associate scientist

Medasource

<div>
 <p>
  <strong>
   Title:
  </strong>
  Associate Scientist I
 </p>
 <p>
  <strong>
   Duration:
  </strong>
  Contract through June 2026
 </p>
 <p>
  <strong>
   Schedule:
  </strong>
  M-F 8-5 Onsite
 </p>
 <p>
  <strong>
   Occupational Summary
  </strong>
 </p>
 <p>
  The Associate Scientist I will support the development, qualification, and execution of analytical methods to
 </p>
 <p>
  enable optimization of processes, formulations and characterization of vaccine products. This incumbent in this
 </p>
 <p>
  position will be involved in pharmaceutical and analytical development for GMP production of vaccine products
 </p>
 <p>
  and therapeutics.
 </p>
 <p>
  <strong>
   Work Performed
  </strong>
 </p>
 <p>
  &bull; Perform pharmaceutical development and successful GMP release including:
 </p>
 <p>
  o Analytical development
 </p>
 <p>
  o Develop product specific release and characterization methods
 </p>
 <p>
  &bull; Quality methods for product release and complete comprehensive characterization of clinical lots
 </p>
 <p>
  &bull; Complete GMP testing in line with OCH and regulatory guidance
 </p>
 <p>
  &bull; Formulation development - developing formulations to stabilize vaccine products
 </p>
 <p>
  &bull; Employ analytical characterization tools to inform product formulation design
 </p>
 <p>
  &bull; Lead formulation &amp; filling of vaccine products including tech transfer &amp; production under GMP
 </p>
 <p>
  conditions
 </p>
 <p>
  &bull; Execute and document development and GMP actitivites in compliance with regulatory requirements
 </p>
 <p>
  &bull; Collaborate closely with other development teams to provide support for development activities and will
 </p>
 <p>
  work diligently with other development functions to understand how the production process changes
 </p>
 <p>
  impact product quality
 </p>
 <p>
  &bull; Compile data and perform analysis and interpretation and draw conclusions regarding progress and
 </p>
 <p>
  results of work, utilizing the data in appropriate decision making; summarize date, present results and
 </p>
 <p>
  propose next steps to advance development
 </p>
 <p>
  &bull; Write and review development reports; writes procols for tech transfer and SOPs for GMP production,
 </p>
 <p>
  and present data to project teams and larger settings
 </p>
 <p>
  <strong>
   Required Qualifications
  </strong>
 </p>
 <p>
  &bull; Knowledge and hands on classwork with analytical methods and/or product formulation
 </p>
 <p>
  &bull; Hands on experience with specific analytical methods (HPLC, immunoassays, biochemical methods),
 </p>
 <p>
  molecular or pharmaceutical product formulation (buffer &amp; excipient screening, thermal stability
 </p>
 <p>
  evaluation, biophysical methods) is preferred.
 </p>
 <p>
  &bull; GMP experience huge plus
 </p>
 <p>
  &bull; Must have the ability to work independently with guidance from senior scientists/managers
 </p>
 <p>
  &bull; Demonstrated ability in solving moderately complex analytical problems with guidance from senior
 </p>
 <p>
  development scientists
 </p>
 <p>
  &bull; Strong oral and written communication skills
 </p>
</div>


Associate Scientist

Syngene International Limited

<div>
 Date: 29 Sept 2025
 <br/>
 <br/>
 Location:
 <br/>
 <br/>
 Kolthur Shamirpet, Medchal, TG, IN, 500078
 <br/>
 <br/>
 Division: Discovery Services
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 Job title: Associate Scientist
 <br/>
 <br/>
 Job location: Hyderabad
 <br/>
 <br/>
 Job grade: 8-I
 <br/>
 <br/>
 About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
 <br/>
 <br/>
 <em>
  At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit
  <br/>
  <br/>
 </em>
 Mandatory expectation for all roles as per Syngene safety guidelines
 <br/>
 <br/>
 <ul>
  <li>
   Overall adherence to safe practices and procedures of oneself and the teams aligned.
  </li>
  <li>
   Contributing to development of procedures, practices and systems that ensure safe operations and compliance to company&rsquo;s integrity &amp; quality standards.
  </li>
  <li>
   Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
  </li>
  <li>
   Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
  </li>
  <li>
   Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
  </li>
  <li>
   Compliance to Syngene&rsquo;s quality standards at all times
  </li>
  <li>
   Hold self and their teams accountable for the achievement of safety goals.
  </li>
  <li>
   Govern and Review safety metrics from time to time.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Core Purpose Of The Role
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Personnel handling this profile will be responsible for conducting reactions and delivering final compounds within a fast turnaround time, meeting the specific requirements of both the project and Syngene. The candidate should be capable of independently designing the synthetic scheme for any target and solve chemistry problems. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Role Accountabilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Expected to design a synthetic scheme for any given target and to be proactive in identifying rate limiting steps along with the mitigation strategy.
  </li>
  <li>
   The candidate should be well versed in using literature search engines and predictive synthesis tools
  </li>
  <li>
   Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipment&rsquo;s&rsquo;
  </li>
  <li>
   Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment
  </li>
  <li>
   Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially.
  </li>
  <li>
   The candidate should be capable of meeting Syngene&rsquo;s productivity expectations (# of compounds/month, # of steps/month and productivity index of around 1.5) without compromising on safety and quality.
  </li>
  <li>
   The candidate should be capable of synthesizing the final compounds at a faster turnaround time.
  </li>
  <li>
   The candidate should have excellent analytical interpretation and purification skills.
  </li>
  <li>
   Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms.
  </li>
  <li>
   Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety.
  </li>
  <li>
   Attend all mandatory trainings and update training records as and when trainings are completed.
  </li>
  <li>
   Always ensure confidentiality.
   <br/>
   <br/>
  </li>
 </ul>
 Syngene Values
 <br/>
 <br/>
 All employees will consistently demonstrate alignment with our core values.
 <br/>
 <br/>
 <ul>
  <li>
   Excellence
  </li>
  <li>
   Integrity
  </li>
  <li>
   Professionalism
   <br/>
   <br/>
  </li>
 </ul>
 Specific requirements for this role
 <br/>
 <br/>
 <strong>
  Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   8-10 years.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Skills And Capabilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms.
  </li>
  <li>
   Should be capable of designing synthetic schemes and troubleshooting synthesis problems independently.
  </li>
  <li>
   Should be excellent in purification and analytical interpretation skills.
  </li>
  <li>
   Familiar with operations of relevant apparatus - instrument / equipment.
   <br/>
   <br/>
  </li>
 </ul>
 Education
 <br/>
 <br/>
 <ul>
  <li>
   M.Sc in general or organic chemistry.
  </li>
 </ul>
</div>


fairlife, LLC

<div>
 fairlife, LLC is a Chicago-based nutrition company that creates great-tasting, nutrition-rich and dairy products to nourish consumers.
 <br/>
 <br/>
 With over $3B in annual retail sales, fairlife's portfolio of delicious, lactose-free, real dairy products includes:
 <strong>
  fairlife&reg; ultra-filtered milk
 </strong>
 ;
 <strong>
  Core Power&reg;
 </strong>
 High Protein Shakes, a sports nutrition drink to support post-workout recovery;
 <strong>
  fairlife&reg; nutrition plan&trade;
 </strong>
 , a nutrition shake to support the journey to better health.
 <br/>
 <br/>
 A wholly owned subsidiary of The Coca-Cola company, fairlife, LLC has been recognized by both Fast Company and Nielsen for its industry leading innovation.
 <br/>
 <br/>
 To learn more about fairlife and its complete line of products, please visit fairlife.com.
 <br/>
 <br/>
 <strong>
  job purpose
 </strong>
 : The Associate Scientist will be applying scientific principles, conducting research experiments, and producing reliable test results. The primary objectives of this position are to resolve technical challenges, develop new products, improve existing products, validate testing methods, or enhance efficiency. The candidate should be comfortable working with a team and should have a passion for creativity and innovation within a fast-paced environment.
 <br/>
 <br/>
 The successful candidate will learn to interpret and apply scientific findings to dairy systems, to translate findings into innovative manufacturing processes and products.
 <br/>
 <br/>
 <strong>
  responsibilities:
  <br/>
  <br/>
 </strong>
 To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
 <br/>
 <br/>
 <ul>
  <li>
   Design and conduct benchtop experiments and perform tests according to research plan.
  </li>
  <li>
   Up-scale trials from benchtop to pilot plant and perform tests according to research plan.
  </li>
  <li>
   Design and execute shelf-life studies on selected products including routine analysis and sensory evaluations.
  </li>
  <li>
   Keeping up to date with relevant scientific and technical developments.
  </li>
  <li>
   Analyzing and summarizing research data.
  </li>
  <li>
   Presenting scientific findings to the R&amp;D team and to other functions when needed.
  </li>
  <li>
   Consistently deliver concise, accurate and complete reporting of work in the specified format (written and/or electronic).
  </li>
  <li>
   Operating benchtop and pilot plant equipment.
  </li>
  <li>
   Adhering to GMP and other safety regulations.
  </li>
  <li>
   Maintaining a safe, clean, and sanitary work area.
  </li>
  <li>
   Organizing, storing, and handling all chemical substances, fluids, and compressed gases according to safety instructions.
  </li>
  <li>
   Ensuring that safety guidelines are adhered to at all times within the laboratory.
  </li>
  <li>
   Cleaning, sterilizing, maintaining, and calibrating laboratory equipment.
  </li>
  <li>
   Providing technical support when necessary.
  </li>
  <li>
   Performing other duties assigned by supervisor.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  skills/qualifications required:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Master's Degree in food science with either a focus on dairy science or a working experience in dairy
  </li>
  <li>
   Previous working knowledge related to at least one of the following: food science, product recipe/formulation, process research, experimental design and/or plant trials.
  </li>
  <li>
   1+ years' experience in a lab/ pilot plant environment.
  </li>
  <li>
   Hands-on experience operating electrical and non-electrical laboratory equipment.
  </li>
  <li>
   In depth knowledge of QHSE management systems, preventative measures, and laboratory best practices.
  </li>
  <li>
   Ability to handle ambiguity and work in a fast paced, entrepreneurial environment.
  </li>
  <li>
   Working knowledge of MS Office Suite and database systems.
  </li>
  <li>
   Excellent verbal and written communication skills
  </li>
  <li>
   Strong analytical skills.
  </li>
  <li>
   Willingness to travel overnight, and to work night and weekend shifts for special projects
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  working conditions and physical requirements:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   8+ hours sitting/standing/walking
  </li>
  <li>
   Ability to lift up to 40 lbs.
  </li>
  <li>
   Exposure to hazards (machinery, flammable liquids, biohazards, etc.), etc.)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  position location:
 </strong>
 Chicago, IL
 <br/>
 <br/>
 <strong>
  reports to
 </strong>
 : Director, R&amp;D
 <br/>
 <br/>
 <strong>
  travel requirements:
 </strong>
 15%
 <br/>
 <br/>
 <strong>
  exempt/nonexempt:
 </strong>
 exempt
 <br/>
 <br/>
 <ul>
  <li>
   Base pay offered may vary depending on geography, job-related knowledge, skills, and experience. A full range of medical, financial, and/or other benefits, dependent on the position, is offered.
   <br/>
   <br/>
  </li>
 </ul>
 Base pay range:
 <br/>
 <br/>
 $90,000&mdash;$120,000 USD
 <br/>
 <br/>
 <em>
  fairlife, LLC is an equal opportunity employer. We do not discriminate on the basis of
 </em>
 <em>
  race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. All qualified applicants and employees will be given equal opportunity. Selection decisions are based on job-related factors.
  <br/>
  <br/>
 </em>
 <em>
  In addition to its nondiscrimination commitment, the Company will also provide reasonable accommodation of qualified individuals with known disabilities unless doing so would impose an undue hardship on the Company. If you have a disability and would like to request accommodation in order to apply for a position with us, please email
 </em>
 <em>
  careers@fairlife.com
 </em>
 .
 <br/>
 <br/>
 <em>
  <strong>
   For Recruitment Agencies
   <br/>
   <br/>
  </strong>
 </em>
 <em>
  At fairlife, we manage the majority of our hiring internally through our dedicated Talent Acquisition team, which is actively engaged in direct candidate sourcing. Most of our roles are filled through applications submitted via our careers site or through direct outreach by our team.
  <br/>
  <br/>
 </em>
 <em>
  As our recruitment is primarily handled in-house, we work only occasionally with external agencies, and only those on our existing, pre-approved vendor list. At this time, we are not reviewing or expanding that list.
  <br/>
  <br/>
 </em>
 <strong>
  <em>
   Unsolicited resumes or submissions from external agencies not authorized by our Talent Acquisition team will be considered direct candidate applications. As such, fairlife will not assume responsibility for any placement fees associated with these submissions.
   <br/>
   <br/>
  </em>
 </strong>
</div>


Aragen life sciences

<div><div><div><h6 class="jobSectionHeader"><b>LOCATION</b></h6><div>
Hyderabad, India</div></div><div><h6 class="jobSectionHeader"><b>
DEPARTMENT</b></h6><div>
Chemistry Solutions</div></div></div><div></div><div><div><b><br>
Years of experience:</b> to</div><div><b>
Salary Range:</b> INR to (Annual)</div><p></p><div><b><br>
Scope</b></div><p><b><br>
This role is responsible for client projects by route designing and synthesis of molecules as per client specifications, independently or through supervision of a team of chemist.</b></p><p><b>
Responsibilities</b></p><p><b>
 Set-up and execute reactions for synthesis of target molecules</b></p><ul><li><div><b>
Understand the project requirements and deliverables from manager as specified by the client</b></div></li><li><div><b>
Understand the reaction protocol and search literature as required</b></div></li><li><div><b>
Efficiently delegate work and monitor team members for effective planning, execution and delivery</b></div></li><li><div><b>
Understand and discuss the MSDS (Material Safety Data Sheet) with team members</b></div></li><li><div><b>
Identify and mitigate any potential safety risk with the help of supervisor</b></div></li><li><div><b>
Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage and minimum wastage</b></div></li><li><div><b>
Ensure parallel execution of multiple reactions</b></div></li><li><div><b>
Monitor the reaction by observing progress by using analytical techniques</b></div></li><li><div><b>
Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality</b></div></li><li><div><b>
 </b><b>Analyze analytical data, evaluate and interpret results from the synthesis and report</b></div></li><li><div><b>
Meet productivity benchmarks on number of reactions / number of steps / number of compounds / quality / compounds purity / project timelines</b></div></li></ul><ul><li><b> Improve delivery efficiency and quality through project management</b></li></ul><ul><li><div><b>
Support project manager in finalizing the estimation of the project by identifying relevant literature, proposing appropriate synthetic route/ reaction design and by assessing project risks and challenges</b></div></li><li><div><b>
Prepare weekly / monthly/ final reports as required</b></div></li></ul><ul><li><b>Ensure safety at work through enforcement of good laboratory practices</b></li></ul><div></div><ul><li><div><b>
Follow safety and quality systems in the labs</b></div></li><li><div><b>
Maintenance and usage of equipment/apparatus/instruments as per SOPs and general housekeeping norms</b></div></li></ul><p><b>
 Maintain records, data integrity and IP confidentiality</b></p><ul><li><div><b>
Document reactions executed, research findings/ observations accurately in lab note books as per client requirements to ensure data integrity</b></div></li><li><div><b>
Maintain strict IP confidentiality and adhere to all related policies</b></div></li><li><div><b>
To prepare final reports as required</b></div></li><li><div><b>
Identify and report non-compliance of LNB guidelines update by junior team members</b></div></li></ul><div></div><div><b><br>
 Ensure high morale and skill development of team:</b></div><div></div><ul><li><div><b>
Improve knowledge of organic chemistry (particularly synthesis) / Analytical techniques etc. through ono on one discussions with supervisor/ regular classroom trainings/ project trainings/ further education programs etc.</b></div></li><li><div><b>
Guiding a teams of chemists to meet productivity/ quality targets.</b></div></li><li><div><b>
Train and develop team members, regularly review their performance</b></div></li></ul><div></div><div><b><br>
Functional/ Technical Skills</b></div><div></div><ul><li><div><b><br>
Knowledge of Chemistry &amp; Execution</b></div></li><li><div><b>
Knowledge of Safety Protocols</b></div></li><li><div><b>
Knowledge of IP &amp; Confidentiality and Data Integrity</b></div></li><li><div><b>
Ability to conduct cost benefit analysis and optimum usage of resources</b></div></li></ul><div></div><div><b><br>
Required Educational Qualification &amp; Relevant experience</b></div><div></div><div><b><br>
Msc (Organic/ Medicinal Chemistry) with 1 - 5 years of relevant experience</b></div><div></div><div><b><br>
Or</b></div><div></div><div><b><br>
Ph.D. / PDF (Organic/ Medicinal Chemistry) with 1 &ndash; 3 years of relevant experience</b></div><div></div><div><b><br>
Additional Requirements</b></div><div></div><div><b><br>
Candidates with their research publications in leading journals would be preferred</b></div><p></p><p><b><br>
Additional Responsibilities:</b></p><p><b>
Reporting Team</b></p><ul><li><b>
Reporting Designation:</b></li><li><b>
Reporting Department:</b></li></ul><p><b>
Educational qualifications preferred</b></p><ul><li><b>
Category:</b></li><li><b>
Field specialization:</b></li><li><b>
Degree:</b></li><li><b>
Academic score:</b></li><li><b>
Institution tier:</b></li></ul><p><b>
Required Certification/s:</b></p><p><b>
Required Training/s:</b></p><p><b>
Required work experience</b></p><ul><li><b>
Industry:</b></li><li><b>
Role:</b></li><li><b>
Years of experience:</b></li></ul><p><b>
Key Performance Indicators:</b></p><p><b>
Required Competencies:</b></p><p><b>
Required Knowledge:</b></p><p><b>
Required Skills:</b></p><p><b>
Required abilities</b></p><ul><li><b>
Physical:</b></li><li><b>
Other:</b></li></ul><p><b>
Work Environment Details:</b></p><p><b>
Specific requirements</b></p><ul><li><b>
Travel:</b></li><li><b>
Vehicle:</b></li><li><b>
Work Permit:</b></li></ul><p><b>
Other details</b></p><ul><li><b>
Pay Rate:</b></li><li><b>
Contract Types:</b></li><li><b>
Time Constraints:</b></li><li><b>
Compliance Related:</b></li><li><b>
Union Affiliation:</b></li></ul></div></div><p></p>

Alnylam

<div><div><b>Overview<br>
</b></div><div></div><div>The Research Department at Alnylam Pharmaceuticals is seeking a Principal Associate Scientist to join our High Throughput In Vitro team within the RNAi Discovery group. This dynamic, interdisciplinary team drives the discovery and development of novel RNAi therapeutics&mdash;from target identification through lead candidate selection.<br>
</div><div></div><div>The ideal candidate will bring a strong background in in vitro research and biological sciences, along with a robust technical skillset and enthusiasm for scientific innovation. Success in this role requires excellent organizational and interpersonal skills, the ability to manage multiple projects, and a commitment to learning and sharing new techniques.<br>
</div><div></div><div>We are looking for a detail-oriented, motivated team player who thrives in a fast-paced, goal-driven environment and is eager to contribute to Alnylam&rsquo;s mission of transforming the treatment of human disease through RNAi therapeutics.<br>
</div><div></div><div>This position is lab-based <b>onsite </b>and will be primarily located in Cambridge, MA.<br>
</div><div></div><div><b>Summary of Key Responsibilities<br>
</b></div><div></div><ul><li>Conduct a wide range of in vitro siRNA research studies to evaluate RNAi compounds using biochemical, molecular, and cell-based assays.
</li><li>Plan, coordinate, and execute day-to-day high-throughput in vitro experiments, including transfection, RNA extraction, qPCR, data upload, and statistical analysis.
</li><li>Design, perform, and interpret experiments independently and collaboratively, providing critical troubleshooting and technical insight.
</li><li>Maintain and culture various cell types (iPSCs, primary cells, immortalized cell lines) to support research objectives and facilitate high-throughput siRNA screening through qPCR and cell-based assays.
</li><li>Ensure accurate data recording, analysis, and timely reporting, preparing clear and detailed experimental summaries, documentation, and presentations.
</li><li>Identify and resolve technical challenges, contributing to the ongoing optimization and development of experimental protocols.
</li>Operate and maintain automated instrumentation and robotic systems to support high-throughput (384-well) screening workflows.<br>
<li>
</li></ul><div></div><div><b>Qualifications<br>
</b></div><div></div><ul><li>BS/MS in Biology, Molecular/Cell Biology, Biochemistry, or related field with 5&ndash;8 years of relevant experience, preferably in an industrial or biotech environment
</li><li>Proficiency in mammalian cell culture, including maintenance and transfection of immortalized and primary cell lines
</li><li>Skilled in molecular biology techniques for RNA, DNA, and protein quantification (qPCR, dPCR, Western blotting, ELISA, immunoprecipitation)
</li><li>Prior experience or strong understanding of nucleic acid&ndash;based therapeutics (siRNA, ASO, CRISPR) highly desired
</li><li>Hands-on experience with laboratory automation systems, including liquid-handling platforms such as PerkinElmer JANUS, Beckman i7, or similar
</li><li>Strong knowledge of experimental design, data interpretation, and scientific troubleshooting
</li><li>Highly detail-oriented, organized, and capable of managing multiple projects in a fast-paced, dynamic environment
</li><li>Demonstrated ability to collaborate and communicate effectively with cross-functional teams and stakeholders
</li>Proficiency with Microsoft Office (Excel, Outlook, PowerPoint, Word) and GraphPad Prism<br>
<li>
</li></ul><div></div><p><b>U.S. Pay Range
</b></p><p><b>$93,800.00 - $140,600.00
</b></p><p>The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
</p><p>Alnylam&rsquo;s robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
</p><p><i>Learn more about these and additional benefits offered by Alnylam by visiting the </i><i>Benefits section of Nebula </i><i>.</i></p></div>

Principal Associate Scientist, RNAi Discovery

AbbVie

<div><b>Company Description</b><p><br>
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 &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.</p><b><br>
Job Description</b><p><br>
Possesses an understanding of sample management processes and works closely with scientists and project managers to ensure samples are received and transferred to frozen storage in accordance with SOPs and study protocols. Supports colleagues in laboratory operations and biological sample testing. Develops independence in performing routine work and ability to organize, manage and set priorities for multiple tasks. Demonstrate the ability to document according to good documentation practices, communicate observations and escalate issues effectively.</p><p><b>
Essential Functions:</b></p><ul><li>
Work in a cross-functional team to meet business needs.</li><li>
Log shipments and receive samples for clinical and/or toxicology trials, in accordance with priority and in accordance with SOPs and regulations. Work with applicable team members to resolve any sample discrepancies as necessary.</li><li>
Safely works with biological matrix (e.g. plasma, urine, blood, etc) in a biohazard level 2 laboratory.</li><li>
Document and maintain sample chain of custody such as shipment, sample receipt and condition records per SOP.</li><li>
Manage the maintenance/calibration of cooling devices to ensure all samples are appropriately stored. Ensure alarms from temperature monitoring system are addressed within expected timeframes.</li><li>
Support bioanalytical testing through sample preparation such as tissue dissection, solvent and reagent preparation, along with maintaining chemical and reagent inventories.</li><li>
Support laboratory operations with instrumentation such as deactivation, retirement, and disposal.</li><li>
Performs work assignments accurately and in a timely and safe manner.</li><li>
Performs self and peer review of the data for accuracy and compliance.</li><li>
Ensure compliance with current SOPs and training.</li></ul><br>
<b>
Qualifications</b><br>
<p></p><ul><li>
Bachelor&rsquo;s degree (preferably life sciences related) or equivalent years of experience required</li><li>
Must have 1-3 years of sample processing experience in a GLP regulated environment.</li><li>
An expert in the end-to-end sample lifecycle.</li><li>
Proficient with applicable LIMS software.</li><li>
Proven ability to work autonomously and develop ideas/solutions to improve operations</li><li>
Must have demonstrated experience in cross-functional team environment (specifically IT, Bioanalysis, Clinical Systems)</li></ul><p><b>
Preferred Skills:</b></p><ul><li>
Knowledge of applicable regulatory requirements</li><li>
Ability to understand and independently apply Good Laboratory Practices (GLPs) to everyday work</li><li>
Ability to utilize Microsoft Excel and Word to perform tasks</li><li>
Ability to use electronic laboratory notebook and Laboratory Information Management System (e.g. Watson LIMS, StarLIMS, etc)</li><li>
Good written and oral communication skills</li><li>
Time management and project management skills</li><li>
Problem solving and troubleshooting abilities</li><li>
Ability to work in a collaborative work environment with a team</li><li>
Strong organization, attention to detail, and multi-tasking skills</li><li>
Ability to lift boxes up to 20 lbs</li></ul><br>
<b>
Additional Information</b><p><br>
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
</p><ul><li><p>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
</p></li><li><p>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
</p></li><li><p>This job is eligible to participate in our short-term incentive programs.
</p></li><li><p>This job is eligible to participate in our long-term incentive programs
</p></li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company&rsquo;s sole and absolute discretion, consistent with applicable law.</p><div></div><p>
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.</p><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

Associate Scientist II

IDEXX Laboratories

<div></div><div><div><div><div><div><div>Location</div>
 <div></div>Westbrook, ME
</div></div><div><div><div>Category</div>
 <div></div>Research &amp; Development</div></div></div></div></div><div></div>
<br><div><div><p>The <b>R&amp;D Discovery and Technology Futures Team</b> at IDEXX Laboratories is seeking an innovative early career <b>Associate Scientist</b> to assist in designing the next generation of IDEXX products. In this highly collaborative role, you will join a group of talented, technically focused individuals working together to deliver paradigm-shifting technologies that enable the development of next generation diagnostic assays. The successful candidate will be innately inquisitive, comfortable with evaluating high-risk/high-reward opportunities, and thrive in multi-disciplinary environments.</p><p></p><p>
In this role, you will contribute to early-stage ideation and evaluation of innovative assay designs and formats for product extensions across our various detection platforms. You will join and work closely with a scientifically diverse team including staff with expertise in biochemistry, synthetic chemistry, and systems engineering to develop transformative assay concepts, translate them into assay embodiments, and determine their feasibility for the detection of exciting new biomarkers coming through our pipeline.</p><p></p><div><b>
What You&rsquo;ll Do:</b></div><ul><li><p>
Perform a variety of novel and traditional biomarker assays, including immunoassay (e.g., ELISA and immunofluorescence), enzyme activity, nucleic acid detection, etc.</p></li><li><p>
Contribute to the design, development, and early-stage feasibility assessment of new assay formats and embodiments.</p></li><li><p>
Design experiments and new protocols, analyze complex data sets, and troubleshoot around failure modes.</p></li><li><p>
Communicate data, complex analytical methods, and project impact cross-functionally.</p></li><li><p>
Collaborate closely with other team members within the group and broader R&amp;D organization to drive results.</p></li></ul><p></p><div><b>
What You Need to Succeed:</b></div><ul><li><p>
Bachelors in Biochemistry, Chemistry, Bioengineering, Biomedical Engineering, or related fields with 3-5 years of relevant experience in industry or academic lab</p></li><li><p>
Technical knowledge and experience running ELISA immunoassays is required</p></li><li><p>
Exposure to other immunoassay formats and nucleic acid detection is highly desirable</p></li><li><p>
Ability to quickly learn new skills and technologies, pivot around new strategies, and prioritize critical experiments to meet timelines.</p></li><li><p>
Ability to clearly communicate data to a wide range of audiences and convey impact on a broader scale</p></li></ul><p></p><div><b>
What you can expect from us:</b></div><ul><li><p>
Base salary range starting at $62,000 based on experience</p></li><li><p>
Opportunity for annual cash bonus</p></li><li><p>
Health / Dental / Vision Benefits Day-One</p></li><li><p>
5% matching 401k</p></li><li><p>
Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more</p></li></ul><p></p><p>
If you&rsquo;re looking for a role that&rsquo;ll challenge you, offer a variety of work and learning, while helping an amazing industry, we&rsquo;d love to hear from you!</p><p></p><div><b><br>
Why IDEXX:</b></div><p>
We&rsquo;re proud of the work we do because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people.</p><p></p><p>
So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement.</p><p></p><p>
Let&rsquo;s pursue what matters together.</p><p></p><p><i>
IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply.</i></p><p></p><p><i>
IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited</i> <i>by local, state, or federal laws.</i></p><p></p><p><i>
While we appreciate our staffing partners, we are unable to accept unsolicited agency resumes.</i></p><p></p><p><i>
 </i><i>#LI-CAG</i></p></div></div>

Next Generation Immunoassay, Associate Scientist

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