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<h3>Job Description</h3>
Job DescriptionObjectivePerspective Therapeutics is seeking a highly motivated hands-on scientist with expertise in&nbsp;sterile injectable drug products to join our dynamic CMC drug product team. This role is critical in supporting the development of sterile injectable formulations and drug product process development from early development through scale-up and commercial manufacturing. The successful candidate will play a pivotal role in developing and optimizing injectable radiopharmaceutical formulations and associated manufacturing processes in a cGMP-compliant environment. Working in a fast-paced, integrated, and multidisciplinary environment, the successful candidate is expected to collaborate cross-functionally while also delivering strong independent contributions that support product advancement to late-stage clinical development and commercialization.Objective
<ul>
<li>Serve as the technical subject matter expert (SME) for formulation and drug product process development.</li>
<li>Conduct formulation/process development studies, including comparability, stability, and compatibility assessments.</li>
</ul>
<ul>
<li>Lead scale-up and technology transfer activities to support manufacturing.</li>
<li>Draft detailed study plans to ensure that work is performed efficiently and in a scientifically sound manner</li>
<li>Monitor experiments (e.g. process development, formulation optimization) and ensure complex data are interpreted in a scientifically correct way</li>
<li>Support filter and container closure integrity validation studies and other special studies as necessary.</li>
<li>Collaborate with cross-functional teams including Analytical, Quality, Regulatory, and Manufacturing.</li>
<li>Author formulation and process development reports, study protocols, and regulatory CMC module 3 documentation to support late-stage IND and NDA submissions.</li>
<li>Ensure all work is performed in accordance with company policies, procedures and safety standards. </li>
<li>Ensure documents follow relevant regulatory standards (e.g., FDA, USP, ICH) and CMC guidelines.</li>
<li>Troubleshoot and propose scientifically sound solutions in collaboration with internal teams.</li>
<li>Provide technical support during regulatory inspections and audits, as needed.</li>
</ul>
QualificationsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.Education/Experience
<ul>
<li>Ph.D. or M.S. or B.S. in Pharmaceutics, Chemistry, or related field</li>
<li>5-7 years of hands-on experience in formulation development and sterile drug product process development using quality by design (QbD) principles.</li>
<li>Strong understanding of aseptic processing, formulation characterization, excipient compatibility, and container-closure systems</li>
<li>Experience with QbD principles and risk-based development approaches.</li>
<li>Pharmaceutical product life cycle management</li>
<li>Deep expertise in regulatory frameworks (FDA, EMA), and clinical/commercial manufacturing.</li>
<li>Familiarity with GMP quality systems and electronic document management systems.</li>
<li>Experience in radiopharmaceuticals or isotope-based therapeutics is strongly preferred.</li>
</ul>
Knowledge / Skill / Ability
<ul>
<li>Ability to prepare detailed study protocols and interpret complex data sets across multiple techniques.</li>
<li>Excellent communication skills, including the ability to explain technical concepts to cross-functional teams.</li>
<li>Prior radiochemistry experience and knowledge of radioactive material handling are a plus.</li>
<li>Strong organizational skills, with the ability to manage multiple priorities and meet tight deadlines.</li>
<li>Work independently and proactively in a highly matrixed environment.</li>
</ul>
Work Environment&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; &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; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
<ul>
<li>Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.</li>
<li>May be required to sit or stand for long periods of 8+ hours a day while performing duties.&nbsp; </li>
<li>Willingness to complete safety training within allotted time limits, and work in a team-based environment.</li>
<li>May require travel to Iowa up to 10%.</li>
</ul>
 &nbsp;
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Lead Scientist - Sterile Formulations Development

<h3>Job Description</h3>
Job Description
Job Summary Product Development Scientist-&nbsp;Dietary Supplements, Confectionery Nutraceuticals Gummi World is a fast-growing nutraceutical manufacturer based in Chandler, Arizona. We strive to deliver the highest quality vitamin supplement products to our clients and maintain long-standing relationships with them. We think of each client as our partner, and we do everything we can to help them grow their businesses. When we provide you with the highest level of quality and consistency for your products, it allows you to always provide your customers with the brand they have learned to trust. Gummi World is seeking an accomplished, talented, and dynamic insights-driven leader to be a founding member of our Business Development/&nbsp;Research &amp; Development team. Confectionary experience is required for this role, preferably in starch &amp; starchless gummy formulation, capsules and powders are a plus. The Product Development Scientist will work with the product development team on strategic initiatives to expand the Gummi World&nbsp;supplement&nbsp;product line. This role is responsible for developing products that are delicious, and consistently manufactured while ensuring all safety and quality requirements are met. The Product Development Scientist will have KPI’s in all stages of the&nbsp;process for specified projects spanning, innovation, flavor, collaborating with clients and manufacturers, cost optimization, and commercialization. Responsibilities
<ul>
<li>Develop concepts for the Innovation&nbsp;process</li>
<li>Collaborate with the Regulatory Team on formulations and claim substantiation.</li>
<li>Maintain branded ingredient and raw material database</li>
<li>Research potential ingredients based on physical properties such as solubility for particular form factors.</li>
<li>Follow up with R&amp;D and Business Development&nbsp;teams on samples, prototypes, and test batches.</li>
<li>Help with the development of different pack-out options for existing products.</li>
<li>Lead product tastings, evaluations, etc., and analyze/record results in a statistical/analytical manner.</li>
<li>Scope secondary contract manufacturers to match existing formulations</li>
<li>Support Quality in new product specifications, change controls and label initiation forms.</li>
<li>Contribute to innovation, troubleshooting, and brainstorming ideas in a team environment for future platform growth in key consumer needed state areas.</li>
<li>Understand customer needs, business needs, and strategy by attending and participating in cross-functional team meetings.</li>
<li>Forge relationships with key suppliers, and purchasing team to keep abreast of upcoming trends, to solicit and secure opportunities for new food ideas, technologies, ingredients, and packaging materials.</li>
<li>Maintain professional and technical knowledge by attending regulatory training, educational workshops, reviewing professional publications, establishing personal networks, and participate in professional societies.</li>
<li>Support company growth initiatives</li>
</ul>
Requirements
<ul>
<li>Bachelor's Degree (BA/BS) from a 4-year accredited college or university in Food Science, Biology, Engineering, Chemistry or Equivalent BS degree, with 5+ years of experience in R&amp;D, Product Development, Manufacturing and/or Quality Assurance in food and/or supplement industry is preferred.</li>
<li>Must have advanced knowledge in more than one of the aforementioned formats (Confectionary, starch &amp; starchless gummies, formulations, Capsules, powders etc.) is required as well as having a proven track record developing clean (i.e. short ingredient list) and delicious food that meet specific requirements on a large scale.</li>
<li>Must have strong interpersonal and presentation skills, ability to work in a team environment as well as independently, and have the ability to manage numerous projects simultaneously in a high-paced environment while staying in control under pressure.</li>
<li>Must have excellent analytical, written, and organizational skills with the ability to manage complex technical information and have an industry-leading understanding of ingredient functionality, product evaluation, health and nutrition, food manufacturing processes, microbiology, quality assurance principles, and market research practices.</li>
<li>Preferred candidates must have demonstrated technical sales experience with a wide range of clients.&nbsp;</li>
</ul>
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Product Development Scientist - Dietary Supplements, Confectionery Nutraceuticals

<h3>Job Description</h3>
Job DescriptionThis role will serve as a business representative for laboratory IT systems and will be responsible for mentoring laboratory personnel on the use of electronic lab systems as well as supporting internal and external audits as a laboratory IT system subject matter expert. Key Objectives/Deliverables:
<ul>
<li>Performs or supports Laboratory with the validation of laboratory equipment and software systems.</li>
<li>Supports the establishment and maintenance of the validated state of software-based computerized systems in use in the laboratory.</li>
<li>Act as business owner and contact SME for QC laboratory IT systems.</li>
<li>Responsible for collecting data and authoring periodic review documents for laboratory information systems.</li>
<li>Provide oversight and support continuous improvement of quality systems as they relate to laboratory informatics.</li>
<li>Apply knowledge of quality principles, cGMP, and laboratory systems towards the development and execution of local procedures, training courses, and practices.</li>
<li>Assist in improvement of quality systems by creating or revising worksheets, developing, or updating laboratory execution system documentation, updating laboratory methods, and maintaining other lab documentation systems.</li>
<li>Responsible for method management in the QC Laboratory, specific to scripted or coded methods.</li>
<li>Supports and/or leads investigations, CAPA and change control initiatives.</li>
<li>Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.</li>
<li>Ability to work in a lab environment including wearing appropriate PPE and other safety related equipment or considerations.</li>
</ul>
Requirements (Education, Experience, Training):
<ul>
<li>Bachelor’s degree in a computer science, life science, or applied science with at least five (5) years of demonstrated relevant experience in a GMP lab.</li>
</ul>
Preferred attributes but not required:
<ul>
<li>Experience with computer systems including Microsoft Office suite, laboratory information management systems.</li>
<li>Investigation and deviation management experience.</li>
<li>Demonstrated proficiency in computer system validation.</li>
<li>Experience with compliance requirements and regulatory expectations.</li>
<li>Demonstrated accuracy and proficiency in analytical skills.</li>
<li>Strong oral and written communication skills and demonstrated through documentation and presentation skills.</li>
<li>Demonstrated strong interpersonal interaction skills.</li>
</ul>
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Laboratory IT Associate

<h3>Job Description</h3>
Job Description
Job Title:&nbsp;Chemical Technician II Location:&nbsp;Corning NY Duration:&nbsp;12+ Months Top 3 Required Skills:
<ul>
<li>Experience with chemical inventory management systems (CISPro Biovia or similar)</li>
<li>Strong organizational and attention-to-detail skills</li>
<li>Knowledge of chemical handling and safety procedures</li>
</ul>
Must-Have Skills:
<ul>
<li>Proficiency with computer-based inventory systems and data management</li>
<li>Ability to conduct regular inventory audits and maintain accurate records</li>
<li>Experience labeling, storing, and organizing chemicals and laboratory materials</li>
<li>Understanding of Standard Operating Procedures (SOPs) and compliance regulations</li>
<li>Effective communication and collaboration with cross-functional teams</li>
</ul>
Requirements:
<ul>
<li>Experience managing laboratory or chemical inventories</li>
<li>Proficiency with data entry and computer-based tracking systems</li>
<li>Strong attention to detail and accuracy</li>
<li>Ability to follow safety and compliance standards for chemical handling</li>
<li>Excellent organizational and communication skills</li>
</ul>
Company DescriptionElevaIT is a certified and values driven Service-Disabled Veteran owned global staffing and IT professional services firm serving Fortune 1000 clients with customized and scalable workforce solutions. Leveraging talent intelligence analytics, our scalable recruiting platform puts diversity, equity, inclusion, and belonging (DEIB) at the forefront of everything we do. 
<h3>Company Description</h3>
ElevaIT is a certified and values driven Service-Disabled Veteran owned global staffing and IT professional services firm serving Fortune 1000 clients with customized and scalable workforce solutions. Leveraging talent intelligence analytics, our scalable recruiting platform puts diversity, equity, inclusion, and belonging (DEIB) at the forefront of everything we do.

Chemical Inventory Technician

<h3>Job Description</h3>
Job Description
Description HistoWiz is the largest online histopathology company, based in New York City. Our mission is to help biomedical researchers find cures by accelerating histopathology and enabling global collaboration.
Since inception in 2013, we have doubled our month-over-month sales, driven primarily by customer referrals. We are profitable, won numerous awards and are funded by prestigious investors, including Y-Combinator and Zhenfund. We are seasoned scientists with experience at leading academic institutions and have published high impact research in top journals of biomedicine. We have just completed our Series A and are now looking to scale our business significantly in the coming years.
HistoWiz has over 3,000 paying customers globally from top academic institutions (e.g. MSKCC, Harvard, Stanford, HHMI) and pharmaceutical companies (e.g. CRISPR, Johnson &amp; Johnson, Regeneron). We process tissue specimens and digitize all of the results, hosting our client’s data on a proprietary platform, PathologyMapTM . This platform not only enables industry-leading turnaround time for diagnosis, but also online viewing, sharing and search. No other platform like this exists, so we are truly building something new that can bridge scientists, doctors, and patients from all over the world to conquer life-threatening diseases collaboratively instead of individually. This online platform also contains the world’s largest collection of pathology data and the first network of top pathologists.
We are looking for highly motivated Research Associate to join our fast-growing team. Under the general direction and supervision of the Director of Laboratory Operations, the Research Associate will effectively apply a working knowledge and skill of designated Research Associate-related duties and tasks, in support of the Department as a whole, to complete the daily assigned Histology workload. &nbsp;
Requirements
<ul>
<li>Research and review the literature to find the best antibodies for IHC and IF</li>
<li>Design and recommend processes, systems, and operational changes to increase efficiency and effectiveness</li>
<li>Maintain laboratory organization and team priorities to complete projects with client-expected turnaround time</li>
<li>Lead project update meetings with clients</li>
<li>Design experiments and interpret results, while thinking critically about research projects</li>
<li>Write IHC validation reports for pharma clients</li>
<li>Coordinate in ordering supplies and maintain inventory for the AIR department</li>
<li>Develop new protocols and assays, including Multiplex mIF panels</li>
<li>Troubleshoot quality issues and work with pathologists to QC slides</li>
<li>Oversee and perform biomarker and equipment validations</li>
<li>Perform IHC, IF and ISH via RNAScope independently</li>
</ul>
Position Requirements:
<ul>
<li>Bachelors degree in scientific field preferred</li>
<li>Tech-savvy, fast learner. We use a proprietary, digital LIMS system</li>
<li>Strong verbal and written communication skills</li>
<li>HTL or QIHC licenses, a plus</li>
<li>Experience working at a biotech&nbsp;preferred</li>
</ul>
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Research Associate

<h3>Job Description</h3>
Job Description
Who We Are Dudek is a leading environmental, planning, and engineering firm that help public and private clients plan, design, and build projects that improve communities’ built and natural infrastructure. Founded in 1980, Dudek has grown steadily to more than 800 professionals across the U.S. and received the Top Workplace Award for 2024. As a 100% employee-owned company, Dudek’s culture rewards smart, productive team members with ownership, professional development, and financial benefits. We seek creative, pragmatic problem-solvers working at the intersection of science, engineering, regulations, and multiple stakeholders’ interest to help clients achieve project goals. We encourage collaboration, sustainability, and innovation. At Dudek, we abide by shared values: Trust:&nbsp; We trust each other to use good judgment. Respect:&nbsp; We act professionally and treat each other fairly. Teamwork:&nbsp; We come together, share openly, and apply diverse perspectives. Fun:&nbsp; We take our work seriously…not ourselves. Well-Being:&nbsp; We care about each other’s health, safety, and total wellness. Our culture is the foundation of who we are and how we work. Learn more about our culture. About The Job We are seeking qualified, experienced Archaeological Field Technicians for various archaeological projects throughout California on an on-call/as-needed basis. Immediate needs in the northern and central California regions. However, we also have a number of additional opportunities throughout other areas of California and other states. Candidates could be connected with our Oakland, Sacramento, or Auburn offices although proximity to an office is not a determining factor. Learn more about the projects you will have the opportunity to shape. Who You Are To thrive at Dudek, you should be comfortable with accountability, collaboration, flexibility while being a resourceful and independent thinker. We look for curious, solution-focused people who can adapt quickly to an ever-changing industry. There is no single way to solve a problem, so we encourage innovation. Duties and Responsibilities (may include some or all of the below):&nbsp; 
<ul>
<li>Archaeological survey, excavation, and monitoring</li>
</ul>
Minimum Requirements
<ul>
<li>Bachelor’s degree in Archaeology or Anthropology</li>
<li>Current valid driver’s license and the ability to safely operate a 4wd vehicle</li>
<li>Must have the ability to be insured to drive a vehicle and/or current auto-insurance</li>
<li>Must possess a valid driver’s license and have active personal automobile liability insurance by first day of employment.</li>
</ul>
* As a federal contractor, successful candidates are required to pass the following pre-employment requirements prior to beginning employment: pre - employment drug test and background check. Preferred Qualifications
<ul>
<li>Experience with a wide range of archaeological field methods including pedestrian survey, testing/evaluation, and monitoring</li>
<li>Ability to operate field equipment, including GPS equipment, cameras, and tablets</li>
<li>Physical ability to carry equipment and supplies (up to 40 lbs.) and walk or hike for long hours during fieldwork</li>
<li>Understanding and willingness to safely accommodate difficult weather and other environmental conditions and challenges</li>
<li>Willingness to travel to a project location for several consecutive days</li>
<li>Completed an accredited field school certification</li>
<li>Previous archaeological survey experience in California or adjacent areas, and experience recording a variety of site and isolate types in the region</li>
<li>Knowledge of and experience using ESRI Collector</li>
</ul>
Physical Requirements Working Conditions: 
<ul>
<li>This job operates in an outdoor or office-based environment and this role routinely uses standard office equipment such as computers, phones, printers, etc.</li>
<li>This job requires project site visits which are based outdoors which can include excessive noise, uneven walking surfaces, extreme weather, moving vehicles and equipment.</li>
</ul>
Physical Requirements: The physical demands described here are representative of those that must be met in order to successfully perform the essential functions of the job.
<ul>
<li>This job may require working on a computer, sitting or standing for long periods of time in an office or remote office setting.</li>
<li>Employees must be capable of bending, squatting, climbing ladders, and lifting up to 35 lbs. unassisted; 50lbs in a team lift (two or more employees).</li>
<li>This job requires attending meetings, both in person and virtually as well as speaking on the phone with government agency representatives, members of the public, and others. Speaking, hearing and listening are required.</li>
<li>Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.</li>
<li>Outdoor activity may involve walking/trekking in uneven terrain over long distances in extreme weather conditions for extended periods of time.</li>
</ul>
&nbsp; Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Proposed Salary Range: $21.00-$31.00/hourly* *Final agreed upon compensation will be based on a variety of factors including but not limited to an individual’s related experience, education, certifications, skills, and work location. Perks of Being a Dudekian At Dudek we will provide you with a competitive salary in an environment that promotes growth, career development, and a flexible work–life balance. Dudek offers an array of benefits, from medical, dental, and vision coverage, to the discretionary bonuses, based on firmwide, divisional, and individual performance. We also offer a yearly merit review, an employee stock ownership program, and dog friendly offices! To honor our key value of well-being, Dudek provides generous Paid Time Off (PTO) packages for both salaried and hourly employees. If you’re tired of an overly bureaucratic decision-making process and want to be part of a work culture that puts its employees first, speak with your recruiter to learn more about the great perks of being a Dudekian. *As-needed and part-time employees are eligible for our 401(k) plan, sick leave, and our Employee Assistance Program (EAP). As-needed and part-time employees have the option of additional benefits like medical benefits and ESOP participation provided they meet minimum hours worked during the 12-month look back measurement period. &nbsp;Speak with your recruiter to learn more. Dudek is an Equal Opportunity Employer.&nbsp; Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, disability, protected veteran status, or other characteristics protected by applicable law. Dudek is a U.S.-based employer. All positions are based in the U.S. and require U.S. work authorization.
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Archaeological Field Technician On-Call - Northern California

<h3>Job Description</h3>
Job DescriptionIEEE/Wi-Fi Standards Research Engineer About Ofinno: Ofinno is a leading research and development lab headquartered in Reston, Virginia, specializing in advancing communication and media standards. Our team’s innovative work has led to significant contributions to technologies such as 5G cellular, Wi-Fi, and media compression. Ofinno holds strategic partnerships and licensing agreements with several of the world’s leading technology companies that use such technologies. At Ofinno, we foster an environment of collaboration and excellence, where researchers can focus on delivering breakthroughs that shape the future of technology. Position Overview: As an IEEE/Wi-Fi Standards Research Engineer, you will play a pivotal role in advancing Wi-Fi technologies and standards. This position focuses on researching and optimizing Wi-Fi transmission and reception mechanisms, as well as developing novel algorithms based on IEEE 802.11, 802.15, and 802.19 protocols. Your work will contribute to the development of new features in Wi-Fi and Wi-Fi/Cellular coexistence technologies, positioning Ofinno as a leader in the Wi-Fi standards landscape. You will actively participate in IEEE and other relevant standards bodies, helping shape the future of wireless communication and ensuring the alignment of business priorities with emerging technologies. Key Responsibilities:&nbsp; As an&nbsp;IEEE/Wi-Fi Standards Research Engineer, you will:&nbsp;&nbsp;
<ul>
<li>Research and optimization of advanced&nbsp;Wi-Fi&nbsp;transmission and reception mechanisms.&nbsp;</li>
<li>Develop novel enhanced algorithms based on IEEE 802.11, 802.15, and 802.19 protocols.</li>
<li>Provide patentable and&nbsp;standardization-oriented&nbsp;solutions for implementation of new features in Wi-Fi and Wi-Fi/Cellular coexistence technologies.&nbsp;</li>
<li>Participate in IEEE and other relevant standards bodies to help drive advanced solutions to support&nbsp;Ofinno&nbsp;business priorities.&nbsp;&nbsp;</li>
<li>Write and present technical contributions to standards bodies, including IEEE 802.&nbsp;</li>
<li>Support the entire patent process from start to end.&nbsp;</li>
<li>Interact with and present to clients.</li>
<li>Possess expert knowledge of communication theory and IEEE 802 standards related technologies such as wireless local area network (WLAN) Wi-Fi (802.11n/ac/ax/be/bn, 802.11ad/ay), ZigBee, UWB, IEEE 802.15, 802.19 coexistence, V2X, multi-band, MIMO, Wi-Fi based positioning(802.11az), Wi-Fi sensing (802.11bf), cellular systems (e.g., 3GPP standards), or advanced spatial multiplexing mechanisms.&nbsp;&nbsp;</li>
</ul>
Based on your experience and qualifications, you may join us as a Senior Engineer, Staff Engineer, Senior Staff Engineer, or Principal Engineer. Qualifications:
<ul>
<li>Master's degree in Electrical Engineering or related field; Ph.D. is strongly preferred.</li>
<li>5+ years of experience with IEEE standards</li>
<li>A proven&nbsp;record of successful contributions to IEEE standards and activities&nbsp;</li>
<li>A proven record of developing patents related to wireless communication systems,&nbsp;Wi-Fi standards, IEEE 802.11, or 3GPP standards&nbsp;&nbsp;</li>
<li>Experienced in&nbsp;WLAN/Wi-Fi, cellular systems (e.g., 3GPP standards), or unlicensed spectrum</li>
<li>Experience developing physical/MAC layer protocols/procedures – channel access mechanism (e.g., LBT/FBE), OFDM/OFDMA, MIMO, dual-band operation, channel access mechanisms for&nbsp;mmWave&nbsp;frequencies, multi-beam operation, positioning, power saving techniques&nbsp;&nbsp;</li>
<li>Experience developing use cases and requirements for next generation Wi-Fi, Zigbee, UWB, and wireless personal area network (WPAN) communications</li>
<li>Experience with link-level/system-level simulation/optimization of wireless systems, protocol layer design, and network signaling&nbsp;</li>
</ul>
<ul>
<li>Have a theoretical understanding of network performance, queuing analysis, and spectral efficiency</li>
</ul>
What else you should know: Our people are our&nbsp;business.&nbsp;We know you&nbsp;have to&nbsp;see it to believe it, but here are some of the perks you can count on:&nbsp;
<ul>
<li>401(K) matching – We help you plan and save for retirement with a 401(K) matching program that’s available on day one.&nbsp;&nbsp;</li>
<li>Free&nbsp;healthcare plans – Ofinno covers full premiums for you and&nbsp;your family on select healthcare plans, including employer HSA contributions if applicable.&nbsp;</li>
<li>Free food – Our kitchen is always fully stocked, including lunch, protein bars, fruit, sodas, coffee and tea.&nbsp;&nbsp;</li>
<li>Unlimited Paid Time Off – Our lives are enriched by family time, vacations and personal time, so we offer unlimited paid time off and sick leave.&nbsp;&nbsp;</li>
<li>On-campus gym – Unwind, reduce stress and feel great – even when you’re at work.&nbsp;</li>
<li>Please discuss with our great People Ops team about additional benefits offered.&nbsp;</li>
</ul>
What Now?&nbsp; What are you waiting for? We hope you will click on the link and forward your credentials to us today.&nbsp;All your information will be kept confidential according to EEO guidelines. &nbsp;
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IEEE/Wi-Fi Standards Research Engineer

<h3>Job Description</h3>
Job Description
Job Description: The Geotechnical Department Manager will oversee the planning, coordination, and delivery of geotechnical projects across industrial, commercial, and residential sectors. This leadership role is responsible for departmental operations, strategic planning, quality control, financial oversight, and staff development. The manager will collaborate with clients, internal teams, and external partners to ensure timely and high-quality project execution.
Key Responsibilities:
<ul>
<li>
Strategic Planning Budgeting: Develop long-term goals and department business plans; manage annual capital and departmental budgets; support overall organizational strategy.
</li>
<li>
Business Development Client Engagement: Collaborate with business development teams on proposals; network to enhance visibility; define project tasks, schedules, and resource requirements.
</li>
<li>
Department Oversight Team Management: Monitor team productivity and chargeability; lead day-to-day operations; maintain a positive work environment; mentor and develop staff.
</li>
<li>
Project Delivery Quality Assurance: Lead the delivery of geotechnical and construction materials testing projects; ensure compliance with QA/QC standards; coordinate with architects, engineers, and consultants.
</li>
<li>
Policy Compliance: Establish and enforce department-specific policies and procedures; ensure adherence to internal standards and regulatory compliance.
</li>
<li>
Cross-Functional Collaboration: Coordinate with HR and IT on staffing and technology needs; work with other department heads on scheduling and resource allocation.
</li>
<li>
Financial Management: Oversee project budgets, invoices, software/equipment expenses; review client billing, collections, and identify revenue opportunities.
</li>
<li>
Client Contract Management: Consult with clients on geotechnical site requirements; oversee contracts and change orders; maintain communication throughout project lifecycle.
</li>
<li>
Additional Duties: Lead special initiatives and support company-wide objectives as assigned.
</li>
</ul>
Proficiencies:
<ul>
<li>
Budgeting, financial oversight, and invoicing
</li>
<li>
Project and personnel management
</li>
<li>
Proposal writing and business development
</li>
<li>
Microsoft Office Suite
</li>
<li>
Regulatory compliance in Michigan geotechnical standards
</li>
<li>
Communication and stakeholder management
</li>
</ul>
Qualifications:
<ul>
<li>
Bachelor’s degree in Civil Engineering or related field
</li>
<li>
10+ years of progressive experience in civil/geotechnical engineering
</li>
<li>
Active or eligible Michigan P.E. License
</li>
<li>
Experience managing multi-disciplinary projects and engineering teams
</li>
<li>
Knowledge of applicable codes, standards, and software
</li>
<li>
Proven track record of successful project delivery and client satisfaction
</li>
</ul>
Job Details: Security Clearance Required: No Visa Sponsorship: Not considered Location: Primarily local; travel to project sites required Relocation Assistance: Limited Compensation: Not disclosed Employment Type: Full-time, Monday–Friday, 8 AM–5 PM (with required overtime) Physical Requirements: Occasional lifting (up to 25 lbs), field visits, general office and site conditions
Key Skills: geotechnical, civil, budgeting, leadership, QA/QC, client-management, Microsoft Office, project-delivery, mentoring, proposal-writing

Geotechnical Department Manager

<h3>Job Description</h3>
Job Description
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. &nbsp;
The Senior Scientist in the Cell Science Department is responsible for the development and optimization of CHO-based processes for the production of biotherapeutics. This role requires broad expertise and the ability to contribute to both drug discovery and development projects. A strong interest in bench work and hands-on experience with mammalian cell culture is essential. This position requires a full-time onsite presence at our Redmond, WA location. Responsibilities:
<ul>
<li>Design and execute cell line development workflows, including vector design, transfection, clone screening, and selection for stable expression.</li>
<li>Perform cell culture experiments involving mammalian cells (e.g., CHO cells) under sterile, aseptic conditions.</li>
<li>Develop and optimize expression systems, including promoters, selection markers, and gene amplification strategies for high-yield production.</li>
<li>Screen and characterize clones for productivity, stability, growth characteristics, and product quality attributes using molecular and biochemical assays.</li>
<li>Collaborate with project teams and downstream process development scientists to execute protocols, experimental plans, critical production batches, and technology transfers.</li>
<li>Manage and prioritize multiple projects while supporting and coordinating with other departments to advance company objectives and develop scalable, robust culture processes.</li>
<li>Write and review Standard Operating Procedures (SOPs) and technical reports for regulatory filings. </li>
<li>Prepare process transfer documents and cGMP documentation to support the successful implementation of process technologies in clinical and commercial manufacturing operations.</li>
<li>Collaborate with R&amp;D and the manufacturing team in China, participating in meetings and providing technical support as needed.</li>
<li>Availability to work weekend and holiday shifts, as required.</li>
<li>Perform other duties as assigned.</li>
</ul>
 Qualifications:
<ul>
<li>Ph.D. in Cell Biology or a related field, with 5+ years of relevant experience in the pharmaceutical or biotechnology industry.</li>
<li>Strong scientific background in recombinant protein expression, cell line development, cellular metabolism, and media optimization.</li>
<li>Experience in both early- and late-stage bioreactor operations, mammalian stable cell line development, and upstream process development is preferred.</li>
<li>Demonstrated expertise in advanced technologies for cell line development, with a focus on antibody production.</li>
<li>Strong knowledge of FDA regulations and other global health authority requirements related to Investigational New Drug (IND) applications, particularly those concerning single stable clone selection and characterization.</li>
<li>Excellent written, verbal, and interpersonal communication skills.</li>
<li>Proven ability to perform effectively under pressure, meet tight deadlines, and adapt to shifting project priorities and requirements.</li>
<li>Experience with high-throughput automated workstations for clone selection is highly desirable.</li>
</ul>
Compensation and Benefits: The expected base salary range for this position is $90,000 - $140,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills. While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise align strongly with the requirements of the role. &nbsp; SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE. &nbsp; We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. &nbsp; SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply. &nbsp;
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Senior Scientist, Cell Science

<h3>Job Description</h3>
Job DescriptionRincon Consultants is seeking&nbsp;Field Biologists and Botanists to provide as-needed support for projects spanning&nbsp;the Central Coast, from San Mateo to Santa Barbara counties. This is an excellent opportunity for both&nbsp;early-career and experienced biological consultants (2–10+ years)&nbsp;with strong field expertise in&nbsp;Central Coast ecosystems&nbsp;to engage in high-impact work on utility, infrastructure, and development projects. We welcome candidates at all levels of experience and will adjust responsibilities, project complexity, and compensation accordingly.&nbsp;Senior-level applicants&nbsp;will have opportunities to&nbsp;lead field teams, oversee complex compliance efforts, mentor junior staff, and serve as subject matter experts. &nbsp;Overview of Key Duties and Responsibilities:&nbsp;
<ul>
<li>Conduct site assessments, surveys, and habitat evaluations for common and special-status plant and wildlife species and map vegetation communities.</li>
<li>Perform biological monitoring and provide compliance support during construction activities, prepare compliance monitoring reports.</li>
<li>Identify plant species using a dichotomous key, focusing on Central Coast botany.</li>
<li>Map vegetation communities using standard mapping practices and identify sensitive vegetation communities.</li>
<li>Survey, monitor, and assess habitats for special-status species, including but not limited to the following:
<ul>
<li>​​​​California red-legged frog</li>
<li>Foothill yellow-legged frog</li>
<li>California tiger salamander</li>
<li>Western spadefoot</li>
<li>Northwestern and southwestern pond turtles</li>
<li>San Francisco garter snake</li>
<li>Coho salmon</li>
<li>Steelhead</li>
<li>Tidewater goby</li>
<li>California least tern</li>
<li>Western snowy plover</li>
<li>Least Bell’s vireo</li>
<li>White-tailed kite</li>
<li>Northern harrier</li>
<li>Burrowing owl</li>
<li>Vernal pool branchiopods</li>
<li>Monarch butterfly</li>
<li>Smith’s blue butterfly</li>
<li>Crotch’s bumble bee</li>
<li>Regionally occurring special-status plants</li>
</ul>
</li>
</ul>
&nbsp;
<ul>
<li>Prepare preconstruction survey reports and other technical documentation.</li>
<li>Track compliance with mitigation measures and permit conditions, maintaining accurate field reports and monitoring logs.</li>
<li>Collaborate with multidisciplinary teams and provide additional support to the Natural Resources Team as needed.</li>
<li>Work independently or as a project/task lead depending on experience.</li>
<li>Wetland delineation and regulatory permitting experience is a plus.</li>
</ul>
 This Job Might Be for You If You Have the Following:&nbsp;
<ul>
<li>Bachelor’s or Master’s degree in biology, botany, ecology, environmental science, or a related field.</li>
<li>2–5+ years&nbsp;of biological fieldwork required.</li>
<li>Expertise in Central Coast ecosystems, including experience with compliance monitoring, habitat assessments, vegetation monitoring, and species-specific surveys.</li>
<li>Prior approval through the U.S. Fish and Wildlife Service or California Department of Fish and Wildlife as&nbsp;Designated Biologist, Species Specific Monitor or General Biological Monitor&nbsp;for any of the above listed species is highly desirable.</li>
<li>Familiarity with&nbsp;federal and state environmental laws, including but not limited to federal and state Endangered Species Acts, and the California Environmental Quality Act, as well as incidental take permits, Clean Water Act permits, Lake and Streambed Alteration Agreements, regulatory compliance oversight, and development/implementation of mitigation measures.</li>
<li>Demonstrated experience with&nbsp;the species listed above, including surveying and monitoring in occupied habitats and securing project approvals is highly desirable.</li>
<li>Excellent&nbsp;verbal and written communication skills, including strong technical writing experience preparing field reports, monitoring logs, and preconstruction survey documentation.</li>
<li>Ability to&nbsp;hike 6–8 miles per day&nbsp;in often difficult terrain and variable weather conditions while carrying 25 lbs.</li>
<li>Ability to work&nbsp;10–12+ hour days, as needed.</li>
</ul>
 Rincon Consultants is an award-winning leader in providing quality environmental consulting services throughout California and is recognized as a ‘Best Environmental Services Firm to Work For’ by the Zweig Group. We partner with clients in sectors such as transportation, energy and infrastructure, sustainability, climate change, oil and gas, water, commercial, private development, and government. Our 500+ associates in 13 offices located in Northern, Central, and Southern California are dedicated professionals who combine their passion with our purpose. The base pay for this as-needed position ranges from&nbsp;$32.00–$65.00 per hour, depending on experience, qualifications, and responsibilities.&nbsp;Entry-level candidates will fall within the lower portion of the range, while&nbsp;more experienced professionals may be considered for higher-level assignments and compensated accordingly. At Rincon, our salary ranges are based on market median of similar jobs, according to third party salary benchmark surveys. The base pay that is actually offered will take into account internal equity and also may vary depending on the candidate’s job-related knowledge, skills, and experience. Individuals offered employment must successfully complete a pre-employment drug screening as a condition of employment. Additionally, those hired who may be assigned to federal projects will be subject to further drug testing, including screening for cannabinoids (THC/marijuana), in compliance with the Drug-Free Workplace Act of 1988 and other applicable federal regulations, which take precedence over California state and local laws. &nbsp;
Rincon Consultants, Inc does not accept unsolicited applicant/candidate resumes from search firm recruiters and/or temporary agencies that do not have a signed contract and specified work order with Rincon Consultants. Further, such resumes received will be deemed the sole property of Rincon Consultants and no fees will be paid in the event Rincon Consultants subsequently hires such individual. Rincon Consultants is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
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