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<h3>Job Description</h3>
Job DescriptionJob Summary
This is an entry-level professional role in which the employee applies basic chemistry principles, theories, and concepts to assigned tasks where established precedents exist. The position involves developing solutions to problems of limited scope and complexity using foundational scientific knowledge. The role supports laboratory and operational activities while maintaining a strong commitment to safety, quality, and teamwork, and works under general supervision.
Minimum Qualifications Required
<ul>
<li>
Bachelors or Masters degree in Chemistry or a related scientific field
</li>
<li>
Zero to two years of relevant experience in an industrial or research laboratory setting
</li>
<li>
Ability to work under general supervision and follow established protocols
</li>
<li>
Strong written and verbal communication skills
</li>
<li>
Commitment to safety, quality standards, and collaborative teamwork
</li>
</ul>
Preferred Qualifications
<ul>
<li>
Hands-on experience with analytical instrumentation and sample preparation
</li>
<li>
Experience in oilfield chemistry, chemical manufacturing, or industrial analytical laboratories
</li>
<li>
Strong problem-solving skills with attention to detail
</li>
</ul>

Chemist

<h3>Job Description</h3>
Job Description
Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics.

We are seeking a Senior Research Associate to join our DNA &amp; Strain Construction team in Boston, MA. The ideal candidate will have a proven track record designing and constructing plasmids, using different assembly strategies. They will be a key contributor to our team, working closely with other DNASC team members using the latest molecular biology and automation techniques to help advance our high throughput DNA construction pipeline, at the same pushing the limits of DNA assembly capabilities. They will also work closely with Asimov’s Synthetic Biology, High Throughput and Cell Line Development teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the foundation for engineering biology.

About the Role:
<ul>
<li>
Conduct PCR, Golden Gate or Gibson Assembly, plasmid purification, and sequencing prep to validate DNA constructs, both manually and in high-throughput using liquid handlers (e.g., Echo, Bravo, Hamilton STAR) following Standard Operation Procedures (SOPs)
</li>
<li>
Contribute to vector assembly design, and remediation plans.
</li>
<li>
Work with your manager to generate regulatory reports to support our customers’ needs.
</li>
<li>
Maintain accurate sample tracking and documentation in LIMS to ensure data integrity and reproducibility.
</li>
<li>
Assist with large-scale plasmid preparations (LSPs) to support internal and external projects.
</li>
<li>
Collaborate with scientists and other RAs to troubleshoot workflows, improve efficiency and develop new initiatives within the team.
</li>
<li>
Work as part of a multifunctional team, you’ll partner with synthetic biologists on the DNASC team as well as members of the Cell Line Development, Synthetic Biology and Software Development teams.
</li>
</ul>

About You:
<ul>
<li>
You have a B.S. or M.S. degree in biology, biochemistry, biological engineering, or a related field.
</li>
<li>
Deep bench experience is necessary to be successful in this role, and you will have 3+ years of biopharma experience.
</li>
<li>
You value teamwork and are motivated to contribute to the team’s goals.
</li>
<li>
Working as part of a highly integrated research team is exciting to you.
</li>
<li>
Automation experience is a plus but a desire to learn to develop automation of lab experiments is a must.
</li>
<li>
You will have independently or collaboratively designed an assembly plan to generate plasmids using either Gibson or Golden Gate.
</li>
<li>
You have experience, outside of coursework, with modern molecular biology and/or microbiological techniques such as various DNA assembly methods (Golden Gate, Gibson), PCR, colony picking, and DNA preps.
</li>
<li>
Being detail-oriented isn’t just a sound bite for you, it’s part of your DNA.
</li>
<li>
Experience with optimizing cloning protocols (PCR, Gibson, and especially Golden Gate) and basic mammalian cell culture techniques is a plus.
</li>
<li>
Experience extracting data using scripts from large databases or desire to learn is a plus.
</li>
<li>
We’re big on tools here! We’re happy to train you but if you know your way around Benchling, LIMS, Google Drive, and Excel, it’ll help you come up to speed quickly.
</li>
</ul>

We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.
Compensation Range: $85K - $90K

Senior Research Associate, DNA & Strain Construction

<h3>Job Description</h3>
Job DescriptionDIHO Consulting USA is seeking a Geotechnical Engineer on behalf of our client for their Southeast Louisiana Area offices.
The successful candidate will provide engineering and consulting services for a wide variety of projects and clients, primarily in the Energy Market Sector. Our client offers training and support necessary for career advancement, with the objective of developing the candidate into a departmental management role. Their Southeast Louisiana operations are well established in the local market and have an experienced engineering support staff in place.
We are looking for a candidate with excellent communication skills, a strong desire for career advancement, and sound leadership qualities.
Responsibilities
<ul>
<li>Prepare technical proposals.</li>
<li>Execute geotechnical engineering project assignments.</li>
<li>Work with and provide mentorship to engineering support staff.</li>
<li>Manage and coordinate geotechnical field and laboratory assignments.</li>
<li>Perform engineering analyses and prepare reports.</li>
<li>Maintain client expectations for project quality and schedule.</li>
</ul>
Requirements
<ul>
<li>Bachelors Degree in Civil Engineering.</li>
<li>PE License or active EIT Certification.</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
Benefits
This position includes a comprehensive benefits package provided by our client, which includes:
<ul>
<li>Flexible work schedule.</li>
<li>Health, Vision, Dental, Disability, and Life Insurance.</li>
<li>401(k) Retirement Program with up to 4% employer match after eligibility period.</li>
<li>120 hours of Paid Time Off (PTO) annually.</li>
<li>9 company-paid holidays.</li>
</ul>

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Do you have a passion for restoring and protecting natural landscapes? The Forest Preserve District is looking for a dedicated Natural Resource Manager / Restoration Ecologist II (full-time, 40 hours per week) to help steward our prairies, wetlands, woodlands, and wildlife for future generations.
This rewarding full-time position blends leadership with hands-on fieldwork and offers the opportunity to make a lasting impact across all Forest Preserve District management sites. You'll work alongside a skilled team of natural resource professionals while helping guide restoration efforts, support staff and volunteers, and engage the public in environmental education.
What You'll Do
<ul>
<li>Play a key role in restoring and managing prairies, wetlands, and forests throughout the District.</li>
<li>Lead and support Restoration Ecologist I staff, seasonal and part-time employees, interns, AmeriCorps members, and volunteers.</li>
<li>Coordinate volunteer groups and assist with training Volunteer Land Stewards.</li>
<li>Participate in prescribed burns, invasive species control, seed collection, planting, and habitat restoration projects.</li>
<li>Assist with management of Afton and Afton South Prairie Wetland Banks in compliance with U.S. Army Corps of Engineers requirements.</li>
<li>Prepare monthly natural resource management reports and contribute to long-term land management goals.</li>
<li>Support public outreach and education programs, including field trips, college partnerships, and summer environmental education camps.</li>
<li>Work independently and collaboratively with Natural Resource Management and Maintenance teams to ensure safe, effective operations.</li>
<li>Participate in required safety training and help maintain a safe, clean, and professional work environment.</li>
</ul>
What We're Looking For
<ul>
<li>At least 2 years of experience in natural resource management, ecological restoration, or a related field.</li>
<li>Bachelor's degree in biology, ecology, environmental science, natural resource restoration, or a related discipline (or equivalent experience).</li>
<li>Strong working knowledge of Midwest flora and fauna.</li>
<li>Ability to work outdoors in varying weather conditions and perform physically demanding tasks, including lifting up to 50 pounds.</li>
<li>Experience using power tools, chainsaws, and land management equipment.</li>
<li>Strong communication skills and the ability to work well with staff, volunteers, and the public.</li>
</ul>
Preferred Qualifications
<ul>
<li>Valid Illinois Class "A" Driver's License.</li>
<li>Illinois Prescribed Fire Burn Certification.</li>
<li>Illinois Department of Agriculture Pesticide Applicator's License.</li>
<li>Experience with land management, restoration, and maintenance equipment.</li>
<li>Knowledge of Illinois native plant and wildlife communities.</li>
</ul>
Compensation &amp; Benefits
Hourly Pay Range:
<ul>
<li>$25.69 - $27.10 (hiring range)</li>
<li>Up to $29.28 (top of range)</li>
</ul>
Benefits Include:
<ul>
<li>Health insurance through Blue Cross Blue Shield of Illinois (or buyout option)</li>
<li>Dental and vision insurance</li>
<li>Term life insurance</li>
<li>Illinois Municipal Retirement Fund (IMRF) public pension</li>
<li>Paid time off available after 6 months</li>
</ul>
Why Join Us?
This is more than a job-it's a chance to protect natural spaces, mentor future conservationists, and serve the community through meaningful environmental work. If you're passionate about land stewardship and ready to grow your career in natural resource management, we encourage you to apply.
 
I understand that employment may be conditioned upon successfully passing a background check. 
I hereby affirm that the information provided on this application and accompanying resume, is true and complete. I understand that any false or misleading representations of omissions on the application or during the hiring process may disqualify me from further consideration for employment and may result in discharge even if discovered at a later date.
I hereby authorize DeKalb County Government to conduct or participate in an investigation of personal background, work history, licensure, and police record as may be necessary to verify the information provided in this application and to determine my fitness to hold the position for which I have applied.
I hereby authorize persons, schools, my current employer (if applicable) and previous employers and other organizations to provide DeKalb County Government with any requested information regarding my application or suitability for employment, and I completely release all such persons or entities from any and all liability related to the provided or use of such information.

Natural Resource Manager / Restoration Ecologist II

<h3>Job Description</h3>
Job DescriptionEmpirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines is seeking a chemist with an interest in solid-phase oligonucleotide synthesis and analytics. This is an excellent opportunity for a highly motivated, creative scientist to be a vital member of our team.Responsibilities:
<ul>
<li>You will be responsible for supporting the synthesis, purification, and characterization of oligonucleotides and their conjugates, and optimizing methodologies to support the development of siRNA medicines. The ideal candidate will have experience in organic and analytical chemistry and both upstream and downstream oligonucleotide manufacturing processes. A key focus of this role will be developing scalable processes suitable for technology transfer to CDMOs. You will be expected to –</li>
<li>Perform solid-phase synthesis, purification, and characterization of oligonucleotides</li>
<li>Develop and optimize scalable upstream (synthesis) and downstream (purification, formulation) manufacturing processes</li>
<li>Support process development activities to enable successful technology transfer to CDMOs</li>
<li>Analyze, interpret, and clearly communicate synthetic and analytical data</li>
<li>Present findings to senior staff and cross-functional teams</li>
<li>Troubleshoot and refine synthesis and purification protocols</li>
<li>Manage multiple projects simultaneously in a fast paced environment</li>
<li>Support GLP related activities and IND-enabling process development efforts</li>
</ul>
Requirements:
<ul>
<li>This position requires a BS in Chemistry with at least 12 years of relevant industry experience, or an MS in Organic Chemistry, Biochemistry, or Chemical Engineering with at least 7 years of relevant experience, or a PhD with at least 3 years of relevant experience.</li>
<li>Industry experience in solid-phase oligonucleotide synthesis is preferred, as well as familiarity with both upstream and downstream oligonucleotide manufacturing processes</li>
<li>Minimum 1 year of experience working in a cGMP environment with demonstrated understanding of cGMP principles</li>
<li>Hands-on proficiency with analytical instrumentation such as NMR, LC-MS, and RP-HPLC</li>
<li>Demonstrated ability in analytical and purification method development using RPIP-HPLC, AEX-HPLC, UV, MALDI, and HRMS</li>
<li>Background in process development and technology transfer to CDMOs, including development of scalable purification and formulation methodologies</li>
<li>Working knowledge of tangential flow filtration (TFF) method development</li>
<li>Experience supporting GLP studies and familiarity with regulatory expectations for IND-enabling work</li>
<li>Experience with lyophilization and aseptic fill/finish operations</li>
<li>Applicants must have authorization to work in the U.S.</li>
</ul>
The estimated annual base salary range for this role is $110,000 to $160,000. Individual compensation decisions will be based on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills.&nbsp; We offer a wide range of benefits including a retirement savings plan (with company match), paid vacation, holidays, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans. About Empirico: Empirico is a clinical-stage biotechnology company that discovers and develops siRNA medicines designed to mimic naturally-occurring genetic variants that confer beneficial effects on health and disease. Empirico’s two foundational and proprietary technology platforms - the Precision Insights Platform™ for genetically-validated target discovery, and the siRCH™ platform for the discovery and development of siRNA medicines - enable Empirico and its collaborators to rapidly advance programs from the discovery and validation of novel targets to clinically-viable therapeutics. Empirico’s exceptional internal capabilities, augmented by those of its partners, are driving the advancement of a growing and differentiated pipeline of wholly-owned and partnered programs for a broad range of common diseases with unmet medical need. Empirico is headquartered in San Diego, CA with a major second R&amp;D site in Madison, WI. We’re striving to build a strong culture of inclusivity, transparency and collaboration at Empirico, where our diverse and equitable workforce is empowered to contribute to our mission. We always seek the best candidate for the position and encourage you to apply even if your experience or qualifications don’t match up exactly with the job description. Empirico is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. To All Agencies: Please do not contact any employee of Empirico about this position. All resumes submitted by agencies to any employee of Empirico via-email or in any form and by any method will be deemed the sole property of Empirico, unless such agencies were engaged by Empirico for this position and a valid agreement is in place.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Senior Scientist - CMC

<h3>Job Description</h3>
Job Description
Our technician job involves testing raw materials and finished products, maintaining equipment, and supporting research and development or quality control teams. Specific roles can include Product Development Lab Technician or Coatings Application Lab Technician and responsibilities often require a variety of skills and adherence to safety protocols. (This position required HS diploma.) Training will take place on first shift, then will transfer permanently to 2:00 p.m. to 10:30 p.m. shift. Must have previous chemical, batch and/or paint blending experience. 
&nbsp;
<ul>
<li>Supporting color matching, product development, or coatings application projects.</li>
<li>Performing quality control tests on production samples.</li>
<li>Maintaining and troubleshooting laboratory equipment.</li>
<li>Collaborating with other teams and adhering to safety and quality standards.</li>
</ul>
&nbsp;
<ul>
<li>Education: A high school diploma or GED is often the minimum, but some positions require a bachelor's degree in a science-related field like chemistry or chemical engineering.</li>
<li>Experience: Entry-level positions may require little to no experience, while others may ask for 1-3 years in a lab environment.</li>
<li>Skills: General laboratory skills, data review, and the ability to follow instructions are essential. Specialized skills like using specific equipment or understanding regulations may also be necessary depending on the role.</li>
</ul>
&nbsp;
Company DescriptionRapidly expanding facility with ongoing anticipated growth focused on quick response to customer orders. 
<h3>Company Description</h3>
Rapidly expanding facility with ongoing anticipated growth focused on quick response to customer orders.

Chemical Laboratory Technician - 2nd Shift

<h3>Job Description</h3>
Job Description
Palermo Villa Inc. is looking for a high-energy, poised, and confident individual to assist in the development of concepts, products, and optimization projects through Palermo's vigorous consumer-driven R&amp;D process.
Associate Food Scientist Fulltime Milwaukee, WI $55,000-$60,000 Annually 
Who you’ll work for…
While most companies that sell Pizza have no real connection to Italy, Palermo’s passion for food and family reaches all the way back to the country where Pizza was born. “Papa Palermo” carried the cherished recipes to America from Sicily!
Innovation is at the heart of who we are. We use an entrepreneurial, forward-thinking approach resulting in high quality products that are consistently recognized by both the industry and consumers.
Our commitment to quality has made Palermo’s a leader in private label frozen Pizza and contract manufacturing!
Perks…
<ul>
<li>20 free Pizzas per month</li>
<li>Opportunity for training and career advancement</li>
<li>Paid Time Off and Floating Holiday of your choice</li>
<li>401k &amp; Roth with company match and fully vested on the 1st of the Month after Hire</li>
<li>Fantastic benefit offering starting on the 1st of the Month after Hire</li>
</ul>
Where you’ll work…
<ul>
<li>Located in Milwaukee’s Menomonee River Valley, Villa Palermo is a state-of-the industry manufacturing facility that adjoins our company headquarters.</li>
<li>Our high-tech pizza manufacturing operations include an on-site bakery to produce best-in-class crusts, robotic packaging equipment, and a 24-hour shipping and receiving facility.</li>
</ul>
When you’ll work…
<ul>
<li>The Associate Food Scientist role works predominantly day shift hours with occasional nights/weekends to complete projects.</li>
</ul>
What you’ll do…
<ul>
<li>Execute Product Development and/or improvement projects including formulating finished product and sub-assembly for pizzas.</li>
<li>Prepare small-scale samples for testing, document study results according to company procedures, and maintain a clean and organized environment with accurate recordkeeping.</li>
<li>Demonstrate strong knowledge of food science best practices to test materials, develop formulas improvements and/or new formulas, and prepare lab sheets.</li>
<li>Assist with PR events, food shows, food presentations and production presentations.</li>
</ul>
Why you’ll be successful…
<ul>
<li>Proven ability to provide support to the organization in the areas of food technology, product design, food manufacturing, and food safety.</li>
<li>Utilizing knowledge from your Bachelor’s Degree in Food Science, Biology, Chemistry, Culinary and any experience with food manufacturing, major food companies or restaurant industry.</li>
<li>Organized and methodical approach to problem solving – often in a time-sensitive, tight-deadline situation where accuracy is critical.</li>
<li>Passionate lifelong learner with a strong interest in mastering new techniques in the culinary arts and food science.</li>
<li>Team player with excellent communication skills ready to work hard to ensure the whole Palermo’s team succeeds.</li>
</ul>
How to join our team…
Let us learn a little more about how you'll fit on our team <a href="https://take.surveys.ci/s/PALEF7E657/79266" target="_blank">https://take.surveys.ci/s/PALEF7E657/79266</a>

Associate Food Scientist

<h3>Job Description</h3>
Job DescriptionSalary: 

Research Study Technical - Clinvet South Dakota
Our Story 
Clinvet South Dakota is a global veterinary contract research organization (CRO) that conducts preclinical and clinical trials to evaluate the safety, metabolism, and efficacy of animal health products. Clinvet SD is part of the Clinglobal group, which focuses on animal health and consists of various CROs dedicated to supporting innovation and product development.
Primary Job Role:
As a Research Study Technical Support, your primary responsibility will be to oversee the health and care of our livestock production animals, including swine, cattle, poultry, and more. You will also assist with routine basic study activities and provide support to the research team.
This position requires routine standing, moving, and lifting for extended periods of time.
Job Specific Duties and Responsibilities
<ul>
<li>Observe animals regularly, recognizing and reporting changes in eating or drinking habits, general behaviors, and outward signs of disease or abnormal appearance.</li>
<li>Provide basic animal husbandry for study animals, such as feeding and watering animals according to schedules and feeding instructions.</li>
<li>Do facility laundry and clean, organize, maintain, and disinfect animal rooms and facilities</li>
<li>Record and/or maintain animal health data or other data necessary for the operation of the facility or study conduct.</li>
</ul>
Provide routine assistance in study activities, common and more advanced technical procedures, and record-keeping responsibilities, following prescribed procedures and instructions, such as:
<ul>
<li>Handling and restraining animals</li>
<li>Observing and reporting changes in behaviors</li>
<li>Assist in collecting specimens</li>
<li>Recording and maintaining animal health data</li>
<li>Assist with administering medications and treatments</li>
<li>Mixing, dispensing, and storing feeds and special diets</li>
<li>Assist with transferring animals, equipment, and supplies</li>
</ul>
Qualifications, Training, and Experience Requirements:
<ul>
<li>No prior experience is required; however, candidates with relevant experience and education are encouraged to apply.</li>
<li>Experience in the operation of skid loader, tractor, and ability to drive livestock trailers is preferred.</li>
</ul>
Physical Requirements:
The employee must communicate effectively by talking, listening, reading, and writing professionally.
Employee must hold a valid drivers license.
At all times, the employee must be sober and free from the influence of any substances, including alcohol and legal recreational drugs, which could impair the ability to ensure the safety of animals, other staff members, and the quality of work.
Ability to regularly lift and maneuver up to 50 pounds.
Ability to remain on your feet and in constant motion for the duration of an eight-hour shift.
Salary and Benefits:
This position offers a starting hourly rate of $18.00. Salary is commensurate with experience and qualifications.
As a full-time employee, you will be eligible for Clinvet's insurance offerings, including health, dental, vision, short-term and long-term disability, and life insurance.
You will also be eligible to participate in the Clinvet 401(k) retirement plan, with the company matching up to 4% of your pay after one year of employment.
This position provides paid time off (PTO) and offers time and a half for working on holidays.
Other Information:
The position of Research Study Technical Support is a full-time role requiring 40 hours of work per week.
This position requires working rotating weekends and holidays, as well as overtime, depending on company needs.
A typical schedule for this position is from 8 AM to 5 PM.

Clinvet SD provides equal employment opportunities to all employees and applicants for employment. 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. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Research Study Technical Support

<h3>Job Description</h3>
Job DescriptionCordenPharma 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 &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. Our People VisionWe strive for excellence. We share our passion. Together, we make a difference in patients' lives.

SUMMARY
Performs and leads analytical research and development activities for the purpose of designing/improving a manufacturing process or technology as well as producing clinical trial batches by performing the following duties.

ESSENTIAL DUTIES AND RESPONSIBILITIES
Include the following. Other duties may be assigned.

<ul>
<li>Leads large and/or multiple teams to accomplish technology transfers and/or development projects.</li>
<li>Applies analytical and organic chemistry skills to the improvement of processes.</li>
<li>Responsible for participating in the budget process of research projects and/or technology transfers.</li>
<li>Initiates and executes the development of new and innovative analytical chemistry and methodology. Provides written analytical procedures and reports to support manufacturing and regulatory needs. Lead analytical technology transfer activities associated with a method or project.</li>
<li>Develops a comprehensive understanding of internal, corporate, and ICH stability guidelines to provide support to the Corden Stability Program</li>
<li>Develops and applies analytical techniques at a process scale (e.g., process chromatography)</li>
<li>Responsible for the analytical sections of process procedures</li>
<li>Develops key technologies and transfer strategies that function well in a manufacturing environment.</li>
<li>Plans and formulates aspects of analytical research and development proposals such as objectives or purpose of project, applications that can be utilized from findings, cost of project, equipment, and human resource requirements.</li>
<li>Identifies analysis points and develops methods, and procedures for monitoring projects. Devises and completes method validation studies.</li>
<li>Practices excellence in verbal and written communication skills to update management and clients on the current statuses of each project. Maintains documentation such as analysis data and procedures and progress reports in accordance with GLP and company policies.</li>
<li>Submits patents, presents at scientific conferences and company -wide forums, and publishes in scientific journals.</li>
<li>Investigates new analytical technologies and equipment with the aim of practical utilization in new and existing manufacturing processes.</li>
<li>Develops expertise in key advanced analytical techniques.</li>
<li>Analyzes batches of drug substance intermediates and raw materials to be used in clinical registration program.</li>
<li>Proposes analytical specifications for control of raw materials, intermediates, in-process testing, and drug substances for in-house use and regulatory filings.</li>
<li>Participates in manufacturing site activities, such as troubleshooting and analytical problem solving.</li>
<li>Develops thorough understanding of QEH&amp;S principles and regulatory affairs. Impacts analytical process development in at least two areas.</li>
<li>Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste.</li>
</ul>

LEADERSHIP &amp; 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 chemical processes. Expected to work interactively and collaboratively in a project team environment both internally and with clients.

May directly lead 1 – 5 employees. Carries out leadership responsibilities in accordance with Corden policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraise performance, reward and discipline employees; address complaints and resolve problems.

SAFETY &amp; ENVIRONMENTAL RESPONSIBILITIES
Every individual is personally responsible for the safety and environmental aspects of his or her 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.

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 (PhD) in Chemistry plus 3 years’ experience; or lower degree with 7 years related experience; or equivalent combination of education and experience.

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, clients, public groups, and/or boards of directors.

MATHEMATICAL SKILLS
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply statistical concepts such as significant figures, frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.

REASONING ABILITY
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form, and deal with several 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; and taste 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 frequently uses toxic and/or caustic chemicals as well as high potent compounds, and there is a risk of exposure. The employee is occasionally exposed to moving mechanical parts, outside weather conditions, and risk of electrical shock. 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.

<ul>
<li>Scientific leadership in analytical chemistry for API synthesis</li>
<li>Presentation and persuasion skills</li>
<li>Training and facilitation skills</li>
<li>Developed written and verbal communication skills</li>
<li>Complete understanding of cGMP and GLP requirements</li>
</ul>
 
SALARY
Actual pay will be based on your skills and experience.
BENEFITS
<ul>
<li>401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service </li>
<li>Accident Plan</li>
<li>Critical Illness Insurance</li>
<li>Dental Insurance</li>
<li>Disability Insurance</li>
<li>Employee Assistance Program</li>
<li>Flexible Spending Account</li>
<li>Health Insurance PPO/HSA</li>
<li>Hospital Indemnity Plan</li>
<li>ID Theft Protection</li>
<li>Life Insurance</li>
<li>Paid Parental Leave</li>
<li>Tuition Reimbursement</li>
<li>Wellness Program</li>
<li>Vacation – Three Weeks 1st Year</li>
<li>Vision Insurance</li>
</ul>

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 on February 13, 2026

Principal Analytical Chemist

<h3>Job Description</h3>
Job DescriptionJob Summary
The Chemical Service Technician is responsible for providing safe, reliable, and effective technical service support to customers within assigned territories. This role supports sales and customer operations by executing system assurance plans, assisting with new application start-ups, and maintaining chemical treatment systems. The technician plays a critical role in identifying customer needs, resolving technical issues, and ensuring consistent service delivery while adhering to safety and quality standards.
Key Responsibilities
<ul>
<li>
Provide routine technical service support to assist with executing customer system assurance plans
</li>
<li>
Support start-up of new chemical applications for both existing customers and new accounts
</li>
<li>
Deliver technical support by identifying customer issues, troubleshooting problems, and escalating as needed
</li>
<li>
Perform required chemistry testing, accurately log and report data, and maintain product inventories at customer sites
</li>
<li>
Install, calibrate, and maintain chemical feed systems and process monitoring equipment
</li>
<li>
Maintain safe, compliant, and efficient service operations at customer locations
</li>
<li>
Travel within assigned territory as required
</li>
</ul>
Minimum Qualifications
<ul>
<li>
High school diploma or equivalent
</li>
<li>
Valid drivers license with an acceptable motor vehicle record
</li>
<li>
Minimum age requirement to operate company vehicles
</li>
<li>
Ability to work independently and follow established service procedures
</li>
<li>
Immigration sponsorship not available
</li>
</ul>
Preferred Qualifications
<ul>
<li>
Associates degree or trade school certification
</li>
<li>
Previous technical service, field support, or field operations experience
</li>
<li>
Strong mechanical aptitude
</li>
<li>
Experience in water treatment or specialty chemical industries
</li>
<li>
Working knowledge of boilers, cooling towers, and wastewater treatment systems
</li>
<li>
Practical computer skills, including familiarity with standard office software and ability to learn internal systems
</li>
<li>
Demonstrated ability to work autonomously, manage multiple tasks, and maintain a strong work ethic
</li>
</ul>
Physical Requirements
<ul>
<li>
Ability to lift, push, pull, or carry up to 55 pounds
</li>
<li>
Role is safety-sensitive and may be subject to drug and alcohol testing
</li>
</ul>

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