Senior Process Engineer / Senior Validation Specialist at Baxter
Jayuya, Puerto Rico, USA -
Full Time


Start Date

Immediate

Expiry Date

21 Nov, 25

Salary

0.0

Posted On

21 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Professional Development

Industry

Electrical/Electronic Manufacturing

Description

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.

Responsibilities

WHAT YOU’LL BE DOING

Performs, coordinates, and exercises functional authority for planning, organization, control, integration, and completion of engineering maintenance and process upgrade tasks within area of assigned responsibility. Use project management tools to achieve cost reduction results per the strategic plan on every budget process. Coordinates Plant schedule and resources within the assign manufacturing area.

  • Coordinates activities concerned with technical developments, scheduling, and resolving engineering design and test problems.
  • Directs integration of technical activities and products.
  • Evaluates and approves design changes, specifications, and drawing releases.
  • Controls expenditures within limitations of project budget.
  • Prepares interim and completion project reports.
  • Active participation on budget cycle updating, cost impact and QLP process.
  • Assists, trouble shoots, give technical support to all assigned equipment and personnel.
  • Develops, implements systems or projects, procedures and policies to assure the compliance with cGMP’s, Safety and FDA regulations.
  • Creates, reviews and implements changes to specifications and SOP’s.
  • Audits all areas under responsibility assuring the compliance, cGDP’s, specifications, SOP’s, and procedures.
  • Supports and assists in the trouble shoot of projects and equipment as required. Also assists validations process.
  • Completes all documentation and reports on a timely basis as required (daily, weekly, monthly and annually).
  • Keep and develop strong working team, manufacturing maintenance environment.
  • Should be able to work at any shift when its required. (eg. shutdowns, extraordinary, holidays, events).
  • Good and strong supervisions skills.
  • Able to work with many projects and handle multiple tasks at the same time.
  • Request and order all materials required on a timely basis to ensure an efficient performance of the department.
  • Must be able to communicate effectively at all Plant Levels.
  • Willing to travel.
Loading...