Senior Associate, Quality Control Data
Company Description Boehringer Ingelheim is a global, research-driven biopharmaceutical company focused on advancing healthcare and innovation for both humans and animals. With more than 54,000 colleagues worldwide, the company fosters a collaborative culture where diverse teams work together to deliver impactful therapies and solutions. Team members are encouraged to grow their careers while contributing to scientific progress and better patient outcomes. Boehringer Ingelheim promotes an inclusive environment where people are valued for their skills, ideas, and potential and are invited to move their careers and lives “#LifeForward.”
Role Description The Senior Associate, Quality Control Data is a full-time, on-site role based in Winterville, GA. This position is responsible for managing, reviewing, and reporting quality control (QC) data to support manufacturing, testing, and release of products in compliance with internal standards and regulatory expectations. Day-to-day activities include collecting and organizing laboratory data, verifying data accuracy, performing data trending and analysis, and preparing QC reports for internal stakeholders and audits. The role also involves supporting investigations and deviations with data-driven insights, maintaining documentation and data integrity within electronic systems, and collaborating with QC analysts, QA, and production teams to ensure timely and compliant decision-making. The Senior Associate may contribute to method improvements, data management process optimization, and training of colleagues on QC data practices and systems.
Qualifications
• Demonstrated experience with quality control data management, including data review, trending, and reporting in a GxP or regulated environment.
• Strong analytical and problem-solving skills, with the ability to interpret complex laboratory data and support investigations and root-cause analysis.
• Proficiency with data and documentation systems (e.g., LIMS, ELN, ERP, or similar electronic quality and lab systems) and good understanding of data integrity principles.
• Solid knowledge of quality principles, laboratory practices, and relevant regulatory requirements (e.g., FDA, EMA, cGMP) applicable to pharmaceutical or biopharmaceutical operations.
• Effective communication and collaboration skills, with the ability to work cross-functionally with QC, QA, manufacturing, and technical support teams.
• Strong attention to detail, organizational skills, and the ability to manage priorities and timelines in a fast-paced, on-site laboratory and production environment.
• Bachelor’s degree in a scientific discipline (such as Chemistry, Biology, Biochemistry, or related field); an advanced degree or equivalent experience is an advantage.
• Relevant experience in pharmaceutical, biopharmaceutical, or animal health quality control; prior experience in a senior or lead QC data role is preferred.
Pharmaceutical Manufacturing
Pharmaceutical Manufacturing
Full-time