This is whereyour work makes a difference.

What youll be doing

Shift time: Monday to Friday 10:00h-18:30h EST

• Provide front line day-to-day assistance on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality.

• Support during assigned Shift, with the requirement to support plant overtime and planned shutdowns when applicable.

• Provide technical assistance on review and approval of department-related procedural changes, product quality concerns, reinspections, new product introductions, and protocols.

• Support timely follow-up on quality exceptions and their preventative/corrective actions.

• Support initiation/investigation and approvals of non-conformance events in the Trackwise system.

• Act as SME for Electronic Batch Record (EBR) and SPC or equivalent experience.

• Perform change control assessments/executions and approvals.

• Ensure control of defective WIP materials (quarantine, retention, and disposal areas) to keep segregation, movement, documentation, and timely follow-up within the plant in sync with regulatory and compliance requirements.

What youll bring

Required:

• University Degree or equivalent experience, Bachelor of Science or equivalent experience.

• 3-5 yearsexperience in manufacturing and quality roles.

• Prior experience working in a GMP setting.

• Knowledge of cGMP, ISO, and regulatory standards.

• Diligent with the ability to work effectively under pressure.

• Strong written and verbal communication abilities, negotiation capabilities, and the capacity to collaborate with individuals at every level of the organization.

• Ability to build positive relationships and partner with internal and external collaborators.

• Strong ability to balance multiple priorities.

• Strong analytical and problem-solving skills with critical thinking abilities.

• Intermediate to Advanced proficiency in MS Office Suite.

Preferred:

• 5+ years with exposure to various areas of the manufacturing environment.

• Experience in pharmaceutical, healthcare, or food manufacturing environments.

• Experience with continuous improvement methodologies, Lean 6S, Kaizen, TPM, DMAIC.

Join us in our mission to make a global impact with your outstanding skills and dedication to quality!

We understand that compensation is an important factor as you consider the next step in your career. At Baxter,we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated salary range for this position is $86,400 - $129,600 annually, which reflects base salary as wellas estimated target payout under the Management Incentive Compensation Plan. Individual pay will bedetermined based upon skills, expertise and experience, and the incentive, which is contingent upon company andindividual performance outcomes. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

This posting is for a current existing vacancy within our organization. We are actively seeking qualified candidatesto fill this open position. If you are interviewed for this position, we will advise you within 45 days of the interview
as to whether or not you were successful in obtaining the position. Information submitted as part of the jobapplication process will be kept on file for 3 years from the date of submission in accordance with legislative
requirements.

As part of our recruitment process, Baxter Corporation may use AI tools to assist screening candidates and assistin evaluating candidate qualifications. All final hiring decisions are made by the hiring manager and recruitmentteam