biological scientist

University of Florida

<p></p><div><div><p><b>JOB NO:</b></p>
<div>537904</div><br>
<p><b>WORK TYPE:</b></p>
<div>Staff Full-Time</div><br>
<p><b>LOCATION:</b></p>
<div>Main Campus (Gainesville, FL)</div><br>
<p><b>CATEGORIES:</b></p>
<div>Health Care Administration/Support</div><br>
<p><b>DEPARTMENT:</b></p><div>
29030000 - MD-BIOCHEM - MOLECULAR BIOL</div></div><br>
<div>
<div><div><div><div><b>CLASSIFICATION TITLE:</b></div>
<div>
<p>Biological Scientist III</p></div><br>
</div><br>
<div><div><b>CLASSIFICATION MINIMUM REQUIREMENTS:</b></div>
<div>
<p>Bachelor&acirc;&euro;&trade;s degree in biology or a related field and seven years of experience or Master&acirc;&euro;&trade;s degree in biology or a related field with five year of experience.</p>
<p>
Doctoral degree in biology or related field with two years of experience preferred.</p></div><br>
</div><br>
<div><div><b>JOB DESCRIPTION:</b></div>
<div>
<p>Project Management:</p>
<ul><li>Oversee research projects requiring method development, and delivery of results to customers using the Mass Spectrometry facility.</li></ul><br>
<ul><li>Review &amp; approve CE and GC/MS data generated by other lab members.</li></ul><br>
<ul><li>Manage technical staff involved in mass spectrometry services</li></ul><br>
<ul><li>Extract, collect MS data, analyze and review and evaluate research findings of customer samples according to established facility standard operating procedures (SOP)</li></ul><br>
<ul><li>Be proficient regarding glycogen storage diseases, specifically Lafora disease and Pompe disease</li></ul><br>
<p></p>
<p>
Scientific Writing and Dissemination</p>
<p>
Participate in scientific conferences to learn about new MS developments.</p><ul><li><br>
Lead or contribute the writing of manuscripts and data presentations.</li></ul><br>
<ul><li>Disseminate of research results and developments at internal and external scientific meetings and in peer-reviewed scientific publications</li></ul><br>
<ul><li>Disseminate research results and methodology, specifically the methods sections for client publications or grant applications.</li></ul><br>
<p></p>
<p>
Creation and Maintenance of SOPs</p>
<ul><li>Design, write, implement and maintain CE and GC/MS SOPs, protocols and research methods; resolve conceptual problems by troubleshooting and researching.</li></ul><br>
<ul><li>Develop, troubleshoot and implement new sample extraction and analysis methods by CE &amp; GC/MS</li></ul><br>
<ul><li>Oversee the implementation of new methods by coordinating with other lab members in the establishment of said new methods.</li></ul></div><br>
</div><br>
<div><div><b>EXPECTED SALARY:</b></div>
<div>
<p>$65,000 - $70,000 per year, commensurate with experience and education</p></div><br>
</div><br>
<div><div><b>REQUIRED QUALIFICATIONS:</b></div>
<div>
<p>Advanced degree in Biology or closely related field and three years of relevant experience working with glycogen storage disease mouse models.</p></div><br>
</div><br>
<div><div><b>PREFERRED:</b></div>
<div>
<ul><li>A highly organized multi-tasker who pays attention to detail and values research integrity</li></ul><br>
<ul><li>3 years of research experience in mass-spectrometry including at least 3 years of direct experience in GC-MS equipment, technologies, and analysis.</li></ul><br>
<ul><li>Demonstrated computer skills for the analysis of metabolomics data is required.</li></ul><br>
<ul><li>Previous experience in processing and analyzing large datasets (i.e., metabolomics data, NGS data, genome annotation or developing analysis pipelines).</li></ul><br>
<ul><li>Experience with mouse colonies and drug deliver.</li></ul>
<ul><li>Experience in the field of pre-clinical glycogen storage diseases.</li></ul><br>
<ul><li>Ability to work independently yet be a team player.</li></ul></div><br>
</div><br>
<div><div><b>SPECIAL INSTRUCTIONS TO APPLICANTS:</b></div>
<div>
<p>In order to be considered, you must upload your cover letter, resume, and at least two (2) professional references.</p>
<p>
Application must be submitted by 11:55 p.m. (ET) of the posting end date.</p></div><br>
</div><br>
<div><div><b>HEALTH ASSESSMENT REQUIRED:</b></div> <div>No</div></div></div><br>
</div>
</div><p></p><div><p><b>ADVERTISED:</b></p>
<div>19 Nov 2025</div> Eastern Standard Time<br>
<p><b>APPLICATIONS CLOSE:</b></p>
<div><div>26 Nov 2025</div></div>
Eastern Standard Time</div></div><p></p>

Biological Scientist III

State of Florida

<div><p>Requisition No: 864918</p>
<p>Agency: Florida Fish and Wildlife Conservation Commission</p>
<p>Working Title: F&amp;W BIOLOGICAL SCIENTIST III - 77000796</p>
<p> Pay Plan: Career Service</p>
<p>Position Number: 77000796</p>
<p>Salary: $1,730.77 biweekly + benefits</p>
<p>Posting Closing Date: 12/02/2025</p>
<p><b>Total Compensation Estimator </b><b>Tool</b></p>
<div><b>
Employment is contingent upon a successful completion of a background check</b></div>
<div><b>
Anticipated Vacancy</b></div>
<div>
Position Number: 77000796</div>
<div>
Position Title: <b>Fisheries &amp; Wildlife Biological Scientist III</b></div>
<div>
Biweekly Rate of Pay: $<b>1,730.77 + benefits</b></div>
<div>
Supervisor: Cason Pope</div>
<div>
Supervisor contact information for inquiries: 941-833-2555, Andrew.Pope@MyFWC.com</div>
<div>
Broadband Code: <b>19-1023-03</b></div>
<div>
Class Code: <b>5074</b></div>
<div>
Position location: Babcock-Webb WMA Field Office, 29200 Tuckers Grade, Punta Gorda, FL 33955
</div><div>Region: Southwest</div>
<div>
County: Sarasota</div>
<div>
Working hours: Monday &ndash; Friday, 8:00-5:00, evenings and weekends as required</div>
<div>
List of any subordinates supervised: 1 Fish and Wildlife Technician
</div><div>Residency Requirement: Required to reside within 25 miles of the Babcock-Webb WMA field office.</div><br>
<div></div>
<div><b>
Our Organization:</b></div>
<div>
The FWC envisions a Florida where fish and wildlife are abundant and thriving in healthy and connected natural landscapes with vital working lands and waterways; where natural resources are valued and safely enjoyed by all; and wherein natural systems support vibrant human communities and a strong economy.</div><br>
<div></div>
<div>
Our Mission: Managing fish and wildlife resources for their long-term well-being and the benefit of people.</div><br>
<div></div>
<div>
Every organization has an identity that is forged not only by what it does, but by how it conducts itself. The values embedded in our mission and expressed in the vision of the FWC are to make quality decisions by being dynamic, science-informed, efficient, ethical, collaborative and committed to the vitality of the state and its environment.</div><br>
<div>
</div><div>The Division of Habitat &amp; Species Conservation is comprised of six Sections and two offices. This position works within the Wildlife and Habitat Management Section of the Florida Fish and Wildlife Conservation Commission&rsquo;s Division of Habitat and Species Conservation.</div><br>
<div></div>
<div><b>
Minimum qualifications:</b> A high school diploma and 6 years professional experience in a closely related biological field or laboratory program is required.</div>
<div><b>
Preferred qualifications</b>: A Bachelor of Science degree in a relevant field. Florida Certified Prescribed Burn Manager with experience conducting prescribed burns in Florida.</div>
<div>
Answers to qualifying questions must be validated in the application, resume and cover letter.</div><br>
<div></div>
<div><b>
Knowledge, Skills, and Abilities</b>: Incumbent must have excellent verbal and written communication skills and be able to work well with team members and members of the public.</div><br>
<div>
</div><div>Other required knowledge, skills and abilities include:</div>
<ul>
<li>knowledge of wildlife ecology, game management, wildlife and habitat surveying and inventory</li>
<li>knowledge and experience with the application of prescribed fire</li>
<li>knowledge and experience with the chemical and/or mechanical control of vegetation</li>
<li>knowledge and experience in GIS programs</li>
<li>ability to identify common and imperiled species</li>
</ul><ul><li>ability to write technical reports</li>
<li>ability to operate outdoors under inclement weather conditions</li>
<li>ability to work productively unsupervised</li>
<li>strong interpersonal skills to effectively interact with cooperators, coworkers, and constituents</li>
</ul><ul><li><div><ul><li>ability to supervise and motivate field staff
</li><li>skilled in use of Microsoft Office software (e.g. Word, Excel, etc.)</li></ul></div></li><br>
</ul>
<div></div><div><b>Description of Duties:</b></div>
<div>
An exciting opportunity exists for a Fisheries and Wildlife Biologist to join a team of employees within FWC&rsquo;s Wildlife and Habitat Management Section in managing a lead Wildlife Management Area (WMA). FWC&rsquo;s Southwest Region is seeking a motivated applicant that is willing and able to work outdoors in a variety of conditions throughout the year in fulfillment of their job responsibilities. Primary responsibilities include direct involvement in the development and implementation of management programs for Orange Hammock WMA. This position will be responsible for leading the prescribed burn program on the WMA, which includes managing the area&rsquo;s prescribed burn team. Job duties also include public hunt management, biological data collection, wildlife surveys, invasive non-native plant control, infrastructure maintenance, and other various habitat management techniques. This position is also responsible for coordination of the development and periodic revision of long-range, comprehensive management plans, annual work plans, budget proposals, area regulations, and reports. The incumbent will also be working with other staff throughout the region to enhance wildlife habitat and promote compatible recreational use for the general public.</div><div></div><p><br>
The State of Florida is an Equal Opportunity Employer/Affirmative Action Employer, and does not tolerate discrimination or violence in the workplace.</p>
<p>Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (1-866-663-4735). Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation.</p>
<p>The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act.</p>
<p><b>VETERANS&rsquo; PREFERENCE. </b>Pursuant to Chapter 295, Florida Statutes, candidates eligible for Veterans&rsquo; Preference will receive preference in employment for Career Service vacancies and are encouraged to apply. Certain service members may be eligible to receive waivers for postsecondary educational requirements. Candidates claiming Veterans&rsquo; Preference must attach supporting documentation with each submission that includes character of service (for example, DD Form 214 Member Copy #4) along with any other documentation as required by Rule 55A-7, Florida Administrative Code. Veterans&rsquo; Preference documentation requirements are available by clicking here. All documentation is due by the close of the vacancy announcement.</p></div>

F&W BIOLOGICAL SCIENTIST III

US Pharmacopeia

<div>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
 <br/>
 <br/>
 USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds&mdash;regardless of background&mdash;to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
 <br/>
 <br/>
 <strong>
  Brief Job Overview
  <br/>
  <br/>
 </strong>
 This is a hands-on, non-supervisory position in USP-India's Biologics laboratory. In this position, the scientist will spend 80-100% of the time in laboratory and will perform bioassays and binding for various biologics product class such as recombinant proteins and mAbs, perform vaccine and cell and gene therapy (CGT) functional characterization assays, and viral assays. Scientist will be responsible for hands-on execution of projects which can be collaborative testing of reference standards, characterization of biological products, method development and validation for development of standards (Documentary Standards, Physical Reference Standard &amp; Performance Standards). Responsible for supporting activities related to India Biologics laboratory.
 <br/>
 <br/>
 <strong>
  How will YOU create impact here at USP?
  <br/>
  <br/>
 </strong>
 As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
 <br/>
 <br/>
 Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
 <br/>
 <br/>
 <ul>
  <li>
   Proficient in in vitro cell based relative potency.
  </li>
  <li>
   Proficient in handling cell lines and primary cells. Experienced in functional activity and immunogenicity assays.
  </li>
  <li>
   Experienced in method qualification and validation, protocol, and report writing.
  </li>
  <li>
   Plans and executes research projects under supervision.
  </li>
  <li>
   Works with cross-functional teams within the organization to solve/support both technical and
   <br/>
   <br/>
  </li>
 </ul>
 process-related issues.
 <br/>
 <br/>
 <ul>
  <li>
   Keeps abreast of current trends and developments in related scientific field.
  </li>
  <li>
   Seeks out innovative ways to apply knowledge or skills to improve protocols and results
  </li>
  <li>
   Assists team lead in planning, implementing, and evaluating laboratory procedures/systems
  </li>
  <li>
   Supports in departmental trainings as applicable.
  </li>
  <li>
   Attends scientific seminars and conferences
  </li>
  <li>
   Supports lab management activities
  </li>
  <li>
   Follows GLP and QMS practices. Recommend improvement to systems and all other supporting
   <br/>
   <br/>
  </li>
 </ul>
 activities as assigned by the team lead. Participates in internal and external audits.
 <br/>
 <br/>
 <ul>
  <li>
   Aligns with USP's mission, and complies with USP's guidelines and other requirements
  </li>
  <li>
   Performs other duties as assigned.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Who is USP Looking For?
  <br/>
  <br/>
 </strong>
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 <br/>
 <br/>
 MSc. in Biochemistry, or related Biological Science field with 3-6 years of Industrial experience in bio pharmaceutical product development and quality testing, relative potency assays, mAb functional assays, expertise in flow cytometry, and primary cell culture. Able to analyze and interpret data using appropriate statistical software/methods and calculation for relative potency determination.
 <br/>
 <br/>
 <ul>
  <li>
   An equivalent combination of education and experience may be substituted. Laboratory experience must include expertise developing and validating assays, and QMS knowledge and experience.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Desired Preferences
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Working experience in the biotechnology/biopharmaceutical industry strongly preferred.
  </li>
  <li>
   Demonstrated research, technical, and analytical skills, as well as the ability to take highly technical scientific information and make recommendations.
  </li>
  <li>
   Ability to learn new technologies and strong computer, scientific, and organizational skills.
  </li>
  <li>
   Good written and verbal communication skills, time management skills as well as interpersonal skills.
  </li>
  <li>
   Individual must possess the ability to handle multiple priorities in fast-paced environment.
  </li>
  <li>
   Experience with reference materials development is a plus.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Supervisory Responsibilities
  <br/>
  <br/>
 </strong>
 None, this is an individual contributor role.
 <br/>
 <br/>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 <br/>
 <br/>
 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP
 <br/>
 <br/>
 <strong>
  Job Category
 </strong>
 Chemistry &amp; Scientific Standards
 <br/>
 <br/>
 <strong>
  Job Type
 </strong>
 Full-Time
</div>


Scientist II, Bioassay

Systems Planning and Analysis, Inc. (SPA)

<div>Overview:
<div>
Systems Planning and Analysis, Inc. (SPA) delivers high-impact, technical solutions to complex national security issues. With over 50 years of business expertise and consistent growth, we are known for continuous innovation for our government customers, in both the US and abroad. Our exceptionally talented team is highly collaborative in spirit and practice, producing <i>Results that Matter</i>. Come work with the best! We offer opportunity, unique challenges, and clear-sighted commitment to the mission. SPA: Objective. Responsive. Trusted.</div><div></div><div><br>
The Joint, Office of the Secretary of Defense, Interagency Division (JOID) provides expert support services to a range of customers spanning across the Department of Defense, Federal Civilian, and international markets. JOID provides a diverse portfolio of analytical and programmatic capabilities to help our customers make informed decisions on their most challenging issues.</div><div></div><div><br>
JOID assists the Defense Threat Reduction Agency (DTRA) in developing leading edge technologies to counter WMD in support of Combatant Commands (CCMDs) and transitioning these technologies to military services CCMDs. SPA provides expertise across the full range of chemical, biological, radiological, nuclear, and high-yield explosives (CBRNE) WMD, Counter Improvised Threat and Countering Threat Network technologies to support understanding, detection, identification, characterization, denial, control, disabling, defeating, disposing, safeguarding the force, managing consequences, and test and evaluation in support of military and civilian operations.</div><div></div><div><br>
We have a near-term need for a Junior Biologist (Vaccines) to provide onsite support out of Lorton, VA.</div>
Responsibilities:
<div>
This position provides Assistance and Advisory Support (A&amp;AS) to the Defense Threat Reduction Agency (DTRA) Chemical and Biological (CB) Defense Department Medical S&amp;T Division &ndash; Vaccines Branch (RD CBMV). The candidate will provide scientific and project management support to maximize client support for therapeutic technology development. Will serve as a technical/scientific resource on projects by providing R&amp;D analysis to DTRA CBMV with emphasis on biological threats. Provide A&amp;AS on basic principles of biology/microbiology with a focus on viral replication, antiviral strategies (especially broad-spectrum strategies), and small molecule/peptide discovery and preclinical development, including Phase I clinical trials where appropriate. Work on advanced, complex technical projects requiring state-of-the-art technical or industry knowledge of early drug discovery, bioinformatics, medicinal chemistry, high-throughput screening technologies, applications of Artificial Intelligence/Machine Learning (AI/ML), and <i>in vivo</i> and <i>in vivo</i> (small and large animal) studies to assess efficacy and safety. Prepare technical documentation and presentations to explain the approach, associated assumptions, and conclusions of scientific investigations. Review proposals, technical reports, experimental or theoretical techniques, scientific studies, and statements of work to ensure technical validity and evaluate current and emerging biological medical defense technologies. Assist leadership with decision making analysis. Evaluate all project aspects, including design, development, execution, and implementation of biological medical countermeasure research and development. Apply understanding of capability gaps and assist in setting project and product-level strategy and priorities, ensuring portfolios are responsive and mapped to program goals.</div>
Qualifications:
<div><b>
Required:</b></div><ul><li>
Master's degree in Biology, Microbiology, or related field</li><li>
3+ years of experience in a related scientific field, including research</li><li>
Demonstrated scientific research and development experience</li><li>
Excellent communication skills (oral and written)</li><li>
Active DoD Secret Clearance</li><li>
Able to work fully onsite based on client needs</li></ul><div><b>
Desired:</b></div><ul><li>
PhD in Biology, Microbiology, or related field</li><li>
Experience in chemical and biological medical defense as part of the DoD research and development enterprise</li><li>
Experience with DoD Chemical and Biological Defense Program (CBDP) and DoD acquisition policies</li><li>
Prior vaccine development industry experience</li><li>
Experience with bioinformatics and AI/ML techniques for applications in drug discovery and screening of candidate compounds</li></ul></div>

Junior Biologist - Vaccines

<div>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare.
 <br/>
 <br/>
 USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work&mdash;an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
 <br/>
 <br/>
 <strong>
  Brief Job Overview
  <br/>
  <br/>
 </strong>
 This is a hands-on, non-supervisory scientific position the Global Biologics department. The incumbent is responsible for providing support for the development of USP documentary standards and reference standards for biological products such as peptides, Oligonucleotides, protein, carbohydrates, Complex Biologics, Vaccines, Antibiotics, and advanced therapies. The incumbent will provide quality and technical review of scientific documents for accuracy, clarity and compliance, manage and track reference standard stability program and organize efforts for continuous process improvements. The incumbent will also focus on supporting the reference standard suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports for confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in time-bound manner.
 <br/>
 <br/>
 <strong>
  How will YOU create impact here at USP?
  <br/>
  <br/>
 </strong>
 In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.
 <br/>
 <br/>
 <strong>
  The Sr. Scientist -I (RSS-Review) Has The Following Responsibilities
  <br/>
  <br/>
 </strong>
 Roles and Responsibilities
 <br/>
 <br/>
 <ul>
  <li>
   Performs technical and quality reviews of documents to ensure a high level of document quality and compliance before QA review
  </li>
  <li>
   Manages and tracks efforts for continuous process improvements.
  </li>
  <li>
   Develops and reviews SOP&rsquo;s, Operation Manuals, and training documents.
  </li>
  <li>
   Assists in investigations of quality related issues resulting from customer complaints to include root cause analysis, corrective action identification, action planning, and implementation monitoring.
  </li>
  <li>
   Supports the day to day operation of the reference standard stability program.
  </li>
  <li>
   Works with internal stakeholders to develop new and innovative standards for analytical analysis of biological products.
  </li>
  <li>
   Communicates and maintains working relationships with cross functional USP departments regarding assigned projects
  </li>
  <li>
   Supports day to day operations of the RS Stability (CSU) program covering the USP Biologics RS catalog inventory.
  </li>
  <li>
   Reviews RS testing history and drafts test protocols for CSU studies and submits to labs based on designated testing requirements and schedules.
  </li>
  <li>
   Liaisons and Assists laboratories to ensure CSU testing is completed as per protocol and in timely manner.
  </li>
  <li>
   Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use.
  </li>
  <li>
   Compiles, assess current and historical stability testing data and prepare stability trend reports in a time-bound manner.
  </li>
  <li>
   Support the maintenance and updation of various databases documenting laboratory data and program determinations on suitability and Stability interval updates.
  </li>
  <li>
   Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Supporting Quality Assurance and Reference Standard Evaluation in the investigation of unexpected stability testing results
  </li>
  <li>
   Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps.
  </li>
  <li>
   Prepare, present and discuss regular work updates with Team Lead and other team members
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Who is USP Looking For?
  <br/>
  <br/>
 </strong>
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 <br/>
 <br/>
 <ul>
  <li>
   PhD. degree in Biochemistry/Biology/Pharmacy, or a related field Minimum of 7 to 10 years, or Masters degree in Biochemistry/Biology/Pharmacy or a related field with 11 to13 years of years of commensurate industrial experience.
  </li>
  <li>
   Demonstrated experience in Techical review of analytical documents in Quality Assurance.
  </li>
  <li>
   Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc.
  </li>
  <li>
   Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development.
  </li>
  <li>
   Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays.
  </li>
  <li>
   Excellent technical writing, presentation and oral communication skills are required.
  </li>
  <li>
   Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Desired Preferences
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Knowledge of USP products and services is highly desirable.
  </li>
  <li>
   Operates collaboratively at all levels of the organization in a highly technical environment.
  </li>
  <li>
   Must be able to work in a fast-paced environment and respond to shifting priorities.
  </li>
  <li>
   Well-developed interpersonal, negotiation, conflict-resolution and listening skills.
  </li>
  <li>
   Must possess the ability to multi-task and to work effectively with a team.
  </li>
  <li>
   Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality.
  </li>
  <li>
   Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Supervisory Responsibilities
  <br/>
  <br/>
 </strong>
 No
 <br/>
 <br/>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 <br/>
 <br/>
 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
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 <strong>
  Job Category
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 Chemistry &amp; Scientific Standards
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  Job Type
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 Full-Time
</div>


Senior Scientist I, Documentary Standards (Reviewer)

Hope Global School

<div><h3 class="jobSectionHeader"><b>Job Description</b></h3>
<div>Post Graduate Teacher (PGT) in Biology is responsible for teaching advanced biological concepts to senior secondary students. The teacher develops lesson plans, conducts experiments, and explains complex topics such as genetics, ecology, and human physiology. They inspire students toward careers in science, prepare them for board examinations, and ensure conceptual clarity. The PGT Biology teacher promotes scientific thinking and environmental awareness among learners.</div>
<h3 class="jobSectionHeader"><b>Key Responsibilities</b></h3>
<ul><li>Design and deliver engaging lessons aligned with academic curriculum standards.</li>
<li>Conduct laboratory experiments ensuring student safety and proper supervision.</li>
<li>Assess students through assignments, tests, and practical evaluations regularly.</li>
<li>Maintain updated knowledge of modern biological research and discoveries.</li>
<li>Guide students in science projects and participation in academic competitions.</li>
<li>Create and use multimedia teaching aids for enhanced concept understanding.</li>
<li>Collaborate with other faculty for interdisciplinary teaching and curriculum development.</li>
<li>Support students&rsquo; career counseling and preparation for competitive examinations.</li>
</ul><h3 class="jobSectionHeader"><b>Skill &amp; Experience</b></h3>
<ul><li>Strong knowledge of cell biology, genetics, and ecological principles.</li>
<li>Excellent classroom communication and scientific explanation abilities.</li>
<li>Proficient in using digital tools for interactive biology instruction.</li>
<li>Effective classroom management and motivational teaching strategies.</li>
<li>Ability to design innovative experiments and practical demonstrations.</li>
<li>Strong analytical and mentoring skills for student academic growth.</li>
</ul>
<p><b>Note:</b> Salary depends on experience and skills and is paid in local currency.</p></div>
<br><div></div><div><ul><li><div><div>Date Posted</div>
<div>November 16, 2025</div>
</div></li><div></div><li><div><div>Location</div>
<div><div>Agra, India
</div></div></div></li><div></div><li><div><div>Offered Salary:</div>
 <div>428000 - 680000 / year</div>
</div></li><div></div><li><div><div>Expiration date</div>
<div>August 19, 2026
</div></div></li><div></div><li><div><div>Experience</div>
<div>2 Year
</div></div></li><div></div><li><div><div>Gender</div>
<div>Both
</div></div></li><div></div><li><div><div>Qualification</div>
<div>Master&rsquo;s Degree</div></div></li></ul></div>

PGT- BIOLOGY

Bristol Myers Squibb

<div><b>Working with Us</b><br>
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.<br>
<br>
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .<br>
<br>
<b>Scientist, Predictive Biology and AI</b><br>
<br>
<b>LOCATION
</b><br>
<br>
Seattle, Brisbane CA, San Diego CA, Cambridge MA, Princeton NJ
<br>
<br>
<b>Overview
</b><br>
<br>
The Predictive Biology and AI (PBAI) team within BMS Research develops and applies cutting-edge methods to address patient needs and answer fundamental questions in Oncology, Neuroscience, and other application areas. We work closely with our wetlab partners to both test and deliver our predictions into the pipeline as well as integrate the data they generate into our models. We seek a collaborative AI expert possessing skills spanning machine learning and statistics as well as a passion for addressing unmet patient needs. The successful candidate will thoughtfully evaluate and adapt state-of-the-art AI models and techniques to challenges in cell engineering and target discovery. The role offers the opportunity to impact directly the delivery of truly transformational and life-changing therapies in key diseases of unmet medical need.<br>
<br>
<b>Responsibilities
</b><ul><li>Apply, adapt, and in some cases create multi-modal foundation models such as large language models (LLMs), diffusion models, and encoder architectures to answer biological domain-specific questions</li><li>
Address real-world biological modeling challenges such as data sparsity, class imbalance, noise, experimental bias, and heterogeneity of effects</li><li>
Thoughtful model evaluation that incorporates appropriate benchmarks, statistical tests, and problem understanding to support technical and business decisions</li><li>
Work in close collaboration with partners across the organization including wet-lab scientists, Research IT, and other computational scientists to broaden the impact of AI developments</li><li>
Maintain and share up-to-date knowledge of modern advances in the field, including presenting work at public conferences</li></ul><b>
Basic Qualifications
</b><ul><li>Bachelor's Degree 5+ years of academic / industry experience</li><li>
Or Master's Degree 3+ years of academic / industry experience</li><li>
Or PhD No experience required</li></ul>
<b>Preferred Qualifications</b>
<ul><li>A Ph.D. with 0+ years industry research experience or an M.S. with 3+ years industry research experience in computer science, statistics, computational biology, or another quantitative field</li><li>
Expert-level understanding of and experience using deep learning tools and approaches (transformer-based encoders/decoders, LLMs, reinforcement learning, etc.) as demonstrated through publications or projects</li><li>
Hands-on experience leading the building and scaling of deep learning training pipelines on multi-GPU computational infrastructure using PyTorch, Huggingface, and/or other tools</li><li>
Knowledge of or the ability to learn biological concepts and data types, including the ability to work and communicate effectively with biologists</li><li>
Excellent verbal and written communication skills. Fluent verbal and written English language skills prerequisite</li><li>
Experience building agentic workflows is a plus</li><li>
Prior experience in pharmaceutical application areas is a plus</li></ul>
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
<br>
<br>
<b>Compensation Overview:</b><br>
<br>
Brisbane - CA - US: $141,150 - $171,042<br>
Cambridge Crossing: $141,150 - $171,042
<br>
Princeton - NJ - US: $122,740 - $148,732
<br>
San Diego - CA - US: $135,010 - $163,605<br>
Seattle - WA: $135,010 - $163,605<br>
<br>
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
<br>
<br>
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
<br>
<br>
Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
<br>
<br>
<b>Uniquely Interesting Work, Life-changing Careers</b><br>
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.<br>
<br>
<b>On-site Protocol</b><br>
<br>
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
<br>
<br>
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
<br>
<br>
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
<br>
<br>
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
<br>
<br>
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.<br>
<br>
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
<br>
<br>
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</div>

Scientist, Predictive Biology and AI

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