Sr Engineer Projects
hace 7 meses
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission.
Your role at Baxter:
Responsible for crafting, developing, implementing, and evaluating efficient, cost-effective projects and technologies. In addition to provide technical support and service to responsibilities areas, the incumbent may also perform the following functions: supervising, requisitioning, documenting, validating and trainings.
Your team:
We develop quality products with the patient in mind, so our marketing efforts are also patient centric. That means you can be proud of our work and the value we provide to people every day.
As a large, multinational organization, you could expand your knowledge through collaboration with a variety of individuals, exposure to different facets of our portfolio, and an encouraging leadership team that encourages ongoing development.
What you'll be doing:
Provide a wide range of work to fully support the manufacturing processes and products in Aibonito. Implement, plan, and coordinate inter-departmental activities related to new equipment, equipment and process improvements and product support. Responsible for the diverse range of project activities related to equipment and process design and development, introduction, studies development process, and validations.
Participate in multifunctional projects to give with plant manufacturing strategies.
Use standard and advanced technical principles such as PFMEA, 5 Why’s, Fish Bone, DMAIC, to analyze and resolve process related issues.
Works under minimal supervision to identify manufacturing improvement opportunities and respond to request for assistance.
Implementation and validation of all capital projects (end-to-end) of the facility and manufacturing areas.
Review User Requirements Specifications and Scope of Work documents for bidding purposes.
Write, execute and/or support SAT, FAT, IQ, SQ, OP and PQ.
Generate and coordinate FOC/COB for assigned projects. Ensure on-time closing.
Support Manufacturing Departments in the selection and/or implementation of MIP Projects.
Manage resources to clearly set workload priorities to effectively achieve project and production milestones.
Plan, coordinate, and execute equipment installation and startup. Provide documented evidence of requirements of mentioned activities such as Change Control, EMP, JSA, Work Permits etc.
Plan, coordinate, and execute validation activities. Provide documented evidence of validated submissions, equipment, control systems and manufacturing processes.
Present and defend to FDA (and all other regulatory bodies) validation protocols, results, and documentation.
Clear understanding of company validation approach for equipment/process and computer software systems.
Get along with Divisional and International Facilities/Offices, outside Consultants and Suppliers to provide Aibonito with the best available technical support.
Coordinate Change Controls, equipment, product, or process validations, by acting independently to achieve desired goals.
Perform and assist in the implementation of new product introductions, existing product design modifications, manufacturing improvements giving direct support on change process as change control owner and /or action owner on local or divisional projects.
Strong negotiation skills required, ability to work with minimal direction on multiple projects at the same time.
Promote a zero-harm workplace and assure that required EHS resources are available and that all applicable EHS practices and rules are being followed by supervised employees.
Observe data privacy and confidentiality rules at all times.
What you'll bring
EDUCACIÓN Y/O EXPERIENCIA (EDUCATION AND/OR EXPERIENCE):
Bachelor’s Degree in Engineering or Science Field and 3-5years related experience in manufacturing or project engineer in a closely related industry.
MS engineering and 1-2 years related experience.
IDIOMA (LANGUAGE):
Bilingual (Spanish and English) written and verbal.
DEMANDA FISICA (PHYSICAL DEMANDS):
Light Work : Exerting up to 20 pounds of force occasionally and/or a 10 pounds of force frequently, and/or a negligible amount of force constantly to move objects. Physical demands requirements are more than those for Sedentary Work. Even though the weight lifted may be only a negligible amount, a job should be rated Light Work: (1) when it requires walking or standing to a significant degree; or (2) when it requires sitting most of the time but entails pushing and/or pulling of arm or leg controls; and/or (3) when the job requires working at a production rate pace entailing the constant pushing and/or pulling of materials even though the weight of those materials is negligible.
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