Technical Project Manager – Validation Services

🔥 0 minutes ago

🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🤓 Technical Project Manager

👻 Ghost score 11%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

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• No salary listed.

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Sartorius

WebsiteLinkedInAll Job Openings

10,000+ employees

🏭 Manufacturing

💼 Consulting

📦 Logistics

Manufacturing • Consulting • Logistics

Sartorius is a leading international partner of life sciences research and biopharmaceutical manufacturing. The company focuses on simplifying progress from drug discovery to manufacturing, thereby improving access to better medicine. Sartorius provides innovative laboratory instruments and consumables through its Lab Products & Services division for research and quality control in pharmaceutical and biopharmaceutical companies, as well as academic research institutes. Its Bioprocess Solutions division offers a broad product portfolio centered on single-use solutions, aiding customers in the safe and efficient manufacturing of biotech medications, vaccines, and cell and gene therapies. Headquartered in Göttingen, Germany, Sartorius operates globally with around 60 production and sales sites and employs approximately 14,600 people.

📋 Description

• Lead validation projects from customer requirement gathering through execution • Translate customer needs into test plans • Coordinate with validation laboratories • Approve quotes and supervise project completion • Connect customers, validation laboratories, and sales for transparent communication and coordinated execution • Provide technical consultancy and conduct risk assessments using validated scientific methods and risk-based approaches • Generate leads, manage opportunities, and win deals with sales • Present validation capabilities at conferences, events, and customer meetings • Enhance market visibility, position Sartorius as a thought leader, and generate qualified leads

🎯 Requirements

• Bachelor’s degree in Biotechnology, Microbiology, Chemistry, or Biological Sciences • 3+ years of experience in single-use bioprocess validation projects or related technical project management • Strong understanding of drug manufacturing processes and regulatory compliance, including GMP concepts • Keen focus on data integrity and documentation standards compliance • Customer service-oriented mindset with a proactive and target-driven work style • Strong negotiation and solution-selling skills • Ability to influence internal and external cross-functional stakeholders • Excellent communication skills, with fluency in English and Spanish • Team-oriented and collaborative problem solving • Willingness to travel up to 25%

🏖️ Benefits

• Remote work arrangement • Opportunity to work with cross-functional experts • Career advancement in a dynamic global environment

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