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<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>Competitive salary</li>
<li>Free uniforms</li>
</ul>
 Austin Wildlife Rescue is hiring full-time Seasonal Animal Care Technicians to start ASAP and to work through mid-August with the option to stay through the end of October, and with the potential to stay on beyond October based on job performance. Technicians work directly with a variety of native Texas wildlife, including mammals, birds and reptiles. Job Location * Rehabilitation Center 111 Elbow Bend, Elgin, TX 78621 Responsibilities/Duties: * Cleaning cages * Feeding animals * Administering medications * Maintaining care plans for injured animals, * Providing direction/guidance to interns and volunteers * Assisting the public with animals they bring to our facility. ** This is a very physical job that requires a lot of movement and lifting. Requirements/Preferences: * Proof of a tetanus vaccination within the past 10 years is required. ** Rabies vaccines are optional and are at the expense of the employee. Benefits/Perks: * Accrued paid sick-time off * AWR staff t-shirts provided **Hands-on experience working with amazing native Texas wildlife *About Austin Wildlife Rescue: The mission of Austin Wildlife Rescue is to rehabilitate and release orphaned, injured, and sick wild animals and to educate the public to coexist with wildlife. We accept native Texas wildlife into our care. Our Intake location is in Austin. There we take in the majority of the animals in our care, over 9,000 per year! Our Rehabilitation Facility is located in Elgin, which is where the animals are transported to and stay until they are ready to be released.

Seasonal Animal Care Technician-HIRING NOW FOR FULL TIME DAY!

<h3>Job Description</h3>
Job DescriptionBenefits/Perks
<ul>
<li>Ability to grow with the Company</li>
<li>Competitive Compensation</li>
<li>Flexible Scheduling</li>
<li>Career Growth Potential</li>
<li>A variety of work</li>
</ul>
Job SummaryWe are seeking geotechnical/construction materials testing field and laboratory technicians to join our team in Tampa, Florida! We are a Florida based consulting company specialized in geotechnical engineering and environmental services. As a geotechnical/construction material testing field and/or laboratory technician, you will be responsible for performing a variety of construction materials (soils, concrete and others) testing, project specific observations and site assessment duties under direct supervision and/or from detailed procedures.&nbsp; Responsibilities Primary responsibilities will include but are not limited to: 
<ul>
<li>Performing testing and sampling of soils, concrete, pavement, and other construction materials at active construction sites and/or in the laboratory.</li>
<li>Reviewing construction plans to determine the testing required, and track testing performed.</li>
<li>Communicating with client and project team on construction progress and testing results.</li>
<li>Preparing daily field reports of construction activities and testing results.</li>
<li>Other duties may be assigned.</li>
</ul>
Qualifications
<ul>
<li>High school education or Equivalent.&nbsp;</li>
<li>Experience performing construction materials testing / inspections is preferred, but not required.</li>
<li>Experienced professionals are highly encouraged to apply.&nbsp; &nbsp;</li>
<li>Must have basic math, calculator and computer skills.</li>
<li>Ability to communicate and interact effectively in verbal &amp; written communication.</li>
<li>Must be able to read and understand work plans.&nbsp;</li>
<li>Must be able to work off shifts and overtime .</li>
<li>Valid Driver's License and reliable driving record (required).</li>
<li>Ability to lift, move, push, and pull 30 to 50 pounds. </li>
</ul>
&nbsp;

Geotechnical/Construction Materials Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Are you an innovative and self-motivated data scientist with a passion for leveraging AI/ML in computational protein design? Join AbbVie's Discovery Biotherapeutics team as a Senior Scientist, where you'll have the opportunity to work on groundbreaking technologies for discovering and developing novel biotherapeutics.
About the Role
In this pivotal role, you will utilize your expertise in AI/ML and computational protein design to drive the development of cutting-edge biotherapeutics. You'll have access to leading modeling tools and collaborate with a cross-functional team focused on protein production and characterization.
Key Responsibilities
<ul>
<li>Develop and implement state-of-the-art AI/ML methodologies for computational protein design, including fine-tuning protein language models and generative protein design.</li>
<li>Stay abreast of advancements in NLP, ML, and generative AI to build novel tools that enhance therapeutic discovery and development.</li>
<li>Collaborate with internal experts to optimize the computational discovery infrastructure, offering both individual and team-based innovative solutions.</li>
<li>Communicate complex scientific ideas effectively to both technical and non-technical audiences, fostering collaboration across multidisciplinary teams.</li>
</ul>
Qualifications 
<ul>
<li>BS, MS, or PhD in Chemistry, Computer Science, Machine Learning, Cheminformatics, Chemical Engineering, or related fields, with typically 10-12+ years (BS), 8-10+ years (MS), or 0-4+ years (PhD) of experience.</li>
<li>Proven track record in developing machine learning models for chemical and biological data, including AI/ML-enabled molecular generation and affinity prediction.</li>
<li>Proficiency in programming languages such as Python and experience with cloud computing capabilities.</li>
<li>Strong analytical and problem-solving skills, with demonstrated creativity and the ability to contribute individually and collaboratively.</li>
<li>Experience in modeling protein sequence, structure, and function and a history of related scientific publications.</li>
<li>Versatile communicator who can elucidate complex ideas to non-specialists and commitment to continuous improvement and innovation. &nbsp;</li>
</ul>
Position will be hired based on level of experience- Senior Scientist I or Senior Scientist II.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job may be eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, Computational Protein Design - AI/ML

<h3>Job Description</h3>
Job Description
Matrix has been named a Zweig Group 2025 Best Firm to Work For! 
 
About Matrix: Matrix Design Group, Inc., an employee-owned planning, engineering, and environmental consulting firm is actively seeking a GIS Analyst in our Denver, Colorado Springs, Phoenix, and San Antonio offices. As an employee-owned company we are committed to fostering, cultivating, and preserving a culture of diversity, respect, and excellence. Our strengths of service, innovation, and skill are a result of that belief. We have a friendly, collegial, cooperative atmosphere and offer a full range of benefits including medical, dental, vision, disability, and life insurance; holiday, vacation, and sick leave; training and education; 401(k) and an Employee Stock Ownership Plan (ESOP). Matrix employees are encouraged to participate in employee wellness programs, social committees, and community outreach programs. We strive to employ highly motivated people with excellent communication and applied problem-solving skills who desire to advance their talents and skills.
Salary Range: $62,000.00 to $73,000.00 Annually. Salary will be dependent upon experience. 
Job Summary:
Responsible for creating and analyzing digital mapping data using Geographic Information Systems (GIS) to support company-wide efforts in product planning, design, and implementation. Essential functions and competencies may be adjusted to be commensurate with applicant experience and skillset. 
Essential Functions:
<ul>
<li>Performs spatial analyses and creates information products from GIS and related software.</li>
<li>Produces presentation quality maps using cartographic design standards for public, client, and internal usage.</li>
<li>Catalogs and inventories GIS data, including metadata creation.</li>
<li>Develops and edits large and complex GIS databases.</li>
<li>Maintains a high attention to detail on concurrent tasks, while meeting challenging deadlines.</li>
<li>Uses GIS techniques to provide a better understanding of certain variables in a given geographic location. </li>
<li>Relies on experience and judgment to plan and accomplish goals.</li>
<li>Creates and manages data to support 3D visualization.</li>
<li>Develops and maintains ArcGIS Online and StoryMaps to express planning concepts and alternatives.</li>
<li>Develops custom web applications using ArcGIS Experience Builder and ArcGIS API for JavaScript.</li>
<li>Acquires and designs field collection applications using ArcGIS Field Maps and similar software platforms. </li>
<li>Assists with client, customer, or official contacts and communication pertaining to specific assignments or meetings.</li>
</ul>
Competencies:
<ul>
<li>Proficiency with Esri’s GIS mapping software, particularly ArcGIS Pro with Spatial Analyst and 3D Analyst extensions, ArcGIS Experience Builder, ArcGIS Field Maps and Survey123 for ArcGIS.</li>
<li>Proficiency in MS Office Suite.</li>
<li>Working knowledge of various relational database management systems (RDBMS).</li>
<li>Strong verbal and written communication skills.</li>
<li>Working knowledge of AutoCAD Civil 3D with the ability to perform basic editing tasks.</li>
<li>Analytical and problem-solving skills.</li>
<li>Ability to take direction and work independently.</li>
<li>A working understanding of programming languages.</li>
<li>Familiarity with a variety of the field’s concepts, practices, and procedures. A background in asset management, planning, water resources, or similar fields is a plus.</li>
<li>Familiarity with ArcGIS Model Builder and/or Python scripting for automating geoprocessing.  </li>
</ul>
Education and Experience:
<ul>
<li>Bachelor’s degree from accredited program in GIS, geography, planning, computer science, engineering, geology, or related field. An associate degree or GIS certification may also be acceptable if the work experience is commensurate with this position. A master’s degree is a plus. </li>
<li>Minimum of two (2) years of experience with demonstrated GIS responsibilities. Additional experience is a plus.</li>
<li>Experience implementing GIS solutions for asset management, land use planning projects, and water resources (hydrology &amp; hydraulics) is preferred.</li>
<li>Experience working in the engineering and/or planning consulting fields is preferred.</li>
<li>Geographic information System Planning (GISP) Certificate is a plus.</li>
<li>Valid driver's license, in conjunction with successfully passing the Company’s MVR.</li>
</ul>
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
Physical Demands:
While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 10 pounds.
The noise level in the work environment is usually moderate.
Matrix Design Group, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, color, religion, sex, national origin, or protected veteran status, and will not be discriminated against based on disability. 
The expected salary range for this position is displayed in accordance with the Colorado Equal Pay for Equal Work Act. The final agreed upon compensation is based on individual education, qualifications, experience, and work location. 
Any applicant with a qualifying physical or mental disability who believes s/he requires a reasonable accommodation for any part of the application process should contact us at 719-575-0100 for assistance. 
How to Apply:
Please apply online at <a href="http://www.matrixdesigngroup.com/careers" target="_blank">http://www.matrixdesigngroup.com/careers</a>

GIS Analyst

<h3>Job Description</h3>
Job Description
The Associate Investigator is a member of the General Toxicology group in our AAALAC-accredited and GLP-compliant facility. The Associate investigator will be responsible for conducting studies which includes protocol reviews, in-life data collection (both electronically and written), collecting biological samples, and performing procedures according to Standard Operating Procedures (SOPs). Job Responsibility The duties include, but are not limited to the following: • Ensure the welfare of laboratory rodents in the testing facility. • Uphold study integrity. • Careful handling/restraint of laboratory rodents. • Test material administration by various routes of exposure, e.g. dietary, oral gavage, intraperitoneal injection, subcutaneous injection. • Determining and recording animal body weights, clinical observations, holding for eye exams, and other in-life study functions. • Collecting biological samples which can include, urine, feces, and blood (tail venipuncture). • Data collection using manual and electronic methods (including Provantis and Microsoft software systems). • Collecting, recording, documenting, and reporting results with a high degree of accuracy and precision in a timely manner. • Understanding and following all relevant SOPs, GLPs, and safety guidelines. • Learning and refining new laboratory skills as applicable. • Maintaining study records and data in in a well-organized manner. • Communicating effectively with Study Directors, Supervisors, attending Veterinarians, and other relevant staff members within the company. • Assisting other Associates and completing other tasks as assigned. • Working weekends, holidays, and or external hours on a rotating schedule. Job Requirements • B.S. degree in animal science, biology, or related field or an equivalent of a combination of applicable work experience and higher education. • 2-5 Years of relevant experience. • Ability to work both independently and in a team setting with minimal supervision. • Proficient with Microsoft Office software programs. Physical Demands • Employees must be able to lift, move, manipulate, and/or hold heavy objects up to 50 pounds. This includes work materials, equipment, animal cage racking systems, and/or transporting equipment on wheels. • Must be able to perform procedures which require talking, hearing, standing, or sitting for long periods of time, entering data into a computer database(s), using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing personal safety equipment (PPE) according to Corteva Agriscience's and/or OSHA standards. • Must be able to frequently hold rodent species firmly while utilizing fine motor skills. Work Environment • Most of the tasks required for this position will be conducting in a secured and locked animal vivarium. When entering the vivarium individuals must wear safety glasses with side shields, laboratory coats or scrubs, and shoe coverings. The use of a respirator (usually a particulate filtering mask) is required in areas/rooms where research animals are being housed or handled. Please note: If the employee had visited another animal facility on the same day as work, has had contact with companion-/pet-/wild-rodents, or had contact with snakes/reptiles/birds of prey that are fed rodents, the employee must shower and have a complete change of clothing prior to entering Corteva Agriscience’s animal vivarium. • Employees will be working individually and/or in groups in small animal housing rooms, examination rooms, or special purpose procedures rooms. • Work in a research environment, which requires the use of sharp objects (e.g. needles) and working around mechanical parts such as rodent caging systems, watering systems, cage washing systems. • Working with or near known or unknown toxic chemicals and/or biological hazards. • The employee will work regularly with live animals requiring the use of appropriate PPE to prevent exposure to allergens, biohazards, and/or test material hazards. &nbsp;
Company DescriptionFrontier Science Partnerships is a full-service scientific and business alliance partner, providing outsourced staffing to expand your company’s research, production, and business service capabilities. 
<h3>Company Description</h3>
Frontier Science Partnerships is a full-service scientific and business alliance partner, providing outsourced staffing to expand your company’s research, production, and business service capabilities.

General Toxicology Associate Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Analytical Research &amp; Development team is seeking a talented, highly motivated candidate with experience in small molecule structure elucidation.&nbsp; As part of the Predictive Stability and Structure Elucidation team, the successful candidate will be responsible for designing, developing, and implementing analytical methods for the characterization of small molecules with an emphasis on mass spectrometry-based methods.&nbsp; The candidate will collaborate with analytical and cross-functional teams to build an understanding of process impurities and degradation pathways for small molecule APIs.&nbsp;
The successful candidate will be expected to act as a lead scientist in their area of expertise, critically evaluate relevant scientific and regulatory advances, and integrate this knowledge into research and development programs.&nbsp; Candidate should possess an understanding of their core discipline and use that expertise to support early phase development of drug substance and drug product and collaborate across the global Analytical R&amp;D organization and with cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), Quality Assurance (QA), and CMC-Regulatory. 
Responsibilities:
<ul>
<li>Utilize cutting-edge mass spectrometry techniques, including high-resolution MS, MS/MS, ion mobility-MS, and 2DLC-MS, to characterize small molecule active pharmaceutical ingredients, intermediates, starting materials, and impurities.</li>
<li>Identify, develop, and implement novel analytical methods for the characterization of pharmaceuticals with an emphasis on LC-MS and analytical characterization to drive discovery projects through the research and development pipeline.</li>
<li>Be responsible for leading the structure elucidation aspects of a project while collaborating with cross-functional project teams to advance programs through the development pipeline.</li>
<li>Support new product development with advanced method development and validations, technical transfer packages, and generation of technical data in support regulatory requirements.</li>
<li>Be highly autonomous and productive in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor.</li>
<li>Formulate conclusions and design follow-on experiments based on multidisciplinary data.</li>
<li>Initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a research and development program.</li>
<li>Communicate and collaborate with cross-functional groups and departments.</li>
<li>Routinely demonstrate scientific initiative and creativity in research or development activities and maintain a high level of productivity in the lab.</li>
</ul>
Qualifications 
<ul>
<li>Bachelors, Masters, or Ph.D. in Analytical Chemistry typically with a minimum of 12 (BS), 10 (MS), or 4 (Ph.D.) years related industry experience.</li>
<li>Extensive experience in designing mass spectrometry experiments for the characterization of peptides, proteins, and/or oligonucleotides and a strong understanding of instrument theory and operation.</li>
<li>Strong technical background in analytical chemistry, excellent analytical problem-solving skills. Capable of independently developing and troubleshoot analytical methods.</li>
<li>Practical knowledge of organic structure, functional groups, chemistry, and modern spectroscopic techniques as applied to small-molecule analytical analysis.</li>
<li>Hands-on experience with NMR spectroscopy a plus.</li>
<li>Self-motivated, hard-working, detail-oriented individual able to work in a fast-paced team environment.</li>
<li>Experience in the use of computerized data handling systems.</li>
<li>High-quality written and oral communication skills and ability to interact effectively with interdisciplinary scientists and engineers.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist II , Mass Spectrometry

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
Job Summary:
We are seeking a skilled and detail-oriented Protein Purification Associate Scientist to join our US Protein Department. This role involves executing downstream processing activities including protein purification, characterization, and documentation. The ideal candidate will have a solid background in biochemistry, biotechnology, or a related field, along with hands-on experience in protein purification techniques in a laboratory or manufacturing setting. 
Key Responsibilities:
<ol>
<li>Perform protein purification using a variety of chromatography techniques such as affinity, ion exchange, size exclusion, and hydrophobic interaction. </li>
<li>Prepare buffers and reagents following SOPs and project-specific protocols. </li>
<li>Characterize protein products using SDS-PAGE, Western Blot, HPLC, UV spectroscopy, BCA assay, and other analytical methods. </li>
<li>Maintain accurate, complete, and timely documentation of experimental procedures and results. </li>
<li>Troubleshoot and optimize purification protocols as needed to improve yield and purity. </li>
<li>Collaborate closely with upstream, analytical, and quality teams to ensure project timelines and specifications are met. </li>
<li>Assist in the revision and creation of SOPs, batch records, and technical reports. </li>
<li>Support additional tasks and projects as assigned by the department supervisor. </li>
</ol>
Qualifications:
<ol>
<li>BS/MS in Molecular Biology, Cellular Biology, Biochemistry or related field with 1+ years of relevant experience in protein purification/characterization.</li>
<li>Familiarity with AKTA systems and chromatography software is a strong plus. </li>
<li>Strong organizational and documentation skills, with attention to detail and data integrity. </li>
<li>Ability to work independently and as part of a team in a fast-paced environment. </li>
<li>Excellent problem-solving and communication skills. </li>
<li>Experience in a CRO or CDMO setting is preferred. </li>
</ol>
#GS
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Protein Purification Associate Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Position Overview: Virology Team – Product Development, Science &amp; Technology
AbbVie’s Product Development, Science &amp; Technology Virology team is seeking dynamic candidates to support both pipeline and commercially available products. This role encompasses a broad range of responsibilities across the product lifecycle, from late-stage process development and BLA/NDA submissions to ongoing market support. &nbsp; Successful candidates will demonstrate a passion for science, a focus on impactful solutions, and a dedication to elevating AbbVie’s contributions to healthcare.
Key responsibilities for the role:
<ul>
<li>Viral Control Strategies: Develop and implement comprehensive viral control strategies, ensuring adherence to quality and regulatory standards.</li>
<li>Innovative Solutions: Lead the innovation and optimization of new methods, techniques, and experimental approaches to address challenges in viral safety, control, and testing.</li>
<li>Cross-Disciplinary Collaboration: Build and maintain effective collaborations with various scientific disciplines. Your work will focus on establishing improved process conditions, enhancing viral control, and refining regulatory strategies.</li>
<li>Continuous Improvement: Foster an environment of open, honest, and candid communication to drive creative, continuous improvements across the team.</li>
<li>Patient Impact: Demonstrate a strong commitment to AbbVie's mission, striving to make a meaningful impact on the patients we serve.</li>
<li>Virology Support and Method Enhancement: Provide expert support in virology, particularly involving animal-sourced APIs. Execute and refine quantitative Polymerase Chain Reaction (qPCR) and in vitro cell culture virus infectivity assays for continuous improvement.</li>
<li>Scientific Documentation: Author and review scientific reports and regulatory submissions, ensuring they meet regulatory and accuracy standards.</li>
<li>BSL-2 Facility Operations: Conduct research involving potentially biohazardous viruses in BioSafety Level 2 (BSL-2) facilities, strictly adhering to safety protocols to maintain a secure laboratory environment.</li>
<li>Literature Application and Problem Solving: Stay informed of the latest scientific literature and apply theoretical frameworks to effectively and efficiently solve problems.</li>
</ul>
Qualifications 
Qualifications
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ph.D. in Virology or similar field.
 Preferred Skills:
<ul>
<li>qPCR Expertise:&nbsp;Proficiency in the development, execution, optimization, and troubleshooting of quantitative Polymerase Chain Reaction (qPCR) methods.</li>
<li>Cell Culture and Microscopy:&nbsp;Strong skills in cell culture techniques and microscopy, crucial for viral studies and analysis.</li>
<li>Molecular Biology and Aseptic Technique:&nbsp;Solid background in molecular biology and adeptness in aseptic techniques to ensure contamination-free experiments.</li>
<li>Immunofluorescence:&nbsp;Experience with immunofluorescence techniques for the detection and analysis of viral components.</li>
<li>Viral Clearance Procedures:&nbsp;Understanding and application of viral clearance methodologies to ensure product safety.</li>
<li>Problem Solving:&nbsp;Ability to anticipate, recognize, and effectively resolve problems within laboratory and project settings.</li>
<li>cGMP Environment Proficiency:&nbsp;Experience working in current Good Manufacturing Practice (cGMP) environments to ensure compliance and high-quality outputs.</li>
<li>Cross-Functional Teamwork:&nbsp;Ability to effectively collaborate within a Cross Functional Team (CFT) environment to achieve project goals.</li>
<li>CMC Regulatory Knowledge:&nbsp;Familiarity with Chemistry, Manufacturing, and Controls (CMC) regulatory issues, crucial for successful product development and compliance.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​&nbsp;Salary: $94,000&nbsp;- $178,500
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We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
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This job is eligible to participate in our short-term incentive programs.&nbsp;​​
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Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
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Senior Scientist, I Virology ( On-site, North Chicago, IL )

<h3>Job Description</h3>
Job Description
Recruiters please do not contact this job poster. Please be advised: Solvias does not accept unsolicited resumes or services from third-party recruitment agencies. In the event, a recruiter or agency submits a resume or candidate without an agreement we shall explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited resumes, including those submitted to Company employees, shall be deemed the property of the Company.
Solvias is an internationally recognized provider of integrated solutions in contract analytical research, development, and manufacturing. The company offers a broad spectrum of services and solutions in the Pharmaceutical, Biotech, Medical Device, Cell &amp; Gene Therapy (CGT), and Cosmetic industries. With headquarters near Basel, Switzerland, about 800 highly qualified employees take pride in putting science at the heart of serving customers to bring safer and better products to market faster. 
Position Overview 
Located at our large molecule headquarters in RTP, North Carolina, the Principal Scientist will be the Subject Matter Expert (SME) for the Cell-Based bioassay department. They will oversee resource allocation (personnel, equipment, space, operating resources). Principal Scientists are scientifically renowned leaders in their representative field of work. They represent Solvias within their focused technology and field of work to the inside and outside world. Principal Scientists participate in continuous improvement processes around CBBA work, making sure that in-house developed methods and services are state of the art and of exceptional quality. Principal Scientists will attend conferences and perform talks, present posters, network, and support sales activities in road shows and customer interactions/visits. They may also actively publish scientific work performed at Solvias with the goal of increasing outside visibility of the services and quality available at Solvias. Additionally, Principal Scientists perform and/or lead other scientists to achieve excellent work results with high scientific complexity. They plan, manage, and support both Non-GMP and GMP analytical work. The Principal Scientist ensures that the work is performed smoothly and according to scope. This position is a team member in the Large Molecule &amp; Advance Therapy Medicinal Products Services in a Good Manufacturing Practices (GMP) laboratory environment. This position will report to the Director, Cell-based Bioassay &amp; Analytical Chemistry.
Critical Performance Areas 
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<li>Continuously improves developed methods and services, pursuing innovation and optimization.</li>
<li>Collaborates with the US Commercial team to strengthen Solvias' brand recognition in North America.</li>
<li>Represents Solvias within the CBBA team, both internally and externally.</li>
<li>Oversees and supports highly complex CBBA analytical work, ensuring compliance with cGMP standards.</li>
<li>Provides expertise in method development, service improvements, and automation. Leads innovation in new methodologies using cutting-edge technologies and scientific advancements.</li>
<li>Develops automation and quality improvement solutions for analytical projects, addressing both internal and external customer needs.</li>
<li>Prepares scientific documents, presenting results and expert recommendations to clients.</li>
<li>Engages with project teams and scientific experts to foster collaboration and knowledge exchange.</li>
<li>Serves as the CBBA Subject Matter Expert (SME).</li>
<li>Maintains technical and scientific expertise required for role effectiveness.</li>
<li>Leads the development of new methods and services, actively driving innovation.</li>
<li>Applies technical expertise to support customer acquisition and retention efforts.</li>
</ul>
 Essential Job Functions
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<li>Ensures compliance with GMP regulations, SOPs, and quality standards.</li>
<li>Investigates deviations, non-conformities, OOS results, change controls, and other quality events under GMP.</li>
<li>Trains and mentors scientists, analysts, and new employees.</li>
<li>Enhances lab workflows through process improvements and automation.</li>
<li>Collaborates with Team Leads, cross-functional teams, and customers.</li>
<li>Provides scientific guidance for method development and optimization.</li>
<li>Identifies and applies cutting-edge scientific advancements.</li>
<li>Aligns activities with the CBBA Director and supports sales efforts to increase visibility.</li>
<li>Adheres to Solvias’ Quality Management System and HSE requirements.</li>
<li>Applies automation and operational excellence principles to ensure high-quality results.</li>
<li>Reports potential bottlenecks, barriers, or complaints to the CBBA Director.</li>
<li>Maintains industry knowledge and technical expertise for continuous improvement.</li>
<li>Consults with the CBBA Director and project teams on method and service development.</li>
<li>Ensures compliance with task specifications and instructions.</li>
<li>Provides technical insights for customer quotations.</li>
</ul>
Requirements 
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<li>M.S. or Ph.D. Life Sciences with 7+ years relevant experience or B.A/B.S. with 15+ years relevant experience. </li>
<li>Experience working in GMP or GLP environment.</li>
<li>Strong experience in method development, qualification, and validation of CBBA, ELISA, and other emerging technologies.</li>
<li>Client management experience in a CRO/CDMO is preferred.</li>
</ul>
 Other Desired Skills/Abilities 
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<li>Excellent organizational skills, ability to work independently and collaboratively in a team environment.</li>
<li>Strong written and verbal communication skills.</li>
</ul>
NOTE: This job description is not intended to be all-inclusive. Individuals may perform other related duties to meet the ongoing needs of the organization. 
Disclaimer: Solvias North America does not currently offer relocation packages or sponsor work visas. All applicants must have the legal right to work in the location of the job posting.

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