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HomeCompaniesEde1ea78 34fc 4920 A043 335c6e96f763 19000101 000001Principal Purification Chemist

Principal Purification Chemist

Ede1ea78 34fc 4920 A043 335c6e96f763 19000101 000001 · Boulder, CO, US, Boulder, CO · Active · $122,000–$153,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyEde1ea78 34fc 4920 A043 335c6e96f763 19000101 000001
TitlePrincipal Purification Chemist
Normalized title-
Department / team-
LocationBoulder, CO, United States
Work model-
Employment typeFull Time
Salary$122,000–$153,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-05-13 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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Linked records

CompanyEde1ea78 34fc 4920 A043 335c6e96f763 19000101 000001
Sourceb71f96f4-5822-4f43-b725-e1cc7c3a5577
ATS providerADP Workforce Now Recruiting

Description

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. SUMMARY Responsible for providing strong technical leadership and documentation support for development and GMP manufacturing processes. Responsible for the planning and execution of multi-step preparative chromatography from laboratory to full commercialization. Emphasis is on the creative application of a full range of literature and theoretical concepts, from a diverse range of chemistry to the design and implementation of cost-effective processes for the manufacture of Corden pharmaceuticals. Works within a team-oriented environment with professionals from a variety of disciplines. Conducts research, analysis, synthesis, experimentation, and documentation for such purposes as process development, implementation, registration, validation, and process improvement. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned. Ensures that the purification chemistry is capable of meeting cost, yield, throughput, quality/purity, and QSHE goals on assigned processes in GMP plant production Leads the technical progress of large and/or multiple teams to accomplish the development, transfer, or implementation of technology at a lab or plant scale Develops and supports scalable purification processes and provides technical expertise and support during lab or GMP plant operations Responsible for supplying management with specific project data to facilitate the budgeting process for the development, transfer, or implementation of technology Develops and executes procedures, processes, and methods for solutions to purification and technical problems on lab and plant scale Conducts research and development to improve manufacturing processes Troubleshoots purification processes running in lab and GMP plant manufacturing Possesses an individual area of technical expertise, which others consult them for advice Adheres to GDP and SOPs in all aspects of work LEADERSHIP & BUDGET RESPONSIBILITIES 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. Leads team in the development, troubleshooting, transfer, and improvement of purification and analytical processes. Gives regular reports to, and actively solicits feedback from, management. SAFETY & ENVIRONMENTAL RESPONSIBILITIES 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. QUALITY RESPONSIBILITIES 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. QUALIFICATIONS 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. EDUCATION and/or EXPERIENCE Doctoral Degree (Ph.D.) in Chemistry and one year of postdoctoral experience, preferably specializing in Purification Chemistry, plus five years of experience; or equivalent combination of education and experience in a Pharmaceutical or Fine Chemical Manufacturing environment. 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. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to comprehend and apply principles of advanced calculus, modern algebra, and advanced statistical theory. Ability to work with concepts such as limits, quadratic and exponential equations, and proofs of theorems. REASONING ABILITY Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.,) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS 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. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to work with hands; reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT 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. While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. CORE COMPETENCIES 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. Demonstrates a positive attitude Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports Experience in the purification of Peptides Thorough knowledge of all plant-scale purification unit operations, scale-up, and plant design considerations An understanding of chemical reactivity, process hazards, cross reactivity, side products, and waste streams, especially for processes they support Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects Assumes reasonable risk in trying out new, self-generated ideas Proactive approach to problem identification and resolution Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or proposing improvements 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 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 Demonstrates skills in negotiation and influencing others Thorough working knowledge of regulatory issues in pharmaceutical manufacturing including cGMPs, PSM, OSHA, EPA requirements, and process hazard analysis; can interpret regulatory laws, and propose, defend, and implement cost-effective solutions Computer skills, in the areas of Microsoft Office Products – Word, Excel, PowerPoint, statistical analysis programs, Laboratory Information Management System (LabVantage), electronic notebook system (Signals), Openlab, Smartsheets, and business systems (SAP) Develops special expertise in products and processes; acknowledged as an expert in one or more technical areas both within and outside site Creates clear, concise goals, and strategies that support individuals’ development and the site’s mission; actively participates in proposing and setting purification/Process Chemist Group and Manufacturing Department goals Routinely demonstrates a proactive approach to problem identification and resolution Understands Corden’s business goals and contributes technically to its strategy development Interacts with management in developing project objectives and site strategies; advises management regarding technical opportunities and advances SALARY Actual pay will be based on your skills and experience. BENEFITS 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service Accident Plan Critical Illness Insurance Dental Insurance Disability Insurance Employee Assistance Program Flexible Spending Account Health Insurance PPO/HSA Hospital Indemnity Plan ID Theft Protection Life Insurance Paid Parental Leave Tuition Reimbursement Wellness Program Vacation – Three Weeks 1st Year 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 June 15, 2026

Full job record

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    "requisitionDescription": "<div><div><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;' data-pasted=\"true\"><strong><span style=\"font-family: verdana,sans-serif;\">CordenPharma </span></strong><span style=\"font-family: verdana,sans-serif;\">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&rsquo;s lives.</span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">&nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids &amp; Carbohydrates, Injectables, Highly Potent &amp; 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.</span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;margin-top:2.0pt;'><span style=\"font-family: verdana,sans-serif;\"><strong>&nbsp;</strong></span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;margin-top:2.0pt;'><span style=\"font-family: verdana,sans-serif;\"><strong><span style=\"font-size:16px;text-transform:uppercase;\">Our People Vision</span></strong></span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">We strive for excellence. We share our passion. Together, we make a difference in patients&#39; lives.</span></p><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">SUMMARY</span></h2><h2 style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;line-height:14.0pt;'><span style=\"font-size: 15px; font-family: verdana, sans-serif; text-transform: none; font-weight: normal;\">Responsible for providing strong technical leadership and documentation support for development and GMP manufacturing processes. Responsible for the planning and execution of multi-step preparative chromatography from laboratory to full commercialization. Emphasis is on the creative application of a full range of literature and theoretical concepts, from a diverse range of chemistry to the design and implementation of cost-effective processes for the manufacture of Corden pharmaceuticals. Works within a team-oriented environment with professionals from a variety of disciplines. Conducts research, analysis, synthesis, experimentation, and documentation for such purposes as process development, implementation, registration, validation, and process improvement.</span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">ESSENTIAL&nbsp;DUTIES&nbsp;AND RESPONSIBILITIES</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">Include the following. Other duties may be assigned.</span></p><div style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Ensures that the purification chemistry is capable of meeting cost, yield, throughput, quality/purity, and QSHE goals on assigned processes in GMP plant production</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Leads the technical progress of large and/or multiple teams to accomplish the development, transfer, or implementation of technology at a lab or plant scale</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Develops and supports scalable purification processes and provides technical expertise and support during lab or GMP plant operations&nbsp;</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Responsible for supplying management with specific project data to facilitate the budgeting process for the development, transfer, or implementation of technology</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Develops and executes procedures, processes, and methods for solutions to purification and technical problems on lab and plant scale</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Conducts research and development to improve manufacturing processes</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Troubleshoots purification processes running in lab and GMP plant manufacturing</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Possesses an individual area of technical expertise, which others consult them for advice</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Adheres to GDP and SOPs in all aspects of work</li></ul></div><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">LEADERSHIP &amp; BUDGET&nbsp;RESPONSIBILITIES</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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. Leads team in the development, troubleshooting, transfer, and improvement of purification and analytical processes. Gives regular reports to, and actively solicits feedback from, management.</span></p><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">SAFETY &amp; ENVIRONMENTAL RESPONSIBILITIES</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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.</span></p><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">QUALITY RESPONSIBILITIES</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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&rsquo;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.&nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\"><br></span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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.</span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">&nbsp;</span></p><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">QUALIFICATIONS</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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.</span></p><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">EDUCATION and/or EXPERIENCE</span></h2><h2 style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;line-height:14.0pt;'><span style=\"font-size: 15px; font-family: verdana, sans-serif; text-transform: none; font-weight: normal;\">Doctoral Degree (Ph.D.) in Chemistry and one year of postdoctoral experience, preferably specializing in Purification Chemistry, plus five years of experience; or equivalent combination of education and experience in a Pharmaceutical or Fine Chemical Manufacturing environment.</span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">LANGUAGE SKILLS</span></h2><h2 style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;line-height:14.0pt;'><span style=\"font-size: 15px; font-family: verdana, sans-serif; text-transform: none; font-weight: normal;\">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. Ability to effectively present information to top management, public groups, and/or boards of directors.</span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">MATHEMATICAL SKILLS</span></h2><h2 style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;line-height:14.0pt;'><span style=\"font-size: 15px; font-family: verdana, sans-serif; text-transform: none; font-weight: normal;\">Ability to comprehend and apply principles of advanced calculus, modern algebra, and advanced statistical theory. Ability to work with concepts such as limits, quadratic and exponential equations, and proofs of theorems.</span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">REASONING ABILITY</span></h2><h2 style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;line-height:14.0pt;'><span style=\"font-size: 15px; font-family: verdana, sans-serif; text-transform: none; font-weight: normal;\">Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.,) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables.</span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">CERTIFICATES, LICENSES, REGISTRATIONS</span></h2><h2 style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;line-height:14.0pt;'><span style=\"font-size: 15px; font-family: verdana, sans-serif; text-transform: none; font-weight: normal;\">Domestic and international travel required.</span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">PHYSICAL DEMANDS</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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.</span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\"><br></span></p><h2 style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;line-height:14.0pt;'><span style=\"font-size: 15px; font-family: verdana, sans-serif; text-transform: none; font-weight: normal;\">While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to work with hands; reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.</span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">WORK ENVIRONMENT</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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.</span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;'><span style=\"font-family: verdana,sans-serif;\"><br></span></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate.</span></p><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\"><br></span></h2><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><span style=\"font-family: verdana,sans-serif;\">CORE COMPETENCIES</span></h2><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;line-height:14.0pt;'><span style=\"font-family: verdana,sans-serif;\">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.</span></p><div style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Demonstrates a positive attitude</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Experience in the purification of Peptides&nbsp;</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Thorough knowledge of all plant-scale purification unit operations, scale-up, and plant design considerations</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">An understanding of chemical reactivity, process hazards, cross reactivity, side products, and waste streams, especially for processes they support</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Assumes reasonable risk in trying out new, self-generated ideas</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Proactive approach to problem identification and resolution</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or proposing improvements</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">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</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">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</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Demonstrates skills in negotiation and influencing others</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Thorough working knowledge of regulatory issues in pharmaceutical manufacturing including cGMPs, PSM, OSHA, EPA requirements, and process hazard analysis; can interpret regulatory laws, and propose, defend, and implement cost-effective solutions</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Computer skills, in the areas of Microsoft Office Products &ndash; Word, Excel, PowerPoint, statistical analysis programs, Laboratory Information Management System (LabVantage), electronic notebook system (Signals), Openlab, Smartsheets, and business systems (SAP)</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Develops special expertise in products and processes; acknowledged as an expert in one or more technical areas both within and outside site</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Creates clear, concise goals, and strategies that support individuals&rsquo; development and the site&rsquo;s mission; actively participates in proposing and setting purification/Process Chemist Group and Manufacturing Department goals</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Routinely demonstrates a proactive approach to problem identification and resolution</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Understands Corden&rsquo;s business goals and contributes technically to its strategy development</li><li style=\"margin: 0in; font-size: 15px; font-family: verdana, sans-serif;\">Interacts with management in developing project objectives and site strategies; advises management regarding technical opportunities and advances</li></ul></div><h2 style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Verdana\",sans-serif;text-transform:uppercase;'><br></h2><p style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;line-height:normal;' data-pasted=\"true\"><strong><span style='font-size:16px;font-family:\"Verdana\",sans-serif;'>SALARY</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;line-height:14.0pt;background:white;'><span style='font-size:15px;font-family:\"Verdana\",sans-serif;color:#414141;'>Actual pay will be based on your skills and experience.</span></p><p style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;line-height:normal;'><strong>&nbsp;</strong></p><p style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;line-height:normal;'><strong><span style='font-size:16px;font-family:\"Verdana\",sans-serif;'>BENEFITS</span></strong></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service&nbsp;</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Accident Plan</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Critical Illness Insurance</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Dental Insurance</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Disability Insurance</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Employee Assistance Program</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Flexible Spending Account</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Health Insurance PPO/HSA</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Hospital Indemnity Plan</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>ID Theft Protection</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Life Insurance</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Paid Parental Leave</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Tuition Reimbursement</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Wellness Program</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Vacation &ndash; Three Weeks 1st Year</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family: initial;line-height:normal;\"><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>Vision Insurance</span></li></ul><p style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;line-height:normal;'><strong>&nbsp;</strong></p><p style='margin-top:2.0pt;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;line-height:normal;'><strong><span style='font-size:16px;font-family:\"Verdana\",sans-serif;color:#414141;'>EQUAL OPPORTUNITY EMPLOYER</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;line-height:14.0pt;'><em><span style='font-size:15px;font-family:\"Verdana\",sans-serif;'>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.</span></em></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;font-size:11.0pt;font-family:\"Aptos\",sans-serif;'><br></p><p style='margin:0in;font-size:15px;font-family:\"Verdana\",sans-serif;'>This post will expire June 15, 2026</p></div></div>\n",
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    "requisitionTitle": "Principal Purification Chemist",
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