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Analytical Chemist for Standards and Stability

2 months ago

Boulder, Colorado, United States CORDEN PHARMA BOULDER INC Full time
Job Overview

Corden Pharma Boulder Inc is committed to fostering an inclusive workplace and provides equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment of any kind based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

As a prominent contract development and manufacturing organization (CDMO), we specialize in the production of active pharmaceutical ingredients (APIs), excipients, and pharmaceutical drug products (DP). With a workforce exceeding 2,600 globally, our services empower pharmaceutical and biotech companies to produce medications aimed at enhancing the quality of life for patients.

Our extensive network across Europe and the U.S. provides tailored solutions across various technology platforms, including Peptides, Lipids, & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We are dedicated to excellence in supporting this network and ensuring the highest quality products for patient well-being.

Position Summary

This role represents an intermediate-level technical professional within the Research and Development (R&D) team. The incumbent will perform analytical tasks with precision and efficiency, supporting the Stability Program and ongoing development projects.

Key Responsibilities
  • Support a continuous manufacturing schedule, with flexibility to work weekends and/or nights as needed.
  • Conduct routine and specialized tests on various samples, including special requests from production and technical teams.
  • Perform calibration of equipment, standardization of titrants, and characterization/qualification of standards as required.
  • Identify and resolve issues with laboratory instruments, and communicate findings and solutions related to processes and materials.
  • Maintain a clean and organized laboratory environment, adhering to safety, regulatory, and chemical hygiene policies, including Good Manufacturing Practices (GMP).
  • Document daily activities using SAP and LIMS, manage material status changes, and initiate incident reports.
  • Oversee the proper management of hazardous and non-hazardous waste generation and accumulation.
  • Participate in R&D and cross-functional team meetings to enhance team collaboration.
Qualifications

To excel in this position, candidates must meet the following qualifications:

  • A Bachelor’s degree from a four-year college or university, or two years of relevant experience and/or training, or an equivalent combination of education and experience.
  • Proficient in reading and comprehending instructions, correspondence, and memos, with the ability to write simple correspondence.
  • Strong analytical skills, with the ability to perform routine calculations and interpret data from various analytical testing techniques.
  • Ability to solve practical problems and navigate a variety of concrete variables in compliance with stringent cGMP standards.
Core Competencies
  • Analytical skills and knowledge of general or organic chemistry.
  • Effective communication and computer skills.
  • Attention to detail and commitment to quality.
Work Environment

The work environment is characterized by occasional exposure to fumes or airborne particles, low levels of toxic or caustic chemicals, and moderate noise levels. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.