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<h3>Job Description</h3>
Job Description
Matrix has been named a Zweig Group 2025 Best Firm to Work For! 
Matrix Design Group, Inc., an employee-owned planning, engineering, and environmental consulting firm is actively seeking a GIS Technician I or II. The position will be filled in our Colorado Springs, Denver, Lone Tree, Phoenix or San Antonio offices. As an employee-owned company we are committed to fostering, cultivating, and preserving a culture of diversity, respect, and excellence.
About Matrix: 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 critical thinking skills who desire to advance their talents and skills.
 
Salary Range: $50,000.00 to $62,000.00 Annually. Salary will be dependent upon experience. 
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>Catalogs and inventories GIS data, including metadata creation.</li>
<li>Develops and edits large and complex GIS databases.</li>
<li>Produces presentation quality maps using cartographic design standards for public, client, and internal usage.</li>
<li>Maintains a high attention to detail on concurrent tasks, while meeting challenging deadlines.</li>
<li>Formulates and solves problems.</li>
</ul>
Competencies:
<ul>
<li>Possesses oral and written communication skills.</li>
<li>Interacts with staff.</li>
<li>Proficient with Esri’s GIS mapping software, particularly ArcGIS Pro.</li>
<li>Proficient with Microsoft Office Suite.</li>
<li>Competent with ArcGIS Model Builder.</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. </li>
<li>Zero to two (0) – (2) years of experience with demonstrated GIS responsibilities. Additional experience is a plus.</li>
<li>Experience working in the engineering and/or planning consulting fields is preferred.</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 office 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.
This position may also require field data collection surrounding the office or travel to remote locations. While performing the field duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee will also regularly be required to walk and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 40 pounds.
 
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. 
 
Any applicant with a qualifying physical or mental disability who believes they require 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 Technician

<h3>Job Description</h3>
Job Description
Saratoga Medical has a Part-time (PRN) opening for a Medical Physicist to work at VA Medical Center. Position is 208 hours an annually. We offer a competitive salary and the wonderful opportunity to care for and provide services to our military members.
 
Performance Work Statement (PWS) Overview
<ul>
<li>Provide on-site coverage for radiation oncology services.</li>
<li>Conduct QA testing, equipment calibration, dosimetry, and support.</li>
<li>Follow standards of the American College of Radiology, ASTRO, and AAPM.</li>
<li>Maintain consistent staffing and arrange replacements as needed.</li>
<li>Detailed QA processes and performance expectations included.</li>
</ul>
 
Licensure &amp; Certification:
<ul>
<li>Must hold a Therapeutic Radiological Physicist license (any U.S. State, Territory, or DC).</li>
<li>Must hold or obtain Florida licensure.</li>
<li>Required: Certification by the American Board of Radiology (ABR) in Medical or Therapeutic Medical Physics.</li>
</ul>
 
Experience:
<ul>
<li>Must have hands-on experience with: (Varian Linear Accelerators, IGRT, Eclipse &amp; ARIA systems, MapCheck 3, CT Simulator, Superficial X-ray equipment.</li>
<li>Must complete CEUs and VA-required training (HIPAA, harassment, suicide prevention, etc.).</li>
<li>Must pass required health screenings (TB, MMR, Varicella, Influenza, bloodborne pathogens).</li>
</ul>
Saratoga Medical Center, Inc. is an equal opportunity employer and will not discriminate in recruiting, hiring, training, promotion, transfer, discharge, compensation or any other term or condition of employment on the basis of race, religion, color, age (over age 39), sex, national origin, or on the basis of disability if the employee can perform the essential functions of the job, with a reasonable accommodation if necessary.

Medical Physicist

<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
</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, I Virology ( On-site, North Chicago, IL )

<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 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 Biologics Drug Product Development group within AbbVie is a global organization responsible for developing and characterizing drug product formulations and manufacturing processes for biologic therapeutics (antibodies, antibody-drug conjugates (ADCs), neurotoxins, and novel biologic formats) from preclinical development through clinical proof of concept. We have an exciting opportunity available for an Associate Scientist I/II to join our team at our Bay Area site in South San Francisco, CA. This position requires an onsite presence and involves lab-based functions. Successful candidates will thrive in a collaborative lab environment.
Key responsibilities include:&nbsp;
<ul>
<li>Execute formulation composition and drug product process development studies for sterile liquids and lyophilized dosage forms</li>
<li>Manufacture drug product formulation batches for evaluating formulation stability and/or to support animal studies</li>
<li>Conduct stability studies to enable selection of formulation composition and container closure for liquid and lyophilized dosage forms for protein therapeutics</li>
<li>Conduct clinical in-use studies to guide dose solution administration</li>
<li>Analyze data, interpret results and draw conclusions from multistage experiments; note significant deviations and propose relevant new experiments</li>
<li>Use data analytics to optimize workflows, data entry, and data digitalization</li>
<li>Generate high-quality data based on sound scientific principles and document results in electronic lab notebook</li>
<li>Effectively organize and present scientific data in presentations and document studies by authoring reports that support regulatory filings.</li>
<li>Support functional technical initiatives by investigating and developing novel experimental approaches and/or technologies in the field of drug product development</li>
<li>Maintain oversight of day-to-day laboratory activities; manage inventory of raw materials and drug product packaging and manufacturing supplies; coordinate ordering, shipping, and receiving</li>
</ul>
Qualifications 
<ul>
<li>Degree in chemistry, chemical engineering, biochemistry, pharmaceutical sciences or equivalent
<ul>
<li>For Associate Scientist I: Bachelor’s degree and typically 0-3 years of experience</li>
<li>For Associate Scientist II: Bachelor’s degree and typically 3-5 years of experience or Master’s degree and typically 0-2 years of experience.</li>
</ul>
</li>
<li>Strong technical background encompassing protein chemistry and protein handling</li>
<li>Technical ability to execute and troubleshoot experiments through rational and critical thinking.</li>
<li>Hands-on experience with analytical techniques used for protein characterization and stability testing</li>
<li>Must be highly organized and detail-oriented.</li>
<li>Eagerness to learn and apply new scientific techniques.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Strong collaborative skills for working effectively within the team.</li>
<li>Prior experience in protein formulation development, lyophilization process development, drug delivery, or analytical functions is highly preferred.</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>​​This is an on-site opportunity located in the South SF office of AbbVie.&nbsp;</li>
<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>

Associate Scientist I/II, Biologics Drug Product Development

<h3>Job Description</h3>
Job DescriptionDescription:
Carry out routine day-to-day quality control testing of Water, Raw Materials, Bulk, Finished Products and Stability samples in the Quality Control Laboratory. Perform routine chemical testing by such means as HPLC, GC, FTIR, UV Spectrophotometry, Titrations and other physical and chemical techniques. Review note books and generate test data reports. Write and revise SOPs. Prepare protocols, perform testing for special investigations and write scientific reports.
<ul>
<li>Performs routine laboratory testing of raw materials, bulk products, finished products and stability samples.</li>
<li>Performs routine chemical testing by such means as HPLC, GC, FTIR, UV Spectrophotometry, Titrations and other physical and chemical techniques.</li>
<li>Assists QC staff in determining whether or not Ferndale products meet release and stability specifications.</li>
<li>Performs instrument calibration.</li>
<li>Writes scientific reports, prepares protocols, and generates analytical test data reports.</li>
<li>Implements new chemical testing procedures as needed.</li>
<li>Trains chemistry staff as needed.</li>
<li>Writes and revises SOPs as requested by management.</li>
<li>Performs laboratory cleanup.</li>
<li>Troubleshoots analytical equipment and methods.</li>
<li>Makes recommendations that may impact the QC Department.</li>
<li>Reviews notebooks and test data.</li>
<li>Occasionally contacts outside suppliers and contract labs.</li>
<li>All other duties as assigned.</li>
</ul>
Requirements:
Must have 1-2 years experience in analytical chemistry. Knowledge of equipment, supplies, components, and technical areas that are utilized in the chemical laboratory, i.e. HPLC, UV-VIS, balance, FT-IR, GC, pH meter, viscometer, etc.
Requires a Bachelor of Science in Chemistry or a closely related field or an equivalent combination of education and experience.
 
Position requires pre-placement drug screen/ physical and background check.
 
EO Employer 
E-verify Participant.

Chemist

<h3>Job Description</h3>
Job DescriptionSalary: DOE 
About Us: Willmer Engineering is an award-winning consulting firm specializing in geotechnical engineering, environmental services, and construction materials testing. With over 40 years of experience, we've contributed to significant infrastructure projects across the U.S., including:
<ul>
<li>Hartsfield-Jackson Atlanta International Airport Geotechnical support for modernization efforts.</li>
<li>Atlanta BeltLine Clear Creek Sewer Basin Environmental and geotechnical services.</li>
<li>GDOT I-75/I-575 Northwest Corridor Project Transportation infrastructure development.</li>
<li>Fort Lauderdale-Hollywood International Airport Geotechnical investigations.</li>
<li>City of Atlanta Watershed Management Projects Comprehensive geotechnical and environmental services.</li>
</ul>
Position Overview: Join our dynamic team to work on diverse projects involving complex geotechnical challenges. Responsibilities include conducting site investigations, designing solutions, and collaborating with multidisciplinary teams to ensure project success.
 
Key Responsibilities:
<ul>
<li>Conduct geotechnical investigations and develop project scopes.</li>
<li>Prepare clear and concise reports.</li>
<li>Provide construction-phase services and reporting.</li>
<li>Coordinate with other disciplines to meet project timelines.</li>
<li>Perform field observations and QA/QC inspections.</li>
</ul>
Qualifications:
<ul>
<li>B.S. in Civil Engineering (Geotechnical preferred); M.S. a plus.</li>
<li>E.I.T. certification preferred.</li>
<li>23 years of relevant geotechnical experience.</li>
<li>Experience with DOT projects is advantageous.</li>
<li>Strong written and verbal communication skills.Glassdoor+1willmerengineering.com+1</li>
</ul>
Compensation &amp; Benefits:
<ul>
<li>Competitive salary, commensurate with experience.</li>
<li>Comprehensive benefits package, including Health, Dental, Vision, Life Insurance, Short/Long-Term Disability.</li>
<li>401(k) plan, Profit Sharing, and PTO.</li>
</ul>
Join Our Team: If you're ready to advance your career in a collaborative and growth-oriented environment, apply now. Visit willmerengineering.com or contact Becky Chapman at <a href="mailto:hr@willmerengineering.com" target="_blank">hr@willmerengineering.com</a> for more information.

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