scientist ii

Microsoft

<div>
 
 Overview
 
 
 
 We are seeking a passionate and technically skilled Data Scientist II to join the Commerce &ndash; Platforms, Data, and Experiences (PDX) team. This team plays a pivotal role in shaping Microsoft&rsquo;s commerce data strategy, building scalable data platforms, and delivering actionable ML driven insights that drive business transformation across the ecosystem.
 
 
 As a Data Scientist II in PDX, you will work at the intersection of data engineering, data processing, and machine learning to solve complex business problems. You will collaborate with cross-functional teams to design experiments, build predictive models, and develop scalable solutions that enhance decision-making and customer experiences by producing descriptive, diagnostic, predictive and prescriptive insights.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Design and implement advanced analytics solutions to support commerce data platform initiatives including analytics based on Machine Learning Models.
 </li>
 <li>
 Partner with engineering and product teams to define data requirements and ensure high-quality data pipelines.
 </li>
 <li>
 Conduct exploratory data analysis, feature engineering, and model evaluation using structured and unstructured datasets.
 </li>
 <li>
 Ensure the models built are operable, scalable, extensible and performant.
 </li>
 <li>
 Develop dashboards, visualizations, and storytelling artifacts to communicate insights to stakeholders.
 </li>
 <li>
 Lead experimentation efforts to evaluate new features, forecasting, data quality and anomaly detection systems.
 </li>
 <li>
 Build extensible solutions on LLM models to improve productivity of engineers across the commerce organization.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s or Master&rsquo;s degree in Computer Science, Statistics, Mathematics, or related field.
 </li>
 <li>
 2+ years of experience in data science, analytics, or applied machine learning.
 </li>
 <li>
 Proficiency in Python, SQL, and ML frameworks (e.g., Scikit-learn, TensorFlow, PyTorch).
 </li>
 <li>
 Experience with cloud platforms (Azure preferred) and big data technologies.
 </li>
 <li>
 Strong understanding of statistical modeling, predictive analytics, and experimentation design.
 </li>
 <li>
 Excellent communication and stakeholder management skills.
 </li>
 <li>
 Demonstrated experience leveraging AI tools and technologies to enhance engineering effectiveness, coupled with a strong curiosity and commitment to continuous learning in the field of Artificial Intelligence.
 
 
 </li>
 </ul>
 This position will be open for a minimum of 5 days, with applications accepted on an ongoing basis until the position is filled.
 
 
 Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance with religious accommodations and/or a reasonable accommodation due to a disability during the application process, read more about
 
 requesting accommodations.
 
</div>

Data Scientist II

Anvia Therapeutics

<div>
 
 
 Job Title: Scientist II- Immunology
 
 
 
 
 Location: NYC
 
 
 
 
 About Us:
 
 
 
 Anvia Therapeutics is a dynamic and innovative biotech company dedicated to developing small molecule inhibitors targeted at treating inflammatory and autoimmune diseases. We foster a collaborative environment where scientific excellence and creativity drive our mission to develop impactful medicines.
 
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a highly motivated immunology Scientist to drive hypothesis-driven in vitro immunology research in a fast-paced and innovative drug discovery environment. The successful candidate will design, develop, and execute complex cellular assay systems, including primary human immune cells, patient-derived samples, and disease-relevant cell lines to support immune pharmacology and mechanism-of-action (MoA) studies across inflammatory disease programs such as IBD, rheumatoid arthritis, and dermal inflammation.
 
 
 
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Design and execute hypothesis-driven cellular assays to support immune pharmacology, target validation, and MoA studies.
 </li>
 <li>
 Develop, optimize, and validate complex in vitro assay systems using primary immune cells, patient-derived samples, and disease-relevant or engineered cell lines.
 </li>
 <li>
 Perform functional immune assays including cell activation, proliferation, cytokine production, signaling, and cytotoxicity, using both primary and cell-line&ndash;based systems.
 </li>
 <li>
 Contribute to immune pharmacology assessments, including compound potency, pathway modulation, selectivity, and translational relevance.
 </li>
 <li>
 Apply a strong mechanistic understanding of immune and inflammatory signaling pathways to guide assay design and data interpretation.
 </li>
 <li>
 Utilize flow cytometry, ELISA/MSD/other cytokine/chemokine profiling techniques, protein- and signaling-based assays, and related techniques to generate high-quality, reproducible data.
 </li>
 <li>
 Analyze, interpret, and clearly communicate experimental results to project and leadership teams.
 </li>
 <li>
 Troubleshoot and refine experimental systems to improve robustness, scalability, and biological relevance.
 </li>
 <li>
 Maintain accurate experimental records using electronic laboratory notebooks.
 </li>
 <li>
 Collaborate closely with lead discovery, chemistry, translational, and external partners to advance program milestones.
 </li>
 <li>
 Stay current with emerging immunology technologies and incorporate innovative methodologies where appropriate.
 </li>
 </ul>
 
 
 
 
 
 Required Qualifications
 
 
 <ul>
 <li>
 PhD in Immunology, Biology, Biotechnology, Molecular Biology, or a related field with 2+ years of relevant experience.
 </li>
 <li>
 Hands-on experience developing and executing complex cellular assays using primary immune cells, patient-derived samples, and cell line&ndash;based systems.
 </li>
 <li>
 Experience working with functional immune readouts, including flow cytometry&ndash;based phenotyping and signaling assays, and cytokine measurement (ELISA/MSD/other).
 </li>
 <li>
 Demonstrated expertise in protein-level analysis of signaling pathways, including Western blotting and related biochemical techniques used to assess pathway activation, inhibition, and mechanism of action.
 </li>
 <li>
 Strong understanding of cell signaling pathways relevant to immune and inflammatory biology.
 </li>
 <li>
 Proven ability to independently design experiments, troubleshoot assays, and manage multiple priorities.
 </li>
 <li>
 Proficiency with data analysis and visualization tools (e.g., GraphPad Prism, FlowJo, Excel).
 </li>
 <li>
 Excellent written and verbal communication skills.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Experience supporting immune pharmacology and MoA characterization in early drug discovery.
 </li>
 <li>
 Background in inflammatory or autoimmune disease biology (IBD, RA, dermatology preferred).
 </li>
 <li>
 Familiarity with assay validation, quantitative potency assessment and translational biomarker analysis/ identification.
 </li>
 <li>
 Experience working in a fast-paced, innovative biotech environment.
 </li>
 </ul>
 
 
 
 
 Why Join Us?
 
 <ul>
 <li>
 Be part of a passionate team making a difference in biotech innovation.
 </li>
 <li>
 Collaborative and dynamic work environment.
 </li>
 <li>
 Hands-on experience with state-of-the-art technologies.
 </li>
 <li>
 Opportunities for professional development and advancement.
 </li>
 <li>
 Competitive compensation and benefits.
 </li>
 </ul>
 
 
 
 
 The salary range for this position is $115,000-$150,000 per year. The actual compensation offered will be based on factors such as relevant experience, education, and skills. In addition to base salary, we offer a comprehensive benefits package, including health insurance, paid time off, and retirement plan options.
 
 
 
 
 
 Anvia Therapeutics is an equal opportunity employer. We do not discriminate against any employee or applicant for employment because of race, creed (religion), color, national origin, sex (including gender identity and sexual orientation), age, disability, marital status, citizenship status, military status, genetic information, or any other characteristic protected by federal, state, or local law.
 
 
 
 
 
 Our employment decisions are based on merit, qualifications, and business needs. We are committed to providing a work environment free from discrimination, harassment, and retaliation, and we undertake affirmative action efforts to promote equal opportunity for all employees and applicants.
 
 
 
 
</div>

Scientist II, Immunology

Thermo Fisher Scientific

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
How will you make an impact?
 
You'll perform sophisticated analyses to ensure product quality and safety in our laboratories. As a QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through commercial release. You'll work with analytical instruments and technologies while making a meaningful impact on patient health through precise quality control testing. 
 
Working with cross-functional teams, you'll execute validated test methods, participate in method development and validation activities, investigate out-of-specification results, and maintain detailed documentation of analyses. You'll contribute to continuous improvement initiatives and help establish robust analytical processes while adhering to cGMP requirements and safety standards.
We have 2 positions available.
A Day in the Life:<ul><li>
Perform testing on In-Process, DS release, DP release, DS stability, DP Stability, and various other non-routine samples, ensuring timely delivery for projects</li><li>
Participate in analytical method validation/transfer, method establishment/qualification routine and stability analysis.</li><li>
Conduct GMP testing in an analytical laboratory environment using Separation Techniques, BioAssay Analysis and Compendia test methods (i.e. Reverse Phase, SEC, Titer concentration, iCE, pH, Osmolarity, Residual DNA, Appearance)</li><li>
Compiles data for documentation of test procedures, prepares reports. Ensures all testing processes, monitoring, and departmental documentation meet SOPs and cGMP regulatory standards.</li><li>
Participate in the development of new concepts, techniques, and standards. Involved with assisting in the preparation of CoAs.</li><li>
Recognize and report out-of-specification/ out-of-trend results to laboratory management; recommend solutions.</li><li>
Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines</li><li>
Partake in laboratory activities, including safety inspections and client audits in a timely matter.</li></ul><div>
Keys to Success: 
<ul><li>Advanced degree with no prior experience, or Bachelor's degree with 2 years of experience in a GMP regulated laboratory environment performing analytical testing</li><li>Preferred Fields of Study: Chemistry, Biology, Biochemistry, or related scientific field</li><li>Expertise in analytical techniques such as HPLC, GC, CE, ELISA, PCR, and other bioanalytical methods</li><li>Proficient in aseptic techniques and environmental monitoring procedures</li><li>Strong knowledge of cGMP regulations and quality control requirements</li><li>Experience with laboratory information management systems (LIMS) and quality management systems</li><li>Excellent documentation practices and attention to detail</li><li>Strong problem-solving and analytical skills</li><li>Ability to work both independently and collaboratively</li><li>Proficiency with Microsoft Office applications</li><li>Strong written and verbal communication skills</li><li>Ability to lift up to 30 pounds and stand for extended periods</li><li>Willingness to wear required PPE including lab coat, safety glasses, and gloves</li><li>May require flexible scheduling including occasional weekend work</li><li>Experience with method validation and transfer activities preferred</li><li>Knowledge of data integrity requirements and good documentation practices</li><li>Demonstrated ability to investigate out-of-specification results and author technical reports</li></ul></div>
Excellent Benefits<ul><li>
Benefits &amp; Total Rewards | Thermo Fisher Scientific</li><li>
Medical, Dental, &amp; Vision benefits-effective Day 1</li><li>
Paid Time Off &amp; Designated Paid Holidays</li><li>
Retirement Savings Plan</li><li>
Tuition Reimbursement</li></ul>
OTHER<ul><li>
Relocation assistance is NOT provided</li><li>
Must be legally authorized to work in the United States now or in the future, without sponsorship.</li><li>
Must be able to pass a comprehensive background check, which includes a drug screening</li></ul></div>

QC Scientist II

AAA Auto Club Enterprises

As our Data Scientist II, you will act as an internal business consultant to help optimize every facet of this organization. You will solve problems and answer questions – using data – for other departments to help us reduce costs, reduce errors, and be a better organization for our 18 million members.
 
What You’ll Do
 
Every day, you will help solve business problems presented to us by stakeholders using data. You will get a scenario or problem, such as, “We need to reduce cycle times,” and then pull, analyze, and interpret data relevant to that scenario.
 You will pull data from SQL databases. You will analyze and interpret data using Python, R, or other tools. You will determine patterns or trends and their statistical significance to the problem. To visualize the data, you will use Tableau.
 Once you have done your analysis, paired with a data engineer, you will present your findings to the stakeholder and confirm, refute or simply acknowledge a hypothesis. Your work may be implemented or may develop into something else.
 This role is remote, but you must be able to report to the Coppell, TX, office for 2 collaboration days every month.
 
What You’ll Need
 
To thrive in this role, you must have a solid foundation of statistics and data analysis. You must be able to describe a project where you pulled data, analyzed it, identified trends or patterns, determined significance, and delivered insights or recommendations to the business. What was your approach? What tools did you use and why? Did you get to the root cause of the issue? Did you confirm or refute a hypothesis? You must be able to speak to your involvement and decisions at each stage.
 For pulling data, we use SQL so you must be proficient with this tool. To curate and analyze data, we use a variety of languages and programs: Python, R, and even Excel. You can choose whatever tool helps you best, but you must be proficient in either Python or R.
 Excellent communication skills and an attitude of flexibility are a must. Very often, we get into the data, and some aspect takes longer than we thought, or we have to pivot and change how we approach a problem. A dashboard works better than a model, perhaps. Then you have to explain to the stakeholder or the team why you made that change or why the deliverable is taking longer than expected. It’s all about being creative in your approach and communicating that frequently and clearly to people who may be less tech or data-savvy than you.
 You have worked previously with an Agile team or understand these concepts. You expect to participate in daily standup meetings, you’ll complete your projects or stories during our bimonthly sprints, and you’re ready to meet frequent deployment deadlines.
 
Remarkable benefits: 
<ul>
<li>Health coverage for medical, dental, vision</li>
<li>401(K) saving plan with company match AND Pension</li>
<li>Tuition assistance</li>
<li>PTO for community volunteer programs</li>
<li>Wellness program</li>
<li>Employee discounts (membership, insurance, travel, entertainment, services and more!)</li>
</ul>
Auto Club Enterprises is the largest federation of AAA clubs in the nation. We have 14,000 employees in 21 states helping 17 million members. The strength of our organization is our employees. Bringing together and supporting different cultures, backgrounds, personalities, and strengths creates a team capable of delivering legendary, lifetime service to our members. When we embrace our diversity – we win. All of Us! With our national brand recognition, long-standing reputation since 1902, and constantly growing membership, we are seeking career-minded, service-driven professionals to join our team.
 
"Through dedicated employees we proudly deliver legendary service and beneficial products that provide members peace of mind and value.”
 
AAA is an Equal Opportunity Employer

Wonderful Pistachios & Almonds

<div>
 
 Company Description
 
 
 
 Wonderful Pistachios &amp; Almonds is the largest vertically integrated pistachio and almond processor in the world. Located in California's Central Valley, our nuts are Non-GMO Project Verified and sustainably harvested, providing a smart, healthy choice for consumers around the world. Our facilities are equipped with the most advanced processing technology available, allowing us to efficiently sort, grade, process, roast, flavor, and package billions of nuts each year. We are committed to providing the highest-quality nuts to our customers and consumers worldwide.
 
 
 
 Job Description
 
 
 
 SUMMARY OF POSITION
 
 
 The Food Scientist II supports R&amp;D initiatives ranging from new product development and innovation to product quality improvement, sensory analysis, shelf-life evaluation, and regulatory compliance. The role requires applying strong technical and scientific principles to drive innovation, ensure product excellence, and independently manage projects from concept through commercialization. The position demands comfort with ambiguity, initiative in problem-solving, attention to detail, and the ability to translate complex challenges into actionable solutions.
 
 
 
 Essential Duties And Responsibilities
 
 
 
 <ul>
 <li>
 Apply food science and engineering principles to deliver technical and innovative solutions for pistachio, almond, and nut-based products.
 </li>
 <li>
 Independently manage complex technical projects, taking initiative to identify challenges, link cross-functional insights, and drive progress amid ambiguity.
 </li>
 <li>
 Use ingredient functionality expertise to improve existing product quality and develop innovative new products. Lead feasibility trials and commercial scale-ups to resolve processing challenges.
 </li>
 <li>
 Assess new technologies for roasting, seasoning, and nut-based product applications, driving innovation, solving technical challenges, and keeping pace with industry trends.
 </li>
 <li>
 Manage regulatory compliance activities by maintaining accurate nutrition, ingredient, and labeling information for all products and ensuring alignment with domestic and international requirements.
 </li>
 <li>
 Apply sensory science methodologies to assess product quality, conduct discrimination and descriptive analysis, and generate actionable recommendations.
 </li>
 <li>
 Conduct data-driven shelf-life studies; evaluate correlations between organoleptic changes, lipid oxidation, and packaging film properties. Recommend shelf-life extension strategies.
 </li>
 <li>
 Maintain detailed project documentation, specifications, reports, and data archives.
 </li>
 <li>
 Support and promote a safe, healthy, and compliant work environment.
 </li>
 <li>
 Drive product and process advancement through creativity, adaptability, and initiative.
 </li>
 <li>
 Build effective cross-functional relationships and collaborate with marketing, sales, and operations to ensure successful commercialization and continuous improvement initiatives.
 
 
 </li>
 </ul>
 
 Skill Requirements
 
 
 
 Language skills
 
 
 <ul>
 <li>
 Excellent written and verbal communication skills are necessary.
 </li>
 <li>
 Ability to communicate and interact with all levels of the organization, including senior management, customers, consumers, and regulatory officials.
 
 
 </li>
 </ul>
 
 Mathematical Skills
 
 
 
 <ul>
 <li>
 Exhibit strong analytical Skills (math and Excel)
 </li>
 <li>
 Ability to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions, and decimals, along with computing ratios and percentages
 
 
 </li>
 </ul>
 
 Computer Skills
 
 
 
 <ul>
 <li>
 Proficient in Excel and Word applications.
 </li>
 <li>
 Understanding of Oracle and Discoverer reporting tools.
 
 
 </li>
 </ul>
 Pay range: $91,000.00 - $124,500.00/yr
 
 
 
 Qualifications
 
 
 
 QUALIFICATIONS EDUCATION and/or EXPERIENCE
 
 
 <ul>
 <li>
 BS or Bachelor&rsquo;s or Master&rsquo;s degree in Food Science, Food Engineering, Chemical Engineering, or related field.
 </li>
 <li>
 Minimum 5 years of relevant industry experience.
 </li>
 <li>
 Proven ability to work independently, manage multiple priorities, and navigate ambiguity while taking ownership of projects from ideation to execution.
 </li>
 <li>
 Strong interpersonal, communication, and problem-solving skills.
 </li>
 <li>
 Hands-on, self-motivated, and results-oriented with a collaborative and innovative mindset.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 All your information will be kept confidential according to EEO guidelines.
 
 
 EEO is the law - click here for more information
</div>

Food Scientist II

Institute of Obstetrics and Gynaecology, MMC.

The Project Research Scientist II (Medical) will be responsible for:&middot; Providing support to research nurses in recruitment of study subjects anddata collection.&middot; Ensuring data accuracy and completion (both manual and digital)&middot; Entering data into database, manage and maintain effective record keeping data&middot; Providing support to project office operations performing a variety ofstandard administrative duties including typing of official documentsensuring high quality and accuracy of work&middot; Keeping track of project with update reports&middot; Any additional work related to current project and other related projects asinstructed by the PIEssential qualifications and experienceMBBS / BVSc / BDS with three years&rsquo; post qualification experienceOrMBBS / BVSc / BDS + Post Graduate Degree (MD/MVSc./MDS/MPH) or anyequivalent degree, including integrated PG degreesOrMBBS/BVSc/ BDS with PhDDesirable qualifications and experience1. Postgraduate degree or diploma in clinical trial management2. Experience as a project scientist in at least one research project involvingfunding agencies like ICMR, DBT, DST, SERB, Welcome Trust, GatesFoundation, etcSkills<ul><li>Proficient knowledge of data, data dictionary, database, research data</li><li>workflow, etc.</li><li>Basics of biomedical research including informed consent process</li><li>Well versed in recording the data</li><li>Excellent reading comprehension and strong written as well as verbal</li><li>communication skills, including good command of English is required</li><li>Good understanding of needs for project and job responsibilities</li><li>Proficiency in using computers (Windows and mac OS), internet,</li><li>troubleshooting, using cloud storage of various types. Good organizational</li><li>behavior and problem-solving skills</li><li>Ability to establish and maintain effective working relationships with co-</li><li>workers and investigators.</li></ul><ul><li>Schedule of selection (subject to change)</li><li>Last date of receiving applications: 27 Dec 2025 at 5 PM.</li><li>Screening test/Interview (Interaction with shortlisted candidates) on 29 Dec 2025.</li></ul>Job Type: Contractual / Temporary Contract length: 36 monthsPay: ₹960,000.00 - ₹1,248,000.00 per yearWork Location: In person

Research Scientist II (Medical)

US Pharmacopeia

<div>
 
 Description
 
 
 
 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.
 
 
 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.
 
 
 
 Brief Job Overview
 
 
 
 This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 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.
 
 
 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.
 
 
 
 The Scientist-II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Executes all testing and analysis of data with excellence and essentially no errors.
 </li>
 <li>
 Supporting Verification, GPH, PQM, stability and other departmental teams in terms of testing whenever needed.
 </li>
 <li>
 Responsible for sample archival, sample tracking and chemical inventory tracking in the laboratory.
 </li>
 <li>
 Coordination with supervisor to ensure completion of the projects allotted to the team.
 </li>
 <li>
 Completing the project as per the timelines and troubleshoot the scientific aspects of the projects on need basis.
 </li>
 <li>
 Responsible for performing the calibration of the equipment as per the schedule.
 </li>
 <li>
 Responsible for preparing, executing, and completing IQ/OQ/PQ of new instruments.
 </li>
 <li>
 Ensuring that the chemicals and column etc. are available for the projects and forward the purchase requisitions.
 </li>
 <li>
 Taking up any additional responsibilities assigned by Supervisor from time to time.
 </li>
 <li>
 Ensure all lab safety and GLP practices are maintained in the lab and participate actively in the internal and external audits and certification.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 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
 
 
 The candidate must have strong analytical chemistry knowledge with the ability to analyze, interpret and report effectively on data from a variety of analytical instrumental tests (e.g., HPLC, GC, Wet analytical techniques, spectroscopic techniques). Well-developed organizational and interpersonal skills. Able to establish and nurture relationships with individuals of varying backgrounds, cultures and learning styles.
 
 
 <ul>
 <li>
 Master&rsquo;s degree in chemistry or Pharmacy.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 3 to 6 years with relevant laboratory experience.
 </li>
 <li>
 Proven track record of consistently delivering projects on time and with high quality for API&rsquo;s.
 </li>
 <li>
 Expert in chromatographic analysis, particularly in HPLC.
 </li>
 <li>
 Proficient in other related analytical instrumentation such as Water determination, Loss on drying, Residue on Ignition, Titrations, Spectroscopic analysis (UV, IR etc.,).
 </li>
 <li>
 Knowledge of pharmaceutical testing requirements and test protocols involving compendial methods for reference materials (USP compendia, ICH guidelines, FDA regulations etc.).
 </li>
 <li>
 Must possess effective communication skills, both written and verbal.
 </li>
 <li>
 Expert in Empower software with knowledge on Audit trails and Custom fields.
 </li>
 <li>
 Must possess good technical and analytical skills to independently resolve or troubleshoot issues.
 </li>
 <li>
 Should have a strong understanding of GLP regulations and exposure to external regulatory audits.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Knowledge in other related analytical instruments (GC, Thermal, Elemental analysis, Mass analyzers etc.), Electronic Laboratory Notebook, ERP, QR coding system will be an added advantage.
 </li>
 <li>
 Understanding monograph procedures and participating in compendial methods for reference materials (USP, FCC, NF, etc.).
 </li>
 <li>
 Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&amp;D, or a contract pharmaceutical analytical laboratory testing organization is a plus.
 </li>
 <li>
 Awareness of GLP regulations, QMS, ISO/IEC 17025 and exposure to external regulatory audits is desirable.
 </li>
 <li>
 Ability to embrace and lead change. Extremely adaptable.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 Benefits
 
 
 
 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..
 
 
 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
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Scientist II, RSL

Search 1478+ Scientist ii jobs near you this January. New roles added regularly across leading industries. Apply today.

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