- Collaborate with managers to develop analytical methods (LC-UV and/or LC-MS) for purity analysis and impurity characterization of small molecules, peptides, PMOs, and PPMOs.
- Provide analytical support for internal discovery and development activities, including stability sample analysis, forced degradation sample preparation, and characterization.
- Draft and review analytical protocols and reports for in-house analytical tasks, and compile analytical source documents for regulatory submissions.
- Perform regular maintenance on analytical equipment, HPLC systems, balances, pH meters, etc., and assist in setting up new instruments.
- Foster a culture of collaboration, innovation, and cutting-edge research focused on scientific excellence, open communication, and continuous improvement.
- Ph.D. in Chemistry or related field with at least 1 year of experience, or an MS degree with over 5 years of relevant experience in analytical development within the pharmaceutical/biotech sector. The job title will be determined based on the candidate's experience level.
- Hands-on experience in method development using HPLC and MS (e.g. TOF, QTOF, etc.) is essential.
- Preferred experience in method transfer, qualification, and validation of chromatographic methods (HPLC, GC, LC-MS, CE, etc.).
- Good understanding of current Good Manufacturing Practices (cGMPs) or Good Lab Practices (GLP) is beneficial.
- Knowledge of analytical support for early discovery and formulation development is advantageous.
- Ability to effectively prioritize tasks, meet tight deadlines, and thrive in a fast-paced and dynamic team environment.
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Scientist I/II, Analytical Development - Boston, United States - PepGen
Description
Scientist I/II, Analytical Development
The Scientist in Analytical Development plays a crucial role in PepGen's Analytical Development group. This position offers great opportunities to utilize cutting-edge instruments for researching potential drug candidates to develop groundbreaking therapies for patients with neuromuscular conditions. The selected candidate will be responsible for leading method development, providing analytical support for in-house drug discovery and development projects, and collaborating closely with experienced CMC and discovery teams. The role involves developing and validating analytical methods for various chemical entities such as peptides, oligos, and PepGen's proprietary Enhanced Delivery Oligonucleotides (EDOs) to ensure high-quality therapies for patients. The position is laboratory-based and requires on-site presence five days a week.
Responsibilities:
Requirements:
About the Team:
We are a team of dedicated and innovative scientists focused on analytical development and quality control of the revolutionary EDO platform at PepGen. Our team values transparent communication and is seeking a collaborative team member who shares our values and enthusiasm for the potential of our EDO platform to make a meaningful impact on patients' lives.
About PepGen
PepGen is a biotech company advancing next-generation oligonucleotide therapies for neuromuscular diseases. Our goal is to harness the potential of nucleic acid therapeutics through our proprietary Enhanced Delivery Oligonucleotide (EDO) platform. We are rapidly expanding our team at our U.S. headquarters in Boston, Massachusetts, and exploring the application of this technology across various indications.
EEO Statement
PepGen is an Equal Opportunity Employer dedicated to fostering a diverse workforce. We welcome applications from qualified individuals without regard to race, color, religion, national origin, age, gender, sexual orientation, disability, or veteran status.
Recruitment & Staffing Agencies: PepGen does not accept unsolicited agency resumes. We are currently partnering exclusively with The Bowdoin Group for all our recruitment needs. Thank you.