Technical Services Manager (m/f/d)

Our offerAdragos Pharma Jura is currently seeking an experienced manager to lead the Technical Services department. As a team leader, you will be responsible for engineering, maintenance, and facility management. Your mission will be to ensure the reliability and safety of the cleanroom production environment, processing and laboratory equipment, GMP storage operations, and site infrastructure.As the Technical Services Manager, you will be an integral part of the site management team. Your role will involve supporting the company’s transition and growth to provide our clients with pharmaceutical products for niche markets worldwide.We Offer You:At Adragos Pharma Jura, we offer a competitive salary based on experience and qualifications. Additionally, you will have the opportunity to play a leading role in a dynamic and stimulating work environment, collaborating with different departments to support the company’s continuous growth. At Baccinex, we place great importance on work-life balance and encourage the professional development of our management team through individual development programs.Your profileCommunication and Collaboration Skills: Must be a persuasive communicator, an active listener, and capable of collaborating with other functions, even in challenging situations.Team Management Experience: Proven experience in leading, developing, and managing a team of employees.Structured and Analytical Approach: Dynamism, curiosity, and a structured and analytical approach are essential for problem-solving.Knowledge of Regulated Sectors: Experience in regulated sectors to understand regulatory requirements and quality systems.Technical Training and Field Experience: At least a basic technical training in engineering, complemented by higher education (e.g., HES/ES engineer, federal certificate/diploma) or field experience. Experience in cleanroom production, clean utilities, and/or aseptic filling line equipment is an advantage.cGMP Environment Experience: More than 15 years of relevant direct experience, preferably over 5 years in a pharmaceutical or food production environment compliant with Good Manufacturing Practices (cGMP).Equipment and Infrastructure Knowledge: Practical knowledge of the entire lifecycle of pharmaceutical processing equipment, utilities, and facility infrastructure systems, as well as basic practical knowledge of process controls.Budget Planning: Experience in developing and planning OpEx/CapEx budgets is required.IT Skills: Proficiency in IT tools such as Maintenance Planning and Building Management Systems (BMS), as well as Alarm Monitoring and Control Systems (EMS).Outsourced Work Management: Proven ability to manage outsourced work and services while ensuring the quality and safety of executed tasks.Language Proficiency: Proficiency in both French and English is an asset.Your missionSupervision and Prioritization of Activities: Oversee and prioritize activities to support daily manufacturing processes, adhering to the department’s schedule and objectives.Performance Monitoring and Staff Motivation: Responsible for tracking the department’s Key Performance Indicators (KPIs) and motivating the team.Equipment and Facility Management: Manage equipment design requirements, FAT/SAT installation, and commissioning as part of the product line redesign.Maintenance and Operations Management: Oversee the planning and execution of shutdowns, alarm management, pest control, spare parts management, automation programs, as well as the management and archiving of GMP-related data.Site Infrastructure: Ensure the maintenance, renovation, and cleanliness of facilities.Strategic Planning and Budgeting: Responsible for the site’s strategic plan for investment projects, managing operational and capital budgets.Business Continuity and Contract Management: Ensure business continuity to support manufacturing operations, continuous utility services, and facility usage. Maintain a network of external contractors and service providers, managing contracts.Compliance and Safety: Ensure overall compliance with site policies and procedures, GMP, ESS, and other relevant regulations and directives. Foster a compliance-focused mindset within the organization, holding individuals personally accountable for their own compliance and safety.ContactIf you are ready to contribute within a CDMO and participate in the constant evolution of the pharmaceutical industry, we invite you to submit your CV via our online form along with a cover letter highlighting your relevant experience and the reasons why you are interested in this position. At our company, equal opportunities are paramount, and we encourage candidates from all backgrounds to apply.In case of questions, please reach out to #J-18808-Ljbffr