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<h3>Job Description</h3>
Job Description
MERL is looking for a research intern to develop efficient transformer-informed stochastic MPC to control net-zero energy buildings. This is an exciting opportunity to make a real impact in the field of cutting-edge deep learning and predictive control on a real system. Publication of results produced during the internship is desired. The expected duration of the internship is 3-6 months with a flexible start date.
The Ideal Candidate Will Have:
<ul>
<li>Significant hands-on experience with stochastic MPC
<ul>
<li>Publications in SMPC are a strong plus</li>
</ul>
</li>
<li>Fluency in Python and PyTorch</li>
<li>Understanding of probabilistic time-series prediction</li>
<li>Experience with convex programming
<ul>
<li>Convex formulations of MPC/SMPC problems are a strong plus</li>
</ul>
</li>
<li>Completed their MS, or &gt;50% of their PhD program</li>
</ul>
Mitsubishi Electric Research Labs, Inc. "MERL" provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, MERL complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
MERL expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of MERL’s employees to perform their job duties may result in discipline up to and including discharge.
Working at MERL requires full authorization to work in the U.S and access to technology, software and other information that is subject to governmental access control restrictions, due to export controls. Employment is conditioned on continued full authorization to work in the U.S and the availability of government authorization for the release of these items, which might include without limitation, obtaining an export license or other documentation. MERL may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to MERL facilities and information systems, as MERL deems appropriate, to ensure practical compliance with applicable employment law and government access control restrictions.

Internship - [research keywords here]

<h3>Job Description</h3>
Job Description
Come join CCRM Fertility, a global pioneer in fertility treatment, research, science, specializing in IVF, fertility testing, egg freezing, preimplantation genetic testing, third party reproduction and egg donation. As a member of CCRM Fertility’s diverse team of professionals, you will be a part of helping families grow and changing lives. We take pride in providing our employees with meaningful employment, a supportive culture, and a well-balanced personal &amp; work life alignment. For more information, visit <a href="http://www.ccrmivf.com" target="_blank">www.ccrmivf.com</a>
Location Address: 
Department: IVFLaboratory
Work Schedule: Monday – Friday (8:00am – 4:30pm)
What We Offer Our Team Members:
<ul>
<li>Generous Paid time-off (PTO) and paid holidays</li>
<li>Medical, Dental, and Vision Insurance</li>
<li>Health benefits eligible the first day of the month following your start date.</li>
<li>401(k) Plan with Company Match (first of the month following 2 months of service)</li>
<li>Basic &amp; Supplement Life Insurance</li>
<li>Employee Assistance Program (EAP)</li>
<li>Short-Term Disability</li>
<li>Flexible spending including Dependent Care and Commuter benefits.</li>
<li>Health Savings Account</li>
<li>CCRM Paid Family Medical Leave (eligible after 1 year)</li>
<li>Supplemental Options (Critical Illness, Hospital Indemnity, Accident)</li>
<li>Professional Development, Job Training, and Cross Training Opportunities </li>
<li>Bonus Potential</li>
</ul>
What You Will Do:The Senior Embryologist will be responsible for performing all procedures in the IVF Laboratory under the direction of the IVF Laboratory Supervisor. The Senior Embryologist must demonstrate knowledge and skills related to the various procedures performed in the IVF Laboratory. The Senior Embryologist reports directly to the IVF Lab Supervisor.
<ul>
<li>Perform daily, weekly, and periodic function checks and maintenance on equipment and trouble shoot equipment problems and make appropriate decisions for repair, with guidance.</li>
<li>Follow appropriate blood borne pathogen handling and disposal procedures.</li>
<li>Perform all aspects of media/medium preparation with sterile technique for each case and documents the lots used.</li>
<li>Process semen for IVF procedures according to IVF lab protocol.</li>
<li>Assist physician during egg retrievals and is able to locate and assess all oocytes retrieved in a timely manner. Able to trim oocytes without trauma or injury to the oocytes.</li>
<li>Adhere to the IVF lab’s double signature and check system when performing procedures to ensure correct identity of eggs, sperm, and embryos.</li>
<li>Document all patients’ results into the IVF Lab information system (LIS).</li>
<li>Perform daily fertilization checks which includes “cleaning” embryos with minimal trauma (insemination cases) to observe fertilization.</li>
<li>Assess fertilization by observation of pronuclei and polar bodies.</li>
<li>Perform freezing and thawing of human embryos according to IVF lab protocol with a high survival rate.</li>
<li>Perform oocyte inseminations according to IVF lab protocol.</li>
<li>Able to hyal and strip oocytes for ICSI with minimal trauma.</li>
<li>Perform Intracytoplasmic Sperm Injection (ICSI) according to IVF lab procedures resulting in high fertilization rates.</li>
<li>Assist physician with embryo transfer and ensures proper identification of the patient with a “time-out” before the transfer.</li>
<li>Assist physician during PESA, MESA and TESE procedures by locating and processing sperm found according to IVF lab procedures.</li>
</ul>
<ul>
<li>Perform biopsy procedures, including trophectoderm biopsy, resulting in high number of embryos returning a test result. Embryos biopsied result in a high survival rate when thawed and an acceptable implantation rate when transferred.</li>
<li>Other duties as assigned.</li>
</ul>
What You Bring:
<ul>
<li>Bachelor’s Degree in Biology, Chemistry, or Microbiology required.</li>
<li>Medical technology licensure/certificate required if Embryologist completed a medical technology university-based program.</li>
<li>5+ years’ experience in laboratory or scientific research required (Med laboratory preferred).</li>
<li>Computer and database experience preferred.</li>
</ul>
Working Conditions:The physical demands described here are representative of those which should be met, with or without reasonable accommodation (IAW ADA Guidelines), by an employee to successfully perform the essential functions of this job. This job operates in a professional office and clinical setting. This role routinely uses standard office equipment such as computers, including computer keyboards and mice; telephones; photocopiers; scanners; filing cabinets. While performing the duties of this job, the employee is regularly required to communicate with others. The employee is frequently required to sit; will occasionally stand and/or walk; use hands and fingers to grasp, pick, pinch, type; and reach with hands and arms. Employees should have the visual acuity to perform an activity such as: preparing and analyzing data and figures, viewing a computer terminal, extensive reading, and operation of standard office machines and equipment. 
CCRM’s Compensation: The salary range represents the national average compensation for this position. The base salary offered will vary based on location, experience, skills, and knowledge. The pay range does not reflect the total compensation package. Our rewards may include an annual bonus, flexible work arrangements, and many other region-specific benefits.
Pre-Employment Requirements:All offers of employment are conditional upon the successful completion of the CCRM Fertility onboarding process, including verification of eligibility and authorization to work in the United States. This employer participates in the E-Verify Program in order to verify the identity and work authorization of all newly hired employees.
Equal Employment/Anti-Discrimination: We are an equal-opportunity employer. In all aspects of employment, including the decision to hire, promote, discipline, or discharge, the choice will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Senior Embryologist

<h3>Job Description</h3>
Job DescriptionRole Summary
<ul>
<li>Responsibilities: You will be responsible for devising and performing statistical analysis plans and then communicating the methodologies and results of these to our clients in the healthcare sector</li>
<li>Salary: $73,000 to $76,000 depending on qualifications and previous experience</li>
<li>Benefits: Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous vacation allowance, private medical and dental insurance, 401K plan with up to a 5% employer contribution, life insurance, full funding and study leave for external training and more</li>
<li>Role Type: Full-time, permanent </li>
<li>Start Date: We are currently recruiting for start dates throughout 2025, including May, June and July, and you will be asked to state your availability on your application form</li>
<li>Application Deadlines: Whilst there are no set application deadlines, we strongly recommend applying as early as possible. The role, or particular start dates, may close when suitable candidates are found</li>
<li>Location: This role is available in our Boston office </li>
</ul>
About the Role
Our Statistics team provide statistical and analytical expertise across Costello Medical, devising statistical analysis plans and performing data analysis within R, Excel, Stan, SQL and BUGS software. They are also responsible for communicating the methodologies and results in both written and oral formats to drug and device manufacturers, and doctors. The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as basic statistical analysis of individual patient data, regression analysis, survival analysis and complex Bayesian network meta-analysis using both standard and emerging methods.
You will work in project teams alongside colleagues from all specialities to ensure that statistics projects are completed to an exceptionally high standard, on time and in line with client expectations. You will receive training in the technical aspects of the role, project management skills and effective client communication. Delivering project work requires close collaboration with clients and, following a successful induction period, you will increasingly participate in client calls and face-to-face meetings with external stakeholders. 
Our team typically work on several projects at one time and the results of each analysis can feed into publications, value materials, health economic models or health technology assessment submissions. You will therefore be exposed to a wide variety of our services and a broad range of therapeutic areas. To read more about our recent articles and publications, please visit our website: <a href="https://www.costellomedical.com/research/articles-publications/" target="_blank">https://www.costellomedical.com/research/articles-publications/</a>
Hybrid Working Policy: We believe that having face-to-face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. At the same time, we recognize that homeworking can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments. Therefore, we offer flexible working arrangements that allow our colleagues to work from home for up to half of the time, measured across a 2-week rolling period.
A Day in the Life of a Statistician
To learn more about a typical day for a Statistician at Costello Medical, please click here: <a href="https://www.costellomedical.com/day-in-the-life/statistician.html" target="_blank">https://www.costellomedical.com/day-in-the-life/statistician.html</a>
Career Profile
We offer many opportunities for personal and professional development at Costello Medical. Please click below to read firsthand accounts from our colleagues about their time with the company: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/</a>
About Costello Medical
Costello Medical is a rapidly growing global healthcare agency specializing in medical communications, market access and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies and charitable organizations. We have been listed in the Top 100 Best Companies to Work For list since 2017 and were proud to receive B Corporation accreditation in 2022. Please click here to learn more about us, our work and our mission: <a href="https://www.costellomedical.com/" target="_blank">https://www.costellomedical.com/</a>
Requirements
About You
The successful candidate will be someone who enjoys problem solving and thinking outside the box to develop innovative solutions. In line with the company’s values, you will be passionate about improving patient outcomes by applying your statistical knowledge and technical skills to the healthcare industry.
Essentialrequirements for the role are:
<ul>
<li>A degree level or higher qualification in a scientific or mathematical discipline (minimum GPA 3.3) with a focus on statistics and data analysis. </li>
<li>Proficiency in the R programming language, and the willingness and ability to rapidly develop your programming skills</li>
<li>The technical and mathematical ability, coupled with the written and oral communication skills, to explain complex techniques and results to non-experts</li>
<li>A willingness to trial, explore or recommend new software or techniques that may suit specific projects</li>
<li>A high degree of accuracy and attention to detail, along with the ability to maintain a high level of customer service and the quality of deliverables under multiple competing demands</li>
<li>A high level of organisation, with the flexibility to respond to changing deadlines</li>
<li>The ability to use your initiative and work independently, in addition to working collaboratively within project teams</li>
<li>Excellent written English, which will be assessed during the selection process</li>
</ul>
Desired requirements for the role are:
<ul>
<li>A Masters degree or PhD in a scientific or mathematical discipline </li>
<li>Experience with Python Stan, SQL</li>
<li>Experience in and/or knowledge of medical data, clinical processes or trials</li>
</ul>
Joining Costello Medical from Academia
At Costello Medical, we warmly welcome applicants from academia who are looking to transitioning into a role within a commercial, industry-based setting. We understand the unique perspectives and valuable skills that academic professionals bring to our team. To support your career change, we offer comprehensive training, mentorship programs, and a work culture that fosters collaboration, growth and innovation. We are committed to facilitating a smooth transition and helping you thrive in an industry-based setting.
Many of our team members have successfully made this transition, and they share how their expertise has been transformed into fulfilling, impactful careers with us. Learn more here: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/joining-from-academia/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/joi…</a>
Benefits
What We Offer
Alongside our award-winning company culture, where every team member is celebrated, respected, and has their voice heard, our comprehensive benefits package includes:
<ul>
<li>A starting salary of $73,000 to $76,000 per annum, depending on your qualifications and previous experience, as well as a discretionary profit share bonus paid twice per year. Please note that we have established salary bands that ensures a fair and consistent approach for all applicants, eliminating the need for individual negotiations</li>
<li>23 days’ vacation leave increasing by 1 day each year to a maximum of 27 days. 6 public holidays plus 1 floating vacation day to use on a holiday of your choosing</li>
<li>Flexible, reasonable working hours and the chance to work from home for up to half of your working time</li>
<li>Private medical insurance with a company contribution, as well as dental and vision cover and life insurance</li>
<li>Retirement savings via a 401k plan with up to a 5% employer match</li>
<li>Paid funding for external education and study leave</li>
<li>Paid and unpaid sabbaticals based on length of service</li>
</ul>
Please click here to learn about our full reward package and the other benefits of working for Costello Medical: <a href="https://www.costellomedical.com/careers/benefits-package-in-the-us/" target="_blank">https://www.costellomedical.com/careers/benefits-package-in-the-us/</a>
The Application Process
You are required to submit your resume and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your resume should clearly state the dates of all qualifications and grades achieved where applicable.
Our recruitment process includes a telephone interview with a member of our Talent Acquisition team. Following this, you will also be sent a technical assessment, using R programming, and a proofreading exercise that we ask you to complete in your own time. If successful, you will be invited to an interview which will include a short presentation you can prepare for in advance. Our standard recruitment process lasts around 6 weeks, however, this can be adapted if necessary.
As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Please click here to learn more.
Please note that, whilst we embrace AI to innovate and improve processes, your role may involve confidential data that cannot be uploaded to AI. Therefore, it is important for us to assess your own skills and abilities, so we recommend that you do not rely solely on this technology to generate any application materials.
Visa Sponsorship
We welcome applications from international candidates, but we are unfortunately unable to provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we are able to consider those on a temporary visa, such as an OPT visa

Statistician

<h3>Job Description</h3>
Job DescriptionJob Description
The Clean Room Assembler performs a variety of tasks ranging from repetitive to non-repetitive production to assemble component parts into assemblies, sub-assemblies, or completed units. This role requires adherence to standard operating procedures and may involve conducting quality inspections on the processing line in accordance with quality specifications.
Responsibilities
<ul>
<li>Assemble component parts into assemblies, sub-assemblies, or completed units using standard operating procedures.</li>
<li>Conduct quality inspections on the processing line in accordance with quality specifications.</li>
<li>Apply basic skills and techniques to complete routine tasks within the assigned area.</li>
<li>Maintain appropriate licenses, training, and certifications.</li>
<li>Adhere to all quality guidelines and work under close supervision.</li>
<li>Ensure all work is reviewed for accuracy and deviations from the norm are approved by the supervisor before proceeding.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in assembly processes.</li>
<li>Experience working in a cleanroom environment.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Understanding of standard operating procedures and scientific methods.</li>
</ul>
Why Work Here?
Join a team that prioritizes quality and precision, offering a supportive work environment where all employees are encouraged to develop their skills and maintain necessary certifications. Experience a collaborative work culture that values accuracy and adherence to guidelines.
Work Environment
The role is based in a cleanroom environment, requiring adherence to specific dress codes and operating procedures. Employees work on routine assignments under close supervision, ensuring accuracy and compliance with quality standards.
Pay and Benefits
The pay range for this position is $17.90 - $19.40/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Chicopee,MA.
Application Deadline
This position is anticipated to close on Jun 26, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<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 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 
Independently generate precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.
Responsibilities:&nbsp;
<ul>
<li>Perform routine tasks competently and independently, and generate reliable and consistent results.</li>
<li>Design, develop, and optimize robust analytical methods using separations-based techniques (HPLC, icIEF, CE-SDS)</li>
<li>Analyze and critique results, noting significant deviations.</li>
<li>Troubleshoot experiments and instrumentation.</li>
<li>Learn and understand new experimental techniques.</li>
<li>Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences.</li>
<li>Place data in proper scientific context by consulting and citing relevant literature.</li>
<li>Demonstrate technical proficiency in his/her field.</li>
<li>Impact projects predominantly through lab and/or pilot plant based activities.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</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 (no additional experience).</li>
<li>Theoretical and practical knowledge to carry out job function.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Familiarity with statistical tools for data analysis, Empower software and regulatory guidelines.</li>
<li>Experience leading the qualification and validation of analytical methods in accordance with ICH, FDA, and USP guidelines, ensuring methods are suitable for late-phase development and regulatory submissions.</li>
<li>Experience with authorship and review of technical reports, standard operating procedures (SOPs), and validation protocols.</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 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>

<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 DescriptionSalary: $53,000 - $56,000 per year 
Overview
The Initiative for a Competitive Inner City (ICIC) is a national nonprofit founded in 1994 by Harvard Business School professor Michael Porter. ICIC drives inclusive economic prosperity in under-resourced communities through innovative research and programs to create jobs, income, and wealth for local residents. Informed by our research, ICIC has developed and supported highly effective initiatives for underserved businesses to meet entrepreneurs most pressing needs. At ICIC, you will work with talented, creative, and committed professionals in a collaborative culture dedicated to excellence and innovation.
 
Position Summary
ICIC is seeking a high-performing full-time Research Analyst who will work closely with senior research staff to lead and support research projects on local economic development and business growth issues and manage engagements with a diverse set of clients. The Research Analyst will report directly to the Senior Vice President and Director of Research.
Duties and Responsibilities
<ul>
<li>Conduct primary research using surveys, interviews, and qualitative and quantitative analysis.</li>
<li>Compile and synthesize data and information from public and private sources, including literature reviews using secondary data sources.</li>
<li>Perform quantitative analysis involving large and small datasets.</li>
<li>Support other staff with research projects from idea stage through completion.</li>
<li>Support senior staff with writing research grant proposals.</li>
<li>With supervision from senior staff, prepare reports and presentation materials for external and internal audiences, including writing, editing, and dissemination.</li>
<li>With supervision from senior staff, develop and support design of data visualizations.</li>
<li>Support senior staff in identifying new research opportunities.</li>
<li>With supervision from senior staff, manage research projects, ensuring that they meet rigorous research standards and are grounded in theory.</li>
<li>Other duties as assigned.</li>
</ul>
 
Qualifications
<ul>
<li>Strong academic performance with coursework or work experience in the social sciences or related fields, such as economics, business, geography, urban planning, political science, sociology, public policy, or a similar discipline.</li>
<li>Some experience in a research or consulting position is desirable but not required.</li>
<li>Demonstrated experience using and analyzing datasets.</li>
<li>Excellent writing, editing, and oral communication skills, including ability to summarize and synthesize complex information accurately and concisely.</li>
<li>Strong analytical skills.</li>
<li>Ability to convey complex information visually.</li>
<li>Ability to work collaboratively with research staff and staff from other units within the organization.</li>
<li>Demonstrated ability to work on projects independently.</li>
<li>Flexibility with changing priorities.</li>
<li>Ability to manage multiple tasks and projects simultaneously and successfully meet deadlines.</li>
<li>Ability to learn independently and solve research problems creatively.</li>
<li>Minimal travel may be required.</li>
</ul>
The ideal candidate will be committed to ICICs mission and bring a strong passion for research and analytics. They will have a solid understanding of economic development issues and demonstrate the ability to manage multiple projects at once while taking initiative to drive them to successful completion. Were seeking someone who thrives in a team environment and has a proven track record of effective collaboration.
This is a full-time remote position. We are currently able to employe candidates working from any of the following states: AL, AR, CA, CO, CT, DC, DE, FL, GA, IL, KY, MA, MD, MI, NC, NJ, NY, OH, OR, PA, TX, and VA.
Benefits include:
<ul>
<li>Three weeks of vacation per year to start, with an additional day added for each year of service up to 5 years</li>
<li>Thirteen days of paid holidays, half days on Fridays before long weekends, plus one floating holiday</li>
<li>Ten days of paid sick leave and two days paid personal leave each calendar year</li>
<li>Health, Dental, Vision Insurance (70% paid by ICIC)</li>
<li>401(k) Retirement Plan with employer matching up to 4% after the first year of employment</li>
<li>Up to 16 weeks of paid Parental leave</li>
<li>Individual Professional Development benefit of $1000 each year</li>
</ul>
ICIC is dedicated to fostering a diverse and inclusive organization. We provide equal opportunity for all persons seeking employment without regard to race, age, color, religion, gender identity, family status, sexual orientation, military status, national origin, disability, or any other characteristic as established by law.
ICIC participates in E-Verify to confirm that all new hires are authorized to work in the U.S. Please see the Participation Poster and Right to Work Poster for more information.
 remote work

Research Analyst

<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

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