
QA Inspector
Baxter International Inc., Saint Paul, MN, United States
Your Role at Baxter
Responsible for endorsing process and product quality, efficacy, and safety through routine assessment of plant operations and finished products. Ensure adherence to regulatory and procedural requirements governing those operations and products.
Your Team
The Quality team collaborates to uphold product quality and safety, working strategically to solve operational challenges and continuously improve processes.
Responsibilities
Monitor product quality through visual and functional testing and maintain knowledge of sampling plans.
Promote process control by supporting equipment and process validations, including product checks that validate studies.
Implement World Class Manufacturing Strategies, including Statistical Process Control (SPC), and generate and interpret SPC control charts.
Ensure accuracy of measuring and testing equipment through calibrations.
Perform periodic audits of manufacturing practices and local procedures.
Initiate and coordinate procedural changes resulting from audits.
Assist with corrective and preventive actions and track expectations.
Participate as team leader, facilitator, or major contributor in Process Management Team improvement initiatives.
Qualifications
Knowledge of GMP documentation.
Demonstrated attention to detail and accuracy.
Good communication skills.
General knowledge of quarantine and warehouse operations helpful.
May be required to work flexible hours and overtime on short notice.
High school diploma with 1+ years related experience or 0 years related experience allowed.
Experience in pharmaceutical or biotech industry helpful.
Familiarity with cGMP and FDA requirements preferred.
Compensation
Base salary range: $44,800 to $61,600. Actual salary may vary based on skills, experience, role tenure, business line, and geographic location.
Benefits
Baxter offers medical and dental coverage starting on day one, life and disability insurance, 401(k) with company match, ESPP, Flexible Spending Accounts, educational assistance, paid holidays, paid time off ranging from 20 to 35 days, family and medical leave, paid parental leave, commuting benefits, employee discounts, employee assistance program, and childcare benefits.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity, protected veteran status, or disability status.
Reasonable Accommodations
Baxter is committed to providing reasonable accommodations to individuals with disabilities. Applicants requesting accommodations should contact the hiring team with the nature of the request and contact information.
Recruitment Fraud Notice
Baxter has identified employment scams where fraudulent parties pose as Baxter employees or recruiters. Applicants are advised to verify contact information through official Baxter channels.
#J-18808-Ljbffr
Responsible for endorsing process and product quality, efficacy, and safety through routine assessment of plant operations and finished products. Ensure adherence to regulatory and procedural requirements governing those operations and products.
Your Team
The Quality team collaborates to uphold product quality and safety, working strategically to solve operational challenges and continuously improve processes.
Responsibilities
Monitor product quality through visual and functional testing and maintain knowledge of sampling plans.
Promote process control by supporting equipment and process validations, including product checks that validate studies.
Implement World Class Manufacturing Strategies, including Statistical Process Control (SPC), and generate and interpret SPC control charts.
Ensure accuracy of measuring and testing equipment through calibrations.
Perform periodic audits of manufacturing practices and local procedures.
Initiate and coordinate procedural changes resulting from audits.
Assist with corrective and preventive actions and track expectations.
Participate as team leader, facilitator, or major contributor in Process Management Team improvement initiatives.
Qualifications
Knowledge of GMP documentation.
Demonstrated attention to detail and accuracy.
Good communication skills.
General knowledge of quarantine and warehouse operations helpful.
May be required to work flexible hours and overtime on short notice.
High school diploma with 1+ years related experience or 0 years related experience allowed.
Experience in pharmaceutical or biotech industry helpful.
Familiarity with cGMP and FDA requirements preferred.
Compensation
Base salary range: $44,800 to $61,600. Actual salary may vary based on skills, experience, role tenure, business line, and geographic location.
Benefits
Baxter offers medical and dental coverage starting on day one, life and disability insurance, 401(k) with company match, ESPP, Flexible Spending Accounts, educational assistance, paid holidays, paid time off ranging from 20 to 35 days, family and medical leave, paid parental leave, commuting benefits, employee discounts, employee assistance program, and childcare benefits.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity, protected veteran status, or disability status.
Reasonable Accommodations
Baxter is committed to providing reasonable accommodations to individuals with disabilities. Applicants requesting accommodations should contact the hiring team with the nature of the request and contact information.
Recruitment Fraud Notice
Baxter has identified employment scams where fraudulent parties pose as Baxter employees or recruiters. Applicants are advised to verify contact information through official Baxter channels.
#J-18808-Ljbffr