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Roche Holding AG recherche un responsable de production capable de superviser les opérations GMP et le personnel au quotidien, en assurant le respect des pratiques cGMP et des standards de qualité.
Le candidat idéal possède une expérience en biotechnologie ou en pharmacie, des compétences en leadership et une capacité à résoudre rapidement les problèmes techniques et procéduraux. Poste en horaires décalés dans nos installations de Singapour.
Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte.
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
The Opportunity
This position has overall accountability for hands-on, daily supervision of manufacturing operations and personnel while in full compliance with current Good Manufacturing Practices (cGMPs) and Roche’s corporate principles, quality policies and standards.
Key Responsibilities:
Work effectively within the management team to execute goals, objectives and tasks to achieve desired results.
Responsible for the hands-on, daily supervision of GMP manufacturing operations and personnel within the manufacturing site(s).
Responsible for all day to day operations in the GMP manufacturing suite, as assigned. Specific responsibilities will include:
Hands on supervision and support of manufacturing staff.
Create and revise batch records, standard operating procedures (SOPs) and other supporting documents in compliance with cGMP guidelines.
Timely review of completed manufacturing documentation (batch records, forms and logbooks etc.).
Schedule manufacturing staff to ensure manufacturing timelines are met.
Review production schedule and priorities to establish shift assignments.
Ensure required levels of safety, quality and productivity are met.
Provide assistance in problem solving of manufacturing process issues.
Timely reporting, investigation and resolution of manufacturing deviations.
Provide expertise in cross-functional coordination and issue resolution.
Coordinate equipment maintenance activities.
Make recommendations to management on matters relating to human resources, budget and department operations.
Has contact with internal personnel and outside representatives concerning scheduling of specific projects or contracts.
May be involved in conducting briefings and participating in meetings for internal and external representatives concerning immediate area of responsibility.
Lead cross-functional improvement initiatives and closure of audit commitments.
Participate in all aspects of personnel management (interviewing, training, coaching and developing).
Preferred
Safety, Health & Environment:
Comply with all RSTO’s Safety, Health & Environmental (SHE) requirements, never put oneself and others at safety & health risks, and report any workplace accidents, near misses and hazards as soon as practicable.
Observe all RSTO’s site security measures at all times, and report any suspicious characters/objects & damaged security mechanisms to Site Security immediately.
Lean Production System:
Embody PT Lean Production System (LPS), while fostering and advocating a continuous improvement mindset and culture throughout the organization, by encouraging experimentation and learning.
Who You Are
Degree in Life Sciences or Engineering discipline (or equivalent)
Minimum 5 years of related working experience or equivalent holders with combination of education and related work experience
3 or more years in managing teams in biotechnology or pharmaceutical operating environment is preferred
Knowledge of GMP systems and biologics production process
Good interpersonal and communication skills
Excellent leadership skills in team-based environment
Demonstrated advanced troubleshooting skills for resolution of process and equipment problems
Prepared to work on 12-hour shift schedule
Must be able to carry heavy loads of up to 25kg
Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial.
Construisons ensemble un avenir plus sain.
Roche est un employeur offrant l'équité en matière d'emploi.