analytical scientist

Altair

<div>
 
 Transforming the Future with Convergence of Simulation and Data
 
 
 
 
 Analytical Scientist
 
 
 
 
 Job Summary
 
 
 
 Our client in Ann Arbor, MI is looking for an Analytical Scientist. This is a contract position.
 
 
 
 What You Will Do
 
 
 
 Our Client's Motor North America&rsquo;s Materials Research Department is looking for an Analytical Scientist.
 
 
 The primary responsibility of this role is to support in-house analytical projects in the field of materials R&amp;D. The position requires staying abreast of analytical techniques relevant to all fields of battery, catalyst, fuel cell, thermal and functional materials. The candidate must be able to work efficiently within a diverse group of scientists and engineers in a collaborative research environment, while performing analytical support functions geared towards the generation of new intellectual property and academic publications.
 
 
 
 What You Will Be Doing
 
 
 
 <ul>
 <li>
 Provide analytical support to in-house teams utilizing instruments such as XRD, XPS, SEM, TGA/DSC, and various other spectroscopic techniques commonly utilized in R&amp;D laboratories.
 </li>
 <li>
 Utilize information shared by our teams on their materials and identify optimum analytical pathways.
 </li>
 <li>
 Develop workflows to efficiently curate analytical data for the materials you are tasked.
 </li>
 <li>
 Timely reports and presentations to respective research teams, analytical leads and management.
 </li>
 <li>
 Help draft invention disclosures for patent application, publish original research articles and attend conferences to communicate with external research communities.
 </li>
 <li>
 Manage the equipment, servicing, lab spaces and safety aspects for your analytical tools.
 </li>
 <li>
 Provide support in general department administrative tasks related to analytical equipment and spaces.
 
 
 
 </li>
 </ul>
 
 Basics
 
 
 
 <ul>
 <li>
 B.Sc. degree in Materials Science, Chemistry, Chemical Engineering or related Analytical fields.
 </li>
 <li>
 Experience in scientific research processes, laboratories, simple data management and organization.
 </li>
 <li>
 Experience with fundamental analytical techniques (ideal but not critical), such as XRD, XPS, SEM, etc.
 </li>
 <li>
 Self-motivated individual with initiative and drive for overcoming technical challenges.
 </li>
 <li>
 An understanding in scientific writing needs and/or presenting in scientific settings (like conferences).
 </li>
 <li>
 Proficient in the use of Microsoft 365 (Word, Power Point and Excel minimum) for reporting purposes.
 
 
 
 </li>
 </ul>
 
 Preferred
 
 
 
 <ul>
 <li>
 Knowledge in the fields of batteries, catalysis, fuel cells, thermal or functional materials.
 
 
 
 </li>
 </ul>
 
 How You Will Be Successful
 
 
 
 <ul>
 <li>
 Envision the Future
 </li>
 <li>
 Communicate Honestly and Broadly
 </li>
 <li>
 Seek Technology and Business &ldquo;First&rdquo;
 </li>
 <li>
 Embrace Diversity and Take Risks
 
 
 
 </li>
 </ul>
 
 What We Offer
 
 
 
 <ul>
 <li>
 Competitive Salary
 </li>
 <li>
 Comprehensive Benefit Package
 </li>
 <li>
 401(k) with matching contributions
 </li>
 <li>
 Paid Time Off
 </li>
 <li>
 Employee Discounts
 </li>
 <li>
 Free training on all Altair products
 
 
 
 </li>
 </ul>
 
 Why Work With Us
 
 
 
 Altair is a global technology company providing software and cloud solutions in the areas of data analytics, product development, and high-performance computing (HPC). Altair enables organizations in nearly every industry to compete more effectively in a connected world, while creating a more sustainable future. With more than 3,000 engineers, scientists, and creative thinkers in 25 countries, we help solve our customer&rsquo;s toughest challenges and deliver unparalleled service, helping the innovators innovate, drive better decisions, and turn today&rsquo;s problems into tomorrow&rsquo;s opportunities.
 
 
 
 Our vision is to transform customer decision making with data analytics, simulation, and high-performance computing.
 
 
 
 For more than 30 years, we have been helping our customers integrate electronics and controls with mechanical design to expand product value, develop AI, simulation and data-driven digital twins to drive better decisions, and deliver advanced HPC and cloud solutions to support unlimited idea exploration. To learn more, please visit altair.com
 
 
 
 Ready to go? #ONLYFORWARD
 
 
 
 At our core we are explorers; adventures; pioneers. We are the brains behind some of the world&rsquo;s most revolutionary innovations and are not only comfortable in new and unchartered waters, we dive headfirst. We are the original trailblazers that make the impossible possible, discovering new solutions to our customer&rsquo;s toughest challenges.
 
 
 Altair is an equal opportunity employer. Our backgrounds are diverse, and every member of our global team is critical to our success. Altair&rsquo;s history demonstrations a belief that empowering each individual authentic voice reinforces a culture that thrives because of the uniqueness among our team.
</div>

Analytical Scientist

Dr. Reddy's Laboratories

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 
 
 
 
 
 
 We are seeking a highly skilled Analytical Specialist in to join our Research and Development team for Nasal and Inhalation Division for developing, validating the analytical methods and evaluation of sameness studies for Nasal and Inhalation products.
 
 
 
 
 You are responsible to
 
 
 
 <ul>
 <li>
 Develop, validate, and transfer analytical methods for Nasal and Inhalation products, including spray characterization techniques (SP, PG, DSD) and inhalation-specific techniques (APSD, DDU, Pump Delivery) along with assay and impurity methods .
 </li>
 <li>
 Should be well versed with the planning and conducting experiments for the PoP BE/sameness studies
 </li>
 <li>
 Perform Drug Master File/Literature review, procure relevant materials, and stay updated with industry developments.
 </li>
 <li>
 Execute analytical activities as per defined procedures, document data.
 </li>
 <li>
 Conduct method validation studies and transfer validated methods to Quality Control (QC) department/
 </li>
 <li>
 Ensure proper maintenance, calibration, and operation of laboratory equipment in compliance with Good Laboratory Practices (GLP) standards.
 </li>
 <li>
 Maintain accurate documentation, organize work area, and adhere to Standard Operating Procedures (SOPs) to ensure compliance with internal and external auditing requirements.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 Masters in Science/ Organic chemistry/ Pharmaceutical Sciences
 
 
 
 
 
 Minimum work experience:
 
 7-101years of experience in analytical method development, validation and sameness studies.
 
 
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 
 <ul>
 <li>
 Have work experience on Formulation Development and expertise in inhalation/injectable dosage form.
 </li>
 <li>
 Understanding on Abbreviated New Drug Application (ANDA) filing requirements.
 </li>
 <li>
 Strong understanding of regulatory guidelines and industry standards related to pharmaceutical product development and analysis.
 </li>
 </ul>
 
 
 Behavioral Skills
 
 
 
 
 <ul>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 Strong analytical and problem-solving abilities.
 </li>
 <li>
 Ability to work collaboratively with own team and cross-functional teams.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking an experienced Analytical Specialist specializing in Mass Spectrometry to develop sensitive and robust methods for quantifying genotoxic impurities (Like: Nitrosamines) in drug substances and products. This role involves method development, validation, troubleshooting, and resolving method-related issues. Your expertise in Mass Spectrometry will be crucial in creating accurate impurity profiles through comprehensive analysis.
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 
 <ul>
 <li>
 You will be responsible for developing sensitive and robust methods to quantify genotoxic impurities in drug substance and products. This involves selecting appropriate quantitation modes, validating methods, and transferring them to QC sites. Your role includes troubleshooting and resolving method-related queries and issues, ensuring quality robust method development.
 </li>
 <li>
 You will be responsible for identifying impurities in stress and stability studies, correlating data based on Mass and fragmentation, and developing methods for screening leachables in Parental formulations. The goal is to create accurate impurity profiles through comprehensive analysis.
 </li>
 <li>
 You will respond to regulatory deficiencies related to Mass spec techniques, provide quantitation support for plant samples, and perform structure confirmation activities for working/reference standards and impurities. Anticipating potential queries from regulatory authorities/customers and proposing relevant measures for timely responses are crucial aspects of this role.
 </li>
 <li>
 You will be responsible for training new team members, preparing Standard operating procedure (SOPs) and guidelines, conducting incident/investigation analysis, identifying Corrective Action Preventive Action (CAPA) and root causes, and ensuring adherence to safe work practices. Maintaining Good Manufacturing practices (GMP) in laboratory and conducting preventive maintenance of instruments are essential for meeting minimum operating standards.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 Post Graduation in Pharma/Physics
 
 
 
 
 
 Minimum work experience:
 
 8-10 years of experience
 
 
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 
 <ul>
 <li>
 Able to understand the mass spectrometry principles and Liquid chromatography principles.
 </li>
 <li>
 Good hands-on experience on Liquid chromatography-mass spectrometry (LC_MS), Tandem mass spectrometry (MS/MS) and High resolution mass spectrometry (HR-MS) techniques.
 </li>
 <li>
 Excellent skill set on method development, sample preparation, matrix interference removal and validation of quantitative methods in API and formulations.
 </li>
 <li>
 Experience on extractable and leachable, analytical method development, validations &amp; transfers.
 </li>
 <li>
 Good documentation practices and laboratory practices.
 </li>
 <li>
 Sound knowledge and understanding of FDA regulations governing pharmaceuticals.
 </li>
 </ul>
 
 
 Behavioral
 
 
 Skills
 
 
 
 
 <ul>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 Ability to work with cross functional teams.
 </li>
 <li>
 Strong analytical and problem-solving abilities.
 </li>
 <li>
 Leadership skills to motivate and mentor the team.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable Division for developing and validating analytical methods for injectable products, ensuring compliance with the regulatory requirements, conducting literature reviews, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. This role demands a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer.
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 
 <ul>
 <li>
 You will be responsible Analytical method development and validation of injectable products.
 </li>
 <li>
 You will be responsible to perform the Drug Master File/Literature review and procure the relevant columns and standards in order to initiate the analytical method development. Stay updated with the latest literature and industry developments in the field.
 </li>
 <li>
 You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department.
 </li>
 <li>
 You will be responsible to execute analytical activities as per defined procedures, document the data and send the respective record of analysis to group leader/analytical expert for the review and release in order to provide the approved results to formulation team.
 </li>
 <li>
 You will be responsible for analytical method development for drug products for various tests mentioned in the specification in order to analyse the product development batches for the prototype screening.
 </li>
 <li>
 You will be responsible for analytical method validation activities at the manufacturing sites providing method development reports to verify the validation parameters and ensure the execution of method validation as per the regulatory requirement in order to provide the authentic analytical validation report for the regulatory filing.
 </li>
 <li>
 You will be responsible for analytical method transfer to plant locations successfully in order to train the Quality Control (QC) team on the methods for the Exhibit and commercial batch analysis at plant.
 </li>
 <li>
 You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results.
 </li>
 <li>
 You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy.
 </li>
 <li>
 You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions.
 </li>
 <li>
 You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 Masters in Science/ Organic chemistry/ Pharmaceutical Sciences
 
 
 
 
 
 Minimum work experience:
 
 5 years of experience in analytical method development
 
 
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 
 <ul>
 <li>
 Have work experience on Process scale up of Injectable Products.
 </li>
 <li>
 Have work experience on Formulation Development and expertise in inhalation/injectable dosage form.
 </li>
 <li>
 Understanding on Abbreviated New Drug Application (ANDA) filing requirements.
 </li>
 <li>
 Experience in Process Optimization (Manufacturing) and Technology Transfer.
 </li>
 <li>
 Strong understanding of regulatory guidelines and industry standards related to pharmaceutical product development and analysis.
 </li>
 <li>
 Proven experience in method validation and documentation in compliance with regulatory requirements.
 </li>
 </ul>
 
 
 Behavioral Skills
 
 
 
 
 <ul>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 Strong analytical and problem-solving abilities.
 </li>
 <li>
 Ability to work collaboratively with own team and cross-functional teams.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

Analytical Scientist Injectable

Veranova

<div>
 
 Discover Veranova:
 
 
 
 At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
 
 
 Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.
 
 
 Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.
 
 
 
 Role Overview:
 
 
 
 The Structure Characterization Analytical Scientist will have expertise in structural elucidation of drug substances, impurities and degradants through rapid and efficient characterization of synthetic molecules by NMR, chromatography and mass spectrometry analysis. The successful candidate will have a strong foundation in analytical chemistry and spectroscopy, with hands-on laboratory experience. A background in organic chemistry is highly desirable for interpreting complex structures and reaction mechanisms.
 
 
 
 Core Responsibilities:
 
 
 
 <ul>
 <li>
 Exercise sound technical judgment in the planning, execution, and analysis of experiments to determine structural identification of pharmaceutical actives and related substances including forced degradation for impurity enrichment, 2D NMR, high-resolution MS, HPLC and GC method development.
 </li>
 <li>
 Implement characterization approaches for the preparation, isolation, and identification of low-level impurities in a drug development environment.
 </li>
 <li>
 Author analytical test methods, protocols, reports, relevant SOPs and regulatory documents as needed.
 </li>
 <li>
 Develop and apply qNMR methods for accurate quantification of drug substances and impurities.
 </li>
 <li>
 Support method development, qualification, transfer, and validation activities for analytical procedures.
 </li>
 <li>
 Provide support for cGMP manufacturing campaigns, ensuring compliance with regulatory requirements and documentation standards.
 </li>
 <li>
 Communicate technical findings and results to both internal and external stakeholders, including clients and regulatory bodies.
 </li>
 <li>
 Collaborate with key partners including chemistry development scientists, quality control and regulatory affairs teams to ensure successful project delivery.
 </li>
 <li>
 Mentor and develop scientific staff. Ensure continued technical and professional growth of department members, encourage efforts towards excellence and knowledge sharing.
 </li>
 <li>
 Maintain and troubleshoot NMR and LCMS instrumentation (e.g., Orbitrap, Q-TOF, Triple Quad).
 
 
 
 </li>
 </ul>
 
 Qualifications:
 
 
 
 
 Required
 
 
 
 <ul>
 <li>
 Ph.D. or M.S. in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, or related field. Demonstrated mastery of one or more subject areas related to structural characterization.
 </li>
 <li>
 Strong hands-on experience with 2D NMR, HR-MS.
 </li>
 <li>
 3+ years of hands-on experience in structural characterization of impurities for active pharmaceutical ingredients under cGMP&rsquo;s.
 </li>
 <li>
 Strong knowledge of organic structure elucidation &ndash; forced degradation, MS, NMR, etc., with the ability to train/mentor colleagues.
 </li>
 <li>
 Excellent communication, organizational, and leadership skills with ability to work independently and in a team environment.
 </li>
 <li>
 Well organized with good problem-solving skills, a high level of attention to detail and have a passion for delivering high quality data in a fast-paced environment
 
 
 
 </li>
 </ul>
 
 Preferred
 
 
 
 <ul>
 <li>
 Experience with regulatory submissions and GMP/GLP environments.
 </li>
 <li>
 Experience with structural characterization of larger synthetic molecules including peptides and oligonucleotides.
 </li>
 <li>
 Risk assessment and development of trace level methods for potential GTI and nitrosamines.
 
 
 
 </li>
 </ul>
 
 Salary Range
 
 : $90,000 - $135,000 annual base salary
 
 
 
 Our Commitment:
 
 
 
 <ul>
 <li>
 Health &amp; Wellness: Comprehensive health &amp; wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
 </li>
 <li>
 Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.
 </li>
 <li>
 Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
 </li>
 <li>
 Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don&rsquo;t meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.
 
 
 
 </li>
 </ul>
 
 Additional Information:
 
 
 
 Applicants for this role must be authorized to work in the United States without further employer sponsorship.
 
 
 Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.
 
 
 All your information will be kept confidential according to EEO guidelines.
 
 
 Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
 
 
 All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .
 
 
</div>

Analytical Scientist - Structural Characterization

GenScript

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

Analytical Associate Scientist/Scientist

Biocon Biologics

<div>
 Roles &amp; Responsibilities:Execution of experiments for analytical method development/ qualification/ transfer, in-process/ stability sample testing, biosimilarity analysis and for evaluation of new high throughput formats of testing using chromatography (HPLC/UPLC), electrophoresis /capillary electrophoresis, UV spectrophotometer, Solo-VPE and other high-end analytical tools. Sample analysis in GC, Atomic absorption spectroscopy (AAS), Charged Aerosol Detector (CAD) etc. Glycan analysis.Sequential and logical planning of experiments. Record the experiment details (procedure, controls, analyses, and observation of the experiments) accurately and completely following good documentation practices in electronic laboratory notebook.Compilation, and interpretation of experimental data Communication of data to cross-functional teams, compilation of data for reports and participate in internal group meetings.Prepare documents such as method development reports, protocols, instrument operation procedures, author change controls and deviations.Perform literature survey of assays, support in experimental design based on historical data and troubleshooting of experimentsMaintain equipment and instruments in coordination with instrumentation team and support installation of new equipment and prepare Equipment/Instrument operating proceduresRegularly track inventory of consumables/ critical reagents and making sure they are ordered and follow-up of the ordered material and support in laboratory maintenance.Participate in QMS related activities.
 
 Education:Degree in life sciences such as biology, biochemistry, biotechnology, analytical chemistry or closely related fieldM.Pharma/M.Sc/M.Tech with 3-8 years of research experience
 
 Required Experience:Experience in leading biopharmaceutical organizations, contributing to high-impact research and development initiatives.Strong expertise in chromatographic techniques including Ion Exchange (IEC), Reverse Phase (RP), Size Exclusion (SEC), and Hydrophilic Interaction Chromatography (HILIC) for protein therapeutics. Glycan analysis. Additional experience in excipient analysis using ELSD, CAD, and MS platforms is highly valued.Hands-on experience with a wide range of analytical instruments, such as HPLC, UPLC, Capillary Electrophoresis (CE), UV-Vis Spectrophotometer, SoloVPE, Octet, Maurice, GC and AAS etc. Higher order structure analysis techniques (CD spectroscopy, DSC, DLS, SEC-MALS, FTIR). Demonstrated ability to contribute to experimental design and troubleshooting within collaborative, cross-functional team environments.Skilled in data analysis using instrument-specific software, with working knowledge of statistical tools for method evaluation and interpretation.Thorough understanding of regulatory guidelines including ICH, WHO, and USP for method development, qualification, transfer, and validation. Proficiency in electronic laboratory notebook (eLN) systems is also preferred.Effective communicator and team player, capable of articulating scientific concepts, challenges, and solutions clearly.Familiarity with Empower Method Validation Manager is an added advantage
</div>

Analytical Development Scientist (Non PhD)

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