Senior Bioanalytical Scientist
3 weeks ago
We are seeking a highly experienced Senior Bioanalytical Scientist to join our Quality Control team at AmplifyBio. As a key member of our team, you will be responsible for developing, optimizing, and validating analytical procedures for product release, stability, and process characterization.
Key Responsibilities- Lead analytical development projects and collaborate with R&D groups and clients to develop robust and fit-for-purpose analytical procedures using HPLC and/or LC-MS technologies.
- Write and execute protocols for analytical procedure development, qualification/validation, and technology transfer, and draft/review written reports.
- Perform routine and non-routine biological, biochemical, and chemical test methods for product in process, lot release, and stability purposes.
- Set the example for QC colleagues to work in accordance with guidelines and requirements established by FDA Good Manufacturing Practices (cGMP), Good Documentation Practices (cGDP), Code of Federal Regulations (CFR), and other applicable regulatory guidance.
- Contribute to the QC laboratory maintenance and lab operations systems, and work with QC management to promote the continuous improvement of QC operations procedures and systems.
- Bachelor's degree in biological sciences, biotechnology, or a related field of study with a minimum of 10 years of experience in a related field, or a graduate-level degree with 5 years of relevant experience.
- Minimum 4 years of experience in a QC laboratory operation or analytical development role in a regulated laboratory operation.
- Highly experienced and knowledgeable biological science laboratory professional with in-depth knowledge of HPLC and/or LC-MS for GMP use, including assay qualification/validation, technology transfer, and troubleshooting.
- Expected to maintain rigor and high quality of execution and documentation required by GMP and other regulatory agencies.
- The candidate should enjoy operating in an exceptionally dynamic and cooperative environment that is goal-driven to achieve time-sensitive objectives.
- Is highly dedicated to mentoring team individuals, motivating team success, and contributing in a collegial manner to the entire company.
- Able to communicate clearly and concisely, both verbally and in the form of written reports, including drafting and review of protocols, SOPs, batch records, and regulatory documentation to support clinical development.
- Ability to work in a fast-paced environment and flexible.
AmplifyBio is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work, a preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike, and, most recently, an expansion into manufacturing services for cell, gene, and mRNA-based therapeutics.
We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work. From a wellness program to financial planning and legal assistance, we make sure to take care of our own.
We are an equal opportunity employer and value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), sexual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law.
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