Associate Scientist I

About the role

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.

Requirements

• 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
• Reasonable Accommodations
• Recruitment Fraud Notice

Benefits

Additional Information

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.

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