Project Manager, Small Molecule Drug Discovery

ClinicalPro is seeking a Project Manager, Small Molecule Drug Discovery for a leading organisation specialising in Small Molecule research located in the USA.

This individual will be responsible for acting as an expert in small molecule drug discovery and offering guidance on lead series’ physiochemical characteristics, potency, and selectivity optimisation.

Must be eligible to work in the USA.

Responsibilities

• Ability to deliver massive, complicated, small molecule projects—or major chunks of projects—right the first time.
• Leadership skills in leading cross-functional teams.
• Capable of managing, delegating, and assigning tasks to internal team members.
• Knowledge of the specification, selection, testing, commissioning, troubleshooting, and qualification phases of the equipment life cycle.
• Excellent interpersonal and communication abilities.
• Good teamwork and collaboration.
• The capacity to weigh several choices and decide on a leading strategy.
• Working within the project’s and department’s budgetary and time restrictions.
• Keeping up with industry changes and best practices; participating in professional or technical organisations.
• Communicates with other technical departments to make sure that new and related products successfully transfer technology.
• Expertise in the support of projects involving biologics, vaccines, or sterile products.
• For the delivery of assets and project realisation, prior knowledge with engineering design, equipment operation, vendor interaction, risk assessment, process safety, and industry advice is crucial.
• Must be familiar with the requirements for unit operations, Hazard Analysis, and the operation, commissioning, and certification of equipment.
• Knowledge of the specification, selection, testing, commissioning, troubleshooting, and qualification phases of the equipment life cycle.
• Skills in analysis and problem-solving.
• Working with clients, vendors, and design engineers to complete projects for customers in the biotech and pharmaceutical industries requires experience with process facility design and construction in clean rooms, labs, and the life sciences.
• Offer your knowledge and experience for projects including process equipment, utilities, and facility design.

Skills and Requirements

• Experience working on API, Oral Solid Dosage, Biologics, Vaccine, or Sterile Projects in a GMP.
• Bachelor’s or master’s degree in engineering.
• For the delivery of assets and project realisation, it is crucial to have 15+ years of project management/process engineering expertise that includes engineering design, equipment operation, vendor interaction, risk assessment, process safety, and industry advice.
• Senior-level experience designing, commissioning, and starting up biopharmaceutical facilities.
• Collaborating with customers, suppliers, and other design engineers to complete projects for biotech and pharmaceutical clients.
• Specifying unit activities, doing a Hazard Analysis, and operating, commissioning, and qualifying equipment.
• Excellent interpersonal and communication abilities.
• Good teamwork and collaboration.
• The capacity to communicate with various stakeholders in support of capital project delivery.
• It is necessary to have prior biotech/pharma industry experience.
• Strong leadership and project management abilities are preferred (ability to interact with a team and manage them under time constraints).
• Very driven, organised, and takes professional initiative.
• Working in a tough, quick-paced atmosphere.

Apply

If you’re interested in this position, apply now to send us an updated copy of your CV, or give us a call right away.

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