64 Drug Discovery Jobs - Page 2

Role & Responsibilities Will be responsible for managing Discovery projects end to end. Facilitate project team meetings and ensure accuracy and adequacy of documentation of project issues and action items. Handle minimum 3-4 (Early stage / Lead Optimization stage) internal or external programs and additional responsibilities (w.r.t processes / in-house applications). Co-ordinate project planning with respect to time and cost. ; co-ordinate with various functions of a project team for budget projections for approval and tracking of budgets/costs spent vs approved, assessing and reporting impact of variances. Lead and co-ordinate with respective functions for shipments, identifying reimbursable for monthly billing to clients (wherever applicable) and outsourcing studies (Non-GLP, GLP, GMP). Monitor resource allocation and utilization for assigned programs in consultation with function heads/Project team leads. Assess scope changes and risks to program delivery; flagging issues, making recommendations in consultation with team and executing agreed actions Provide timely communication of project/program status, issues and challenges to stakeholders and senior management Preferred candidate profile M.Sc. / M. Pharm / MTech & MBA with 4-6 years in project management with PMP certification, preferably from biotechnology/ Pharmaceutical sector Candidate with project management experience in Discovery Sciences would be preferred; should be adept at managing project milestones, budget and stakeholders. Should have excellent communication skills. ; Should have good negotiation skills & must have experience in MS project, MS Excel

Prolim is seeking an Application Engineer, Advanced, in the field of computational chemistry and multiscale modeling. You are an enthusiastic team player with a computational background in biology, chemistry, or physics. As part of Simcenter CULGIs dynamic and multidisciplinary team, you will support the customer to achieve their objectives. You will be responsible for the day-to-day execution of individual projects, executing simulation tasks ensuring quality results, reporting on their progress, and delivering successful and valuable solutions to the customer. You will interact with the customer to support the management of their expectations. Responsibilities Interfaces with customers during the execution of the projects Provides information to the development team to improve our software solutions Writes/updates scripts to support and enhance the creation of simulation tasks Proactively communicates the status on all projects Apply appropriate tools to analyze, identify, and resolve technical problems Required Knowledge/Skills, Education, and Experience A B.Tech Biotechnology/Chemistry , MSc Biotechnology /Chemistry / Ph.D. degree in computational science in either biology or chemistry Ability to work on multiple projects simultaneously Ability to communicate complex technical concepts clearly and effectively Problem-solving and reasoning skills Excellent written, verbal, and interpersonal communication skills Preferred Knowledge/Skills, Education, and Experience Previous role as RD engineer is a plus Commercial or professional industrial experience is a plus. Having experience in multiscale modeling and/or computational chemistry is a plus

About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and optimize Route of Synthesis (RoS) for novel medicinal drugs. Synthesize and purify medicinal compounds using advanced laboratory techniques. Conduct laboratory experiments to test the efficacy and safety of synthesized compounds. Analyse data from various analytical techniques to assess compound quality and properties. Improve the physicochemical properties of existing drugs to enhance performance and stability. Collaborate with other scientists and departments to advance drug development projects. Follow strict health and safety guidelines to ensure a safe working environment. Review and interpret the structure and purity of chemical compounds using modern analytical tools. Knowledge & Experience Bachelors in Medicinal Chemistry with Masters in Medicinal Chemistry, Organic Chemistry, or a related field. With M.Sc. (2 to 4 years of Experience) At least 2 years of hands-on experience in chemical synthesis within a pharmaceutical or biotech setting. Proficiency in modern synthetic techniques and analytical methods (e.g., NMR, HPLC, MS). strong problem-solving skills and the ability to design efficient synthetic routes. Excellent laboratory skills, including safe handling of chemicals and operation of laboratory equipment. Ability to work collaboratively in a team-oriented environment. Excellent written and verbal communication skills. Detail-oriented with strong organizational skills. Commitment to continuous learning and staying current with scientific advancements. Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans .

Job Description: We are seeking a highly motivated and skilled Medicinal Chemist with the industrial experience of 2 to 5 years to join our dynamic research and development team in Bengaluru. The candidate will be responsible for the design, synthesis, and characterization of novel chemical entities (NCEs) in accordance with client specifications and internal guidelines, contributing significantly to our drug discovery programs. Key Responsibilities: Synthesize and characterize novel NCEs efficiently and independently, adhering to client specifications. Apply broad knowledge of modern organic chemistry and synthetic methodologies to complex chemical problems. Execute various synthetic reactions, including but not limited to: heterocyclic chemistry, metal-catalyzed reactions, air/moisture-sensitive reactions, and hydrogenations, carrying out multi-step synthesis as required. Utilize a wide range of techniques for synthesis and purification, including chromatographic methods (e.g., MPLC, HPLC). Perform spectroscopic characterization of novel compounds using techniques such as NMR, LCMS, HPLC, and IR. Maintain accurate and up-to-date Lab Note Books in accordance with client specifications and internal guidelines. Generate final reports and other scientific documents as needed. Demonstrate a strong understanding of systems and processes pertaining to safety, health, and environmental regulations. Strictly adhere to EHS (Environmental, Health, and Safety) guidelines, maintaining a zero-tolerance policy for non-compliance. Required Candidate Profile: Education: M.Sc. in Organic Chemistry or Chemistry. Experience: 2 to 5 years of experience in Synthetic Chemistry (Small Scale). Interview Details (Walk-in Drive): Date: 5 th July'25 Time: 9:00 AM to 3:00 PM Interview Venues: Bengaluru: Aurigene Pharmaceutical Services Ltd. 39-40 Hosur Road KIADB Industrial Area, Phase 2, Electronic City, Bengaluru, Karnataka 560100 Hyderabad: Aurigene Pharmaceutical Services Ltd. Bollarum Road, Jaya Prakash Narayan Nagar, Miyapur, Telangana 500049, India Mandatory Documents to Carry for Interview: Your latest resume. Last three months' salary slips. Salary revision letter (if applicable). 3 Passport-size photographs. Note: The final job posting location will be Bengaluru, regardless of the interview location.

We are hiring Trainers/ Faculty/ Lecturer for our Pune branch to teach topics clinical research, medical coding, drug discovery Pharmacovigilance. Contact 9856963895 Eligibility : Msc(microbiology), Bpharm, Mpharm, Pharm D

Industry Engineering Engineering Design R&D Quality Qualification M.Sc Key Skills Green Field Projects UPLC R&D Synthesis HPLC R&D Developed PDR Brownfield M.Sc Chemistry We are looking for a skilled R&D professional with 4 to 9 years of experience to join our team in the Employment Firms/Recruitment Services industry. The ideal candidate will have a strong background in synthesis and be able to work independently. Roles and Responsibility Develop and implement new methods for chemical synthesis. Conduct experiments and analyze data to optimize processes. Collaborate with cross-functional teams to achieve project goals. Design and develop new equipment and facilities for chemical synthesis. Troubleshoot issues and improve existing processes. Maintain accurate records of experiments and results. Job Requirements Strong knowledge of chemical synthesis and related techniques. Ability to work independently and as part of a team. Excellent problem-solving and analytical skills. Good communication and interpersonal skills. Ability to prioritize tasks and manage time effectively. Familiarity with laboratory equipment and safety protocols.

Required skills : - Experience in computational biology and bioinformatics related areas is a must. - MS/PhD in Bioinformatics, Biostatistics, Mathematics, Computer Science, Computational biology or similar, with a strong publication record. - A strong understanding of statistical principles behind the current best practices in computational biology - Experience in computational biology and bioinformatics related areas is a must. - A strong understanding of statistical principles behind the current best practices in computational biology - Proven experience in drug discovery and development is essential preferably in industrial setting - Expertise in the use of a high-level programming language such as R, Python or Perl for complex data analysis. - Programming, web application programming, or relational database experience are pluses. - Proven expertise in defining and validating computational approaches to generate hypotheses using multivariate, Bayesian and machine learning approaches - Ability to generate in-silico experimental workflows and in-depth knowledge in proprietary and public biological databases, methods and tools.

aganitha cognitive solutions is looking for Scientist (Computational Chemistry / Materials & Molecular Modeling) to join our dynamic team and embark on a rewarding career journey Conduct innovative research and experiments to develop new knowledge, products, or technologies within a specialized scientific field Design, plan, and execute scientific studies while ensuring compliance with safety and ethical standards Collect, analyze, and interpret data using advanced tools and methodologies to draw valid conclusions Prepare detailed technical reports, research papers, and documentation for internal use and external publication Collaborate with cross-functional teams, including engineers, analysts, and other scientists, to achieve project goals

You Get To Collaborate On Work closely with discovery specialists, disease area scientists and in vivo team members. Handling of laboratory animals like rat, mice, Guniea Pig and Rabbits. Dose administration to experimental animals by different routes and small animals surgery (like cannulations, CSF fluid collection) and handling, followed by compound dose preparation, administration to experimental animals. Contributing to the ongoing drug discovery programs by conducting in vivo DMPK studies for NCEs with a good knowledge of in vivo animal models. Data generation, analysis, compilation, report preparation. Regular uploading of the data. Conduct statistically supported data (analysis using win online) and deliver results in a timely manner to enable informed decision-making Understanding systems, processes, and compliance. Prepare, review, and deliver scientific presentations for internal/external use. Participate in cross-functional team activities, add value to research projects through creative ideas. Learn from top-notch drug discovery scientists across the world and opportunity to get trained in people skills. PK-PD studies in rat and mice of NCE. Who will thrive in this role M.Pharm / M.S in Pharmacology with 3-5 years of research experience in either academic or industrial R&D setting. Deep understanding in pharmacokinetics, physiology along with in vivo disease model development and testing. Prior experience in small animal handling, dosing through different routes of administration, dissections and tissue harvesting, tissue processing Fair understanding about the drug discovery process. Excellent organizational, interpersonal, and problem-solving skills Experience of working with different cross functional teamsExcellent oral and written communication skillsStrong work ethic; scientific curiosity; can-do, will-do attitude. Experience in using electronic lab notebook system. If you don't meet all of the requirements listed here, we still encourage you to apply. No job description is perfect, and we might find an even more suitable opportunity that matches your experience.

Role & Responsibilities Will be responsible for managing Discovery projects end to end. Facilitate project team meetings and ensure accuracy and adequacy of documentation of project issues and action items. Handle minimum 3-4 (Early stage / Lead Optimization stage) internal or external programs and additional responsibilities (w.r.t processes / in-house applications). Co-ordinate project planning with respect to time and cost. ; co-ordinate with various functions of a project team for budget projections for approval and tracking of budgets/costs spent vs approved, assessing and reporting impact of variances. Lead and co-ordinate with respective functions for shipments, identifying reimbursable for monthly billing to clients (wherever applicable) and outsourcing studies (Non-GLP, GLP, GMP). Monitor resource allocation and utilization for assigned programs in consultation with function heads/Project team leads. Assess scope changes and risks to program delivery; flagging issues, making recommendations in consultation with team and executing agreed actions Provide timely communication of project/program status, issues and challenges to stakeholders and senior management Preferred candidate profile M.Sc. / M. Pharm / MTech & MBA with 4-6 years in project management with PMP certification, preferably from biotechnology/ Pharmaceutical sector Must have commercial /product launch experience Candidate with project management experience in Discovery Sciences would be preferred; should be adept at managing project milestones, budget and stakeholders. Should have excellent communication skills. ; Should have good negotiation skills & must have experience in MS project, MS Excel

Role & Responsibilities Conduct original research on AI applications, focusing on machine learning algorithms and data-driven methodologies. Design, implement, and evaluate innovative algorithms to solve complex problems in various domains. Collaborate with cross-functional teams to integrate research findings into production systems and prototypes. Analyze and interpret large datasets to extract meaningful insights and validate research hypotheses. Stay current with the latest developments in the AI field and contribute to scholarly publications. Mentor junior researchers and contribute to a collaborative and stimulating research environment. Skills & Qualifications Must-Have Master's degree or PhD in Computer Science, Artificial Intelligence, or related field. Strong knowledge of machine learning and AI algorithms. Proficiency in Python programming for AI applications. Experience in statistical modeling and data analysis techniques. Hands-on experience with natural language processing (NLP) methods. Preferred Familiarity with deep learning frameworks such as TensorFlow or PyTorch. Experience in conducting peer-reviewed research and publications. Excellent problem-solving skills and creativity. Benefits & Culture Highlights Collaborative and innovative work environment that nurtures creativity. Opportunities for professional development and continuous learning. Supportive team culture valuing diversity and inclusion.

Drug Discovery - In Vitro Pharmacology: Ph.D. in Bio-chemistry / Molecular Biology / Pharmacology / Biotechnology with 10 years industry experience or Ph.D. + post-doctoral fellowship with 6-8 years in drug discoveryresearch. Knowledge: Good understanding of overall drug discovery process; exposure to multiple therapeutic a reas In-depth understanding of all aspects of in vitro pharmacology as applicable to new drug d iscovery Basicunderstanding of biologics development like mAbs, ADC, etc Skills: Ability toestablish cost effective biochemical and cell based assays by using differentkinds of readouts like absorbance, luminescence, fluorescence and HTRFtechnologies. Ability to screenNCEs in biochemical and cell based assays Statistical applications and dataanalysis Good communication and management skills Competencies: Expertise and specializationin developing target based biological assays for NCEs and their screening Ability toinitiate, test and adapt new assay and screening methodologies Focused; driven to finish set goals within strict timelines

Chemveda is hiring for Ph.D Chemistry Freshers for our Discovery Chemistry Team Qualification - Ph.D Chemistry (2024,2025 passed outs) Department - Discovery Synthesis Position Name - Senior Research Associate Work Location - Hyderabad Key Skills and Competencies: Experience in Organic Synthesis/Multi-step Synthesis Handling reactions from mg to KG scale. Sound Knowledge of isolation, separation & purification techniques. Experience in characterization and identification of Organic molecules using spectroscopy techniques like NMR, IR, LCMS, HPLC. Positive and confident individual with strong work ethics. Team player and good communication skills Interested candidates can share their profiles with ramasatish.uppuluri@chemvedals.com or Whatsapp - 9100490347

Develop the scientific & strategic direction of the synthesis research business, overseeing drug discovery initiatives, managing research teams, ensuring the effective administration & growth. Required Candidate profile Ph.D. in Chemistry with 12+ years in CRO/ process development/ chemical synthesis with flair of senior research leadership role would be an ideal fit. Willing to work at the lab and be a mentor. Perks and benefits Best of CTC, additional perks and benefits

Aragen is hiring for Research Associate / Senior Research Associate / Associate Scientist for Hyderabad location Department: Synthesis R&D Qualification: M.Sc . (Organic Chemistry/ Medicinal Chemistry) Experience: 2- 10 Years into the CRO industry Role Description Set-up and execute reactions for synthesis of Targeted molecules/ Compounds Conducting day-to-day synthesis activities, including designing and executing experiments, analyzing data, and contributing to project advancement in the laboratory setting. Qualifications 1.Experience in Synthesis R&D (min 1year) 2.Strong background in organic synthesis, medicinal chemistry, or related field 3.Hands-on experience in executing chemical reactions in mg to gm scale and to synthesize required quantities of molecules/ compounds as per client specifications using efficient route and techniques 4.Proficiency in analytical techniques for compound characterization using NMR, LCMS, HPLC. 5.Expertise in writing Electronic Lab Notebook & detail-oriented approach to work and documentations 6.Master's or Ph.D. in Chemistry or relevant discipline 7.Experience in the CRO industry Please share your CV if you have above skillset only " sanjana.tulasiram.c@aragen.com "

Dear Chemists! "Aragen" is widely hiring Chemists with 2-10 Yrs of Discovery Synthesis experience for Hyderabad. Date of SCHEDULED WALK IN DRIVE - 21-06-2025 Time: 08:00 AM to 12:00 PM Interview Venue: Survey No 125 & 126, IDA Mallapur, Mallapur Campus, MLR-3, Hyderabad-500076

Shares in Eurofins Scientific are listed on the Euronext Paris Stock Exchange (ISIN FR0014000MR3, Reuters EUFI.PA, Bloomberg ERF FP). Discovery One Overview Integrated Drug Discovery, Discovery One, brings together the breadth of functional expertise across the entire Eurofins Discovery organization and combines a wealth experienced drug discovery and program management expertise to design, implement and deliver from idea to IND enabled on behalf of the client. In combining all the chemistry, biology, ADME, pharmacology, safety and toxicology capabilities of Eurofins Discovery, and using our extensive drug discovery expertise and experience, as well as exceptional program management services, Discovery One brings high value, complementary consultative support to enable the client. The virtual project team of Scientific Project Leads and Program Managers, drives the project internally and externally to a successful conclusion and hopefully project renewal. The Project Coordinator/Manager would oversee and coordinate chemistry-focused projects managed by DiscoveryOne but executed at Eurofins Advinus. This role will also support Program Managers in the planning, execution, and assessment of different programs within DiscoveryOne. The Project Coordinator will facilitate effective communication and collaboration across multiple sites and ensure that projects are delivered on time, within scope, and in compliance with contractual requirements. They will also collaborate closely with Program managers, Scientific Project Leads, Client Services teams, Laboratory Operations teams, and other personnel to ensure that the goals, objectives, and outcomes of the program are achieved. Additionally, they will interact with internal and external stakeholders to offer information, feedback, and support. Essential Duties and Responsibilities Project Coordination: Oversee and manage the day-to-day activities of Chemistry-focused projects, ensuring smooth execution and timely delivery Act as the primary point of contact between the different teams and sites involved in the project Ensure seamless coordination between DiscoveryOne, and the Chemistry teams across different sites Review and verify contractual requirements to ensure they are being met Work with legal and finance teams to ensure compliance with contract terms, deliverables, and payment schedules Monitor project progress and ensure deadlines are met Maintain and update program databases and records Collaboration and Support to DiscoveryOne Program Management team (Study Coordination): Provide administrative support to program managers Assist in the development and execution of program strategies and activities Responsible for processing orders from clients and organizing materials for project implementation, from quote and sales order generation to study completion Facilitate communication between program managers and internal client services and operations teams, keeping program managers informed of study status, turnaround times and delays or potential issues and operations teams informed of client requirements Initiate and track studies under DiscoveryOne, ensuring timely study activation and data delivery Maintain and update program databases and records Monitor study/project progress and ensure deadlines are met Perform other duties as assigned Qualifications Education Associates or Bachelors degree in Chemistry or equivalent; or more than 3 years related experience and/or training in project management; or equivalent combination of education and experience. Proven project management ability, with excellent follow-up and close-out skills Experienced in writing and interpreting documents such as standard operating procedures, instructions, and contracts and agreements with demonstrated attention to detail Knowledge of integrated drug discovery process and bringing drugs to market in Pharma or Biotech is preferred Experience in Microsoft Dynamics AX Software and Laboratory Information Management System (LIMS) is preferred Preferably from the CRO industry Strong organizational and time management skills Excellent written and verbal communication Ability to work independently and in a team environment Coordinate with team members from different regions to meet deadlines and program milestones Demonstrate adaptability in accommodating flexible working hours to support a seamless collaboration environment Detail-oriented with strong problem-solving abilities Mentality/ Skills Strong organizational and time management skills Excellent written and verbal communication Ability to work independently and in a team environment Coordinate with team members from different regions to meet deadlines and program milestones Demonstrate adaptability in accommodating flexible working hours to support a seamless collaboration environment Detail-oriented with strong problem-solving abilities

The candidate should have excellent knowledge of modern synthetic methodology including asymmetric synthesis, heterocyclic chemistry, catalysis and the reaction mechanism is expected. Should be expert in synthetic problem solving/troubleshooting skills. Excellent communication skills including face to face and virtual interactions with team and clients. Must have exceptional Presentation skills. The candidate should maintain an accurate scientific notebook, draft concise written reports for publications.

Bhagwan Mahaveer Cancer Hospital & Research Centre is looking for Senior Resident Radiation Oncology to join our dynamic team and embark on a rewarding career journey. Patient Care: Provide comprehensive medical care to patients under the supervision of attending physicians Perform physical examinations, diagnose medical conditions, develop treatment plans, and monitor patient progress Clinical Supervision: Supervise and provide guidance to junior residents, interns, and medical students in their clinical duties Assist in their training, evaluation, and professional development Hospital Rounds: Conduct regular hospital rounds to assess patients, review test results, and discuss treatment plans with the healthcare team Coordinate and communicate patient care plans with nurses, specialists, and other healthcare professionals Medical Procedures: Perform or assist in various medical procedures, such as venipuncture, wound care, suturing, and bedside procedures Ensure adherence to sterile techniques, safety protocols, and best practices Medical Documentation: Maintain accurate and up-to-date medical records, including patient history, physical examination findings, treatment plans, and progress notes Ensure compliance with legal and regulatory requirements Patient Education: Educate patients and their families about their medical conditions, treatment options, and preventive measures Provide counseling on lifestyle modifications, medication management, and post-discharge care instructions Interdisciplinary Collaboration: Collaborate with other healthcare professionals, including nurses, pharmacists, therapists, and social workers, to ensure coordinated and holistic patient care Participate in interdisciplinary team meetings and contribute to care planning Continuity of Care: Facilitate smooth transitions of care between inpatient and outpatient settings Coordinate follow-up appointments, referrals, and discharge planning to ensure continuity of care and optimal patient outcomes Medical Research and Education: Stay updated with the latest medical advancements, evidence-based practices, and clinical guidelines Engage in research activities, present at conferences, and contribute to medical education and scholarly activities Quality Improvement: Participate in quality improvement initiatives to enhance patient safety, clinical outcomes, and healthcare delivery Identify areas for improvement, implement evidence-based practices, and contribute to quality assurance programs Professional Development: Engage in continuing medical education (CME) activities, attend conferences, and pursue opportunities for professional growth Maintain licensure and board certification requirements

Required skills : - Experience in computational biology and bioinformatics related areas is a must. - MS/PhD in Bioinformatics, Biostatistics, Mathematics, Computer Science, Computational biology or similar, with a strong publication record. - A strong understanding of statistical principles behind the current best practices in computational biology - Experience in computational biology and bioinformatics related areas is a must. - A strong understanding of statistical principles behind the current best practices in computational biology - Proven experience in drug discovery and development is essential preferably in industrial setting - Expertise in the use of a high-level programming language such as R, Python or Perl for complex data analysis. - Programming, web application programming, or relational database experience are pluses. - Proven expertise in defining and validating computational approaches to generate hypotheses using multivariate, Bayesian and machine learning approaches - Ability to generate in-silico experimental workflows and in-depth knowledge in proprietary and public biological databases, methods and tools.

Role & responsibilities Lead medicinal chemistry strategies for the design, synthesis, and optimization of novel drug candidates. Execute SAR (Structure-Activity Relationship) strategies to improve potency, selectivity, and overall drug-like properties. Drive hit-to-lead and lead optimization efforts across multiple discovery programs. Incorporate AI-driven drug design and computational modeling into medicinal chemistry workflow. Manage external collaborations with CROs' and academic partners to scale compound synthesis and profiling. Partner closely with biology, pharmacology, DMPK, and analytical chemistry to integrate data and advance candidates efficiently Analyse experimental results, generate hypotheses, and make data-driven decisions to guide programs. Build and mentor a team of medicinal chemists, fostering scientific innovation and Professional growth. Remain hands-on in chemistry when needed, applying creativity and rigour to overcome key design challenges. Preferred candidate profile PhD in Organic or Medicinal Chemistry (or a related discipline) with 10+ years of industry experience in drug discovery. Demonstrated leadership in advancing small molecules or peptides into the clinic. Deep expertise in synthetic chemistry, drug design, and SAR optimization. Exposure to AI-based drug discovery, computational chemistry, or fragment-based design. Solid understanding of DMPK, pharmacology, and safety assessment in early development Familiarity with patent strategy and regulatory considerations for small-molecule therapeutics Proven ability to manage cross-functional projects and external partnerships Excellent communication, leadership, and decision-making skills

Hi, Greetings from Biophore India Pharmaceuticals!! We are hiring for Synthesis R&D /Process R&D/CRO Experience: 3 to 6 Years Qualification: M. Sc ( Organic Chemistry) Walk In date : 19th November 2024, Tuesday . Timings : From 10:00 AM to 02:00 PM . Preferable Male Candidates only If any one not able to attend the interviews , share your CV to " recruitments@biophore.com "

Hi , WE are hiring for Leading ITES Company for SAS Programmer & CDB Programmer ( J Reviewer/Python/SAS) Role & responsibilities: 1.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 2. Develop library of reusable checks working closely with data engineers and config specialists. 3. Collaborate with cross functional teams in creating business rules and automated check library across TAU. 4. Serves as a technical resource for creating data analytics to help with data validation and cleaning. 5. Provide programming expertise for data cleaning to efficiently ensure high quality data. 6. Ensure accurate delivery by creating macros for Standard listings for the department based on specifications. 7. Develop programs that generate CRF and Query metrics, including ad-hoc Sponsor and internal programming requests. 8. Ability to set up and configure analytics for coding reports, safety review and any risk-based monitoring activities. 9. Operational experience in pharmaceutical drug development with significant direct exposure to clinical development and data operations required for the reporting of clinical trial data (e.g. data review, regulatory submissions, safety updates, etc.) 10. Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable 11. Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle), 12. EDC build and/or clinical data management experience preferred 13. Experience in AWS preferred 14. Experience setting up automated validation is preferred 15. Knowledge of Data lake and creating interactive Dashboards are preferred 16. Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.) To Apply, WhatsApp 'Hi' @ 9151555419 Follow the Steps Below: >Click on Start option to Apply and fill the details >Select the location as Other ( to get multiple location option ) a) To Apply for above Job Role ( Nagpur ) Type : Job Code # 85 b) To Apply for above Job Role ( Bangalore ) Type : Job Code # 86

The Wireless Network Security, IT IS_CNS_Wireless Network_Cisco role involves working with relevant technologies, ensuring smooth operations, and contributing to business objectives. Responsibilities include analysis, development, implementation, and troubleshooting within the Wireless Network Security, IT IS_CNS_Wireless Network_Cisco domain.

Shares in Eurofins Scientific are listed on the Euronext Paris Stock Exchange (ISIN FR0014000MR3, Reuters EUFI.PA, Bloomberg ERF FP). DiscoveryOne Overview Integrated Drug Discovery, DiscoveryOne, brings together the breadth of functional expertise across the entire Eurofins Discovery organization and combines a wealth experienced drug discovery and program management expertise to design, implement and deliver from idea to IND enabled on behalf of the client. In combining all the chemistry, biology, ADME, pharmacology, safety and toxicology capabilities of Eurofins Discovery, and using our extensive drug discovery expertise and experience, as well as exceptional program management services, DiscoveryOne brings high value, complementary consultative support to enable the client. The virtual project team of Scientific Project Leads and Program Managers, drives the project internally and externally to a successful conclusion and hopefully project renewal. The Project Coordinator/Manager would oversee and coordinate chemistry-focused projects managed by DiscoveryOne but executed at Eurofins Advinus. This role will also support Program Managers in the planning, execution, and assessment of different programs within DiscoveryOne. The Project Coordinator will facilitate effective communication and collaboration across multiple sites and ensure that projects are delivered on time, within scope, and in compliance with contractual requirements. They will also collaborate closely with Program managers, Scientific Project Leads, Client Services teams, Laboratory Operations teams, and other personnel to ensure that the goals, objectives, and outcomes of the program are achieved. Additionally, they will interact with internal and external stakeholders to offer information, feedback, and support. Essential Duties and Responsibilities Project Coordination: Oversee and manage the day-to-day activities of Chemistry-focused projects, ensuring smooth execution and timely delivery Act as the primary point of contact between the different teams and sites involved in the project Ensure seamless coordination between DiscoveryOne, and the Chemistry teams across different sites Review and verify contractual requirements to ensure they are being met Work with legal and finance teams to ensure compliance with contract terms, deliverables, and payment schedules Monitor project progress and ensure deadlines are met Maintain and update program databases and records Collaboration and Support to DiscoveryOne Program Management team (Study Coordination): Provide administrative support to program managers Assist in the development and execution of program strategies and activities Responsible for processing orders from clients and organizing materials for project implementation, from quote and sales order generation to study completion Facilitate communication between program managers and internal client services and operations teams, keeping program managers informed of study status, turnaround times and delays or potential issues and operations teams informed of client requirements Initiate and track studies under DiscoveryOne, ensuring timely study activation and data delivery Maintain and update program databases and records Monitor study/project progress and ensure deadlines are met Perform other duties as assigned Qualifications Education Associates or Bachelors degree in Chemistry or equivalent; or more than 3 years related experience and/or training in project management; or equivalent combination of education and experience. Proven project management ability, with excellent follow-up and close-out skills Experienced in writing and interpreting documents such as standard operating procedures, instructions, and contracts and agreements with demonstrated attention to detail Knowledge of integrated drug discovery process and bringing drugs to market in Pharma or Biotech is preferred Experience in Microsoft Dynamics AX Software and Laboratory Information Management System (LIMS) is preferred Preferably from the CRO industry Strong organizational and time management skills Excellent written and verbal communication Ability to work independently and in a team environment Coordinate with team members from different regions to meet deadlines and program milestones Demonstrate adaptability in accommodating flexible working hours to support a seamless collaboration environment Detail-oriented with strong problem-solving abilities Mentality/ Skills Strong organizational and time management skills Excellent written and verbal communication Ability to work independently and in a team environment Coordinate with team members from different regions to meet deadlines and program milestones Demonstrate adaptability in accommodating flexible working hours to support a seamless collaboration environment Detail-oriented with strong problem-solving abilities Additional Information We support your development! Do you feel you dont match 100% of the requirementsDont hesitate to apply anyway! Eurofins companies are committed to supporting your career development. Weembracediversity! Eurofins network of companies believe in strength and innovation through diversity, being anEqual Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page:https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, research services.It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.