Jobs at Bimeda

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.

The QA Associate supports pharmaceutical manufacturing quality systems and continuous improvement. Responsibilities include deviation, complaint, and OOS investigations; batch record review and product release; incoming packaging inspections; internal audits; SOP development; GMP compliance; audit support; laboratory testing coordination; and corrective action follow-up. The role also trains manufacturing personnel, monitors quality metrics, resolves compliance issues, and collaborates with production, vendors, and cross-functional teams.

Lead QA systems and a team to ensure product quality and regulatory readiness. Manage audits, investigations, CAPAs, customer complaints, KPIs, and cross-functional corrective actions to maintain cGMP/QSR/GDP compliance and support product release.

Manage post-approval regulatory maintenance for NADA/ANADA products, compile and submit annual reports, CMC submissions, labeling supplements, and agency correspondence. Maintain regulatory records, ensure cGMP and regulatory compliance, perform regulatory reviews, determine reporting categories, coordinate state registrations and GMP documentation, and prepare electronic submissions to FDA-CVM.

Territory-based sales role selling Bimeda equine pharmaceutical and nutritional products to veterinarians, large equine operations and distributors. Develop and maintain high-level relationships, execute sales plans, use CRM and sales reports, attend events, provide market intelligence, and meet territory sales and budget targets while collaborating with commercial, technical, and marketing 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.

Six-month, full-time QA intern responsible for scanning, uploading, filing, reviewing, and purging documents in a document management system (Zen). Maintain organized physical and digital filing, perform document checks for completeness and compliance, and support office teams with accurate recordkeeping.

Lead global ownership of SAP S/4HANA, QAD, and Salesforce platforms; govern implementations and partners; build platform roadmap; ensure integration, release governance, and stakeholder engagement across 30+ entities.

Lead and improve EHS programs across multiple sites, ensuring OSHA/EPA compliance, conducting inspections, audits, incident investigations, risk assessments, training, and reporting. Drive environmental compliance, collaborate with operations for safety culture, support plant changes, and report metrics to senior leadership.

Lead and execute deviation investigations for aseptic pharmaceutical manufacturing, determine root causes, write corrective/preventive actions, support CAPA implementation, deliver training, and ensure cGMP and regulatory compliance with FDA and Health Canada standards.

Lead the French commercial organisation, set country commercial strategy, grow revenue and margin, manage key account and territory teams, negotiate contracts and rebates, ensure regulatory compliance as the Responsible Person, and collaborate cross-functionally to execute product launches and market opportunities.

Lead Bimeda's commercial entry and growth in Spain and Portugal by building the Iberian commercial strategy and team, driving revenue, margin and market share, managing key accounts and contracts, ensuring regulatory compliance, and collaborating with cross-functional teams to execute launches and commercial plans across livestock and equine portfolios.

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.