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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 
The Process Chemistry in the Small Molecule API (SMAPI) division is responsible for the scale-up of active pharmaceutical ingredients (API) for the use in preclinical and early clinical studies.&nbsp; The Innovative Chemical Technologies group is a part of Process Chemistry and is responsible for developing and enabling new technologies that challenge the status quo in process development.&nbsp; Within the Innovative Chemical Technologies team is the Machine Learning team focused on applying the tools of computational chemistry and data science to improve the speed and efficiency of process development. &nbsp;Training in both practical application of data science and organic synthesis is required.
The Senior Scientist I Chemistry position has these key responsibilities:&nbsp;
<ul>
<li>Develop new tools and models to explain/predict reaction outcomes and enable more rapid reaction discovery and optimization.</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 data science and organic synthesis fields.&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;</li>
<li>Show flexibility in providing support in Process Chemistry as project demands require.</li>
</ul>
Qualifications 
<ul>
<li>A PhD in organic chemistry or chemical engineering or data science. &nbsp;MS in organic chemistry and 5-8 years of experience</li>
<li>Experience using the tools of machine learning to understand/predict reaction outcomes.&nbsp; &nbsp;&nbsp;</li>
<li>Experience with gathering and analyzing large datasets.&nbsp;</li>
<li>General programming experience in Python</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>
 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;$94,000 - $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>

Sr Scientist I - Machine Learning Specialist Process 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 
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

<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
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.

Cleanroom Assembler (1st, 2nd & 3rd shift available)

<h3>Job Description</h3>
Job Description
Gojob is hiring Chemical Mixer / Chemical Assembly for a leading logistics warehouse located in Berea, OH. The primary responsibility of this role is mixing dry and wet in a manufacturing or laboratory setting. Forklift certification is needed for this role. Strict adherence to safety and PPE protocols are a must. You must be willing to submit to a physical for the purposes of wearing a respirator. 
As a Gojobber, you will enjoy weekly pay, excellent communication from recruiters, the opportunity to build a career, health insurance and more!
Shift &amp; Pay:
<ul>
<li>2nd Shift: Sun-Thu, 9:30pm - 6:00am: $21/hr</li>
</ul>
Responsibilities:
<ul>
<li>Accurately kit dry and liquid chemicals according to specified formulations</li>
<li>Ensure all chemicals are correctly labeled and packaged</li>
<li>Safely mix chemicals in precise quantities following detailed instructions and monitor the mixing process to ensure consistency and quality</li>
<li>Strictly adhere to all safety protocols, including the use of PPE and fit testing for respirators</li>
<li>Conduct lock out and tag out procedures</li>
<li>Perform grounding and bonding tasks to prevent static discharge and routine inspections and tests on chemical batches</li>
<li>Maintain accurate records of all kitting and mixing activities including weights and measures for all mixing use scales, balances, and other measuring equipment</li>
<li>Safely operate a forklift to transport chemical containers and other materials</li>
<li>Maintain comprehensive records of all chemical handling activities and prepare production reports as required</li>
</ul>
Qualifications:
<ul>
<li>High school diploma or equivalent; additional technical training or certification in chemical handling is preferred.</li>
<li>Proven experience in a chemical kitting or mixing role.</li>
<li>Knowledge of safety protocols, including PPE usage, fit testing for respirators, lock out and tagout, and grounding and bonding.</li>
<li>Experience operating a forklift.</li>
<li>Strong math skills and attention to detail for calculating weights and measurements.</li>
<li>Good communication and record-keeping skills</li>
<li>Ability to lift and move containers of chemicals, which may weigh up to 50 lbs.</li>
<li>Willingness to wear PPE for extended periods.</li>
<li>Ability to pass a respirator fit test and comply with all PPE requirements.</li>
</ul>
At Gojob, we celebrate workplace diversity. We are proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
To read our Candidate Privacy Information Statement, click here: <a href="https://gojob.com/en_us/privacy-policy/" target="_blank">https://gojob.com/en_us/privacy-policy/</a>
Company DescriptionGojob is the #1 Workforce-As-A-Service platform that leverages Tech and Data to make the labor market more fluid &amp; accessible, and empower workers with dignity. 
<h3>Company Description</h3>
Gojob is the #1 Workforce-As-A-Service platform that leverages Tech and Data to make the labor market more fluid &amp; accessible, and empower workers with dignity.

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