Associate II, Quality Lab

Baxter International Inc.; Round Lake (IL); On-site; USD 68,000 - 94,000; Full time

Benefits offered by this job

Medical, Dental and Vision coverage

160 hours of Paid Time Off and Paid H1

401K match

Employee Stock Purchase Program

Paid Parental Leave

Tuition Reimbursement

Job summary

Baxter International Inc. in Round Lake, IL, is seeking a chemistry- or physical-science professional to perform chemical and physical analyses across the manufacturing process, from incoming materials to finished goods, and to support environmental monitoring programs.

This first-shift role requires occasional weekend work for training, projects, and production support; candidates must not be allergic to penicillin or cephalosporins.

Qualifications

• Bachelor degree in Chemistry or physical science with 2+ years' experience.
• Must have good oral and written communication skills, strong analytical skills and be detail oriented.
• Knowledge of current Good Manufacturing Practices is preferred.
• Advanced laboratory skills with basic knowledge of statistical methods.
• Strong technical problem solving skills.
• Ability to handle multiple tasks concurrently, and in a timely fashion.
• Knowledge of Empower Chromatography Data System and LIMS is preferred but not required.
• Knowledge of GLP, cGMP requirements and familiarity with USP/ICH guidelines is preferred but not required.
• Must demonstrate effectiveness in ability to train others, empowerment, leadership, results orientation, and task completion.
• Ability to work independently and as part of a team, self-motivated, demonstrates adaptability, and possesses a positive attitude in a highly dynamic environment.
• Ability to lift up to 50 pounds when required.
• Occasional weekend work required.
• Must not be color blind.

Responsibilities

• Conduct chemical and physical analysis on raw materials, in-process and final products, and environmental monitoring samples.
• Work under minimum supervision.
• Serve as mentor to Quality Laboratory Associate (QLA) I positions.
• Provide training and work direction for QLA I positions as required.
• Perform review of test data and ensure proper documentation.
• Perform release functions in LIMS or other computerized systems.
• Use laboratory instrumentation (e.g., HPLC, GC) and computer systems to collect and record data.
• Perform advanced chemical assays requiring precise analytical skills and understanding of biology and chemistry.
• Complete all testing, including special project/protocol testing, timely and appropriately.
• Maintain data integrity and ensure compliance with SOPs and FDA, GLP, QSR and cGMP regulations.
• Participate in cross-functional teams to improve production, efficiency, and quality.
• Perform laboratory and manufacturing audits; update plant SOPs as required.
• Perform equipment maintenance and calibrations.
• Document testing in Notebooks, Controlled documents, Forms and LIMS; maintain quality records.
• Follow Baxter SOPs and policies on cGMP and safety; maintain a clean, safe lab area.
• Investigate deviations and write exception/OOL/OOS/OOT documents.
• Support improvement projects using LEAN principles (6S, Kaizen).
• Communicate progress and issues with peers and management; suggest solutions.
• Maintain high standards in quality, customer service and regulatory compliance.

Skills

Chemical analysis

Physical analysis

Analytical thinking

Attention to detail

Oral and written communication

Training and mentoring

Team collaboration

Problem solving

Education

Bachelor degree in Chemistry or physical science

Tools

LIMS

Empower Chromatography Data System

Job description

• Work under minimum supervision.

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.

Your Role at Baxter

This is where your creativity addresses challenges

The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs.

This is a first shift position but will be required to work on weekends to support training of analysts and to support projects and/or production, as required.

A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials.

Your Team at Baxter

Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it's building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation. The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always. The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products. We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable, ethical, and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when there's a new insight or opportunity to improve something. This open dialog builds trust within the team and helps create a better product for our customers.

What we offer from Day One

• Medical, Dental and Vision coverage
• 160 hours of Paid Time Off and Paid Holidays
• 401K match
• Employee Stock Purchase Program
• Paid Parental Leave
• Tuition Reimbursement

What you'll be doing

• Conduct critical chemical and physical analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at the Round Lake manufacturing facility.
• Work under minimum supervision.
• Serve as mentor to Quality Laboratory Associate (QLA) I positions.
• Provide training and work direction for QLA I positions as required.
• Perform review of test data, which includes overall documentation practices.
• Perform release functions in LIMS or other computerized systems.
• Use sophisticated laboratory instrumentation (e.g., HPLC, GC) and computer systems to collect and record data.
• Perform advanced chemical assays requiring precise analytical skills and understanding of biology and chemistry principles.
• Complete all testing, including special project / protocol testing in a timely and appropriate manner.
• Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
• Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings, and improve quality.
• Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
• Perform equipment maintenance and calibrations as required.
• Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records.
• Follow, understand, and comply with Baxter SOP’s and policies on cGMP’s and safety. Maintain a clean, safe, and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas.
• Investigate deviations and write exception/OOL/OOS/OOT documents.
• Support improvement projects and drive efficiency through utilization of LEAN management principles (i.e., 6S, Kaizen, etc.).
• Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise.
• Maintain and meet the highest standards in quality, customer service and regulatory compliance.

What you'll bring

• Bachelor degree in Chemistry or physical science with 2 or more years' experience.
• Must have good oral and written communication skills, strong analytical skills and be detail oriented.
• Knowledge of current Good Manufacturing Practices is preferred.
• Advanced laboratory skills with basic knowledge of statistical methods.
• Strong technical problem solving skills.
• Ability to handle multiple tasks concurrently, and in a timely fashion.
• Knowledge of Empower Chromatography Data System and LIMS is preferred but not required.
• Knowledge of GLP, cGMP requirements and familiarity with USP/ICH guidelines is preferred but not required.
• Must demonstrate effectiveness in ability to train others, empowerment, leadership, results orientation, and task completion.
• Ability to work independently and as part of a team, self-motivated, demonstrates adaptability, and possesses a positive attitude in a highly dynamic environment.
• Ability to lift up to 50 pounds when required.
• Occasional weekend work required.
• Must not be color blind.

Other Duties as Assigned

This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Overtime is worked as required.

We understand compensation is an important factor as you consider the next step in your career. At Baxter,we arecommitted toequitablepay for all employees, and we strive to be moretransparentwith our pay practices. The estimated base salary for this position is $68,000-$93,500 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses.

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.

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and 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, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees.

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 or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Know Your Rights: Workplace Discrimination is Illegal

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information.