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<h3>Job Description</h3>
Job DescriptionHarrington Geotechnical Engineering Inc. (HGEI) has over 50 years of experience in the geotechnical engineering field. With our experts, professional skilled staff and diverse experience, we offer reliable services in an integrated, efficient, and cost-effective service to clients in the public and private sectors. Our services include: Geotechnical Engineering, Geotechnical Engineering Laboratory Materials Testing, Engineering Geology and Environmental Engineering. We are growing and looking for a skilled and detail-oriented Soil Technician to join our team. About the Job: As a Soil Technician, you will be conducting field work and utilizing computer software for the input/output of soil data and geographical information. This position is also responsible for collecting and analyzing soil samples, conducting quality control inspections, and providing valuable insights to support projects. You will also need to demonstrate excellent verbal and written communication skills, positive attitude, good organizational skills, with a strong work ethic. Responsibilities: 
<ul>
<li>Collects soil data and compiles field maps displaying geographical information and the compilation of soils suitability and capability maps for the Soils Resource Mapping Program.</li>
<li>Compiles all background information including topographical maps and aerial photographs for specified mapping areas.</li>
<li>Conducts field work and records specific soils data; collects and processes soil samples in accordance with samples.</li>
<li>Provides technical support for the use of data loggers.</li>
<li>Performs equipment, soils reports and map inventory and facilitates inventory and maintenance schedule for ATV’s, field equipment and logistical supplies.</li>
<li>Maintains liaison with other staff in the Agrifoods Branch, other government departments and agriculture industry groups to acquire data for the completion of field mapping projects.</li>
<li>Prepares activities and attends agricultural fairs and workshops and liaises with public to promote the Soils Resource Mapping Program.</li>
<li>Conducts routine office duties such as annual soils reports, maintaining map inventory and report filing.</li>
</ul>
Requirements: 
<ul>
<li>Minimum 2 to 3 years of experience with proven experience as a Soil Technician or similar role</li>
<li>Strong knowledge of soil surveying and data collection methods/techniques with GIS and related mapping applications software</li>
<li>Familiarity with construction inspection processes and procedures</li>
<li>Proficient in analyzing soil samples in a laboratory setting</li>
<li>Excellent attention to detail and ability to accurately record data</li>
<li>Ability to interpret engineering plans and specifications related to soil conditions</li>
<li>Strong communication skills to effectively collaborate with engineers and construction teams</li>
</ul>
Note: This job description is not intended to be all-inclusive. The employee may be required to perform other related duties as assigned. Competencies: 
<ul>
<li>Written and verbal communication skills</li>
<li>Word processing, spreadsheet and database skills</li>
<li>GPS and GIS usage</li>
</ul>
If you meet the above requirements or know of anyone that maybe suitable to join our team, please apply with your updated resume. We look forward to reviewing your application.

Soil Technician

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJoin a team where science meets purpose!
We’re looking for a detail-oriented and driven Analytical Chemist to support critical testing operations in a fast-paced pharmaceutical environment. If you're passionate about precision, thrive in a collaborative setting, and are ready to make an immediate impact, we want to hear from you.
What You’ll Do
<ul>
<li>Perform routine and advanced chemical testing using cutting-edge techniques and instruments.</li>
<li>Operate and maintain specialized lab equipment including HPLC, GC, ICP, and more.</li>
<li>Lead and support investigations to troubleshoot and resolve analytical issues.</li>
<li>Ensure strict adherence to cGMP standards, data integrity, and documentation practices.</li>
<li>Collaborate with cross-functional teams to support raw material testing and product release.</li>
</ul>
What You Bring
<ul>
<li>Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.</li>
<li>Hands-on experience in the pharmaceutical or biotechnology industry.</li>
<li>Proficiency with analytical instruments such as HPLC, GC, and ICP.</li>
<li>A strong understanding of regulatory compliance and quality standards.</li>
</ul>
Why Join Us?
<ul>
<li>Be part of a mission-driven organization focused on improving patient outcomes.</li>
<li>Work in a collaborative, innovation-focused environment.</li>
<li>Gain exposure to advanced technologies and industry-leading practices.</li>
</ul>
Pay and Benefits
The pay range for this position is $65000.00 - $80000.00/yr.
Health Vision 401 K Dental Relocation Assistant
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Jul 16, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job Description Description:
Job Title: Lab Supervisor Department: Quality Control / Laboratory Reports To: Lab Manager Type: Full-Time 
 
Note: This position requires applicants to successfully pass a pre-employment, as well as an annual pulmonary function test (PFT). This position may expose the employee to isocyanates which are chemicals known to be respiratory irritants and sensitizers. While TSE provides personal protective equipment (PPE) to its employees working around such chemicals, the most current and best available medical data indicate that individuals with pre-existing respiratory conditions including but not limited to asthma, chronic bronchitis, emphysema, and the like are at high risk of experiencing serious, and possibly fatal reactions to isocyanates, even at concentrations below the legally permissible exposure level (PEL). Therefore, due to this direct threat to their safety, TSE does not hire individuals with pre-existing respiratory conditions to work in this position. 
 
Position Summary: The Lab Supervisor supports the Lab Manager in the day-to-day operations of the laboratory within a chemical manufacturing environment. This role ensures effective execution of laboratory processes, supervises lab personnel in the absence of the Lab Manager, and contributes to maintaining ISO 9001 compliance. The Lab Supervisor plays a key role in quality control for raw materials, in-process products, and final finished goods, and also assists with training new team members and scheduling lab activities. 
 
Key Responsibilities:
<ul>
<li>Supervise laboratory staff and daily lab activities in coordination with or in the absence of the Lab Manager. </li>
<li>Assist in scheduling lab shifts and tasks to ensure timely completion of testing and quality activities. </li>
<li>Perform quality control testing on incoming raw materials, in-process batches, and final products, ensuring conformance to company specifications and regulatory standards. </li>
<li>Approve or reject finished products based on lab results and quality standards. </li>
<li>Participate in ISO 9001 quality management system activities, including audits, documentation, and continuous improvement efforts. </li>
<li>Help oversee adherence to safety and compliance protocols within the lab environment. </li>
<li>Provide guidance and training to new lab employees to ensure accurate and consistent testing practices. </li>
<li>Support investigation of non-conformances and contribute to root cause analysis and corrective actions. </li>
<li>Maintain and calibrate lab instruments and ensure accurate recordkeeping of test results and logs. </li>
<li>Assist the Lab Manager in data review, reporting, and development of lab-related procedures and policies. </li>
</ul>
Teamwork is essential for TSE's continued success, so Teamwork is an essential function of every employee's job. Teamwork drives positive results every day. Teamwork promotes positive customer relations and results in exceeding the expectations of our customers. Teamwork benefits every employee since it grows our business and increases our sales. With Teamwork, we all succeed. Without it, we all suffer. Teamwork with co-workers in the same department is just the beginning. Teamwork with every other employee, department and division is the Teamwork that is required to succeed. WE ARE TSE.
Requirements:
Qualifications:
<ul>
<li>Bachelor's degree in Chemistry, Chemical Engineering, or a related scientific field. </li>
<li>3+ years of experience in a chemical laboratory setting; prior supervisory or team lead experience preferred. </li>
<li>Familiarity with ISO 9001 quality systems and documentation practices. </li>
<li>Strong understanding of laboratory safety protocols, chemical testing, and quality control procedures. </li>
<li>Excellent organizational and communication skills. </li>
<li>Proficiency with lab data systems and Microsoft Office Suite. </li>
<li>Ability to lead by example and maintain a team-oriented, high-performance work environment. </li>
</ul>
Working Conditions: This position is primarily based in a laboratory environment and requires the use of appropriate personal protective equipment. Some exposure to chemicals, noise, and equipment is expected.
 
Compensation details: 55000-55000 Yearly Salary
 
PI1f153cc5bb2a-25405-37612465

Lab Supervisor

<h3>Job Description</h3>
Job DescriptionSalary: $45,000-$55,000 
Why DelRicht Research?
 
DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states.
 
DelRicht Research has been recognized as one of New Orleans Top Workplaces for 2023 and 2024!This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction.
 
Healthcare Project Coordinator Main Objective: The Administrative Assistant will assist our Regulatory Team with providing high level, centralized support organizing and running the busy day-to-day operations of our numerous clinical research sites throughout the US. 
 
Outcomes Administrative Assistant is Responsible for Achieving:
<ul>
<li>Key resource in allowing our clinical research sites to provide excellent customer service to our patients, physicians and sponsors</li>
<li>High level of autonomy and responsibility in role</li>
<li>Maintain fast, industry leading study start up times by completing initial trial documents within 3 days of receipt</li>
<li>Evaluate whether sites are in compliance with Regulatory compliance standards</li>
<li>Understand company policies and operating procedures and effectively communicate them to Clients</li>
</ul>
 
Job Description:
The Administrative Assistant will maintain all activities related to the general operations of our clinical research sites and offices including but not limited to:
<ul>
<li>Helps complete documents required to initiate new clinical research trials</li>
<li>Ensures quality documentation and training throughout each clinical trial, including processing clinical trial amendments</li>
<li>Maintains site staff certifications</li>
<li>Responds to client inquiries regarding requests for information</li>
<li>Supports clinical research sites and team cohesion by providing clear and consistent communication regarding clinical trial activities</li>
<li>Assists in the initial set up of new clinical trial Sites</li>
<li>Monitors and maintains equipment used for clinical trials</li>
<li>Computer Skills:
<ul>
<li>Email management</li>
<li>Excellent with Apple computers and all Google Workspace applications</li>
</ul>
</li>
</ul>
 
Skills needed to win:
<ul>
<li>Required: B.S or B.A from any accredited university or equivalent work experience (1-2 years professional experience)</li>
<li>Required: 1+ years administrative and/or assistant experience is a plus</li>
<li>Required:Exceptional organizational skills</li>
<li>Clinical Research or Regulatory experience is not required but always a plus!</li>
<li>Coffee drinkers preferred. Tea drinkers accepted.</li>
</ul>
 
The Right Candidate Will:
<ul>
<li>Be self motivated! Energetic! Positive!</li>
<li>Be remarkably organized</li>
<li>Be skilled at problem solving</li>
<li>Accept ownership of tasks from inception through completion and assume responsibility for personal success</li>
<li>Love efficiency and continuously look for ways to do more with less, improve processes and come in under budget</li>
</ul>
 
The Company Culture You Will Be Part Of:
 
DelRicht Researchs Core Values: Production, Humility, Consistency
 
Production:
<ul>
<li>We deliver on our promises</li>
<li>We have a bias towards action: we value independent problem solving</li>
<li>We proactively over deliver: we can act without being told what to do and we always have new ideas that will be heard and will improve the company</li>
</ul>
 
Humility:
<ul>
<li>We support each other relentlessly</li>
<li>We always have enthusiasm: we exhibit passion and excitement about our work which leads to everyone having a can do attitude</li>
<li>We embrace change: we are excited to always be growing and moving the organization forward which means change is the norm for us</li>
<li>Coachable: we all love to learn, we are willing to be taught and will adapt quickly</li>
</ul>
 
Consistency:
<ul>
<li>We always are able to execute: we get it right the first time and promote touch it once accuracy</li>
<li>We have persistence: we demonstrate the tenacity and willingness to go the distance to get something done</li>
<li>We are calm under pressure: we can maintain stable performance when under heavy pressure or stress</li>
</ul>
 
Our team comes first so here are some of the perks and benefits at DelRicht Research:
<ul>
<li>Medical, Dental, Vision, Short &amp; Long Term Disability and Life Insurance (group rates!)</li>
<li>Generous Paid Time Off that builds throughout your career with the company</li>
<li>No nights or weekends</li>
<li>401K (+ discretionary match/profit sharing)</li>
<li>Exceptional quarterly bonus plan that clearly outlines your bonus potential per quarter and giving the team the visibility and control to maximize earnings by hitting team goals</li>
<li>Job Type: Full-time, 40+hours </li>
</ul>
 
We are an equal opportunity employer and considers all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

Healthcare Project Coordinator

<h3>Job Description</h3>
At Keurig Dr Pepper (KDP), innovation and impact drive everything we do. Guided by our vision — Drink Well, Do Good — our Product Development team leads the charge in delivering breakthrough innovations, driving productivity, and elevating the performance of our portfolio.
This Senior Scientist role within Research and Development will support the beverage product development agenda by executing our product modernization, brand integration, and compliance initiatives across our cold beverage portfolio. The Senior Scientist will work in a dynamic environment to develop and commercialize formulations in support of our strategic objectives. 
 
 
Your work will directly contribute to our mission by refining and improving our portfolio of amazing consumer brands. This is an exciting opportunity to be part of a forward-thinking team that continuously strives to redefine what’s possible in beverage development.
 
 
 
POSITION ACCOUNTABILITIES
<ul>
<li>Leads and develops the product development product strategy to meet the consumer need states across the KDP Cold portfolio (CSD, Juice, Water, Tea, Energy, Sauce, Mixers, and other)</li>
<li>Conducts bench-top work, pilot plant, and manufacturing trials to verify and support formula accuracy and documentation across projects within the KDP portfolio</li>
<li>Leads complex test and research trials to gain insights into key product development challenges and opportunities, writing technical reports, and effectively communicates information within the organization</li>
<li>Conducts feasibility and impact analysis for formula change opportunities</li>
<li>Takes initiative to strategically develop new ideas to build the product pipeline, rooted in brand improvement, technology advancement, and regulatory landscape</li>
<li>Fully understands R&amp;D functions and broadly understands the greater KDP organization</li>
<li>Proactively partners and engages with various functions of R&amp;D (Sensory, Ingredients, Nutrition, Regulatory, Flavor Technology, Packaging, Chemistry, Process Engineering)</li>
<li>Manages and leads complex initiatives with cross-functional peers consisting of across R&amp;D, Marketing, Supply Chain, Sales</li>
<li>Delivers updates on strategic initiatives within business to key stakeholders and senior leaders</li>
<li>Effectively communicates technical information to senior leadership </li>
<li>Proactively identifies and implements opportunities for improvement within function</li>
<li>Maintains accurate and detailed record of laboratory work</li>
<li>Work appropriately and safely in a laboratory environment</li>
<li>Use formulation software to document lab work and formulas </li>
<li>Demonstrate flexibility and resilience in adapting to changing business needs and priorities</li>
<li>Ability to earn trust, maintain positive and professional relationships, and strengthen our culture of inclusion</li>
</ul>
 
 
 
 
Benefits:
 
Our people are the heart of our business, which is why we offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at Keurig Dr Pepper.
 
 
 
 
 
 
Requirements:
 
<ul>
<li>BS in Food Science, Chemical Engineering, MS/MBA is preferred</li>
<li>7 years of experience in a related function within food/beverage (R&amp;D, Quality), CPG, and/or commensurate advanced education </li>
<li>Ability to work independently and in a team environment.</li>
<li>Excellent written and presentation skills</li>
<li>Works independent, excels in team-based culture and collaborates </li>
<li>Skilled in problem solving, with a growth mindset</li>
<li>Ability to travel is required</li>
</ul>
 
 
 
 
 
 
 
 
Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partners brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! 
Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that’s proud of its brands, partnerships, innovation, and growth. Will you join us? 
We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~28,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work.
Keurig Dr Pepper is an equal opportunity employer and affirmatively seeks diversity in its workforce. Keurig Dr Pepper recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law.

Senior Scientist

<h3>Job Description</h3>
Trillium Renewable Chemicals 
Chemical Lab Technician 
Location: Onsite role&nbsp;
 
Trillium Renewable Chemicals is building a more sustainable future through chemistry. We have raised Seed, Series A, and Series B financing rounds and have been featured in Bloomberg, Chemical &amp; Engineering News, won multiple Department of Energy Awards, and were named one of the Top 10 Startups for 2023. Our patented technology converts renewable feedstocks like glycerol to acrylonitrile, a monomer for acrylic fibers, carbon fibers, and other valuable raw materials like ABS (acrylonitrile-butadiene-styrene) plastic. We are building a demonstration scale plant deemed “Falcon” that will begin operations in 3rd Quarter, 2025. The plant will be located at INEOS Nitriles in Port Lavaca, Texas. We are looking for an experienced chemical lab technician to support activities related to the design and operation of Falcon.
 
Responsibilities
<ul>
<li>Conduct chemical and physical laboratory tests of solids, liquids, and gaseous materials.&nbsp;</li>
<li>Prepare chemical solutions for products or processes following standardized formulas.&nbsp;</li>
<li>Maintain a safe work environment by participating in chemical hygiene and safety programs.&nbsp;</li>
<li>Order and inventory materials to maintain supplies.&nbsp;</li>
<li>Maintain and clean laboratory instruments and equipment.&nbsp;</li>
<li>Provide technical support to chemists and engineers.&nbsp;</li>
</ul>
 
Qualifications
<ul>
<li>4+ years of experience in an industrial laboratory setting</li>
<li>Bachelor's degree in a science-based discipline. Biology or Chemistry degree is preferred. </li>
<li>Will consider experienced candidates with associate’s degree or technical certification </li>
<li>Proficient in lab methods and techniques such as GC, spectroscopy, titrations, and handling hazardous materials.&nbsp;</li>
<li>Strong computer skills and experience </li>
<li>Familiarity with following test methods, such as ASTM, EPA, and ISO methods&nbsp;</li>
<li>Must be able to perform work with minimal direct supervision&nbsp;</li>
<li>Eligibility to obtain a Transportation Workers Identification Card (TWIC)&nbsp;</li>
</ul>
 
Physical Requirements&nbsp;
<ul>
<li>Job conditions require standing, sitting, stooping, twisting, crouching, kneeling, and climbing ladders 8-12 hours a day.&nbsp;</li>
<li>Job conditions require the employee to be able to make visual inspections, perceive color differences, and manipulate objects with precise hand and finger movements.&nbsp;</li>
<li>Job conditions require the employee to lift, carry, push, or pull up to 30lbs.&nbsp;</li>
<li>Job conditions require wearing personal protective equipment, especially chemical resistant gloves and full-face respirators. Beards are not permitted at the work site.&nbsp;</li>
</ul>
 
Location and Travel
The Falcon unit will be located at INEOS Nitriles, Port Lavaca, Texas. Depending on the location of the selected candidate, significant business travel will be required to the INEOS site.
 
Salary
$30 - $45 per hour depending on experience&nbsp;

Chemical Lab Technician

<h3>Job Description</h3>
Job Title: Associate Scientist
Location: Oceanside, CA (100% Onsite)
Duration: 2 Months
 
Working Hours: Monday-Friday, 8:30am-5:30pm
Focus: Downstream Process Development
 
Role: The Associate Scientist/Sr Associate Scientist, Purification Process Development (Pivotal and Commercial) role will contribute to all aspects of purification development including process development and process characterization at internal or external facilities for client biologics entities during pivotal and commercial development phases.
 
Specific Responsibilities:
Contribute to experimental design. Plan and execute assigned purification process development laboratory studies. Support process scaleup and implementation in internal and external GMP facilities.
Collect and analyze data from laboratory experiments in compliance with data integrity policy. Author experimental protocols and reports.
Support process transfer to internal and contract manufacturing facilities to produce GMP and non GMP drug substances on time and with high success rate***
Provide technical support for manufacturing atypical event investigations.
Ensure high-quality documentation in electronic laboratory notebooks, protocols and reports.
Mentor junior team members on purification process development strategies, experimental design and execution as well as process transfer.
Help to establish and maintain a state-of-the-art purification lab.
Execute purification platform development and new technology/innovation evaluation and implementation to enable pivotal clinical trials.
Participate in cross functional initiatives as needed.
Adhere to department budget and all training, compliance and safety requirements.
 
Education &amp; Experience:
M.S. with 3+ years or B.S. with 5+ years in a relevant scientific discipline (chemical engineering, biochemistry, bioengineering).
 
Knowledge, Experience and Skills:
Hands-on laboratory operations experience with purification process operations including centrifugation, normal flow filtration, chromatography operations, tangential flow filtration, and virus inactivation/removal is required.
Experience with AKTA chromatography systems and UNICORN software is required
Experience in pivotal stage purification process development, characterization, and implementation in GMP facilities. Antibody drug conjugate experience is a plus.
Excellent communication, technical writing, and presentation skills and aptitude for creative problem solving.
Experience writing CMC sections of commercial regulatory filings (BLA, MAA) and post approval change filings is a plus.
Demonstrated ability to collaborate and influence cross-functionally.
Experience in statistics, design-of-experiments, and data analysis (e.g. JMP, Spotfire).
Working knowledge of lab automation, data management, data science, knowledge management and data protection is a plus
 
Must Have's:
Plan and execute assigned purification process development laboratory studies.
Collect and analyze data from laboratory experiments in compliance with data integrity policy. Author experimental protocols and reports.
Experience in pivotal stage purification process development, characterization, and implementation in GMP facilities
 
Preferred Requirements:
AKTA operation
TFF Filtration/Viral Clearance
Hamilton purification/High-throughput system operation

Associate Scientist

<h3>Job Description</h3>
Top 3 Required skills: 
<ul>
<li>GIS Development with ArcGIS Web App Builder, Able to communicate with Business stakeholders to capture business requirements, Review and Lead the development team work.</li>
<li>Years of experience in each of the must-have skills: 10+</li>
<li>Need to be able to work with other Integration teams to understand and co-ordinate on Integration issues Need to be able to Support team in developing and implementing highly responsive user interface components Need to be Self driven and Self motivated</li>
</ul>
 
Must haves:
<ul>
<li>10+ year of experience in ArcGIS Development and Esri Technologies</li>
<li>Strong working experience with ArcGIS Suites including ArcGIS Desktop/ArcGIS Pro, ArcObjects, ArcSDE, ArcGIS Enterprise, ArcGIS Web App Builder</li>
<li>Experience in GIS based web application development using JavaScript, TypeScript, jQuery, HTML, CSS, Bootstrap</li>
<li>Reviewing application requirements and interface designs.</li>
<li>Supporting team in developing and implementing highly responsive user interface components.</li>
<li>Be able to communicate with End users and understand end-user requirements.</li>
<li>Supporting team in developing and implementing highly responsive user interface components.</li>
<li>Meeting with the development team to discuss user interface ideas and applications.</li>
<li>Monitoring and improving application performance.</li>
<li>Ability to work in team in diverse/ multiple stakeholder environment</li>
<li>Analytical and troubleshooting skills</li>
<li>Excellent communication and collaboration skills to work with business users</li>
</ul>
Good to haves:
<ul>
<li>Working experience with ArcGIS Web Experience Builder</li>
<li>Strong working experience in developing applications using ArcGIS JavaScript 4.x,</li>
<li>Strong working experience in developing Oracle Packages / Procedures / functions &amp; PLSQL</li>
<li>Supporting integrative systems and Integrate data storage solutions.</li>
<li>Extend support in design and create effective applications.</li>
</ul>

Senior GIS Developer

<h3>Job Description</h3>
Job Description: Associate Scientist, Analytical Chemistry – Fort Worth Analytical, Pharma R&amp;D
 
• This laboratory position in the Research and Development Analytical Chemistry department provides support to ophthalmic drug development programs.
• The selected individual will have key responsibility for analytical testing supporting a range of activities including general sample analysis, analytical method development, analytical method validation, method transfer, stability, and investigative studies to trouble-shoot issues.
• The position is laboratory based and will involve support work for internal and external projects.
• The individual provides analysis and evaluation of materials and products at all stages of the product development process.
 
SKILLS AND RESPONSIBILITIES:
 
• Perform analytical chemistry in collaboration with others to develop and validate analytical methodology, including stability-indicating HPLC methods, GC methods, Karl Fischer for new drug substances and products.
• Perform and verify compendia methods when appropriate.
• Generate analytical data for new and existing methods to trouble-shoot issues.
• Assists in the design and execution of clinical phase-appropriate method validation protocols.
• Executes stability studies to support the development of new drug substances or drug products.
• Compiles laboratory data.
• Assists laboratory investigations for aberrant and out-of-specification data.
• With assistance, author technical documents such as method development/validation reports, stability reports, and certificates of analysis.
• Able to maintain laboratory records and provide peer review and approval of quality critical data.
• Able to independently schedule work activities and maintain laboratory supplies and equipment.
• Authors and/or reviews standard operating procedures pertaining to analytical testing and reporting.
• Able to execute investigational studies in collaboration with others to address specific issues.
• Conducts work in compliance with cGMP, safety, and regulatory requirements.
• Provides analysis and evaluation of materials and products at all stages of development and for their area of focus.
Comments for Suppliers:

Analytical Chemist

<h3>Job Description</h3>
Client - Financial Services 
Title - Quantitative Analyst 
Location - NYC, Wilmington DE, Baltimore MD (Hybrid)
Job Description: 
<ul>
<li>Reporting, strategy implementation, strategy validation and ad-hoc analyses including customer segmentation, competitive analysis, sensitivity analysis and modeling, and performance read.</li>
<li>Expand competencies and grow business / industry acumen</li>
<li>Demonstrate the ability to work on complex processes or projects across the end-to-end project cycle.</li>
<li>Gain knowledge to suggest new answers to old questions, develop insights and push the traditional boundaries of the lending industry.</li>
</ul>
 
Key Responsibilities:
<ul>
<li>Under your manager’s limited guidance, you will design, recommend, document and execute consumer credit underwriting and pricing strategies via extracting and analyzing requisite historical customer performance data from multiple disparate systems.</li>
<li>Utilize data query tools (i.e., R, SAS, SQL, MATLAB, Python) and decision tree analytical software to develop, test and execute new strategies.</li>
<li>Leverage traditional regression model and machine learning algorithm to understand the key drivers and estimate customer behaviors by different strategy treatment</li>
<li>Drive profitable business growth via developing strategy optimization framework with full credit-cycle view</li>
<li>Implement Quality Control processes to ensure data accuracy.</li>
<li>Continually enhance existing processes and reporting through automation, quality control, presentation and insights.</li>
<li>Effectively summarize and present results and insights to management.</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor Degree (Graduate Preferred) in a quantitative discipline, such as Engineering, Statistics, Economics, Business Management or Computer Science is preferred.</li>
<li>4+ years of experience in complex, data-driven problem solving. Master’s or PHD degrees may offset experience.</li>
</ul>

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