execute account plans, negotiate pricing, monitor CRM activity, support campaigns and product launches, deliver customer training, identify new business, and provide market and competitor insights. Regular travel across the territory is required.

Oversee and improve multi-site Environmental, Health, and Safety programs in an industrial setting. Ensure OSHA, EPA, and related regulatory compliance; develop policies and training; lead inspections, audits, incident investigations, root cause analyses, and corrective actions. Manage environmental compliance, risk assessments, sustainability initiatives, and safety metrics while advising leadership and supporting operational improvements across equipment, plant, and process changes.

Maintains site quality management and documentation systems, including document control, product release records, retains, SOPs, specifications, and artwork files. Performs incoming inspections, batch record reviews, packaging approvals, inventory release, QC testing, and prepares Certificates of Conformity and Analysis. Supports GMP-regulated pharmaceutical, food, and cosmetics manufacturing while ensuring accurate records, compliance, and process quality.

Leads pharmaceutical solid-dose manufacturing operations for water-soluble powders and tablets. Oversees production, maintenance, staffing, scheduling, budgets, compliance, quality, safety, delivery, and cost targets. Provides technical expertise in blending, milling, compression, coating, filling, and packaging; manages investigations, validations, equipment upgrades, and regulatory interfaces. Develops employees, drives continuous improvement, analyzes capacity and KPIs, and removes production constraints while ensuring FDA cGMP and other regulatory requirements are met.

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.

The QA Associate manages pharmaceutical GMP quality activities, including batch record review, product release, change control, APRs, deviations, CAPAs, complaints, OOS investigations, audits, and inspection readiness. The role supports implementation of e-QMS, LIMS, and electronic batch records; uses quality metrics and trend analysis; improves SOPs and processes; trains manufacturing personnel; and collaborates with Manufacturing, QC, Regulatory, and customer-facing teams.

Lead veterinary vaccine R&D programs from concept through regulatory filing. Design and oversee target-animal efficacy, safety, and immunogenicity studies; author USDA or equivalent regulatory submissions; develop and transfer immunoassays; manage small scientific teams and CRO relationships; mentor scientists; present program and regulatory strategy to senior leadership.

Support production and QC of bacterin and viral aquaculture vaccines: grow cultures, maintain batch records, perform in vivo/in vitro testing, analyze data, investigate deviations, author SOPs, maintain GxP documentation, operate and troubleshoot lab equipment, and liaise with other sites.

Supports vaccine manufacturing by preparing, labeling, packaging, and cleaning production areas and equipment. Maintains accurate temperature and process records, reports equipment malfunctions, follows GMP, SOPs, and safety procedures, assists with warehouse tasks, monitors frequently used inventory, and helps maintain organized production areas. This is a part-time role requiring 15–20 hours weekly and Tuesday and Thursday morning availability.