Search the 53 jobs at Project Farma

As a Consultant in Project Controls Engineering, you will collaborate with clients and teams to ensure successful biomanufacturing projects by producing schedules, budgets, and project reports, while also analyzing project data and maintaining internal tools.

As a CQV Engineering Consultant, you will lead and execute engineering life cycle projects, ensuring high-quality deliverables. Responsibilities include developing technical documentation, mentoring team members, and supporting business development through client engagement and networking.

As a Project Controls Engineer, you will collaborate with various stakeholders to produce project controls deliverables, analyze project data, and enhance decision-making processes within biomanufacturing projects, while embodying a patient focus and team spirit.

The Project Engineer collaborates with various partners and departments to support biomanufacturing projects, focusing on technical delivery, maintaining timelines, and enhancing relationships. Responsibilities include authoring technical documents, executing validation protocols, and developing pharmaceutical programs.

The Project Engineer will create alignment across departments, provide troubleshooting assistance during engineering processes, and produce technical documentation. This role also involves executing validation protocols and addressing project roadblocks, aligned with the company's patient-focused mission.

As a CQV Engineering Consultant, you will lead client projects in the life science sector, coordinating with multiple departments to ensure timely and high-quality project outcomes. You will develop essential technical documentation and mentor internal team members while supporting business development through maintaining professional networks.

As a CQV Engineering Consultant, you will coordinate client projects, providing support in engineering life cycles, ensuring quality deliverables, mentoring team members, and assisting in business development initiatives. You'll develop technical documentation and maintain professional networks to address client needs.

As a CQV Engineering Consultant, you will lead client project initiatives in the life sciences sector, coordinating with cross-functional teams and providing hands-on support. Your responsibilities will include developing technical documentation, mentoring team members, and supporting business development efforts.

As a CQV Engineering Consultant, you'll lead cross-functional projects, develop technical documentation, mentor team members, and drive business development initiatives. Your role involves navigating the engineering lifecycle of advanced manufacturing processes and ensuring timely delivery of high-quality work.

As a Manager, CQV Engineering, you will lead high-performing teams in executing projects, representing Manufacturing Solutions, managing client accounts, and ensuring high-quality project delivery. You will provide technical direction and support for team development while driving strategies for market success and collaboration with clients.

The Senior Project Engineer will facilitate cross-functional alignment, provide hands-on support in engineering life cycles, author technical documentation, execute validation protocols, identify roadblocks, and foster internal and external client relationships. The role requires significant travel and a commitment to the company's patient-focused mission.

The CQV Engineering Consultant will lead engineering project initiatives in the life sciences industry, coordinating client departments, developing technical documentation, mentoring team members, and supporting business development initiatives while ensuring timely high-quality deliverables.

The Senior Project Engineer will coordinate with various departments to support biomanufacturing projects, delivering high-quality work, authoring technical documents, and executing validation protocols, while building relationships with partners and enhancing patient-focused culture.

The Manager will lead and mentor a team at Project Farma, focusing on operational excellence and business development in advanced therapy projects. Responsibilities include providing technical direction in engineering and project management, enhancing team performance, engaging in client relations, and overseeing resource allocation.

The Project Engineer collaborates with partners and contractors in biomanufacturing projects, focusing on technical delivery and project support. Responsibilities include authoring technical documents, executing validation protocols, and maintaining project timelines while fostering relationships and patient-focused culture.

The Project Engineer will collaborate with various teams to support biomanufacturing projects ensuring high quality work and developing industry knowledge. Responsibilities include coordinating with departments, authoring technical documents, executing validation protocols, and maintaining project timelines while fostering relationships with partners.

As a VP of Strategy, you will lead client relationship development, drive growth initiatives, and mentor team members. You’ll provide strategic direction for project delivery, handle client escalations, and manage project schedules. Your expertise in technical operations will ensure successful client setups and enhance team capabilities.

As a Project Controls Engineer, you will support biomanufacturing projects by managing budgets, schedules, risks, and project performance reports. You will analyze project data to facilitate decision-making, and you will maintain strong relationships with clients and team members.

The Project Engineer will create alignment with client departments, support troubleshooting for engineering life cycles, author technical documents, execute validation protocols, and contribute to a patient-focused mission. Key responsibilities also include building relationships with clients and identifying solutions to project challenges.

The Project Engineer will align with various client departments, provide troubleshooting support, create technical documentation, execute validation protocols using GxP practices, and identify solutions to project roadblocks while fostering internal and external relationships.