product manager

business development and application scientist Jobs in Hyderabad

business development and application scientist

formulation development scientist Jobs in Hyderabad

formulation development scientist

formulation scientist

pricing scientist

product development scientist

DFE Pharma

<div>
 
 Did you know that you already know us? Almost every second tablet which is on the global market contains our products. This demands great entrepreneurial power so that we are always looking for people who take ownership and are not afraid of accountability.
 
 
 Now it is your chance to join!
 
 
 
 
 
 We are looking for laboratory based Formulation Scientist(s) with a solid pharmaceutical formulation background (API and excipients) to advise our customers on their formulation challenges. In this role you will formulate final dosage forms for customers with actual or model APIs to support them in their development programs. As part of a team of Formulation Scientists and with our Technical Managers in the market, you will translate customer formulation challenges into mechanistic based formulation protocols, execute the experiments, and report the results for sharing with the customer. You will be working in a new high end Technical Center of Excellence in Hyderabad, India. Do you have this combination of good pharmaceutical formulation knowledge and a drive to deliver relevant solutions for DFE Pharma&rsquo;s customers?
 
 
 
 
 
 
 What we ask
 
 
 <ul>
 <li>
 Experience in developing formulations for the regulated market, with a focus on oral solid dosage forms (like Tablets, Capsules, Granules, Powders, pellets etc.) showcasing strong pharmaceutical formulation development skills.
 </li>
 <li>
 A hands-on experience of handling equipments associated with OSD manufacturing is mandatory.
 </li>
 <li>
 Deriving product development strategy or customer solution based on targeted literature searches, including patent search is desirable.
 </li>
 <li>
 Having a good working knowledge of pharmaceutical process steps (Direct Compression, Wet Granulation, Dry granulation &amp; Wurster coating) and equipment to formulate oral solid dosage forms and execute relevant laboratory experiments.
 </li>
 <li>
 Scale up, Exhibit batches and technology transfer experience is mandatory.
 </li>
 <li>
 Ability to prepare consultative / mechanistic (powder technology) based formulation protocols. Knowledge of various excipients, their role in formulations, usage concentrations etc is a must.
 </li>
 <li>
 Review test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals.
 </li>
 <li>
 Prepare/review master formulas, manufacturing procedures, SOPs, stability protocols/reports, Product Development Reports, QOS, QbR and other CMC documents for regulatory filings.
 </li>
 <li>
 Independent product development and stakeholder management skills to build strong connections with your team, the Technical Managers, and the Innovation &amp; Technical Solutions (ITS) team.
 </li>
 <li>
 Provide recommendations for continuous improvements in practices and systems to improve performance and enhance efficiency and quality.
 </li>
 <li>
 Striving for excellence in everything you do.
 </li>
 <li>
 Stakeholder management skills to build strong connections with colleagues in the team.
 </li>
 <li>
 High proficiency in English (spoken and written).
 </li>
 <li>
 Education qualification: M. Pharm or Ph.D.
 </li>
 <li>
 Min. 8 years of recent technical experience in the pharmaceutical industry, in formulation development of oral solid dosage forms.
 </li>
 </ul>
 
 
 
 
 
 What we offer
 
 
 <ul>
 <li>
 A very international work environment
 </li>
 <li>
 Working in a new high end laboratory facility in Hyderabad, India
 </li>
 <li>
 Continuous learning and development; your development is not only good for your career; we also benefit from it.
 </li>
 <li>
 Excellent remuneration package
 </li>
 <li>
 Short communication and short decision lines
 </li>
 </ul>
 
 
 
 
 
 Vacancy description
 
 
 <ul>
 <li>
 Translate the customer requirements into a solution/recommendation using a Design of Experiments (DoE) approach.
 </li>
 <li>
 Write the required protocols with agreed timelines &amp; outputs (what feasible, what not)
 </li>
 <li>
 Perform experiments with your colleagues in the formulation team and work out the solution within agreed timelines &amp; resources.
 </li>
 <li>
 Interact with internal stakeholders in a multidisciplinary &amp; multicultural set up.
 </li>
 <li>
 Write the required protocols with agreed timelines and outputs (what feasible, what not)
 </li>
 <li>
 Translate the experiment results into reports / presentations.
 </li>
 </ul>
 
 
 
 
 
 Team details
 
 
 <ul>
 <li>
 You will be part of a Formulation team.
 </li>
 <li>
 The formulation team, along with Analytical team, forms our newly established Technical Centre Excellence, led by the CoE Manager and Director.
 </li>
 <li>
 The Technical Centre of Excellence is part of the wider Innovation &amp; Technical Solutions Department of DFE Pharma.
 </li>
 </ul>
</div>

Formulation Development Scientist

Suzhou Nanomicro Tech India

<div>
 
 Nano Micro is a technology startup recognized globally for its leadership in producing spherical, monodisperse particles through proprietary manufacturing processes. These methods enable high-yield, cost-effective production across diverse industries and applications. Meeting purification needs from laboratory to manufacturing scale in both small molecule pharmaceuticals and biopharmaceuticals requires ongoing integration of advancements in chromatography and resin technology, as well as adept management of continually evolving business and scientific challenges.
 
 
 
 
 
 Nano Micro swiftly established itself as an OEM supplier for chromatography vendors worldwide, supporting pharmaceutical and biopharmaceutical purification under various brands. The company has since introduced its own brand internationally, with a strategic focus on India, where it has made considerable market advances and successfully expanded operations within major accounts. This is perfect time a larger team dedicated to increasing market share by penetrating and ramp up volumes within all areas of biopharmaceutical purification.&nbsp;
 
 
 
 Opportunities at Nano Micro
 
 
 
 Nano Micro welcomes candidates from a broad range of disciplines, including sales, business development, and scientific research mainly focusing on application support and scaling up in biopharmaceutical space.
 
 
 
 Commitment to Continuous Improvement
 
 
 
 At Nano Micro, employees are encouraged to seek innovative approaches and embrace new working methods, ensuring continuous advancement for colleagues, clients, and partners.
 
 
 
 Collaborative Environment
 
 
 
 Our workplace fosters cooperation and mutual respect, with a strong emphasis on diversity and inclusivity.
 
 
 
 Professional Development
 
 
 
 Nano Micro prioritizes employee growth by supporting professional development and skill enhancement and provides opportunities throughout the organization. We recognize that learning from setbacks is intrinsic to progress and actively encourage staff to engage in new experiences beyond conventional roles.
 
 
 At Nano Micro, business growth and career development are aligned as employees work to deliver effective resin solutions in all application areas. The company offers competitive pay, performance-based bonuses, and comprehensive benefits in line with startup industry standards.
 
 
 
 
 
 
 NanoMicro &ndash; Career Opportunities
 
 
 
 
 About Us
 
 
 
 NanoMicro is a global startup pioneering&nbsp;
 
 monodisperse chromatography resins
 
 &nbsp;for scalable purification of&nbsp;
 
 peptides, proteins, oligonucleotides, vaccines, and plasma proteins
 
 . With strong OEM partnerships and growing operations in India, we&rsquo;re expanding our team to drive innovation in biopharma purification.
 
 
 
 
 
 
 Open Positions: 2-8years Experience; Location: Ahmedabad, Bangalore and Hyderabad
 
 
 
 
 1. Business Development&nbsp;
 
 
 
 Drive customer engagement and growth in the biopharma market.
 
 
 
 Requirements:
 
 &nbsp;Master&rsquo;s in Life Sciences, experience in BD/technical sales, knowledge of upstream/downstream processes, strong communication, and travel readiness.
 
 
 
 2. Application Scientist&nbsp;
 
 
 
 Support chromatography applications, demos, and training for biopharma customers.
 
 
 
 Requirements:
 
 &nbsp;Master&rsquo;s in Chemistry/life sciences/biopharma, 2-8 years academic or industry experience, strong presentation skills, and 40% travel.
 
 
 
 
 
 Please send your resume to kaushik@nanomicrotech.com
 
</div>

Business Development and Application scientist

Advance Auto Parts

<div>
 
 Job Description
 
 
 
 
 Pricing Scientist
 
 
 
 
 About Advance Auto Parts
 
 
 
 Founded in Roanoke, VA in 1932, Advance Auto Parts is a leading automotive aftermarket retail parts provider that serves both professional installer and do-it-yourself Customers. As of July 13, 2019, Advance operated 4,912 stores and 150 Worldpac branches in the United States, Canada, Puerto Rico, and the U.S. Virgin Islands. The Company also serves 1,250 independently owned CARQUEST branded stores across these locations in addition to Mexico, the Bahamas, Turks, and Caicos and the British Virgin Islands. The company has a workforce of over 70,000 knowledgeable and experienced Team Members who are proud to provide outstanding service to their Customers, Communities, and each other every day.
 
 
 
 About Aap Global Capability Center
 
 
 
 We are continually innovating and seeking to elevate the Customer experience at each of our stores. For an organization of our size and reach, today, it has become more critical than ever, to identify synergies and build shared capabilities. The AAP Global Capability Center, located in Hyderabad, is a step in this strategic direction that enables us to access a larger talent pool, unlock operational efficiencies and increase levels of collaboration.
 
 
 
 About Pricing Team
 
 
 
 The Pricing team is growing its presence in India to help expand our technical, brand, and analytical capabilities across the enterprise. This is a fantastic opportunity to join a team of highly specialized and focused individuals dedicated to driving our brand marketing and eCommerce outcomes in a collaborative environment.
 
 
 Join the Pricing team and start reimagining the future of automotive retail. Disrupt the way consumers buy Auto Parts and join a fast-growing eCommerce team to take on the industry&rsquo;s biggest challenges.
 
 
 The focus here is on our customers -- how we make them happy, earn their trust, and create loyalty. We want to expand our best in class data science capability to predict consumer behavior and ensure we are getting the right return on our investments. Ultimately, the Pricing team is responsible for rapidly developing and deploying solutions that will drive the customer experience and, ultimately, enhance our bottom line as an organization.
 
 
 
 Roles And Responsibilities
 
 
 
 <ul>
 <li>
 Independently develop Analytics solutions / predictive model for pricing and promotions e.g. promotions forecasting, price elasticity models, customer segmentation, discount optimization.
 </li>
 <li>
 Perform statistical analysis for hypothesis testing e.g. A/B testing to predict the impact of pricing changes on test skus/regions.
 </li>
 <li>
 Collaborate with the pricing strategy and insights team to conceptualize and develop the prototype of analytics solutions and partner with Enterprise Data Engineering / Data science teams to scale up and deploy the solutions for enabling optimized pricing decisions
 </li>
 <li>
 Involve in discussions with stakeholders and gather requirements showcasing the analysis, interpretations &amp; findings and scale the solutions to next level
 </li>
 <li>
 Bring in the thought process and independently involve in designing the approach, test and build the algorithm framework, and implement models
 </li>
 <li>
 Forecasting of demand drivers using Structural Time Series and Na&iuml;ve Bayes approach and also by analyzing the impact of micro-economics factors on category/region performance
 </li>
 <li>
 Build intelligent systems to capture and model the vast amount of behavior data to enrich the content understanding with behavioral information for promotional strategies
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 <ul>
 <li>
 4 to 8 years of relevant experience as Sr. data scientist or pricing scientist in retail/ecom analytics in similar industry and business function.
 </li>
 <li>
 Masters/PhD in management science, data science, economics, mathematics from reputed institutes is a must.
 </li>
 <li>
 Should have strong fundamental understanding of price elasticity, price-demand curves, econometrics and optimizations techniques.
 </li>
 <li>
 Strong applied knowledge of machine learning covering the landscape of classification, regression and with in-depth interpretation of outcomes for pricing and promotions
 </li>
 <li>
 Advance level proficiency in python/R, PowerBI, Snowflake/SQL and cloud technologies
 </li>
 <li>
 Ability to effectively communicate and explain the analytical model approach and output with the business stakeholders
 </li>
 <li>
 Experience of developing a powerful storyline to provide meaningful insights for senior leadership consumption
 </li>
 <li>
 Applicants should have strong fundamental understanding and research experience in Data Wrangling, Statistical Analysis, Predictive Modeling using Machine Learning (Regression and Classification), Clusters Segmentation, Time Series Forecasting (ARIMA, SARIMAX) etc.
 
 
 </li>
 </ul>
 
 California Residents Click Below For Privacy Notice
 
 
 
 https://jobs.advanceautoparts.com/us/en/disclosures
 
 
 We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age national origin, religion, sexual orientation, gender identity, status as a veteran and basis of disability or any other federal, state or local protected class.
</div>

Pricing 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 dynamic and experienced Scientist in Process Engineering in Active Pharmaceutical Ingredient (API) development with proven expertise in scaling up or down technologies to meet production demands. Proficient in Process and Chemical Engineering, adept at troubleshooting complex projects, facilitating technology transfer, and optimizing operations.
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 
 <ul>
 <li>
 You will be responsible to review of journals and patents.
 </li>
 <li>
 You will be responsible for feasibility study of the Process, Process Optimization, Lab Validations, Technology Transfer to plant and identify and evaluate the reaction parameters
 </li>
 <li>
 You will be responsible for staying up to date with relevant scientific and technical developments. Execute experiments efficiently with high reproducibility.
 </li>
 <li>
 You will be responsible for interpretation of analytical and spectral data to ensure quality and regulatory compliance.
 </li>
 <li>
 You will be responsible to write technical development reports, Quality by Design (QbD) reports, justification reports and Drug Master Filing (DMF) filing related documents.
 </li>
 <li>
 You will be responsible to provide support in scale up batches execution and ensure process reproducibility at scale.
 </li>
 <li>
 You will be responsible for ensuring lab safety and process safety.
 </li>
 </ul>
 
 Qualifications
 
 Educational qualification:
 
 M.Sc/ M.Pharma
 
 
 
 
 
 Minimum work experience:
 
 3-5 years of Experience in API Manufacturing
 
 
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 M.Sc/B.Tech/M.Tech
 
 
 
 
 
 Minimum work experience:
 
 3-5 years of Experience in API Manufacturing
 
 
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 
 <ul>
 <li>
 Have work experience on Process scale up of Active Pharmaceutical Ingredients.
 </li>
 <li>
 Experience in Process Optimization (Manufacturing)
 </li>
 <li>
 Experience in Process Intensification
 </li>
 <li>
 Experience in Operational Excellence
 </li>
 <li>
 Experience in Chemical Process Engineering
 </li>
 <li>
 Experience in Technology Transfer
 </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>

Process R&D Scientist

Sandoz India Pvt Ltd

<div>
 
 Job Description
 
 
 
 
 Your Key Responsibilities:
 
 
 
 
 Your Responsibilities Include, But Not Limited To
 
 
 
 <ul>
 <li>
 Independently plan, organize, perform and document scientific experiments /GMP testing /manufacturing plant activities under minimal supervision; handle several activities at a time
 </li>
 <li>
 -Take over responsibility for and utilize special tools /equipment or specialized facilities as an expert; schedule and perform maintenance and qualification of instruments / equipment -Proactively identify conflict situations and contribute to solutions
 </li>
 <li>
 -Work according to appropriate standards for quality, ethics, health, safety, environment protection, and information security; lead initiatives to ensure continuous improvement. Documentation of raw data, evaluate and interpret results; propose and actively support the design of next experiments.
 </li>
 <li>
 Review and verify raw data generated by others; approval of tests / experiments performed by others. Write protocols, scientific reports or lab procedures based on templates or SOPs under minimal supervision. For technical development units: Develop new methods or optimize existing methods/processes (lab or plant); contribute to development and implementation of new technologies
 </li>
 <li>
 -For GMP units: ensure compliance to cGMP -For technology-focused roles: Perform information and literature searches under minimal guidance. Actively foster knowledge exchange.
 </li>
 <li>
 Train and coach associate scientists, technicians, temporary employees and employees under training / education -For project-focused role: Participate in function-specific sub teams and fulfill assigned project tasks and responsibilities under supervision -Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.
 </li>
 <li>
 Contributes to some cost center goals and objectives -Design, plan and perform / supervise scientific experiments and contribute to project related scientific /technical activities under minimal supervision (e.g., interpret and report results, generate and evaluate data, draw relevant conclusions, optimize existing methods / processes).
 </li>
 <li>
 Establish innovative solutions for verification and control of critical quality attributes, critical material attributes or critical process parameter in cooperation with other colleagues. Establish control procedures and specifications and review test procedures. Generate scientific documents to hand over to internal and / or external partners (e.g., MST, TechOps, authorities, external companies) and support generation of international registration documents under minimal supervision.
 </li>
 <li>
 If assigned this task, maintenance of infrastructure / equipment and required investments (e.g. system ownership) -Generate lab procedures or SOP&rsquo;s, generate protocols and reports -Lead technical meetings during product development at the local level as well as on the level of SDC network -Report and present scientific /technical results internally and contribute to publications, presentations and patents.
 
 
 </li>
 </ul>
 
 Essential Requirements
 
 
 
 What you&rsquo;ll bring to the role:
 
 
 <ul>
 <li>
 M Pharm with 2-5 years' experience or PhD with 1-3 years' experience
 </li>
 <li>
 Functional Breadth.
 </li>
 <li>
 Operations Management and Execution.
 </li>
 <li>
 Collaborating across boundaries.
 
 
 </li>
 </ul>
 
 Skills
 
 
 
 <ul>
 <li>
 Environment.
 </li>
 <li>
 Experiments Design.
 </li>
 <li>
 Health And Safety (Ehs).
 </li>
 <li>
 Laboratory Equipment.
 </li>
 <li>
 Manufacturing Process.
 </li>
 <li>
 Materials Science.
 </li>
 <li>
 Process Simulation.
 </li>
 <li>
 Project Management.
 </li>
 <li>
 Sop (Standard Operating Procedure).
 </li>
 <li>
 Technical Writing.
 
 
 </li>
 </ul>
 Why Sandoz?
 
 
 Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!
 
 
 With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
 
 
 Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!
 
 
 Join us!
</div>

Scientist - Pharmaceutical Development

Eli Lilly and Company

<div>
 At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
 
 
 The Position Of Principal Technical Services Rep - APIEM Reports To The TSMS Director &ndash; Peptides API EM And Provides Technical Leadership And Expertise In Conjunction With API EM Contract Manufacturer Personnel In The Reliable Supply And Commercialization Of Medicines With Safety First And Quality Always By
 
 
 <ul>
 <li>
 Developing and sustaining process knowledge in order to ensure the execution of the appropriate product, process, and operational control strategy at the Contract Manufacturer (CM).
 </li>
 <li>
 Direct and Indirect interaction with CM personnel to ensure reliable supply via the CM execution of the operational control strategy.
 </li>
 <li>
 Participation with internal or CM resources in technical transfer, process validation, and process data monitoring.
 </li>
 <li>
 Adherence to the expectations of the Lilly Red Book when carrying out interactions with API EM&rsquo;s CMs.
 
 
 
 </li>
 </ul>
 
 Key Objectives/Deliverables
 
 
 
 The candidate will be responsible for process monitoring, response to issues, and improvements where necessary. A strong understanding of manufacturing principles and Lilly systems is required to ensure those same standards are applied to the external contract manufacturers.
 
 
 The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. The position requires working cross-functionally within the site and other functions to deliver on technical objectives.
 
 
 
 Build and Sustain Process Team Relationships
 
 
 
 <ul>
 <li>
 Utilize past experiences with unit operation control to provide insight and feedback to members of the Lilly / CM Joint Process Team (JPT).
 </li>
 <li>
 Employ excellent communication skills to manage internal and external relationships.
 </li>
 <li>
 Build and maintain relationships with development and central technical organizations.
 </li>
 <li>
 Operate with &lsquo;Team Lilly&rsquo; in mind - including coaching and mentoring of peers and other scientists.
 
 
 
 </li>
 </ul>
 
 Develop and Sustain Process Knowledge
 
 
 
 <ul>
 <li>
 Provide technical oversight and stewardship for peptide manufacturing processes.
 </li>
 <li>
 Ensure that processes are compliant, capable, in control, and maintained in a validated or qualified state.
 </li>
 <li>
 Enable the development and maintenance of process knowledge infrastructure such as validated process monitoring spreadsheets
 </li>
 <li>
 Review and track key process parameters (i.e. CPP&rsquo;s, rOPP&rsquo;s, IPC, etc.)
 
 
 
 </li>
 </ul>
 
 Provide Process Support
 
 
 
 <ul>
 <li>
 Leads resolution of technical issues including those related to control strategy and manufacturing.
 </li>
 <li>
 Ensure proper characterization of processes and products and ensure effective documentation of the process description, measures, acceptable ranges, and specifications (and the justification of these measures, acceptable ranges, and specifications).
 </li>
 <li>
 Understand, justify and document the state of validation with data that evaluate the capability of the manufacturing process to meet its stated purpose.
 </li>
 <li>
 Identify systemic issues affecting production and reliable supply from CMs
 </li>
 <li>
 Lead or participate in root cause analysis and CAPA development
 
 
 
 </li>
 </ul>
 
 Process Optimization &amp; Continuous Improvement
 
 
 
 <ul>
 <li>
 Influence and implement the network technical agenda and drive continuous improvement.
 </li>
 <li>
 Maintaining peptide processes in a state of compliance with US and global regulations
 </li>
 <li>
 Understanding the scientific principles required for manufacturing intermediates and drug substances, including the interaction of chemistry and equipment.
 </li>
 <li>
 Support development and technical analysis for on-going continuous improvement activities.
 </li>
 <li>
 Review and identify cost reduction opportunities, as well as process capacities and bottlenecks.
 </li>
 <li>
 Assist in prioritization of opportunities with respect to overall business objectives.
 </li>
 <li>
 Perform and promote optimization of unit operation cycle time, loading, and yield performance.
 
 
 
 </li>
 </ul>
 
 Basic Requirements
 
 
 
 <ul>
 <li>
 Bachelor of Science in Chemistry or Biochemistry
 </li>
 <li>
 5+ years of demonstrated experience and proficiency with GMP pharmaceutical manufacturing and working knowledge of regulatory expectations.
 </li>
 <li>
 Demonstrated ability to function in a team environment as a technical leader and as a member of teams.
 </li>
 <li>
 Demonstrated ability to manage and prioritize competing priorities and to appropriately communicate verbally and in writing to various audiences.
 
 
 
 </li>
 </ul>
 
 Additional Preferences
 
 
 
 <ul>
 <li>
 Successful application of root cause analysis and systematic problem solving
 </li>
 <li>
 Knowledge and experience with Regulatory requirements
 </li>
 <li>
 Knowledge of data management practices across manufacturing
 </li>
 <li>
 Enthusiasm for changes, team spirit and flexibility
 </li>
 <li>
 Ability to influence and communicate to diverse groups on business, or technical issues within the site and function
 </li>
 <li>
 Proficiency in delivering complex tasks and/or tasks that are cross-functional
 </li>
 <li>
 Demonstrated Project Management skills and ability to coordinate complex projects
 
 
 
 </li>
 </ul>
 
 Other Information
 
 
 
 <li>
 The normal schedule for this position is Monday-Friday, 8 hours/day. However, teleconferences may routinely occur outside of these hours due to the time zones of contract manufacturers. Some off-shift work (night/weekend) may be required to support 24/7 operations
 </li>
 <li>
 Tasks require entering manufacturing and laboratory areas and will require wearing appropriate PPE.
 </li>
 Some travel (&lt;25%) is required. International travel may be required to support process start-ups, troubleshooting, and commercial manufacturing.
 
 
 Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
 
 
 Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
 
 
 #WeAreLilly
</div>

API EM TS/MS Mfg. Scientist – Peptides

Amgen

<div>
 
 Join Amgen&rsquo;s Mission of Serving Patients
 
 
 
 At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
 
 
 Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
 
 
 Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
 
 
 
 Job Summary
 
 
 
 The Discovery Chemistry Group Leader will provide scientific and strategic leadership to a synthetic chemistry research team focused on making intermediates and analogs in support of our drug discovery efforts. This role is accountable for designing and executing research strategies that support pipeline progression, innovation, and scientific excellence within Amgen&rsquo;s Small Molecules portfolio. The Discovery Chemistry Group Leader will mentor scientists, drive cross-functional collaboration, and ensure that chemistry efforts align with organizational priorities.
 
 
 In your daily work, you will:
 
 
 <ul>
 <li>
 Lead project teams to meet program goals.
 </li>
 <li>
 Develop and implement robust synthetic strategies to access analogs and intermediates on scales ranging from milligrams to kilograms.
 </li>
 <li>
 Oversee experimental design and data generation. Interpret results, author technical protocols and reports.
 </li>
 <li>
 Collaborate with the Medicinal Chemistry and Synthetics Separation teams to ensure seamless execution of discovery chemistry projects
 </li>
 <li>
 Contribute to resource allocation and project planning
 </li>
 <li>
 Represent the group in project reviews and scientific discussions.
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 Provide mentorship to staff for technical growth and career development
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 Recruit and retain top scientific talent
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 Stay abreast of emerging scientific trends, technologies, and competitor activities.
 
 
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 </ul>
 
 Basic Qualifications
 
 
 
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 Master&rsquo;s degree and 12+ years of Scientific experience; Or
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 Doctorate degree PhD and 8+ years of Scientific experience
 
 
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 </ul>
 
 Preferred Qualifications
 
 
 
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 PhD in Synthetic Organic Chemistry with extensive experience performing independent scientific research
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 Minimum of ~15 years of industry research experience, with at least 5 years in a leadership or people management role.
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 Proven record of scientific innovation and project delivery in a discovery chemistry environment.
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 Demonstrated experience leading discovery chemistry teams and collaborating across various research functions.
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 Strong background in experimental design, data analysis, and scientific communication.
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 Ability to translate complex scientific data into actionable insights and development strategies.
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 Exceptional leadership, mentoring, and interpersonal skills.
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 Proficiency in managing multiple priorities and driving results in a dynamic research environment.
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 </ul>
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Senior Principal Scientist – Discovery Chemistry

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