Jobs at Bimeda

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.

Manage a sales territory and designated key accounts across veterinary and agricultural trade sectors. Build customer and key opinion leader relationships, achieve sales and financial targets, negotiate commercial terms, execute account plans and seasonal campaigns, analyze CRM and market data, support marketing initiatives, deliver product training, report pharmacovigilance issues, identify new business, and maintain customer ordering and debt management.

Oversee and improve multi-site Environmental, Health, and Safety programs in an industrial setting. Develop policies, training, audits, inspections, risk assessments, and regulatory compliance initiatives covering OSHA, EPA, environmental permits, hazardous materials, waste, air quality, and water pollution prevention. Lead incident investigations, root cause analysis, corrective actions, sustainability efforts, and safety culture initiatives while reporting EHS metrics to leadership. The hybrid role requires three onsite days weekly, occasional U.S. travel, and periodic night or weekend support.

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.

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 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.

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.