Jobs at Hovione

Performs and coordinates pharmaceutical quality control activities, including analytical testing, method development, validation, transfer, investigations, documentation, and data review. Ensures compliance with GMP, GLP, regulatory requirements, and client specifications. Uses HPLC, GC, laboratory information systems, and analytical software; supports equipment qualification, audits, CAPAs, training, continuous improvement, and cross-functional collaboration.

Plans and designs cGMP-compliant manufacturing processes for pharmaceutical intermediates and finished products. Prepares and reviews GMP documentation, supports risk assessments, reports operational abnormalities, and leads non-complex projects with guidance. The role also coordinates with internal and customer teams, monitors process trends and KPIs, and trains manufacturing personnel on process-related tasks while following HSE and company procedures.

Designs, deploys, and maintains global enterprise and OT network infrastructure across LAN, WAN, WLAN, SD-WAN, VPN, firewall, and wireless environments. Responsibilities include monitoring performance, troubleshooting complex incidents, implementing network security controls, supporting infrastructure projects, maintaining documentation, and securing connectivity for SCADA, PLC, and MES systems. The role also collaborates with cybersecurity, automation, engineering, and manufacturing teams while ensuring compliance with GxP, audit, and internal security requirements.

Build and maintain data architecture, data lakes, data products, analytics, reporting, and machine learning solutions. Partner with stakeholders to identify use cases, engineer and analyze structured and unstructured data, implement monitoring and lifecycle management, and communicate insights through visualizations. Ensure data quality, governance, compliance, and reliable delivery using cloud technologies, especially AWS, alongside SQL, Python, and business intelligence tools.

Designs and leads complex engineering projects in pharmaceutical manufacturing environments. Responsibilities include defining user requirements, developing and approving engineering designs, managing technical procurement, budgets, schedules, risks, and resources, and supervising construction, commissioning, qualification, and integration. Ensures GMP, regulatory, environmental, health, and safety compliance while driving continuous improvement, resolving technical issues, supporting audits, and coordinating multidisciplinary teams and suppliers.

Leads pharmaceutical manufacturing operations for highly potent compounds, ensuring cGMP, HSE, quality, customer, and production-schedule compliance. Manages people, equipment, processes, budgets, metrics, documentation, audits, complaints, validation, and continuous improvement. Coordinates recruitment, training, performance management, and departmental goals while supporting customer requirements and regulatory readiness.

Manage pharmaceutical quality assurance activities in a GMP-regulated CDMO environment. Responsibilities include maintaining the QMS, overseeing deviations, CAPAs, change controls, validation, audits, inspections, documentation, supplier qualification, quality oversight of manufacturing, and continuous improvement. The role collaborates across manufacturing, quality control, regulatory affairs, procurement, and external suppliers while supporting compliance, inspection readiness, and quality training.

Performs pharmaceutical quality control testing for raw materials, intermediates, finished products, and client projects. Responsibilities include analytical method transfer and verification, investigations of deviations and OOS/OOT results, CAPA support, equipment and laboratory systems maintenance, audit support, KPI reporting, and continuous improvement. The role also provides technical guidance and collaborates with cross-functional teams to ensure GMP and regulatory compliance.

Lead Hovione’s global pharmaceutical quality and compliance strategy across sites and functions. Responsibilities include inspection readiness, internal audits, health authority inspections, customer audits, remediation, management reviews, quality risk governance, and continuous improvement. The role requires influencing site and global stakeholders, driving transformation programs, strengthening quality culture, and maintaining regulatory rigor across a matrix organization.

Supports the design, implementation, optimization, and compliant operation of pharmaceutical manufacturing processes. Prepares GMP documentation, conducts risk assessments, investigates deviations, implements CAPAs, supports audits and tech transfers, trains operations personnel, and contributes to process improvement, productivity, and project execution under the guidance of lead process engineers.

Performs and supervises qualitative and quantitative analytical testing for pharmaceutical compounds and products. Leads method development, specification creation, method transfer, investigations, corrective actions, and complex analytical projects under GMP, HSE, and regulatory requirements. Collaborates with clients, supports audits, evaluates materials and suppliers, trains colleagues, resolves technical problems, manages risks, and contributes to scientific innovation and intellectual property development.

Leads process and detailed design engineering for pharmaceutical and chemical facilities, ensuring GMP, EHS, constructability, operability, cost, and schedule compliance. Oversees PFDs, P&IDs, equipment specifications, layouts, utilities, multidisciplinary interfaces, safety reviews, contractor deliverables, design controls, and change management. Manages and develops engineering teams while serving as the project design authority and coordinating with project managers, vendors, OEMs, production, QA, and EHS stakeholders.

Leads pharmaceutical manufacturing process design, implementation, optimization, scale-up, technical transfers, and production support. Ensures cGMP, HSE, quality, cost, schedule, and regulatory compliance while managing resources, documentation, risk assessments, CAPAs, maintenance, audits, and facility improvements. Acts as lead process engineer for complex customer projects, mentors engineers, supports commercial assessments and capital projects, and applies simulation and data-mining methods to improve productivity and manufacturing performance.

Responsible for ensuring cGMP and GDP compliance across pharmaceutical projects and products, managing quality systems, supplier qualification, audits, regulatory interactions, change controls, and product quality issues. The Qualified Person authorizes batch release and certification for APIs, medicinal products, investigational products, and intermediates while supporting continuous improvement and maintaining compliance with applicable legislation and marketing authorizations.

Leads commissioning, qualification, and validation activities for pharmaceutical engineering projects. Develops CQV plans, standards, SOPs, and technical documentation; coordinates design, commissioning, qualification, and GMP compliance activities. Supports audits and regulatory inspections, resolves complex equipment and systems issues, supervises internal and outsourced engineers, and mentors junior staff. Coordinates engineering, validation, manufacturing, QA, and IT teams through project delivery and equipment handover.

Supports Learning and Development processes, including needs analysis, training design, content creation, LMS administration, learner support, feedback analysis, and continuous improvement. Collaborates with subject matter experts and contributes to L&D projects and governance activities while following internal guidelines and safety standards.

Leads assembly, commissioning, qualification, and handover of facilities, utilities, and process equipment for pharmaceutical capital projects. Manages engineering teams, contractors, budgets, schedules, KPIs, and continuous improvement initiatives. Ensures compliance with cGMP, HSE, FDA, EMEA, ICH, ISPE, and ISO requirements. Coordinates cross-functional qualification activities, oversees documentation, manages deviations and CAPAs, and supports audits while developing team capabilities and maintaining operational and financial performance.

Scientist leading technical development of drug-device combination products from concept through manufacturing. Responsibilities include solving technical challenges, selecting methods, developing procedures, analyzing data, preparing documentation, supporting GMP and audit activities, improving processes, generating intellectual property, communicating with clients, and training technical staff. The role requires a scientific or engineering degree and pharmaceutical R&D or operations experience, with expertise in process development, drug products, formulation, unit operations, modeling, or engineering.

Performs quality control laboratory activities for pharmaceutical raw materials, intermediates, and finished products. Organizes sample analysis, maintains GMP and HSE compliance, records laboratory data, calibrates equipment, investigates atypical results and deviations, supports audits, and collaborates with internal teams using QC systems. The role requires pharmaceutical GMP laboratory experience, relevant scientific qualifications, strong communication, English proficiency, and shift availability.

Lead facility master planning, architectural design authority, and end-to-end project execution for regulated industrial facilities. Translate business and operational needs into scalable designs, define GMP-compliant layouts and cleanroom zoning, coordinate multidisciplinary teams, manage budgets, schedules, risks, suppliers, and regulatory requirements, and support continuous improvement, sustainability, and advanced engineering standards. Provide technical guidance to internal and external design teams across global facilities.