field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<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 
A Scientist II position is available within the Biologics Process Development Department at the Antibody Drug Conjugate Center of Excellence in Waltham, MA. The group is responsible for developing and supporting cell culture and purification 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 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>Develop recovery and purification process that utilizes clarification, chromatography, and membrane filtration technologies for monoclonal antibodies, bispecifics, and antibody drug conjugates (ADC).</li>
<li>Proactively seek opportunities to come up with innovative solutions to cater challenging business problems through creative solutions.</li>
<li>Design and execute process development and characterization activities, impurity and viral clearance studies.</li>
<li>Build experimentally verified fit for purpose mathematical models for downstream purification processes.</li>
<li>Provide deeper understanding of process performance using appropriate experimental and modeling tools.</li>
<li>Highly independent and productive in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor.</li>
<li>Work collaboratively and cross-functionally with colleagues in other functional areas (Analytical Development, Discovery, Manufacturing and Quality).</li>
<li>Conceive, investigate and execute scientific research and development to significantly improve platform processes and workflows, develop new methods, build technical expertise and intellectual property, and deepen scientific understanding.</li>
<li>Proactively seek out new information and opportunities to advance our technologies and pipeline.&nbsp; Critically evaluate relevant scientific, regulatory and business advances and integrate this knowledge.</li>
<li>A primary author of publications, presentations, regulatory documents and/or primary inventor of patents.</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 8 years of experience, or Master’s Degree or equivalent education with typically 5 years of experience.</li>
<li>Education background in chemical engineering, biomedical engineering, biochemistry, biochemical engineering, or biotechnology is preferred.</li>
<li>Experience in areas of purification process development is preferred.</li>
<li>Demonstrate excellent communication skills and specifically illustrate strong oral and written technical communications.</li>
<li>Seamlessly present research outcomes to multifunctional teams</li>
<li>Demonstrated problem-solving skills and capability to overcome complex issues.</li>
<li>Demonstrated success in coordinating and executing important projects to achieve business goals.</li>
<li>Must have a “results-oriented” work ethic and a positive “can-do” attitude with a strong sense of urgency and self-motivated desire to achieve.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Scientist II, Process Development

<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 a detail-oriented Microbiologist&nbsp;to support environmental monitoring and analytical testing. Responsibilities will include:&nbsp;
<ul>
<li>Total organic carbon testing</li>
<li>Endotoxin and bioburden testing</li>
<li>Environmental monitoring sampling
<ul>
<li>Surface, Water, and Air</li>
</ul>
</li>
<li>General lab duties
<ul>
<li>Cleaning, Stocking, Cold Room 5S, etc.</li>
</ul>
</li>
<li>Data verification and review</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>GMP Experience&nbsp;</li>
<li>Experience in a Quality Control Microbiology Lab</li>
<li>Experience with LIMS and&nbsp;Electronic laboratory notebooks</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>Associate’s degree with 3+ years of experience OR</li>
<li>Bachelor's degree with 2+ years of experience OR</li>
<li>Master's degree with 0-2 years of experience</li>
<li>Proficiency with MS word and excel</li>
<li>Understanding of experimental design and scientific methodology in order to interpret results and draw conclusions</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Visit on Site to Meet with the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, and on the second shift is Wednesday through Sunday. The hours are 2 pm-10:30 pm. Training is on the first shift before transmitting to the second shift. Candidates living within a commutable distance of Andover, MA, and the surrounding areas are encouraged to apply.&nbsp;
<ul>
<li>Excellent full-time benefits including 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 client’s 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.

QC Microbiologist Scientist II (2nd Shift Wed-Sun)

<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 
Discovery Biotherapeutics and Genetic Medicine (BGM) at Abbvie is seeking a highly motivated Principal Research Scientist to join the Cell and Functional Biology group at the AbbVie Bioresearch Center (ABC) site based in Worcester, MA. &nbsp;This role will be responsible for the design and execution of screening strategies employed to advance promising biotherapeutics from early exploration through lead optimization. &nbsp;Close partnerships with cross-functional colleagues will be required to drive transformative ideas to the clinic. The ideal candidate should possess experience in large molecule screening strategy design including vitro cell-based assays, with a strong experience in functional assay development and high-throughput screening.
Job Responsibilities:
<ul>
<li>Develop in vitro functional assays leveraging diverse signaling pathways to transition early therapeutic ideas into enabled biotherapeutics campaigns.</li>
<li>Design and employ strategic screening funnels for biotherapeutic discovery campaigns, performing detailed analysis of complex data sets for key insights guiding decision-making processes in research projects.</li>
<li>Identify and integrate cutting-edge technologies and methodologies into screening and assay development, anticipating future trends in drug discovery.</li>
<li>Foster strong cross-functional collaborations with therapeutic area partners to promote the generation of innovative ideas and solutions which support organizational objectives.</li>
<li>Present and explain research findings and strategies clearly and effectively, preparing scientific reports, publications, and presentations for varied audiences.</li>
<li>Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment.</li>
</ul>
Qualifications 
<ul>
<li>BS with 12+ years of experience or MS with 10+ years of experience or PhD 4+&nbsp;years of experience in Biology, Molecular and Cellular Biology, or another related field.</li>
<li>Extensive experience in biotherapeutic discovery and screening.</li>
<li>Demonstrated ability to inspire team members to achieve their best performance, fostering a positive and productive team environment.</li>
<li>Proficiency in developing and optimizing high-throughput screening assays for biotherapeutic candidates, including cellular and immunoassays.</li>
<li>Demonstrated ability to lead cross-functional research teams, manage projects, and effectively communicate with stakeholders.</li>
<li>Experience with state-of-the-art screening technologies and data analysis tools.</li>
</ul>
Desirable:
<ul>
<li>Experience with HTS and enabling automation platforms</li>
<li>Experience in managing relationships with Contract Research Organizations (CROs) and external partners.</li>
<li>Experience with enterprise data capture solutions (GeneData, Dotmatics, Benchling)</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>

Senior Scientist II, Cellular/Functional Biology

<h3>Job Description</h3>
Job Description
Title: Chemical Biology Research Scientist
Hiring Organization: Connexion Systems &amp; Engineering
Compensation, Benefits, and Employment Type
<ul>
<li>Duration: 6+ month contract, with potential for extension or conversion</li>
<li>Pay rate: $64-$68/hr </li>
<li>Job Location: Boston, MA</li>
<li>Schedule: M-F, 1st shift</li>
<li>Job#: bh17622</li>
</ul>
Description:
We are seeking a Research Scientist to join our Chemical Biology group. We aim to treat serious diseases, many with targets difficult to drug. In this lab-based role, this scientist will help deploy novel covalent drug discovery techniques to the identification and validation of ligands for hard-to-target proteins. The ideal candidate is a motivated, detail oriented, life-long learner with expertise in covalent drug discovery and compound screening.
Top requirements: 
<ul>
<li>Skilled in proteomics workflow</li>
<li>Mammalian cell culture</li>
<li>Affinity capture or immunoprecipitation skills</li>
<li>Sample preparation for Mass Spec analysis</li>
</ul>
Key Duties and Responsibilities:
· High throughput compound screening
· Designing, executing and troubleshooting novel screening approaches for covalent ligand discovery
· Proactive verbal and written communication to effectively engage with scientists from different disciplines on the team.
· Collaboratively work with members of the team to coordinate screening staging and timing
Knowledge and Skills:
· Expertise in covalent chemoproteomics and data analysis
· Knowledgeable about concepts of compound binding affinity, selectivity, reactivity and kinetics
· Automation for liquid handling
· Affinity capture methods including immunoprecipitation
· Western analysis
· Cell biology (cell culture, lentiviral based expression)
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.

Chemical Biology Research Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Discovery Biotherapeutics and Genetic Medicine (BGM) at Abbvie is seeking a highly motivated Principal Research Scientist to join the Cell and Functional Biology group at the AbbVie Bioresearch Center (ABC) site based in Worcester, MA. &nbsp;This role will be responsible for the design and execution of screening strategies employed to advance promising biotherapeutics from early exploration through lead optimization. &nbsp;Close partnerships with cross-functional colleagues will be required to drive transformative ideas to the clinic. The ideal candidate should possess experience in large molecule screening strategy design including vitro cell-based assays, with a strong experience in functional assay development and high-throughput screening.
Job Responsibilities:
<ul>
<li>Develop in vitro functional assays leveraging diverse signaling pathways to transition early therapeutic ideas into enabled biotherapeutics campaigns.</li>
<li>Design and employ strategic screening funnels for biotherapeutic discovery campaigns, performing detailed analysis of complex data sets for key insights guiding decision-making processes in research projects.</li>
<li>Identify and integrate cutting-edge technologies and methodologies into screening and assay development, anticipating future trends in drug discovery.</li>
<li>Foster strong cross-functional collaborations with therapeutic area partners to promote the generation of innovative ideas and solutions which support organizational objectives.</li>
<li>Present and explain research findings and strategies clearly and effectively, preparing scientific reports, publications, and presentations for varied audiences.</li>
<li>Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment.</li>
</ul>
Qualifications 
<ul>
<li>BS with 14+ years of experience or MS with 12+ years of experience or PhD +6 years of experience in Biology, Molecular and Cellular Biology, or another related field.</li>
<li>Extensive experience in biotherapeutic discovery and screening.</li>
<li>Demonstrated ability to inspire team members to achieve their best performance, fostering a positive and productive team environment.</li>
<li>Proficiency in developing and optimizing high-throughput screening assays for biotherapeutic candidates, including cellular and immunoassays.</li>
<li>Demonstrated ability to lead cross-functional research teams, manage projects, and effectively communicate with stakeholders.</li>
<li>Experience with state-of-the-art screening technologies and data analysis tools.</li>
</ul>
Desirable:
<ul>
<li>Experience with HTS and enabling automation platforms</li>
<li>Experience in managing relationships with Contract Research Organizations (CROs) and external partners.</li>
<li>Experience with enterprise data capture solutions (GeneData, Dotmatics, Benchling)</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 Scientist I, Cellular/Functional Biology

<h3>Job Description</h3>
Job Description
The Research Associate (RA) is a key member of the R&amp;D team, supporting important research projects and ongoing scientific activities. The RA brings 3-5 years of experience at a life sciences company, academic or medical research organization and is comfortable working in a fast-paced environment. The RA plays an important role assisting the CSO and other team members' conduct of the Company's clinical studies, technical validations, and scientific initiatives associated with CND's suite of neurodiagnostic products and services. The RA helps define research plans in collaboration with team members and performs secondary research on assigned topics. The RA provides key facts and figures for peer-reviewed publications and helps review and ensure all data is accurate and checked. The individual is a strong collaborator and is comfortable interfacing across multiple departments and communicating effectively with various team members. The RA has excellent attention to detail and provides effective written summaries of complex information. The individual also offers key insights on analyses and has experience discussing methods and conclusions with senior leaders in the organization.
Job Responsibilities:
Research Design and Execution
<ul>
<li>Contribute to the design and implementation of research projects </li>
<li>Conduct literature reviews to identify relevant research and methodologies</li>
<li>Support the development of research protocols and procedures </li>
<li>Help collect, analyze, and interpret data from various sources </li>
<li>Maintain accurate records of research activities and data </li>
</ul>
Data Analysis and Reporting
<ul>
<li>Support statistical analyses and other data analysis techniques</li>
<li>Develop figures for effective display of information</li>
<li>Help prepare reports, posters, presentations, and publications summarizing research findings </li>
<li>Aid in publication of manuscripts, abstracts and protocols</li>
</ul>
Collaboration and Communication
<ul>
<li>Work collaboratively with project teams, principal investigators(PIs), other researchers, and team members</li>
<li>Communicate research progress and findings effectively, both orally and in writing </li>
<li>Assist with grant writing and securing funding for research projects </li>
</ul>
Other Duties
<ul>
<li>Play a key role in maintaining the Company's scientific publications library and providing summaries of specific publications when needed</li>
<li>Stay current with advancements in the field and communicate to Company leaders</li>
<li>Assist with laboratory or field research activities when requested</li>
<li>Help manage research budgets and resources Perform literature searches as required and communicate relevant publications and findings to the research team.</li>
<li>Review agendas and abstracts from upcoming or previous scientific meetings and share relevant insights with the research team.</li>
<li>Contribute to additional activities, as needed, that support the goals of the research or study team</li>
<li>Perform other duties as assigned.</li>
</ul>
Knowledge, Skills &amp; Experience:
<ul>
<li>Experience in a research lab focused on innovative scientific advancements</li>
<li>Familiarity with moderately complex statistical methods that apply to applicable clinical studies</li>
<li>Ability to effectively manage multiple tasks and projects</li>
<li>Proficiency in relevant software, statistical packages, and laboratory techniques </li>
<li>Strong analytical and problem-solving skills are essential</li>
<li>Excellent written and verbal communication skills are necessary for effective collaboration and reporting </li>
<li>Strong organizational and time-management skills are needed to manage multiple projects and deadlines.</li>
<li>Ability to work effectively in a team environment.</li>
</ul>
Education, Certifications &amp; Licensures:
<ul>
<li>Master's degree or Ph.D is neuroscience required</li>
</ul>
Other:
<ul>
<li>This position is based in our Boston office (Coolidge Corner, Brookline) and is expected to be in-office at least 3-4 days/week.</li>
</ul>

Research Associate

<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:
The Associate QC Scientist performs laboratory testing within a fast-paced GMP environment in support of one or more of the following areas: raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab investigation reports.
Responsibilities:
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for the department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>2+ years of related work experience in a GMP and Quality Control environment (with knowledge of/experience with techniques such as Infrared (IR), FTIR, UV-vis, SoloVPE, Truscan)</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, Quality Control

<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 Associate QC Scientist performs laboratory testing within a fast-paced GMP environment in support of one or more of the following areas: raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab investigation reports.
The work schedule and hours for this position are Sunday through Wednesday, 4:00pm to 2:30am.
Responsibilities:
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for the department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>2+ years of related work experience</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, Quality Control (2nd shift, Sun-Wed, 4pm-2:30am)

<h3>Job Description</h3>
Outlier helps the worlds most innovative companies improve their AI models by providing human feedback. Are you an experienced Geography expert&nbsp;who would like to lend your expertise to train AI models?

About the opportunity:&nbsp;
<ul>
<li>Outlier is looking for talented &nbsp;Geography expert to help train generative artificial intelligence models</li>
<li>This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you</li>
</ul>
You may contribute your expertise by
<ul>
<li>Assessing the factuality and relevance of domain-specific text produced by AI models</li>
<li>Crafting and answering questions related to Geography</li>
<li>Evaluating and ranking domain-specific responses generated by AI models</li>
</ul>
Examples of desirable expertise:
<ul>
<li>A bachelor's or higher degree in &nbsp;Geography or a related subject</li>
<li>Experience working as a Geography&nbsp;professional</li>
<li>Ability to write clearly about concepts related to &nbsp;Geography&nbsp;in fluent English</li>
</ul>

Payment:
<ul>
<li>Currently, pay rates for core project work by Geography&nbsp;experts range from $20 to $40 per hour USD.&nbsp;</li>
<li>Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.</li>
</ul>

Geography Expertise Sought for AI Training (Part time work from home)

<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’re looking for a detail-oriented and motivated individual to join our team.&nbsp;In this role, you’ll execute routine testing using gel electrophoresis, HPLC, and compendial methods.&nbsp;This is a great opportunity for someone with strong analytical skills and a passion for lab-based work in a collaborative, client-focused environment. Responsibilities include:&nbsp;
<ul>
<li>Execute testing of assigned analysis type for routine sample submissions using gel electrophoresis, HPLC, and compendial methods</li>
<li>Identify and help to resolve equipment and basic test method issues</li>
<li>Develop expertise to serve as a backup executor of a limited number of other analysis types (other test methods)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li>
<li>Provide feedback to client on the performance of existing assays / test methods</li>
</ul>
Qualifications 
<ul>
<li>BS in science (chemistry, pharmacy, or equivalent life sciences degree)
<ul>
<li>1+ years of directly related experience</li>
</ul>
</li>
<li>Prior knowledge and lab experience with HPLC instrumentation and data processing&nbsp;</li>
<li>Prior knowledge and lab experience with&nbsp;compendial analysis</li>
<li>Prior knowledge and lab experience with LC-UV and Empower skills&nbsp;is required</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
</ul>
Additional Details:&nbsp;
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.

177 Science Jobs