Contract Manufacturing Developer

Description

Job Summary: We are seeking a Contract Manufacturing Developer with experience in the veterinary pharmaceutical industry to expand our international presence. Key Highlights: 1. Opportunity for professional growth within a leading company in the sector. 2. Key role in international expansion and consolidation in animal health. 3. Challenging work combining technical and commercial skills. A veterinary pharmaceutical company with 34 years of market experience is looking to add a Contract Manufacturing Developer to its team to further consolidate its position in the animal health industry both in Colombia and across the other 10 countries where it operates. **Required Profile:** **Education**: Degree in Pharmaceutical Chemistry or related fields. **Knowledge**: * Commercial skills with a technical focus * Regulatory affairs (ICA / INVIMA) * Product formulation and development * Management of technical documentation (dossiers, protocols, reports, dossiers) * Technical evaluation of manufacturing capabilities for contract manufacturing * Handling of commercial and technical performance indicators **Experience**: * Minimum 5 years of experience in the veterinary pharmaceutical, pesticide, or related industries, in areas such as development, regulatory affairs, quality, or technical business. **Responsibilities**: * Identify, target, and acquire potential contract manufacturing clients for various product types based on plant capabilities. * Conduct technical and commercial visits to present manufacturing capabilities. * Prepare commercial proposals and preliminary contract manufacturing cost estimates. * Manage the full commercial cycle, including contract closure, commencement of manufacturing, and order replenishments. * Coordinate and prepare dossiers for regulatory procedures before INVIMA: registrations, renewals, modifications, extensions, or certifications. * Support preparation of dossiers for regulatory procedures before ICA or equivalent regulatory bodies. * Prepare and submit technical documents, dossiers, and certifications required by authorities (where applicable). * Respond to INVIMA requests or official notices. * Accompany customer, INVIMA, ICA, or other regulatory authority audits. * Prepare documentary evidence, records, and protocols required for audits. * Manage post-audit action plans in coordination with Technical Management, Quality, and Production. If you are interested in joining one of the most well-positioned companies in the veterinary pharmaceutical industry—with exponential growth—and want to learn and develop professionally, this is your opportunity. Apply now. Position Type: Full-time Education: * Completed Bachelor's degree (Preferred)