associate scientist

Joulé

<div>
 
 
 Job Title:
 
 Associate Scientist &ndash; Product Formulation
 
 
 Location:&nbsp;&nbsp;
 
 Trumbull, CT&nbsp;(100% Onsite)
 
 
 Hours/Schedule:
 
 Monday&ndash;Friday, 8:30 am to 5 pm&nbsp;
 
 
 Type:
 
 Contract
 
 
 Overview
 
 
 The Associate Scientist will support product formulation development through hands-on laboratory experimentation, data analysis, and collaboration with cross-functional teams. This role involves creating and evaluating prototype products, conducting performance and stability testing, and contributing to the commercialization of new consumer product innovations.
 
 
 Responsibilities
 
 <ul>
 <li>
 
 Plan and perform laboratory experiments related to product formulation, validation, and performance testing
 
 </li>
 <li>
 
 Develop experimental designs and work plans to create prototype products that meet performance requirements
 
 </li>
 <li>
 
 Analyze experimental data, draw conclusions, and propose next steps in development plans
 
 </li>
 <li>
 
 Collaborate with packaging, process development, and manufacturing teams during development and commercialization phases
 
 </li>
 <li>
 
 Record and maintain detailed, accurate laboratory notes and experimental documentation
 
 </li>
 <li>
 
 Plan and schedule project tasks, including laboratory testing, third-party evaluations, and consumer trials
 
 </li>
 <li>
 
 Present data, progress, and results to project teams and management
 
 </li>
 <li>
 
 Develop or modify test methods to solve technical problems and evaluate competitive products
 
 </li>
 <li>
 
 Support lab demonstrations, training activities, and customer visits as needed
 
 </li>
 <li>
 
 Maintain laboratory supplies, raw material inventories, and clean, safe work environments
 
 </li>
 <li>
 
 Follow all applicable safety, environmental, and regulatory standards and policies
 
 </li>
 </ul>
 
 Qualifications
 
 <ul>
 <li>
 
 Bachelor&rsquo;s degree in Chemistry required, or Associate&rsquo;s degree with relevant industrial experience
 
 </li>
 <li>
 
 Relevant formulation experience in consumer packaged goods considered a strong advantage
 
 </li>
 <li>
 
 Advanced understanding of detergent chemistry and related testing methods preferred
 
 </li>
 <li>
 
 Experience performing a variety of research experiments and operating laboratory equipment
 
 </li>
 <li>
 
 Proficiency in Microsoft Word, Excel, and database applications
 
 </li>
 <li>
 
 Strong communication skills and ability to collaborate effectively within cross-functional teams
 
 </li>
 <li>
 
 Commitment to safe work practices and adherence to health, safety, and environmental regulations
 
 </li>
 </ul>
 
 Benefits
 
 
 
 System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
 
 
 
 
 
 Ref: #558-Scientific
</div>

Associate Scientist

Medasource

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

Adecco

Quality Control Associate Scientist (Temporary - until February 2026) Basingstoke, UK Full-time, Temporary Contract Are you an experienced Quality Control professional looking to make an impact in a leading life sciences organisation? We have an exciting opportunity for a Quality Control Associate Scientist to join our team in Basingstoke on a temporary basis until February 2026. About the Role As a Quality Control Associate Scientist, you will play a key role in ensuring our products meet the highest standards of quality and compliance. You will carry out a range of QC testing activities in accordance with Oxoid test specifications and methods, supporting the timely and accurate release of products. Key Responsibilities <ul> <li> Perform Quality Control testing in line with Oxoid test specifications, including Level 1, 2, and 3 testing methods. </li><li> Prepare media and manage the use of autoclaves. </li><li> Complete Out of Specification (OOS) reports and assist with investigations. </li><li> Maintain accurate and up-to-date training records. </li><li> Plan, track, and control the progress of products under test, providing reliable availability dates to Planning and Customer Services. </li><li> Proactively alert the QC Team Leader to any potential issues or failures and support follow-up investigations. </li><li> Record all test results within the SAP Quality Management module. </li><li> Conduct equipment checks, cleaning, and audits to ensure compliance with quality standards. </li><li> Manage waste disposal and replenish consumables as required. </li></ul> About You We're looking for someone with: <ul> <li> Previous experience in a Quality Control or laboratory environment (ideally within life sciences, microbiology, or pharmaceuticals). </li><li> Strong attention to detail and a proactive approach to problem-solving. </li><li> Familiarity with SAP Quality Management or similar systems (desirable). </li><li> Excellent organisational and communication skills. </li><li> The ability to work effectively in a fast-paced, team-oriented environment. </li></ul> Contract Details <ul> <li> Location: Basingstoke </li><li> Contract type: Temporary (until February 2026) </li><li> Hours: Full-time </li></ul> Join a team dedicated to maintaining the highest standards of product quality and safety - and help us deliver excellence every day. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

QC Associate Scientist

Regeneron

<div>We are looking for highly motivated Associate Scientists, to join Regeneron&rsquo;s Early Career Exploration Program (ECEP). This program is a full-time opportunity for former Regeneron interns, graduating with a BS in biology, biochemistry, biophysics, chemistry, or related field to find a full-time opportunity at Regeneron post-graduation. The ECEP provides participants with the chance to explore multiple positions across Regeneron&rsquo;s Research &amp; Pre-Clinical Development (R&amp;D) function, all while building strong foundational knowledge in biotechnology.
The ECEP Experience :
Participants will be placed in assignments 3-6 months in length, covering for colleagues on leave of absence, and can have opportunities to explore multiple R&amp;pD functions. The program runs up to 2 years before participants are expected to find permanent placement. This program is intended to be a small cohort, aimed at building a strong entry-level talent pipeline for Regeneron R&amp;pD. Participants will have a centralized manager guiding them throughout their journey, providing them with advice, mentorship and other developmental opportunities.
 We hope you are excited by the opportunity to work with numerous functional groups to come up with innovative approaches to tackle some of the most challenging therapeutic discovery projects being pursued at Regeneron.
 There is no &lsquo;typical&rsquo; day for our ECEP participants, but below are some examples of things you may do during your assignments:
<ul><li>Conducting basic laboratory work including pipetting, culturing, and qPCR
</li><li>Working with automated systems including robotic liquid handlers
</li><li>Maintaining cell cultures
</li><li>Assisting with small and large-scale protein expression using bacteria, insect cells, and other types
</li><li>Participating in journal clubs and data presentation
</li><li>Performing routine molecular biology techniques such as plasmid and bacmid purification and baculovirus production
</li><li>Performing protein biochemical analysis
</li><li>Conducting protein purification (affinity, ion exchange, and size exclusion) and biochemical and biophysical analysis
</li><li>Analyzing experimental data and assessing quality
</li></ul><ul><li>Writing standard operating procedures (SOPs).
</li></ul><ul><li>Maintain adequate inventory of laboratory supplies and reagents. 
</li></ul>This role may be for you if you:
<ul><li>You have a passion for science and innovation with a strong dedication to continual improvement
</li><li>You enjoy working in a fast-paced and deadline driven team environment to discover lifesaving medicines for people with serious medical conditions
</li><li>You have the desire and ability to work on multiple projects in parallel
</li><li>Can multi-task, prioritize work and maintain confidentiality
</li><li>Growth mindset, willingness to be flexible and work in a ever-changing changing environment
</li><li>Comfortability with ambiguity
</li></ul>In order to be considered for the role, you must be a current undergraduate senior, who will be graduating with or have your BS in biology, biochemistry, biophysics, chemistry, or related field by Spring 2026. Participants who are graduating in Fall/Winter of 2025 will also be considered but may have a delayed start date. Hiring preference will be given to former Regeneron R&amp;D interns.
These opportunities are in-person at our Regeneron Headquarters located in Tarrytown, NY.
<div><div><div><div><div><div><div>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries&rsquo; specific benefits, please speak to your recruiter.
 
Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron&rsquo;s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron&rsquo;s on-site policy and expectations for your role and your location. 
 
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually)
</div></div></div></div></div></div></div>$93,900.00 - $153,300.00</div>

International Potato Center (CIP)

<div>
 The International Potato Center (CIP) seeks to recruit a
 
 full-time Scientist
 
 to support the implementation of the
 
 FAO&rsquo;s &ldquo;Additional Financing for Afghanistan Emergency Food Security Project.&rdquo;
 
 The position will be
 
 based in Karnal, Haryana, India
 
 , and will play a key role in strengthening Afghanistan&rsquo;s potato seed systems. The successful candidate will be responsible for arranging potato seed supply to Kabul, developing training materials, and delivering both virtual and in-person training sessions for trainers and farmers on best practices in potato seed production. Additionally, the Scientist will develop protocols for the evaluation of CIP germplasm to identify and advance locally adapted potato varieties and will prepare monthly and annual technical project reports.
 
 
 
 About the role:
 
 This position will be based in
 
 Karnal, Haryana, India
 
 . The selected candidate will be under the direct supervision and guidance of the Principal Investigator of the project.
 
 
 
 Key Responsibilities
 
 
 
 The ideal candidate will mainly focus on these tasks/responsibilities below:
 
 
 <ul>
 <li>
 Provide scientific leadership in the development of training materials and capacity-building programs, both online and in-person, on best potato seed production practices and the participatory evaluation of CIP germplasm using the PVS approach.
 </li>
 <li>
 Oversee and facilitate the supply of CIP advanced germplasm and potato seed of released Indian varieties for adaptability trials and seed multiplication in Afghanistan.
 </li>
 <li>
 Lead the design and supervision of research trials for evaluating potato varieties and CIP germplasm under Afghan conditions.
 </li>
 <li>
 Conduct statistical analyses, synthesize research findings, and ensure the timely preparation of monthly and annual technical reports for donors.
 </li>
 <li>
 Contribute to and/or lead the formulation of new project proposals and funding opportunities related to potato research and development in collaboration with national and international partners.
 </li>
 </ul>
</div>

Associate Scientist (N-25-29)

Aditi Consulting

<div>
 
 
 
 
 Payrate:
 
 
 
 $29.00 - $31.00/hr.
 
 
 &nbsp;
 
 
 
 Summary:
 
 
 
 
 This role involves performing experiments, organizing data, and analyzing results with minimal supervision. The position requires planning, conducting, and monitoring experiments, ensuring data integrity, and compliance with protocols and applicable regulations.
 
 
 &nbsp;
 
 
 
 Responsibilities:
 
 
 
 <ul>
 <li>
 
 
 Monitor or follow established experimental designs and protocols to perform routine tasks and studies
 
 
 </li>
 <li>
 
 
 Plan, conduct, analyze, and record experiments; provide interpretation of data
 
 
 </li>
 <li>
 
 
 Transfer experimental methods from literature to the lab and modify as needed
 
 
 </li>
 <li>
 
 
 Develop and implement new protocols with moderate review
 
 
 </li>
 <li>
 
 
 Engage coworkers in scientific discussions
 
 
 </li>
 <li>
 
 
 Communicate data and interpretations to the work group
 
 
 </li>
 <li>
 
 
 Develop systems to ensure quality data
 
 
 </li>
 <li>
 
 
 Operate standard laboratory equipment and major instruments/techniques
 
 
 </li>
 <li>
 
 
 Troubleshoot equipment and experimental issues effectively
 
 
 </li>
 <li>
 
 
 Contribute to internal/external reports, presentations, regulatory documents, invention disclosures, and/or patents
 
 
 </li>
 <li>
 
 
 Participate in department-wide support efforts such as safety, recruiting, and committees
 
 
 </li>
 <li>
 
 
 Train staff and/or supervise others as needed
 
 
 </li>
 <li>
 
 
 Coordinate and organize resources to complete tasks
 
 
 </li>
 <li>
 
 
 Demonstrate sound judgment and know when to seek input versus acting independently
 
 
 </li>
 <li>
 
 
 Oversee the general operations of the NMR facility and provide hands-on new user instrument training to chemists.
 
 
 </li>
 <li>
 
 
 Maintain the lab&rsquo;s NMR spectrometers and all associated equipment, performing or organizing all necessary calibrations, repairs and upgrades.
 
 
 </li>
 <li>
 
 
 Acquire NMR data for quality control of small molecule drugs, intermediates, and starting materials.
 
 
 </li>
 <li>
 
 
 Collaborate and communicate effectively with a team of chemists and separation scientists.
 
 
 </li>
 </ul>
 
 &nbsp;
 
 
 
 Qualifications:
 
 
 
 <ul>
 <li>
 
 
 Degree in Organic Chemistry, Physical Chemistry, Pharmaceutical Sciences, or a related field.
 
 
 </li>
 <li>
 
 
 General instrumentation experience with the ability to set up Client experiments and calibrate NMR and LC-MS instruments.
 
 
 </li>
 <li>
 
 
 Experience with the operation, troubleshooting, and maintenance of Bruker NMR spectrometers, HPLC and MS equipment (Agilent, Waters).
 
 
 </li>
 <li>
 
 
 Experience using 1D (1H, 13C, 19F, 31P, etc.) and 2D (COSY, TOCSY, NOESY, HSQC, HMBC, etc.) multinuclear solution-state NMR experiments for structure confirmation.
 
 
 </li>
 <li>
 
 
 Ability to run automated acquisition and analysis software programs such as Bruker Topspin or Agilent MassHunter.
 
 
 </li>
 <li>
 
 
 Experience with NMR and LC-MS data analysis packages such as ACD/Spectrus or Mestre Nova.
 
 
 </li>
 <li>
 
 
 Familiarity with the principles of organic chemistry, analytical and separation sciences, and automated liquid handling systems.
 
 
 </li>
 </ul>
 
 &nbsp;
 
 
 
 Pay Transparency:
 
 
 
 
 The typical base pay for this role across the U.S. is:
 
 $29.00 - $31.00 /hour
 
 . Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match,&nbsp; life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law.&nbsp;
 
 
 
 &nbsp;
 
 
 
 
 Consent to Communication and Use of AI Technology:
 
 
 
 
 
 By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. These communications may include information about potential opportunities and information. Message and data rates may apply. Message frequency may vary.
 
 
 
 
 
 You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts. You also acknowledge and agree to Aditi Consulting LLC&rsquo;s use of AI technology during the sourcing process, including calls from an AI Voice Recruiter. AI is used solely to gather data and does not replace human-based decision-making in employment decisions.  Calls may be recorded.
 
 
 
 &nbsp;
 
 
 
 Consent is not a condition of purchasing any property, goods, or services. You may revoke your consent at any time by replying &ldquo;STOP&rdquo; to messages or by contacting
 
 
 
 
 privacy@aditiconsulting.com
 
 
 
 
 .
 
 
 
 
 
 For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our
 
 
 
 
 Privacy Policy
 
 
 
 
 .
 
 
 
 &nbsp;
 
 
 
 #AditiConsulting
 
 # 25 - 23191
 
 
 
 
</div>

GenScript

<div>
 
 
 About GenScript
 
 
 
 
 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
 
 
 
 GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
 
 
 
 
 About ProBio
 
 
 
 
 ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio&rsquo;s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.&nbsp;
 
 
 
 
 Job Summary:
 
 
 
 We are seeking a detail-oriented and proactive
 
 Analytical Associate Scientist or Scientist
 
 to join our US Protein Department. This role involves performing analytical testing and characterization of protein products to support research, development, and production activities. The ideal candidate will have a strong background in analytical chemistry, biochemistry, or biotechnology, with practical laboratory experience and familiarity with regulatory standards.
 
 
 
 Key Responsibilities:
 
 
 <ol>
 <li>
 Perform routine and non-routine analytical testing on protein samples using techniques such as HPLC, SDS-PAGE, ELISA, UV-Vis spectroscopy, and others as required.
 </li>
 <li>
 Prepare reagents, standards, and samples according to established protocols.
 </li>
 <li>
 Record, analyze, and interpret data with accuracy and integrity; prepare detailed reports and documentation.
 </li>
 <li>
 Maintain and calibrate laboratory instruments and ensure compliance with quality standards and safety regulations.
 </li>
 <li>
 Assist in method development, validation, and troubleshooting of analytical procedures.
 </li>
 <li>
 Collaborate with cross-functional teams to support project timelines and deliverables.
 </li>
 <li>
 Participate in the review and update of SOPs, batch records, and other quality documentation.
 </li>
 <li>
 Support continuous improvement initiatives and additional tasks as assigned by the supervisor.
 </li>
 </ol>
 
 
 Qualifications:
 
 
 <ol>
 <li>
 BS/MS in analytical chemistry, biochemistry, biotechnology, or related with 2+ years of relevant experience in protein purification/characterization.
 </li>
 <li>
 Hands-on experience with analytical instruments such as HPLC, SDS-PAGE, ELISA, UV-Vis, or similar is preferred.
 </li>
 <li>
 Strong attention to detail, organizational skills, and commitment to data integrity.
 </li>
 <li>
 Ability to work independently and collaboratively in a fast-paced team environment.
 </li>
 <li>
 Good communication skills and the ability to clearly document and present data.
 </li>
 <li>
 Experience working in a CRO or CDMO setting is an advantage.
 </li>
 </ol>
 
 &nbsp;
 
 
 
 #GS
 
 
 
 &nbsp;
 
 
 
 GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
 
 
 
 
 GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
 
 
 
 &nbsp;
 
 
 
 
 Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.&nbsp;
 
 
 
</div>

Analytical Associate Scientist/Scientist

Search 5729+ Associate scientist jobs near you this November. New roles added regularly across leading industries. Apply today.

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