analytical research chemist

United Pharma Technologies Inc

<div>
 <p>
  <strong>
   Role:
  </strong>
  Analytical Chemist
 </p>
 <p>
  <strong>
   Location:
  </strong>
  Utah, USA
 </p>
 <p>
  <br/>
 </p>
 <p>
  Job Description
 </p>
 <p>
  We are seeking a skilled Analytical Chemist to support laboratory testing activities within a regulated pharmaceutical environment. The ideal candidate will have hands-on experience with analytical techniques, GMP documentation, and pharmaceutical testing to support product development, release, and stability programs.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Key Responsibilities
 </p>
 <ul>
  <li>
   Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products
  </li>
  <li>
   Execute testing using techniques such as HPLC, GC, UV-Vis, FTIR, Dissolution, Karl Fischer, and related methods
  </li>
  <li>
   Support method validation, verification, and transfer activities per ICH guidelines
  </li>
  <li>
   Conduct stability testing and maintain stability chambers as required
  </li>
  <li>
   Prepare, review, and maintain GMP-compliant documentation, including test results, protocols, and reports
  </li>
  <li>
   Investigate OOS, OOT, and deviations, and support CAPA activities
  </li>
  <li>
   Follow SOPs, cGMP, FDA, and data integrity requirements
  </li>
  <li>
   Maintain laboratory instruments, logs, and calibration records
  </li>
  <li>
   Support audits and inspections as needed
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Required Qualifications
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Chemistry, Analytical Chemistry, or related scientific discipline
  </li>
  <li>
   2&ndash;5+ years of experience in an analytical laboratory within the pharmaceutical or biotech industry
  </li>
  <li>
   Strong hands-on experience with HPLC (mandatory)
  </li>
  <li>
   Working knowledge of cGMP, GLP, USP, ICH, and FDA regulations
  </li>
  <li>
   Experience with laboratory documentation and electronic systems (LIMS preferred)
  </li>
  <li>
   Strong attention to detail and data integrity
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Preferred / Nice-to-Have
 </p>
 <ul>
  <li>
   Experience with method development and validation
  </li>
  <li>
   Exposure to stability programs
  </li>
  <li>
   Experience with LC-MS or GC-MS
  </li>
  <li>
   Familiarity with regulatory inspections and audits
  </li>
 </ul>
 <p>
 </p>
</div>


Analytical Chemist

Astrix

<div>
 <p>
  <strong>
   Summary:
  </strong>
 </p>
 <p>
  Our client who is a well respected and growing Specialty Chemical company is looking for a Chemist to perform quality control testing on materials and products within a regulated environment. This is a great opportunity for an experienced Chemist to continue their career in an independent lab based role.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Pay: Starting at $28.00/hr
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Conduct analytical testing per established procedures using laboratory instrumentation and wet chemistry methods.
  </li>
  <li>
   Calibrate, maintain, and verify readiness of laboratory equipment.
  </li>
  <li>
   Provide in-process testing support and ensure clear communication between shifts.
  </li>
  <li>
   Lead OOS investigations and follow up on corrective and preventive actions.
  </li>
  <li>
   Support method optimization, troubleshooting, and specification updates.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Chemistry or related field and 2+ years of laboratory experience.
  </li>
  <li>
   Familiarity with GMP regulations preferred
  </li>
  <li>
   Hands on experience with ONE of the following GC, GC-MS, HPLC, titrations, etc.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Schedule:
  </strong>
 </p>
 <p>
  12 hour schedule (Day and night shift available)
 </p>
 <p>
  <br/>
 </p>
 <p>
  This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
 </p>
 <p>
 </p>
</div>


Frost & Sullivan

<div>
 <p>
  <strong>
   <u>
    About the Role
   </u>
  </strong>
 </p>
 <p>
  Frost &amp; Sullivan is seeking candidates with skills and experience across these solutions, with specific interest in candidates who have applied these skills in one or more segments; e.g. Basic Chemicals, Petrochemicals, Specialty Chemicals, Plastics &amp; Composites, CASE and Construction materials etc.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Responsibilities
   </u>
  </strong>
 </p>
 <p>
  &Oslash; To undertake business-to-business research through telephone interviews and secondary search sources, analyze industry trends and data, and generate client focused reports, briefings, presentations and other project material.
 </p>
 <p>
  &Oslash; To produce high quality project outputs, including sizing markets, generating forecasts, competitive (market share) information and strategic recommendations for our clients.
 </p>
 <p>
  &Oslash; Participate and help in the preparation of consulting proposals for our clients active in the chemicals and materials markets.
 </p>
 <p>
  <strong>
   <u>
   </u>
  </strong>
 </p>
 <p>
  <strong>
   <u>
    Required Competencies
   </u>
  </strong>
 </p>
 <p>
  <strong>
   We&rsquo;re looking for candidates who -
  </strong>
 </p>
 <ul>
  <li>
   &Oslash; The successful candidate will be a Consulting professional with a thorough understanding of business research and consulting methodologies in the Chemicals &amp; Materials sector and proven success of direct client interaction.
  </li>
  <li>
   &Oslash; Strong verbal and written communication.
  </li>
  <li>
   &Oslash; Excellent troubleshooting skills.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualification and Experience
  </strong>
 </p>
 <ol>
  <li>
   &Oslash; A degree-level education or equivalent in Chemistry, Materials Science, Chemical Engineering, Environmental Science or another related discipline.
  </li>
  <li>
   &Oslash; Thorough understanding of research methodologies and/or strategic marketing.
  </li>
  <li>
   &Oslash; Fluency in the written and spoken English language.
  </li>
  <li>
   &Oslash; Ability to forge close working relationships with a commercial acumen and analytical mind.
  </li>
  <li>
   &Oslash; The ability to work autonomously and also effectively in a team environment.
  </li>
  <li>
   &Oslash; A minimum of 3 years in fact-based consulting/market research with a focus on complex ad-hoc studies
  </li>
  <li>
   &Oslash; Consultative thinking, focus on delivering the story, not just the data
  </li>
  <li>
   &Oslash; Strong analytical skills with a sound understanding of and passion for research and consulting
  </li>
  <li>
   &Oslash; Intercultural competence and experience in working closely with teams in a global matrix organisation
  </li>
  <li>
   &Oslash; Proactive thinking
  </li>
  <li>
   &Oslash; Organized, outgoing, and capable of delivering tangible results in a fast-paced and creative environment
  </li>
  <li>
   &Oslash; Attentive to details and showing strategic insights in the delivery of research findings
  </li>
  <li>
   &Oslash; Excellent MS Office and MS Powerpoint skills
  </li>
  <li>
   &Oslash; Data visualization experience like Power BI/Tableau is preferred
  </li>
 </ol>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    What will make you succeed at Frost &amp; Sullivan?..
   </u>
  </strong>
 </p>
 <p>
  <strong>
   You need to be-
  </strong>
 </p>
 <ul>
  <li>
   Wildly curious and entrepreneurial
  </li>
  <li>
   Committed to customer success
  </li>
  <li>
   A self-starter invested in your future
  </li>
  <li>
   A persuasive communicator
  </li>
  <li>
   Deeply Analytical
  </li>
  <li>
   Excited about Disruptive Trends
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Benefits
   </u>
  </strong>
 </p>
 <ul>
  <li>
   A friendly work environment with an &lsquo;open door&rsquo; policy
  </li>
  <li>
   A strong career path with growth opportunities.
  </li>
  <li>
   Be part of a global team that strives for excellence, and fosters an Olympic spirit
  </li>
  <li>
   Feed your intellectual curiosity by collaborating across all levels of the company across the globe
  </li>
  <li>
   Global Recognition - President&rsquo;s Club &amp; Chairman&rsquo;s Club Awards
  </li>
  <li>
   Continuous learning and coaching
  </li>
  <li>
   Flexible work policy
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About Frost &amp; Sullivan
  </strong>
 </p>
 <p>
  Frost &amp; Sullivan, the Transformational Growth Journey Company, has spent more than 60 years partnering with clients to develop transformational growth strategies by focusing on innovation and growth opportunities driven by disruptive technologies, mega trends, emerging markets and new business models. Today, more than ever before, companies must innovate, not only to survive, but thrive in the future. Our Growth Pipeline Management (GPM) system supports clients by identifying and evaluating new growth opportunities and serves as the foundation for continuous growth. This is your opportunity to be part of a revolutionary global team that truly inspires positive global changes by innovating to zero. Learn more about Frost &amp; Sullivan at www.frost.com
 </p>
 <p>
  <br/>
 </p>
 <p>
  <em>
   Frost &amp; Sullivan is committed to a work environment free of all forms of discrimination. Frost &amp; Sullivan recruits and hires without regard to race, color, religion, gender, marital status, age, disability, national origin, veteran status, or sexual orientation
  </em>
 </p>
 <p>
  <em>
   e to overwhelming responses, only short-listed candidates will be
  </em>
 </p>
</div>


Consulting Analyst - Chemicals & Materials

Kenvue

<div><div><div><div><div><div><div><div><p>Kenvue is currently recruiting for a:</p></div></div></div></div></div></div></div>
Scientist Analytical Chemistry<p></p><p><b>
What we do</b></p><p>
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.</p><p></p><p><b>
Who We Are</b></p><p>
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.</p><p></p><p><b>
Role reports to:</b></p>
MANAGER R&amp;D<p></p><p><b>
Location:</b></p>
Asia Pacific, India, Maharashtra, Greater Mumbai<p></p><p><b>
Work Location:</b></p>
Fully Onsite<p></p><p><b>
What you will do</b></p><p>
Kenvue is currently recruiting for:</p><p><br>
</p><p><b>Scientist, R&amp;D Analytical</b></p><p>
This position reports into Principal Scientist, R&amp;D Analytical and is based at Mumbai, India</p><p></p><p><b>
Who we are</b></p><p>
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. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of 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.</p><p><br>
</p><p><b>Role reports to:</b> Principal Scientist, R&amp;D Analytical</p><p><b>
Location:</b> Mumbai</p><p></p><p><b>
What you will do</b></p><p>
The Scientist, R&amp;D Analytical is responsible for performing analytical and stability testing, conducting advanced research activities and utilizing technology and programs to enable Innovation projects:</p><p>
Key Responsibilities</p><ul><li>
Lead and manage analytical research projects in R&amp;D department</li><li>
Develop, optimize, validate and transfer analytical methods to support product development and life cycle management projects</li><li>
Execute developmental stability testing for Drug and Cosmetic products</li><li>
Collaborate with cross-functional teams to drive scientific advancements</li><li>
Provide technical expertise in analytical instrumentation and data analysis</li><li>
Ensure expertise in a wide range of analytical technologies and instrumentation for testing capabilities.</li><li>
Execute the assigned stability testing for shelf-life assessment of stability studies.</li><li>
Participate in method transfer process regarding testing activities.</li><li>
Work on specific research projects, if required.</li><li>
Stay current with industry trends and technologies to drive innovation</li><li>
Support process owners or subject matter experts for assigned responsibilities, critical laboratory processes and quality systems.</li></ul><p></p><p><b>
What we are looking for</b></p><p></p><p>
Required Qualifications</p><ul><li>
Minimum Masters in Chemistry or equivalent science (e.g. Biochemistry, Pharmaceutical Sciences) or Ph.D with 4-8 years of proven working experience in Analytical Chemistry and/or Medicinal chemistry, Quality Control or related functions in healthcare/pharma/FMCG sector with exposure to GMP and Quality environment preferred</li><li>
Proven track record of leading successful scientific projects</li><li>
Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health or Pharmaceutical environment</li><li>
Strong knowledge in UPLC, HPLC, and GC to execute Analytical test method development, validation and optimization in a cGMP environment</li><li>
Solid understanding of analytical and physical testing capabilities, technical skills related to instrumentation principles and working, basic troubleshooting, good documentation practices, data integrity aspects, etc.</li><li>
Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment</li><li>
Excellent communication and collaboration skills</li><li>
Strong experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems.</li><li>
Ability to grasp technical/compliance requirements and execute assigned work to meet the key performance indicators</li><li>
Excellent oral and written communication and articulation skills</li><li>
Challenges the status quo and brings innovative ideas and suggestions</li><li>
Displays technical curiosity and self-initiative to deliver beyond usual activities</li><li>
Good interpersonal skills to partner across functions, sites, and regions</li></ul><p></p><p>
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 identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.</p><p></p><p>
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.</p></div>

Scientist Analytical Chemistry

Dr. Reddy's Laboratories

<div>
 <p>
  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
  <strong>
   Good Health Can&rsquo;t Wait
  </strong>
  .
  <br/>
  <br/>
 </p>
 <p>
  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.
  <br/>
  <br/>
 </p>
 <p>
  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).
  <br/>
  <br/>
 </p>
 <p>
  &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
  <br/>
  <br/>
 </p>
 <p>
  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.
  <br/>
  <br/>
  <br/>
  <br/>
 </p>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <p>
  <strong>
   Job Summary
   <br/>
  </strong>
  <br/>
  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.
  <br/>
  <br/>
  <br/>
  <br/>
  <strong>
   Roles &amp; Responsibilities
   <br/>
   <br/>
  </strong>
 </p>
 <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.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <p>
  <strong>
   Educational qualification:
  </strong>
  Masters in Science/ Organic chemistry/ Pharmaceutical Sciences
  <br/>
  <br/>
  <br/>
  <br/>
  <strong>
   Minimum work experience:
  </strong>
  5 years of experience in analytical method development
  <br/>
  <br/>
  <br/>
  <br/>
  <strong>
   Skills &amp; attributes:
   <br/>
  </strong>
  <br/>
  <strong>
   Technical Skills
   <br/>
   <br/>
  </strong>
 </p>
 <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>
 <p>
  <strong>
   Behavioral Skills
   <br/>
   <br/>
  </strong>
 </p>
 <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.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 <p>
  <strong>
   About the Department
   <br/>
   <br/>
  </strong>
 </p>
 <p>
  <strong>
   Integrated Product Development Organisation
   <br/>
   <br/>
  </strong>
 </p>
 <p>
  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
  <br/>
  <br/>
  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.
  <br/>
  <br/>
  <br/>
  <br/>
  <strong>
   Benefits Offered
   <br/>
  </strong>
  <br/>
  At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
  <br/>
  <br/>
  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.
  <br/>
  <br/>
  <br/>
  <br/>
  <strong>
   Our Work Culture
   <br/>
  </strong>
  <br/>
  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.
  <br/>
  <br/>
  For more details, please visit our career website at
  <strong>
   https://careers.drreddys.com/#!/
  </strong>
 </p>
</div>


Analytical Scientist Injectable

PI Industries Ltd.

<div><div><div><div><div><h2 class="jobSectionHeader"><b>Position Description</b></h2>
</div><div><div>
<div><div><div><div><b>Business Division:</b></div>
<b>R&amp;D
</b></div><div><div><b>Department:
</b></div><b>Analytical</b></div>
<div><h1 class="jobSectionHeader"><b>Location:
</b></h1><b>UDAIPUR</b></div><br>
</div><br>
<div><div><div><b>Position Title:</b></div>
<b>Research Scientist - Analytical</b></div>
<div><div><b>Reporting to (Title):</b></div>
<b>Group Leader</b></div>
<div><div><b>Level:</b></div>
<b>E2- E4</b></div><br>
</div><br>
</div></div></div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Position Purpose</b></h2>
</div><div><ul><li>The Position will be responsible for assisting in analytical method development of assigned project within given timeframe as per Safety and Environmental rules.</li>
<li>Raw materials and finished products analysis. Generating COA and compiling documents. Proactiveness to trouble shoot any complexity during analysis
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Strategic Responsibilities</b></h2>
</div><div><ul><li>To understand the analytical scope of the project assigned.</li>
<li>Inputs in planning of analytical support to R&amp;D and Plant</li>
<li>Timely calibration of assigned instruments</li>
<li>Proper house- keeping and use of PPE&rsquo;s.
</li><li>Use relevant MSDS for safe handling and disposals of toxic chemicals</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Operational Responsibilities</b></h2>
</div><div><ul><li>Assist in analytical method development as per planning.</li>
<li>Co-ordination with R&amp;D for analytical support / development</li>
<li>Authenticity of the result generated.
</li><li>Troubleshooting
</li><li>Data interpretation skills</li>
<li>Analytical Support to kilo lab/pilot plant/manufacturing site during technology transfer</li>
<li>Data compilation and time to time update of KL/ PP plant trials</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Financial Responsibilities</b></h2>
</div><div><ul><li>Contribute to budgetary controls within the area of responsibility.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>People Responsibilities</b></h2>
</div><div><ul><li>Utilization of all available sources for skill up-gradation
</li><li>Actively participation in problem solving sessions/ training programs
</li><li>Coordination and communication with team</li>
<li>To guide subordinates
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Education Qualification</b></h2>
</div><div><div>
Master in Organic Chemistry from a reputed University / Institute</div><br>
</div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Work Experience</b></h2>
</div><div><div>
1-5 year experience</div>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Industry to be Hired from</b></h2>
</div><div><div>
Agro chemicals/fine chemicals/ pharma-API/ Specialty chemicals</div>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Functional Competencies</b></h2>
</div><ul><li>Knowledge of Processes related to EHS
</li><li>Scientific Knowledge_O
</li><li>Data Analysis
</li><li>Compliance &amp; Regulatory Knowledge
</li></ul></div><div><div><h2 class="jobSectionHeader"><b>Interaction Complexity and Team Work</b></h2>
</div><div><div>
<div></div><div><div><div>Contact Person (mention the level/position that the position-holder will interact with)</div> <div>Frequency</div> <div>Nature of Interaction</div><br>
</div><br>
<div></div><div><div>Peer(s):Head of Analytical or Executive in the same or other plant</div> <div>As &amp; when required</div> <div>Telephonic or face to</div><br>
</div><br>
<div></div><div><div>Customer(s): Internal Heads &amp; Managers of other department</div> <div>As &amp; when required</div> <div>face</div>
</div><br>
<div><div>Vendor(s):Not applicable</div> <div>As &amp; when required</div> <div>Telephonic or face to</div><br>
</div><br>
<div></div><div><div>Any other external interactions: GPCB/AEPS</div></div></div></div></div></div></div></div></div><div></div>

Research Scientist - Analytical, PR&D

Eurofins BioPharma Product Testing North America

<div>
 <p>
  <strong>
   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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
   <br/>
   <br/>
  </strong>
 </p>
 <p>
  <strong>
   The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
   <br/>
   <br/>
  </strong>
 </p>
 <p>
  <strong>
   In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
   <br/>
   <br/>
  </strong>
 </p>
 <p>
  <strong>
   In 2024, Eurofins generated total revenues of EUR &euro; 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
   <br/>
   <br/>
  </strong>
 </p>
 <p>
  <br/>
  <br/>
  <br/>
  <br/>
 </p>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products
  </li>
  <li>
   Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus
  </li>
  <li>
   Executing method transfer protocols
  </li>
  <li>
   Performing monthly maintenance of laboratory equipment
  </li>
  <li>
   Working efficiently, documenting work clearly, and performing tests accurately
  </li>
  <li>
   Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
  </li>
  <li>
   Reads and understands analytical procedures (compendial and client supplied) and internal SOPs
  </li>
  <li>
   Processes data, generates reports, and evaluates data
  </li>
  <li>
   Trains others in laboratory procedures
  </li>
  <li>
   Performs laboratory maintenance
  </li>
  <li>
   Communicates with vendors and repair personnel
  </li>
  <li>
   Writes investigations
  </li>
  <li>
   Leads project/test areas and perform method transfers/feasibility studies
  </li>
  <li>
   Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <p>
  <strong>
   The Ideal Candidate would possess:
   <br/>
   <br/>
  </strong>
 </p>
 <ul>
  <li>
   Good dexterity; positive attitude; solution driven
  </li>
  <li>
   Due to the size of the site, employees are required to flex into positions and activities outside their normally assigned duties as workload requires and as trained. These activities require working in all departments including QA, microbiology, chemistry, and general support for laboratory operations
  </li>
  <li>
   Conducts all activities in a safe and efficient manner
  </li>
  <li>
   Performs other duties as assigned
  </li>
  <li>
   Strong computer, scientific, and organizational skills
  </li>
  <li>
   Excellent communication (oral and written) and attention to detail
  </li>
  <li>
   Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  </li>
  <li>
   Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  </li>
 </ul>
 <p>
  <strong>
   Minimum Qualifications:
   <br/>
   <br/>
  </strong>
 </p>
 <ul>
  <li>
   Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
  </li>
  <li>
   1-2 years of previous laboratory experience
  </li>
  <li>
   Authorization to work in the United States indefinitely without restriction or sponsorship.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Additional Information
   <br/>
   <br/>
  </strong>
 </strong>
 <p>
  Position is full-time position, Monday - Thursday 8:00am - 6:00pm, 4*10 schedule.  Candidates currently living within a commutable distance of Portage, MI are encouraged to apply.
  <br/>
  <br/>
 </p>
 <ul>
  <li>
   Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  </li>
  <li>
   Life and disability insurance
  </li>
  <li>
   401(k) with company match
  </li>
  <li>
   Paid vacation and holidays
  </li>
 </ul>
 <p>
  <strong>
   Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
   <br/>
   <br/>
  </strong>
 </p>
</div>


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