3619 Biotechnology Jobs - Page 26

Position: Senior Executive – Quality Assurance & Regulatory Affairs Location: Edapally,Kochi | Employment Type: Full-Time | Experience: 3–6 Years Position Overview: We are seeking a highly motivated Senior Executive – Quality Assurance & Regulatory Affairs to establish and manage the Quality and Regulatory systems for pre-clinical stage drug development program. The role will play a key part in supporting compliance for ongoing R&D and pre-clinical studies, laying the foundation for GxP readiness, and managing early regulatory communications. This is a strategic hands-on role for a professional, passionate candidate about building quality and compliance frameworks from the ground up in a fast-paced startup environment. The person will be working closely with cross-functional R&D teams and leadership to shape the quality culture and regulatory strategy and gets a unique opportunity to become key foundational personnel in a mission driven drug development program. Key Responsibilities: · Establish initial QA systems aligned with GLP and other applicable regulatory guidelines for R&D and pre-clinical environments. · Draft, implement, and maintain Standard Operating Procedures (SOPs) , policies, and work instructions across departments. · Support data integrity , documentation review , and record-keeping for lab notebooks, protocols, study reports, etc. · Coordinate internal audits and prepare the organization for external audits and inspections (CROs, vendors, regulators). · Oversee vendor/CRO qualification , quality agreements, and ensure quality oversight of outsourced pre-clinical activities. · Ensure training compliance for scientific and operational staff on quality systems and regulatory requirements. · Maintain awareness and interpret relevant regulatory guidelines (CDSCO, ICH, US FDA, EMA, etc.) applicable to early-stage drug development. · Prepare and manage regulatory documentation (Pre-IND briefing packages, initial regulatory inquiries, ethics submissions). Qualifications & Skills: · Master’s degree in Pharmacy, Life Sciences, Biotechnology, or related field . · 3–6 years of experience in QA/RA functions in a pharmaceutical, biotech, or CRO environment, ideally in early development/preclinical phase. · Hands-on experience with GLP practices , regulatory compliance , and SOP development . · Familiarity with regulatory frameworks (ICH, OECD, US FDA IND pathways). · Strong organizational skills and attention to detail with the ability to handle multiple responsibilities in a startup setting. · Effective verbal and written communication skills, especially in regulatory and technical documentation. · Strong understanding of Quality Management Systems (QMS), GMP, GLP compliance Certifications (Preferred but not mandatory) · GLP/GMP/GCP Training Certification · Quality Management System (QMS) Certification · Regulatory Affairs Certification Soft Skills · Excellent attention to detail and strong documentation skills. · Proactive and solution-oriented mindset with ability to manage priorities independently. · Strong interpersonal and communication skills. · Capability to work in dynamic startup environments with cross-functional collaboration. Compensation & Benefits · Health Insurance · Second Saturdays & All Sundays Off · Opportunities for Learning & Career Development: To work with International renowned research institutions and pharma companies · Exposure to cutting-edge R&D projects and regulatory strategy · Collaborative & inclusive work culture that values innovation and accountability How to Apply Send your updated CV and cover letter to careers@luxmatra.com with the subject line: Application – Senior Executive – QA & RA

Job Title: MLT Company : MS Clinical Location : Bangalore Job Type : Full-time Experience: 1-2years About MS Clinical : MS Clinical is a dynamic and innovative company dedicated to advancing medical research and improving patient outcomes. We specialize in conducting clinical trials and providing comprehensive medical writing services to pharmaceutical, biotechnology, and healthcare organizations worldwide. Job Description : A lab technician's responsibilities vary depending on the industry and company, but some common duties include: Testing and analyzing samples Lab technicians may test and analyze body fluids, food samples, or new drugs. Operating equipment Lab technicians use a variety of equipment, including microscopes, centrifuges, and automated cell counters. Recording data Lab technicians record data from tests and enter results into patient records. Maintaining equipment Lab technicians keep equipment clean, sanitized, and in good working order. Following safety procedures Lab technicians follow strict safety procedures and ensure the safe removal of waste. Communicating results Lab technicians discuss results with physicians and other senior colleagues. Keeping records Lab technicians keep accurate records of scientific work and results. Writing reports Lab technicians write detailed summaries and reviews of investigations and their findings. Providing technical support Lab technicians may provide technical support to other lab technicians and scientists. Lab technicians may need a bachelor's degree, but some positions may accept an associate degree or certificate. Some states require lab technicians to be licensed Job Types: Full-time, Permanent Pay: ₹20,458.75 - ₹29,738.84 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Yearly bonus Education: Diploma (Required) Language: English (Required) Location: Bengaluru, Karnataka (Required) Application Deadline: 24/07/2025 Expected Start Date: 25/07/2025

Click here to view download Form Department of Plant Breeding and Genetics PAU, Ludhiana Applications are invited on the prescribed form available in the office of undersigned on payment of Rs.200/- in shape of online payment on any working day from 9.00 AM to 5.00 P.M in favour of Comptroller, PAU, Ludhiana along with receipt of online payment and attested copies of certificates for the one post of Project Associate I @ Rs.31000/- P. M. + 16% HRA provided in the scheme “Tackling emerging diseases and insect pests problem in rice through innovative genomic approaches, CSS-24 (PC-6409)" for a period of six months or till the termination of the scheme whichever is earlier. Educational Qualifications B.Sc.(Agriculture)/B.Sc. Horticulture/B.Sc Biotechnology/B.Tech. Biotechnology with minimum OCPA 6.00/10.00 basis or 60% marks. Master's degree in Plant Pathology/ Entomology with minimum OCPA 6.50/10.00 basis or 65% marks and with NET may be recruited as Project Associate I @ Rs.31000/- P. M. + 16% HRA. OR Master's degree in Plant Pathology/ Entomology with minimum OCPA 6.50/10.00 basis or 65% marks and without NET may be recruited as Project Associate I @ Rs.25000/- P. M. + 16% HRA. Note-1: The candidate who does not possess Master’s degree in the relevant subject but possesses Ph.D Degree in the discipline required at Master’s level shall be eligible for the post. Note -2: Desirable qualification: Preference will be given to the candidates having specialization in Plant Pathology. Details for the payment of online application fee:- Name of account - COMPTROLLER PAU RECRUITMENT Saving Account No. - 29380100017259 Name of the Bank - Bank of Baroda, PAU IFSC Code - BARB0PAULUD (0 is zero) The last date for the receipt of applications (duly completed in all respects) in this office is 28-07-2025. Incomplete applications or unsupported by the requisite documents will not be entertained. The candidates should appear for interview on 30-07-2025 at 11.00 A.M . in the office of the undersigned (Room No.114 P.G Building, PAU, Ludhiana). No separate information for interview will be sent. No TA/DA will be paid for attending the interview. Those who had applied earlier in response to this office endst. no. PB-III.AU.2025/ 13611-690 dated 07-07-2025 need not apply again. Head Department of Plant Breeding & Genetics Endst.No:PB-III.AU.2025/ 14212-277 Dated: 21-07-2025

We are seeking a highly qualified Lead Scientist – Organic Fertilizer R&D to drive product innovation, formulation, and lab-to-field implementation of solid and liquid organic fertilizers, including LFOM and FOM. The candidate will lead R&D trials, formulation design, microbial enrichment, and shelf-life improvements. Key Responsibilities Design and develop new formulations for FOM and LFOM, including granules and enriched blends. Conduct lab, greenhouse, and field trials to validate performance and nutrient efficacy. Optimize LFOM drying and solidification technologies without nutrient loss. Lead microbial culture development for nitrogen-fixing, phosphorus-solubilizing, and compost-accelerating strains. Document R&D work for regulatory filings (FCO) and certification audits. Support product registration, eco-certification, and patent documentation. Stay updated with global best practices and lead pilot-scale innovation projects. Qualifications M.Sc./Ph.D. in Soil Science, Agriculture, Microbiology, Biotechnology, or Environmental Science. 5 to 10 years of R&D experience in organic or biofertilizer product development. Strong knowledge of microbial inoculants, composting techniques, fermentation, and drying technologies. Proven success in commercializing new fertilizer products. Ideal Candidate Has A scientific temperament with field validation experience. Knowledge of FCO regulations and product registration process. Experience working with organic certification bodies (e.g., NPOP, OMRI). Reporting To Director – Bhagyashree Green Energy Pvt. Ltd. Perks & Benefits Research funding and lab infrastructure Performance bonus and long-term ESOPs Housing allowance/on-site accommodation Job Types: Full-time, Permanent Pay: ₹500,000.00 - ₹1,500,511.45 per year Benefits: Health insurance Schedule: Day shift Ability to commute/relocate: Junagadh, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: Research & development: 5 years (Required) Work Location: In person

On-site at Cloudnine Hospital 📍 Location: Bangalore 🏢 Company: Cryoviva Biotech Pvt Ltd 🕒 Type: Full-time | On-site 🎓 Eligibility: B.Sc / M.Sc in Biotechnology, Microbiology, Biochemistry or related life sciences (Freshers welcome!) Tasks Key Responsibilities: Educate pregnant women and families about stem cell preservation and its future health benefits. Counsel clients, answer their questions, and help them understand the scientific and emotional value of the service. Coordinate with doctors, gynecologists, and hospital staff to maintain smooth communication and support. Build Relationships with clients and hospital teams to promote awareness and trust in our services. Drive Enrollments by guiding and assisting parents through the decision-making and registration process Requirements Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration

Job Summary : The Research Scientist will perform in vitro assays including cell culture, FACS, ELISA, and data documentation while ensuring SOP compliance and lab maintenance Key Responsibilities Preparation of compound dilutions, cell line maintenance, PBMC isolation, cell seeding in plates for treatment, FACS staining, ELISA, Western Blot. Data analysis and documentation Understanding and training on SOPs for instruments and procedures Maintenance of SOP based calibration schedules and AMC etc for instrumentations. In consultation with supervisor raising change controls for existing SOPs and coordinating with QA to finalize the same. Maintaining lab notebooks and their timely review by the supervisor. Keeping track of reagents and consumables in lab and placing order for new reagents and consumables accordingly. Maintaining schedule for instrument calibration and preventive maintenance. Interact with all stakeholders to enable timely and accurate communication on project progress towards meeting project goals and timelines. Educational Qualification : MSc (Pharmacology/Biotechnology/Life Sciences) Experience : 2+ years of experience in the pharma industry Functional Competencies : Innovative thinking, meticulous in documentation, punctual in project documentation, passion for learning new techniques and assays

Company Description Allied Biotechnology, a fast-growing In-Vitro Diagnostic company, delivers advanced IVD pathology laboratory instruments and consumables at competitive prices. Since 2019, we have been manufacturing IVD products under the "Make In India" initiative with our ALLCARE brand, offering a wide range of products including Clinical Chemistry Reagents, Rapid Test kits, Microbiology products, and POCT Analyzers. Trusted by reputable manufacturers globally, we engage in technical collaborations to provide top-notch diagnostics to the Indian market and beyond. With nearly two decades of industry experience, our Mumbai and Hyderabad sales and service teams, supported by a nationwide distributor network, ensure excellent customer support and satisfaction. Role Description This is a full-time, on-site role located in Mumbai for a Biochemistry Reagent Production Manager. The Manager will oversee the production of biochemistry reagents, ensuring adherence to quality standards and regulatory requirements. Responsibilities include managing daily production activities, coordinating with the R&D, QA, and logistics teams, conducting quality checks, optimizing production processes, and maintaining appropriate documentation. The role requires effective team leadership to meet production goals and deadlines. Qualifications Experience in Biochemistry reagent production and quality control Strong knowledge of regulatory standards and compliance requirements Team leadership and management skills Excellent problem-solving and process optimization abilities Effective communication and coordination with R&D, QA, and logistics teams Relevant degree in Biochemistry, Biotechnology, or a related field Proficiency in relevant software and production management tools Prior experience in the IVD industry is highly desirable

Introduction of Clearstate Clearstate specializes in healthcare-focused market intelligence and strategic advisory services, assisting MedTech companies, biotechnology firms and healthcare service providers in identifying and leveraging market growth opportunities. We are committed to delivering actionable strategies rooted in robust data analytics, built on the basis of market realities, empowering our clients to make informed decisions. Our mission is to provide credible, actionable and granular market insights globally, and provide value-adding advisory tailored to the needs of the MedTech sector. We are seeking highly motivated Associate Manager/ Manager to lead the development and delivery of market data solutions and custom research projects aligned with our business objectives. Responsibilities Project Management Lead a team of analysts in developing global market tracker solutions and custom research projects focused on healthcare market insights Define project requirements, including analytical models, research methodologies, timeline and budgets Ensure project setup, design, and delivery are aligned with client needs, providing actionable, customer-centric insights Innovate and enhance data solutions by conceptualizing new product ideas, additional analyses, and improvements Apply advanced analytical and quantitative tools to extract meaningful business insights Content Development and Project Delivery Deliver high quality data insights with deep domain knowledge expertise in assigned sectors and regions Develop clear, actionable recommendations based on research and analysis Confidently lead client presentations, ensuring clarity and impact Serve as the client engagement lead, communicating project updates and presenting key milestones Client and Stakeholder Engagement Collaborate with client to align on deliverables, ensuring insights meet their needs Engage effectively with various client stakeholders during project delivery and presentations Support business development and marketing initiatives by contributing content and domain expertise For Managers: Lead, appraise and develop team members, fostering skill development and ensuring team success Experience 5+ years in market analysis, market intelligence, or business consulting, with proven project and client management experience (preferably in healthcare or consulting) Qualifications Bachelor’s or Masters’ degree in Science, Business or related fields MBA preferred

Introduction of Clearstate Clearstate specializes in healthcare-focused market intelligence and strategic advisory services, assisting MedTech companies, biotechnology firms and healthcare service providers in identifying and leveraging market growth opportunities. Our data collection approach combines market research techniques, data processing and analytical frameworks. We are committed to delivering actionable strategies rooted in robust data analytics, built on the basis of market realities, empowering our clients to make informed decisions. Our mission is to provide credible, actionable and granular market insights globally, along with value-added advisory tailored to the MedTech sector. The role of the Research Operations Manager will play a critical role in driving Clearstate’s healthcare research and vendor partnership strategy. This role is responsible for overseeing operational activities to ensure the successful execution of market research and business intelligence. This includes managing vendor partnerships, optimizing processes, building and maintaining internal databases and panels, and implementing cost-saving initiatives. Responsibilities Research Operations Management Manage the data collection process by collaborating with project teams to define research needs, set up quota sampling designs, track progress and finalize deliverables Oversee the performance and cost-effectiveness of vendor pools, ensuring continuous evaluation and optimization Identify, screen and onboard new vendors to maintain a robust and reliable vendor pipeline Monitor vendor performance and implement improvement initiatives as needed, to ensure quality and efficiency Market Research Sourcing Strategy Develop and own sourcing strategies based on transparent benchmarking of current performance, cost analysis and growth projections Identify and manage new vendors, growing and curating this vendor pool to ensure a seamless pipeline is essential Identify innovative approaches to improve cost-effectiveness, delivery quality and process efficiency, leveraging technology and strategic collaborations with vendors Partner with internal teams to identify suitable service providers and methodologies, fostering cross-stakeholder engagement Build and maintain internal research panels and databases to enhance in-house research capabilities Conduct vendor and freelancer training sessions to ensure high quality outputs from external partners Experience At least 5 years of relevant experience in market research or consulting services Qualification Bachelor’s or Masters’ degree in Science, Business or related fields

Introduction of Clearstate Clearstate specializes in healthcare-focused market intelligence and strategic advisory services, assisting MedTech companies, biotechnology firms and healthcare service providers in identifying and leveraging market growth opportunities. Our data collection approach combines market research techniques, data processing and analytical frameworks. We are committed to delivering actionable strategies rooted in robust data analytics, built on the basis of market realities, empowering our clients to make informed decisions. Our mission is to provide credible, actionable and granular market insights globally, along with value-added advisory tailored to the MedTech sector. We are seeking highly motivated Analyst/ Senior Analyst to lead the development and delivery of market data solutions and custom research projects aligned with our business objectives. Key Responsibilities: Market Analysis, Tracker Development and Custom Project Delivery Execute market analysis for multi-country global market tracker solutions focused on healthcare market data and insights Analyze datasets by deploying various analytic models, research methodologies (primary and secondary), quantitative tools and modeling techniques Perform secondary research to gather and validate data and insights Engage in in-depth discussions with external stakeholders to understand the market in the context of client’s business objectives Utilize data insights to produce robust analyses and actionable conclusions Develop clear and compelling recommendations for clients based on findings Present findings confidently, clearly and concisely to clients and stakeholders For Senior Analysts: Manage projects and coordinate with teams to achieve client delivery goals within agreed timelines For Senior Analysts: Support client engagements and serve as a client contact when needed Stakeholder Engagement Work with external primary research partners to ensure research aligns with the specified design and meets quality standards Engage directly with clients to deliver data insights and findings, including presenting results and managing client stakeholders as needed Mentoring (Senior Analyst only) Mentor and guide junior analysts, ensuring that they meet performance goals and advance in their careers successfully

R&D Intern – Biomaterials, Mycelium Leather (Unpaid Internship) Location: Remote (with potential on-site requirements) Duration: 3 months Company: MyRei Stipend: Unpaid (Potential for future paid role based on contribution) About MyRei At MyRei , we are developing sustainable, biodegradable, and innovative materials using mycelium and bio-based binders to disrupt the synthetic leather. We are currently in early-stage R&D, prototyping material behavior, and exploring the biofabrication ecosystem to create eco-conscious alternatives for tomorrow. What You'll Work On As a Research & Development Intern , you'll contribute to: Studying research papers and patents on mycelium, algae binders, and bio-inks Reverse-engineering published methods to identify new directions Brainstorming new composite formulations for flexible bio-materials Building detailed mind maps and idea trees from technical literature Supporting our bio-incubation initiatives (possible offline involvement later) Exploring biodegradable alternatives and future design directions for bio-leather Who We’re Looking For Background in Biotechnology / Microbiology / Bioengineering / Material Science Strong interest in biofabrication, biopolymers, or biomaterials Passionate about sustainable alternatives and open to deep research Willingness to work independently and adapt in a dynamic early-stage setup Ideally, hands-on lab experience with fungi or biomaterial cultures is a strong plus Internship Highlights Unpaid role with the potential to transition to a core team or technical R&D head based on contribution Learn startup-level R&D planning, mind mapping, and literature deep dives Remote-first with potential in-person lab work if accepted by any bio incubator All offline expenses (travel, stay, etc.) are self-funded initially If incubated and funded, opportunity to become part of the first technical team Legal & Confidentiality All selected interns must sign an NDA & Confidentiality Agreement to ensure protection of ideas and IP during the research phase. Your ideas and contributions will be documented, credited, and ethically protected. Why Join Us This is not just an internship, it’s a calling for thinkers, tinkerers, researchers, and sustainability enthusiasts who wish to be part of a revolutionary material science startup from the ground up. To Apply: Send a brief note on your interest, background, and any previous relevant experience via DM or email to shaik0abdul0hafeez@gmail.com . Include any research projects or papers you’ve worked on.

Job Title : Smart Connected Products - Manager-S&C GN Management Level: 07 - Manager Location: Bangalore/ Must have skills: Have Experience with leading MedTech solutions effectively by providing value-add to the processes, designs, methodologies, and business models Good to have skills: Have business Acumen to drive actionable outcomes for clients Possess analytical and outcome-driven approach Demonstrate a strategic Mindset to understand shape innovative, fact-based strategies and operating models Ability to communicate and present skills to share the perfect pitch with key stakeholders Have team building skills to collaborate, work and motivate teams with diverse skills and experience to achieve goals Job Summary: As part of the Smart Connected Product Design & Development (SCPDD) team you will create Connected Products based solutions in the MedTech space that provide vital digital intelligence and drive organizational changes for some of the world's best product companies. Roles & Responsibilities: Have business Acumen to drive actionable outcomes for clients Possess analytical and outcome-driven approach Demonstrate a strategic Mindset to understand shape innovative, fact-based strategies and operating models Ability to communicate and present skills to share the perfect pitch with key stakeholders Have team building skills to collaborate, work and motivate teams with diverse skills and experience to achieve goals Demonstrate leadership skills along with strong communication, problem solving, organizational and delegation skills Professional & Technical Skills: At least 10+ years in MedTech and Life Sciences across the value chain with experience to lead Strategic Projects with a global top Pharmaceutical, Medical Devices, Biotechnology or Healthcare Consulting firms Experience with QMS development and alignment from beginning to end of project cycle and be comfortable working with and according to the industry norms and existing processes. Comfortable with platforms including Trackwise, Veeva etc. Experience of developing commercialization strategy and launching medical devices in new markets End to End development of Personal Health Record (PHR) System as per HL7 PHR-S Functional Model Experience with integrating new technologies for EMR & PHR and medical devices Understanding of In-Hospital and remote fetal monitoring system, Remote ECG Monitoring system and Medical Device connectivity with EMR system Understanding of gateway connectivity with EHR, PACS and multiple devices such as C-Arm, Ultrasound, Laser, saline devices etc. Implementation of Healthcare Information System (HIS), Radiology Information System (RIS), Pharmacy Solution & e-Health solution at Healthcare Providers In-depth understanding of Medtech, Digital health, Cybersecurity, Connected Health Strategy (DTx and SaMD), Point of care diagnostics and Digital/Robotics Surgery Experience in business scoping, assessment and planning that includes Blueprinting, business case creation and business process redesign Experience in Project Management: Transform Product Strategies, Product Management, and overall engineering by enabling portfolio alignment with overall business strategy, right products mix with optimal resource utilization and better governance thereby ensuring increased product success Develop assets and methodologies, point-of-view, research or white papers for use by the team and larger community Lead proposals, business development efforts and coordinate with other colleagues to create consensus-driven deliverables. Execute a transformational change plan aligned with client’s business strategy and context for change. Engage stakeholders in the change journey and build commitment for change. Additional Information: Exceptionally organized Detail oriented Good judgement in how to engage with senior stakeholders regarding approvals/ follow ups Strong communication skills Proactive and able to work independently Sensitivity and skill at working with different cultures and styles A highly motivated self-starter About Our Company | Accenture , Experience: 10+ years of Industry Experience Educational Qualification: Engineering background with MBA preferred

Date: 15 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Manufacturing Services Job/Role Description The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene’s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Key Responsibilities At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Common Responsibilities Follow the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment and adhere to the highest standards of quality, integrity & compliance for every work activity. Complete the assigned trainings in a timely manner and comply with the training procedure & training calendar. Attend all assigned mandatory trainings related to data integrity, health, and safety measures. Compliance to Current Good Manufacturing Practices and Good Documentation Practices. Adherence to Standard Operating procedures, Operational control Procedures. Participate in & support the trainings on procedures, protocols, and On-the-Job activities. Follow the discipline of reporting structure at times of escalation. Report nonconformities & deviations to the respective supervisor(s) and/or line manager(s). Participate in & support for on-time initiation & closure of deviations, investigations, CAPA and change controls. Safety And DI Responsibilities Adhere to organizational policies & procedures on EHSS, POSH, Data Integrity and IT security. Always wear the applicable PPEs and adhere to any other Environment, Health, and Safety (EHS) requirements in the workplace for individuals & lab/plant safety. Understand all necessary safety protocols and always follow the same to ensure safety for all. Proactively identify near-misses & potential incidents and communicate to supervisor and/or line manager or through the respective web portals. Specific Responsibilities Follow good aseptic behavior inside Biologics operations facility. Perform all the upstream activities like Assembly preparation, Media Preparation, Vial thaw, Feed preparation and filtration, Bioreactor Operations to Batch Harvest. Monitoring and process control of the specific Operations of the upstream. Maintenance of Quality records. Traceability from raw material till finished product. In-process product sampling and storage. Preparation and review of operation related documents. Perform room owner responsibility for the assigned USP area. Perform equipment/instrument ownership related responsibilities related to USP. Initiate Complaint Slips (work orders) for USP related areas and equipment. Coordinate with QA for line clearance. LNS system monitoring and LN2 tank refilling. Gas Bank Monitoring. Maintaining process area All-time ready for Inspection/ audit purpose. Preparation of general upstream related procedures, protocols, risk assessment and BMRs. Execution of protocols related to upstream related activity and equipment / instrument qualification. General consumable stock review and record maintenance Ensure PM planner and calibration planner are followed. Execution of batch activity as per BMR and report nonconformity to the supervisor. Issuance of annexures, RM, consumables and BMRs. Tracking of work order status and ensuring timely closure. Involve in downstream related activities under supervision of downstream supervisor. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Pls visit us at https://syngeneintl.com/ to know more about us and what we do.

Date: 21 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Manufacturing Services Designation: Senior Research Associate Level: 9- II Job Location: Bangalore The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene’s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Key Result Areas Role-specific Functional Responsibilities: Responsible & accountable towards safety & compliance in all the work activities in the own responsibility area(s). Monitor & confirm that the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment are followed. Adhere to the highest standards of quality, integrity & compliance for every work activity. Complete the assigned trainings in a timely manner and comply with the training procedure & training calendar. Attend all assigned mandatory trainings related to data integrity, health and safety measures. Participate in & support the trainings on procedures, protocols and On-the-Job activities. Compliance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Report nonconformities & deviations to the respective supervisor(s) and/or line manager(s). Participate in & support for on-time initiation & closure of deviations, investigations, CAPA and change controls. Primary Responsibilities Sample analysis for in-process, finished product, stability and miscellaneous samples. Responsible to troubleshoot problems, provide technical guidance, train lab personnel in fundamental lab techniques and procedures as a mentor and coach. Responsible for supporting the routine testing operations, ensuring compliance with regard to observation data sheet along with the analytical data, analysis report and handing over the same on time to QA or the Client. Preparation and review of batch release documents like STPs with observation data sheet, Method transfer and validation protocols etc. Responsible to review of Analytical data, QMS documents related to batch release and stability study activity related documents. Responsible to review the Method transfer, Method validation& Verification protocols. Coordinating and supporting for the review and release of Method transfer, Method validation & Verification activity and its records/reports and results. Responsible to manage a team supporting for routine testing operations, Ensuring Compliance with regard to observation data sheet along with the analytical data, analysis report on time to QA and Customers. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Pls visit us at https://syngeneintl.com/ to know more about us and what we do.

Date: 15 Jul 2025 Location: Bangalore, KA, IN, 560100 Custom Field 1: Essential Functions Job Description Job Role: Procurement Operations Partner Job Location: Bangalore Department: Strategic Sourcing About Syngene Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines: Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’ s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Purpose Responsible for achieving business objectives by ensuring the timely submission of quotations and the uninterrupted supply of essential input materials—including raw materials, kits, consumables, reagents, animals, and stationeries—for the Biology vertical and other assigned business units. Key Responsibilities Market Intelligence/Best Practices: The individual will develop and maintain deep market knowledge in one or more spend categories. They will identify and implement industry best practices to drive value creation and operational efficiency. Strategic Sourcing & Collaboration: Collaborate internally with Biologics Category Leads and external partners in the US and China. Lead both local and global sourcing projects through the strategic sourcing process, culminating in supplier negotiations and contract execution (Category: Biology / Research Services) Procurement Operations Source & select competitive global vendors for raw materials (Biology Category); preparation of detailed comparison statement capturing last PO price, internal estimation, arriving at a negotiation strategy Engage in techno-commercial discussions with local and global vendors on cost, delivery, freight, and other terms Achieve excellence in delivery of materials / animals / services to all projects to meet customer expectations (PR-PO, QUOTIF, etc.) Handle SEZ/EOU documentation, co-ordinate with cross-functional teams for licensing requirements of restricted materials Procurement Operations Vendor Sourcing & Evaluation: Identify and select competitive global vendors for raw materials. Prepare detailed comparison statements including last PO price, internal cost estimates, and formulate negotiation strategies. Techno-Commercial Engagement: Conduct comprehensive techno-commercial discussions with both local and international vendors, covering aspects such as pricing, delivery schedules, freight terms, and other contractual conditions. Operational Excellence: Ensure timely and efficient delivery of materials, animals, and services across all projects to meet customer expectations. Manage procurement processes including PR-PO cycles, QUOTIF evaluations, and related workflows. Regulatory Compliance: Handle SEZ/EOU documentation and coordinate with cross-functional teams to fulfill licensing requirements for restricted materials, ensuring full regulatory compliance. Supplier Identification and Management: The individual in this role will be responsible for identifying, negotiating with, and managing suppliers who provide goods and services aligned with Syngene’s CRO/R&D requirements. This includes developing RFx documents, executing contracts, and adhering to Preferred Supplier Strategies. Strategic Sourcing Initiatives: Lead strategic sourcing efforts such as spend analysis, category management, supply-demand market intelligence, benchmarking, clean-sheet costing, and negotiations. Ensure process compliance and maintain high levels of internal stakeholder satisfaction. Cost Optimization: Drive cost optimization by developing alternate sourcing strategies and leveraging effective negotiation techniques. Finalize contracts that define pricing, discount structures, and rebate mechanisms across categories. MIS Reporting: Prepare and present management reports highlighting key findings, recommendations, and actionable insights. Focus on identifying opportunities for cost savings, operational improvements, and risk mitigation. Vendor Management: Establish and maintain strong relationships with vendors, ensuring adherence to service level agreements (SLAs). Address and resolve disputes, monitor vendor performance, and conduct regular reviews to drive continuous improvement. Engage with critical suppliers to ensure negotiated value is realized and sustained. Educational Qualification Bachelor's degree / BSc with relevant experience (preferably with Biology/Biotechnology as one of the subjects) PG Dip. MM or MBA is an added advantage Technical/functional Skills Strategic & Tactical Sourcing Logistics / SEZ / EOU compliance Vendor evaluation and selection criteria, such as capacity, capabilities, and compliance. Cold chain / temperature-controlled shipments Good knowledge on eco-system / Pharmaceuticals / CRO / CDMO Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience Should have experience in strategic sourcing with a minimum of 2-5 years in pharmaceuticals / life sciences Vendor development, negotiation, and annual rate contract. Identification of supply risks, mitigation plan (proactively execution of the plan) Collaboration, cost optimization, and value creation. Proven skills in negotiation and understanding of commercial law. Market intelligence, benchmarking knowledge, and awareness of best practices. MIS reporting - conversant in generating SAP reports, collating data for analysis. Act as the go-to person for all material & service needs of projects, interfacing b/w vendors and users to obtain and finalize techno-commercial offers. Support strategic initiatives such as – working capital management & digital initiatives like e-procurement, Automations, B2B Integration, etc. Behavioral Skills Partners with Customer Understands customer needs Drives Accountability Stakeholder management skills Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Job Title: Sales & Technical Support Executive – Life Science Products Location: Hyderabad & Kolkata Company: Spark Scientific Pvt. Ltd. About the Company: Spark Scientific Pvt. Ltd. is a rapidly growing organization specializing in advanced scientific instrumentation and laboratory solutions for the life sciences sector. We proudly serve academic institutions, research organizations, and biotech industries across India, offering top-quality products backed by exceptional technical support. Job Description: We are looking for a motivated and technically skilled Sales & Technical Support Executive to join our Hyderabad team. The ideal candidate will have a strong academic background in life sciences and proven experience in both sales and support of laboratory instruments used in molecular biology and analytical labs. Key Responsibilities: Promote and sell life science products such as Gel Documentation Systems, Electrophoresis Units, Chemiluminescence Imaging Systems , and related instruments. Provide pre-sales consultations, technical demonstrations, and post-sales support to clients. Build and maintain strong relationships with stakeholders in academic, research, and industrial laboratories . Conduct product training sessions, technical presentations, and troubleshooting support . Coordinate with internal service engineers and product managers to ensure customer satisfaction. Represent the company at industry exhibitions, conferences, and promotional events . Qualifications & Requirements: Bachelor's or Master's degree in Life Sciences, Biotechnology, Biochemistry , or a related field. 2–5 years of experience in sales or technical support of life science instruments. Hands-on experience with Gel Doc, Electrophoresis, Chemidoc , or similar systems is highly desirable. Strong communication, presentation, and customer engagement skills. Willingness to travel for client visits and product demonstrations. What We Offer: Competitive salary and incentive structure. Opportunity to work with cutting-edge scientific technologies . A supportive and collaborative work environment. Ongoing career development and training opportunities. To Apply: Interested candidates can share their updated resume at hrd@sparksci.in or raheem@sparksci.in

Job title: Field Bioinformatics Scientist Location: Bengaluru, Chennai or Mumbai, India Employment type: Full Time Expand Your Horizons and Promote Advanced Life Science Tools for Future Healthcare with MGI #OMICS FOR ALL #Leading Life Science Innovation About BGI BGI Group was founded in 1999 in China with the vision of using genomics for the benefit of mankind and has since become the largest genomics organization in the world. With over 10,000 employees, BGI operates in more than 100 countries, focusing on research and applications in healthcare, agriculture, conservation, and environmental fields. BGI has a proven track record of innovative, high-profile research, which has generated over 3,800 publications, with 430+ publications in top-tier journals such as Nature, Science and Cell. Additionally, in the field of R&D, BGI was ranked No.1 among corporations in the life science/biotechnology sector in the Asia-Pacific region and No.5 worldwide by Nature Index. About MGI MGI is one of the subsidiaries of BGI Group, it is committed to building core tools and technology to lead life science through intelligent innovation. With a focus on R&D, production, and sales of DNA sequencing instruments, reagents, and related products, MGI provides real-time, panoramic, and full-life-cycle equipment and systems for precision medicine, precision agriculture, precision healthcare, and other relevant industries. MGI is a leading producer and one of the few companies in the world that can independently develop and mass-produce clinical high-throughput gene sequencers, its multi-omics platforms include genetic sequencing, medical imaging, and laboratory automation. Our Mission is to develop and promote advanced life science tools for future healthcare, and to transform people’s lives for the better. We don’t hesitate to make bold decisions that can help us achieve new breakthroughs. We believe that the success of our business will mean a better world for people to live in. Our Message to the world is simple: lead in life science innovation, make everyone’s life healthier and longer. Your duties as an FBS include but are not limited to the following: Design, develop, optimize, and maintain in-house bioinformatics pipelines and various genomics applications. Understand customer research questions and provide appropriate solutions or customized approaches. Respond to technical issues from global sales and customers, providing resolutions and recommendations. Liaise with FAS, FSE, Product Managers, and R&D to provide product feedback, develop customised solutions, and support solution provision. Maintain current knowledge in Sequencing, Bioinformatics, MGI products, and industry trends Evaluate new software/tool suitability for various applications, and apply best-practice statistical and computational methods. Provide technical (FPGA) pre-sales and post-sales support services. Provide training and webinars to customers and the front-end sales team. Assist with document management, including collecting and updating training materials, FAQs, slides, videos, SOPs, and knowledge base content. The successful candidates for this position can demonstrate: Bachelor's degree or above with 3+ years’ experience in academic or industrial settings in Bioinformatics, Computational Biology, Biostatistics or Computer Science, or equivalent experience. Experience in developing next-generation sequencing data analysis methods for DNA,RNA and Long read analysis. Experience with scripting languages, including Python, bash, Perl, C++ and R. Excellent communication skills and ability to describe complex process and result to audiences with diverse backgrounds. Ability to contribute independently and collaboratively, manage progress of assigned tasks, and work in a fast-paced environment. Experience with using version control systems such as Git. Knowledge and experience with a wide range of bioinformatics tools. Proficiency in using Linux operating system such as Ubuntu, Fedora, Centos, etc. Here at BGI, we value people and consider our employees as partners. We have created a transparent, fair, and friendly environment. We implement an agile approach to management, providing each partner with enough independence as well as guidance. We take care of our partners’ physical and mental health and are dedicated to a life-work balance corporate culture. Not only do we bring life science closer to people, but we also participate in various charity programs, advocate for nature preservation, and support equality. We condemn any form of discrimination and are committed to providing job opportunities to everyone regardless of sex, race, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and more. Let’s move to a brighter and more equal future together and deliver #Omicsforall

About Us At RNT Health Insights, we are developing Breakthrough Medical Devices to improve the accuracy of detection of early-stage upper gastrointestinal cancers. Our FDA-Breakthrough designated medical devices help in detecting early-stage gastric and esophageal cancers in real-time during endoscopic procedures, empowering gastroenterologists with split-second insights and improving patient outcomes. Join our multidisciplinary team of engineers, clinicians, and regulatory experts passionate about pushing the boundaries of med-tech, and help deliver life-saving insights in real time. Role Overview We are looking for dedicated Full-Time Medical Data Annotators and Interns to meticulously review and annotate endoscopic video data. Your role will involve accurately labeling medical images and videos to support the development of our AI-assisted cancer detection technologies. You will collaborate closely with our clinical, engineering, and AI teams to ensure high-quality data annotation, directly impacting the accuracy and efficacy of our medical solutions. What You'll Do Review and annotate endoscopic videos and images, accurately identifying and marking abnormalities such as lesions, polyps, ulcers, and areas suspicious for cancer. Follow precise annotation protocols and guidelines to ensure consistency and accuracy of labeled data. Collaborate closely with clinical experts to validate annotations and resolve discrepancies. Assist in quality assurance checks to maintain high standards of annotated datasets. Document annotation processes meticulously, ensuring compliance with medical-device regulatory standards. Provide feedback to improve annotation processes, protocols, and tools. Required Qualifications What We're Looking For: Previous experience with medical data annotation or related annotation activities. Excellent attention to detail, strong observational skills, and patience for repetitive tasks. Basic understanding of human anatomy and pathology, particularly gastrointestinal diseases. Experience working with computer systems, medical imaging software, and annotation platforms. Strong communication and collaboration skills. Preferred Qualifications Bachelor's degree or pursuing a degree in Medicine, Biology, Biomedical Sciences, Biotechnology, Nursing, or a related healthcare field. Familiarity with gastrointestinal endoscopy procedures. Knowledge of medical terminology specific to gastroenterology. Experience with annotation software tools such as Labelbox, CVAT, or similar. Understanding of regulatory considerations in medical data handling (e.g., FDA, ISO 13485). Why You'll Love Working with Us We'll match or exceed industry-standards in compensation to ensure you share in our success. Directly contribute to groundbreaking medical technology that saves lives Work alongside leading clinicians and AI researchers in a fast-paced startup Gain hands-on experience with cutting-edge AI and medical-device technology. Flexible work hours, and a supportive, mission-driven culture

Production & Lab Assistant – Herbal Extraction Location: Gauribidanur, Karnataka Company: Koppex Life Sciences LLP Industry: Natural Ingredients | Herbal Extraction | Life Sciences Job Type: Full-time About Us Koppex Life Sciences LLP is a manufacturer of Natural Functional Ingredients , dedicated to innovation in herbal extraction, natural colors, phyto-APIs , and related R&D. Our mission is to advance health and wellness through science-backed, natural solutions. We are seeking a motivated Production & Lab Associate – Herbal Extraction to support both process operations and analytical testing . Key Responsibilities Assist the senior production team in herbal extraction processes and batch operations. Handle raw materials, monitor process parameters, and document batch data. Conduct sample collection, drying, filtration, and routine in-process quality checks . Handle and operate analytical testing equipment such as pH meters, moisture analyzers, UV-Vis spectrophotometers, and other lab instruments. Assist in basic analytical testing of extracts and ingredients as per SOPs. Support pilot-scale trials and experimental work for the R&D department. Maintain cleanliness, safety, and documentation in both lab and production areas. Qualifications Diploma in Pharmacy, B.Sc. (Chemistry, Biotechnology, Microbiology, or related field), or ITI in a technical/lab-related discipline. 0–2 years of experience in a production or laboratory environment ; freshers are welcome. Basic understanding of herbal raw materials , extraction techniques, and lab testing procedures. The candidate must be willing to relocate to the town near the site. Key Skills Lab and equipment handling Analytical testing basics Process discipline and hygiene Record-keeping and observation Teamwork and adaptability What We Offer Hands-on experience in a natural product manufacturing and R&D setting . Competitive salary with performance-linked growth and accommodation . Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Ability to commute/relocate: Gauribidanur, Karnataka: Reliably commute or planning to relocate before starting work (Required) Work Location: In person Expected Start Date: 01/08/2025

laboratory technician performs various tasks related to testing, analyzing, and maintaining laboratory equipment and samples. Their duties can include collecting and preparing samples, conducting tests, recording results, and ensuring the laboratory environment is safe and organized. Key Responsibilities: Sample Handling: Collecting, labeling, and preparing samples (e.g., blood, urine, tissue) for analysis. Testing Procedures: Performing standardized tests and experiments, often under the guidance of a senior scientist. Data Analysis and Reporting: Analyzing findings, deciphering results, and recording data accurately in specified formats. Equipment Maintenance: Maintaining and calibrating laboratory equipment, ensuring its proper functioning. Safety Compliance: Following safety rules and guidelines, maintaining a safe laboratory environment, and potentially explaining safety procedures to others. Inventory Management: Ordering supplies, stocking shelves, and managing laboratory inventory. Record Keeping: Maintaining detailed records of experiments, results, and inventory. Specific Examples of Lab Technician Roles: Medical Laboratories: Analyzing patient samples (blood, urine, tissue) to diagnose diseases and monitor patient health. Food and Beverage Industry: Testing food and drink samples to ensure quality and detect contamination. Research Labs: Assisting scientists with experiments and data collection in various research fields. Chemical and Biotechnology Labs: Working with chemicals and biological samples in research and development. Required Skills and Qualifications: Technical Skills: Proficiency in laboratory techniques, data analysis, and equipment operation. Job Type: Full-time Pay: ₹12,000.00 - ₹25,000.00 per month

Job Description Position: Medical Coder - Work from Home Ct: HR KAMATCHI - 8925264660 Job Description:Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books. Requirement knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills No of vacancy: 500 Eligibility Nursing GNM/DGNM Life science graduates Pharmacy Physician assistant Bio medical Engineers Bio chemistry Bio technology Bio informatics Micro biology Zoology and Advanced zoology Biology Botany Plant biotechnology Genetics Food and Nutrition Paramedical Physiotherapy M.Sc. Clinical Nutrition M.Sc. Human Genetics M.Sc. Medical Laboratory Technology M.Sc. Medical Sociology M.Sc. Epidemiology M.Sc. Molecular Virology M.Sc. Biostatistics M.Sc. Blood Banking Technology M.Sc. Rgnerative Medicine M.Optom. M.Sc. Genetic Counseling M.Sc. Radiolog Imaging Technology M.Sc. Medical Biochemistry M.Sc, Medical Microbiology M.Sc. Clinical Care Technology M.Sc. Clinical Care Technology M.Sc. Medical Physics B.Sc. - Accident Emergency Care Technology B.Sc. - Audiology speech Language Pathology B.Sc. - Cardiac Technology B.Sc. - Cardio Pulmonary Perfusion Care Technology B.Sc. - Critical Care Technology B.Sc. - Dialysis Technology B.Sc. - Neuro Electrophysiology B.Sc. - M.L.T. B.Sc. - Medical Sociology B.Sc. - Nuclear Medicine Technology B.Sc. - Operation Theatre Anaesthesia Technology Bachelor of Science in Optometry B.Sc. - Physician Assistant B.Sc. - Radiology Imaging Technology B.Sc. - Radiotherapy Technology B.Sc. - Medical Record Science B.Sc. - Respiratory Therapy B.Sc. - Fitness and Lifestyle Modifications Accident Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Salary 15K to 17K (fresher) To 50K (experienced) Pm (Incentives Benefits as per Corporate Standards) 4K fixed hike after six months Other Benefit Pick Up Drop Facility Food Facility Day Shift Weekend Off Reach Us HR KAMATCHI 8925264660 Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Jobs for Passed outs Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital Perks and Benefits Incentives Benefits as per Corporate Standards This job is provided by Shine.com

Location: Gauribidanur, Karnataka Company: Koppex Life Sciences LLP Industry: Natural Ingredients | Herbal Extraction | Life Sciences Job Type: Full-time About Us Koppex Life Sciences LLP is a manufacturer of Natural Functional Ingredients , dedicated to innovation in herbal extraction, natural colors, phyto-APIs , and related R&D. Our mission is to advance health and wellness through science-backed, natural solutions. We are seeking a motivated Production & Lab Associate – Herbal Extraction to support both process operations and analytical testing . Key Responsibilities Assist the senior production team in herbal extraction processes and batch operations. Handle raw materials, monitor process parameters, and document batch data. Conduct sample collection, drying, filtration, and routine in-process quality checks . Handle and operate analytical testing equipment such as pH meters, moisture analyzers, UV-Vis spectrophotometers, and other lab instruments. Assist in basic analytical testing of extracts and ingredients as per SOPs. Support pilot-scale trials and experimental work for the R&D department. Maintain cleanliness, safety, and documentation in both lab and production areas. Qualifications Diploma in Pharmacy, B.Sc. (Chemistry, Biotechnology, Microbiology, or related field), or ITI in a technical/lab-related discipline. 0–2 years of experience in a production or laboratory environment ; freshers are welcome. Basic understanding of herbal raw materials , extraction techniques, and lab testing procedures. Key Skills Lab and equipment handling Analytical testing basics Process discipline and hygiene Record-keeping and observation Teamwork and adaptability What We Offer Hands-on experience in a natural product manufacturing and R&D setting . Competitive salary with performance-linked growth and accommodation. Mandatory Requirement Willing to relocate to Gauribidanur

Date: 14 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Job Title: Digitization Lead. Job Location: Syngene International Limited, Bengaluru About Syngene: Syngene (www.syngeneintl.com) Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries around the world. Syngene’s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240-strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’ s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose Of The Role To act as System SME and ensure compliance activities related to ERP systems ensuring adherence to regulatory requirements and internal policies, thereby supporting quality assurance and data integrity in Syngene’s operational systems. Role Accountabilities Prepare, review, and approve validation deliverables including Impact Assessments, User Requirements Specifications (URS), Functional Requirements Specifications (FRS), and Validation Reports compliant with 21 CFR Part 11, EU Annex 11, and GAMP5 Implementation of ERP systems (Ex SAP, EDMS, Track Wise….) and maintain the system in validated state. Plan and execute installation, operational, and performance qualification (IQ, OQ, PQ) testing to verify system functionality and compliance Collaborate with IT, QA, and business stakeholders during system testing, deployments, and upgrades for ERP systems such as EQMS, Documentum, SAP Assess and manage risks and impacts associated with ERP system changes and new implementations Ensure adherence to company SOPs, regulatory guidelines, and quality standards throughout validation lifecycle Act as subject matter expert during internal and external audits related to ERP system validation and compliance Identify compliance risks proactively and implement corrective/preventive actions Mentor and guide junior team members on validation compliance best practices Manage investigation and closure of deviations and issues arising from validation and audit activities Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience: Experience in validation and compliance of GxP regulated ERP systems including EDMS (Documentum-LSQM), EQMS Trackwise, and other ERP platforms 13-18 Years of domain experience. Demonstrated ability to support audits and manage compliance risks effectively Demonstrated Capability Detail-oriented with strong analytical and problem-solving skills Ability to manage multiple priorities, meet deadlines, and to meet quality norms Skills And Capabilities Experience in preparing and reviewing validation documentation and conducting ERP system qualification testing Strong working knowledge of data integrity, good documentation practices, and regulatory requirements such as 21 CFR Part 11, EU Annex 11, and GAMP5. Excellent communication and stakeholder management skills to work effectively across IT, QA, and business functions Ability to mentor and train junior team members Education Master’s degree in Science, Pharmacy, Biotechnology, B. Tech, or IT-related field Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Date: 14 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Job Description Job Title : Manager Development Quality Assurance (BRDS) Department : Discovery and Development QA Job Location: Bengaluru, India About Syngene: Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene’s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Key Result Areas We are seeking an experienced and dynamic Quality Assurance lead to manage research and development quality assurance division at Bicara Research and Development at Syngene (BRDS). This role will involve implementing Syngene Quality Assurance principles for Biologics development and ensuring compliance to quality systems throughout the life cycle of R&D projects. Mandatory expectation Responsible and accountable towards safety and compliance in all the work activities in the own responsibility area(s). Monitor and confirm that the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment are followed by self and direct reports. Monitor and confirm that self and direct reports adhere to the highest standards of quality, integrity and compliance for every work activity. Complete the assigned training in a timely manner and comply with the training procedure and training calendar and monitor and confirm the same for the direct reports. Attend all assigned mandatory training related to data integrity, health and safety measures, and monitor and confirm the same for the direct reports. Participate and support the training on procedures, protocols and On-the-Job activities. Comply with Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Report nonconformities and deviations to the respective supervisor(s) and/or line manager(s). Participate and support on-time initiation and closure of deviations, investigations, CAPA and change controls. Educational Qualification Masters or Doctorate degree in Pharmaceuticals, Biotechnology, Engineering or any stream of Science. Profile Description This role will be responsible for crafting the allocation methodologies and process flows for Development services. This individual will collaborate actively with Operation units of development services for Bicara to improve alignment and achievement of customer satisfaction and value realization Core Purpose Of The Role Responsible for Quality Systems of Development Services and relevant QA activities. Role Accountabilities Lead Quality Management System activities pertaining to Bicara Research and Development at Syngene. Liaise with Bicara Global Quality to align on quality principles and process flow for discovery and development projects at BRDS. Execute quality risk assessment across different development stages of Biologics Discovery and Development and implement phase appropriate QMS principles. Ensure that OOS, Deviations, Customer Complaints are investigated, reviewed and CAPA implemented in accordance with QMS requirements. Ensure change controls are assessed. Coordinating with Cross functional team other GxP functions for the implementation of Quality Management System (QMS). Training of employees on QMS procedures. Prepare / Review of documentation such as Quality Manual, Site Master Files, SOPs and Quality Agreements. Planning and follow-up of QMS activities for closure within the target timeline for Biologics Operation Units. Preparation of QMS Metrics within BRDS. Preparation and review of risk assessment for Quality activities. Preparation and review of trends as per schedule for all QMS elements as applicable. Liaise with and support the Internal Audit and Continuous Improvement team for the timely closure of the CAPA. Facilitate continuous improvement via QMS to improve the health of the Quality Systems. Participate and coordinate the client and regulatory audits for Biologics Discovery and Development Labs. Development of team skills within Biologic-QA team, motivating, coaching and mentoring direct reports to higher levels of management capabilities. Review of SOPs within QA, periodic review of the SOPs implemented across the functions. Ensure quality compliance against regulatory requirements and revise SOPs as necessary to comply with these regulations. Accountable for reviewing and approving protocols, SOPs, IOPs and documents related development, method qualification, Specifications, Tech-Transfer, etc. Responsible for approval and timely availability of Technology Transfer from Development services to Manufacturing services; Analytical Method and Process Development Transfer documents. Develop role-based training modules for BRDS and ensure training of staff on quality procedures, processes, policies and issue training binders. Implement phase appropriate quality procedures and DI related training across operating units. Review and approval of Quality Assurance procedures in EDMS and TrackWise. Implementation of role-based curricula in Discovery and Development Services and ensure compliance. Approve annual training planner, instrument audit trail and eLN audit trail schedules. Contributing to development procedures, practices, and systems that ensure safe operations and compliance with the company’s integrity and quality standards. Coordination with cross-functional teams to complete the assigned work on time such as data review, report approval, etc. Execute root cause investigation by performing why-why analysis and propose mitigation strategies and implement CAPAs. Responsible for facing audits by clients and regulatory bodies. Lead regular meetings with team members to communicate operational information and objectives. Evaluate team performance periodically and identify areas in need of improvement to implement development strategies. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience 10+ years of experience in driving quality assurance in pharmaceutical/biopharmaceutical industry Skills And Capabilities Proven track record in implementing QMS in biologics development and QC labs. Strong understanding of biologics development process flow including early-stage process development, scale-up and technology transfer. Good knowledge of international quality guidelines applied for biologics drug development including ICHQ, USP, etc. Knowledge of electronic notebooks and should be well versed in TrackWise QMS Software for raising Deviation, Change Control and CAPA. Excellent interpersonal communications with track record of working in dynamic environment

As a Sales Engineer/Sales Executive/Assistant Manager, your role will involve promoting Hi-tech analytical & Sophisticated Instruments to various Research institutions, Universities, Research & Development organizations, and laboratories including Quality Control laboratories. This includes tasks such as pre-sales visits, conducting meetings, delivering presentations, organizing demonstrations, engaging in technical discussions, and providing technical support. To qualify for this position, you should hold an M.Sc. in Chemistry, Physics, Botany, Zoology, Biotechnology, Biochemistry, or Environmental Science. Alternatively, a B.Sc. with combinations such as Chemistry-Physics, Chemistry-Biology, or Chemistry-Biotechnology would be acceptable. A B. Tech in Biotechnology, Electronics, Chemical Engineering, or similar fields is also suitable. Candidates should demonstrate a strong willingness to pursue a career in Marketing, possess a passion for interacting with highly qualified individuals including Scientists, Senior Persons, and Technocrats. Additionally, enthusiasm for travel, self-motivation, and a desire to stay updated with the latest techniques are essential qualities for this role.,