90 Biotech Jobs

As a Product Manager with Life Sciences / Pharma Subject Matter Expertise at our AI-native startup focusing on automation solutions for the pharmaceuticals and life sciences sector, you will play a crucial role in bridging the gap between industry workflows and cutting-edge AI solutions. You will be responsible for leveraging your deep subject matter expertise in Pharma / Life Sciences to drive product strategy and requirements. Your domain knowledge will be instrumental in shaping product features that cater to the specific processes, regulations, and workflows of the Life Sciences, Pharma, Biotech, and MedTech industries. Key Responsibilities: - Utilize your strong expertise in Life Sciences / Pharma / Biotech / MedTech processes, regulations, and workflows to inform product strategy - Translate domain knowledge into actionable requirements and features that align with industry needs - Lead product management activities including roadmapping, discovery, and stakeholder engagement - Demonstrate secondary skills in consulting and account management to enhance the overall product offering - Leverage exposure to digital transformation, workflow automation, and AI-driven products to drive innovation and differentiation Qualifications Required: - Proven experience in product management with a track record of successfully translating domain knowledge into product strategies - Strong understanding of Agile methodologies and the ability to work closely with cross-functional teams - Excellent communication skills to effectively collaborate with engineering, design, and leadership teams - Ability to thrive in a fast-paced, entrepreneurial environment with a focus on continuous growth and learning In addition to the above responsibilities and qualifications, as part of our fast-growing AI startup, you will have the opportunity to take on a full-time role with high ownership. You will be at the forefront of defining and launching AI-first products tailored to pharma workflows. This role offers a collaborative and agile work culture where you will work closely with diverse teams to deliver industry-defining solutions. Join us and be part of an exciting journey filled with growth potential and the chance to make a significant impact in the pharmaceutical and life sciences sector.,

Main responsibilities Organize and implement an instructional program. Identify, choose and implement different teaching methods for all students with various educational backgrounds. Transfer to student's theoretical information, practical skills, methods and techniques. Provide a positive and honest environment for students during class hours. Use media equipment to sustain your course. Establish and maintain good relationships with the college staff, students and their parents. Stimulate analytical and rational thinking. Supervise student's projects. Examine and give students a feedback about their academic activity. Develop and implement a research strategy in a certain field. Participate and coordinate research activities. Write publications about your research activity. Sustain presentations at national and international conferences. Participate at college fairs. Handle student's problems. Act as tutor and offer them moral support. Counsel them concerning their educational development and career choosing. Required skills Excellent written and oral communication skills. Very good interpersonal skills. Intercultural competences. Professional appearance and presentation skills. Computer proficiency. Academic leadership. Problem solving capabilities. Highly organized and efficient in time management. Responsible and reliable.

Develop and implement innovative instructional methods. Develop professional logistics to improvise student performance. Guide, lead and mentor students in research projects. Evaluate, monitor and mentor student academic progress. Create, innovate and implement career-enhancement programs and activities.

Organize and implement an instructional program. Identify, choose and implement different teaching methods for all students with various educational backgrounds. Transfer to student's theoretical information, practical skills, methods and techniques. Provide a positive and honest environment for students during class hours. Use media equipment to sustain your course. Establish and maintain good relationships with the college staff, students and their parents. Stimulate analytical and rational thinking. Supervise student's projects. Examine and give students a feedback about their academic activity. Develop and implement a research strategy in a certain field. Participate and coordinate research activities. Write publications about your research activity. Sustain presentations at national and international conferences. Participate at college fairs. Handle student's problems. Act as tutor and offer them moral support. Counsel them concerning their educational development and career choosing. Required skills Excellent written and oral communication skills. Very good interpersonal skills. Intercultural competences. Professional appearance and presentation skills. Computer proficiency. Academic leadership. Problem solving capabilities. Highly organized and efficient in time management. Responsible and reliable. Excellent teaching skills. Willingness to assist and support students.

As a Sr. Technical Architect, you will be responsible for designing and delivering complex enterprise-scale Salesforce solutions for Customers in the Health industry. You will collaborate with teams across different stakeholders to realize a vision and ensure customer success. Your role will involve becoming a deep Health Cloud Domain and Product expert, leading the technical design and implementation of Salesforce solutions, and ensuring compliance with industry regulations (HIPAA, GxP, etc.) and alignment with business goals. You will support the full implementation lifecycle, from scoping to deployment in an evolving ecosystem consisting of clients and partners. Additionally, you will engage with potential customers during the pre-sales process, understand their business needs, and design tailored Salesforce solutions that align with their objectives. You will work closely with sales team, clients, and technical delivery teams to ensure the proposed solutions are technically sound, deliverable, and fit within the client's business processes. Your responsibilities will include serving as the Sr. Technical Architect for Salesforce Life Sciences Cloud implementations, architecting and designing scalable, secure, and high-performance Salesforce solutions, defining and overseeing data models, security architecture, API integrations, and performance optimization strategies. You will lead a team of architects focused on driving optimized solutions for Health industry clients leveraging Salesforce Health Cloud, Service Cloud, Sales Cloud, and Experience Cloud. Furthermore, you will participate in pre-sales activities such as discovery and technical deep-dive sessions, Proof-Of-Concept development with prospects, estimations, and help in creating release roadmap and timelines. You will connect with Salesforce Product teams to support client implementations, lead functional and technical workshops, and demonstrate leadership skills in designing, delivering, testing, and deploying. In addition to the above, you will play a program architect and advisory role as needed, have expertise in User Journey preparations, User Story reviews, Data Modeling, Apex Design Patterns, LWC, and other modern UI techniques. You will establish trust with the customer's leadership, promote and/or implement standard processes with SFI and Salesforce, and build out sophisticated business processes using native Salesforce Industries technology and the toolkit of the platform and integration tools. To qualify for this role, you must have a Salesforce Certified Technical Architect (CTA) credential, 14+ years of experience in developing technology solutions, and 5+ years of experience in handling client-facing projects in positions of increasing responsibility. You should have proven experience architecting enterprise-level Salesforce solutions in the life sciences or healthcare industry, a strong understanding of compliance and regulatory requirements including HIPAA, GxP, PHI, HL7, and FHIR, and expertise in Salesforce Life Sciences, Health Cloud, Sales/Service/Experience Cloud, and Vlocity Omnistudio. Moreover, you should have knowledge of integration architecture, REST & SOAP APIs, Governor limits involved during integrations, healthcare transformation projects, continuous integration, working with repositories, Apex Design Patterns, Platform Security, Identity and Access Management, Integration Security, Sharing and Visibility, Data Architecture and Management, Architectural Design Patterns, Salesforce/Apex, and experience with modern web and mobile technologies. Strong presentation and communication skills, as well as the ability to develop content for appropriate audiences, are essential for this role. Salesforce Certification, Application & System Architect Certifications are preferred qualifications.,

We have an urgent opening for a Technical Application Specialist (Sales) at Cleansep Systems Pvt. Ltd., an Engineering OEM company based in Thane. As an Application Specialist, your role will involve translating and explaining technical information to customers in the Biotech, Biopharma, Pharma, API/Bulk-drug, and Chemical industries. You will focus on demonstrating how our products and technology can address specific client needs, thereby playing a crucial part in the sales process. In this position, you will be required to provide advice and support to clients across various industries, identify new business opportunities, negotiate contracts, and review performance. You should be capable of engaging with both corporate stakeholders and end users to explain product features, address concerns, and collaborate with internal departments to customize products or services as per customer requirements. The ideal candidate for this role should have prior experience in OEMs catering to Biotech, Biopharma, and API industries. You must possess a strong technical understanding of our products and demonstrate a high level of motivation and discipline to succeed in this dynamic field. Reporting to your superior at the headquarters on a daily basis is essential. This is a full-time position with a competitive compensation range and benefits including cell phone reimbursement, paid sick time, and Provident Fund. The work location is in Thane, and only male candidates are eligible to apply. If you meet the qualifications and are passionate about leveraging technology advancements to drive business growth, we encourage you to apply for this exciting opportunity. Contact Person: Sushmita R. Shukla Contact No.: 9512547218 Email ID: hr.admin@cleansep.com Website: [Insert website] Job Type: Full-time Benefits: Cell phone reimbursement, Paid sick time, Provident Fund Schedule: Day shift Work Location: In person,

We are seeking candidates who have experience in various functions including manufacturing, procurement, R&D, production, vendor management, supply chain management, sales, merchandising, and distribution. The ideal candidate should be enthusiastic about participating in change initiatives and should thrive in a dynamic environment with rapidly evolving priorities. Applicants with at least 2 years of experience in industries such as electrical, electronics, civil, mechanical, biotech, production, medical, footwear, chemical, textile, pulp and paper, food technology, automobile, sports, cosmetics, construction, and any other related fields are encouraged to apply.,

As a Business Development Executive for our leading provider of high-quality scientific products and chromatography solutions, you will be a key contributor to expanding our market presence and driving sales growth. Your role will involve identifying new business opportunities, maintaining client relationships, and achieving sales targets within the scientific sector. Your responsibilities will include generating leads in research institutions, laboratories, and industrial clients, conducting market research to evaluate trends, and managing the entire sales cycle from initial contact to after-sales support. It will be essential for you to develop and nurture relationships with existing and potential clients, understand their needs, and recommend suitable scientific products and solutions. To excel in this role, you must stay informed about the latest scientific product developments, effectively communicate technical information to customers, and prepare customized proposals and quotations. Additionally, tracking sales performance, collaborating with internal teams, attending industry events, and providing exceptional client support are integral parts of your responsibilities. To qualify for this position, you should hold a Bachelor's degree in a science-related field, with a background in scientific research or technical sales being advantageous. Previous experience in business development or sales, particularly in the scientific or technical product sector, will be beneficial. Strong communication skills, goal-oriented mindset, and proficiency in CRM software and Microsoft Office Suite are desirable attributes for this role. If you are a self-motivated individual with a passion for scientific innovation, exceptional problem-solving abilities, and a keen interest in contributing to the growth of the scientific community, we invite you to apply. In return, we offer a competitive salary, performance-based incentives, opportunities for professional growth, and a dynamic work environment with health and wellness benefits. To apply for this exciting opportunity and be part of our team, please send your resume and cover letter to sales@damconscientific.com. Join us in supporting the growth of our scientific product range and making a difference in the scientific community.,

You will work as a production operator/supervisor in a chemical/fermentation plant, where your responsibilities will include operation and supervision of production for fermentation-based biotech products. This will involve tasks such as media preparation, chemical reactor/fermenter set-up, filtration, sampling, and other related activities. The ideal candidate for this position should have a B.Sc or Diploma qualification. This is a full-time job that requires you to work on a variety of shifts including day shift, morning shift, night shift, rotational shift, and weekends. The location of this job is in Surat, Gujarat. Please note that remote work is not available for this position.,

As an Instrumentation Engineer at our leading biotech manufacturing company in Mohali, Chandigarh, specializing in bioprocess equipment, your role will involve overseeing the installation, troubleshooting, and maintenance of control systems integrated into our bioreactors, fermenters, and ultrafiltration systems. Your responsibilities will include configuring, troubleshooting, and maintaining control systems such as PLCs, SCADA, sensors, pumps, and actuators used in biotech and pharma applications. You will be required to assemble, wire, and test PLC and microcontroller-based control panels for bioprocess equipment, ensuring compliance with design specifications and safety standards. Furthermore, you will play a key role in ensuring the proper installation, calibration, and commissioning of bioprocess equipment at client sites. In addition to providing troubleshooting and technical support to diagnose and resolve issues related to control systems and instrumentation failures, you will also be responsible for training client personnel on the safe operation, troubleshooting, and routine maintenance of bioreactors and associated equipment. Occasional travel to customer sites for installation, commissioning, and service visits will be required as part of your role. To excel in this position, you should hold a Diploma/ITI in Electronics & Communication / Instrumentation / Electrical Engineering with at least 2 years of relevant experience in pharma/biotech, biomedical, or industrial automation industry. Proficiency in PLC programming, SCADA systems, sensors, control circuits, and industrial automation is essential. Strong communication skills, the ability to read electrical schematics and interpret mechanical assembly drawings, and a willingness to occasionally travel across India for installations and on-site support are also required. In return, we offer a range of benefits including Provident Fund & ESIC, Health Insurance, Mobile and/or Laptop, Travel Allowance / Daily Allowance, Annual Bonus, Retention Bonus, and Encashable Leaves. If you meet our requirements and are enthusiastic about contributing to the success of our biotech manufacturing operations, we encourage you to apply for this full-time position and join us in optimizing process efficiency and enhancing equipment performance in the biotech industry.,

You should possess a Bachelor's Degree in Science, Biochemistry, Biotechnology, Pharmacy, Bioinformatics, and preferably an MBA from a reputable institute. With 1-7 years of experience, you will be responsible for Cold Calling and B2B Sales within the CRO, CRAMS, Biotech, or Pharma sector. Strong communication skills are essential, coupled with a self-driven and result-oriented mindset. Your role will include identifying and developing new sales opportunities, working closely with the Marketing team to create innovative campaigns, and generating high-quality leads. You should be comfortable initiating conversations with senior professionals and key decision-makers, maintaining detailed communication documentation through CRM tools, and exceeding monthly lead generation quotas. Understanding the healthcare ecosystem and the industry sector is crucial, as you will be interacting with seasoned professionals to create a need for the business offerings. Working collaboratively in a team-based environment, you will take complete end-to-end responsibility to achieve impactful business results. Articulating the value proposition effectively, employing persuasion techniques, and maintaining a never-give-up attitude are key aspects of this role. A proactive and organized approach is essential to meet and exceed the desired business outcomes. Fluency in European languages such as German or Spanish would be advantageous. If you are a high-energy, motivated individual seeking a fast-paced entrepreneurial environment, this opportunity may be the right fit for you. Contact us at hr@clientcurve.com.,

The Regulatory Data & Systems Senior Associate will be responsible for interpreting and executing business requirements, based on a combination of industry best practice and Amgen regulatory processes. This role involves optimizing complex data systems supporting the health authority submission process, while ensuring compliance with regulatory regulations and guidance. The ideal candidate will have a strong background in system analysis and data science/AI in a regulated industry. Roles & Responsibilities: Data Administration/AI: Optimize and maintain the organization's complex data models, ensuring they are integrated, efficient, and compliant with regulatory requirements. Regulatory Business Analysis: Interpret and implement regulatory requirements, ensuring all systems and processes adhere to relevant regulatory requirements and industry best practices. Project Coordination: Assist in planning, tracking, and executing departmental projects and initiatives. Stakeholder Communication: Liaise with internal and external stakeholders to ensure timely and accurate communication regarding regulatory requirements and system updates. Required Knowledge and Skills: Strong interpersonal and teamwork skills, with the ability to interact with business users, technical IT groups, project managers, senior management, outsourced service providers, and vendors. 5+ years" experience as a business analyst, with command of business analysis techniques & tools, as well as SDLC & agile systems development methodologies. Excellent oral and written communication skills; able to organize and present ideas in a convincing and compelling manner. Ability to operate effectively in a matrix environment; team player yet able to work independently with minimal direction. Familiarity with GxP requirements and systems validation. Life Sciences, Biotech, or pharmaceutical industry experience. Preferred Knowledge and Skills: Advanced knowledge of Veeva Vault. Familiarity with global regulatory processes and standards. Proficiency in Agile methodologies, including Scrum or Kanban, to enhance collaboration, efficiency, and adaptability within an Agile work environment. Basic Education and Experience: Bachelors degree and 2 years of directly related experience. Associates degree and 6 years of directly related experience. High school diploma/GED and 8 years of directly related experience. Preferred Education and Experience: Practical experience with regulatory data standards, such as IDMP. 5+ years experience in data management, machine learning, or related fields.,

As a Technical Support Specialist, your primary responsibility will be to address customers" technical issues and complaints in a timely and effective manner. You will collaborate closely with Sales and other Technical Support Specialists to troubleshoot problems and provide solutions. Additionally, you will be required to conduct correlation studies and validations in coordination with customers as needed. Another essential aspect of your role will involve providing training to customers to ensure they are equipped to use our products effectively. Regularly visiting clients to gather feedback and communicate relevant information to the sales team will also be part of your duties. Furthermore, you will participate in regional and national conference calls to update technical issues and contribute to discussions. To qualify for this position, you should hold a Bachelor's degree or higher in Clinical Medicine, Biotechnology, Pharmacy, or a related field. A Master's degree would be highly preferred. You must have a minimum of 3 years of experience working in the IVD Application area, with a focus on disciplines such as immunology, biochemistry, or molecular biology. Proficiency in English as a working language is essential, and strong communication skills are a must. Additionally, we are looking for a hard-working individual who can thrive in a dynamic and fast-paced environment. This position is based in multiple locations, including Delhi, Kolkata, Hyderabad, among others. In addition to the specified responsibilities, you may be assigned other tasks by the company to support our overall objectives.,

The Project Finance Analyst is responsible for ensuring excellence in financial management and controls across assigned projects and portfolio. As an individual contributor, you will work closely with Project Managers to manage project profitability, realization, client reporting, and systems support/maintenance. Your responsibilities will include ensuring revenue recognition and forecasting support throughout the lifecycle of all projects within your assigned portfolios. You will provide business partnering analysis on realization, profitability, budgets & forecasts on assigned projects, supporting Project Managers to identify and develop plans to resolve areas of poor financial performance. It will be your duty to ensure financial excellence targets are met on all assigned projects, including realization, profitability, and maintenance of deferred revenue balance where appropriate. You will liaise with Project Management personnel, offering timely advice, support, and resolution to issues and omissions in the month-end financial process. Providing insight to senior management on project movements compared to forecast and contract on assigned projects will also be part of your responsibilities. Additionally, you will manage the month-end processes on assigned projects related to revenue and forecast management, and project performance. Your role will involve overseeing project finance close-out activities, completing final budget reconciliation in collaboration with PM and other stakeholders, including clients, sites, and third-party vendors. You will ensure compliance with any contracted project finance requirements for completed projects. Developing strong relationships with customers, ensuring timely response to client queries and reporting requests will also be crucial. Moreover, you will be responsible for the timely and accurate setup of projects within the ERP and ensuring timely handover to Project Management. Your contribution to process improvement initiatives within the Project Finance group will be highly valued. To be considered for this role, you should be a graduate in a finance, clinical, or life sciences related field, with relevant experience/qualifications in allied professions also being considered. A minimum of two years" experience within the pharmaceutical/CRO industry or related field is required. Strong financial acumen with a desire to drive business performance and accountability is essential. Proficiency in Microsoft Office, specifically advanced Excel skills, is a must, along with experience with SalesForce/Certinia ERP ecosystem. Novotech is committed to providing a great workplace that promotes gender equality and inclusivity. Flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs, and ongoing development programs are some of the benefits we offer to our team members. We welcome individuals passionate about working in clinical research and biotech, including those who identify as LGBTIQ+, have a disability, or have caring responsibilities. As a Circle Back Initiative Employer, we commit to responding to every application and look forward to contacting you regarding your application.,

As a Quality Engineer with rich experience in manufacturing process equipment for Chemical, Pharma, and Biotech applications, your main responsibility will be to ensure the highest standards of quality are maintained throughout the manufacturing process. This includes conducting quality checks, implementing quality control measures, and identifying areas for improvement to enhance overall product quality. You will work closely with cross-functional teams to address any quality issues that may arise, and collaborate with production teams to implement corrective actions. Your expertise will be crucial in developing and maintaining quality standards that meet industry regulations and customer expectations. The ideal candidate will have a proven track record in quality engineering within the manufacturing industry, particularly in the Chemical, Pharma, and Biotech sectors. Strong attention to detail, analytical skills, and a commitment to continuous improvement are essential for success in this role. This is a full-time position that requires you to work in person at the designated work location. If you are passionate about quality engineering and have the necessary experience in manufacturing process equipment, we would love to hear from you.,

Join the rapid growth with Genuine Biosystem! Genuine Biosystem, a leader in providing cutting-edge Rapid Cards, is expanding its reach and looking for dynamic, driven individuals to promote our products across Tamil Nadu. We are hiring Sales Cum Application Executives who are passionate about innovative products and eager to make a difference in the biotechnology, healthcare, IVD, biochemistry, and microbiology industries. As a Sales Cum Application Executive, you will have the opportunity to work across various business verticals and be part of a revolutionary product line in biotechnology/IVD. What we offer: - Attractive Salary & Incentives: Competitive remuneration plus additional incentives for every sale. - Training & Support: Comprehensive product training and ongoing support to ensure your success. - Flexible Work Environment: Manage your schedule and work at your own pace. - Career Growth: Opportunity to grow within the organization. - Cutting-Edge Products: Work with high-quality, trusted rapid cards used by healthcare professionals. What we're looking for: - Experienced sales professionals passionate about healthcare, IVD, or biotech products. - Excellent Communication Skills: Ability to effectively connect with healthcare professionals and clients. - Self-Motivated: A go-getter who can drive results and achieve targets. - Reliability: Consistent performance in meeting targets and maintaining relationships. - Local Knowledge: Familiarity with Tamil Nadu's healthcare market is a plus. Why Genuine Biosystem - Known for high-quality products and reliable service. - Rapid Cards trusted by healthcare professionals with proven success in diagnostics. - Be part of a forward-thinking company in a rapidly growing industry. Ready to make an impact Apply today by sending your resume to info@genuinebiosystem.com or admin-hr@genuinebiosystem.com. Contact us at 6383066400 or 7200349594.,

As a Sales Leader/Manager in the Pharma Filtration industry, you will be responsible for driving B2B/OEM sales of validated filtration products to pharmaceutical API/formulation and biotech plants. Your role will involve managing and growing key accounts, identifying and converting new business opportunities, and engaging with decision-makers across different segments. You will lead technical discussions, maintain an active sales pipeline, and collaborate with internal teams to tailor customer-centric solutions. Key Responsibilities: - Drive B2B/OEM sales of validated filtration products such as depth filters, membrane cartridges, and process housings. - Manage and grow key pharma/biotech accounts through consultative, solution-driven filtration systems. - Identify and convert new business opportunities in API, formulation, sterile injectables, and biotech segments. - Engage with decision-makers including Plant Heads, QA/Validation Teams, Utility Heads, and Engineering Managers. - Lead technical discussions on DQ/IQ/OQ/PQ, filter integrity testing, and documentation support. - Maintain an active sales pipeline, ensure timely follow-ups, and contribute to revenue growth. - Collaborate with internal product and application teams to develop customer-centric solutions. - Participate in technical presentations, trade shows, plant audits, and industry events. Must-Have Skills & Experience: - 3-8 years of sales or business development experience in filtration, CIP/WFI utility systems, or sterile process solutions. - Proven ability to close deals with pharma clients and strong knowledge of process filtration. - Comfortable with validation protocols (DQ/IQ/OQ/PQ), documentation cycles, and cleanroom compliance. - Excellent client-facing, presentation, and negotiation skills. - Willingness to travel frequently (domestic and occasional international). - A Bachelor's degree in engineering or pharmaceuticals is preferred. If you have the relevant experience and skills in technical sales of filtration systems for the pharmaceutical industry, we encourage you to apply for this exciting opportunity. Please note that only shortlisted candidates will be contacted. Thank you for your interest in this position.,

Role & responsibilities Timely completion of designs, and Process engineering deliverables. Adherence to Dept./Discipline Working Instructions and Quality Systems. Overview of work progress and work-hour usage. Working within company budgets Meet client expectations and maintain long-term relationship with client. Attend to clients feedback and any complaints Preferred candidate profile A degree in Chemical Engineering Discipline with Minimum 18 to 25 years in Process Department of a consultancy organization or technical services department of a Pharmaceutical/ Biotech/Lifesciences. Candidate should possess knowledge in carrying out basic and detailed engineering work. The experience can be from any Pharmaceutical/ Biotech/ Chemical projects. Candidate should have knowledge of following: Performing process calculations like heat & mass balance, Utility sizing for API, OSD and Biotech Projects. Pharma Process Equipment data sheet preparation Line sizing, relief load & PSV calculation. Exposure of simulation softwares such as HYSYS, ASPEN. Preparing Process Flow Diagrams (PFDs) and Piping and Instrument Diagrams (P&IDs). Reviewing all aspects of design and construction for consistency and safety, including leading Hazop and PHA Reviews Process engineering calculations such as Thermal rating of heat exchangers, and hydraulics

Design, build, and support data ingestion, transformation, and delivery pipelines across structured and unstructured sources within the enterprise data engineering. Manage and monitor day-to-day operations of the data engineering environment, ensuring high availability, performance, and data integrity. Collaborate with data architects, data governance, platform engineering, and business teams to support data integration use cases across RD, Clinical, Regulatory, and Commercial functions. Integrate data from laboratory systems, clinical platforms, regulatory systems, and third-party data sources into enterprise data repositories. Implement and maintain metadata capture, data lineage, and data quality checks across pipelines to meet governance and compliance requirements. Support real-time and batch data flows using technologies such as Databricks, Kafka, Delta Lake, or similar. Work within GxP-aligned environments, ensuring compliance with data privacy, audit, and quality control standards. Partner with data stewards and business analysts to support self-service data access, reporting, and analytics enablement. Maintain operational documentation, runbooks, and process automation scripts for continuous improvement of data fabric operations. Participate in incident resolution and root cause analysis, ensuring timely and effective remediation of data pipeline issues. Create documentation, playbooks, and best practices for metadata ingestion, data lineage, and catalog usage. Work in an Agile and Scaled Agile (SAFe) environment, collaborating with cross-functional teams, product owners, and Scrum Masters to deliver incremental value Use JIRA, Confluence, and Agile DevOps tools to manage sprints, backlogs, and user stories. Support continuous improvement, test automation, and DevOps practices in the data engineering lifecycle Collaborate and communicate effectively with the product teams, with cross-functional teams to understand business requirements and translate them into technical solutions Must have Skills: Build and maintain data pipelines to ingest and update metadata into enterprise data catalog platforms in biotech or life sciences or pharma. Hands-on experience in data engineering technologies such as Databricks, PySpark, SparkSQL Apache Spark, AWS, Python, SQL, and Scaled Agile methodologies. Proficiency in workflow orchestration, performance tuning on big data processing. experience in data engineering, data operations, or related roles, with at least 2+ years in life sciences, biotech, or pharmaceutical environments. Experience with cloud platforms (e. g. , AWS, Azure, or GCP) for data pipeline and storage solutions. Understanding of data governance frameworks, metadata management, and data lineage tracking. Strong problem-solving skills, attention to detail, and ability to manage multiple priorities in a dynamic environment. Effective communication and collaboration skills to work across technical and business stakeholders. Strong problem-solving and analytical skills Excellent communication and teamwork skills Experience with Scaled Agile Framework (SAFe), Agile delivery practices, and DevOps practices.

Key Activities: Performs product complaints statistical excursion trending deep dives Understand customer / patient use of Amgen s packaged and/or distributed mechanical and/or electromechanical products Understand manufacturing processes for Amgen s packaged and/or distributed products. Maintain close interaction with multiple functions including Quality (e. g. complaints, device quality, product quality, external supplier quality, manufacturing quality, quality engineering) and contribute to product / device design improvements Collaborate with other safety functions to support integrated surveillance of Amgen products from both quality and safety s perspectives Prepares and interprets adverse events and product complaints data supporting integrated product surveillance activities Prepares product and process surveillance metrics for internal safety and quality governance forums Pulls complaints and/or adverse events data to support ad-hoc analysis and regulatory inquiries Perform data verification of complaints data pulled for inspection requests Applies analytical skills to evaluate complex situations using multiple sources of information Contribute to technology innovation initiatives related to post market surveillance, including AI/ML and automation opportunities Contribute to improvements in trending methodologies and process improvement opportunities Support audits and inspections as appropriate Knowledge and Skills Required Knowledge and Skills: Quality and/or manufacturing experience in biotech or pharmaceutical industry Complaints or complaints trending within a development, manufacturing, or post-market environment Knowledge of product complaints and adverse events intake and processing process Ability to pull and create product complaints and/or adverse events data per request Knowledge of medical devices or combination products, ideally Class II and Class III Data querying skills and experience with data visualizations tools such as Tableau, Power BI, or Python Preferred Knowledge and Skills: Proven experience with mechanical and/or electromechanical medical devices Knowledge of combination products and medical devices, including device safety monitoring regulations and standards Ability to perform data analysis and derive insights Education & Experience (Preferred) Degree in Engineering or Life Science 5-9 years of quality and/or manufacturing experience as an engineer in the biotech or pharmaceutical industry 2+years of experience in complaints or complaints trending within a development, manufacturing or post-market environment, working with medical devices or combination products, ideally Class II and Class III Experience with statistical trending methodology, preferably complaints Strong data analysis experience and a passion for finding correlations across different datasets Experience with data querying and business intelligence tools Strong presentation and teamwork skills

Key Responsibilities: Literature Management Process - Perform review of literature results retrieved and imported into literature citation management system on a weekly basis and determine if minimum criteria for ICSR is met for marketed products Perform review of literature results to determine if article contains new aggregate safety information in support of the periodic report and/or signal detection Determine whether full text article needs to be ordered and order them if further information is needed to confirm if the citation meets criteria for ICSR or for signal detection Flag articles containing new aggregate safety information for TA Safety to perform secondary review Request Local Safety Officer to provide English translation if the article is not in English Notify business partner of articles received, if applicable Perform retrospective quality checks on the quality of the literature review performed by team Support audits and inspections Collaborate with Case Management and TA Safety on process improvement initiatives Proactively proposes and system and process improvement ideas Provide training and onboarding to junior staff Perform Quality checks on literature reviews performed by other staff Periodic Reporting Process - May assist with quality control of periodic reporting activities as required. Extract list of citations for inclusion in periodic reports Key Activities Responsible for routine review of literature articles as part of the global literature surveillance process Assist with quality control of periodic reporting activities Support audits and inspections by extracting requested citations from literature citation management system Knowledge and Skills Knowledge of product profiles for products assignment Ability to identify literature articles containing ICSR criteria or aggregate safety findings supporting signal detection Ability to order full text articles where needed Ability to receive feedback from Case Management and TA Safety and optimize quality of literature review Demonstrate knowledge of global aspects of pharmacovigilance Strong knowledge of processes and global regulations for pharmacovigilance and literature surveillance Ability to effectively manage competing priorities and timelines Strong knowledge of literature citation management systems and platform used to configure search strategies Experience in use of AI and prompts would be useful CONTRIBUTION: Ensures Amgen remains in compliance and maintains high quality global literature review process Responsible for the timely completion of review of weekly literature results Education & Experience (Basic) 8-13 years of pharmaceutical, biotech or regulatory authority experience in a research and development setting Knowledge of bibliographic databases and direct literature review experience (preferred)

Evalueserve is a global leader in delivering innovative and sustainable solutions to a diverse range of clients, including over 30% of Fortune 500 companies. With a presence in more than 45 countries across five continents, we excel in leveraging state-of-the-art technology, artificial intelligence, and unparalleled subject matter expertise to elevate our clients" business impact and strategic decision-making. Our team of over 4,500 talented professionals operates in countries such as India, China, Chile, Romania, the US, and Canada. Our global network also extends to emerging markets like Colombia, the Middle East, and the rest of Asia-Pacific. Recognized by Great Place to Work in India, Chile, Romania, the US, and the UK in 2022, we offer a dynamic, growth-oriented, and meritocracy-based culture that prioritizes continuous learning and skill development, work-life balance, and equal opportunity for all. Our Insights and Advisory team plays a crucial role in providing strategic guidance and data-driven insights to organizations. By analyzing market trends, consumer behavior, and business data, our team helps decision-makers make informed choices that can positively impact their organization's performance and bottom line. We work across diverse industries and sectors like Technology, Industrials, Energy, Chemicals, Life Sciences, and Logistics, including market research, strategy, sales and marketing, R&D, and more. As a member of Evalueserve, you will be responsible for Pharma Business research and Strategy Consulting support. Your tasks will include defining problem statements and initial hypotheses, designing optimal research approaches with a mix of research techniques (e.g., primary/secondary/basic modeling), structuring and presenting data and results using relevant frameworks, arriving at key messages/highlights addressing key objectives for Executive Leadership consumption, presenting research results to clients, handling client queries, and actively participating and contributing to team discussions on project-specific areas. We are seeking individuals with proven experience in strategy consulting and advisory within the pharmaceutical and biotech sectors, with a strong track record across key project types including opportunity assessment, competitive benchmarking, portfolio optimization, M&A due diligence, go-to-market planning, and go/no-go decision frameworks. The ideal candidate will have deep expertise in primary market research (both qualitative and quantitative), with the ability to apply advanced analytical models and strategic frameworks for data synthesis, trend identification, and triangulation of insights. The successful candidate will demonstrate the ability to quickly grasp client objectives and deliver high-impact solutions independently or as part of cross-functional teams, ensuring timely and high-quality execution. Additionally, they should be skilled in developing strategic reports and executive-level presentations, delivering actionable insights and clear recommendations tailored for senior leadership and C-suite stakeholders. Strong working knowledge of key pharma and medical data sources, analytical mindset, excellent communication skills, strong interpersonal skills, and proficiency in MS Office Suite are essential requirements for this role. Minimum qualifications include M.Tech./M.Pharm/B.Pharm/B.Tech (Biotech)/B.E(Biotech)/MBA and 6+ years of relevant experience in business research in a Pharmaceutical/Life Sciences Consulting Organization. Please note that the job description provided above serves as an informative reference for the tasks you may be required to perform. It is not an integral component of your employment agreement and is subject to periodic modifications to align with evolving circumstances. Accuracy and authenticity of the information provided are crucial for your candidacy and will be verified during the Background Verification Process. For further information about our culture and what it's like to work with us, please reach out to us at careers@evalueserve.com.,

The Regulatory Affairs - International Business role at Nexaa VRA Lifescience Pvt Ltd is a full-time position based in Dehradun. As a Regulatory Affairs professional, you will play a crucial role in ensuring compliance with international regulatory agencies. Your responsibilities will include preparing and submitting regulatory documents, staying updated on regulations and guidelines, liaising with international business partners, and providing guidance on regulatory requirements and strategies. You will be actively involved in managing regulatory submissions, reviewing product labels and marketing materials, and collaborating with various teams to ensure adherence to regulatory standards. To excel in this role, you should possess a strong understanding of international regulatory affairs, compliance, and submission processes. Experience in preparing, reviewing, and submitting regulatory documents is essential. Additionally, familiarity with different regulatory guidelines and requirements is key. Effective written and verbal communication skills are necessary for this position. The ability to work both independently and as part of a team is crucial. A Bachelor's degree in Life Sciences, Pharmacy, or a related field is required. Prior experience in the biotech or pharmaceutical industry would be advantageous. Attention to detail and excellent organizational skills are also important qualities for success in this role. Join Nexaa VRA Lifescience Pvt Ltd on its journey of purpose and progress in the international pharma space.,

We are looking for a QA Project Manager with a focus on Quality Assurance. Experience as a Project Manager in Life Sciences, Biotech, or Biosimilar Industry is essential for this role. The ideal candidate will be responsible for planning, coordinating, and implementing projects within the allocated budget, timeline, and scope. You will be required to effectively monitor project progress and provide updates to stakeholders, clients, or team members. Responsibilities include setting project timelines, monitoring deliverables, updating relevant stakeholders on project progress, and coaching project team members with assigned tasks. Qualifications: - Bachelor's Degree or equivalent experience - Strong business acumen in project planning and management - Excellent verbal, written, and organizational skills - Preference for candidates with experience in CGT driven companies Key Skills: - Project planning & execution: Managing timelines, resources, and deliverables across multiple projects - Risk management: Identifying, mitigating, and managing technical, regulatory, and operational risks - Cross-functional leadership: Coordinating across R&D, clinical, regulatory, manufacturing, and commercial teams - Background in life sciences (e.g., molecular biology, biochemistry, pharmacology) - Understanding of biotech R&D pipelines: Drug discovery, preclinical, clinical trials, and regulatory pathways - Ability to translate scientific data into actionable plans - Aligning project goals with company strategy and commercialization milestones If you meet the specified requirements and have the necessary experience, we encourage you to apply for this position.,

You will be responsible for overseeing and managing the end-to-end production and operations at the plant. Your role will involve ensuring product quality by regularly monitoring and adhering to standards, maintaining proper labeling, packaging, and batch traceability protocols, and enforcing GMP and GHP practices. You will need to implement cost-control measures to reduce wastage and improve efficiency, ensure on-time production and dispatch, and handle operational issues promptly with a proactive approach. In this position, you will also be coordinating with vendors for timely supply of raw materials and packaging, contributing to product improvement, supporting new flavor or product development, and setting up SOPs for smooth operations. You will investigate and resolve customer complaints, ensure the final product meets quality benchmarks, manage a team and assign work effectively, conduct QC of the final product, and manage NPD and RND activities. The qualifications and skills required for this role include a Bachelors or Masters degree in Food Technology, Biotech, or a related field, along with at least 3 years of experience in a food or beverage manufacturing environment, preferably with exposure to fermented products. Strong knowledge of food safety, GMP, and plant operations is essential, and familiarity with lean manufacturing and continuous improvement practices is a plus. Excellent problem-solving, team management, and communication skills are also important for this role. This is a full-time position with a day shift and fixed shift schedule. A performance bonus is included in the benefits package. The ability to commute or relocate to Bangalore, Karnataka is preferred for this role. As part of the application process, you will be asked about what interests you about working for the company. The work location is in person.,