QA Inspector

Baxter•St Paul, MN

About The Position

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. Your Role At Baxter: Responsible for endorsing process and product quality, efficacy, and safety through the routine assessment of plant operations and finished products. Responsible for ensuring adherence to the regulatory and procedural requirements that govern those operations and products. Your team: When you join the Quality team you belong to a group that never shies away from a challenge and truly believes that teamwork makes jobs great. Motivated by work that is never the same from one day to the next, this team powers through internal processes to create products that they deeply believe in. Individuals within the quality organization are encouraged to think strategically about how to best-solve any issues at hand. Baxter remains positive, confident, and resilient as it approaches new challenges and strives to create the best possible product for the client, always.

Requirements

Knowledge of GMP documentation.
Demonstrated attention to details and accuracy required.
Must have good communication skills.
Associates with 0 years related experience or High School diploma with 1+ years related experience.

Nice To Haves

General knowledge of quarantine and warehouse operation helpful.
Experience in a pharmaceutical or Biotech industry helpful.
Familiarity with cGMP and FDA requirements preferred.

Responsibilities

Monitor product quality through the performance of required visual and functional testing.
Maintain a working knowledge of statistically based Sampling Plans and their applications.
Promote process control through activities in support of equipment and process validations. These activities are primarily product checks that support or refute validation studies.
Monitor processes through the implementation of World Class Manufacturing Strategies, including Statistical Process Control (SPC).
Responsible for generating and interpreting SPC control charts.
Ensure the accuracy of measuring and testing equipment through the performance of calibrations.
Perform periodic audits of manufacturing practices and local procedures. Procedural changes in response to these audits may be initiated and coordinated by the QA inspector.
Support the corrective and preventive action program by assisting with expectation situations.
Promote continuous improvement through participation (i.e. team leader / facilitator or major contributor) in Process Management Team program.

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
Time-off benefits such as 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