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<h3>Job Description</h3>
Job DescriptionGIS Technician I *Local to Richmond, VA only please *This position is 100% onsite during the training period. After training is completed, it will transition to a hybrid schedule with 2 days/week onsite Description:
<ul>
<li>Works in GIS and database applications which model electric utility distribution systems and fiber optic cables. </li>
<li>Requires understanding of functional business processes as they relate to design, construction and operations and working understanding of data attributes that support these business processes. </li>
<li>Requires ability to create a connected model that replicates the electric distribution system. </li>
<li>Performs and manages QA/QC processes. </li>
<li>Must be available to work emergency and planned overtime.</li>
<li>Editing GIS to display Fiber cable, as it is installed</li>
</ul>
 Education/Certification:
<ul>
<li>GIS education or certification</li>
</ul>
 Proper email communication will only be done to and from @astyra.com email addresses. Please ensure you are communicating with approved Astyra recruiters by checking this point when receiving offers and messages from us. Please ensure you are communicating within these guidelines and proper channels for the quickest possible interview consideration! #AC

GIS Technician I

<h3>Job Description</h3>
Job Description
We are LOTTE BIOLOGICS! Delivering Therapies That Enable a Healthier World. 
A new company, built on 80 years of tradition. We embody our core values of being Inspired by Science, Embracing Diversity, Fostering Talent, and Connecting Lives. Our mission is to be the most trusted partner in the industry, with high standards of quality and continuous innovation, to reliably deliver benefits for patients worldwide. 
Position Summary
The Engineer/Scientist, Manufacturing Science and Technology (MSAT) will report into the Development organization. The Engineer/Scientist will support upstream cell culture clinical manufacture of biopharmaceutical drug substance produced at the LOTTE Biologics Syracuse facility. The MSAT group supports a large-scale, cell culture, and purification facility. This position provides resolution of complex problems associated with manufacturing of biopharmaceutical drug substance and/or newer modalities. The Engineer/Scientist will contribute to a dynamic and highly collaborative team environment. The Engineer/Scientist will be required to work independently, with minimal supervision, to develop and deliver on appropriate objectives and priorities, overcome obstacles, and deliver results within established timelines. This position is a team-based position that may require work on evenings, weekends, and holidays.
Duties &amp; Responsibilities
<ul>
<li>Troubleshoot process-related manufacturing issues on the floor by leveraging strong upstream and/or downstream process knowledge to ensure quality of the product and compliance according to regulations</li>
<li>Proactively identify and make formal recommendations for opportunities to improve process performance, productivity, robustness, quality, business process, and safety through on-floor observation and through active collection, routine process and data monitoring/review, and statistical analysis of process performance data/trends</li>
<li>Drive improvements to completion and provide regular data updates to management to track process performance</li>
<li>Use different data trending and statistical analysis tools to complete process review, modeling, principal component analysis, and multivariate analysis</li>
<li>Author process-related Change Controls and applicable effectiveness checks</li>
<li>Author Quality Events (QEs) with a view toward providing thorough root cause analysis, making a product impact assessment, and provide recommendations for effective Corrective Action and Preventive Action (CAPA)</li>
<li>Support continued process verification program activities including authoring process monitoring plans, leading statistical alert event investigations, out-of-tolerance events, and support data lifecycle activities for internal and client needs, as applicable</li>
<li>Support authoring, review, and approval of manufacturing retrospective reports for inclusion in Annual Product Review(s) and Annual Quality Product Review(s), as applicable</li>
<li>Perform process facility fit, lead process technical transfers of new molecules and lead implementation of product/process transfers, including support of engineering, clinical, and process validation (PV) studies, as appropriate</li>
<li>Author technical documents and whitepapers, risk and impact assessments, Process Performance Qualification (PPQ) protocols and reports, provide floor coverage support for critical operations, and ensure that PV samples are collected and submitted</li>
<li>Support and lead process development, process characterization, and process technical transfer activities from laboratory to manufacturing scales, including author/review of study protocols and final reports for studies required in Manufacturing, as applicable</li>
<li>Support and lead implementation of new technologies and procedures from Development into Manufacturing, as applicable</li>
<li>Support regulatory changes and filings through change control authorship and management, filing authoring and review, and data collection and analysis, as applicable</li>
<li>Review cGMP documentation including Standard Operating Procedures (SOPs) and Manufacturing Batch Records (MBRs), as required</li>
<li>Serve as designee for Manager as directed when training and qualifications are appropriate</li>
</ul>
Education &amp; Experience
<ul>
<li>Degree in Biology, Chemistry, Biochemical or Chemical Engineering, or related industry experience: Minimum of a B.Sc/B.Eng with 6+ years, M.Sc./M.Eng degree with 4+ years, or Ph.D degree with no experience (0 years)</li>
</ul>
Knowledge, Skills, Abilities
<ul>
<li>Prior experience with technical support of cGMP/Biologics manufacturing facility and/or cGMP investigations (R&amp;D, technology transfer, manufacturing) is preferred</li>
<li>Prior experience in or knowledge of cell culture, recovery, and/or purification of biopharmaceutical drug substance in a manufacturing environment is preferred</li>
<li>The candidate must have demonstrated verbal, written, and communication skills including ability to present complex information clearly and concisely, with a successful proved history of working with technical teams</li>
<li>Experience should include technical support of a cGMP biologics manufacturing facility, including strong knowledge and engineering leadership for drug substance processing equipment, manufacturing support, and technology transfer</li>
<li>Prior experience in/knowledge of cell culture, recovery, and/or purification of biopharmaceutical drug substance in a manufacturing environment is required</li>
<li>Technical writing and data presentation abilities are requirements</li>
<li>Demonstrated leadership skills, and the ability to interact with diverse groups and teams is preferred</li>
<li>Project management skills (organization, collaboration, multi-tasking and communication), attention to detail, and the ability to perform well in a team-based environment is preferred</li>
<li>Prior experience in leading cGMP investigations using formal Root Cause Analysis tools is preferred</li>
<li>Prior experience with SOPs, cGMPs, and the know-how to work within a regulatory environment is required</li>
<li>Prior experience facilitating/participating in Risk Assessments is preferred</li>
</ul>
Physical Demands
<ul>
<li>Position requires repetitive use of hands and wrist (computer work), and infrequent lifting of items not to exceed 50 lbs</li>
<li>Occasional bending, twisting and stooping to allow for gowning into classified environment is required</li>
</ul>
Work Environment
<ul>
<li>Position is primarily office based with occasional work in a classified GMP manufacturing environment</li>
<li>Position is a team &amp; project-based position that will require occasional shift work, weekends, and holidays</li>
</ul>
Travel
&lt;5% travel required for this position 
Target Bonus
10%
Work Location:
East Syracuse, NY 
New York Pay Range$76,000—$113,000 USD
We are an Equal Employment Opportunity ("EEO") Employer. 
We believe that women, people of color, veterans and LGBTQ communities must participate in the work we do, so we strongly encourage applications from people with these identities or who are members of underrepresented communities!  If this is the work that you want to do, in a culture of inclusion and excellence with the goal of making our world to be a healthier place, then please apply today!

Engineer/Scientist, Manufacturing Science and Technology (MSAT)

<h3>Job Description</h3>
Job Description
JOB DESCRIPTION: Senior drivers handle Interstate moves (out-of-state), Intrastate (in-the-state), packing and Higher End Moves. Energetic, personable and safe. Must enjoy meeting people and be deeply familiar with area nuances, such as back roads and traffic patterns.
An ideal candidate has background in dispatching and warehouse. This position will ask for more than just driving and moving. We want someone who can grow with the company in multiple areas.
 DUTIES AND RESPONSIBILITIES:  Use route navigation apps and have knowledge of area  Interact with customers in a professional manner  Work occasional evenings and weekends  Complete daily maintenance checks on Trucks and notify manager of any issues  Drive in inclement weather, such as rain and snow  Maintain electronic logs to track routes
QUALIFICATIONS:  Must have valid Class D Driver’s License  Must have a clean driving record and reliable vehicle to drive to and from work
SKILLS:  Ability to manage time and routes for a streamlined experience  Familiarity with GPS devices or map apps  Minimum of one year driving experience  Open and transparent communication  Strength to lift 70 pounds plus bending and twisting  Work well independently and with a team

Senior Driver

<h3>Job Description</h3>
Job Description
Do you have a deep passion for financial markets?
Are you driven by creativity and a willingness to learn and develop your knowledge in markets and content production?
Bravos Research is a leading investment research and financial media company. We help investors navigate global markets with data-driven market research and video content.
Our investment strategy combines macro and technical analysis. We look at economic data and signals from stocks, currencies, and credit markets. Technical analysis helps us time the market, ensuring we make decisions with the highest probability of success.
As a Research Associate at Bravos Research, you will play a key role in creating high-quality investment research and video content:
<ul>
<li>Research: Assist in producing research covering a wide range of asset classes through macroeconomic, and technical analysis</li>
<li>Video Content Production: Develop scripts for video content to communicate complex market insights in an engaging, accessible way for clients</li>
<li>Chart Production: Create visually appealing charts using Excel for various Bravos Research products and clients</li>
<li>Social Media: Contribute to social media content creation and management</li>
</ul>
Requirements
<ul>
<li>Education: Undergraduate degree in Commerce, Finance, or Economics.</li>
<li>Experience: 1–2 years in a research role is preferred.</li>
<li>Skills:</li>
<ul>
<li>Deep understanding of macroeconomic cycles and their impact on financial markets</li>
<li>Knowledge of technical analysis, including the ability to interpret charts, patterns, and key indicators such as moving averages, RSI, and support/resistance levels</li>
<li>Proficiency in Microsoft Excel</li>
<li>Strong data visualization skills</li>
<li>Strong written and verbal communication skills</li>
<li>Ability to manage multiple projects in a deadline-driven environment. </li>
</ul>
</ul>
<ul>
<li>Must be comfortable working fully remote.</li>
</ul>
----------
How to Apply
To apply, submit your resume and a cover letter that tells us about yourself, what you can bring to Bravos Research, and how this role fits in your future.
Tell us about something you’ve done, something that’s relevant to the work we do, or something you're passionate about. 
We want to hear your unique voice of why you want to work with us and see some creativity and effort. Generic or AI-generated cover letters will be disregarded.
As part of our application process, we'll ask candidates to complete a non-paid trial task: writing a 800-word video script. This exercise is representative of the day-to-day responsibilities of our research team.
We look forward to hearing from you!

Research Analyst

<h3>Job Description</h3>
Job DescriptionJob Title: Supervisor Laboratory Medicine- Geisinger Medical Center Muncy (GMCM) - Full time - Days Location: Muncy, Pennsylvania Job Category: Diagnostic Services, Lab Schedule: Days Work Type: Full time Department: Laboratory Administration Division Date Posted: 12/01/2024 Job ID: R-70236 Job SummaryJoin our team at Geisinger Medical Laboratories. You can find your passion for caring and innovation as a team member in our state-of-the-art laboratories. Our mission is to provide exceptional patient care through innovative, efficient, and high-quality laboratory services. Job Duties
Leads and coordinates the daily operations of assigned section in conjunction with leadership. Plans, organizes and directs the activities of the section personnel to provide optimal, cost-effective delivery of services in accordance with departmental standards of quality, productivity, system-wide integration and standardization.
<ul>
<li>Supervises technical and administrative operations of assigned laboratory section.</li>
<li>Including maintaining a staff of qualified personnel to assure quality service is provided.</li>
<li>Selects, instructs and develops employees through careful interviewing, comprehensive training, delegation, and supportive coaching.</li>
<li>Conducts performance appraisals; ensures training and orientation of new hires, evaluates employee competency in an on-going manner.</li>
<li>Participates with Lab Information Technology Team and doctoral directors to plan and oversee all laboratory information system functions in support of hospital and group practice work processes.</li>
<li>Ensures staff is adequately trained in all computer applications required for their positions Ensures the provision of timely and efficient workflow in support of group practice quality and turnaround time standards of excellence.</li>
<li>Delegates appropriate tasks daily to assure equitable workload and adequate coverage of all responsibilities.</li>
<li>Prepares schedule to ensure adequate and appropriate staffing to meet service demands and maintain productivity standards.</li>
<li>Prepares and monitors annual operating budget for section cost centers.</li>
<li>Collaborates the planning of equipment purchases and leases with the Anatomic Pathology Operations Director.</li>
<li>Supervises analysis of cost for materials and negotiation of contracts to obtain favorable prices.</li>
<li>Oversees section purchasing, receiving, and inventory management to reduce costs.</li>
<li>Assures section's compliance with applicable regulations and accrediting standards.</li>
<li>Actively supports the Quality Program and takes a leadership role in facilitating change to realize noticeable error reduction and service improvement.</li>
<li>Provides appropriate administrative and transcription support to Pathologists for research projects, Tissue Arrays and the annual laboratory program.</li>
</ul>
 Work is typically performed in a clinical environment. Accountable for satisfying all job specific obligations and complying with all organization policies and procedures. The specific statements in this profile are not intended to be all-inclusive. They represent typical elements considered necessary to successfully perform the job. Additional competencies and skills outlined in any department-specific orientation will be considered essential to the performance of the job related to that position.
 Position Details
Education Qualification and Details &nbsp;
Medical Laboratory Scientist:&nbsp;
<ul>
<li>Bachelor of Science degree from an accredited college/university AND successful completion of an&nbsp;ASCP/NAACLS-accredited&nbsp;Medical Technology/Medical Laboratory Science program OR;&nbsp;</li>
<li>Bachelor of Science degree from an accredited college/university with a major in biological, chemical, physical or clinical laboratory science AND ASCP categorical certification OR;&nbsp;</li>
<li>Bachelor of Science degree from an accredited college/university with a major in biological, chemical, physical, or clinical laboratory science AND at least two years' experience in a role equivalent to that of a Medical Laboratory Technician (MLT) in a clinical laboratory&nbsp;</li>
</ul>
<ul>
<li>Hiring Incentive: This position qualifies for a $12,500 SIGN ON BONUS&nbsp; for eligible candidates</li>
<li>Required Experience: 6 years experience</li>
</ul>
Geisinger cares about not only its patients and members but also about you and your family. We offer a competitive compensation and benefits package to ensure that you and your loved ones can maintain good health, achieve financial stability, and excel both personally and professionally. We believe in creating a diverse and inclusive environment where all employees can be their authentic selves. To learn more: <a href="https://jobs.geisinger.org/diversity&amp;nbsp" target="_blank">https://jobs.geisinger.org/diversity&amp;nbsp</a>;
Benefits of working at Geisinger:
<ul>
<li>Full benefits (health, dental and vision) starting on day one&nbsp;</li>
<li>Three medical plan choices, including an expanded network for out-of-area employees and dependents&nbsp;&nbsp;</li>
<li>Pre-tax savings plans with healthcare and dependent care flexible spending accounts (FSA) and a health savings account (HSA)&nbsp;&nbsp;</li>
<li>Company-paid life insurance, short-term disability, and long-term disability coverage&nbsp;&nbsp;</li>
<li>401(k) plan that includes automatic Geisinger contributions&nbsp;&nbsp;</li>
<li>Generous paid time off (PTO) plan that allows you to accrue time quickly&nbsp;&nbsp;</li>
<li>Up to $5,000 in tuition reimbursement per calendar year&nbsp;&nbsp;</li>
<li>MyHealth Rewards wellness program to improve your health while earning a financial incentive&nbsp;&nbsp;</li>
<li>Family-friendly support including adoption and fertility assistance, parental leave pay, military leave pay and a free Care.com membership with discounted backup care for your loved ones&nbsp;&nbsp;</li>
<li>Employee Assistance Program (EAP): Referrals for childcare, eldercare, &amp; pet care. Access free legal guidance, mental health visits, work-life support, digital self-help tools and more.&nbsp;&nbsp;</li>
<li>Voluntary benefits including accident, critical illness, hospital indemnity insurance, identity theft protection, universal life and pet and legal insurance&nbsp;&nbsp;</li>
</ul>
 EducationHigh School Diploma or Equivalent (GED)- (Required), Bachelor's Degree- (Preferred) ExperienceMinimum of 6 years-Related work experience (Required), Minimum of 1 year-Managing people, processes, or projects (Preferred) Our Purpose &amp; ValuesOUR PURPOSE &amp; VALUES: Everything we do is about caring for our patients, our members, our students, our Geisinger family and our communities. KINDNESS: We strive to treat everyone as we would hope to be treated ourselves. EXCELLENCE: We treasure colleagues who humbly strive for excellence. LEARNING: We share our knowledge with the best and brightest to better prepare the caregivers for tomorrow. INNOVATION: We constantly seek new and better ways to care for our patients, our members, our community, and the nation. SAFETY: We provide a safe environment for our patients and members and the Geisinger family We offer healthcare benefits for full time and part time positions from day one, including vision, dental and domestic partners. Perhaps just as important, from senior management on down, we encourage an atmosphere of collaboration, cooperation and collegiality. We know that a diverse workforce with unique experiences and backgrounds makes our team stronger. Our patients, members and community come from a wide variety of backgrounds, and it takes a diverse workforce to make better health easier for all. We are proud to be an affirmative action, equal opportunity employer and all qualified applicants will receive consideration for employment regardless to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.PandoLogic. Keywords: Medical Laboratory Supervisor, Location: Muncy, PA - 17756 , PL: 599809060

Supervisor Laboratory Medicine- Geisinger Medical Center Muncy (GMCM) - Full time - Days

<h3>Job Description</h3>
Job DescriptionJob Description The Role: Title: In vivo research associate, Immunology and Pharmacology Job summary: The PharmaEssentia Innovation Research Center is building a world-class new drug discovery team in Boston area. We are seeking a highly motivated in vivo research associate to support in vivo experiment (rodent), including MTD studies, Efficacy studies, PK/PD studies and tissue harvest. You will also be asked to maintain and expand cancer cell lines to support the in vivo tumor model studies and conduct hand-on dosing and procedure support for mice pharmacology studies. In addition, you may need to support all aspects of laboratory operation to maintain a highly productive vivarium/laboratory. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), aims to leverage our current expertise in oncology and immunology therapeutic areas to identify and develop novel therapeutic opportunities. Therefore, we are recruiting talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs through disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. PIRC offers a competitive benefit package, including a competitive 401k match, medical/dental/eye care benefits, and other benefits. Summary of Key Responsibilities:
<ul>
<li>Hand-on execute subcutaneous tumor model studies from cancer cells expansion, implantation (in mice), tumor measurement, group randomization and administration of test articles. </li>
<li>Hand-on support all mice pharmacology study procedures, including but not limiting to dosing and tissue harvest.</li>
<li>Follow PIRC IACUC program/protocols and standard operating procedures (SOPs) for all animal procedures.</li>
<li>Maintain and expand cancer cell lines for human xenograft tumor and mouse syngeneic tumor models. </li>
<li>Data process and graphing for the internal team update presentation.</li>
</ul>
Essential Qualifications:
<ul>
<li>B.S. or higher degree in immunology, pharmaceutical sciences or related scientific field</li>
</ul>
&nbsp;SkillPerformed in the last 2 years (includes training)In vitro assayELISANot required, good to knowMSDNot required, good to knowFACSNot required, good to knowHusbandry&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Aseptic TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Micro-Isolator TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Restraint &amp; HandlingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Room ChecksNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cage ChangeNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Injections/ Administration&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubcutaneousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntraperitonealMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntravenousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntramuscularNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Oral GavageNot required, good to knowBlood Withdrawal&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Tail BleedMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cardiac PunctureMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubmandibularMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; RO BleedNot required, good to knowEuthanasia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; CO2 OverdoseMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cervical DislocationMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; DecapitationNot requiredAnimal Preparation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; ShavingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear TaggingNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear Punching/ NotchingNot requiredImplantation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Xenograft SCMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Mammary Fat Pad&nbsp;Good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; TrocarNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Anesthesia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Isoflurane AnesthesiaNot required, good to knowLab OperationsGeneral Organizing lab spaceMustReceiving/stocking suppliesMustAny other duties that may ariseMustMammalian Cell CultureStandard mammalian cell culture procedures and associated aseptic techniques in addition to maintenance of tissue culture facilitiesMustMedia and buffer preparation, culture initiation, propagation, and cryopreservation of cells, including primary human and mouse cells and cell lines as well as adherence to quality control schedules for ensuring consistency of cell culture materials.Must &nbsp; EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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BCuKsdi8dH

In-vivo Research Associate, Immunology and Pharmacology

<h3>Job Description</h3>
Job Description
Coatings Engineer / Chemical Engineer – Automotive Tier 1 ???? Location: Alabama | ???? $95K – $125K
Join a Growing Automotive Products Manufacturer!
 Full benefits, 401k match, PTO, relocation assistance &amp; more!
We’re looking for a Technical Coatings Engineer with a deep knowledge of Understanding in Automotive Coatings (wash, rinse, e-coat, paint).
We are a well-established Tier 1 Automotive Supplier of Exterior and Interior Automotive Stampings and Assemblies
???? Key Responsibilities:
<ul>
<li>Understanding of Coatings and Applications for Stamped Steel Parts</li>
<li>Lead New Product / Project Programs for Stamped Metal Parts</li>
<li>Collaborate with Customers, Production and Engineering Teams</li>
<li>Conduct Root Cause Analysis and Determine Effective Counter Measures</li>
<li>Support Prototype Builds and Program Launches</li>
<li>Champion New Equipment Installations for Technical Assembly</li>
<li>Knowledge of Fanuc Robots or Robotics is a Plus!</li>
<li>Help Advise New Program Launches</li>
<li>Assign work to Junior Engineers and Track Progress</li>
<li>Manage Overall Project Goals and KPI’s</li>
<li>Maintain Program Budget’s</li>
<li>Must have Excellent Reporting Capability and Methodology</li>
</ul>
✅ Requirements:
<ul>
<li>Automotive experience Preferred with (PPAP, APQP, AIAG, Stamping Die’s), understanding of TS16949</li>
<li>Bachelor’s degree with 1 -3 years in Automotive Coatings / Chemical Engineering</li>
<li>Strong Communication, Analysis, and Problem-Solving Skills</li>
<li>CAD/SolidWorks, MS Project</li>
<li>Knowledge and Ability to Make Quick Decisions</li>
<li>BS in Chemical Engineering or Manufacturing Engineering or Equivalent</li>
</ul>
???? Perks:
<ul>
<li>Competitive pay + bonus potential</li>
<li>Full medical, dental, vision coverage</li>
<li>401k match, PTO, paid holidays</li>
<li>Minimal travel + lifestyle perks</li>
<li>Excellent growth &amp; promotion potential</li>
</ul>
???? Join a high-growth company where innovation, quality, and leadership are valued!
???? Call Top Dog Engineers: 601.607.8217

Coatings Engineer / Chemical Engineer

<h3>Job Description</h3>
Job DescriptionWanted: Geotechnical Engineer - Senior, Project, and Associate Levels Don't Miss Out On This GREAT Opportunity. Apply today! This Jobot Job is hosted by: Stephen Niedringhaus Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $100,000 - $170,000 per year 
A bit about us:
 ** HIRING - Experience Geotechnical Engineer - Senior, Project, and Associate Levels Don't Miss Out On This GREAT Opportunity. Apply today! ** Award-winning Geotechnical and Civil Engineering Firm continues to grow. We have a lot of work that needs to be done and done right! If you want to join a "Family-Like" company, do not wait, apply today. For almost 60 years, we have built our reputation as a trusted consultant for some of the most challenging and recognizable construction, and Civil &amp; Geotechnical Engineering projects across Southern California because we do things a little differently! Our projects range from private developers and residential projects to high-profile public works infrastructure projects. Don't miss out on this excellent career opportunity. Interviews are going on now. 
Why join us?
 Geotechnical Engineers - Senior, Project, and Associate Levels 
<ul>
<li> Competitive Base Salary - $100,000 to $170,000 depending on experience and qualifications</li>
<li> Flexible Work Schedules - Work | Life Balance!!!</li>
<li> "Family-Like" Work Atmosphere!!!</li>
<li> Accelerated Career Growth!!!</li>
<li> Medical, Dental, Vision, Life Insurance, HSA contributions, and matching 401(k)</li>
<li> Profit Sharing Bonus</li>
<li> Paid Holidays</li>
</ul>
 And so much more!!! 
Job Details
 You will join our growing team of Engineers and Geologists. Key Responsibilities and Duties 
<ul>
<li> Join a dynamic team of engineers and geologists</li>
<li> Oversee and design geotechnical field investigations (drilling, sampling, lab testing)</li>
<li> Analyze subsurface and geologic data for modeling and design</li>
<li> Perform geotechnical analyses for slope stability, liquefaction, foundation capacity, etc.</li>
<li> Prepare detailed geotechnical reports and design recommendations</li>
<li> Manage projects from proposal to delivery and client coordination</li>
<li> Use specialized software for analysis, mapping, and design</li>
<li> Collaborate with interdisciplinary teams across civil, structural, and pavement engineering</li>
</ul>
 Must-Have and Preferred Skills: 
<ul>
<li> Must have: California Professional Engineer (PE) license and B.S. in Civil Engineering</li>
<li> 8+ years of geotechnical engineering experience</li>
<li> Strong expertise in geotechnical investigations, analysis, and design</li>
<li> Proficiency with software such as LPILE, Slope/w, FLAC, CPet-IT, SHAFT, PYWALL</li>
<li> Experience preparing technical geotechnical reports</li>
<li> Project management experience including budgeting, proposals, and scheduling</li>
<li> Familiarity with AutoCAD and ESRI ArcGIS</li>
<li> GE license or Master’s in Geotechnical Engineering (preferred)</li>
</ul>
 Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Geotechnical Engineer - Senior, Project, and Associate Levels

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to perform testing and evaluations of raw materials, bulk, and finished products following written procedures. The role involves ensuring compliance with GMP requirements and maintaining accurate documentation records. You will develop an understanding of various testing methodologies and maintain neat and organized work areas.
Responsibilities
<ul>
<li>Perform testing and evaluations of raw materials, bulk, and finished products in accordance with written procedures.</li>
<li>Ensure test results meet current specifications prior to completion and approval.</li>
<li>Troubleshoot out-of-specification situations and perform batch adjustments as needed.</li>
<li>Maintain compliance with current regulatory expectations and practices, such as USP.</li>
<li>Document monthly Key Quality Incidents and out-of-specification situations, determining root causes and suggesting solutions.</li>
<li>Utilize data to focus improvement efforts, ensuring customer requirements and regulatory regulations are met.</li>
<li>Understand and maintain a culture of 'lean action' within the department.</li>
</ul>
Essential Skills
<ul>
<li>4-year degree in Chemistry.</li>
<li>0-2 years of quality control industry experience in pharma, cosmetics, or food.</li>
<li>Proficiency in laboratory techniques such as wet chemistry, FTIR, and quality control.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with solution preparation, wet chemistry titrations, HPLC, GC, and UV is a plus.</li>
</ul>
Work Environment
This Quality Control Chemist position is based at the Minneapolis site, with hours from Friday to Sunday, working 12-hour shifts. This weekend schedule totals 36 hours, with potential opportunities for full 40-hour work weeks depending on sample and workload availability. The role requires working independently overnight, with a counterpart available at the other facility. The position involves moderate to high physical activity and exposure to various fragrances indoors. Candidates should be able to respond and adapt to changes in the work environment and work in a high-paced environment. Benefits include accruable PTO, holiday pay, and sick pay.
Pay and Benefits
The pay range for this position is $25.00 - $26.00/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 Minneapolis,MN.
Application Deadline
This position is anticipated to close on Sep 1, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Chemical TechnicianJob Description:
We are seeking a dedicated Chemical Technician to join our Compliance and Support team at a plant in Wilsonville. This role primarily involves supporting operations and environmental aspects within a power plant, with a focus on unit-specific tests and silica testing. As you gain experience, you will also maintain two water treatment plants. This position is integral to ensuring the proper operation of the plant's facilities, which include the power plant, water treatment plant, and sewage treatment plant.
Responsibilities:
<ul>
<li>Perform technical and analytical services essential to the proper operation of a power-generating plant.</li>
<li>Operate and maintain a water treatment plant to ensure consistent demineralized water production.</li>
<li>Manage boiler water chemistry to support water/steam cycle operations.</li>
<li>Operate and maintain wastewater treatment equipment to ensure discharge compliance.</li>
<li>Conduct water sampling and analysis for pH, conductivity, sodium, silica, and various other parameters.</li>
<li>Calibrate and maintain continuous instrumentation.</li>
<li>Manage various chemical feed systems for optimal operation.</li>
<li>Log data, analyze, and respond to critical plant operations.</li>
</ul>
Essential Skills:
<ul>
<li>BS degree in Chemistry or another field of science with a minimum of 12 semester hours in Chemistry.</li>
<li>2+ years of industrial lab experience.</li>
<li>Knowledgeable about water treatment processes, pH reading and monitoring, and environmental testing.</li>
<li>Experience and competency in the use, calibration, and maintenance of laboratory instrumentation and equipment.</li>
<li>Familiarity with water analysis, pH, conductivity, and simple calibrations.</li>
<li>Ability to troubleshoot mechanical systems.</li>
<li>Broad knowledge of analytical, inorganic, environmental, and water chemistries.</li>
<li>Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.</li>
<li>Ability to read and understand schematic diagrams and identify plant water process problems.</li>
</ul>
Additional Skills &amp; Qualifications:
<ul>
<li>Hazmat training is a plus.</li>
<li>Familiarity with chemicals and safety certifications is advantageous.</li>
<li>Values continuous learning and teamwork.</li>
<li>Ability to work with limited supervision and adapt to changing work duties.</li>
<li>High initiative and good communication skills.</li>
<li>Willingness to learn from existing chem techs and demonstrate flexibility and reliability.</li>
</ul>
Work Environment:
The Chemical Technician will work primarily inside the power plant, with 98% of their time dedicated to this environment. Standard work hours are Monday to Friday, 6:30 AM to 3:00 PM, with rotating weekends approximately once a month. Call-ins are scheduled based on workload, with prior notice provided. Candidates should have a foundational understanding of basic chemical processes, hazardous waste, and chemical process safety according to OSHA standards. Initial training will take place in the lab for up to two weeks.
Job Type &amp; Location:
This is an on-site position based in Wilsonville, Alabama.
Pay and Benefits
The pay range for this position is $25.00 - $40.00/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 Wilsonville,AL.
Application Deadline
This position is anticipated to close on Aug 22, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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