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<h3>Job Description</h3>
Job Description JOB SUMMARYWe are seeking a highly motivated Laboratory Research Assistant to support in vitro studies and biochemical assays in a pharmaceutical/biotechnology environment. The ideal candidate will have strong experience in aseptic animal tissue culture techniques and molecular biology methods, with the ability to work independently and collaboratively in a fast-paced research setting. This role requires excellent problem-solving skills, attention to detail, and a commitment to scientific integrity and compliance. KEY DUTIES
<ul>
<li>Initiate and complete routine in vitro studies independently, interpreting outcomes and proposing follow-up experiments.</li>
<li>Assist in the design and execution of non-routine cell-based and biochemical assays; conduct exploratory experiments.</li>
<li>Perform literature searches and extract relevant information from published protocols.</li>
<li>Operate and maintain laboratory equipment independently; troubleshoot effectively.</li>
<li>Communicate work clearly in oral and written formats; contribute to protocols, procedures, and technical reports.</li>
<li>Maintain accurate and up-to-date electronic lab notebooks.</li>
<li>Ensure compliance with regulations, SOPs, and safety policies; maintain proper records.</li>
<li>Report and treat data with integrity and ethics.</li>
</ul>
REQUIRED SKILLS
<ul>
<li>Proficiency in aseptic animal tissue culture techniques.</li>
<li>Strong foundation in molecular biology techniques including:</li>
<li>Nucleic acid extraction</li>
<li>RT-PCR</li>
<li>Western Blot</li>
<li>ELISA</li>
<li>Transfection</li>
<li>Ability to design, execute, and interpret experiments in these areas.</li>
<li>Proven problem-solving ability and eagerness to learn.</li>
<li>Ability to evaluate and incorporate new technologies into research.</li>
<li>Strong written and verbal communication skills for concise and accurate reporting.</li>
<li>Proficiency with data analysis software (Microsoft Excel, GraphPad Prism).</li>
<li>Ability to work effectively in a highly collaborative environment.</li>
</ul>
EDUCATION &amp; EXPERIENCE
<ul>
<li>Master’s degree in a related scientific discipline OR Bachelor’s degree with 3+ years of relevant experience.</li>
<li>Background in pharmaceutical, biotechnology, or CRO environments highly desirable.</li>
<li>Non-PhD applicants required. </li>
</ul>
 
Education: Bachelors Degree 
Company DescriptionCompunnel Inc., established in 1994; is a leading provider of Staffing, IT/Software, e-Learning/Training, Business Intelligence, and Cloud Solutions. A leader in contingent and permanent workforce solutions, we also provide temp-to-hire staffing, project-based/SOW staffing, and payroll services to our esteemed clientele which includes Fortune 500 companies of diverse industry segments. Ranked as one of the largest staffing firms in the US which is our primary service market; we also have a significant presence in Europe and Asia. As a national service provider in the US, we are serving our customers all major states and regions; thereby generating numerous job opportunities for prospective employees in their preferred locations of choice. We have witnessed multi-fold YOY growth, and continuously adding a large pool of talented resources to our employee base every year. Our extensive experience in hiring professionals of multiple in-demand skill sets (IT, Engineering, Healthcare, Admin-Clerical, Finance, Professional, Light Industrial, etc.) further makes Compunnel a wider and preferred platform for people to pursue their careers in the US. We welcome people from all walks of life and cultures, and we support workforce diversity by providing equal employment opportunities to people without any discrimination based on race, color, gender, religion, national/ethnic region, disability, or any other basis. 
<h3>Company Description</h3>
Compunnel Inc., established in 1994; is a leading provider of Staffing, IT/Software, e-Learning/Training, Business Intelligence, and Cloud Solutions. A leader in contingent and permanent workforce solutions, we also provide temp-to-hire staffing, project-based/SOW staffing, and payroll services to our esteemed clientele which includes Fortune 500 companies of diverse industry segments. Ranked as one of the largest staffing firms in the US which is our primary service market; we also have a significant presence in Europe and Asia. As a national service provider in the US, we are serving our customers all major states and regions; thereby generating numerous job opportunities for prospective employees in their preferred locations of choice.\r\n\r\nWe have witnessed multi-fold YOY growth, and continuously adding a large pool of talented resources to our employee base every year. Our extensive experience in hiring professionals of multiple in-demand skill sets (IT, Engineering, Healthcare, Admin-Clerical, Finance, Professional, Light Industrial, etc.) further makes Compunnel a wider and preferred platform for people to pursue their careers in the US. We welcome people from all walks of life and cultures, and we support workforce diversity by providing equal employment opportunities to people without any discrimination based on race, color, gender, religion, national/ethnic region, disability, or any other basis.

Scientist

<h3>Job Description</h3>
Job DescriptionSalary: $18.96 
Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Fisheries Observer!!

A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is recruitingReef Fish and ShrimpFisheries Observersto work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Southeast Fisheries Science Center (SEFCS) aboard commercial fishing vessels.

The primary goals of the governments shrimp and reef fish observer programs are to provide quantitative biological, vessel, and gear-selectivity information for the southeastern shrimp fishery and Gulf of Mexico reef fish fishery. Observers deploy on commercial shrimp and reef fish vessels operating in the Gulf of Mexico and South Atlantic.If you ever wanted to make a difference, this is how.

Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between the fishing industry and fisheries scientists like yourself. In order to facilitate cooperation, fisheries observers collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen.Commit to the journey!

Click toLearn More about Becoming a Fisheries Observer

Observers record detailed information on the gear and fishing activity of the vessels. Observers work on deck on vessels ranging from 30 to 90 on trips roughly ranging from 1 to 45 days collecting data on fish catch and bycatch, and incidental takes such as marine mammals, seabirds and marine turtles. After attending a 3-week paid training in-person training in Galveston, TX observers are deployed from ports throughout the Gulf of Mexico and southern Atlantic states. Gear types assessed include but are not limited to shrimp trawl, bottom longline, modified buoy gear, bandit reel, and handline. Training projected for end of March/ April timeframe.

Accommodations and meal reimbursement during in person session of training are provided.Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety.

This is a challenging job, and candidates must be mentally prepared to be away from home without access to internet or cellular telephone signal for multiple days and often weeks at a time. Candidates must be physically able to handle heavy lifting, working odd hours, and spending long days in rough seas. Many crews speak limited English compounding the effects of loneliness and isolation on long trips. Observing provides an excellent career in marine biology, as observers are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs.

Compensation:Observersstarting pay is $18.96/hour. Dependent on enrollment in our H&amp;W benefit, observers may also be eligible for anadditional $4.93/hourfor the first 40 hours worked on each calendar week for a total of$23.89 hour. This is a fulltime position with benefits.Annually, observers earn between $35K - $55K a yeardependent on their availability to deploy offshore and their personal sea day accomplishments. Observers will be paid a minimum of 8 hours for each calendar day offshore and are also eligible for additional compensable activities while on land.

AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits.Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus.

Travel is reimbursedin accordance with federal travel guidelines at an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate.

Minimum Qualifications:
<ul>
<li>A bachelor's degree from an accredited college or university with a major in one of the natural sciences and a minimum of 30 semester hours or equivalent in the biological sciences</li>
<li>At least one undergraduate course in math or statistics.</li>
<li>All relevant course work must have been performed at a level acceptable for credit at the candidates academic institution.</li>
<li>Experience with data entry on computers.</li>
<li>Observer candidates must be U.S. citizens, or be legally authorized to work in the U.S.</li>
<li>Candidates must be physically able, as determined by a licensed physicians certification to perform observer duties.</li>
<li>Your own transportation is required.</li>
</ul>

Preferred Qualifications:
<ul>
<li>At-sea experience</li>
<li>The ability to work independently and live in close quarters with little to no communication for purposes other than safety status check-ins for up to 8 weeks. (phone, internet, email and other amenities are unavailable at-sea)</li>
<li>Coursework with dichotomous keys</li>
</ul>

Homeport:
Applicants must be currently living, or be willing to live within 50 miles of the New Orleans, LA

Contact:
If you would like to apply for one of these exciting new openings, please click the following linkCareers Pageto submit the following information.

<ul>
<li>Resume</li>
<li>Cover Letter detailing sea and fish experience.</li>
<li>3 to 5 academic/professional references (name, email address and phone number)</li>
<li>Unofficial copies of your college (or high school if applicable) transcripts.</li>
</ul>

All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to theTalent Teamor 774-770-5833

An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
 
Must be able to work in the U.S. VEVRAA Federal Contractor Request Priority Protected Veteran Referrals Equal Opportunity Employer

Reef Fish and Shrimp Fisheries Observer - New Orleans, LA

<h3>Job Description</h3>
Job DescriptionCompany Description
We are Olsson. We engineer and design solutions that improve the world around us. As a company, we promise to always be responsive, transparent, and focused on results – for our people, our clients, and our company.
We're a people-centric firm, so it's no surprise our greatest asset is our people. The impact this creates is an environment that encourages our people to grow and be creative with their talents. This approach builds a culture that is uniquely Olsson. It allows us to grow our people as we grow our business. This, in turn, creates a lasting impact on the world around us.
Job Description
As one of our student interns on the Geotechnical team you will perform meaningful, hands-on, real-world work that will transform your classroom experience and help you envision your future career. Your experience will involve assisting our geotechnical engineering staff putting together geotechnical reports and appendices. You'll get an introduction to Olsson's culture that will help you evaluate our firm as a career choice. This position may occasionally assist with working in the lab and in the field performing various types of testing and reporting.
Freshman and sophomores are encouraged to apply. 

Qualifications
You are passionate about:
<ul>
<li>Working collaboratively with others</li>
<li>Having ownership in the work you do</li>
<li>Using your talents to positively affect communities</li>
</ul>
You bring to the team:
<ul>
<li>Strong communication skills.</li>
<li>Ability to contribute and work well on a team.</li>
<li>Proficiency in Microsoft Excel, Word, and Outlook.</li>
<li>Problem-solving and decision-making skills.</li>
<li>The ability to work in a constant state of alertness and safe manner.</li>
<li>The ability to work during the school year in addition to the summer.</li>
</ul>

#LI-DNI



Additional Information
Olsson specializes in engineering and design, client advisory services, planning, field services, and environmental. Improving the world has been our mindset from the very beginning, back when Olsson first opened for business in 1956. And it will be our mindset for years to come.
As an Olsson employee, you will:
<ul>
<li>Receive a competitive 401(k) match</li>
<li>Be empowered to build your career with tailored development paths</li>
<li>Have the possibility for flexible work arrangements</li>
<li>Engage in work that has a positive impact on communities</li>
<li>Participate in a wellness program promoting balanced lifestyles</li>
</ul>
In addition, full-time employees will receive our traditional benefits package (health care, vision, dental, paid time off, etc.) and the opportunity to participate in a bonus system that rewards performance.

Olsson is an Equal Opportunity Employer. We encourage qualified minority, female, veteran, and disabled candidates to apply and be considered for open positions. We do not discriminate against any applicant for employment or any employee because of race, color, religion, national origin, sex, sexual orientation, gender identity, gender, disability, age, military status, or other protected status.
Olsson understands the importance of privacy and is committed to protecting job applicants' personal information. Pursuant to the California Consumer Privacy Act, as amended by the California Privacy Rights Act (collectively, the "CCPA"), this notice explains Olsson's practices regarding the collection, use, and disclosure of personal information for job applicants residing in California. Please read this Notice carefully to understand our privacy practices.
For more information about the types of information we collect and how we use it in connection with your general access and use of our website, please review our general California Privacy Notice here.

Student Internship - Geotechnical

<h3>Job Description</h3>
Job Description
Field Scientist / Field Geologist – Environmental Remediation 
Location: Carlsbad, New Mexico
Employment Type: Full-Time
About the Role We are seeking a motivated Field Scientist / Field Geologist to support environmental remediation projects throughout New Mexico’s oilfield regions. Based in Carlsbad, this role is field-focused and central to the investigation and cleanup of soil and groundwater contamination. You will apply technical expertise, regulatory knowledge, and field leadership to ensure compliance with New Mexico Environment Department (NMED) requirements while contributing to environmental restoration efforts that matter to both the community and industry. This is a great opportunity for someone to get their foot in the door and grow within the environmental consulting industry.
Key Responsibilities
<ul>
<li>Conduct field investigations including soil, groundwater, surface water, and vapor sampling in accordance with NMED/EPA standards.</li>
<li>Oversee remediation activities including excavation monitoring, confirmatory sampling, and adaptive in-field decision-making.</li>
<li>Supervise drilling operations (direct-push, auger, and monitoring well installations) and ensure proper chain-of-custody and documentation.</li>
<li>Lead environmental site assessments (Phase I &amp; II ESAs), spill response, and post-cleanup verification.</li>
<li>Operate field instruments such as PID/FID meters, water-quality probes, GPS units, and GIS software.</li>
<li>Prepare accurate daily field logs, sampling documentation, and regulatory-ready reports.</li>
<li>Coordinate with subcontractors, drilling crews, clients, and project managers to ensure smooth field operations and effective remediation strategies.</li>
<li>Adhere strictly to health and safety plans (HAZWOPER, HASP) in active oilfield environments.</li>
</ul>
Required Qualifications
<ul>
<li>Bachelor’s degree in Geology, Environmental Science, Earth Sciences, or related field.</li>
<li>2–4 years of field experience in environmental consulting or remediation.</li>
<li>Demonstrated experience working on New Mexico environmental sites with knowledge of NMED regulations and reporting requirements.</li>
<li>Strong technical writing and reporting skills; proficiency in Microsoft Office.</li>
<li>Valid driver’s license with clean record.</li>
<li>OSHA 40-hour HAZWOPER (or ability to obtain).</li>
</ul>
Preferred Qualifications
<ul>
<li>Oilfield remediation experience (spill response, soil excavation, groundwater recovery).</li>
<li>Familiarity with regulatory communications to NMED.</li>
<li>Experience with ISNetworld or Veriforce compliance systems.</li>
<li>GIS mapping or digital field data platforms.</li>
<li>First Aid/CPR certification and mechanical troubleshooting ability.</li>
</ul>
Working Conditions
<ul>
<li>Primarily outdoor work in oilfield and remote environments under varying weather conditions.</li>
<li>Frequent travel to regional project sites, with occasional overnight stays.</li>
<li>Physical requirements include lifting up to 50 lbs., standing for long periods, and navigating uneven terrain.</li>
</ul>
Why Join Us
<ul>
<li>Full benefits: health insurance, 401(k) with company match, paid time off, and training.</li>
<li>Diverse project exposure across all phases of environmental remediation—from investigation to site closure.</li>
<li>Opportunity to directly contribute to environmental restoration in one of the nation’s most active oilfield regions.</li>
<li>Supportive culture built on safety, technical expertise, and professional growth.</li>
<li>A career-building role for those ready to learn, grow, and advance.</li>
</ul>
Please Note:
<ul>
<li>Candidates must be authorized to work in the U.S, no sponsorship is available. </li>
<li>Relocation reimbursement is not available.</li>
<li>Must live within commuting distance of Carlsbad, NM.</li>
<li>Must be available to start within 2–3 weeks of offer.</li>
</ul>

Field Geologist / Scientist - Earth Systems R&R

<h3>Job Description</h3>
Job DescriptionJob Title: ChemistJob Description
We are seeking a dedicated Chemist to join our team, focusing on processing and analyzing a variety of samples using high-performance liquid chromatography (HPLC). These samples will include different food products, vitamins, cosmetics, and more.
Responsibilities
<ul>
<li>Process and analyze samples using HPLC.</li>
<li>Work with a diverse range of samples including food, vitamins, and cosmetics.</li>
<li>Apply wet chemistry techniques and analytical skills in sample processing.</li>
</ul>
Essential Skills
<ul>
<li>Minimum of 2 years' experience in HPLC.</li>
<li>Proficiency in wet chemistry and analytic techniques.</li>
<li>Strong understanding of high-performance liquid chromatography.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Ability to work effectively as part of a team.</li>
</ul>
Work Environment
The position operates Monday through Friday, from 8:00 AM to 5:00 PM, with flexibility required for potential shifts from 7:00 AM to 4:00 PM or 9:00 AM to 6:00 PM. The team is committed to growth, aiming to increase its current headcount.
Job Type &amp; Location
This is a Contract to Hire position based out of Harrisburg, PA.
Pay and Benefits
The pay range for this position is $30.00 - $34.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Harrisburg,PA.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
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.

Chemist

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Summer Intern, Agentic Systems will support discovery research at Arrowhead Pharmaceuticals by contributing to the development of advanced AI systems that assist scientific research and decision-making. This internship offers hands-on experience building and testing AI-driven tools that support data exploration, evidence synthesis, and hypothesis generation in a collaborative research environment. The intern will work alongside computational and scientific teams to explore how autonomous AI systems can accelerate research workflows and support therapeutic discovery.
This is an 11-week Summer Internship Program paying $27.00 per hour and requires full-time, on-site work five days per week at the designated location.
Responsibilities
<ul>
<li>Support the design and development of AI-driven systems that assist with research analysis and scientific reasoning.</li>
<li>Contribute to building and testing autonomous or semi-autonomous AI workflows that integrate data from multiple sources.</li>
<li>Assist with literature review, data retrieval, and evidence synthesis using AI-enabled tools.</li>
<li>Help develop summaries, visualizations, or reports that communicate insights generated by AI systems.</li>
<li>Collaborate with computational and scientific team members to refine workflows and improve usability.</li>
<li>Participate in testing, iteration, and evaluation of AI systems to improve performance and reliability.</li>
<li>Present progress updates and findings during team meetings.</li>
<li>Support documentation and knowledge-sharing related to AI tools and workflows.</li>
</ul>
Requirements
<ul>
<li>Currently pursuing a PhD in Computer Science, Computational Biology, Bioinformatics, Data Science, or a related quantitative field.</li>
<li>Proficiency in Python, with experience building analytical pipelines or AI-driven applications.</li>
<li>Familiarity with large language models (LLMs) or AI-based automation tools.</li>
<li>Basic understanding of biological or biomedical research concepts.</li>
<li>Strong problem-solving and analytical skills.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Ability to collaborate effectively in a cross-functional research environment.</li>
<li>Excellent verbal and written communication skills and ability to collaborate in a cross-functional research environment.</li>
</ul>
Preferred 
<ul>
<li>Experience working with agent-based or multi-step AI workflows.</li>
<li>Familiarity with API integration and external data sources.</li>
<li>Exposure to scientific or biomedical data platforms.</li>
<li>Experience creating dashboards, reports, or automated summaries.</li>
<li>Strong interest in applying AI to scientific research or drug discovery.</li>
</ul>
California pay range $11,440—$11,440 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Summer Intern, Agentic Systems

<h3>Job Description</h3>
Job Description
Job Description
<ul>
<li>
This position is in the Biologics Purification Development team of the Product Development Science &amp; Technology department at Bioresearch Center.
</li>
<li>
Will be involved with all aspects of protein purification and protein chemistry to support biopharmaceutical process development. 
</li>
<li>
Execute high throughput scale down robotic purification as part of early and late stage process development, viral clearance, process characterization, and continuous process improvement studies.
</li>
<li>
Perform data acquisition and analysis, and documentation in electric lab notebooks.
</li>
<li>
Will develop economical, robust steps for recovering the target protein from bioreactor harvests using chromatography, filtration, and other separation techniques; developing downstream purification processes to be transferred to manufacturing; and perform laboratory scale process characterization studies.
</li>
<li>
Perform various bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.
</li>
<li>
As appropriate, the candidate may supply technical support for pilot and/or GMP manufacturing of clinical materials.
</li>
<li>
Execute new technology/innovation evaluation for purification process.
</li>
</ul>
Qualifications:
<ul>
<li>
PhD in Chemical Engineering, Biotechnology, Biochemistry, or Chemistry with 0-2 yrs. experience; OR
</li>
<li>
MS with 4-6 yrs of experience 
</li>
<li>
Strong biological scientific understanding.
</li>
<li>
Experience with chromatography and filtration for biologics purification
</li>
<li>
Possess strong written, oral, and collaborative skills in order to effectively communicate experimental procedures and results.
</li>
<li>
Experience with bioanalytical assays and methods preferred
</li>
<li>
Internship or corporate experience
</li>
<li>
Laboratory hands on skills
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Biologics Purification Scientist

<h3>Job Description</h3>
Job DescriptionWe are seeking a detail-oriented Electronics Assembly Technician to join our team. This role involves performing a wide variety of electronic and electro-mechanical assembly operations in a clean room environment.Key Responsibilities:
<ul>
<li>Perform bench-level electronic and electro-mechanical assembly using skilled hand techniques and/or automated production equipment</li>
<li>Interpret technical specifications, drawings, and documentation</li>
<li>Follow established methods and sequences for wiring, component installation, hand soldering, and cable harnessing</li>
<li>Set up and adjust assemblies while holding tight tolerances to blueprint specifications</li>
<li>Maintain clean room standards and procedures</li>
</ul>
Qualifications:
<ul>
<li>Experience working in a clean room environment</li>
<li>High School Diploma or equivalent with a minimum of 4 years of relevant experience OR</li>
<li>Associate’s Degree (or post-secondary education) with 0–2 years of related experience</li>
<li>Strong attention to detail and ability to work from technical documentation</li>
</ul>
This is a great opportunity for someone who enjoys hands-on assembly work in a precision-driven environment. #INDNashua #ZipNashuaCompany DescriptionWe are HW Staffing, and our mission is to “Connect Great People with Great Companies.” Collectively, we are revolutionizing how staffing services support the employee and client. HW Staffing jobs encompass meaningful work, a sense of purpose with career development, and a welcoming community. Our jobs inspire and reward independence. Our organizational culture of teamwork and inclusivity supports our spirit and commitment to helping people. Together we can help people find meaningful work - we’re just getting started #wearehwstaffing 
<h3>Company Description</h3>
We are HW Staffing, and our mission is to “Connect Great People with Great Companies.” Collectively, we are revolutionizing how staffing services support the employee and client. HW Staffing jobs encompass meaningful work, a sense of purpose with career development, and a welcoming community. Our jobs inspire and reward independence. Our organizational culture of teamwork and inclusivity supports our spirit and commitment to helping people. Together we can help people find meaningful work - we’re just getting started #wearehwstaffing

Clean Room Assembly NH

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The&nbsp;Associate Director, Statistics - Oncology&nbsp;provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients.
This role will work a hybrid schedule in one of the AbbVie locations:
<ul>
<li>Lake County, IL</li>
<li>South San Francisco, CA</li>
</ul>
Responsibilities
<ul>
<li>Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission.</li>
<li>Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans.</li>
<li>Represent function/department on project team(s) to provide statistical input to compound/drug development and drive alignment with functional management. Partner with other functions (Clinical, Regulatory, Patient Safety, and GMA, etc.) to create development strategies for assigned projects.</li>
<li>Demonstrate extensive understanding of statistical concepts and methodology. Propose novel statistical methodological approaches to design of scientific studies. Provide sufficient detail to allow programming implementation. Ensure that all statistical analyses specified in scientific protocols and analysis plans are conducted appropriately.</li>
<li>Train and mentor staff on statistical methodology and operations. May supervise contract statisticians or junior statisticians. Gain expertise in innovative statistical methods. Assist functional leaders in recruiting qualified personnel and arranging training opportunities for professional development of staff.</li>
<li>Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.</li>
<li>Act as the liaison for statistical issues on AbbVie collaborative studies with CROs, academic institutions, government agencies, steering and/or data monitoring committees, joint ventures or licensing collaborators. Build external scientific connections which foster professional development and promote the reputation of the Statistics Department.</li>
<li>Ensure that all applicable regulatory requirements for work processes are met. Critically review regulatory submission documents. Participate in discussions with regulatory agencies as needed. Validate external statistical software to ensure compliance with SOPs and regulatory requirements</li>
<li>Significant Work Activities:&nbsp;Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required</li>
</ul>
Qualifications 
<ul>
<li>MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics, Biostatistics, or a highly related field.</li>
<li>High degree of technical competence and excellent communication skills, both oral and written</li>
<li>Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others</li>
<li>Able to manage project timeline and quality of deliverables</li>
<li>Able to build strong relationship with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo</li>
<li>Have strong leadership skills and experience in working/managing cross-cultural or oversea teams</li>
<li>Pharmaceutical or related industry knowledge required, including experience and understanding of drug development and life-cycle management in the regulated environment.</li>
<li>(SSG) Experience leading safety-related projects (eg, ISS, benefit-risk assessment, signal detection)</li>
<li>(GMA Stat) Competence in experimental and RWE study design, descriptive statistics, inferential statistics, statistical modeling, and statistical programming. Knowledge of methodologies for confounding control and bias minimization in observational studies preferred.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Director, Statistics

<h3>Job Description</h3>
Job DescriptionGeotechnical Engineer (P.E.) - Mid - Senior Level Geotechnical Engineer (P.E.) Position Overview We are seeking a highly skilled Geotechnical Engineer (P.E.) to join our engineering team. The ideal candidate will be responsible for conducting geotechnical investigations, analyzing soil and rock properties, and designing foundation systems for various construction projects. This role is crucial in ensuring the stability and safety of structures through thorough analysis and innovative engineering solutions. Key Responsibilities
<ul>
<li>Conduct geotechnical investigations and site assessments for construction projects</li>
<li>Analyze soil and rock samples to determine engineering properties</li>
<li>Design foundation systems including shallow and deep foundations</li>
<li>Evaluate slope stability and design retaining walls as needed</li>
<li>Perform material testing and manage construction materials testing (CMT)</li>
<li>Prepare geotechnical reports and project documentation</li>
<li>Collaborate with project managers and other engineering disciplines</li>
<li>Ensure compliance with relevant codes, standards, and regulations</li>
</ul>
Qualifications
<ul>
<li>Bachelor's degree in Civil Engineering or Geotechnical Engineering</li>
<li>Professional Engineer (P.E.) license is required</li>
<li>Minimum 5 years of experience in geotechnical engineering</li>
<li>Strong knowledge of foundation design, slope stability, and retaining wall design</li>
<li>Experience with material testing and construction materials</li>
<li>Familiarity with geotechnical software and engineering tools</li>
<li>Excellent analytical and problem-solving skills</li>
<li>Strong communication and teamwork abilities</li>
</ul>
 - For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. CyberCoders will consider for Employment in the City of Los Angeles qualified Applicants with Criminal Histories in a manner consistent with the requirements of the Los Angeles Fair Chance Initiative for Hiring (Ban the Box) Ordinance.This job was first posted by CyberCoders on 11/18/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. &nbsp;CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at <a href="mailto:Benefits@CyberCoders.com" target="_blank">Benefits@CyberCoders.com</a> to make arrangements.

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