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<h3>Job Description</h3>
Job DescriptionOverview:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.&nbsp;&nbsp;&nbsp; &nbsp;Position:&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;&nbsp;Scientist II - Chemistry / Formulation ChemistLocation:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Middletown, VA - 22645Duration:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp; &nbsp; 6 Months&nbsp;Job Type:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Temporary Assignment&nbsp;Work Type:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;Onsite&nbsp; &nbsp;Shift Timings:&nbsp; &nbsp;Monday to Friday 08:00 AM to 05:00 PM&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;Summary&nbsp;We are&nbsp;seeking a senior Chemist to assist our clients Water Analysis Instruments manufacturing organization. The candidate will support the ongoing transfer to regular manufacturing of water-based chemical solutions including pH buffers, chemical reagents, and ion-specific variants. Project work will focus on updating and optimizing the manufacturing process of these solutions. This hands-on position requires problem-solving, teamwork, excellent communication, and experience in reagents manufacturing processes.&nbsp;&nbsp;Responsibilities&nbsp;
<ul>
<li>Design, test, and manufacture lab solutions.</li>
<li>Optimize current solution manufacturing processes to improve quality, reduce costs, improve regulatory compliance, and resolve documentation issues.</li>
<li>Oversee production of solutions, review documentation, and collaborate with team and facilities to streamline processes.</li>
<li>Review and update production documentation; work with Quality and SMEs to align instructions to actions.</li>
<li>Apply process metrics and KPIs to identify areas of improvement and characterize process enhancements.</li>
<li>Perform root-cause investigations on systems and components to correct problems and improve product quality and reliability.</li>
<li>Interface with Manufacturing, Technical Operations, Compliance, Quality, Purchasing, and Product Management groups.</li>
</ul>
Required Skills
<ul>
<li>Bachelor’s or Master’s degree in Chemistry or Chemical Engineering.</li>
<li>Strong knowledge of electrochemistry, formulation science, chemical processes, and process engineering principles.</li>
<li>Strong hands-on experience in Technical Writing</li>
<li>Minimum 3 years of manufacturing experience within an ISO 13485 environment.</li>
<li>Knowledge and experience in Analytical Chemistry.</li>
<li>Knowledge and experience with conductivity, water testing, ISE design, electrode manufacture, ionic strength adjustment solutions, and titration.</li>
<li>Familiarity with Bill of Materials (BOM).</li>
<li>Excellent problem-solving skills and attention to detail.</li>
<li>Excellent communication and interpersonal skills.</li>
<li>Ability to work independently and manage multiple projects simultaneously.</li>
<li>Ability to communicate and work well in cross-functional team environments.</li>
<li>Adept at working in a fast-paced setting and acting with urgency.</li>
</ul>
TekWissen® Group is an equal opportunity employer supporting workforce diversity.&nbsp; 
TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.
Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.
TekWissen® is an equal opportunity employer supporting workplace diversity.&nbsp;

Formulation Chemist

<h3>Job Description</h3>
Job DescriptionSalary: $45,000 - $50,000/year 
Magnolia Plantation &amp; Gardens, one of the nations oldest and most visited historical public gardens, is seeking a Wildlife Center Manager to lead the management and operations of the Wildlife Center. This role involves training and overseeing the Wildlife Center team and volunteers, ensuring effective animal care through operant conditioning techniques, and spearheading new programming initiatives to enhance guest engagement and education. The Wildlife Center Manager will also be responsible for maintaining animal enclosures, supporting veterinary care, and serving as the primary point of contact for facility coordination and program evaluation.
 
What you will be doing:
<ul>
<li>Offer dynamic leadership to direct reports and volunteers and create schedules that maximize guest interactions. Ensure staff receive appropriate training and safety guidance.</li>
<li>Engage with guests and stakeholders regarding the Wildlife Center and its mission, animal care programs and conservation initiatives such as supporting Marketing and media requests that relate to Animal Care.</li>
<li>Collaborate with the Education department in the design and implementation of programs related to the Wildlife Center for tour groups, on-site events, school groups, and pop-ups.</li>
<li>Establish and maintain animal husbandry protocols and procedures that meet and/or exceed all SCDNR, USDA, USFWS, and community standards. Update and maintain animal health, behavior, and training records.</li>
<li>Coordinate the purchase, pick-up, and ordering of supplies and food.</li>
<li>Perform daily husbandry duties for a wide range of animal species including but not limited to reptiles such as snakes and alligators, birds of prey, carnivores such as a bobcat.</li>
<li>Observe animal behavior to be able to interpret and distinguish signs of unusual behavior which may indicate illness/injury.</li>
<li>Perform deep cleans, routine maintenance, upkeep, and small-scale repairs of enclosures and holding areas as needed. On occasion requiring the use and operation of a compact tractor.</li>
<li>Manage reconfiguration of enclosures and habitat development; install and maintain appropriate perching and enclosure accessories essential to species-specific husbandry requirements.</li>
<li>Maintain tools and equipment used in daily animal care and exhibit maintenance.</li>
<li>Represent a team-player spirit when assigned other duties as required. </li>
</ul>
 
Who you are:
<ul>
<li>You are wildly passionate about animals and educating the public. Youve got a degree in a relevant field such as but not limited to Biology, Ecology, or Animal &amp; Veterinary Science and 3+ years of experience (internships and volunteer work included) in a captive wildlife setting. Experience from a zoo, aquarium, nature center or comparable facility is preferred!</li>
<li>Youve got a strong knowledge of the natural history of the southeastern USA, including identification, ecology, and conservation. You have the ability to interpret unique adaptations and behavior for a wide variety of native species found within the region.</li>
<li>You are comfortable connecting with a wide variety of people, and do so by flexing your presentation style to meet the unique needs and backgrounds of the people youre with</li>
<li>Youre tech savvy, and utilize technology to not just streamline and automate process, but to collect data to support decisions regarding the care and interactions with animals.</li>
<li>As Magnolia is a tourist attraction, this position may require long-days and/or work on the weekends as needed. Were mindful that in order for you to be the most effective in your role, its important that you balance that work with time to rest, so we offer generous PTO and other benefits to support you.</li>
</ul>
 
Employee Benefits:
<ul>
<li>Magnolia realizes the importance of a healthy work/life balance and offers a generous amount of PTO, Sick Days &amp; Paid Holidays.</li>
<li>Happy Birthday.. off! If you are scheduled to work on your special day, you can request 8 hours of pay.</li>
<li>Magnolia contributes 80% of medical premiums for employee-only coverage and 40% to all other levels of coverage.</li>
<li>No cost $10,000 life &amp; accidental death and dismemberment (AD&amp;D) insurance.</li>
<li>401K retirement plan matching at 3%.</li>
<li>If enrolled in our medical plan, access to covered MinuteClinic and Teledoc services are offered to you free or at a lower cost. Covered medical participants can also enjoy Peerfit (helps you stay active with monthly credits that can be redeemed for group fitness classes), Wellness tools (health assessment and online programs to help you meet your goals), Discount program (helps you save on health products and services), 24/7 Employee Assistance Program (helps in all aspects of life, from emotional well-being, legal and financial help), behavioral telehealth/virtual providers and services, no-cost diabetic meters and enhanced maternity program. Plan participants are also offered free, online will preparation with claimant support services and emergency travel assistance.</li>
</ul>
Employee Discounts
<ul>
<li>Experience our history, horticulture and nature with your loved ones! Employees can host their immediate family members (on non-scheduled working days) to Magnolia! This includes free admission to the gardens and to all tours. If immediate family members visit during an employee's scheduled working day, eligible family members are welcome to visit the gardens with free admission. Please contact the Welcome Center for more information.</li>
<li>Save 50% on all on-site venue rentals (includes standard fees), 40% off at our charming Gift Shop and meal discounts at our impeccable Peacock Cafe!</li>
<li>Employees and their immediate family members can join Community Events for free!</li>
<li>Enjoy discounted pricing for Magnolia's prime Special Events.</li>
<li>Earn your Reciprocal Admission Pass after your first 90 days! This gold pass allows you and one guest free admittance to over 40 participating attractions such as: SC Aquarium, SpiritLine Cruises, Charleston County Parks, Children's Museum of the Lowcountry and many more!</li>
<li>Team Members are provided company branded uniform items at no cost!</li>
</ul>
Training &amp; Development
<ul>
<li>No-cost continuing education training for current licenses that benefit both you and MPC.</li>
<li>Limitless internal training and development opportunities!</li>
</ul>
Additional Perks
<ul>
<li>It really pays! Referral bonus for an employee's referral that is hired and completes three months of service. $500 for full-time hires and $250 for part-time hires.</li>
<li>6mi of Biking and Walking Trails for you to use.</li>
</ul>

Wildlife Center Manager

<h3>Job Description</h3>
Job DescriptionSalary: $85K-$110K 
 
Mason Interactive | Hybrid (3 days in office) | $85K-$110K
 Who We Are
Mason Interactive is a 30-person full-service digital agency with offices in Brooklyn and Charlotte. We work with clients in education, fashion, wellness, and luxury across all channels: paid search, paid social, SEO, programmatic, creative, and affiliate.
 
What You'll Do
<ul>
<li>Own paid search performance. No hand-holding. You will manage campaigns across a diverse client base, identify growth opportunities, and speak up when you see potential. Our client services team handles client calls so you can focus on what matters: driving results.</li>
<li>Collaborate across channels. Work with our SEO, paid social, programmatic, and creative teams to build integrated campaigns that actually work together for your clients .</li>
<li>Think like an owner. Take full accountability for performance. Challenge strategies when data says otherwise. Push for better results.</li>
</ul>
 
What You Need
<ul>
<li>5+ years managing paid search campaigns with proven results</li>
<li>Agency experience juggling multiple clients and collaborating across teams</li>
<li>Advanced Google Ads &amp; Microsoft Ads expertise</li>
<li>Owner mentality - you take responsibility and drive improvements</li>
<li>Detail-oriented but not afraid to speak up about big picture opportunities</li>
<li>Self-motivated - thrives in hybrid environment with minimal oversight</li>
</ul>
 
What We Offer 
<ul>
<li>Competitive salary $85K-$110K plus discretionary bonuses for driving client growth</li>
<li>Hybrid flexibility 3 days Brooklyn office, 2 days remote</li>
<li>Full benefits offerings-health, dental, vision, 401(k) matching</li>
<li>Growth budget for certifications and training</li>
<li>Collaborative culture work with specialists across all digital channels</li>
<li>Diverse clients from universities to luxury brands to wellness companies</li>
</ul>
 
Apply now to join our Brooklyn team.
Mason Interactive is an equal opportunity employer.

Senior Paid Search Manager - Brooklyn, NY

<h3>Job Description</h3>
Job DescriptionSalary: $100K - $125K, DOE 
Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to partner in the global effort to improve lives through innovative science with an experienced workforce. We can offer you the chance to build on your skills and knowledge whileworking among experts in their fields and with cutting-edge instrumentation. 
 
Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment. We aim to recruit the best people who stand out among their peers and embody our Core Values:
 
Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. imble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients.
 
We currently have a role available for aExperienced Pharma Biochemist at our South San Francisco site.
 
Job duties include, but are not limited to:
<ul>
<li>Support Bio-Analysis sample preparation, design and perform mass-spec analysis as well as data analysis/interpretation from in-vivo studies from triple-quad mass spectrometers (Sciex 7500).
<ul>
<li>Experience operating, maintaining Sciex 7500 Qtrap, triple-quad mass spectrometers, or Orbitrap instruments is required.</li>
<li>Must be able to work independently to design and execute experiments, and has a track record of conceiving creative solutions in the lab to answer complex questions.</li>
<li>Must be proficient in troubleshooting mass spec and LC systems from common vendors.</li>
<li>Experience with cell culture, PK, and Bio-Analysis of ADC drugs from complex matrices (plasma, tissue).</li>
</ul>
</li>
</ul>
<ul>
<li>Characterization of recombinant proteins, antibodies, and ADCs using intact-MS and peptide mapping for routine QC using high-res mass spec platforms (Oribtrap).
<ul>
<li>Must have a minimum of 5-8 years of hands-on laboratory experience working with mass spectrometry focused approaches in a discovery setting to support drug development.</li>
<li>Extensive hands-on experience operating and maintaining LCMS instrumentation as well as SEC/HIC or U/HPLC systems, and proficient in the software used for data analysis (Protein Metrics, Skyline, Biopharma Finder) is required.</li>
<li>Experience in analytical characterization using SEC/HIC, U/HPLC, cIEF, CE, as well as experience running nano-LCMS instruments for proteomics is desirable.</li>
</ul>
</li>
<li>Work closely with a team of scientists to support the development, optimization, and execution of analytical assays for protein characterization and bioanalysis to guide large molecule therapeutic design.
<ul>
<li>Experience with high throughput plate-based assays working on both large and small molecules is beneficial.</li>
</ul>
</li>
<li>Collaborate with the team to meet timelines and deliverables.
<ul>
<li>The successful candidates demonstrates a "can-do" attitude and brings innovative ideas to challenging projects to contribute to a collaborative and cross-functional organization</li>
</ul>
</li>
<li>Perform general lab maintenance and instrument calibrations.
<ul>
<li>Must be experienced with molecular biology, analytical techniques, and general lab practices, and presenting and interpreting complex datasets in Excel and Prism.</li>
</ul>
</li>
<li>Maintain a high level of productivity in a laboratory setting, this role is 100% on site in South San Francisco and is lab based, but will have opportunities to represent data with project teams. 
<ul>
<li>Experience with analyzing and reporting analytical data, presenting data to colleagues and collaborators, and being a subject area expert in mass spec and analytical approaches is highly advantageous.</li>
<li>Experience with R for data visualization is advantageous.</li>
</ul>
</li>
</ul>
 
Job requirements include, but are not limited to:
<ul>
<li>Minimum of a BSc with 8 years industry experience or MSc with 5 years industry experience in a mass spec focused lab on antibodies/ADCs/ proteomics or a PhD in a relevant scientific discipline focused on mass spec and ADCs. </li>
<li>Team player mentality with strong written and verbal communication skills. Must have good organizational skills and must be detail oriented.</li>
<li>The ideal candidate will be enthusiastic and self-motivated, with the strong interpersonal, communication, and organizational skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery.</li>
</ul>
 
This job posting will close by 10/31/2025 date or when a candidate is identified, whichever comes first.

Experienced Pharma Biochemist

<h3>Job Description</h3>
Job DescriptionSalary: 
Formulation Chemist-Research and Development
 
About Rowe Casa Organics:
From the beginning, Rowe Casa Organics has been on mission to provide safe, natural, and non-toxic products that you can trust.
 
In 2017, sisters Jill and Alicia embarked on a mission seeking greater health and wellness for their families. Frustrated by the lack of transparency and truly safe, effective options, Jill Rowe took matters into her own hands by making our very first product, Elderberry Immune Support. Today, Rowe Casa Organics produces over 300 products to help people thrive in their health, wellness, and lifestyle. From wellness necessities and household essentials to the finest of self-care, each product that we offer is crafted with the utmost quality, care, and love.
 Job Summary:
 
The Formulation Chemist is a hands-on, in-lab research and development roleresponsible for formulating, testing, and supporting the development of clean-labelcosmetic products dietary supplements. This position focuses on lab bench work tosupport the companys product innovation pipeline as well as continuous improvementon existing products, formulations, scaling for mass production and technical transfer.The Formulation Chemist plays a critical role in creating prototypes, preparing samples,conducting experiments, and recording detailed formulation data to support compliance,quality, and innovation efforts. 
 
This role is essential to developing stable, effective, and scalable formulations that alignwith the companys natural and organic standards.
 Reports to: Director of Product Innovation
 
Key Responsibilities:
 
Development of cosmetics, personal care products and dietary supplement development in various formats, using organic and natural ingredients.
<ul>
<li>Assist in weighing, blending, and mixing sample batches using liposomes, emulsions, or standard blending techniques.</li>
<li>Prepare and test formulas for taste, texture, and dispersion.</li>
<li>Record theoretical yield, ingredient weights, and processing conditions for all test batches.</li>
<li>Help identify ingredient compatibility or solubility issues and communicate findings to directors.</li>
<li>Maintain detailed lab notebooks and digital records for all formulation trials and revisions.</li>
<li>Assist in creating batch record data, sample tracking sheets, and formulation change documentation.</li>
<li>Follow all cGMP lab procedures and support readiness for internal or external audits.</li>
<li>Assist in developing a wide range of cosmetic products, including lotions, serums, oils, cleansers, scrubs, balms, deodorants, and shampoos/conditioners.</li>
<li>Weigh, mix, and prepare lab batches based on provided formulation guidelines.</li>
<li>Adjust formulations based on lab observations and feedback from the R&amp;D team.</li>
<li>Record formulation data and observations including pH, viscosity, color, texture, and separation.</li>
<li>Support testing of formulations for performance, stability, and compatibility with packaging.</li>
<li>Maintain clean and organized lab space, ensuring proper labeling and retention of all samples.</li>
<li>Perform other duties as assigned. </li>
</ul>
Qualifications:
<ul>
<li>Bachelors degree in chemistry, Nutritional Sciences or a related scientific field.</li>
<li>25 years minimum of hands-on formulation experience in dietary supplements, cosmetics, personal care. Natural and organic formulation experience. </li>
<li>Understanding of emulsion systems, pH, natural preservatives, surfactants, botanical extracts, and supplement bioavailability. </li>
<li>Familiarity with good lab practices (GLP), cGMP manufacturing requirements, and cosmetic/supplement regulations.</li>
<li>Strong attention to detail and a disciplined approach to documentation.</li>
<li>Proficient in Excel and lab software/tools for formulation tracking, and calculations.</li>
<li>Comfortable working independently in a lab setting and experience operating R&amp;D Laboratory equipment used in formulation development.</li>
<li>Strong communication skills, self-motivated, curious, and excited to work with natural, organic, and innovative ingredients.</li>
</ul>
 
Bonus Skills (Preferred, not required):
<ul>
<li>Knowledge of functional fragrance/aromatherapy principles or essential oil compatibility.</li>
<li>Familiarity with global cosmetic regulations (EU, Canada, Australia) and supplement market trends.</li>
</ul>
Rowe Casa Organics is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, national origin, age, disability, or any other legally protected status.

Formulation Chemist-Research and Development

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes products to determine chemical and physical properties.</li>
<li>Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed.</li>
<li>Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.</li>
<li>Performs data generation, analysis and more complicated problem solving with a minimal rework.</li>
<li>Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.</li>
<li>Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Chemist II

<h3>Job Description</h3>
Job DescriptionSalary: 
About IPinfo
 
IPinfo is a leading provider of IP address data, including geolocation, VPN and residential proxy detection, mobile carrier data and over 20 other context tags. Our API handles over 120 billion requests a month, and we also license our data for use in many products and services you might have used. We're a fast growing bootstrapped business with a global team of around 60 people, and offer data products including IP geolocation, IP to company, carrier detection, and VPN detection. Our customers include Cloudflare, T-Mobile, SpaceX, DemandBase, Clearbit, and many more. We also sponsor academic conferences such as ACM IMC and ACM CoNEXT to connect with fellow researchers.
 
 
How We Work
 
We have an ambitious team, spread all over the globe. We sync up on a monthly all-hands Zoom call, and most teams do a call together every 1-2 weeks. Everything else happens asynchronously, via Slack, GitHub, Linear, and Notion. That means you can pick the hours that work best for you, to allow you to be at your most productive.
 
During the research internship you work within the research team to extract deep knowledge from our data, collaborate with fellow researchers on academic research papers, and discuss ideas at academic Internet measurement conferences.
 
To thrive in this environment you'll need to have high levels of autonomy and ownership. You have to be resourceful and able to work effectively in a remote setup.
 
 
Responsibilities
 
We collect more than 75TB of Internet data every week, including BGP, DNS, ping and traceroute data from more than 1200 servers around the world. Our research team is at the forefront of analyzing and evaluating this data to ensure it finds its way into our producs - IP geolocation, VPN detection, our IP tags and more.
 
During the research internship you will be working on a well-defined research/data analysis project which allows you to collaborate with the research and data teams at IPinfo. The goal of the internship is to gather novel insights, gain new knowledge in data analysis, processing, and Internet measurements, and present your results within the group. During your internship at IPinfo you will be a full member of the research team. Towards the end of your internship you will be evaluating the results and assess possible publication venues (academic conferences, journals, published report,). Check out <a href="https://ipinfo.io/research" target="_blank">https://ipinfo.io/research</a> to find example research projects at IPinfo.
 
 
Skills and Experience
 
<ul>
<li>Currently pursuing a PhD in computer science, data science, statistics, or a related field</li>
<li>Proficiency in programming languages such as Python or Go; data analysis using SQL, pandas, or R</li>
<li>Excellent analytical skills with the ability to collect, organize, analyze, and disseminate information with attention to detail and accuracy</li>
<li>Experience with data visualization tools and techniques</li>
<li>Strong communication skills and the ability to translate data into actionable insights</li>
<li>Commitment to continuous learning and improvement - curious, flexible, believing it can be done better</li>
<li>Optionally publication track record in networking or security conferences (e.g., ACM IMC, ACM SIGCOMM, ACM CoNEXT) or journals (e.g., ACM SIGCOMM CCR, IEEE/ACM Transactions on Networking)</li>
</ul>
 
 
What we offer
 
<ul>
<li>Summer 2026 internship between May and October 2026 (minimum duration: 3 months)</li>
<li>Opportunity to make measurable impact and operate with autonomy</li>
<li>100% remote team and work environment</li>
<li>Flexible working hours</li>
<li>Paid internship </li>
<li>Interesting and challenging work </li>
</ul>
 
 
Application deadline
 
The application deadline for the 2026 summer research internship is January 31, 2026. Earlier applications are preferred.

Research Intern

<h3>Job Description</h3>
Job DescriptionJob Title: Analytical ChemistLocation:&nbsp;Mason, OH&nbsp;
Must Have
<ul>
<li>1. Person to prep samples for MicroCT Lab, weigh samples, place in carousel/conveyor and . check status of acquisition/analysis. 2. The individual will also interact with the instrument’s GUI to setup samples, verify scan regions and initiate sample acquisition. This person will spend their time in the MicroCT and/or Surface Science labs. There will be office space within the lab to setup a laptop and monitor. 3. He/She will be using basic tools like punches and scalpels to prep samples and will have to become familiar with our project tracking system, our image acquisition system and our analysis methods. 4. This person has to be comfortable with detailed prep work and have good communication skills and general computer usage skills (Outlook/Teams/Powerpoint/Excel).</li>
</ul>

Analytical Chemist at Mason, OH

<h3>Job Description</h3>
Job DescriptionSalary: $30 - $40 hourly 
Job Title: Wet Process Chemist
 
Company Overview
VerAvanti is an innovative medical device company specializing in precision imaging catheters and interventional tools. We plan on becoming the Intravascular eyes for coronary Interventionalists. Our mission is to advance healthcare through cutting-edge technology that enables minimally invasive diagnostics and treatments. We foster a collaborative environment where ones creativity and attention to detail, drive our success in developing life-changing products. VerAvanti has a vertically integrated nanofabrication division, which supplies nanofabricated parts using chemical and semiconductor processes to our medical device arm.
 
Job Summary
We are seeking a Wet Processing or Electroplating Chemist to join our nanofabrication team. This position is responsible for overseeing chemical control of electroplating and wet chemistry process operations. This includes electroplating bath maintenance, wet chemical analysis, waste treatment oversight, and preparation of acids, bases, and other process solutions. The chemist ensures stable plating performance, environmental compliance, and safe chemical management practices across operations. This position is manufacturing product 75% of the time. This position will work side by side with the existing process owner who is promoting to another project. They will train on techniques and proven processes from this person over weeks while slowly taking over ownership and offering improvements as time goes on. This position has the unusual benefit of the existing process owner available for training and questions as the responsibility shifts. VerAvanti offers opportunities for equity participation, competitive benefits, and professional growth in a dynamic healthcare-focused environment.
 
Key Responsibilities
<ul>
<li>Perform daily and weekly analysis of plating baths (nickel, gold, cobalt, copper, etc.) using titration, spectroscopy, and pH/conductivity measurement.</li>
<li>Maintain chemical balance and prescribe corrective additions to ensure bath stability and product quality.</li>
<li>Prepare new acid, base, and buffer solutions for production lines and laboratory testing.</li>
<li>Monitor chemical concentrations, temperature, and agitation rates to sustain plating consistency.</li>
<li>Manage hazardous waste accumulation areas, perform waste segregation, label drums, and coordinate disposal in compliance with EPA, RCRA, and local regulations.</li>
<li>Maintain chemical inventory, track expiration dates, and ensure appropriate storage and labeling of acids, caustics, and solvents.</li>
<li>Operate and calibrate laboratory testing equipment (pH meters, analytical balances, spectrophotometers).</li>
<li>Maintain documentation for chemical analysis, waste manifests, and SDS compliance.</li>
<li>Support continuous improvement initiatives to optimize bath life, reduce waste, and minimize environmental impact.</li>
<li>Collaborate with production engineers to troubleshoot plating defects (adhesion, porosity, color variation).</li>
<li>Train technicians on safe handling of acids, bases, and cyanide or heavy-metal-containing solutions</li>
</ul>
 
Qualifications
<ul>
<li>Bachelors degree in Chemistry, Chemical Engineering, or related field (Associate degree with experience acceptable).</li>
<li>25 years of experience in electroplating, surface finishing, or wet chemical processing.</li>
<li>Strong knowledge of inorganic chemistry, electrochemistry, and acid/base reactions.</li>
<li>Familiarity with EPA hazardous waste management and wastewater treatment chemistry.</li>
<li>Experience with analytical techniques such as titration, XRF, AAS, or ICP preferred.</li>
<li>Proficiency with MS Office and laboratory data systems for recording and reporting.</li>
<li>Demonstrated adherence to safety protocols and use of PPE in laboratory or plating environments</li>
</ul>
 
Required Skills and Attributes
<ul>
<li>Not bothered by the smell of non-harmful fumes of the job, such as Acetic Acid (vinegar smell), Acetone, IPA.</li>
<li>Maintain the highest degree of documentation honesty and integrity that is paramount to quick root cause analysis and process controls.</li>
<li>Ability to pay attention to processing details and to double check oneself several times an hour.</li>
<li>Ability to lift 50 pounds while wearing PPE.</li>
<li>Crisp communication skills, with the ability to present ideas clearly to technical and non-technical stakeholders.</li>
<li>Proven team player who thrives in collaborative settings and contributes to group problem-solving.</li>
<li>Optimistic, trusting and sincere in ones team.</li>
<li>Proficiency in Microsoft Office Suite and engineering analysis tools (e.g., FEA software).</li>
</ul>
 
What We Offer
<ul>
<li>Competitive market salary commensurate with experience.</li>
<li>Comprehensive healthcare benefits, including medical, dental, and vision coverage.</li>
<li>Generous Paid Time Off (PTO) policy to support work-life balance.</li>
<li>Equity participation opportunities allowing you to share in the company's success.</li>
<li>Professional development resources, including training and conference attendance.</li>
<li>A supportive, inclusive workplace with flexible hours and opportunities for advancement.</li>
</ul>
 
If you are a driven person with a motor for transforming healthcare through precision work, we encourage you to apply. Please submit your resume and a portfolio of relevant work to Bamboo HR link or visit our careers page. We are an equal opportunity employer.

Wet Process Chemist

<h3>Job Description</h3>
Job DescriptionSalary: 
Join Luxaviation USA as a Senior Charter Broker
 
Luxaviation Group delivers excellence in a comprehensive range of business aviation services tailored to our clients and partners. We are committed to the highest safety standards and strive to create a fulfilling work environment by fostering genuine, open, and engaging relationships with passionate professionals.
 
To strengthen our presence in the U.S. market, Luxaviation USA is actively seeking an experienced Senior Charter Broker, ideally based in or with a strong network in New York, Los Angeles, Miami, or Houston.
 
About the Role
As a Senior Charter Broker, you will be responsible for developing and managing a portfolio of high-net-worth and corporate clients. You will play a key role in the end-to-end coordination of on-demand charter flights from quote to execution ensuring a flawless client experience.
 
Key Responsibilities
<ul>
<li>Proactively develop and manage a high-value client portfolio (UHNWI, corporate accounts, family offices, etc.)</li>
<li>Identify and convert new business opportunities through strategic networking and industry intelligence</li>
<li>Build and deliver bespoke commercial offers and charter quotes in a competitive environment</li>
<li>Negotiate, close, and manage contracts tailored to client needs with the highest service standards</li>
<li>Oversee the complete charter process: from flight planning, aircraft sourcing, and coordination to post-flight follow-up</li>
<li>Collaborate with flight operations, crew, and handling agents to ensure operational excellence</li>
<li>Provide high-touch client service including VIP meet &amp; greet when relevant</li>
<li>Be available for on-call duties (evenings/weekends on a rotating basis)</li>
<li>Ensure proper invoicing, payment follow-up, and budgetary compliance for each operation</li>
</ul>
 
Profile and Qualifications
<ul>
<li>Minimum 5 years of experience in private jet charter brokerage or a similar high-end sales role</li>
<li>Proven track record of closing deals and managing demanding clients</li>
<li>Strong understanding of charter operations and aircraft performance</li>
<li>Exceptional interpersonal, communication, and negotiation skills</li>
<li>Strategic, autonomous, and results-driven mindset</li>
<li>Fluent English required; Spanish or any additional language is an advantage</li>
<li>Ability to work under pressure, with discretion and a client-first attitude</li>
<li>Strong organizational and reporting skills</li>
<li>Valid drivers license and ability to pass background checks</li>
</ul>
 
What We Offer
<ul>
<li>A competitive compensation package including base salary + attractive commissions based on performance</li>
<li>A key role within a globally recognized aviation group</li>
<li>Access to Luxaviations worldwide fleet and resources to support your success</li>
<li>A dynamic and supportive team with international reach</li>
</ul>

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