research scientist

Ortiv-Q3

Department: Formulation &amp; DevelopmentPosition: Sr. Research Scientist / Research ScientistNo. Position: 2Experiences: 3.0 Years to 5.0 Years (Relevant)Qualification: M. Pharma (Pharmaceutical)Job Description:Candidate must have experiences in Topical Formulation (Ointment/Gel/Cream).In Regulated Market (US/EU).Hands-On experiences in Topical Products execution at manufacturing site.Address: Ortiv-Q3 Research Pvt. Ltd., B-202-207, 2nd floor, Ratna Business hub Survey No 439 of Navapura, Sanand City, Ahmedabad - 382210 Landmark Opp. Bharat Petrol pump, Nr. Sanathal Circle.HR DEPARTMENTOrtriv-Q3Ahmedabad (Gujarat)Mob: +91 7676707801Landline: +91 7801961755 (Ext): 211Email: Talent.acquisition@ortiv.inJob Types: Full-time, PermanentPay: From &#8377;300,000.00 per yearBenefits:<ul><li>Commuter assistance</li><li>Flexible schedule</li><li>Food provided</li><li>Health insurance</li><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul>Work Location: In person

Research Scientist

Nammo

<div>Nammo Defense Systems, Inc., a defense contractor, is the primary USA operation of the Nammo Group (Nammo AS). Nammo Defense Systems Inc. (NDS) develops, manufactures, and supports Shoulder Launched Munitions (SLMs), energetic material solutions such as aircraft emergency escape systems, actuation devices, rocket motors, warheads, and composite solutions including carbon fiber tubes and composite aerospace structures. 
 
JOB OVERVIEW: 
The Scientist within the Research Department team will serve as a subject matter expert for various production composite propellants and liners. The individual will conduct and supervise projects involving formulating, raw ingredient testing, lab scale mixing, batch size scale up, propellant property testing, and data reduction/analysis. 
The position will report to and take direction from the Propellant, Explosives and Pyrotechnic Supervisor but will also work closely with the cross-functional program teams to support production programs. 
 
How you will be rewarded as our Scientist: 
<ul><li>Competitive compensation</li><li>Monday-Thursday work week working four 10-hour days (off on Fridays)</li><li>Generous paid time off and Holiday Pay</li><li>Medical, Dental and Vision Insurance</li><li>401(K), employee assistance programs, health savings account</li></ul>
 
KEY RESPONSIBILITIES: 
<ul><li>Apply chemical principles to safely analyze and conduct experiments on propellants, pyrotechnics, and/or explosives to meet program requirements or to make production improvements.</li><li>Develop and/or modify formulas, processes, procedures, and techniques to manufacture propellant.</li><li>Develop methods and analyzes and to create tests compositions to understand and modify chemical, physical, mechanical, ballistic, and hazard properties.</li><li>Establish optimal trade-off of propellant properties by modifying composition to achieve objectives.</li><li>Serve as a principal investigator to resolve propellant production issues.</li><li>Follow standard laboratory practices and safety procedures.</li><li>Coordinate and schedule support work for other departments.</li><li>Make oral presentations outlining/summarizing progress on selected projects and programs to both internal and external customers.</li><li>Prepare technical reports detailing work progression and results.</li><li>Provide labor, equipment, and material estimates for laboratory work required to support production projects.</li><li>Assign/delegate work to technicians and junior chemists.</li><li>Provide training to technicians to perform chemical weigh out, small scale propellant mixing, laboratory testing, mechanical property testing, and burn rate testing.</li><li>Review results of experiments and analyses performed by other scientists or technicians.</li><li>Perform Statistical Process Control charting and predictive modelling to identify propellant performance and/or property trends.</li><li>Follow standard practices and safety procedures.</li><li>Strictly adhere to all safety policies and procedures to ensure a safe working environment.</li></ul>
 
LEVEL OF DECISION MAKING 
This position requires daily autonomous decision-making capabilities when working with both internal and external customers. 
 
SKILLS &amp; QUALIFICATIONS: 
Required: 
<ul><li>Proficient with Microsoft Office, Word, Excel, and Power Point.</li><li>Experience with various lab instruments for analysis and testing of energetic materials.</li><li>Working knowledge of energetic material regulations and safe handling/measurement.</li><li>Ability to work effectively and communicate well with the cross-functional NDS Mesa Team.</li><li>Must have a strong work ethic and be well organized to manage multiple projects simultaneously.</li><li>Must be able to wear safety equipment such as respirators or self-contained breathing apparatus.</li><li>Must be able to exert up to 50 lbs. of force in the course of normal work.</li><li>Must have the ability to obtain and maintain ATF Processor license.</li></ul>
 
COMPETENCIES: 
<ul><li>Excellent communication and collaboration skills.</li><li>Strong attention to detail</li><li>Strong problem-solving and critical-thinking abilities.</li><li>Ability to work in fast-paced environments.</li><li>Leadership or teamwork abilities.</li></ul>
 
WORKING CONDITIONS: 
<ul><li>Full-time on-site position.</li><li>This position may require travel on an as-needed basis</li><li>This position may require working in diverse settings and conditions.</li></ul>
 
**Note**: Due to US Export Control laws and regulations; applicants selected for employment must show proof of a U.S. Person status before employment may begin. 
Our values are the fundamental principles guiding the way we do business and interact with stakeholders.

DEDICATION: We are enthusiastic and creative, always searching for the best solutions. 
PRECISION: We are reliable and accurate in our technology, processes and business. 
CARE: We are inclusive and open-minded, always encouraging team spirit and cooperation.

Nammo and its subsidiaries provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to 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.

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.

**Note**: Due to US Export Control laws and regulations; applicants selected for employment must show proof of a U.S. Person status before employment may begin.</div>

Randstad USA

<div>
 
 
 Clinical Research Scientist
 
 
 
 
 100% Remote (Need to live on East Coast or Midwest)
 
 
 
 
 (Monday-Friday) Flex hours 40 per week
 
 
 
 
 Pay: $86.00 an hour
 
 
 
 
 12 month contract opportunity
 
 
 
 
 Must bachelors degree, 7-10 years of clinical research experience and experience with lupus.
 
 
 
 
 
 
 As a subject matter expert, the Clinical Research scientist (CRS) partners with the Medical Director to provide scientific, clinical, strategic, and operational input to an early or late-stage clinical development program. The CRS contributes to data interpretation, study designs, regulatory documents, and publications as well as providing scientific input into pipeline programs. The CRS closely collaborates with other internal functions as well as external partners, such as contract research organizations and medical experts.
 
 
 Within the frame of the clinical development of new medicines, the Clinical Research Scientist is responsible for
 
 
 
 
 
 Managing assigned activities within clinical study independently
 
 
 
 
 
 providing clinical/scientific input and gathering necessary information from other areas to Clinical Development Plans for one or more molecules or indications
 
 
 
 
 
 Work in close partnership with CROs and other vendors in clinical and medical data review and participating in operational excellence of the execution of the project in collaboration with GCO
 
 
 
 
 
 Work on the design of Clinical trial concepts, study protocols, assessment schedules, patient information material as well as final clinical study reports
 
 
 
 
 
 Work on the relevant sections of the common technical document dossier
 
 
 
 
 
 Help to design and structure the content of relevant Advisory Board Meetings
 
 
 
 
 
 Writes scientific rationale for clinical trial protocols, including most recent literature citations
 
 
 
 
 
 Drives creation and annual update of IB liaising with Toxicology, Pharmacology, Safety, Regulatory and Medical &amp; Communication Experts
 
 
 
 
 
 Works closely with Medical Communications to ensure all relevant documentation is updated with new medical information, including assuming responsibility for the incorporation of additional information into the Investigator Brochure.
 
 
 The Clinical Research Scientist is an individual contributor with analytical skills, strategic thinking, and a growth mindset.
 
 
 
 
 
 Ability to work both independently and collaboratively on assigned tasks or projects of increasing complexity with scientific rigor in a fast-paced, team-based matrix environment.
 
 
 
 
 
 Expert knowledge of scientific principles and concepts
 
 
 
 
 
 Aptitude to interpret and to integrate data, including, clinical safety and efficacy data, pharmacokinetics, biomarker and next generation sequencing data
 
 
 
 
 
 Moderate medical or clinical knowledge and experience in clinical development/ operations with the capacity to monitor labs and other clinical data from clinical trials
 
 
 
 
 
 Experience in product &amp; clinical development (minimum of 3 years, with at least 5 years in a comparable setting in biopharma, preferred)
 
 
 
 
 
 Capability to perform literature searches and to utilize library services, digest the information, and synthesize the key take-away points
 
 
 
 
 
 Strong communication skills - verbal, written and listening, with the knack to contribute to abstracts/publications
 
 
 
 
 
 Record of having completed or significantly contributed to scientific work or project
 
 
 
 
 
 Strong presentation skills and adapting to a variety of audiences
 
 
 
 
 
 Normally receives no instruction on routine work and only general instruction on new assignments
 
 
 
 
 
 Educational and/or work experience in the respective therapeutic area (eg Neurology or Immunology) is strongly desirable.
 
 
 
 
 
 Experience in analysis and interpretation of clinical data and a working knowledge of biostatistics, ICH-GCP, and regulatory requirements for clinical studies.
 
 
 
 
 
 Excellent written/verbal communication and presentation skills.
 
 
 
 
 
 High level of organizational and project management skills.
 
 
 
 
 
 Experience interacting with development operations (clinical operations, regulatory, QA) and clinical investigators.
 
 
 Bachelor's Degree required, preferred in Science with a minimum of 7+ (minimum) years of experience in product &amp; clinical development in Clinical Development or 9+ in a comparable setting in the pharmaceutical industry.
 
 
 
 
 
 
 MilliporeSigma is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to his/her Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual made a good faith report of discrimination.
 
 
</div>

Clinical Research Scientist

University Of Washington

<div>Job Description
As a UW employee, you have a unique opportunity to change lives on our campuses, in our state and around the world. UW employees offer their boundless energy, creative problem-solving skills, and dedication to build stronger minds and a healthier world.
UW faculty and staff also enjoy outstanding benefits, professional growth opportunities and unique resources in an environment noted for diversity, intellectual excitement, artistic pursuits, and natural beauty.
<div>The UW Department of Pediatrics is dedicated to improving the health of all children and adolescents by educating physician leaders of the future, advancing research, advocating for children and providing the nation's best pediatric clinical care. We are committed to building a diverse and inclusive faculty and staff.
</div><div><div><div><div>The UW Department of Pediatrics' Division of Genetic Medicine , has an outstanding opportunity for a Temporary Research Scientist 1. The goal of the laboratory is to investigate the factors that contribute to brain health, development, and resilience across the lifespan. This includes the investigation of neuroprotective strategies for the injured neonatal brain, as well as how early life events alter susceptibility to later injures.
The Research Scientist/Engineer will provide research, data, and administrative support to research studies within the NNL, which is currently involved in multiple basic science studies in animal models of neonatal brain injury. This will include assisting our senior research scientist and lab manager in lab maintenance (cleaning and organizing the laboratory space, ordering and receiving supplies necessary for experiments, preparing and scheduling experiments, and writing laboratory protocols), performing experiments (animal handling, surgical support, behavioral testing, and directly performing in vitro work and biochemical analyses), and data curation, analysis, and manuscript preparation.
JOB DUTIES
<ul><li>Research (40%)
<ul><li>Basic neuroscience research techniques: nucleic acid isolation, quantitative PCR, western blotting, PCR and Sanger sequencing, and other established techniques
</li><li>Surgery assistance and post-surgery care
</li><li>Behavioral testing
</li><li>Slice culturing (plating and maintaining brain slice cultures)
</li><li>Processing experimental samples for biochemical analyses
</li></ul></li><li>General Research Support (20%)
<ul><li>Cleaning and organizing the laboratory space
</li><li>Ordering and receiving supplies necessary for experiments
</li><li>Scheduling and preparing for experimental tasks
</li><li>Writing protocols for laboratory responsibilities and data processing methods
</li><li>Expertise: stay up to date on research related to their projects by reading the literature and attending selected seminars
</li><li>Perform other research duties as required such as: protocol implementation and trouble shooting
</li><li>Data presentation: summarize research results in presentations for lab meetings as well as for use in public presentations and publications
</li><li>Maintain appropriate research documentation and databases
</li></ul></li><li>Sample Handling and Management (40%)
<ul><li>Periodic inventory of existing and past samples.
</li><li>Ensure laboratory documentation is up-to date for stored samples
</li><li>Care of neonatal study animals in the appropriate animal care facility including animal handling, husbandry, drug injections, tissue and blood sampling and processing.
</li><li>Sample intake and processing: label, track, process neonatal hypoxic&#8208; ischemic encephalopathy in ferrets and rodents.
</li><li>Statistics and data processing (ie: GraphPad, Excel)
</li><li>Operating imaging software for further collection/processing (ie: rview, ImageJ, NDP)
</li><li>Academic writing and publishing
</li></ul></li></ul>MINIMUM REQUIREMENTS
<ul><li>Bachelor&rsquo;s degree in a related field and one year of relevant experience,
OR Equivalent combination of education/experience.
</li></ul>DESIRED QUALIFICATIONS
<ul><li>Experience with neuroscience research
</li></ul><ul><li>Knowledge of long read sequencing platforms and techniques
</li><li>Interest cellular and molecular neuroscience
</li><li>Able to work independently and as part of a multidisciplinary team
</li><li>Demonstrated practical experience and proficiency in basic neuroscience procedures
</li><li>Ability to communicate experimental results clearly using strong computer skills in Word, Excel and PowerPoint
</li><li>Attention to detail and strong organizational abilities
</li></ul></div></div></div></div>Compensation, Benefits and Position Details
Pay Range Minimum:
$24.67 hourly
Pay Range Maximum:
$27.00 hourly
Other Compensation:
<ul><li></li></ul>Benefits:
For information about benefits for this position, visit https://hr.uw.edu/benefits/wp-content/uploads/sites/3/2018/02/benefits-professional-staff-librarians-academic-contract-covered-exempt-20250130-a11y.pdf
Shift:
First Shift (United States of America)
Temporary or Regular?
This is a temporary position
FTE (Full-Time Equivalent):
0.00%
Union/Bargaining Unit:
Not Applicable
About the UW
Working at the University of Washington provides a unique opportunity to change lives &ndash; on our campuses, in our state and around the world.
UW employees bring their boundless energy, creative problem-solving skills and dedication to building stronger minds and a healthier world. In return, they enjoy outstanding benefits, opportunities for professional growth and the chance to work in an environment known for its diversity, intellectual excitement, artistic pursuits and natural beauty.
Our Commitment
The University of Washington is proud to be an affirmative action and equal opportunity employer . All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, age, protected veteran or disabled status, or genetic information.
To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 or dso@uw.edu .
Applicants considered for this position will be required to disclose if they are the subject of any substantiated findings or current investigations related to sexual misconduct at their current employment and past employment. Disclosure is required under Washington state law .</div>

Research Scientist 1 (Temporary)

DataAnnotation

<div>
 We are looking for a Research Scientist (Chemistry) to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
 
 
 In this role you will need to hold an expert level understanding of chemistry. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.
 
 
 
 Benefits
 
 
 
 <ul>
 <li>
 This is a full-time or part-time REMOTE position
 </li>
 <li>
 You&rsquo;ll be able to choose which projects you want to work on
 </li>
 <li>
 You can work on your own schedule
 </li>
 <li>
 Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work
 
 
 </li>
 </ul>
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Give AI chatbots complex chemistry questions and evaluate their outputs
 </li>
 <li>
 Evaluate the quality produced by AI models for correctness and performance
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Fluency in English (native or bilingual level)
 </li>
 <li>
 Detail-oriented
 </li>
 <li>
 Solid knowledge of general, organic, and physical chemistry concepts
 </li>
 <li>
 A current, in progress, or completed Masters and/or PhD is preferred but not required
 
 
 </li>
 </ul>
 
 Notes
 
 
 
 Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Only applicants in the United States will be considered for this role. This is an independent contract position.
 
 
 #chem
</div>

Research Scientist (Chemistry)

Cholayil Private Limited

<div>
 
 
 Location:
 
 Chennai
 
 
 
 Company:
 
 Cholayil Private Limited
 
 
 
 Experience Required:
 
 2&ndash;5 Years
 
 
 
 Industry:
 
 Toiletries, Cosmetics, Personal Care, Pharmaceuticals
 
 
 
 Qualification:
 
 M.Sc. in Chemistry
 
 
 
 🔍 Role Overview
 
 
 
 We are seeking a dedicated and experienced
 
 Junior Research Scientist &ndash; Quality
 
 to join our team at Cholayil Private Limited. The ideal candidate will bring deep expertise in quality control and assurance, with a strong foundation in analytical chemistry and regulatory compliance. This role is pivotal in maintaining the highest standards of product quality and safety across our portfolio.
 
 
 
 
 🧷 Key Responsibilities
 
 
 
 <ul>
 <li>
 Independently manage instrumental and chemical analytical laboratories with precision and discipline.
 </li>
 <li>
 Lead analytical method development and validation for new and existing products.
 </li>
 <li>
 Conduct stability studies to evaluate product shelf life and performance under various conditions.
 </li>
 <li>
 Implement and maintain Quality Management Systems (QMS) and support internal and external audits.
 </li>
 <li>
 Oversee document and data control to ensure traceability and regulatory compliance.
 </li>
 <li>
 Prepare and submit documentation for drug/product licensing in accordance with regulatory guidelines.
 </li>
 <li>
 Ensure full compliance with:
 </li>
 <li>
 Drug &amp; Cosmetics Act &amp; Rules
 </li>
 <li>
 GMP/GLP standards
 </li>
 <li>
 Weights and Measures Act &amp; Rules
 </li>
 <li>
 Compile and maintain product dossiers for regulatory and commercial purposes.
 </li>
 <li>
 Train and mentor quality personnel in laboratory systems, documentation practices, and compliance protocols.
 </li>
 </ul>
 
 
 
 🧠 Desired Skills &amp; Attributes
 
 
 
 <ul>
 <li>
 Strong analytical and problem-solving skills
 </li>
 <li>
 Excellent documentation and organizational abilities
 </li>
 <li>
 Familiarity with regulatory frameworks and audit processes
 </li>
 <li>
 Effective communication and team leadership capabilities
 </li>
 <li>
 Commitment to continuous improvement and quality excellence
 </li>
 </ul>
 
 
</div>

Junior Research Scientist

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