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<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking an experienced professional with a strong background in analytical method development and technology transfer within a GMP-regulated environment. This role primarily supports our client by performing routine GMP sample testing, method validation, and bioassay execution. In addition to technical responsibilities, this individual will serve as a group leader, overseeing a team of Eurofins PSS employees embedded within the client’s operation.
Primary Responsibilities:
<ul>
<li>Perform complex GMP release and stability assays, including cell-based functional assays such as PCR, ELISA, and NGS.</li>
<li>Support method transfer, qualification, and validation of bioassays for lot release and characterization of cell and gene therapy products and critical materials.</li>
<li>Author and review SOPs, technical reports, and other documentation in compliance with regulatory standards.</li>
<li>Collaborate with cross-functional teams on method development, product/process characterization, comparability studies, and technical investigations.</li>
<li>Analyze, trend, and interpret data to assess and maintain consistent assay performance and method robustness.</li>
</ul>
Leadership Responsibilities:
<ul>
<li>Supervise and support the daily performance of the Eurofins PSS team.</li>
<li>Assist in the recruitment and onboarding of new team members.</li>
<li>Communicate administrative updates and reinforce company vision and values.</li>
<li>Ensure high standards of quality, efficiency, and GMP compliance in all laboratory operations.</li>
<li>Manage shift coverage, scheduling, and resource allocation.</li>
<li>Support employee growth through performance discussions and development planning.</li>
<li>Maintain a balanced role between hands-on technical work and leadership duties.</li>
<li>Cultivate a positive team culture, encouraging collaboration, accountability, and continuous improvement.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in a scientific discipline with 3–8 years of relevant experience, or a Master’s degree with 2–5 years of experience.</li>
<li>Proven experience in analytical method validation in alignment with GMP regulations.</li>
<li>Demonstrated success in the transfer of analytical methods into GMP-regulated laboratories.</li>
<li>Hands-on experience performing routine sample testing in a GMP environment.</li>
<li>Strong knowledge of regulatory expectations related to method lifecycle management (e.g., FDA, EMA).</li>
<li>Excellent written and verbal communication skills; able to work collaboratively within cross-functional teams.</li>
<li>Self-motivated, highly organized, and detail-oriented with strong problem-solving capabilities.</li>
<li>Previous laboratory supervision or leadership experience is preferred.</li>
<li>Experience with potency assays (e.g., cell-based assays, ELISA) is a plus..</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
The position is full-time and permanent,&nbsp;Monday-Friday, 8 am-5 pm,&nbsp;with overtime as needed.&nbsp;Candidates living near or in&nbsp;Cambridge, MA,&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Group Lead - Sample Testing & Method Transfer (GMP)

<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 
Purpose:
As the mAb lead for clinical programs, this position will be responsible for supporting regulatory approval of biologics drug substances by leading technical teams throughout Phase 1, Phase 2, and Phase 3 development and authoring Chemistry, Manufacturing, and Controls (CMC) filing content.
&nbsp;Responsibilities:
<ul>
<li>Accountable for driving CMC development plans in collaboration with technical functions and in alignment with overall program objectives.</li>
<li>Ensures technical rigor and is accountable for team performance and technical deliverables of the project.</li>
<li>Leads technical issue resolution and implements robust solutions that are aligned cross-functionally.</li>
<li>Ensures phase appropriate control strategy based on timelines and project risks.</li>
<li>Schedules technical team meetings, develops agendas, issues program highlights, and drives project timelines to ensure successful process development and regulatory submission.</li>
<li>Works with the functional area leads to assemble content for technical reviews.</li>
<li>Apprises CMC and PDS&amp;T management of plans and risks through regular communications and periodic reviews throughout development.</li>
<li>Responsible for the preparation and review of regulatory filings. Responds to urgent regulatory queries.</li>
<li>Serves as spokesperson for the drug substance CMC project team on cross-functional product teams and ensures information flow among line functions.</li>
<li>Manages projects utilizing a matrix management approach.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree with at least 14 years of relevant experience; Master’s Degree with at least 12 years of relevant experience; or PhD with at least 6 years of relevant experience. &nbsp;</li>
<li>Demonstrated knowledge of regulatory requirements and strong technical knowledge of biologics process and analytical development from early development through commercialization including process characterization studies, process scale-up, and technology transfer.&nbsp;</li>
<li>Must demonstrate excellent scientific writing and verbal communication skills, including experience authoring technical and regulatory documentation.</li>
<li>Prior experience must include leadership in technical roles and demonstrated ability of problem solving on difficult technical problems.</li>
<li>Prior experience working in highly matrixed teams and demonstrated leadership skills to influence and guide teams in achieving CMC deliverables while balancing scientific, quality, and compliance requirements.</li>
<li>Strong project management skills with ability to manage multiple programs.&nbsp;</li>
</ul>
 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.​ 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>

Principal Research Scientist I, CMC Sciences Biologics Development and Launch (BDL)

<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 
Purpose:
Abbvie Product Development Science and Technology (PDS&amp;T) Analytical Development – Waltham is responsible for CMC analytical development activities for antibody drug conjugates (ADCs). We are building a team of highly skilled scientists and technical leaders in ADC development to drive the advancement of targeted cancer therapies to improve patient’s lives. The Analytical Development- Waltham team is responsible for late-phase to commercial method development, optimization, validation, advanced characterization, process development support, regulatory authoring, and control strategy for ADCs. The team works cross-functionally with process development, regulatory, and quality within the Abbvie network and with contract manufacturing organization and contract laboratories. The Analytical Development – Waltham team is searching for an analytical lead responsible for optimizing and delivering robust methods, reliable results to support process development, designing and implementing automation technologies for mAbs and ADCs. This role requires a strategic thinker with a strong technical analytical background and the ability to lead an analytical team, manage complex projects, and effectively communicate cross-functionally. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
Responsibilities:
<ul>
<li>
<ul>
<li>Lead analytical team, translating development objectives into actionable analytical activities.</li>
<li>Provide technical expertise to analysts in physiochemical analytical methods such as SEC, CE-SDS and iCIEF.</li>
<li>Establish collaborations across the organization to support method optimizations and transfers to PDST analytical teams.</li>
<li>Design and implement robust automation technologies to provide efficient data collection and analysis.</li>
<li>Manage and prioritize analysis to support multiple ADC programs.</li>
<li>Interpret and identify data trends in key analytical release and stability assays.</li>
<li>Act as the principal contact for all stakeholders and balance conflicting expectations between PDS&amp;T and Analytical areas.</li>
<li>Communicate project strategy, key issues, and risks to relevant teams and escalate risks and facilitate resolution within/across functional areas.</li>
</ul>
</li>
</ul>
Qualifications 
<ul>
<li>
<ul>
<li>PhD in analytical chemistry or related field with 8 years of related experience; Master’s Degree with 14 years of related experience</li>
<li>Technical expertise in CMC analytical chemistry</li>
<li>Demonstrated ability to function as a principle investigator, generating original technical ideas and research or development strategies</li>
<li>Interacts well with diverse groups within function and maintains strong working relationships with internal and external collaborators.</li>
</ul>
</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job 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>

Principal Research Scientist II, Analytical Development ( On-site, Waltham MA)

<h3>Job Description</h3>
Job DescriptionJob Title: Bench Scientist Location: Andover, MA Duration: 12 Months+ Remarks: Schedule: Monday - Friday 9 am - 5 pm Pay Range: $40.50/Hour. on W2 Job Description 
<ul>
<li>Provide support for the development and implementation of state-of-the-art mass spectrometry and proteomics technologies to improve understanding of mechanism of action of drug candidates, safety profiles of Client therapeutics, or identification and quantitation of biomarkers.</li>
<li>Combine protein biochemistry and bioanalytical workflows to support complex sample preparation methodologies that will be integrated with the entire suite of protein mass spectrometry-based detection systems.</li>
<li>Independently following protocols and executing experiments with an analytical mindset to deliver high-quality data across multiple portfolio projects.</li>
<li>Partnering with senior scientist and key stakeholders to design key experiments and assist data analysis and interpretation.</li>
</ul>
 Position Responsibilities:
<ul>
<li>Contribute to the design of experiments and independently perform sample preparation using various extraction, protein digestion and purification techniques for mass spectrometry analysis.</li>
<li>Develop "fit-for-purpose" assays and bioanalytical workflows, balancing rigor aProductst study goals to ensure timely delivery of high-quality data.</li>
<li>Work with different types of samples (biological fluids, tissues) from pre-clinical species.</li>
<li>Assist in data analysis and interpretation, communicate results to team members.</li>
<li>Contribute to the setup, troubleshooting, and maintenance of liquid chromatography and mass spectrometry instrumentation and/or other laboratory equipment.</li>
<li>Maintain scientific and ethical standards, including appropriate record-keeping and compliance.</li>
</ul>
 Education and Experience:
<ul>
<li>B.S./M.S. in biological sciences, biochemistry, or related fields.</li>
<li>Recent graduate with 1 to 3 years of experience.</li>
<li>Excellent oral and written communication skills, with the ability to collaborate effectively within a team environment.</li>
<li>Demonstrated ability to perform complex sample preparation workflows (preferably for biological mass spectrometry) with minimal supervision.</li>
<li>Experience working in a laboratory environment.</li>
<li>Well-organized, self-motivated, and able to multitask with attention to detail.</li>
<li>Willingness to learn and a strong work ethic.</li>
<li>Works well independently and in a matrix environment.</li>
</ul>
 What is the minimum education experience required?:
<ul>
<li>B.S./M.S. in biological sciences, biochemistry, or related fields.</li>
</ul>
<ul>
<li>Recent graduate with 1 to 3 years of experience.</li>
<li>Excellent oral and written communication skills,</li>
<li>Experience working in a laboratory environment.</li>
<li>Well-organized, self-motivated, and able to multitask with attention to detail.</li>
</ul>
 #sczr2

Bench Scientist

<h3>Job Description</h3>
Job Description
We are currently recruiting for a Research Data Analyst to join Crosby Advisors. In this position, you will play a vital role in contributing to the investment performance of the team by working closely with investment professionals across CA. 
POSITION DUTIES / ACCOUNTABILITIES:
<ul>
<li>Provide general researchsupport to Crosby Advisors</li>
<li>Conduct a variety of analyses across the fundamental, quantitative, and data science disciplines gather and analyze industry data, interpret results, form conclusions and reflect results</li>
<li>Work closely with investors on various proprietary research projects to support the investment process</li>
<li>Streamline data collection and data management</li>
</ul>
The Skills and Experience
<ul>
<li>Strong Microsoft Excel/VBA skills and an aptitude for technology and working with (and presenting) data</li>
<li>Experience with financial databases like Bloomberg and FactSet</li>
<li>Exhibited experience/interest/skill in fundamental industry analysis</li>
<li>Exhibited experience/interest/skill in quantitative analysis</li>
<li>Exhibited experience/interest/skill in data science</li>
<li>Excellent communication, presentation and writing skills and is able to clearly articulate research findings</li>
<li>A commitment to the integrity of the scientific method</li>
</ul>
QUALIFICATIONS:
Competencies
<ul>
<li>Interpersonal Skills - the capacity to relate effectively across organizational levels </li>
<li>Communication - capacity to message in writing and verbally in manner suitable to the audience</li>
<li>Critical Thinking - demonstrating the capacity to analyze qualitative and quantitative information identifying patterns and nuance enabling the making of investment decisions</li>
<li>Professional Ethics - acting with integrity and respect focusing on responsibility and sound professional conduct</li>
<li>Continuous Learning - remains open to self-improvement, learning and professional development</li>
<li> Ability to adjust to changing business situations or demands, being open to change</li>
</ul>
Education and Experience
<ul>
<li>Bachelor’s Degree or equivalent required, A graduate degree in a financial or investment related discipline, a hard science, mathematics, or a CFA charter, are a plus.</li>
<li>10+ years of work experience, preferably in areas related to security investing, financial statement analysis, accounting, valuation, economics or statistics</li>
</ul>
Skills and Knowledge
<ul>
<li>Detail-oriented with strong problem-solving skills </li>
<li>Demonstrated financial analysis and valuation skills</li>
<li>Strong time management, organizational, and prioritization skills. </li>
<li>Excellent interpersonal, written and verbal communication skills </li>
<li>Proactive and positive attitude, highly motivated, self-directed with minimal daily supervision</li>
<li>Demonstrated flexibility in adapting to new and varying situations</li>
</ul>
Crosby Advisors is an equal opportunity employer. We believe that the most effective way to attract, develop and retain a diverse workforce is to build an enduring culture of inclusion and belonging.

Research Data Analyst

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
An associate scientist II position is available within the Cell Culture group of the BioProcess Development Department at AbbVie Bioresearch Center in Worcester, MA. The group is responsible for developing and supporting cell culture manufacturing processes for early and late phase clinical programs. We strive for speedy delivery of quality processes that are high yield, amenable to efficient manufacturing operations, robust and provide desirable product quality attributes. The group interacts closely with other development groups, along with Manufacturing and Discovery. The selected candidate will be involved in cell culture media development, process development, process characterization, tech transfer and scale-up. We are seeking for an enthusiastic, creative scientist that can work independently and as part of a dynamic team environment.
Key Responsibilities:
<ul>
<li>Cultivate CHO cells in suspension at different bench-top scales (e.g. deep well plates, shake flasks, bioreactors) in fed-batch and perfusion modes.</li>
<li>Prepare cell culture media following recipes.</li>
<li>Execute experiments following established experimental procedures and assist in the interpretation of results.</li>
<li>Apply DoE and other statistical tools for the design and interpretation of experiments.</li>
<li>Maintain clear, accurate and timely documentation.</li>
<li>Effectively communicate scientific data and concepts to internal audiences through reports and presentations.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, and GMP compliance.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree, or equivalent education, with typically 3 or more years’ experience or Master’s Degree or equivalent education</li>
</ul>
Preferred Experience:&nbsp;
<ul>
<li>B.S. in biochemical/chemical engineering or life sciences related disciplines with 3+ years of experience; or M.S. in biochemical/chemical engineering or life sciences related disciplines.</li>
<li>Proven experience working aseptically in cell culture processes.</li>
<li>Proven experience working at bench-top bioreactor scale.</li>
<li>Proven experience to independently analyze and present results.</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.​ Salary: ​$58,656- $107,500
</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>

Associate, Scientist II

<h3>Job Description</h3>
Job Description
Kovalus Separation Solutions (KSS) is looking for Chemical Operators to join our team. We provide on the job training and a great team atmosphere. The right person must be open to learning, taking constructive feedback, and have the drive to be successful. In this role you will follow detailed chemical mix instructions, processes, and procedures to create membrane solution. Kovalus offers excellent health benefits, 401k with an automatic 3% contribution from the company, 10 paid holidays, sick time, and 3-weeks of vacation. In addition to these great perks, there is opportunity for growth within the company. 
This role is not available for Sponsorship.
Shifts Currently Available: Nights
What You Will Do In Your Role 
<ul>
<li>Operate simple equipment and sophisticated PLC-controlled equipment. </li>
<li>Use a variety of hand &amp; power tools, work instructions, and test equipment to perform a series of operations to correctly mix membrane solutions. </li>
<li>Prepare, sample, transfer, clean up, and dispose of chemicals used. </li>
<li>Report issues with quality, processes, equipment, and materials to management </li>
<li>Perform data-collection, record-keeping and update production logs. </li>
<li>Comply with all policies, guidelines and regulatory requirements per the KSS Quality/Manufacturing/Safety/HR Systems </li>
</ul>
The Experience You Will Bring 
Requirements: 
<ul>
<li>Experience handling and/or mixing chemicals, product ingredients, or food ingredients. </li>
<li>Maintain a strict adherence to safety rules and regulations, including wearing all required PPE. </li>
<li>Perform tasks such as lifting up to 50lbs, walking, climbing, stooping, standing, pushing and/or pulling for duration of assigned 12-hour shift. </li>
<li>Wear all PPE which includes hearing protection, eye protection, and safety toe work shoes. </li>
<li>Complete job functions in a wet environment </li>
</ul>
What Will Put You Ahead 
<ul>
<li>Experience utilizing hand and power tools. </li>
<li>Previous experience operating machinery </li>
<li>Experience recordkeeping </li>
</ul>
 Sun, Mon, Tues, every other Wed: Nights 6pm-6:15am

Chemical Operator 3

<h3>Job Description</h3>
Job Description
Job Description
<ul>
<li>
Provide support for the development and implementation of state-of-the-art mass spectrometry and proteomics technologies to improve understanding of mechanism of action of drug candidates, safety profiles of novel therapeutics, or identification and quantitation of biomarkers.
</li>
<li>
Combine protein biochemistry and bioanalytical workflows to support complex sample preparation methodologies that will be integrated with the entire suite of protein mass spectrometry-based detection systems.
</li>
<li>
Independently following protocols and executing experiments with an analytical mindset to deliver high-quality data across multiple portfolio projects.
</li>
<li>
Partnering with senior scientist and key stakeholders to design key experiments and assist data analysis and interpretation.
</li>
<li>
Contribute to the design of experiments and independently perform sample preparation using various extraction, protein digestion and purification techniques for mass spectrometry analysis.
</li>
<li>
Develop "fit-for-purpose" assays and bioanalytical workflows, balancing rigor against study goals to ensure timely delivery of high-quality data.
</li>
<li>
Work with different types of samples (biological fluids, tissues) from pre-clinical species.
</li>
<li>
Assist in data analysis and interpretation, communicate results to team members.
</li>
<li>
Contribute to the setup, troubleshooting, and maintenance of liquid chromatography and mass spectrometry instrumentation and/or other laboratory equipment.
</li>
<li>
Maintain scientific and ethical standards, including appropriate record-keeping and compliance.
</li>
</ul>
Qualifications:
<ul>
<li>
B.S./M.S. in biological sciences, biochemistry, or related fields.
</li>
<li>
Recent graduate with 1 to 3 years of experience.
</li>
<li>
Excellent oral and written communication skills, with the ability to collaborate effectively within a team environment.
</li>
<li>
Demonstrated ability to perform complex sample preparation workflows (preferably for biological mass spectrometry) with minimal supervision.
</li>
<li>
Experience working in a laboratory environment.
</li>
<li>
Well-organized, self-motivated, and able to multitask with attention to detail.
</li>
<li>
Willingness to learn and a strong work ethic.
</li>
<li>
Works well independently and in a matrix environment.
</li>
<li>
Schedule: Monday - Friday 9am - 5pm
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionMaterials Scientist - Aerospace - Technical Ceramics- Relocation available! This Jobot Job is hosted by: Matt Swaneveld Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $100,000 - $150,000 per year 
A bit about us:
 We are a leader in manufacturing advanced materials and are known for our custom designed technical solutions. Due to growth, we are looking for a Materials Scientist to assist in our well structured engineering department. As a Materials Scientist, you will be responsible for developing and testing new materials, analyzing and improving existing materials, and ensuring that all materials meet our high standards of quality and performance. This is a challenging and exciting role that requires a deep understanding of ceramics, materials, raw material testing, and scientific principles. If you have a background in technical ceramics and are looking to take the next step in your career, please read on! 
Why join us?
 
<ul>
<li> We are an industry leader with an assortment of versatile advanced material products</li>
<li> Stable company with well over 50+ years behind us</li>
<li> Great starting salary </li>
<li> Comprehensive benefits package including health/dental/wellness/and more</li>
<li> 401K+ employee match </li>
<li> Relocation assistance package if needed</li>
</ul>
 
Job Details
 Qualifications: 
<ul>
<li> Bachelor's degree in Materials Science, Ceramics, or a related field (Master's / PhD preferred) </li>
<li> Industry experience with Aerospace/Defense/ITAR/Medical</li>
<li> 9+ years of experience in ceramics, materials, or a related field</li>
<li> Potential to obtain a government security clearance</li>
<li> Strong knowledge of scientific principles and research methods</li>
<li> Experience with raw material testing and analysis</li>
<li> Excellent problem-solving skills and attention to detail</li>
<li> Strong communication and collaboration skills</li>
<li> Ability to work independently and as part of a team</li>
<li> Experience with advanced scientific equipment and techniques</li>
<li> Ability to write technical reports and present findings to management and other stakeholders</li>
</ul>
 Responsibilities: 
<ul>
<li> Conduct research and development activities to create new materials that meet our specific needs and requirements</li>
<li> Analyze and improve existing materials to enhance their performance, durability, and reliability</li>
<li> Perform raw material testing to ensure that all materials meet our quality standards</li>
<li> Collaborate with other scientists and engineers to develop new products and improve existing ones</li>
<li> Use advanced scientific equipment and techniques to analyze and test materials</li>
<li> Keep up-to-date with the latest developments in materials science and technology</li>
<li> Write technical reports and present findings to management and other stakeholders</li>
</ul>
 If you are a skilled and experienced Materials Scientist with a passion for innovation and a commitment to quality, we want to hear from you. This is an exciting and rewarding opportunity to work in a dynamic and fast-paced environment, where you will have the opportunity to make a real impact on the manufacturing industry. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Senior Materials Scientist

<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>

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