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<h3>Job Description</h3>
About Outlier
Outlier is the worlds leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities.
 
We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by:
<ul>
<li>Evaluate AI-generated content for factual accuracy and relevance in Chemistry.</li>
<li>Develop and answer Chemistry-related questions to refine AI understanding.</li>
<li>Assess and rank AI responses based on scientific rigor.</li>
</ul>
Required expertise and qualifications:
<ul>
<li>Education: Masters degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled)</li>
<li>Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&amp;D contributions</li>
<li>English Proficiency: Ability to read and write with minimal errors</li>
<li>Bonus Skills: AI model training experience is not required but helpful</li>
</ul>

Payment:
<ul>
<li>Currently, pay rates for core project work by Chemistry&nbsp;experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below)</li>
<li>Opportunities for higher-paying research projects based on performance.</li>
</ul>

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.&nbsp;

Chemistry Tutor (Part time work from home)

Research Scientist (Part time work from home)

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

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate – II Location: Lexington, MA, 02421 Duration: 6+ months Schedule: Monday-Friday, 8:30 am – 5 pm, May need to work outside of standard hours sometimes (evenings/weekends) Pay Range: $45 - 48/Hour. on W2 NOTES: Industry experience is preferred; Pharma experience is a plus. Life sciences degree (Biology, Biochemistry, Biotechnology, etc.) is required. MUST HAVE job-related tissue culture and metabolic assay experience; functional genomics (siRNA/CRISPR) experience a plus. MUST HAVES: 1) Experience in working with scientists to follow required protocols 2) Proficient at tissue culture and cell-based functional assays, with metabolic assays strongly preferred 3) Communication/Organization Purpose: To provide technical laboratory research support of projects focused on target validation using human in vitro models in metabolic functional assays such as Seahorse, lipolysis, and glucose uptake. Essential Functions: Work with scientists to conduct lab-based studies to support project efforts • Perform tissue culture work with human cell lines to develop and optimize workflows for in vitro target validation using mid-throughput (96-384 well plate) assays • Support project management efforts in standard operating procedure creation, sharing knowledge and skills, and fostering cross-functional teamwork • Engage in effective communication with colleagues within Client. Physical Requirements: No overnight travel required: • Work with human cell lines and common molecular biology reagents in a laboratory environment that may include hazardous chemicals and blood borne pathogens • Functions may require some morning, evening, or weekend hours outside of standard business hours Qualifications: • Bachelor's degree with 3-5 years of experience post-degree; relevant experience may be substituted as appropriate. Title is dependent on qualifications. • Tissue culture experience is required—including strong aseptic technique, BSL2 stewardship, and troubleshooting • Experience with cell-based screening systems and lab automation • Metabolic disease understanding is a plus • Experience with human primary cells (adipocyte, skeletal myoblasts) is a plus • Experience with automated laboratory equipment, complex machinery, and familiarity of high throughput data production principles are a plus • Ability to carry out complex protocols required • Experience in basic molecular biology techniques required • Experience working in a team environment required, industry (CRO, pharmaceutical, biotech) experience is preferred • Fluency in spoken and written English is a prerequisite for the role • Role requires proactive communication skills and cross-cultural understanding to interact within a global organization • Must be comfortable in asking for clarification and offering suggestions • Other desirable skills include advanced cellular imaging and/or high throughput data collection skills, and ability to interpret interdisciplinary data • Must love to learn, be ambitious, and be determined to contribute to improving patients' well-being. #sczr2

Research Associate II

<h3>Job Description</h3>
Job Description
Autumn Harp, Inc. is a private-label, custom manufacturer of cosmetics and personal care products. The company’s state of the art facility provides premium service and creative solutions to product development and manufacturing of skincare, color cosmetics and lip care products, in service to the personal care industry. Our OTC facility provides support to clients who range from major global corporations to independent brands. Autumn Harp fosters a diverse company culture and celebrates the uniqueness of our employees and are committed to an inclusive and respectful work environment. Autumn Harp is proud to be an equal opportunity employer.
We are seeking a Production Lab Manager to join our talented and diverse Quality Team in an environment with a strong commitment to internal and external customer service. Reporting to the Vice President, Technical, the Lab Production Manager will be responsible for overseeing the start-up and operations of a newly established industrial microbiology and analytical lab. The ideal candidate will play a pivotal role in decision-making processes related to equipment selection, installation and validation, workflow design and optimization, while ensuring that all products meet the highest quality standards. The ideal candidate will have a strong entrepreneurial attitude and an initiative-taking work ethic. The individual will be instrumental in ensuring the efficient functioning of the lab, adherence to industry and regulatory standards, and the timely delivery of high-quality results to support Production.
Key Responsibilities:
<ul>
<li>Ensure strict adherence to safety protocols and aseptic techniques in the laboratory. Maintain a safe working environment for all lab personnel.</li>
<li>Conduct sample preparation and product testing as required to support Production OSCOT.</li>
<li>Supervise and mentor lab staff, providing guidance and support in their day-to-day activities. Facilitate training programs for lab personnel on equipment usage and aseptic techniques. Foster a collaborative and productive work environment among team members.</li>
<li>Evaluate, select, procure, install, and validate relevant lab equipment.</li>
<li>Oversee equipment maintenance, calibration, and troubleshooting activities.</li>
<li>Develop and implement efficient and compliant analytical and microbiological testing processes, protocols, and validations.</li>
<li>Streamline workflows to maximize efficiency and productivity and minimize turnaround times while continuously assessing laboratory procedures for accuracy, reliability, and efficiency.</li>
<li>Assist in achieving ISO 17025 accreditation and continuously monitor industry standards and regulations to ensure compliance.</li>
<li>Manage the Production laboratory budget and resources.</li>
<li>Analyze experimental data and results, preparing comprehensive reports for internal and external stakeholders. Interpret analytical and microbiological findings, providing insights and recommendations based on the results.</li>
<li>Consult as needed with other departments, such as Production, Quality, R&amp;D, Customer Service and/or Product Safety.</li>
</ul>
Required Skills and Experience:
<ul>
<li>PhD preferred, bachelor’s degree in biology, chemistry or related field with appropriate experience accepted</li>
<li>Have a proven track record with outstanding leadership skills and professionalism</li>
<li>5+ years of experience in a microbiology laboratory that conducts traditional microbiological testing, preferably in the consumer goods, food and beverage, or pharmaceutical industry</li>
<li>In-depth knowledge of and experience using aseptic techniques in a traditional microbiological laboratory (e.g., culture media preparation, plating/inoculation, incubation, enumeration, and identification.)</li>
<li>Familiarity with Biosafety levels, including demonstrating proficiency in standard microbiological practices and techniques for working with agents requiring BSL-2 containment.</li>
<li>Strong analytical and critical thinking skills, with attention to detail and accuracy.</li>
<li>Excellent leadership and team management abilities, with a focus on fostering a positive work environment.</li>
<li>Experience with or willingness to learn how to operate analytical equipment such as HPLC, GC-FID, ICP-OES, and FT-IR.</li>
<li>Familiarity with regulatory and quality requirements for laboratories in the OTC and personal care fields.</li>
<li>Strong communication skills, both verbal and written, for effective collaboration with team members and stakeholders.</li>
<li>Familiarity with LIMS, ELN, and/or ERP software systems as well as all Microsoft Office applications (Word, Excel, Outlook, Teams, PowerPoint, etc.)</li>
<li>Detail-oriented and possess the ability to multi-task</li>
</ul>

Production Lab Manager

<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>

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