60 Purification Jobs

This job is based in Australia at one of Australia's leading research and teaching universities, UNSW. The campus offers a vibrant life with a strong sense of community and inclusion. Working at UNSW means being part of a workplace where the best individuals come together to do their best work. The School of Chemistry at UNSW plays a crucial role in teaching over 2000 undergraduate students annually across different faculties. It offers four undergraduate programs leading to majors in chemistry, taught in five specialized teaching laboratories focusing on First Year, Synthetic, Analytical, and Physical Chemistry. The Research Associate (Level A) position at UNSW involves contributing to the research efforts of the university, particularly in the area of medicinal chemistry. The role offers a salary range of $110K to $117K per year, along with 17% Superannuation and annual leave loading. It is a full-time position for 7 months, requiring 35 hours per week. Reporting to Professor Naresh Kumar, the Research Associate will work independently or as part of a team on collaborative research projects in medicinal chemistry. Responsibilities include conducting research on targeted compounds, synthesis, purification, and structural modifications to optimize biological activity. The role also involves drafting manuscripts for peer-reviewed journals, participating in conferences, and supervising research students. To be successful in this role, candidates should hold a PhD in organic chemistry or a related discipline, or possess relevant work experience. They should demonstrate a commitment to staying updated with discipline knowledge, conducting high-quality research, and working collaboratively. Excellent interpersonal skills, communication abilities, and a strong commitment to UNSW's values and safety policies are essential. Applicants are required to address the selection criteria in their applications. The deadline for applications is May 5th, 2025. Interested candidates can apply online through the university's website. UNSW is an equal opportunity employer and encourages applications from diverse backgrounds. More information about working at UNSW can be found at www.unsw.edu.au.,

We are looking for a Chemistry Research Intern who is eager to learn best laboratory practices, assist in ongoing research activities, and contribute to experimental workflows to drive innovation at altM. The candidate will get hands-on exposure to organic synthesis, characterization techniques, and cross-functional research environments, working closely with senior scientists and engineers. Responsibilities include supporting lab-scale synthesis and formulation activities, assisting in purification and characterization of compounds using instruments such as NMR, GC-MS, HPLC, and IR, helping prepare reagents, setting up reactions, and monitoring experimental progress. The role also involves maintaining accurate lab records, inventory, and data logs, staying curious and engaged, with support provided for literature review, method development, and data interpretation over time, as well as adhering to safety protocols and best practices in lab settings. Requirements for the role include being a student or recent graduate with a Bachelors or Masters in Chemistry (preferably Organic or Applied Chemistry), with prior lab and project experience and internships being a nice-to-have. Strong theoretical and practical knowledge of organic chemistry principles and techniques, proficiency in using lab equipment and analytical instruments, excellent problem-solving skills, attention to detail, strong communication and interpersonal skills, with the ability to collaborate effectively in a team, commitment to safety, compliance, and ethical conduct in scientific research, and the ability to work from our lab in Bangalore with a willingness to travel for fieldwork or partner projects. The compensation and benefits offered include competitive cash compensation, negotiable for the right talent and qualifications.,

As a postdoctoral fellow in Professor Ashim Rai's lab at Ahmedabad University, you will be conducting experimental research focused on the biophysics of Salmonella-host cytoskeleton interactions. The research project aims to uncover the molecular mimicry mechanisms employed by Salmonella pathogenic factors to manipulate host cell cytoskeletal networks. Your role will involve designing and executing experiments using interdisciplinary approaches such as reconstitution biology, fluorescence spectroscopy, and DNA nanotechnology. Proficiency in fluorescence microscopy and spectroscopy is essential for this position. Your responsibilities will include designing and conducting experiments in cytoskeletal research, analyzing a diverse range of experimental data, preparing manuscripts for publication, writing grants for research funding, and mentoring PhD and undergraduate students. You will be expected to leverage your expertise in protein expression and purification using bacterial and insect cell systems, as well as your experience in time-lapse fluorescence imaging and the use of a fluorescence spectrophotometer. The ideal candidate for this role should hold a PhD degree in Biochemistry or Biophysics with a strong publication record in high-impact peer-reviewed journals. Prior experience in cytoskeletal biology would be advantageous. Ahmedabad University is committed to providing a research-driven and project-based learning environment within the Division of Biological and Life Sciences. If you are a motivated and self-driven individual with a passion for biophysics research, we encourage you to apply for this exciting opportunity. Please submit your CV and cover letter to Professor Ashim Rai via email at ashim.rai@ahduni.edu.in. Duration of the position: 36 months.,

As a Team Member in Chemical Research & Development at the Research & Development department, specifically in the Peptide Synthesis sub-department, your primary role is to perform chemical synthesis of molecules. This involves process development, process validation, and transferring the processes to production units. Your responsibilities include conducting literature searches, collecting MSDS, performing lab experiments, documenting experimental results, and interpreting spectral data. You will also be responsible for maintaining various documents such as patents, literature, and analytical reports. Collaborating with analytical chemists and DQA on analytical results and methods is an essential part of the role. To ensure the smooth functioning of the lab, you will need to account for chemical usage, availability of raw materials, and perform calibration of lab equipment like weighing balance, pH meter, and driers. Keeping track of regular solvents, reagents, and managing effluent generation from lab experiments are also part of your duties. In addition, you will be required to perform Manual Solid Phase Peptide Synthesis of Peptides on various scales, ranging from medium to commercial scale with minimal supervision. This includes purification of solid phase products, CGMP activities, synthesis of impurities, and degradation impurity standards for analytical method development and validation. Safety awareness and implementation are crucial aspects of this role, and you must strictly adhere to Good Laboratory Practices and Laboratory Safety Norms. Continuous learning and staying updated with industry trends are essential for success in this position. To qualify for this role, you should have an M.Sc. in Organic Chemistry and a minimum of 2 years of experience in the R&D Department of an API manufacturing company. Preferred qualifications include 6 years of experience and knowledge of Process R&D and scale-up processes. In terms of competencies, you should have a strong understanding of coupling reagents, documentation, GLP, safety compliances, plant scale-up, solid phase synthesis, solution phase synthesis, and purification. Behavioral competencies such as results orientation, customer centricity, collaboration & teamwork, problem-solving, planning, and communication are also essential for this role. Continuous learning and professional development are encouraged to excel in this position.,

You have hands-on work experience in mammalian cell culture, microbial cell culture, and molecular biology areas. You are proficient in therapeutic protein expression and purification using E.coli or yeast expression systems. Your expertise includes molecular biology techniques such as molecular cloning, primer designing, expression vector generation, characterization, and related molecular biology techniques. You have a background in generating CHO-based stable monoclonal cell lines for mAb/therapeutic protein production. Your experience also covers single cell cloning, fed-batch study, cell bank preparation (RCB, MCB, WCB, EPCB), and characterization. You will collaborate with multiple teams, Contract Research Organizations (CRO), Contract Development and Manufacturing Organizations (CDMO) for technology transfer. You will work according to Standard Operating Procedures (SOP), design experiments, and troubleshoot any arising problems. It is crucial for you to maintain proper experimental documentation records in Laboratory Notebook (LNB) and Electronic Laboratory Notebook (ELN) specific formats.,

Role & responsibilities Maintains and documents proper records / log book / BPCRs / Reports as per GDP Handling of Chromatography, sterilization & Filtration techniques. Coordination with other department VIZ. engineering, QA, QC and R&D for smoothly execution of Technical Documents. Coordination with QA for timely issuance, completion, filling of BPCR and other GMP documents. Preparation of Performance Verification and PQ and commissioning protocol Understanding & execution of work in line with cGMP. Preparation of SOP, BPCR and other Technical Documents. Handling of QMS Documents, Handling of DMS. Execution of Training related activities of DSP area. To ensure the timely dispensing of raw material and Handling of SAP. To support in qualification activities of DSP area. Execution of Process validation batches. Filling of all records, Change Controls and QMS related Documents associated with DSP area. Execution of IQ, OQ, PQ of equipments of downstream area. Ensuring complete in-process quality control and continuous improvement in process capabilities. Investigating the OOS.OOT and handling process validation& cleaning validation. Plan and actively oversee team and shift activities to meet the production requirements Location: Plasma Fractionation Centre Preferred candidate profile : Biotechnology- Male Candidate Perks and benefits Transportation Facilities Subsidized Canteen Facilities

Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (JRF) in a time bound research project for a temporary period, purely on contractual basis as per the following details. Position Junior Research Fellow (JRF) Number of Vacancy 01 Project Title High temperature corrosion and mechanical behavior of AM fabricated Haynes 282 alloy Department Mechanical Engineering Project Tenure 3 years Job Description The project aims to investigate the corrosion behavior and high temperature mechanical behavior of additively manufactured Haynes 282 alloy. Knowledge about Selective Laser Melting, corrosion, Fatigue, microstructural characterization is required. Strong communication and writing skills are desirable. Essential Qualification Minimum requirement: B.Tech in Mechanical Engineering/Materials Engineering/ Materials and Metallurgical Engineering with a valid GATE score. Desirable: M.Tech in Mechanical Engineering/ Materials Engineering/ Materials and Metallurgical Engineering with a valid GATE score. Age Limit JRF-28Yrs. Age relaxation The upper age limit is relax-able up-to 5 years in the case of candidates belonging to scheduled castes/tribes/OBC, women and physically handicapped candidates. Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m. Principal investigator Dr. Devasri Fuloria Assistant Professor Senior (Grade I) School of Mechanical Engineering Vellore Institute of Technology Vellore, Tamil Nadu - 632014 Send your resume along with relevant documents pertaining to the details of qualifications, GATE/NET score card, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (5/08/2025) through online http://careers.vit.ac.in Please note that the CV should include contact details (address, mobile phone no., email ID), date of birth, qualifications mentioned clearly. Complete information regarding publications of research papers in SCI Journals should be mentioned in the CV. Incomplete applications will be rejected. No TA and DA will be paid for appearing in 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.

As an individual with hands-on work experience in mammalian cell culture, microbial cell culture, and molecular biology, you will be responsible for various tasks related to therapeutic protein expression and purification utilizing E.coli and yeast expression systems. Your expertise should encompass molecular biology techniques such as molecular cloning, primer designing, generation of expression vectors, and characterization of related molecular processes. Moreover, your role will entail working on the development of CHO-based stable monoclonal cell lines dedicated to mAb/therapeutic protein production. Proficiency in single cell cloning, conducting fed-batch studies, preparing cell banks (RCB, MCB, WCB, EPCB), and their subsequent characterization will be highly valued. Collaboration with multiple teams, Contract Research Organizations (CROs), and Contract Development and Manufacturing Organizations (CDMOs) for technology transfer will be a crucial aspect of your responsibilities. Adhering to standard operating procedures (SOPs), designing experiments, troubleshooting issues as they arise, and ensuring meticulous maintenance of experimental documentation records in LNB and ELN specific formats will also be expected from you.,

* Implement and manage production processes for injectable DPI and liquid injection product. * Ensure all operations comply with GMP and regulatory requirements. * Prepare daily reports and update process documentation consistently Required Candidate profile * Knowledge of Peptide synthesis, Purification & Lyophilization operation. * Operation of reactor, Nutsche filter, centrifuge * Handling experience of equipment Lyophilizer and Autoclave

Plan and conduct multi-step organic syntheses to develop novel molecules.Work closely with cross-functional teams, including medicinal chemists,biologists, and analytical scientists to advance drug discovery projects. Required Candidate profile - Experience in medicinal chemistry or CRO environment, preferably in drug discovery, or custom synthesis. - Proficiency in synthetic organic chemistry.

As a Senior Chemist in the Pharma Manufacturing Industry located in Vatva, Ahmedabad, your role will involve utilizing your M.Sc. in Organic Chemistry and 5 to 8 years of experience in API / Intermediates manufacturing within the pharmaceutical sector. Your responsibilities will include hands-on experience in the synthesis of APIs and intermediates, conducting literature searches using platforms such as SciFinder, Chemical Abstracts, Free Patent Online, and Journals. You will be involved in feasibility studies, route selection for synthesis, multi-step synthesis, yield improvement, and cost reduction strategies. Additionally, you will be responsible for tasks such as extraction, purification, distillation, lab validations, process development with strong documentation including Tech reports, process safety reports, and cost sheets. Furthermore, you will lead technology transfer from the laboratory to kilo lab and plant scale, while coordinating with IPR, Regulatory Affairs, and QA departments. Proficiency in tools like Chemdraw / Chemsketch is essential for this role. Please note that only male candidates from the Pharma Manufacturing Industry will be considered for this position. If you are seeking a challenging full-time, permanent role that requires your expertise in organic chemistry and pharmaceutical manufacturing, we look forward to receiving your application. With Regards, Himani(HR) 9377165778,

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. Now is the perfect time to build a larger team dedicated to increasing market share by penetrating and ramping up volumes within all areas of biopharmaceutical purification. 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 the biopharmaceutical space. At Nano Micro, employees are encouraged to seek innovative approaches and embrace new working methods, ensuring continuous advancement for colleagues, clients, and partners. The workplace fosters cooperation and mutual respect, with a strong emphasis on diversity and inclusivity. Nano Micro prioritizes employee growth by supporting professional development and skill enhancement, providing opportunities throughout the organization and actively encouraging staff to engage in new experiences beyond conventional roles. Nano Micro is currently looking for motivated life science scientists to join their India Field Applications Scientist team focused on Biopharmaceuticals. The ideal candidate should be outgoing, confident, and possess strong communication and presentation skills. The candidate should be able to work independently and as part of an energetic sales team that supports research in life sciences, instrumentation, protein purification, separation devices, molecular synthesis, and Organic slime-resistant nano-filtration solutions. The team provides scientific expertise to researchers, labs, and manufacturing sites across India, prioritizing customer needs with their Chromatography Resin portfolio. The primary responsibilities include delivering field-based and remote scientific engagement with customers, developing expertise with protein filtration and purification instruments, and effectively communicating customer feedback to support innovation and market demands. Qualifications for this position include a Masters or PhD in Chemistry, Immunology, Bioengineering, or related field, with Field Application Scientist experience strongly preferred. Candidates should have 5+ years of experience in advanced academic or industry settings, with experience in applications such as vaccines, insulin, plasma proteins, mAbs, oligonucleosides, immunomodulators, GLP-1 peptides, etc. Strong written, verbal, public speaking, interpersonal, and organizational skills are essential, and candidates should be willing to travel 40-60% within the country. To apply, send your resume to srinivas@nanomicrotech.com.,

Role & responsibilities Expertise in carrying out Multi-step synthesis of organic molecules from milligram to multi-gram scales and their characterization. Responsible for the development efficient synthetic process, which leads to better yields and quality of the product, with less cycle time and cost. Capturing proper learning of the project & would be responsible for maintaining the confidentiality of the project as per the IPR guidelines. Scaling up of process and technology transfer from lab to plant and trouble shooting at the time of scale up. Interpretation of analytical reports like HPLC, GC, NMR, LCMS, IR, GCMS. Knowledge of designing route of synthesis for target molecule. Carried out experiments in laboratory and optimize process in terms of Regulatory Affairs (RA), Safety, cost and time effectiveness. Strong knowledge on process validation in laboratory and demonstration in plants. Adept at preparing documents like Technology transfer document (TTD), Process development report (PDR), presentations and reports for review meetings. Process validation and optimization with QBD. Preparing documents like Solubility chart, Material balance, Green card, Hold time study, Details of process, MSD. Literature search .through Sci-finder and Reaxys Ability to handle linear and parallel multi-step organic synthesis Experienced with purification techniques like thin layer & column chromatography, Crystallization and distillations. Structural elucidation through NMR (1H, 13C), IR, Mass (LC/MS, GC/MS). Good Co ordination with Cross functional teams as well as team mates. Accurate record keeping in laboratory notebook (LNB) and (ELN).

Production: Execute production batches, ensure GMP, manage documentation QA: Ensure cGMP, Issuance and retrievals and manage records. QC: Analyze biopharma samples & maintain Documentation R&D: Prepare stocks and buffers, extract proteins & analyze.

Eligibility : M.Sc / M.tech (Life Sciences / Biotechnology) Probation Period : 3 Month (For junior post only) Technical Skills : Various Extraction Techniques Purification techniques General PCR RAPD RFLP Karyotyping SDS PAGE Blotting General Skills : Complete knowledge of MS Office Standardisation of SOP Sample flow management English (Reading and Writing) Candidate must have a personal Laptop

Responsibilities: Perform chemistry reactions & record data follow lab safety practices work for novel chemistry targets working with team spirit Office cab/shuttle Health insurance Annual bonus Provident fund

As a Senior Chemist in the Pharma Manufacturing Industry based in Vatva, Ahmedabad, you will be responsible for the synthesis of APIs and intermediates. Your role will involve conducting feasibility studies, selecting synthesis routes, and implementing multi-step synthesis processes to improve yield and reduce costs. You will utilize your expertise in conducting literature searches using platforms such as SciFinder, Chemical Abstracts, and Free Patent Online, as well as referring to various journals. Additionally, you will be involved in extraction, purification, and distillation processes, along with conducting lab validations. Strong documentation skills are essential for this role, including the preparation of technical reports, process safety reports, and cost sheets. You will also play a key role in technology transfer activities from the laboratory to kilo lab and plant scale. Collaboration with departments such as IPR, Regulatory Affairs, and QA will be crucial in ensuring compliance and quality standards are met. Proficiency in tools like Chemdraw and Chemsketch will be beneficial for this role. Please note that this position is open to male candidates with a background in the Pharma Manufacturing Industry. If you have a Master's degree in Organic Chemistry and possess 5 to 8 years of relevant experience in API and intermediates manufacturing within the Pharma industry, we encourage you to apply for this full-time, permanent position. For further details or to express your interest, please contact Himani (HR) at 9377165778. Thank you.,

Job Purpose To lead and oversee operations of a 20 TPD Compressed Biogas (CBG) plant using agri-residue and other feedstock, ensuring efficient production, safety, and regulatory compliance. Experience 5–8 years in plant operations, preferably in biogas or process industries, with 3+ years in a leadership role. Experience in handling Agri-residue and gas purification preferred. Qualification Bachelor’s in Chemical/Mechanical/Environmental Engineering. Responsibilities Manage plant operations, maintenance, and production targets. Monitor process performance, troubleshoot issues, ensure compliance, and maintain safety standards. Coordinate with vendors, staff, and authorities . Key Technical Competencies Knowledge of anaerobic digestion, gas upgrading (e.g., PSA), CBG compression, and instrumentation. Skilled in maintenance planning, safety protocols, biomass handling, and performance reporting.

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF-PM-ECRG Funded Project in the School of Bio Sciences and Technology (SBST), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “miR146a-loaded exosomes in suckerin patch for targeted diabetic wound healing via IRAK1 suppression” Qualification : Essential qualification: M. Tech / M. Sc in Biotechnology/ Biochemistry Preferred qualification: The candidates must have qualified GATE (with currently valid score)/CSIR-UGC NET including lectureship (Assistant Professorship) or 2 years of research experience and publications relevant to the proposed project title The selection and administration of the research fellow will be as per terms and conditions laid down by ANRF. Mandatory Skills : Candidates having knowledge in exosome isolation, extraction, purification, rDNA technology, protein expression & purification, cell culture techniques and animal handling. Stipend : Rs. 37,000/- per month plus HRA as per rule. No. of Vacancies : 01 Age Limit (if any) : Not exceeding 27 years i.e. Age must be from 18 to 27 years Sponsoring Agency : ANRF (Prime Minister Early Career Research Grant), Ministry of Science & Technology, Government of India. Duration : 3 years (36 Months) Principal Investigator : Dr. Kanagavel Deepankumar, Associate Professor –Grade I, Department of Biotechnology, School of Bio Sciences & Technology, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Applicants must apply online at http://careers.vit.ac.in by 15/07/2025 and email a single PDF containing the CV, statement of purpose detailing the motivation for working in the research project, essential certificates and a passport-size photograph to Dr. Kanagavel Deepankumar ( deepankumar.k@vit.ac.in ) with the subject line: “Application for the ANRF project JRF”. No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview, later which will be intimated through email. The selected candidate will be expected to join at the earliest.

M.Sc. - Organic Chemistry with 5 to 8 years of experience in Pharma Manufacturing Industries. Having Pharma Company experience in APIs & their Intermediates. Literature Search via Scifinder, chemical abstract, Free Patent online & Journals. Required Candidate profile Communication with IPR & Regulatory Affairs & DQA Dept. Development with Extraction, Purification & Distillation of product. Preparation of Process safety report & data analysis of Intermediate & APIs Perks and benefits Negotiable - Depending Upon Candidate & Experience

Role & responsibilities 1. To work on the new process development for the ongoing and new products at bench level. 1. Arranging of raw materials required for the Process development and R & D work from store. 2. To support the Sr. Chemist on the process development work. 3. Monitoring of reactions in R & D lab by TLC or other available methods. 4. Carry out reactions, isolation and purification as per process requirements. 5. Preparation of Batch summary record and daily lab records in R & D Journal. 6. To manage Lab cleaning, Equipment cleaning with the help of Lab assistants. 7. To arrange Glasswares and Raw materials in separate racks with the help of Lab assistants. 8. To arrange RBF setup as per reaction requirements. 9. Sending samples for the required test in the ADL and observing its results. 10. Purification of materials by Column chromatography as per project requirements.

Role & responsibilities Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels. Experience in handling Roller bottles, Cell stacks, TCFs. Experience in working in GMP conditions / production department of viral vaccines. Preparation of SOP, BMR’s, Protocols related to cell culture / virus culture. Experience in virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Preparation of Media, in process solutions using preparation vessels. Preferred candidate profile Candidate should have experience in Cell Culture vaccine 6 days work from office based at Ahmedabad

Job Title: Peptide synthesis Team members; No. of positions: 1 The ideal candidates will possess background and experience in peptide synthesis, process optimization and isolation techniques. Job Description Strong background and hands-on experience in synthetic organic and/or peptide chemistry Independently perform Solid/Solution phase peptide synthesize of complex peptide active pharmaceutical ingredients (APIs) Knowledge in handling of diverse resins for peptide synthesis and associated process Hands on experience on automatic peptide synthesizers such as Biotage MW, Symphony X, Sonata etc is desirable Familiarity with peptide purification techniques is desirable. Able to work in mg to higher scale along with excellent problem solving skills To follow safety rules in all operations in the lab, lab chemicals management, maintain lab instruments and their proper use. Required Qualification : MSc in Chemistry Experience: > 3 to 5 Years in Peptide-API Industry Regards Srinidhi S srinidhi@bvrpc.com

Job Area: Engineering Group, Engineering Group > Hardware Engineering General Summary: As a leading technology innovator, Qualcomm pushes the boundaries of what's possible to enable next-generation experiences and drives digital transformation to help create a smarter, connected future for all. As a Qualcomm Hardware Engineer, you will plan, design, optimize, verify, and test electronic systems, bring-up yield, circuits, mechanical systems, Digital/Analog/RF/optical systems, equipment and packaging, test systems, FPGA, and/or DSP systems that launch cutting-edge, world class products. Qualcomm Hardware Engineers collaborate with cross-functional teams to develop solutions and meet performance requirements. Minimum Qualifications: Bachelor's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 3+ years of Hardware Engineering or related work experience. OR Master's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 2+ years of Hardware Engineering or related work experience. OR PhD in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 1+ year of Hardware Engineering or related work experience. Key Technical skills requirement: Candidate should have deep and sound understating of: Memory basic design understating for different architectures Memory measurement parameters Memory timing/power characterization and compiler engine building with all accuracy parameters involved Memory power views All the LVF/different forms of variation parameter Memory lib w.r.t. parameters/arcs/SDF conditions/variation parameters/QA steps/different formats Different Simulator tools Should have thorough understanding of release process to customers Knowledge of scripting languages such as Shell, Perl Good working knowledge of MS excel, PPT Mentoring skills to Juniors

Job description - Research Associate (Protein Chemistry laboratory) 1. Process development, scale-up and transfer: (Downstream) Undertake on-going referencing and literature reviews and provide strategic inputs to projects at all stages Conduct lab experiments as per the shortlisted methodologies in order to develop & finalize purification processes for various recombinant therapeutic products. Provide own inputs and insights to optimize/improve process Provide samples to analytical labs for testing, collect and file reports of analysis, compile the data and do data analysis for conclusion of experiments Support plant activities as per need Present data in project review meetings Prepare process development report and technology transfer documents Participate in at-scale demo batches and handover as part of technology transfer Jointly monitor purification process at production facility and resolve any queries that may arise during production 2. Materials and equipment management: Oversee installation of new equipment and attend demos Maintain all IQ/OQ/PQ documents Ensure scheduled and breakdown maintenance by coordinating with maintenance team Create and maintain all maintenance/ repair logs Support management of chemical, consumables: o Transfer/store as per set norms o Engage in technical discussions with vendors in order to suggest suitable vendors o Maintain material logs and calculate shortfalls (for order placement) o Post materials required onto SAP 3. Regulatory and compliance: Accurately capture all lab experiments in laboratory notebooks in real-time Adhere to regulatory, SOPs and safety guidelines for all processes Modify SOPs in own area of work Ensure timely closure of regulatory queries by conducting and documenting lab experiments Ensure data integrity in all respects 4. Learning and improvement Attend all mandatory trainings Take initiative to provide inputs (based on expertise/interest) to other on-going projects Take initiatives for self-development and update self on recent developments in own area of work Take initiative to train fresh RAs upon induction or guide them with select lab processes (basis expertise) 5. Compliance management Ensuring GDP compliance Ensuring CC/ IQ/OQ/PQ/CSV of new instrument Ensuring calibration/PM/AMC of equipment Be audit ready and prepare audit responses as per audit points Lab cleanliness, lab maintenance