At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Analyst II QC Potency

In Bayer’s Pharmaceuticals division, we focus on researching, developing, and marketing specialty-focused innovative medicines that provide significant clinical benefit and value, primarily in the therapeutic areas of cardiology, oncology, gynecology, hematology, and ophthalmology. With our innovative products, we seek to achieve therapeutic benefit for patients, while at the same time satisfying the growing requirements of physicians and health insurers. As one of the leading research-based pharmaceutical companies worldwide, we have nearly 50 ongoing development projects in clinical trials.

The primary responsibilities of this role, Analyst II, QC Potency are to:

• Perform analytical testing to support the release, stability, and in process testing of samples or final products to ensure quality in order to support the release of materials for production or products for commercial use;
• Report abnormalities and oversee the discard of expired materials;
• Legibly document test results and complete technical writing for data analysis;
• Review Quality Control documents and LIMS data and evaluate data/interpret trends;
• Contribute toward the development, revision, application, maintenance, validation and review of quality standards, drafting SOPs, and methods for processing and/or ensuring quality in intermediate or finished products;
• Initiates Discrepancy events;
• Perform assay training;
• Address questions during regulatory compliance audits and support inspection-related needs as required;
• Must be able to work overnight hours - 12:30 a.m. - 8:30 a.m.

WHO YOU ARE:

Your success will be driven by your demonstration of our LIFE (Leadership, Integrity, Flexibility, Efficiency) values. Bayer seeks an incumbent who possesses the following:

Required Qualifications

• Bachelor's Degree in a scientific or related discipline;
• Experience working in a cGMP and global regulatory compliance organization is required;
• Knowledgeable with ELISA methods, SDS-PAGE, gel electrophoresis, and/or bioassay;
• Ability to multi-task and ability to be adaptable to changing business requirements in a dynamic corporate environment;
• Skilled with equipment and analytical and/or biological method validation laboratory execution;
• Strong technical writing skills to be able to write reports and SOPs;
• Continuously Improve Integrity and commitment to Company Beliefs and Values

Preferred Qualifications

• Bachelor's degree with 4+ years of industry experience, or Master's degree with 2+ years of industry experience, or an equivalent combination of education and experience.

Employees can expect to be paid a salary between $68,300 to $85,353. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.. This salary range is merely an estimate and may vary based on an applicant’s location, market data/ranges, an applicant’s skills and prior relevant experience, certain degrees and certifications, and other relevant factors.

#LI-AMSUS