CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical and biotech companies manufacture medicines with the ultimate goal of improving people’s lives.
Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being.
OUR PEOPLE VISION
We strive for excellence. We share our passion. Together, we make a difference in patients' lives.
Include the following. Other duties may be assigned.
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Develops and supports scalable purification processes and analytical methods while providing technical expertise and support during lab or plant operations
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Independently plans and executes experiments for the purification of peptides, toward developing a robust commercial process, while working on a project team
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Works effectively in a team-oriented environment
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Presents work orally and in form of written development reports
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Adheres to cGMP and SOPs in all aspects of work
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Demonstrates a clear understanding of technical issues and the requirements of a viable manufacturing process
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Ensures that the purification is capable of meeting cost, yield, throughput, quality, and QSHE goals on assigned processes
Demonstrates positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons.
Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.
Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC’s Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company.
cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
LANGUAGE SKILLS
Ability to read, analyze, and interpret common scientific and analytical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publication that conform to prescribed style and format.
MATHEMATICAL SKILLS
Ability to calculate figures and amounts such as proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. Ability to convert units of measurement.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.
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Demonstrates a positive attitude
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Strong background in Purification Chemistry or a related scientific field
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Working knowledge of regulatory issues in Pharmaceutical Manufacturing including cGMPs, PSM, OSHA, and EPA requirements
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Communicates effectively in writing and verbally within the department
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Computer skills in the areas of Microsoft Office Products – Word, Excel, PowerPoint
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Ability to work interactively within a multi-functional team-oriented environment
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Takes initiative in setting own goals and work plan
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Hands on purification laboratory experience
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Broad technical knowledge in Purification Chemistry and Process Improvement Methodology
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Maintain a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports
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Experience in the purification of Peptides
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A working knowledge of all plant-scale purification unit operations, scale-up, and plant design considerations
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An understanding of chemical reactivity, potential exotherms, cross reactivity, side products, and waste streams, especially for processes they support
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Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues
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Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes
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Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects
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Assumes reasonable risk in trying out new, self-generated ideas
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Proactive approach to problem identification and resolution
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Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective and effective
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Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or proposing improvements
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Ability to provide leadership in all Purification Chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in an interactive, interdisciplinary team environment
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Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the-art technology and applies it to their assignments
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Demonstrates skills in negotiation and influencing others
SALARY
Actual pay will be based on your skills and experience.
BENEFITS
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401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
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Accident Plan
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Critical Illness Insurance
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Dental Insurance
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Disability Insurance
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Employee Assistance Program
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Flexible Spending Account
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Health Insurance PPO/HSA
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Hospital Indemnity Plan
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ID Theft Protection
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Life Insurance
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Paid Parental Leave
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Tuition Reimbursement
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Wellness Program
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Vacation – Three Weeks 1st Year
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Vision Insurance
EQUAL OPPORTUNITY EMPLOYER
Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to 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. Corden Pharma embraces fair hiring practices.
This post will expire 7/24/2026
