17 Characterization Jobs

Job Description. Our Solutions Engineering Physical IP team comprises some of the industry’s leading experts in deep submicron circuit design. This position is a wonderful opportunity for you to work with our custom standard cell design engineering team on innovative technologies. Your work will have a significant lasting impact as the designs will be used in Solutions Engineering products servicing the infrastructure, client, automotive, and IoT market segments.. In this role, you will take significant responsibility for the technical leadership and strategic direction within the team. You will proactively identify and drive improvements in design processes, methodologies, and infrastructure to ensure continued excellence and innovation.. Responsibilities. Lead technical strategy and decision-making for key product or functional areas in standard cell development. Drive improvements to methodologies, tools, and processes, proactively inspiring change across project teams and related functions. Act as a recognized technical guide and mentor within your area, providing guidance and direction to other specialists across the team. Collaborate closely with multiple teams, projects, and partners across Arm, significantly influencing broader organizational outcomes. Develop Arm custom standard cells in the latest, sub-3nm process technology nodes. Co-optimize circuit designs with physical design engineers to improve PPA of Arm cores integrated into best-in-class SoCs. Closely collaborate with the mask design team for optimal layout tuning, library view characterization, modeling, and QA validation using diverse EDA tools. Required Skills And Experience. 10+ years of relevant circuit design experience (for BSEE), 8+ years (for MSEE).. Proven track record of providing technical leadership and strategic oversight on complex projects or across multiple teams.. Significant experience in identifying, designing, and verifying cells specifically targeted to improve core and SoC-level PPA.. In-depth understanding of MOSFET electrical characteristics, transistor-level device physics, PPA tradeoffs, layout, and variability especially at 3nm and below.. Expertise in transistor-level design of static circuits, including state-retaining elements like latches and flops.. Extensive hands-on development experience with standard cell EDA view characterization, modeling, and QA.. Proficiency with standard cell characterization tools and Spice circuit simulators.. Strong proficiency in scripting languages such as Perl or Python.. Demonstrated ability to independently resolve complex design and project issues, influencing decisions across multiple projects or departments.. Ability and willingness to proactively mentor and support the development of team members.. Demonstrated positive attitude, respect for team members, continuous skill development, and ability to handle diverse responsibilities effectively.. Strong analytical skills with the ability to clearly present conclusions and recommendations.. “Nice To Have”. Experience leading multi-functional technical initiatives, influencing senior customers, and handling project timelines and risks.. Exposure to physical design implementation flow and signoff.. Accommodations at Arm. At Arm, we want to build extraordinary teams. If you need an adjustment or an accommodation during the recruitment process, please email accommodations@arm.com . To note, by sending us the requested information, you consent to its use by Arm to arrange for appropriate accommodations. All accommodation or adjustment requests will be treated with confidentiality, and information concerning these requests will only be disclosed as necessary to provide the accommodation. Although this is not an exhaustive list, examples of support include breaks between interviews, having documents read aloud, or office accessibility. Please email us about anything we can do to accommodate you during the recruitment process.. Hybrid Working at Arm. Arm’s approach to hybrid working is designed to create a working environment that supports both high performance and personal wellbeing. We believe in bringing people together face to face to enable us to work at pace, whilst recognizing the value of flexibility. Within that framework, we empower groups/teams to determine their own hybrid working patterns, depending on the work and the team’s needs. Details of what this means for each role will be shared upon application. In some cases, the flexibility we can offer is limited by local legal, regulatory, tax, or other considerations, and where this is the case, we will collaborate with you to find the best solution. Please talk to us to find out more about what this could look like for you.. Equal Opportunities at Arm. Arm is an equal opportunity employer, committed to providing an environment of mutual respect where equal opportunities are available to all applicants and colleagues. We are a diverse organization of dedicated and innovative individuals, and don’t discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.. Show more Show less

Responsibilities: Collaborate with cross-functional teams on product development. Ensure compliance with industry standards and customer requirements. Design memories, characterize performance.

Execute process development activities for pharmaceutical products at laboratory scale Design and implement experiments to optimize manufacturing processes for increased efficiency and product quality Conduct and analyze data from characterization and optimization studies Prepare the documents like PIS, sampling plan and risk matrix for pilot scale batches (Confirmatory batch and exhibit batch manufacturing) Troubleshoot process issues and implement corrective actions Collaborate with cross-functional teams including manufacturing, quality assurance, and regulatory affairs Author and review technical reports, batch records, and standard operating procedures Ensure compliance with cGMP regulations and company policies Participate in technology transfer activities to support scale-up and exhibit batches. Stay current with industry trends and emerging technologies in pharmaceutical process development Present findings and recommendations to group leader. Contribute to continuous improvement initiatives within the department Qualification M. Pharmacy Additional Information

Job Description: Central product engineering role to liaison between R&D, Field engineering teams, along with product engineers within and other product teams. Test new product features through alpha and beta phases, identify and document usage scenarios, conduct Beta testing with interested customer counterparts and ensure successful deployment of new differentiating features. Study and improve usability, applicability and adoption of products, platforms and solutions to meet customer business needs. Diagnose, troubleshoot and resolve complex technical issues on customer installations Deploy and train customers on new implementations and capabilities. Review and analyze feedback on product and solutions performance from customers and other application partners Work directly with Research and Development (R&D) to develop and implement technical roadmap, specifications and validation for improvements and enhancements. Partner with customer technical leaders and Sales to identify business challenges, develop effective technical solutions for new accounts and increase utilization and retention of products on current accounts. Demonstrate creativity in building effecting test scenarios to exercise product features and identify issues as early as possible in development and deployment life cycles. Handle customer escalated situations with calm demeanor and create alternative solutions to un-gate critical engagements and production stop scenarios. Requirements: Typically requires a minimum of 5 years of related experience. Possesses solid background in Spice simulations (HSPICE, FineSim and industry standard simulators) with ability to create and work with spice decks and netlists. Experienced in standard cell characterization and basic concepts of timing (NLDM, CCST, CCSN), power (NLPM, CCSP), noise (CCSN), LVF, AOCV/POCV methodologies. Resolves issues in creative ways. to create usable workarounds and alternative solutions. Exercises independent judgment in selecting methods and techniques to obtain solutions. Executes projects from start to completion. Contributes to moderately complex aspects of a project Determines and develops recommendations to solutions. Works on team-driven or task-oriented projects. Networks with senior internal and external personnel in own area of expertise. Collaborates across various related tools to provide a complete solution to customers. Possesses excellent communication and inter-personal skills.

What You'll Be Doing: Designing and validating custom standard cells, including flip flops, clock gating cells, level shifters, and power gating cells. Optimizing standard cell circuits to achieve better performance, power, and area (PPA). Engaging in hands-on development while mentoring and coaching junior R&D engineers. Collaborating with layout designers to optimize layout parasitics and achieve target PPA. Involving in layout extraction and understanding layout-dependent parameters in the extracted netlist. Implementing, testing, and analyzing circuit design guidelines and methodologies. The Impact You Will Have: Driving innovations in standard cell design that contribute to the success of Synopsys products. Enhancing the performance, power, and area (PPA) of our silicon IP portfolio. Mentoring and developing the next generation of R&D engineers. Collaborating across functions to ensure methodology alignment and optimization. Contributing to the continuous improvement of circuit design methodologies. Supporting the integration of more capabilities into System-on-Chip (SoC) designs, meeting unique performance, power, and size requirements. What You'll Need: Bachelor's or Master's degree in Electrical Engineering or a related field. 10+ years of experience in standard cell library design. Deep understanding of CMOS device characteristics and submicron process nodes. Experience with FINFET/GAA technologies and high sigma variation analysis. Familiarity with layout design and optimization of layout parasitics. Who You Are: Strong analytical and logical skills. Effective communicator and collaborator. Proactive problem solver with a hands-on approach. Mentor and coach for junior engineers. Innovative thinker with a passion for technology.

Introduction As a Hardware Developer at IBM, youll get to work on the systems that are driving the quantum revolution and the AI era. Join an elite team of engineering professionals who enable IBM customers to make better decisions quicker on the most trusted hardware platform in todays market. Your Role and Responsibilities : We are seeking highly motivated DFT engineer to be part of Hardware team. Join a great team of engineering professionals who are involved in development, validation, and delivery of DFT patterns for IBMs microprocessor chip design team. As a member of functional DFT team ( Power on Reset, Architecture Verification Program, Array BIST teams ), you will be required but not restricted to pattern generation, simulation, validation, characterization, delivery to TAE, IBMs Hardware Bring-up and Silicon Debug Your role and responsibilities We are seeking highly motivated DFT engineer to be part of Hardware team. Join a great team of engineering professionals who are involved in development, validation, and delivery of DFT patterns for IBMs microprocessor chip design team. As a member of functional DFT team ( Power on Reset, Architecture Verification Program, Array BIST teams ), you will be required but not restricted to pattern generation, simulation, validation, characterization, delivery to TAE, IBMs Hardware Bring-up and Silicon Debug Required education Bachelors Degree Preferred education Masters Degree Required technical and professional expertise 5-9 years experience in DFT on complex designs involving scan insertion, compression, MBIST, ATPG, simulations and IP integration and validation.Proven expertise in analysing and resolving DRCs/TSVs .Hands-on experience in pattern generation for various fault models, pattern retargeting and debugging techniques to address low coverage issues.Hands-on experience with Gate-Level DFT verification, both with and without timing annotations.Well versed with industry standard test techniques and advanced DFT features like SSN, IJTAG, IEEE 1500, Boundary scan , LBIST and STA constraint delivery .Hands on experience on industry standard tools used for DFT featuresProficiency in scripting languages such as TCL, Perl or Python to automate design and testing tasks.Worked with cross functional teams like design, STA & tester teams for ensuring top quality of DFT deliverables and DFT support and hand offs.Excellent analytical and problem-solving skills, with a keen attention to detail.Strong communication and collaboration skills, with the ability to work effectively within cross-functional teams Fundamentals in micro controller architecture, embedded firmware, functional verification and RTL design . Experience working with ATE engineers for silicon bring up, silicon debug and validation. . Experience in processor flow and post silicon validation Preferred technical and professional experience Hiring manager and Recruiter should collaborate to create the relevant verbiage.

Job Description: Applications are invited for the post of Project Research Scientist – I (Non-Medical) for the ICMR New Extramural (First in the World Challenge) grant in the Centre for Nanobiotechnology (CNBT), at Vellore Institute of Technology (VIT). (No. EM/Dev/FIW/00252/2024 (E-Office-227016)). Title of the Project: First in the World Challenge: A Nasal Spray Formula for Pulmonary Delivery to Control Multidrug-Resistant Tuberculosis MDR-TB Qualification: The candidate must have First class post graduate degrees with PhD degree in relevance to nano technology, nano-delivery, biological therapeutics, pharmaceutical sciences, Biotechnology, Desirable experience: PhD thesis submitted or having Research fellow experience or having previous experience in nano/liposomal formulation, stability and characterization. Stipend: Rs. 56,000 + 10% HRA (Rs. 61,600) per month, stipend will be as per Institute norms. Sponsoring Agency: ICMR, New Delhi Duration: 3 years Principal Investigator: Dr. Natarajan Chandrasekaran, Professor, Higher Academic Grade, Centre for Nanobiotechnology (CNBT), Vellore Institute of Technology (VIT) Vellore – 632 014, Tamil Nadu Co-Principal Investigator: Dr. George Priya Doss C, Professor Grade 1, Department of Integrative Biology School of Bio Sciences and Technology Vellore Institute of Technology (VIT) Vellore – 632 014, Tamil Nadu Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (10/06/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Day to day analytical activities for robust method development for peptide molecules by different techniques (HPLC and GC).Preparation of Analytical Developments Validation Protocol, process scale-up,validation of methods.Interact with customes. Required Candidate profile 10 years of experience in Analytical R&D in Peptide analytical method development, peptide characterization. Worked on Biotechnology, Chemical peptides and proteins related science.

Requirement : Analog Circuit Design Lead Experience Range : 7 - 12 Yrs. Work Location(s) : Bengaluru, Karnataka Candidates who are ready to join Immediately Requirements: Experience in entire Analog IP development including circuit design, layout, AMS verification, and characterization. Must have led the entire Analog IP development cycle and team. Circuit Design implementation of IPs including LDOs, Band Gap reference, Current Generators, POR, ADC/DACs, PLLs, Oscillators, General Purpose IOs, Temperature sensor, SERDES, PHYs, Die to Die interconnect, High-speed IOs, etc. Analog/custom layout design in advanced CMOS process. Ability to understand design constraints and implement high-quality layouts. Conceptualize and implement chip-level mixed signal simulation environments (testbenches, run scripts, etc...). Characterization . Hands-on experience on lower FINFET technology nodes and design/PPA trade-offs

Company Name: Oneiro Lifecare Pvt Ltd Designation: Regulatory Affairs - Sr Officer/Executive - API Location- Ekalbara Plant (Vadodara) Preferred candidate profile Experience: 3 to 5 Years (M.Pharm (Pharmaceutical Chemistry)/ M.Sc. (Chemistry)/ B.Pharm) JOB PROFILE Interdepartmental Coordination: Liaise with cross-functional teams (R&D, QC, QA, Manufacturing, etc.) to gather, review, and consolidate technical information required for regulatory submissions. API Chemistry & Characterization: Provide expert input on molecular chemistry , including impurity profiling , characterization , and Nitrosamine impurity assessment . DMF (Drug Master File) Management: Prepare, maintain, and update DMFs (both Open and Closed Parts) for submission to national and international regulatory authorities. Ensure data integrity and compliance with ICH and other global regulatory guidelines . Regulatory Documentation & Submissions: Prepare, review, and submit CDSCO-specific checklists for New Drug Applications (ND) and SND (Subsequent New Drug) filings for APIs. Regulatory Compliance: Stay current with evolving regulations and guidelines issued by CDSCO, ICH, USFDA, EMA , and other global regulatory bodies. Assist in audits and regulatory inspections by preparing and presenting required documentation. Liaison with Regulatory Authorities: Coordinate with Local FDA & CDSCO Liaison concerned person and other regulatory authorities for smooth regulatory processes and communication. If interested please share updated resume on corporate.hr@exemedpharma.com

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF-SERB funded Core Research Grant (CRG) Project in the School of Chemical Engineering (SCHEME), at Vellore Institute of Technology (VIT), Vellore (Sanction order dated 01 August 2024) Title of the Project : “ Design and Characterization of Novel Hydrodynamic Cavitation Reactor for Wastewater Treatment” Qualification : M. Tech / M.E in Chemical/Environmental Engineering, or a related engineering field with one or two years of experience in water and wastewater treatment is desirable. Describe if any : Candidates having knowledge in conducting lab/pilot scale experiments in wastewater treatment will be given preference. Stipend : Rs. 37,000/- per month + HRA (As per Institute norms). Sponsoring Agency : Science and Engineering Research Board Duration : 3 Years Principal Investigator : Dr. K.Sivagami, Assoicate Professor, School of Chemical Engineering, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (27 /05/2025) through online http://careers.vit.ac.in. No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview later which will be intimated by email. The selected candidate will be expected to join at the earliest.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere For 70 years, our team has driven meaningful innovations in kidney care As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients? that is what Vantive aspires to deliver, We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us At Vantive, you will become part of a community of people who are focused, courageous and dont settle for the mediocre Each of us is driven to help improve patientslives worldwide Join us in advancing our mission to extend lives and expand possibilities, Summary The successful candidate for this role will bring familiarity and experience in characterization and failure analysis of polymeric materials pertinent to use in drug and device industry The role requires the candidate to perform polymer material testing at in-house labs and/or coordinate the testing with external testing labs under minimal supervision The individual will write required reports following pertinent internal and external guidelines that enable the eventual use of polymer materials tested by them in drugs or devices manufactured by Vantive, Essential Duties And Responsibilities, Perform characterization and failure analysis of polymeric materials used in multiple applications such as disposables (e-g filters, dialyzers, polymeric connectors etc ), packaging, and container closure materials and container systems, Employ appropriate techniques/methods to successfully and independently execute assignments within negotiated deadlines, Apply technical theories and principles to projects within area of expertise and select appropriate techniques and procedures to solve problems, Document results in laboratory notebooks/ELN according to established GDP procedures, Maintain laboratory reagents, materials and equipment as directed in good order, Create and update equipment SOPs and analytical procedures, participate in ordering of raw materials, analytical materials or equipment, Maintain knowledge of and apply relevant quality and safety requirements including equipment ownership and qualification, Have a working knowledge and understanding of GDP, GLP, GMP and related regulations and guidelines, Qualifications, Demonstrated hands-on experience in polymer characterization (FTIR, DSC, TGA, MFI, etc ), polymer microscopy and associated sample preparation techniques (microtomy/cryomicrotomy), as well as experience in failure analysis of polymers required, The successful candidate will demonstrate high level of passion and interest in polymer science and applications of that knowledge to be an effective problem solver in an industrial setting, Excellent written and verbal communication skills in English, Ability to effectively contribute as an integral member of a project team, Ability to objectively assess, organize, and clearly communicate information, Ability to interpret available information and make recommendations to resolve technical challenges, Ability to appropriately prioritize work assigned to meet project deliverables in a timely manner, Demonstrate inclusive attitude, collaborate with team members and cross-functional teams for project deliverables, Contribute to efforts beyond own scope of responsibilities to ensure project milestones are met, Provide and accept critical feedback from others in a constructive manner, Adapt to changes and exhibit an agile mindset, Embrace diversity and inclusion, value differences, Education And/or Experience, Mastersdegree in a relevant field (e-g , Material Science/Chemistry, Polymer Science/Chemistry) with 2 yearsof relevant professional experience, PhD candidates with dissertation work relevant to polymer characterization, polymer microscopy and polymer failure analysis are encouraged to apply, Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information To learn how you can protect yourself, review our Recruitment Fraud Notice,

About Intas Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Research Scientist ADL Job Requisitions No : 12812 Job Description Purpose of Job Senior Scientist role in Analytical development laboratory with an experience of 8+ years in biologics or biopharma domain or PhD in any life sciences with 4+ years of biopharma industrial experience In this proposed job role the scientist is expected to carry out analytical characterization and development activities required for biologics product development Method validation and method transfer related documentation will be key responsibility The person will drive the project from analytical front and will be representing analytical team in CFT discussions and project meetings Data interpretation and rationale decision making for analytical data related decisions and prioritizing deliverables will be key KPI Data compilation and presentation of analytical findings to project team and senior management as an when required The person is expected to lead a group of 4-6 scientists and manage daily activities of group, Skill Required Expertise in LC techniques Expertise in HOS techniques Scientific report writing and documentation Data presentation and data analysis Roles and Responsibilites Responsible for analytical method development of LC and HOS techniques, Perform analytical method qualification and write method qualification reports, Perform method validation and method transfer to QC and identified sites for qualified methods, Manages project work and independently executes experiments as and when required Derives interpretation and conclusion of results Plans daily work, records and reviews results and documents to ensure correctness and to fulfil targets on time Coordinates with other team members as per requirement, Perform literature search and develop newer and improved high throughput characterization workflows, Manage team of 4-6 junior scientists and involved in work allotment and daily activity planning, Assessing team performance and assisting senior scientists and managers during review process, Provide timely feedback and training to junior scientists Meeting analytical deliverables timelines set and agreed upon in project meetings, Qualification Required Sc/M Competencies Intas Action Oriented Intas Customer Focus Intas Dealing with Ambiguity Intas Problem Solving Intas Time Management Relevant Skills / Industry Experience Expertise in LC techniques Expertise in HOS techniques Scientific report writing and documentation Data presentation and data analysis Relevant professional / Educational background Any Other Requirements (If Any) Compensation / Reward Location: Ahmedabad, GJ, IN, 382213 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 11 Apr 2025

Principal Engineer – Rock Mechanics Location : Bengaluru, India Business Line : Mining – Global Capability Centre (GCC-IN) – Global Specialist Mining Team WSP is actively seeking a Principal Engineer – Rock Mechanics to join our Global Capability Centre - India (GCC-IN) as part of the Global Specialist Mining Team . Based in Bengaluru , this role will contribute to global mining projects by providing advanced geomechanical analyses and technical support for open pit and underground hard rock mining operations. You will work alongside global experts and project teams to deliver high-quality technical solutions in rock mechanics and numerical modeling, playing a key role in stability assessment, excavation design, and risk mitigation for mining structures. Key Responsibilities Conduct advanced rock mechanics and geotechnical analyses for hard rock open pit and underground mines. Build, calibrate, and interpret 3D geomechanical models using Itasca software (FLAC3D, UDEC, 3DEC, PFC). Perform stress-strain and failure mechanism analysis , including excavation sequence and support system evaluation. Integrate geological, structural, hydrogeological, and geotechnical data into stability and design models. Apply Python scripting to automate modeling workflows, data processing, and output interpretation. Support back-analysis of field failures, incorporating instrumentation data into geomechanical assessments. Collaborate with multidisciplinary and cross-country teams to deliver technically integrated solutions. Prepare detailed technical reports , presentations, and documentation in accordance with international standards. Provide input to proposals and client-facing materials for business development support. Mentor junior engineers and contribute to technical capability building in the team. Uphold WSP’s safety, quality, and innovation standards throughout all work phases. Key Competencies & Technical Expertise Mandatory Skills Proven expertise in rock mechanics and geomechanical modelling for mining applications. Hands-on experience with Itasca software : FLAC3D , UDEC , 3DEC , and/or PFC . Strong working knowledge of Python for technical modeling, automation, or analysis tasks. Proficient in rock mass characterization (RMR, Q-System, GSI) and design of ground support systems. Excellent analytical skills, with the ability to distill complex technical information into concise reports. Strong communication and teamwork skills in a multi-disciplinary, global context. Desired Skills Experience in excavation sequence modelling, convergence prediction, and numerical back-analysis. Familiarity with geotechnical instrumentation and monitoring data interpretation. Exposure to international mining projects across various geotechnical regimes. Experience with data visualization or analysis tools (e.g., Jupyter, Pandas, GIS platforms). Qualifications Bachelor’s degree in Mining Engineering . Master’s or Ph.D. in Geomechanics , Rock Mechanics , or Geotechnical Engineering , with a mining specialization. 8 to 16 years of direct mining industry experience , focused on rock mechanics and geotechnical engineering for underground and open pit mines. Join WSP’s GCC-IN Global Specialist Mining Team and contribute to technically challenging, high-value mining projects across the globe—leveraging advanced geomechanics, innovation, and collaboration.

Senior Engineer – Rock Mechanics Location : Bengaluru, India Business Line : Mining – Global Capability Centre (GCC-IN) – Global Specialist Mining Team WSP is actively seeking a Senior Engineer – Rock Mechanics to join our Global Capability Centre - India (GCC-IN) as part of the Global Specialist Mining Team . Based in Bengaluru , this role will contribute to global mining projects by providing advanced geomechanical analyses and technical support for open pit and underground hard rock mining operations. You will work alongside global experts and project teams to deliver high-quality technical solutions in rock mechanics and numerical modeling, playing a key role in stability assessment, excavation design, and risk mitigation for mining structures. Key Responsibilities Conduct advanced rock mechanics and geotechnical analyses for hard rock open pit and underground mines. Build, calibrate, and interpret 3D geomechanical models using Itasca software (FLAC3D, UDEC, 3DEC, PFC). Perform stress-strain and failure mechanism analysis , including excavation sequence and support system evaluation. Integrate geological, structural, hydrogeological, and geotechnical data into stability and design models. Apply Python scripting to automate modeling workflows, data processing, and output interpretation. Support back-analysis of field failures, incorporating instrumentation data into geomechanical assessments. Collaborate with multidisciplinary and cross-country teams to deliver technically integrated solutions. Prepare detailed technical reports , presentations, and documentation in accordance with international standards. Provide input to proposals and client-facing materials for business development support. Mentor junior engineers and contribute to technical capability building in the team. Uphold WSP’s safety, quality, and innovation standards throughout all work phases. Key Competencies & Technical Expertise Mandatory Skills Proven expertise in rock mechanics and geomechanical modelling for mining applications. Hands-on experience with Itasca software : FLAC3D , UDEC , 3DEC , and/or PFC . Strong working knowledge of Python for technical modeling, automation, or analysis tasks. Proficient in rock mass characterization (RMR, Q-System, GSI) and design of ground support systems. Excellent analytical skills, with the ability to distill complex technical information into concise reports. Strong communication and teamwork skills in a multi-disciplinary, global context. Desired Skills Experience in excavation sequence modelling, convergence prediction, and numerical back-analysis. Familiarity with geotechnical instrumentation and monitoring data interpretation. Exposure to international mining projects across various geotechnical regimes. Experience with data visualization or analysis tools (e.g., Jupyter, Pandas, GIS platforms). Qualifications Bachelor’s degree in Mining Engineering . Master’s or Ph.D. in Geomechanics , Rock Mechanics , or Geotechnical Engineering , with a mining specialization. 6 to 12 years of direct mining industry experience , focused on rock mechanics and geotechnical engineering for underground and open pit mines. Join WSP’s GCC-IN Global Specialist Mining Team and contribute to technically challenging, high-value mining projects across the globe—leveraging advanced geomechanics, innovation, and collaboration.

Role & responsibilities Understanding business of bioprocessing technologies, clone development, upstream and downstream processing, assay biology, and characterization techniques Understand the analytical requirements of Biologics, Biosimilars, Vaccines, fusion proteins, peptides Develop and implement strategic sales plans to achieve revenue targets within the biopharmaceutical sector. Identify and pursue new business opportunities with biopharma clients Build and maintain strong relationships with existing clients, understanding their needs and ensuring exceptional customer satisfaction. Collaborate with cross-functional teams including technical experts, marketing, and operations to tailor solutions that meet client requirements. Keep abreast of industry trends, market dynamics, and competitor activities to identify potential opportunities and threats. Prepare and deliver presentations, proposals, and contract negotiations to secure new business partnerships. Provide regular updates and reports on sales performance, market trends, and client feedback to senior management. Ability to work independently and collaboratively in a fast-paced, dynamic environment. Demonstrated ability to think strategically and execute tactical sales plans to drive revenue growth. Preferred candidate profile communication, negotiation, and presentation skills Strong understanding of bioprocessing technologies, clone development, upstream and downstream processing, assay biology, and characterization techniques Willingness to travel as required to meet with clients and attend industry events.

We are seeking a highly motivated and experienced Study Director to oversee chemical characterization studies within our research and development team. The ideal candidate will have a strong background in analytical chemistry, extensive knowledge of chemical characterization techniques, and a proven track record in managing complex projects. Key Responsibilities: - Lead and manage chemical characterization studies, including planning, execution, and reporting of results. - Develop study protocols and ensure compliance with regulatory guidelines and internal standards. - Coordinate and communicate with cross-functional teams. - Analyze and interpret data, preparing comprehensive reports and presentations for internal and external stakeholders. - Mentor and train junior staff in scientific techniques and best practices. - Ensure that laboratory safety protocols are followed and maintain a clean and organized work environment. - Stay current with industry trends and advancements in chemical characterization methodologies. Qualifications: - Ph.D. or equivalent degree in Chemistry, or a related field. - A minimum of 10 years of experience in chemical characterization or a similar role within a laboratory setting. - Expertise in techniques such as LCMS - QTOF, GCMS, NVR, ICPMS, IC and other relevant analytical methods. - Strong project management skills with the ability to lead multiple projects simultaneously. - Excellent communication, organizational, and problem-solving abilities. - Familiarity with regulatory requirements and guidelines in the pharmaceutical or biotechnology industry. This position offers a competitive salary and benefits package, along with opportunities for professional growth and development. If you are passionate about advancing scientific research and thrive in a collaborative environment, we encourage you to apply. Roles and Responsibilities 1. Oversee and manage chemical characterization studies from initiation to completion, ensuring adherence to regulatory standards and internal protocols. 2. Design study plans and methodologies that are scientifically sound and aligned with project objectives, including the selection of appropriate analytical techniques and equipment. 3. Coordinate with cross-functional teams, including project managers, chemists, and quality assurance personnel, to ensure effective study execution and communication. 4. Review and approve study protocols, analytical methods, and reports to ensure accuracy, compliance, and scientific integrity. 5. Provide technical expertise and guidance related to chemical characterization, including the interpretation of analytical data and results. 6. Ensure that all studies are conducted in compliance with Good Laboratory Practice (GLP) and other relevant regulations. 7. Manage study budgets and timelines, identifying potential risks and implementing mitigation strategies to ensure successful project delivery. 8. Train and mentor staff on appropriate methodologies and regulatory requirements related to chemical characterization studies. 9. Participate in project meetings, presenting study findings and progress updates to stakeholders, and incorporating feedback into study design and implementation. 10. Maintain up-to-date knowledge of industry trends, emerging technologies, and regulatory changes affecting chemical characterization and related fields. 11. Facilitate communication with regulatory agencies as needed, providing data and documentation to support submissions and inquiries. 12. Contribute to the continuous improvement of departmental processes and methodologies, ensuring best practices are followed in study design and execution.