Sr Quality Tech, Receiving & Inspection

Baxter International Inc.•Round Lake, IL

1d•$51,200 - $70,400•Onsite

About The Position

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.

Requirements

Associate’s degree in a related discipline or equivalent work experience plus 3 year related experience.
Good writing and verbal communication skills, and problem-solving skills are required.
Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements.
Understanding of cGMPs and GDP procedures.
20/30 vision in at least one eye with or without corrective lenses.
The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision.
The candidate must not be allergic to Penicillin or Cephalosporin drugs.
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

Nice To Haves

Preferred experience with material inventory management systems.

Responsibilities

Performs daily quality review of raw material documentation to ensure that materials being received are produced in accordance with Company methodology, procedures, and standards.
Serves as a lead and mentor to the remainder of the team.
Acts as the SME for Receiving & Inspection processes and supports process improvement projects.
Manages raw material tracking log and scheduling work for R&I technicians.
Manages RLDD Stability schedule and sends out Stability notices.
Creates reassay and expiration report on a monthly basis.
Completes GME and Labvantage setups for materials.
Supplier Quality (SQ) responsibilities to include SCAR (Supplier Corrective Action Request) writing and review; Reduced testing of materials - new and periodic review; SQ approval of raw material part records; and Risk Action and Mitigation (RAM) review for Round Lake Drug Delivery.
Performs R&I procedure and training code revisions in document system.
Completes Certification of Documentation Review (CDR) process for raw materials to implement them in the plant systems.
Submit and manage purchase orders in Coupa system.
Manages quotes and sends samples to external testing labs.
Complete and manage R&I Preventive Maintenance (PM) records in the Maximo system.
Attends various Tier and Cross-Functional meetings as the R&I representative.
Will work in Non-Cephalosporin, Cephalosporin, and Penicillin facilities as needed.
Serve as a positive influencer and mentor to the R&I Quality Technicians.

Benefits

medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
educational assistance programs
paid holidays
paid time off ranging from 20 to 35 days based on length of service
family and medical leaves of absence
paid parental leave
commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)
childcare benefits