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.

Summary:

The Analytical Compliance Associate supports quality and compliance projects associated to laboratory activities and processes transformation. He/she demonstrates knowledge and experiences of GMP standards and ability to apply technical and quality knowledge. The Analytical Compliance Associate also uses his/her technical skills to efficiently review R&D activities to ensure the highest level of quality of technical results.

Essential Duties and Responsibilities:

Maintain schedules for periodic reviews of test method assays in collaboration with the management and analytical SMEs. Monitor tasks progress and identify potential planning risks.

Manage change control activities related to test method assay periodic reviews and updates in accordance with project needs and agreed timelines.

Contribute to R&D analytical activities by reviewing experiments within her/his area of technical expertise.

Support analytical projects through effective collaboration in documentation management.

Contribute to the continuous improvement of quality processes within R&D analytical laboratories.

Qualifications:

Minimum requirements:

Knowledge of small molecules analytical projects.

Organizational skills with demonstrated attention to detail.

Ability to apply a logical and methodical approach to analytical and quality processes and to formulate sound recommendations.

Good understanding of GMP standards in a laboratory environment.

Ability to work on multiple tasks simultaneously while meeting deadlines.

Strong interpersonal skills with the ability to collaborate effectively within cross-functional teams.

Quality-oriented mindset.

Education and Experience:

Master in Science degree (e.g. Analytical Chemistry, Organic chemistry, Biochemistry, Bio-engineering, Pharmaceutical Science).

Minimum of 2-6 years of experience in pharmaceutical industry (R&D, manufacturing…)

Demonstrated expertise in reviewing analytical chemistry data (e.g. experiments, reports).

Good knowledge of GMP requirements.

Fluent in spoken and written English is mandatory.

Knowledge of Trackwise is an asset

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.

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, please click on the link here and let us know the nature of your request along with your contact information.

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. To learn how you can protect yourself, review our Recruitment Fraud Notice.