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<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 
This position will focus primarily on drug substance (active pharmaceutical ingredient) programs in a dynamic environment from pre-clinical through first-in-human clinical stages. The individual will independently create phase-appropriate analytical methods to facilitate process development, assess stability, control manufacturing impurities, and enable release testing of pre-clinical and clinical drug substances. They will work closely with synthetic organic chemists in Process Chemistry to establish appropriate proposed regulatory starting materials, design efficient control strategies, support reaction troubleshooting, and identify manufacturing impurities or degradants. Candidates should be comfortable discussing organic chemistry topics relevant to analytical chemistry, such as stereoisomers, common functional groups, and pKa values. Experience with chromatographic analysis (such as HPLC or GC) is preferred but not required. Experience with analysis of peptides and solid-phase peptide synthesis (SPPS) is preferred but not required.
Responsibilities:
<ul>
<li>Apply analytical separation and detection modes for complex impurity profiling of pharmaceutical drug substances to further the understanding of emerging non-GMP and cGMP manufacturing processes.</li>
<li>Responsible for leading the analytical aspects of a project while working with other functional areas to advance projects through the development pipeline.</li>
<li>Utilize understanding of a range of analytical techniques to conduct research and development studies related to small-molecule drug substances, intermediates, starting materials, impurities, and impurity profiling.</li>
<li>Support new product development with advanced method development and validation, technical transfer packages, and generation of technical data in support regulatory requirements.</li>
<li>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>May initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a research or development program.</li>
<li>Process, interpret, and visualize data to facilitate project team decisions.</li>
<li>Communicate and collaborate with cross-functional groups and departments, especially process chemistry, process engineering, and technical operations.</li>
<li>Routinely demonstrate scientific initiative and creativity in research or development activities and maintain a high level of productivity in the lab.</li>
<li>Responsible for method development, testing procedures, and implementation of analytical control strategies to help the advancement of drug discovery candidates.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, and GxP compliance, where applicable.</li>
</ul>
Qualifications 
<ul>
<li>Bachelors, Masters, or Ph.D. in Analytical Chemistry typically with minimum 10 (BS), 8 (MS), or 0 - 2 (Ph.D.) years related industry experience.</li>
<li>Strong technical background in chemistry, excellent analytical problem-solving skills. Capable of independently developing and troubleshoot analytical methods.</li>
<li>Demonstrated experience with HPLC analysis and method development preferred along with expertise and fundamental understanding of spectroscopic techniques.</li>
<li>Comfortable discussing organic chemistry topics within analytical R&amp;D and with partner functions. Hands-on experience with synthetic organic chemistry preferred.</li>
<li>Experience with analysis of peptides and solid-phase peptide synthesis (SPPS) is preferred but not required.</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>
<li>Practical knowledge of organic structure, functional groups, chemistry, and modern spectroscopic techniques as applied to small-molecule analytical analysis.</li>
<li>Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance.</li>
<li>Learns fast, grasps the "essence" and can change course quickly where indicated.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality</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, Drug Substance Analytical R&D

<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 Description
Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that IMPACTS mission!
A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape.
Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset – Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees.
This position will be responsible for performing non-research molecular testing to rapidly identify and characterize potential pathogenic bacterial and viral threat agents. Ensures incoming biological samples are processed and triaged maintaining chain of custody. Performs and interprets a variety of specialized tests and strains, detection, and identification of pathogenic microorganisms. Prepares written and oral reports, answers questions, troubleshoot and makes recommendations to the supervisor for inclusion in comprehensive reports on test findings. Maintains and operates equipment including performing calibrations, adjustments, and to operate equipment and instruments properly and in a safe manner. Participates in cross training related to bioterrorism and other public health emergencies. Additionally, will be responsible for maintaining knowledge and skills related to position and program and to carry out all procedures in accordance with proper handling and storage of various biological materials. Must be available 24/7/365 to respond in case of emergency. Rotating weekends and some holidays are required. Kindly be aware that drug screening is a mandatory condition of employment for this position.
REQUIRED QUALIFICATIONS: 
Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences.
REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training. Biological Safety Level (BSL)-3 experience is highly desirable.
This position supports a federal contract which requires that all employees and job applicants hold a valid Green Card or US Citizenship at the time of application. 
#LI-OnSite
A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status.

Associate Scientist I Chicago

<h3>Job Description</h3>
Job Description
Job Title: Operator I - 2nd Shift Location (On-site, Remote, or Hybrid?): Irvine, CA (onsite) Contract Duration: Contract until 02/13/2026 Work Hours: 3PM - 11:30PM
Operator I Job Description
This is a non-exempt position. This position is responsible for the production of high quality medical devices within a cleanroom environment.
<ul>
<li>Working under close supervision, may perform a combination of assembly, repair, and test operations on medical Catheters.</li>
<li>Maintain Compliance and Quality while performing routine assignments according to standardized procedures.</li>
<li>Be able to clearly communicate ideas, problems and solutions.</li>
<li>Maintain a positive attitude when interacting with internal customers and external customers.</li>
<li>Follow safety guidelines while onsite.</li>
<li>As an FDA regulated company, maintaining accurate documentation ensures all parts are traceable and quality issues can be addressed.</li>
<li>Have the ability to read, comprehend, and follow written procedures; understand and follow verbal instructions.</li>
<li>Ability to handle and maneuver small components and parts under microscope.</li>
<li>Ability to seat and stand for long periods of time.</li>
<li>Able to perform repeated tasks such as grab, pinch, pull, twist.</li>
</ul>
Sought after experience:
<ul>
<li>Manual Assembling of medical devices.</li>
<li>Assemble and use tools under the microscope for long periods of time.</li>
<li>Hand soldering.</li>
<li>Cleanroom environment.</li>
<li>Maintain written and electronic documentation.</li>
</ul>
Company DescriptionOverview TechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal. We serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and project outsourcing needs of clients nationwide. Striving to create personal relationships with clients, TechLink Systems becomes a virtual extension of clients’ own in-house capabilities to help achieve new levels of growth, productivity, and competitiveness. We also have national recruiting 
<h3>Company Description</h3>
Overview\r\n\r\nTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal. \r\n\r\nWe serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and project outsourcing needs of clients nationwide. Striving to create personal relationships with clients, TechLink Systems becomes a virtual extension of clients’ own in-house capabilities to help achieve new levels of growth, productivity, and competitiveness. \r\n\r\nWe also have national recruiting

Assembler (Clean room/Microscope) 2nd shift $19.75hr - OL0816

<h3>Job Description</h3>
Job Description
Why join us?
Parabilis Medicines is a highly distinctive young biopharmaceutical company whose intention is to grow over time into the ranks of major therapeutics companies. Our foundational platform of Helicon™ therapeutics are peptides capable of efficient cell entry and modulation of both protein-protein and protein-DNA interactions. Through Helicon therapeutics, Parabilis is poised to revolutionize the medical possibilities for patients by precisely drugging intracellular targets long understood to be significant drivers of disease but never before drugged due to the limitations of existing drug modalities to act within the cell.
An important distinctive element of Parabilis is our lead program FOG-001, the company's first-in-class TCF-blocking β-catenin inhibitor. This compound is approximately 18 months and ~50 patients into our early development program for patients with advanced solid tumors, most importantly colorectal cancer. There are few products in the ecosystem with the medical and economic potential of FOG-001. Parabilis is fully leveraging the unprecedented potential Helicons present by deploying proprietary, custom-built machine learning and computational methods as part of its discovery and development process. Parabilis Medicines has raised more than $500 million to date from leading life sciences investors. Parabilis Medicines is headquartered in Cambridge, Mass.
What's the opportunity?
We are seeking a highly motivated Principal Associate Scientist with experience in cellular and molecular biology techniques for drug discovery. In this role, you will have opportunities to characterize different cellular activities for our novel HeliconTM peptides and help us develop this new drug modality for cancer and other diseases with unmet medical needs. Ideal candidates will be energetic and passionate, with a breadth of cell-based assay and molecular biology experience, along with a demonstrated ability to drive and deliver results, and an interest in working in a dynamic, fast-paced environment. As part of this role, you will:
<ul>
<li>Develop and perform cellular and molecular biology assays for intracellular targets to screen and evaluate drug activity and mechanism of action</li>
<li>Contribute to transition of lead helicons to development candidate status and IND-enabling experimentation</li>
<li>Accurately record, analyze, and present data to team and company leadership</li>
<li>Collaborate across functional teams to efficiently identify drug candidates and move them to the clinic</li>
<li>Contribute to, and be a part of, an exciting and dedicated group of people pushing the forefront of oncology therapeutics</li>
</ul>
What you'll need to be successful:
<ul>
<li>BS. or M.S. in cancer biology or related field with 10+ years of relevant industry experience</li>
<li>Proficiency in a broad range of biochemical, molecular and cellular techniques including (but not limited to): mammalian cell culture, western blotting, qPCR, transfection, flow cytometry etc.</li>
<li>Hands-on experience developing and performing biochemical and cell-based assays such as HTRF/AlphaLISA/MSD/NanoBRET/HiBiT is required</li>
<li>Hands-on experience in performing high-throughput screening using cellular readouts is required</li>
<li>Experience with data upload and organization onto a data management system such as Dotmatics is required</li>
<li>Hands-on experience with CRISPR and/or RNAi to evaluate gene function is required</li>
<li>Hands-on experience with immunofluorescence and confocal microscopy is preferred</li>
<li>Experience in managing relationships with collaborators or CROs is required</li>
<li>Innovative, creative, inquisitive, motivated researcher with strong problem-solving skills</li>
<li>Excellent written and oral communication skills with a proven track record of publications</li>
<li>Able to work on-site and attend in-person meetings</li>
</ul>
Core Values
Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit.
<ul>
<li>Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.</li>
<li>In(ter)dependent. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.</li>
<li>Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.</li>
<li>All-In. We're All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.</li>
</ul>
As an equal opportunity employer, Parabilis Medicines values diversity and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.
30 Acorn Park Drive | Cambridge, MA 02140 | <a href="http://www.parabilismed.com" target="_blank">www.parabilismed.com</a>

Principal Associate Scientist, Cancer Biology

<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 Scientist II, Drug Substance Process Development, will be an instrumental team member of the NBPS group. The primary roles of this position are to perform drug substance downstream/purification process development and optimization studies for natural and recombinant proteins (including neurotoxins) from bacterial cultures.
The desired candidate will have a good understanding of purification concepts and methodology and hands-on work experience with biologics purification process development, including process chromatography, ultrafiltration/diafiltration. The ability to demonstrate a significant level of hands-on experience in several of these areas is expected. Additional responsibilities include data analysis, troubleshooting process and equipment, lab inventory and organization, maintaining detailed records of batches and experiments. The successful candidate will perform laboratory work, develop productive collaborations and communications with other groups across scientific disciplines and be motivated to innovate and succeed in a fast-paced, collaborative environment.
Key Responsibilities:
<ul>
<li>Hands on laboratory bench work to develop and prepare biologics product candidates for various groups with tight timelines.</li>
<li>Perform and support design and execution of experiments for drug substance purification process.</li>
<li>Independently operate and have sound knowledge of TFF system and AKTA chromatography skid systems. Position requires proficient knowledge and hands on experience of clarification equipment as well.</li>
<li>Routine down-stream purification operations relating to AKTA chromatography system prep: system set-up, assembly/disassembly, system clean-up, in process sampling, buffer preparation, and ability to troubleshoot operational and equipment issues</li>
<li>Knowledge of HPLC instrument operations and method development is also preferred but not required.</li>
<li>Must be willing to work with and handle potent neurotoxins and in-process samples that contain neurotoxin and neurotoxin expressing organisms. Learn and develop a safety mindset and adhere to safety procedures regarding neurotoxin handling. Ability to perform all operations and manipulation under a biosafety laminar flow hood.</li>
<li>The scientist must complete training consistent with safety, technical, operational, process, and other skill/ knowledge requirements for the position. Maintain all training to current status. Support safety program and ensure safety in all routine and new operations.</li>
<li>Follow study protocols or batch records and execute experiments independently (or minimal supervision) at small and large scales.</li>
<li>Author and edit development batch records and associated standard operating procedures.</li>
<li>Communicate and work closely with members from different teams within process development and analytical development groups to foster a collaborative environment for advancement of projects. &nbsp;</li>
<li>Assist the team in maintaining laboratory equipment, supply inventory, and organization.</li>
</ul>
Qualifications 
<ul>
<li>BS or MS in Pharmaceutical Sciences, Microbiology, Biochemistry, Biochemical/chemical engineering, or closely related field.</li>
<li>Scientist II minimally requires a Master’s degree with 5 years, or Bachelor’s degree with 7 years of relevant industry experience.</li>
<li>Must have in depth knowledge of protein chemistry, chromatography, and purification principles</li>
</ul>
<ul>
<li>Hands-on experience in the operation of TFF and purification AKTA chromatography system is required.</li>
<li>Proven ability to work independently, effectively plan and organize work activities, and prioritize task completion to meet project deadlines in a fast-paced environment is required.</li>
<li>Must have a team-centric mindset in order to integrate seamlessly in a team setting when working/collaborating with other members within the group and with other groups.</li>
<li>Excellent oral and written communication skills is required as is experience with documentation of experimental plans, analyzing data and generating high quality technical reports.</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 in Irvine, CA that will work directly with Toxins in a lab-based environment.&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.​​&nbsp;Salary: $82,500 - 157,500</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>

Scientist II, Drug Substance Purification Development

<h3>Job Description</h3>
Job Description
Stampede Culinary Partners is on the hunt for a Food Research and Development Chef-a culinary specialist ready to revolutionize the future of food!
WHY JOIN US?
This is a full-time position offering competitive pay and a comprehensive benefits package that includes:
<ul>
<li>Health, dental, and vision insurance</li>
<li>HSA/FSA options</li>
<li>Short- and long-term disability coverage (STD/LTD)</li>
<li>Life and AD&amp;D insurance</li>
<li>Accident insurance</li>
<li>Group hospital indemnity insurance</li>
<li>Pet insurance</li>
<li>401(k) with company match</li>
<li>Pension plan after 1 year</li>
<li>Floating holidays</li>
<li>Mental health support program</li>
<li>Employee discounts on meat and veggies</li>
<li>Event BBQs and recognition programs</li>
<li>On-site parking and bus route access</li>
</ul>
WONDERING WHO WE ARE?
Stampede Culinary Partners, Inc. is an innovative protein solutions company that focuses on custom protein development and processing. Our customers include leading restaurants, top retailers, leading food service distributors, home delivery customers, and other emerging segments. The ability to satisfy our mission depends largely on our greatest asset, our employees! Our company culture is built on the expertise and experience of all our employees and driven by the 5 pillars that we hold ourselves to daily: perform passionately, challenge directly and respectfully, commit to teamwork, and embrace innovation.
WHAT'S YOUR DAY LIKE?
As our Food Research and Development Chef, you'll immerse yourself in the hands-on creation, testing, and refinement of new food products in our test kitchen. You'll collaborate closely with our Head Chef and Vice President of Technical Innovation and Culinary Development to bring bold ideas to life-starting with bench samples and scaling up to production-ready versions. On any given day, you might be conducting side-by-side trials with QA and Production, improving product attributes like flavor, color, and texture, or analyzing competitor items to ensure our offerings are industry-leading. You'll also contribute to the development of food safety standards, work on cost-conscious innovation, and support our sales and marketing teams in dazzling customers with your culinary creations. From concept to plate, your creativity and technical skill will be at the heart of everything we do.
Here's what we need from you:
<ul>
<li>2+ years of culinary experience</li>
<li>Experience in food preparation</li>
<li>Experience as a research coordinator</li>
<li>Proficiency with computers, including internet software, inventory software, manufacturing software, order processing systems, spreadsheets, and MS Word</li>
<li>Excellent communication and customer service skills</li>
</ul>
READY TO TAKE YOUR CULINARY CAREER TO NEW HEIGHTS?
If you're ready to take your culinary experience beyond the kitchen and into the world of food innovation, apply now to become a Food Research and Development Chef with Stampede Culinary Partners! Our initial application process is extremely quick, easy, and mobile-friendly
 Job Posted by ApplicantPro

Culinary Research and Development 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 
The Process Chemistry department is responsible for the scale-up of active pharmaceutical ingredients (API) for the use in preclinical and early clinical studies.&nbsp; The Separations group is a part of Process Chemistry and is responsible for preparative scale purification of APIs in a GMP environment using reverse phase, normal phase, chiral phase and other types of chromatography.&nbsp; The separations team also works collaboratively to identify trace impurities and deliver other chromatography driven results with our project teams. &nbsp;Training in both separation science as well as organic synthesis is required.
The Senior Scientist II Chemistry position has these key responsibilities:&nbsp;
<ul>
<li>Direct workflow around chromatographic separations to facilitate project goals across different projects, modalities and phases of development.</li>
<li>Keep accurate and current records of research and/or project-related documents according to AbbVie policies.</li>
<li>Staying current with advances in the separations field.&nbsp; Act as advocate to integrate this knowledge into the group’s research efforts.&nbsp; Generate new research or development strategies to effectively address project and divisional goals/needs.&nbsp; Collaborate with functional and technical experts to facilitate scientific achievement.&nbsp;</li>
<li>Show flexibility in providing support in Process Chemistry as project demands require.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree or equivalent education and typically 12 years of experience, Master’s Degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience.</li>
<li>A PhD in organic or analytical chemistry preferred</li>
<li>Experience leading direct reports</li>
<li>Experience with chromatography at large scale and in a GMP environment.</li>
<li>Experience with handling and separating potent compounds</li>
<li>Experience in working with small molecules, antibody drug conjugates, drug linkers and peptides</li>
<li>Experience with machine learning, including the ability to write codes in Python</li>
<li>Track record of seeking out new information in the literature and incorporate this into individual projects as well as the overall program</li>
</ul>
Key Leadership Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance</li>
<li>Learns fast, grasps the “essence” and can change course quickly where indicated</li>
<li>Raises the bar and is never satisfied with the status quo</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality</li>
</ul>
Level and compensation will be commensurate with experience.
 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.​&nbsp;Salary: $106,500 - $202,500
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist II, Chemistry

<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 
Group
AbbVie Biologics Analytical Research &amp; Development (Biologics Analytical R&amp;D) is a global analytical sciences organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products.&nbsp; Our Early Analytical Development team owns analytical strategy, method development, release &amp; stability testing for IND-enabling biologic programs developed internally, partnering closely with Drug Substance, Drug Product, Regulatory Affairs, QA and Process Development Sciences &amp; Technology.
Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologic medicines and spans from the selection of Discovery candidate molecules through the transition of analytical methods and testing to commercial labs to support product launch.&nbsp; We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines.&nbsp; Careers in AbbVie Biologics Analytical R&amp;D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies.&nbsp;
The biologics early analytical development group develops state-of-the-art analytical techniques for analysis of therapeutic proteins and other novel biologic molecules using separation science and other biophysical techniques. We are looking for diverse candidates with strong scientific and leadership experience to join the AbbVie Analytical R&amp;D team and can offer exciting and rewarding career opportunities for these candidates.
Overview
The candidate will focus on development and implementation of analytical assays for the analysis of complex biologics including antibodies, antibody drug conjugates, and new modalities. The candidate will use and develop a variety of analytical techniques including chromatography, electrophoresis, spectroscopy, and automated methods. The successful candidate will contribute to the development and testing of complex and automated assays and will contribute to the continuous improvement and innovation within the group.
Key Responsibilities
<ul>
<li>Effectively function as a scientist, generating original technical ideas and research or development strategies.</li>
<li>Develop and optimize early-stage analytical methods using HPLC/UHPLC, CE-SDS and other separation/biophysical techniques.”&nbsp;</li>
<li>Drive the development of automated workflows for liquid handling platforms to improve method robustness and throughput.</li>
<li>Author CMC analytical sections of IND/IMPD filings and contribute to global regulatory strategy alongside Reg Affairs.</li>
<li>Collaborate daily with DS, DP, QA, late-stage stakeholders, and external CROs to align on method readiness and data packages.</li>
<li>Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.</li>
<li>Independently responsible for project science within his/her area of expertise on one or more project teams leading the method development and validation for complex biologic therapeutics.</li>
<li>Proactively seek out new information in the literature and incorporate this into individual projects as well as the overall program.</li>
</ul>
Qualifications 
<ul>
<li>Ph.D. degree in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences or a closely related discipline or MS degree with 8 years of experience.
<ul>
<li>Qualification for Senior Scientist I: Ph.D. with 0-4 years of experience is required with relevant experience or MS with 8 years of experience.</li>
<li>Qualification for Senior Scientist II: Ph.D. with 4+ years of experience is required with relevant experience or MS with 10 years of experience.</li>
</ul>
</li>
<li>Hands-on expertise with HPLC/UPLC and CE-SDS, plus working familiarity with Hamilton or Tecan liquid-handling platforms.</li>
<li>Working knowledge of cGMP expectations for early clinical materials; routine QC execution is not expected.</li>
<li>Experience applying chemometrics / multivariate data analysis (e.g., PCA, MVM) and statistics to model-based method development.</li>
<li>Demonstrated record of independent thought, creativity and scientific accomplishment (e.g. peer reviewed journal publications, patents).</li>
<li>Must have a solid understanding of protein/oligonucleotide chemistry and biochemistry, particularly as related to biologics drug development.</li>
<li>Strong data and time organization/management skills coupled with strong interpersonal and effective communication skills for facilitating collaborations with a demonstrated ability to lead cross functional process development teams.</li>
<li>Demonstrated scientific curiosity, creativity and comfort operating in ambiguity—key to inventing from scratch.</li>
<li>Effective writer and communication of research or other regulatory materials.</li>
<li>Experience with analytical Multivariate Analytical Procedures development and/or validation a plus.</li>
</ul>
 Additional Information 
<ul>
<li>This is an on-site opportunity based in AbbVie's Abbott Park location in IL.&nbsp;</li>
<li>Leveling will be commensurate to experience.</li>
</ul>
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, Biologics Analytical R&D

<h3>Job Description</h3>
Job Description
Duties &amp; Responsibilities:
<ul>
<li>
Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures.
</li>
<li>
Utilize small hand tools (both manual and electric), manual presses, assembly fixtures, calibrated instruments, measurement equipment, microscopes, and test fixtures.
</li>
<li>
Utilize documentation such as Bill of Materials, product flow charts, work orders, check sheets, visual aids, production reports and assembly drawings to assemble product and record results.
</li>
<li>
May perform soldering, fabricating, crimping, mechanical assembly, sealing, ultra-sonic welding, bonding and gluing with adhesives, Epoxy or RTV.
</li>
<li>
Kitting assemblies using a parts list, scanner and inventory software as required.
</li>
</ul>
Company DescriptionConnexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve. 
<h3>Company Description</h3>
Connexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve.

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