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 an experienced Lead in analytical development who can plan analytical projects based on priorities and established timelines, provide timely analytical delivery for stability testing, test method development/validation, method transfers and other related requests from Research &amp; Development (R&amp;D) or formulation development.
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 &bull; You will have to prepare and review of technical documents e.g. stability reports, method transfer and method validation protocol and reports, etc.
 
 
 &bull; You need to manage communication with stakeholders such as project leaders, product development, analytical teams and other business partners
 
 
 &bull; You need to facilitate productivity improvement through proper planning of analytical activities and resource optimization
 
 
 &bull; You need to co-ordinate and follow up with external labs including training of their staff.
 
 
 &bull; You will need to review of analytical data for accuracy, compliance to quality requirements and completeness e.g. lab notebooks, raw data, system entries, etc.
 
 
 &bull; You will have to review of technical documents such as analytical reports, method transfer /method validation protocols, reports, etc.
 
 
 &bull; You will have to participate in handling and resolution of laboratory non-conformances with related documentation
 
 
 &bull; You will be responsible for analytical methods and process compliance as per quality assurance requirement.
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 Education Qualification -
 
 MSc Chemistry, MSc Food Science, B.Tech/M. Tech in Dairy Technology
 
 
 
 
 
 Minimum experience required
 
 -3-6 years of experience in analytical development department and must have worked on nutritional product portfolio.
 
 
 
 
 
 Skill Attributes
 
 
 Technical Skills
 
 
 
 &bull; Technical expertise related to chemistry, analytical techniques, stability study assessment and advanced research technologies
 
 
 &bull; Efficient in MS Office, Word/Excel/PowerPoint functionalities
 
 
 &bull; Ability to interact with external labs and 3rd party manufacturing site labs to support product development team.
 
 
 &bull; Ability to understand analytical methods defined by global and local bodies
 
 
 &bull; Ability to resolve analytical issue associated with different product matrix.
 
 
 &bull; Should be familiar with analytical methods defined by national and international bodies like Association of Official Agricultural Chemists (AOAC), Bureau of Indian Standards (BIS) etc.
 
 
 &bull; Excellent knowledge of Good Laboratory Practices (GLP), Quality systems, Standard Operating Procedures, latest regulatory trends, and Global regulations as appropriate
 
 
 &bull; Data review, interpretation of analytical data and accurate documentation of laboratory investigations.
 
 
 
 Behavioural Skills
 
 
 
 &bull; Systematic approach and strategic thinking
 
 
 &bull; Possess excellent interpersonal skills, communication, coordination, and time-management skills
 
 
 &bull; Ability to independently handle teams
 
 
 &bull; Excellent oral/written communication and articulation skills
 
 
 &bull; Passion for people development
 
 
 &bull; Ability to prioritize work and change focus quickly
 
 
 &bull; Ability to delegate effectively
 
 
 
 
 
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 Global Generics India
 
 
 
 Global Generics India business journey began in 1986. In the last three decades, we have grown as a trusted name in the healthcare industry and rank as one of the top 10 Pharma Companies in the Indian Pharma Market (IPM) as per IQVIA MAT (November 2022). Our commitment to Lead Ahead has helped us move ranks from 16th position to 10th position (IPM) in the last four years. We are a fast-growing organisation with double-digit growth and significant market share in domestic markets. Currently, we rank among the top 5 in oncology, anti-allergy and gastrointestinal diseases and the top 10 in a few other therapy areas. Our focus is on leveraging our digital capabilities, collaborations, innovations and inorganic opportunities to become the top 5 companies in the Indian Pharma Market.
 
 
 
 
 
 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

Eurofins

<div>Company Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. 
Job Description 
Carry out dissolution and HPLC/UPLC methods. Carry out GC methods. Serve as Subject Matter Expert in lab area of dissolution.<ul><li>Perform daily laboratory duties to include preparing samples, performing analysis, calculating data, recording/reporting data, performing general housekeeping in alignment with 5S standards, and performing other duties as assigned.</li><li>Meet all quality and productivity metrics</li><li>Perform instrument calibration, maintenance, troubleshooting, recognize errors, identify root causes, and maintain excellent working knowledge of laboratory instrumentation.</li><li>Apply the highest quality standard in all areas of responsibility; maintain ISO 17025 quality standards and accreditation for the laboratory.</li><li>Review data, data notebooks, logbooks, and reports to ensure highest quality</li><li>Demonstrate strong client service skills</li><li>Proactively plan and maximize productivity</li><li>Demonstrate strong teamwork and collaboration</li><li>Implement operational improvements</li></ul>
Support and promote company policies and procedures 
Qualifications<ul><li> 
5+ years of relevant laboratory experience</li><li>Experience using Dissolution and/or HPLC, UPLC laboratory instrumentation</li><li>4-year degree in chemistry or related scientific discipline</li><li>Experience working within an established quality system (ISO 17025 preferred)</li><li>Understanding of production laboratory operations</li><li>Detailed-oriented with strong analytical and organizational skills.</li><li>Strong written, verbal and presentation skills along with demonstrated ability to collaborate with others.</li><li>Strong computer, scientific, and organizational skills</li><li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li></ul> 
Additional Information 
Position is full-time, Monday - Friday 1st Shift. with occasional overtime required. Candidates currently living within a commutable distance of Richmond, VA are encouraged to apply. 
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.</div>

GenScript

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

Analytical Associate Scientist/Scientist

JP Techno Park

<ul><li>JOB DESCRIPTION</li></ul>We are seeking a highly skilled Data Scientist along with strong Data Engineering expertise to join Advance Analytics and Modeling team. The ideal candidate will have a proven ability to work with diverse datasets, build machine learning models, and deploy scalable solutions. This role requires proficiency in Python, advanced analytical skills, and experience in developing machine learning models and dashboards in python. The candidate should have experience in deploying machine learning models in production using cloud platforms such as AWS or Azure and workflow orchestration tools like Airflow.Key Responsibilities:<ul><li>Develop and deploy machine learning models for classification, regression, and</li><li>clustering problems.</li><li>Perform statistical analysis to derive actionable insights from data.</li></ul><ul><li>Design and implement predictive analytics solutions to support business decision-</li></ul>making.Docker)translate them into analytical solutions.<ul><li>Design, build, and optimize data pipelines using Airflow.</li><li>Ensure data quality, integrity, and availability through robust ETL processes.</li><li>Work on model deployment using Python-based frameworks and containerization (e.g.,</li><li>Create interactive dashboards using Python libraries to visualize data and results.</li><li>Collaborate with cross functional teams to understand business requirements and</li></ul>Required Skills &amp; Expertise:Technical Skills:<ul><li>Proficiency in Python, advanced Python concepts (object-oriented programming,</li><li>multi-threading, etc.), SQL and Excel.</li><li>Hands-on experience with data visualization tools (e.g., Tableau, Power BI) is a</li></ul>plus.Analytics and Machine Learning:<ul><li>Strong analytical skills and experience in predictive modeling.</li><li>Hands-on experience with machine learning libraries like scikit-learn, TensorFlow</li><li>or PyTorch.</li><li>Ability to work with large datasets and extract meaningful insights to generate</li></ul>output<ul><li>Ability to work on ad-hoc requests to support business needs and derive</li></ul>actionable insightsData Visualization:Streamlit.<ul><li>Experience inn creating dashboards using Python libraries like Plotly, Dash, or</li></ul>Data Engineering:<ul><li>Knowledge of Airflow or similar workflow orchestration tools.</li><li>Expertise in ETL processes and pipeline automation.Model Deployment:</li><li>Familiarity with deploying machine learning models in production using Flask,</li><li>FastAPI, or similar frameworks.</li><li>Experience with containerization and orchestration tools (Docker, Kubernetes.)</li></ul>Tools and Platforms:<ul><li>Experience with version control tools like Git.</li><li>Familiarity with cloud platforms like AWS, Azure, or GCP is a plus.</li><li>Problem-Solving &amp; Communication: Strong problem-solving skills, with the ability to translate complex analytical findings into clear and actionable recommendations.</li><li>Excellent communication and presentation skills, with experience delivering</li><li>insights to senior stakeholders.Candidate Profile:</li><li>Educational Background: Bachelor&rsquo;s/Master&rsquo;s degree in Analytics, Data Science, Economics, Statistics, Engineering, or a related field.</li><li>Professional Experience: At least 5 years of experience in Data Science and Data</li></ul>Engineering.Job Type: Full-timePay: &#8377;1,500,000.00 - &#8377;1,800,000.00 per yearExperience:<ul><li>Data Scientist: 10 years (Required)</li><li>Python: 10 years (Required)</li><li>Analytical Data: 10 years (Required)</li><li>PySpark: 10 years (Required)</li><li>SQL: 10 years (Required)</li><li>Excel: 10 years (Required)</li><li>Data Visualization: 10 years (Required)</li><li>Insurance: 10 years (Required)</li><li>Tableau: 10 years (Required)</li><li>Power BI: 10 years (Required)</li><li>Data Engineering: 10 years (Required)</li><li>machine Learning: 10 years (Required)</li><li>ETL: 10 years (Required)</li><li>Automation: 10 years (Required)</li><li>Flask: 10 years (Required)</li></ul>Work Location: In person

Lead Analytical Data Scientist

NextGen Tides

<div>
 
 
 Company Description
 
 
 
 NextGen Tides is an innovative biotech startup focused on oligonucleotide and peptide synthesis, conjugation technologies, and next-gen modality services (ASO, siRNA, PMO, AOC, etc.). We are building a top-tier, flexible CRO/CDMO platform that enables discovery-to-preclinical workflows for pharma, biotech, and academic partners worldwide.
 
 
 
 
 
 POSITION SUMMARY:
 
 
 The Principal/Senior Scientist, Oligonucleotides will establish Analytical capability in
 
 
 separation science, and characterization within NextGen Tides&rsquo;s oligonucleotides
 
 
 platform supporting synthesis group and customer&rsquo;s requests. In this visible role, the
 
 
 candidate will be responsible for the Analytical and Purification method development of
 
 
 novel modified oligonucleotides multiple modalities including ASO, siRNA, PMO, and
 
 
 ligand-oligo-conjugation leveraging high-throughput automation and screening
 
 
 workflows. This individual will have direct experience with analysis, purification, and
 
 
 analytics of oligonucleotides and nucleoside analogs, as well as demonstrated ability to
 
 
 work as part of an integrated team on multiple projects.&nbsp;He/She will have in depth
 
 
 experience in the field of oligonucleotide/peptide therapeutics with knowledge in
 
 
 chemical structure search tools, purification instrumentation, and analysis methods
 
 
 related to chemically modified oligonucleotides. He/She will interact with all levels of the
 
 
 organization and take on substantial ownership within NextGen Tides&rsquo;s scientific
 
 
 function. The successful candidate will focus on Method Development and Analysis of
 
 
 oligonucleotides, and analytical characterization of multiple modalities. Leading through
 
 
 contributions at the bench, the selected candidate will serve as Lead Oligonucleotide
 
 
 Scientist for Analytical Team.
 
 
 &nbsp;
 
 
 Key Responsibilities
 
 <ul>
 <li>
 Serve as the Lead Oligonucleotide Scientist in cross-functional teams with
 </li>
 </ul>
 
 accountability for oligos purification and analytical analysis.
 
 <ul>
 <li>
 Take a leadership role in maintaining all aspects of analytical/ purification
 </li>
 </ul>
 
 instrumentation and operations in the oligonucleotide laboratory.
 
 <ul>
 <li>
 Develop and maintain standard operating procedures (SOPs) for processing,
 </li>
 </ul>
 
 purification, and analytical characterization to ensure high-quality and
 
 
 reproducible results.
 
 <ul>
 <li>
 Establish and maintain high-throughput automation workflows to support small
 </li>
 </ul>
 
 and mid-scale purification and analysis of ASOs, siRNA, PMO, and ligand-oligo-
 
 
 conjugation with routine and novel next generation amidite synthesis.
 
 <ul>
 <li>
 Establish and routinely perform oligos purification using &Auml;KTA and analytical
 </li>
 </ul>
 
 characterization workflows.
 
 <ul>
 <li>
 Troubleshoot, operate and oversee the interpretation of data from LC-MS as well
 </li>
 </ul>
 
 as analytical and preparative HPLC.
 
 <ul>
 <li>
 Work closely with synthesis and bioconjugation chemists to develop a seamless
 </li>
 </ul>
 
 workflow to support manufacturing of novel targeting ligands (e.g., peptide,
 
 
 antibody, etc).
 
 
 
 
 <ul>
 <li>
 With the growth of NextGen Tides, train and/or build a small team of research
 </li>
 </ul>
 
 associates to support oligos purification and analytical analysis capabilities.
 
 <ul>
 <li>
 supervise and/or lead associates in a cross functional team environment.
 </li>
 <li>
 Demonstrate excellent written and verbal communication skills.
 </li>
 <li>
 Convey novel innovations at the project team level.
 </li>
 </ul>
 
 
 
 
 Qualifications &amp;amp; Experience
 
 <ul>
 <li>
 A doctorate degree in Chemistry, Chemical Biology, Organic/Medicinal
 </li>
 </ul>
 
 Chemistry, or a related field.
 
 <ul>
 <li>
 A minimum of 3+ (Senior Scientist) or 6+ (Principal Scientist) years of firsthand
 </li>
 </ul>
 
 industry experience in modern synthetic chemistry methods particularly in
 
 
 nucleosides, nucleotides, and oligonucleotide synthesis, purification, and
 
 
 analysis in pharmaceutical or biotechnology settings.
 
 <ul>
 <li>
 Direct experience setting up and operating different instruments used in
 </li>
 </ul>
 
 oligonucleotides purification (e.g., &Auml;KTA Avant/Pure with Unicorn Software,
 
 
 tangential flow filtration), analysis (e.g., UPLC, LC/MS, LC/HRMS), and
 
 
 lyophilizes.
 
 <ul>
 <li>
 A dependable contributor to cross-functional teams who embrace a collaborative
 </li>
 </ul>
 
 culture while demonstrating the autonomy and initiative required to deliver on
 
 
 assigned scientific and operational responsibilities.
 
 <ul>
 <li>
 Demonstrated ability to troubleshoot instrumentation and complex scientific
 </li>
 </ul>
 
 problems and adapt to shifting priorities in a fast-paced, quality-driven
 
 
 environment.
 
 <ul>
 <li>
 Prior experience in discovery of therapeutic oligonucleotides is highly desirable.
 </li>
 </ul>
 
 
 
 
 
 Compensation&amp;Benefits
 
 
 <ul>
 <li>
 Competitive base salary + commission
 </li>
 <li>
 Equity incentives for high performers
 </li>
 <li>
 401(k) with employer contribution
 </li>
 <li>
 Health benefits and family medical coverage
 </li>
 <li>
 Vacation &amp; PTO policy
 </li>
 <li>
 Opportunities to grow into principle/VP
 </li>
 </ul>
</div>

Senior Scientist

United Pharma Technologies Inc

<div>
 
 
 Position:
 
 QC Scientist
 
 
 
 Location:
 
 Massachusetts (MA)
 
 
 
 
 
 
 Job Description
 
 
 
 We are seeking a QC Scientist to support analytical testing for monoclonal antibody (mAb) programs. The ideal candidate will be responsible for executing standardised assays, data interpretation, and maintaining high-quality lab practices in a GMP environment.
 
 
 
 
 
 
 Responsibilities
 
 
 <ul>
 <li>
 Perform standardised assays for monoclonal antibodies.
 </li>
 <li>
 Conduct UPLC and CE analyses, glycan analysis, titer, mAb, and peptide mapping.
 </li>
 <li>
 Schedule laboratory work, process analytical data, and interpret results accurately.
 </li>
 </ul>
 
 
 
 
 
 Requirements
 
 
 <ul>
 <li>
 Motivated self-starter with relevant technical laboratory experience.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Experience with Mass Spectrometry.
 </li>
 <li>
 Waters BioAccord experience is a strong plus.
 </li>
 </ul>
 
 
</div>

Quality Control Scientist

Kenvue

<div><div><div><div><div><div><div><div>Kenvue is currently recruiting for a:</div></div></div></div></div></div></div>
Scientist RMC Analytical
What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we&rsquo;re the house of iconic brands - including NEUTROGENA&reg;, AVEENO&reg;, TYLENOL&reg;, LISTERINE&reg;, JOHNSON&rsquo;S&reg; and BAND-AID&reg; that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage &ndash; and have brilliant opportunities waiting for you! Join us in shaping our future&ndash;and yours.
Role reports to:
Principal Scientist RMC Analytical
Location:
Asia Pacific, India, Maharashtra, Greater Mumbai
Work Location:
Fully Onsite
What you will do
Kenvue is currently recruiting for:
Scientist RMC Analytical - Mumbai
Who we are
At Kenvue, part of the Johnson &amp; Johnson Family of Companies, we believe there is extraordinary power in everyday care. Built on over a century of heritage and propelled forward by science, our iconic brands&mdash;including NEUTROGENA&reg;, AVEENO&reg;, TYLENOL&reg;, LISTERINE&reg;, JOHNSON&rsquo;S&reg; and BAND-AID&reg; &mdash;are category leaders trusted by millions of consumers who use our products to improve their daily lives. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers&rsquo; hearts and homes.
What will you do
Position Summary
Scientist RMC Analytical
Support Analytical Qualifications and Specification Management for Raw Materials:
<ul><li>Support Analytical (Raw Material testing &amp; Characterization) projects globally and ensure on time support to various projects in Cosmetic and OTC products.</li><li>
Support Analytical stability testing for qualification projects globally and ensure on time support to various projects in Cosmetic and OTC products.</li><li>
Responsible for the calibration and maintenance of in-house equipment&rsquo;s.
</li><li>Collaborate with external partners for outsourcing activities and ensure the compliance to applicable Kenvue standards</li><li>
Participate in discussions regarding analyzing and interpreting data, drawing conclusions, and arriving at timely technical decisions</li><li>
Responsible for compliance of EOHS &amp; Quality standards in lab</li></ul>
Major Duties &amp; Responsibilities
Tasks/Duties/Responsibilities<ul><li>
Coordination of Raw Material Analytical qualification projects to ensure timely support to internal stakeholders</li><li>
Participate in various meetings with internal and external stakeholders to shape/streamline the processes</li><li>
Participate in raw material related investigations as appropriate to support internal &amp; external manufacturing sites and investigate the OOS results during Analytical qualifications.</li><li>
Draft &amp; review of technical documents like qualification reports, stability reports, technical justifications, analytical method transfer etc.</li><li>
Training and Performance assessment of third-party resources</li><li>
Provide timely updates to reporting manager and provide insights on creating new opportunities for process improvements</li></ul>
Required Minimum Education:
 A minimum of a Master&rsquo;s degree in Analytical/Organic Chemistry or BPharm or MPharm from reputed university
Required Years of Related Experience: 2-5 years in FMCG/Pharma sector
Required Knowledge, Skills and Abilities:
(Include any required computer skills, certifications, licenses, languages, etc.)<ul><li>
Advanced understanding and application of principles, concepts, and practices of Analytical Chemistry is required.</li><li>
Adequate knowledge of GMP, quality systems, SOPs, Global &amp; Country specific Regulatory requirements</li><li>
Technical skills related to interpretation of analytical data and accurate documentation of laboratory investigations and non-conformances.</li><li>
Excellent communication, organizational, and interpersonal skills</li><li>
Experience in an GxP environment is mandatory.</li><li>
Ability to collaborate with internal and external resources to meet project objectives.</li><li>
Proven record of delivering project results</li><li>
Strong analytical and problem-solving skills</li><li>
Proficiency in Microsoft office tools</li></ul>
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.</div>

Scientist RMC Analytical

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