3542 Biotechnology Jobs

Job Summary Are you passionate about solving customer problems, offering Technical solutions and building deeper business relationships that help drive growth for industry leading Consumer Products customers? Joining science and creativity, we are an international collective of thinkers who partner with customers to bring scents, tastes, experiences, ingredients and solutions for products the world craves. If you are skilled at solving complex problems with elegant technical solutions, and have a collaborative approach to exceeding customer expectations, you could be our next Application Specialist! Your Focus As a part of our Application Development team, you will be responsible to work across functions to develop and support products and processes. The role will see you providing technical and functional leadership opportunities and will play a key part in supporting our evolving industry and customer base. The role is based in Hyderabad, India and will report to the Regional Application Leader – Grain Processing. How you will contribute Involve with hands on work at bench and pilot scales. Design, develop, execute, and contribute innovatively to the development of enzyme and yeast products and processes across scale, analyze and interpret data using statistics to make a sound recommendation for specific projects. Collaborate closely with the application scientist to advance the solution while creating and maintaining an up-to-date project data, both at lab and pilot scale. Objectively support the analysis of customer and project samples using physical, bio/chemical and functional assay. Manage the day-to-day lab activities while upholding to the highest standards of Occupational Health and Safety. Interact with cross functional teams including R&D, sales, marketing, legal, procurement and engineering. What you will need to be successful Master`s degree (with 3+ years of Industry experience) or a PhD degree in Biochemistry, Biotechnology, Bio Engineering, Agriculture Engineering or a related area. Strong knowledge and experience of industrial scale fermentation, preferably in the grain based ethanol manufacturing. Experience in executing experiments across scales (Lab-Pilot-Commercial) to assess the performance of enzymes and/or yeast meeting project timelines. Experience with analytical techniques relevant to monitoring the biotechnological process (Proximate, HPLC, GC, Biochemical assay, Viscometry, PSD, micro-DSC, Etc). Proficiency with statistical analysis software such as JMP, SPC, excel, etc., for generating scientific report with objective inferences. Excellent verbal and written communication skills Strong team player with the ability to deliver results in a fast-paced environment. Willingness to travel upto 20% across ASPAC, including to customer commercial facilities. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Job Summary : Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we’re looking for experienced professionals to join us as we prepare to launch of our newest office in Hyderabad, India . This is more than just a job. It’s an opportunity to be part of something from the very beginning. You’ll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects. Why Join Medpace in Hyderabad? Be a Founding Member : Help establish and lead operations at our newest location. Immediate Impact : Your experience will directly influence Medpace’s growth in the region. Career Growth : As the office grows, so will the leadership and advancement opportunities. Global Reach : Work on cutting-edge clinical trials with international teams and top-tier sponsors. Strong Culture : Join a company known for its stability and commitment to professional development. Support & Infrastructure : While the Hyderabad office is new, you’ll be backed by the global resources and processes of a well-established CRO. If you’re looking for a new challenge, and want to be part of building something meaningful while advancing your career with a company that’s investing in your region — we’d love to hear from you. Help shape the future of Medpace in Hyderabad. Apply today. Responsibilities : Collect, analyze and document user requirements; Design, modify, develop and support software applications; Participate in software validation process through development, review, and/or execution of test plan/cases/scripts; Create software applications by following software development life-cycle, which includes requirements gathering, design, development, testing, release, and maintenance; Communicate with team members regarding projects, development, tools, and procedures; Utilize skills in development areas including object oriented programming (C#), databases (SQL) web applications (ASP.NET); and Potential opportunities to lead software development projects. Qualifications : Bachelor's Degree in Computer Science; Familiarity of technologies such as C#, Angular, Webservices, Git, relational databases; Experience in Entity Framework, Azure DevOps is advantageous; Understanding of software development life cycle (SDLC) and software release management; Prior experience modernizing systems to a cloud-based platform (Azure) is a plus; Excellent analytical, written and oral communication skills in English; and Prior experience developing mobile application (iOS/Android) is a plus. Medpace Overview : Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

About Wellness Extract: Wellness Extract is a leading Canadian healthcare company committed to bridging the gap between premium healthcare and science-backed natural wellness. With a growing global footprint and a strong focus on natural supplements, we are now expanding our product innovation capabilities in India with a special focus on Ayurvedic and nutraceutical product lines. Whom we are looking for: We are looking for a visionary and hands-on Product Development Manager to join our India operations and lead the development of new supplements rooted in Ayurvedic wisdom and aligned with our existing portfolio of tocotrienols, astaxanthin, GG, CoQ10, colostrum, and detox products. Key Responsibilities:  Lead new product ideation based on Ayurvedic principles and scientific validation.  Identify market trends and gaps in USA, Canada, and UK.  Collaborate with Ayurvedic experts, R&D labs, and clinical researchers.  Source high-quality, ethically harvested ingredients.  Coordinate regulatory compliance (FSSAI, AYUSH, FDA, Health Canada).  Manage documentation, product claims, specifications, and SOPs.  Support marketing with USPs, positioning, and launch strategies. Qualifications & Skills:  Bachelor’s/Master’s in Pharmacy/ Food Science / Ayurveda / Biotechnology / Related.  5+ years in nutraceutical or Ayurvedic supplement development.  Experience launching products for USA, Canada, or UK.  Knowledge of Indian and global regulatory frameworks.  Exposure to clinical trials and patented/branded ingredients.  Strong documentation and project management abilities.  Passion for clean-label, sustainable, and innovative health products. What We Offer:  Opportunity to work with a global wellness brand.  Innovation-driven, collaborative culture.  Competitive salary and other benefits.  International exposure and flexible work environment.

Quality Assurance Officer – Certification & Regulatory Compliance Job Purpose To manage and ensure compliance / documentation with all food safety, quality, and regulatory standards by obtaining, maintaining, and renewing certifications including FSSAI, Halal, Kosher, Non-GMO, RSPO , and others as required by the business or market. This role ensures the unit’s products and processes meet global and domestic certification standards. Key Responsibilities Certification & Compliance Management Coordinate and maintain all third-party certifications including FSSAI license, Organic, renewal , Halal , Kosher , Non-GMO , RSPO , and any client-specific audits. Liaise with certification bodies, consultants, and authorities to prepare for audits, respond to non-conformities, and submit required documentation. Maintain a certification calendar and ensure timely application/renewal to avoid compliance lapses. Documentation & Recordkeeping Develop, implement, and maintain robust documentation systems for compliance, including SOPs, traceability records, declarations, and internal audit logs. Ensure product labels, claims, and packaging materials meet regulatory and certification standards. Prepare and submit regulatory filings and declarations (e.g. FSSAI Form C, RSPO annual communications). Quality Assurance & Auditing Conduct internal audits to verify compliance with applicable standards (e.g. Halal hygiene protocols, RSPO supply chain models, etc.). Identify gaps and propose corrective/preventive actions (CAPA) to achieve and maintain compliance. Support product and process traceability for Non-GMO and RSPO Mass Balance/Segregated systems. Training & Awareness Conduct internal training for production, procurement, and QA teams on certification standards and hygiene requirements. Build cross-functional awareness of requirements such as halal compliance zones, allergen management (Kosher), and raw material integrity (Non-GMO). Reporting & Communication Generate monthly reports on compliance status, certification timelines, audit outcomes, and risk assessments. Support client documentation requests (e.g., Kosher certificate copies, Halal declarations, GMO-free certificates, etc.). Qualifications & Experience Bachelor’s/Master’s Degree in Food Technology, Microbiology, Biotechnology, or related field. 2–5 years of experience in food industry QA or regulatory compliance, preferably in a manufacturing setup. Experience handling FSSAI, Halal, Kosher, RSPO, or Non-GMO certifications is mandatory. Job Type: Permanent Pay: ₹20,000.00 - ₹45,000.00 per month Willingness to travel: 50% (Preferred) Work Location: In person

Company Description Credence Genomics is is a leading provider of clinical genomics services, utilizing next generation sequencing technology to provide diagnostics and analytical support. Medisequence Private Limited is the subsidiary located in Chennai, India. Role Description This is a Technical Support Executive Duties and Responsibilities mentioned below : · Product Documentation and Literature · Quality Management System (QMS) · Product Performance Monitoring · Customer Complaints Management · Training and Process Familiarization · Technical Support for Site Implementations · Site Implementation Documentation · R&D Documentation Management Qualifications: Master's in life sciences · M Tech · M Sc. - Biotechnology & Genetic Engineering · M Sc. - Molecular Biology Experience: · At least 1 year Laboratory experience in Molecular Biology · Experience in implementation of Quality Management System Skills: · Team Player · Excellent communication skills · Good knowledge in writing and speaking English · Presentation Skills · Computer skills- general (Internet, Email, office package) Send your CV to hr@credencegenomics.com, to book an Interview. Note: Preference for Immediate Joiners only! Work Location : In Person Shift: · Day shift Job Type: Full-time Shift: Day shift Application Question(s): Do you have at least 1 year laboratory experience in molecular biology? Do you have experience in working or implementation of quality management system? Language: English (Preferred) Work Location: In person

Company Description Credence Genomics is is a leading provider of clinical genomics services, utilizing next generations sequencing technology to provide diagnostics and analytical support. Medisequence (Pvt) Limited is the subsidiary located in Chennai, India. About the Role: This is a Field Application Specialist role located on-site in Chennai at Medisequence (Pvt) Limited Key Responsibilities: 1. Product Workflow Expertise 2. On-Site Implementation 3. Customer & Technical Support 4. Quality Management & Standardization 5. Operational Support Qualifications: Master's in life sciences · M Tech · M Sc. - Biotechnology & Genetic Engineering · M Sc. - Molecular Biology Experience : · At least 1 year experience in molecular biology laboratory (academic or industry) · At least 1 year experience in PCR, DNA Extraction, DNA Sequencing, Nanopore Sequencing · Familiar with ISO15189 or NABL quality management system Skills: · Team Player · Excellent communication skills · Good knowledge in writing and speaking English · Presentation Skills · Computer skills- general (Internet, Email, office package) Send your CV to hr@medisequence.com, to book an Interview. Note: Preference for Immediate Joiners only! Shift: Day shift Job Type: Full-time Shift: Day shift Work Days: Monday to Friday Weekend availability Application Question(s): Do you have 1 year experience in PCR, DNA Extraction, DNA Sequencing(desirable), Nanopore Sequencing(desirable) ? Do you have 1 year experience in molecular biology laboratory (academic or industry)? Are you familiar with ISO15189 or NABL quality management system? Can you join immediately? Work Location: In person

Key Responsibilities:  Perform routine microbiological testing of raw materials, in-process samples, finished products, and water systems (e.g., TOC, endotoxin, bioburden, sterility).  Conduct environmental monitoring (viable and non-viable particle counts, surface swabbing, personnel monitoring) in cleanrooms and controlled areas.  Perform validation activities including media fill simulations, cleaning validation, and method validation.  Identify and investigate out-of-specification (OOS) and non-conformance issues in collaboration with QA/QC.  Maintain accurate and complete microbiological records, logs, and documentation as per cGMP.  Prepare microbial cultures, maintain microbial stock cultures, and carry out identification of microorganisms.  Participate in internal and external audits and assist in CAPA implementation related to microbiology.  Ensure laboratory instruments and equipment are calibrated, maintained, and validated as per schedule.  Assist in the development and revision of SOPs, protocols, and microbiological methods.  Support continuous improvement and training initiatives within the microbiology lab. Key Skills Required:  Attention to detail and strong documentation practices  Analytical and critical thinking  Familiarity with microbiology software systems (LIMS, etc.)  Ability to work independently and in teams  Good communication and reporting skills Qualification:  B.Sc./M.Sc. in Microbiology, Biotechnology, or related field.  2–5 years of experience in a pharmaceutical microbiology lab, preferably sterile manufacturing.  Good knowledge of current Good Manufacturing Practices (cGMP), GLP, and regulatory guidelines (e.g., WHO, EU, USFDA).  Hands-on experience in microbial limit testing, sterility testing, and EM techniques.  Proficiency in data recording, documentation, and handling microbiology lab equipment. Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Schedule: Day shift Experience: Microbiology: 2 years (Preferred) pharmaceutical microbiology lab: 1 year (Preferred) sterile manufacturing: 1 year (Preferred) microbial limit testing: 1 year (Preferred) sterility testing: 1 year (Preferred) EM techniques: 1 year (Preferred) Work Location: In person

Post code: PAT-I Post Name: Project Associate I (PAT-I) Number of posts: 01 Essential Qualification: Master's degree (M.Sc.) in Microbiology/Biotechnology Preferred experience: Work experience in scientific communication writing, publication and information dissemination Emoluments: (a) ₹. 31,000/- + HRA for those candidates who have qualified CSIR-UGC / ICAR / ICMR NET including lectureship/assistant professorship or GATE or those who have qualified National level examinations conducted by Central Government Department like DBT/DST or equivalent and/or their Agencies/Institutions (b) ₹ 25,000/- + HRA for others who do not fall under (a) above Job description: Selected candidate will work in the CSIR-sponsored project entitled “ Jigyasa 2.0 Programme with the concept of Virtual lab Integration (CJVL) ”. The candidates are expected to work in scientific communication, writing, publication, lab analytical work and information dissemination. Age limit: 35 years as on the date of interview (age relaxation as per CSIR rule). Other details: Duration: This position is purely temporary and the appointment will be given up to 31st March, 2026. It does not confer any right or claim for absorption in CSIR-CSMCRI. This post is purely temporary and co-terminus with the project (upto 31.03.2026). The engagement of a project staff in different projects either in the CSIR - Central Salt & Marine Chemicals Research Institute, Bhavnagar or different Laboratories/Institutes of CSIR taken together shall not exceed 06 years in any case. It would, therefore, not confer any right/claim implicit or explicit for any candidate for claiming extension or absorption in CSIR-CSMCRI, Bhavnagar. Interview Details: Interested candidates should appear before the Selection Committee for an interview/written test at CSIR-Central Salt and Marine Chemicals Research Institute, G. B. Marg, Bhavnagar-364002 (Gujarat) on 22nd August 2025; Friday at 10.00 AM in the institute. Required Documents: Please bring an application with full particulars, including: Full name and postal address with email and phone number (application form attached), Date of birth and recent photograph. Educational qualifications and experience (if any) with photocopies of certificates/testimonials. Also, bring the following original documents (compulsory): Certificates and mark sheets (Degree/Diploma, etc.) of educational qualifications and proof of date of birth mentioned in the application (degree certificate is compulsory). GATE/NET Score Card, validity of the score, and details of seminars/projects done in the Master’s course. Experience certificates and testimonials. "No Objection Certificate" from the present employer if employed in a Government/Semi-Government or Autonomous Organization. For queries, please email drchaudhary@csmcri.res.in. No TA/DA will be provided for attending the interview.

Job Summary Are you passionate about solving customer problems, offering Technical solutions and building deeper business relationships that help drive growth for industry leading Consumer Products customers? Joining science and creativity, we are an international collective of thinkers who partner with customers to bring scents, tastes, experiences, ingredients and solutions for products the world craves. If you are skilled at solving complex problems with elegant technical solutions, and have a collaborative approach to exceeding customer expectations, you could be our next Application Specialist! Your Focus As a part of our Application Development team, you will be responsible to work across functions to develop and support products and processes. The role will see you providing technical and functional leadership opportunities and will play a key part in supporting our evolving industry and customer base. The role is based in Hyderabad, India and will report to the Regional Application Leader – Grain Processing. How You Will Contribute Involve with hands on work at bench and pilot scales. Design, develop, execute, and contribute innovatively to the development of enzyme and yeast products and processes across scale, analyze and interpret data using statistics to make a sound recommendation for specific projects. Collaborate closely with the application scientist to advance the solution while creating and maintaining an up-to-date project data, both at lab and pilot scale. Objectively support the analysis of customer and project samples using physical, bio/chemical and functional assay. Manage the day-to-day lab activities while upholding to the highest standards of Occupational Health and Safety. Interact with cross functional teams including R&D, sales, marketing, legal, procurement and engineering. What You Will Need To Be Successful Master`s degree (with 3+ years of Industry experience) or a PhD degree in Biochemistry, Biotechnology, Bio Engineering, Agriculture Engineering or a related area. Strong knowledge and experience of industrial scale fermentation, preferably in the grain based ethanol manufacturing. Experience in executing experiments across scales (Lab-Pilot-Commercial) to assess the performance of enzymes and/or yeast meeting project timelines. Experience with analytical techniques relevant to monitoring the biotechnological process (Proximate, HPLC, GC, Biochemical assay, Viscometry, PSD, micro-DSC, Etc). Proficiency with statistical analysis software such as JMP, SPC, excel, etc., for generating scientific report with objective inferences. Excellent verbal and written communication skills Strong team player with the ability to deliver results in a fast-paced environment. Willingness to travel upto 20% across ASPAC, including to customer commercial facilities. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

On-site at Cloudnine Hospital 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 Types: Full-time, Permanent, Fresher Pay: ₹300,000.00 - ₹400,000.00 per year Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Application Question(s): When are you available to start working with us? Work Location: In person

Cryoviva Biotech Pvt Ltd New INSIDE SALES EXECUTIVE (Fresher - Biotech) Noida, India Employee Inside Sales, Sales Clerks On-site at Cloudnine Hospital Location: Noida 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 ID: 14606738 Cryoviva Biotech Pvt Ltd 51-200 employees Hospitals

We are looking for a detail-oriented and experienced Senior QC Microbiologist to join our Quality Control team. In this role, you will oversee microbiological testing and ensure that raw materials, in-process samples, and finished pharmaceutical products meet regulatory and internal quality standards. Key responsibilities include conducting environmental monitoring, water testing, bioburden analysis, endotoxin testing, and microbial identification. You will be responsible for reviewing and approving microbiological data, investigating out-of-specification (OOS) or out-of-trend (OOT) results, and leading root cause analyses. The Senior QC Microbiologist will also play a critical role in maintaining GMP compliance and assisting during regulatory audits and inspections. The ideal candidate has a strong background in microbiology, with at least 5 years of experience in a pharmaceutical or biotechnology QC lab. Proficiency in aseptic techniques, microbiological instrumentation (e.g., endotoxin reader, particle counter), and good documentation practices is essential. Familiarity with compendial methods (USP, EP) and regulatory requirements (FDA, EMA) is highly desirable. As a senior team member, you will mentor junior staff, ensure laboratory best practices, and contribute to continuous improvement initiatives within the QC function. Job Types: Full-time, Permanent Pay: ₹600,000.00 - ₹700,000.00 per year Schedule: Day shift Work Location: In person

Post- Executive Assistant Location- Near Grand Venice Mall, Greater Noida( 2.3 KMs from Pari Chowk) Qualification- Bio-Technology, Bio-Science, Medical Bio-technology or related field Job Roll- Assisting Students for joining paid Training courses, Counseling of candidates to pay & join, Data Follow-ups by calling, Conversion of Students to pay Type of Job- Part-Time, 4 Hours, 11AM to 3PM, Flexible( Evening hours also OK) Salary- Rs.5000- Rs.8,000 Language- English Fresher- OK Students- OK Company Description Nanofludiks Research Pvt Ltd is a cutting-edge biotechnology company incubated at Jawaharlal Nehru University (JNU), New Delhi. The company is a JNU spinoff founded under the Atal Incubation Centre – JNU Foundation for Innovation (AIC-JNUFI), a government-supported initiative launched in May 2019 under the Atal Innovation Mission – NITI Aayog. Nanofludiks is among the select 18 biotech-focused companies nurtured within AIC-JNUFI’s vibrant academic–entrepreneurial ecosystem. The company has developed a cloud-based biological data analytics platform with applications in healthcare, infectious disease research, and vaccine/drug development. Role Description This is a part-time on-site role located in Gautam Buddha Nagar for an Executive Assistant specialized in Bio-Technology, Data Follow-Ups, and Student Counseling. The Executive Assistant will be responsible for providing executive administrative assistance, managing expense reports, and offering executive support. Additionally, the role will involve enhanced communication and administrative assistance duties, including following up on data and counseling students. Qualifications Executive Administrative Assistance, Administrative Assistance, and Expense Reports skills Experience in Executive Support and Communication Excellent organizational and multitasking abilities Strong interpersonal and communication skills Ability to work on-site in Gautam Buddha Nagar Experience in the biotechnology sector is a plus Bachelor's degree in a relevant field is preferred Apply @WhatsApp 9818625731 www.nanofludiks.com

The University of Hong Kong Apply now Ref.: 532746 Work type: Full-time Department: School of Public Health (22400) Categories: Research Staff Hong Kong Research Assistant II/ I and Senior Research Assistant in the Division of Public Health Laboratory Sciences, School of Public Health (Ref.: 532746) (to commence as soon as possible on a one-year temporary term or two-year fixed-term contract, with the possibility of renewal subject to funding availability and satisfactory performance) The applicants should possess a Bachelor's or Postgraduate degree in Biomedical Sciences, Microbiology, Biotechnology, or related disciplines. Experience in handling microbial pathogens in BSL2 laboratories would be an advantage. We seek applicants who are team players, have a strong sense of responsibility and independent thinking ability. The appointee will work in the laboratory and in the field to study influenza and coronaviruses virus-host interactions. Enquiries about the duties of the post should be sent to Professor H.L. Yen at hyen@hku.hk. A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits. The appointment on fixed terms will attract a contract-end gratuity and University contribution to a retirement benefits scheme, totalling up to 10% of basic salary. The University only accepts online applications for the above post. Applicants should apply online and upload an up-to-date CV. Review of applications will commence as soon as possible and continue until October 30, 2025 , or until the post is filled, whichever is earlier. Advertised: Jul 31, 2025 (HK Time) Applications close: Oct 30, 2025 (HK Time) Back to search results Apply now Whatsapp Facebook LinkedIn Email App

Profile : Research Associate – R&D (Biochemistry & Hematology) Location: Ghitorni New Delhi Salary : 20,000 to 25,000 (Based On Interview) Experience : 0 to 6 Months Key Responsibilities Design and execute experimental protocols for the development of diagnostic assays in clinical biochemistry and hematology. Perform wet lab work including reagent formulation, sample preparation, assay optimization, and troubleshooting. Develop, validate, and standardize biochemical and hematological test methods. Evaluate analytical performance parameters such as precision, accuracy, sensitivity, specificity, linearity, and stability. Prepare and maintain experimental documentation, lab notebooks, and technical reports. Collaborate with cross-functional teams including QC, manufacturing, and regulatory affairs for tech transfer and validation. Assist in drafting SOPs, protocols, validation plans, and scientific documentation for regulatory submissions (e.g., ICMR, CDSCO, US FDA). Support comparative studies with reference methods and competitor products. Maintain laboratory instruments, ensure calibration and preventive maintenance as per GLP. Stay updated with recent advancements in clinical diagnostics and regulatory guidelines. Required Qualifications & Skills M.Sc. / M.Tech in Biochemistry, Biotechnology, Hematology, Life Sciences or related field. 0–3 years of hands-on R&D experience in clinical diagnostics. Sound understanding of biochemical reactions, enzyme kinetics, and hematological principles. Experience in using analyzers like spectrophotometers, hematology analyzers, and auto-analyzers. Knowledge of method validation and regulatory documentation (e.g., CLSI guidelines). Strong analytical, problem-solving, and data interpretation skills. Proficiency in scientific writing and documentation. Familiarity with ISO 13485, CDSCO regulations is an advantage. Preferred Qualities Self-motivated with a strong passion for innovation and diagnostics. Detail-oriented, organized, and capable of working independently and in teams. Good communication and presentation skills.

Junior Research Fellow (JRF) Position Last Date for applying : 10-08-2025. Online Interview on 13-08-2025 Company Description: Opto-Biomedical Microsystem (OBMS) Laboratory https://www.obmslab.com/ is a research and development laboratory located in Raurkela and is an integral part of the Department of Biotechnology and Medical Engineering, National Institute of Technology Rourkela https://nitrkl.ac.in/SRICCE/Career. https://nitrkl.ac.in/docs/Career/ProjectFelow/2025/25072025143524449.pdf Job descriptions: The OBMS LAB is focused on developing instruments for biomedical applications including screening, diagnosis, monitoring, and point-of-care diagnostics. OBMS also focuses on image and signal analysis for drug screening and testing applications. The lab further focuses on the fabrication of microfluidic devices. Lab is equipped with: high-end Workstation (32 GB Graphics card ADA) GPU, High-Speed Imaging Camera (Upto 14000 Frames per seconds), Polarized He-Ne laser source 20 mW, High Power white light sources, Multiple Vibration Isolation Optical Table, Various Optical and opt mechanics components, Various 3D printers (Industrial grade Bambu Labs, Creality 3D printer, Resin 3D printer, High Power Laser Engraver 40 Watts), etc. Responsibilities and Role Description: This is a full-time on-site role for a Junior Research Fellow (2 years) https://nitrkl.ac.in/docs/Career/ProjectFelow/2025/25072025143524449.pdf at OBMS Laboratory. The successful candidate will be expected to work on developing and testing instruments for biomedical applications, microfluidic devices, and image and signal analysis. They will also be responsible for conducting research and publishing results. Interested candidates can apply by filling out the applications: NITR/SR/2025/Advt./23BM060/L/051 The successful candidate also has the provision to enroll Ph.D. at NIT Rourkela if all criteria's are fulfilled. The position is available from the sponsored project titled "Innovating Indigenous Portable Microfluidic Absorption Flow Cytometer for Multi-diseases Detection at Point-of-Care" under @ANRF / SERB, India. Qualifications Having Experience in dealing with Optical components, Applied physics, Optics, Microfluidics is having potential edge in the recruiting process. Experience in developing and testing biomedical instruments and microfluidic devices Experience in image and signal analysis Ability to conduct research and publish results Strong understanding of biomedical applications and technology Excellent written and verbal communication skills Bachelor's or Master's degree in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Physics, or related field Experience working in a research laboratory is a plus Ability to work as part of a team. Interested Individuals reach out me at Dr. Earu Banoth Fulbright Fellow-2019 Senior Member IEEE and OPTICA Assistant Professor Dept. Of Biotechnology Medical Engg NIT Rourkela, banothe@nitrkl.ac.in Phone: +91 8861543837/ 661-246-2299

Click here to download Form College of Basic Scs. & Humanities PAU, Ludhiana NOTICE Applications from the eligible candidates are invited for the position of One Junior Research Fellow on contractual basis @ Rs. 31,000/- per month + 16% HRA provided in the scheme entitled “DBT-BUILDER-Punjab Agricultural University Interdisciplinary Life Science programme for Advance Research and Education” CSS-46 (PC-6349)” (Financed by Government of India, Ministry of Sciences & Technology, DBT, New Delhi). The desirous candidates fulfilling the qualifications/ experience should send their applications to Dean, College of Basic Sciences & Humanities, PAU, PIN-141004 on the prescribed proforma complete in all respect alongwith attested copies of the testimonials and bank draft amounting to Rs.200/- in favour of Comptroller, PAU, Ludhiana. Qualification for the position of Junior Research Fellow i . B.Sc./ B.Sc Medical/ Biochemistry /Life Sciences/ Biotechnology/ B.Tech. Biotechnology with minimum OCPA 6.00/10.00 basis or 60 % marks. ii . M.Sc. in Biochemistry/ Biotechnology/ Molecular Biology/ Life Sciences/ Microbiology with minimum OCPA 6.5/10.00 or 65 % marks. Note-I: The candidate, who does not possess Master ’s degree in the relevant subject but possess Ph.D. degree in the discipline required at Master’s level, shall be eligible for the post. Note-II: Applicants having post graduation degree in subjects mentioned above, but having Bachelor degree with three years must have passed the NET by ARS, DBT, CSIR/ UGC NET or GATE. Desirable Qualification The candidates holding the experience of conducting biochemical experiments associated with biotic and abiotic stress/ hands on molecular biology techniques and bioinformatics tools/ soil microbiology will be preferred. "The candidates should ensure that they fulfill the qualifications by the last date of submission of application ." The fellowship is purely temporary and initially awarded for period of six months which may be extended for piece meals period of six months at a time or till the termination of the scheme whichever is earlier. The last date for the receipt of applications duly complete in all respects in this office is 13.8.2025 by 3.00pm. The incomplete applications unsupported by the requisite documents will not be entertained. The date of interview will be intimated later on PAU website i.e. www.pau.edu. No TA/DA will be paid for attending the interview. The Junior Research Fellow if leave the University shall have to give one-month notice or one-month salary in lieu of that notice period. Sd/- Dean College of Basic Scs. & Humanities Endst. No. A-2/2025/ 9615-9714 Dated: 01.08.2025

Company Description The Aspire Biozymes specializes in producing high-quality papain products, including Ultra Refined Papain Powder (URPP) and Stabilized Liquid Papain (SLP). Our commitment to quality and innovation makes us a leader in the industry, dedicated to delivering superior products to our clients worldwide. Role Description This is a full-time, on-site role located in Tiruppur for a Sales and Marketing Associate. The Sales and Marketing Associate will be responsible for developing and executing sales strategies, conducting market research, engaging with customers, and providing excellent customer service. The role also includes training new team members, managing client accounts, and driving marketing campaigns to enhance brand awareness and sales performance. Eligibility Masters in Business Administration or related Field. Qualifications Excellent Communication and Customer Service skills. Proven experience in Sales. Strong skills in Training and Sales & Marketing. Ability to develop and execute marketing strategies. Excellent interpersonal and relationship-building skills. Proficiency in using CRM software and other sales tools. Relevant experience in the biochemistry or biotechnology field is a plus.

Company Description Autocal Solutions Pvt. Ltd. is a leading Pan India company specializing in Calibration, Validation, and HVAC activities. Established in 2002, we offer localized support and services across various regions, continuously expanding our laboratory network to meet customer needs nationally and internationally. We are accredited by NABL as per ISO/IEC 17025:2005, with laboratories located in Vasai, Pune, and Nashik. Our expertise includes Calibration, Validation, PLC Validation, Food Testing, Microbiological Testing, Air Testing, and Water Testing. Role Description This is a full-time on-site role for a Technical Manager - Microbiology, located in Mumbai. The Technical Manager - Microbiology will oversee and manage the day-to-day microbiological testing activities, including supervising the technical team, developing testing methodologies, ensuring compliance with regulatory standards, and maintaining laboratory quality assurance. Additional responsibilities include performing microbiological tests, interpreting test results, training staff, and continually enhancing laboratory processes and procedures. Qualifications Experience in Microbiological Testing, understanding of microbiological techniques, and methodologies Familiarity with regulatory standards and compliance requirements related to microbiology Leadership and team management skills Excellent problem-solving and analytical skills Strong written and verbal communication skills Ability to work independently and manage multiple tasks efficiently Experience in the calibration, validation, and testing industry is highly beneficial Bachelor's or Master's degree in Microbiology, Biotechnology, or related fields

Job Title: Zebrafish Housing Systems & Devices Service Technician 📍 Location: Gami Industrial Park, Navi Mumbai 💼 Company: Zebrafish India About the Role Zebrafish India is looking for a motivated and technically skilled Service Technician to join our team. The role involves installation, servicing, and maintenance of zebrafish housing systems and related devices, while also supporting sales operations and client communication. If you are a local candidate from Navi Mumbai with a background in biotechnology and a passion for hands-on technical work, we’d love to meet you! Key Responsibilities Installation, servicing, and maintenance of zebrafish housing systems and devices. Conduct regular service visits and resolve technical issues for clients. Travel 5–10 days per month for onsite service and installations. Manage client calls, provide technical support, and maintain service logs. Assist in sales support activities, demonstrations, and client follow-ups. Collaborate with the internal team to ensure timely execution of projects. Ensure compliance with company service and safety standards. Qualifications Education: B.Sc. in Biotechnology (Post Graduates are over qualified and requested not to apply) CV should mention current address (Full Address). Experience: Freshers or candidates with relevant technical/service experience are welcome. Strong troubleshooting and problem-solving skills. Good communication skills in English, Hindi, and Marathi. Must be a local candidate from Navi Mumbai or nearby areas. Compensation Salary: ₹12,000 per month (fixed) Incentives: ₹3,000 for every successful installation or service Travel: 5–10 days/month (company-covered) TA/DA will be in addition to the above incentive. (Overall package per year with incentives will go to 20000/- per month. Why Join Us Opportunity to work with India's leading zebrafish research solutions provider. Hands-on technical training and growth in the life sciences industry. Competitive incentive structure for high performers. Commited candidates will see growth from Service Technician to Service Manager Position with fast promotion in reponsibilities and package. But, those who prefer money over learning will not be preferred. Candidates should be unmarried, freshers and local residents of Navi Mumbai. Travelling will be all over India. 📩 How to Apply: Send your CV to info@zebrafishindia.in with the subject line "Application – Service Technician" .

Job Description : We are looking for the candidates who are good at, 1 Performing sample testing using basic methods (Titration, Culture maintenance, etc) and aseptic handling. 2 Performing microbial analysis of various samples, like a water sample. 3 Titrimetric analysis of raw material, In-process and finished material. 4 Up keeping the general maintenance of laboratory equipment under a quality assurance and standard operating procedures. 5 Sampling and testing of lab utilities including but not limited to bioburden. 6 Preparation of volumetric solutions/media/buffers. 7 We are looking for candidates with, good communication skills and good handwriting. 8 An incumbent who is highly organized and with an attention to details 9 Exposure of audits and good documentation practices will be an added advantage. Note : Freshers can also apply, Male or Female. Job Types: Full-time, Fresher or Expd. Qualification : B.Sc or M.Sc Computer skills: MS Office. Good Written Communication skills. Salary : Rs. 4 lakhs per Annum to 9 LPA Contact : Mr Vasanth Managing Director 7259549756 / 8722187029 Karnataka Information Solution No.6, Ground Floor, ASVNV Bhavan, Opp FKCCI Bldg, K.G Road, Majestic, Bangalore Ph : 080 - 22260106

Company Description Astam Diagnostics Private Limited, part of ASTAM group of companies, was established on February 17, with the vision of providing diagnostics at the doorstep. Committed to delivering quality diagnostics at affordable prices, we manufacture In-Vitro Diagnostics kits and reagents, all managed by experienced professionals from the diagnostics field. With a robust sales and distribution network rooted in 20 years of industry experience, Astam Diagnostics ensures accessibility and reliability in diagnostic services. Role Description This is a full-time, on-site role for a Business Development Manager – Medical Devices located in New Delhi. The Business Development Manager will be responsible for identifying new business opportunities, developing and maintaining client relationships, conducting market research, and driving sales growth. Additional responsibilities include coordinating with internal teams to align on strategy, preparing sales reports, and participating in industry events and trade shows. Qualifications Experience in business development, sales, and client relationship management Knowledge of the medical devices industry, particularly In-Vitro Diagnostics Strong analytical skills, including market research and data analysis Excellent verbal and written communication skills Ability to work independently and as part of a team Bachelor’s degree in Business, Marketing, Biotechnology, or a related field; advanced degree is a plus Experience with project management and strategic planning

University: Delft University of Technology Country: Netherlands Deadline: 2025-09-15 Fields: Mechanical Engineering, Chemical Engineering, Applied Physics, Fluid Dynamics, Materials Science Are you passionate about unraveling the mysteries of complex fluid flows and eager to contribute to groundbreaking research with real-world applications in healthcare, industry, and energy? If you aspire to deepen your expertise in experimental fluid dynamics and make a tangible impact on society, the PhD positions in Experimental Investigation of Inertial Dense Suspensions at TU Delft may be the perfect next step for your academic journey. Inertial Dense Suspensions (IDeS) are a cornerstone of both natural phenomena and industrial processes, appearing in contexts as diverse as blood circulation, waste management, additive manufacturing, and energy storage. Despite their prevalence, these flows remain poorly understood, hindering our ability to predict and control them with accuracy. This knowledge gap has significant implications: for instance, current models can misestimate the pressure drop in suspension pipe flows by up to 40%, complicating the design and operation of critical systems. The challenge arises because these flows do not fit neatly into traditional categories of laminar or turbulent regimes, instead occupying a complex middle ground characterized by unique inertial phenomena. As part of the ERC Advanced Grant project IDeS, TU Delft is seeking two highly motivated PhD candidates to join a dynamic research team dedicated to advancing our understanding of densely-laden pipe flows. The successful candidates will contribute to experimental investigations that push the boundaries of current knowledge, utilizing state-of-the-art measurement techniques and analytical tools. About The University Or Research Institute Delft University of Technology (TU Delft) stands as a beacon of scientific and engineering excellence, renowned globally for its pioneering contributions to water management, biotechnology, and sustainable innovation. Located in the vibrant city of Delft, Netherlands, TU Delft offers a stimulating academic environment where creativity and collaboration thrive. The university’s Faculty of Mechanical Engineering is particularly distinguished for its cutting-edge research and high-tech laboratory facilities, fostering a culture of interdisciplinary cooperation and societal engagement. TU Delft is committed to diversity, inclusivity, and the professional growth of its students and staff, providing comprehensive support for international researchers relocating to the Netherlands. Research Topic and Significance Also See PhD in Systems Engineering for Sustainable Energy in Manufacturing at TU Delft PhD Opportunity in Symbolic AI and Reasoning Under Uncertainty at TU Delft Postdoctoral Opportunity in Applied Planning and Scheduling Under Uncertainty for Offshore… Netherlands – PhD in Silicon-Based Electrodes for Lithium-Ion Batteries at TU Delft Fully Funded PhD and Postdoctoral Opportunities in Catalysis Research at TU Delft The focus of this research is on the experimental investigation of inertial dense suspensions—complex multiphase flows where suspended particles significantly influence fluid behavior. These suspensions defy conventional fluid dynamics paradigms, exhibiting phenomena such as particle-induced fluctuations, gradual transitions to turbulence, and shear-induced migration. Understanding these mechanisms is vital for improving the design and efficiency of systems across multiple industries, from medical devices to energy infrastructure. The project’s outcomes will not only advance fundamental science but also enable the development of more reliable predictive models, facilitating innovation and sustainability in key sectors. Project Details The two available PhD positions, funded by the ERC Advanced Grant project IDeS, offer distinct but complementary research trajectories: – PhD 1 will employ advanced optical techniques, such as volumetric flow measurement (e.g., Lagrangian particle tracking or tomo-PIV), to quantify near-wall behavior and model particle-induced fluctuations. This work includes investigating how these fluctuations interact with the onset of turbulence. – PhD 2 will focus on ultrasound imaging velocimetry combined with shadowgraphy to study shear-induced migration of particles, developing models that account for variables such as volume fraction, particle size, Reynolds number, and density ratio. Both positions are based in the Process & Energy (P&E) department within TU Delft’s Mechanical Engineering faculty, which boasts a comprehensive suite of flow facilities and advanced measurement modalities, including MRI and ultrasound systems dedicated to multiphase research. Responsibilities include conducting experimental research, publishing in peer-reviewed journals, presenting at international conferences, and mentoring undergraduate and master’s students. Professional development is supported through a range of technical and non-technical courses. Candidate Profile Ideal Applicants Should Possess – An MSc degree in Mechanical Engineering, Chemical Engineering, Applied Physics, or a closely related field. – A strong background in (multiphase) fluid dynamics. – Demonstrated experience with experimental research and a drive to advance state-of-the-art techniques. – Proficiency in image and data processing using Python or Matlab. – Excellent written and spoken English skills. – Creativity, self-motivation, and the ability to work effectively within a multidisciplinary team. TU Delft values diversity and encourages applicants from all backgrounds to apply, ensuring a fair and inclusive selection process. Application Process Interested candidates should submit their applications no later than 15 September 2025 via the official TU Delft application portal: https://careers.tudelft.nl/job/Delft-Two-PhD-Positions-Experimental-Investigation-of-Inertial-Dense-Suspensions-2628-CD/826454302/ Required Application Materials – Curriculum vitae – Motivation letter detailing relevant research skills and motivation for pursuing this PhD project – Diplomas and transcripts of BSc and MSc studies, including certified grade lists – Names and contact details of at least two academic referees (preferably including the MSc thesis supervisor) Applications should be addressed to Prof. C. Poelma. For further information about the position, research project, or application procedure, prospective applicants may contact Prof. C. Poelma at C[dot]Poelma[at]tudelft[dot]nl. Conclusion This is a unique opportunity to join a world-class research team at TU Delft and contribute to cutting-edge advancements in the understanding of inertial dense suspensions. If you are driven by scientific curiosity and a desire to make a meaningful impact, you are encouraged to apply. For more opportunities like this, explore similar positions and stay updated with the latest academic openings. Want to calculate your PhD admission chances? Try it here: https://phdfinder.com/phd_admission_chance_calculator/ Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee!

About Immuneel Immuneel Therapeutics Private Limited is a pioneering start-up company leading the charge in cell therapy and personalized immunotherapy for patients in India and the world. For more details, please refer www.immuneel.com We Pursue, with Purpose, to serve our Patients (3 Ps) by Connecting within, collaborating globally and Creating (3 Cs) solutions. Our flexible, diverse, and vibrant team is bringing together best practices and innovations in the field of cell and gene therapy. Working at Immuneel promises the excitement of an agile startup on a critical mission. Proudly Indian in solutioning, yet global in outlook, we are keen to collaborate. We value diversity including in experience and perspectives. We value work-life balance and believe that having fun on the job is integral to achieving the right results. We pride ourselves on providing an open environment and our mission resonates with humanity everywhere. At Work, we are: Passionate in driving patient outcomes: We are passionately committed to doing the RIGHT thing to achieve the best outcomes for our patients through innovation, agility and performance orientation. We put the impact on the patient above all else. Responsible and accountable: We demonstrate ownership and accountability for our actions. We make timely and well-informed decisions, learning from our performance. Transparent, honest, and supportive in how we work together: We insist on integrity and respect for the individual. We demand excellence. Our performance management is focused on excellence through timely and constructive feed-forward. Inclusive and flexible: We are full of life and embrace all opportunities to collaborate and work together. We are excited about the collective knowledge and expertise that we share. “Being and thinking different” is valued. Immuneel prides itself as an organization that is keeping pace with best practices in organization design. Our role-based organization incorporates global trends in human capital that promote focus on work and greater nimbleness. Our role-based structure allows you to be cherished by the work you do and bring value to your work rather than designations, our organization is simplified into a flat, non-hierarchical, millennial, organization where you may fully inherit the role you play in the organization and are recognized by the accountability you take and the work you deliver. Immuneel’s employees are integral to our quest to develop and deliver high quality engineered cell and gene therapies in India. We believe that our culture provides an environment for employees to excel and find purpose. The strength of our team is every bit as important as our cutting-edge technology and we invest in clear compensation and comprehensive benefits for our employees. People for us, are not resources, but our capital. If you are a talented professional, an out-of-box thinker with a zeal to help change, and passionate about healthcare, we invite you to join us and be a part of a historic initiative in India. Interested to be a part of the next revolution in cancer treatment? Send your resume to careers@immuneel.com 1. Role Title: Analyst / Specialist - Regulatory Affairs (CMC and Operations) 2. Department/Function: Regulatory Affairs 3. Reporting Structure: Reports to: Regulatory Affairs Direct Reports: Individual Contributor 4. Role Summary: The ideal candidate will play a critical role in managing and supporting regulatory submissions, ensuring compliance with global regulatory requirements, and maintaining the highest standards of operational excellence in regulatory processes. This role requires strong organizational skills, a high level of attention to detail, and the ability to collaborate across cross-functional teams. 5. Key Responsibilities: Regulatory CMC and operations Prepare, review and submit regulatory applications , including but not limited to Clinical Trial Applications, IND, MA applications, Test licence NoC, Import licence applications, IND, IMPD for cell and gene therapy products to CDSCO and respective regulatory agencies in other geographies. Prepare, review and submit regulatory applications, including but not limited to Form B1, Form C3, Form C5 to RCGM. Any other regulatory compliance documentation related to RCGM. Prepare, review and submit regulatory applications, including but not limited to Form 27 applications, Form 30 applications, WHO GMP applications, COPP applications to KDCD. Any other regulatory compliance documentation related to KDCD. Should be able to manage all IBSC/GTAEC (if required) related assignments. Prepare, review and submit response to various queries received from CDSCO/RCGM/KDCD/Other regulatory agencies. Follow up for various regulatory applications submitted to CDSCO/RCGM/KDCD/Other regulatory agencies in terms of seeking acknowledgements, queries, response to queries and approvals. Expertise in handling the online submissions on RCGM/SUGAM/NSWS portals. Very well versed with CTD/eCTD requirements for M1, M2, M3, M4 and M5 of the dossier. And ACTD requirements for Part I, Part II, Part III and Part IV of the dossier. Should have understanding about the regulatory compliance with respect to life cycle management (LCM) activities and changes made to the approved products. Engage in cross functional activities such as audit management and compliance. Government Affairs Liaison with CDSCO Zonal Office (Bengaluru, Karnataka), KDCD, RCGM office, IBSC Committee as assigned. Establish working relationship, facilitate discussions and follow up with the above regulatory bodies. Regulatory Intelligence : Stay updated on Indian as well as Global regulatory requirements and changes in regulatory guidelines for Biologics and CGT products. Stay updated in developers of CGT and the competitive intelligence of similar CGT product development in India as well as globally. Communicate changes and their implications to relevant cross functional teams to ensure regulatory compliance. 6. Competencies Required: Technical CDSCO Regulations: Deep understanding of the Drugs and Cosmetics Act, 1940, and related rules, guidelines, and circulars issued by the CDSCO. Drug Development Lifecycle: Knowledge of the entire drug development process, from preclinical research to life cycle management (LCM). Clinical Trials: Familiarity with clinical trial regulations, including Good Clinical Practices (GCP) and the New Drugs and Clinical Trials Rules, 2019. Drug Approval Process: Understanding of the procedures for obtaining marketing authorization for new drugs, including dossier preparation and submission. Pharmacovigilance: Knowledge of pharmacovigilance regulations and guidelines for reporting adverse drug reactions. Behavioural Adaptable, Team Player, Collaborative, Empathetic, (Good) Listener, Persuasive, Ethical, Resourceful, Self Motivated, Result Oriented, Organised, Persistent, Conceptual, Information Seeker, Enthusiastic, Committed, Hard Working. Soft Skills: Liaison & Negotiation: Ability to effectively communicate and negotiate with regulatory officials/partners, build rapport, and address their queries. Technical Writing: Excellent writing skills to prepare clear, concise, and accurate regulatory documents, such as applications, submissions, and responses to queries. Presentation Skills: Ability to present information effectively to internal and external stakeholders, including regulatory agencies, cross functional teams and partners. Interpersonal Skills : Strong interpersonal skills to interact with colleagues, superiors, and external stakeholders in a professional and collaborative manner. Critical Thinking: Ability to analyse complex regulatory requirements and identify potential challenges. Problem-Solving : Ability to find solutions to regulatory issues and address queries from CDSCO efficiently. Attention to Detail: Meticulous approach to ensure accuracy and completeness of regulatory documents. 8. Qualifications: Educational Qualification: Bachelors or Masters degree in Life Sciences, Pharmacy, Biotechnology, or a related field. Experience: 2-5 years of experience in regulatory affairs (CMC + Operations), or a related field. Extensive experience in handling regulatory applications to DCGI, RCGM, KDCD and other regulatory agencies. 9. Working Conditions: Role Type: Full Time Work Hours: 9:00 AM to 6:00 PM for the General Shift and 2:00 PM to 11:00 PM for the Post-Noon Shift (on a rotational basis). There will be two days off each week, which may not necessarily fall on a Saturday or Sunday. Travel Requirements: Occasional Base Location: Bengaluru. Office Location address - Immuneel Therapeutics Private Limited, 8th Floor, Mazumdar Shaw Medical Center, Narayana Health City, Bommasandra Industrial Area, Bangalore - 560099

Job Summary: We are seeking an experienced and proactive Sales Manager to drive Pan India sales of pharmaceutical-grade consumables and sterile handling solutions, including RTP/Alpha-Beta Ports, Single-Use Bags for Bioprocessing, and CSM/EPDM Gloves. The ideal candidate must have strong industry knowledge, experience in cleanroom or containment equipment sales, and an established network within biotech, pharmaceutical, and CDMO sectors. Key Responsibilities: Develop and execute Pan India sales strategies for consumables used in biopharmaceutical manufacturing and aseptic processing. Manage the complete sales cycle: lead generation, technical discussions, proposal submission, negotiations, and order closure. Build and nurture strong relationships with procurement, engineering, production, and QA teams in pharmaceutical companies, CDMOs, and research institutes. Promote and sell: RTP (Rapid Transfer Ports) and Alpha-Beta Ports for aseptic and containment applications. Single-Use Bags and components used in upstream/downstream bioprocessing. CSM/EPDM Gloves and related consumables used in isolators and RABS. Provide techno-commercial support, including presentations, product demos, and validations. Collaborate with application specialists, service teams, and OEM partners for customized solutions and smooth implementation. Monitor market trends, customer feedback, and competitor activity to refine product and pricing strategies. Maintain accurate CRM records, prepare reports, and manage a robust sales pipeline. Required Skills & Qualifications: Bachelor’s degree in Pharmacy, Biotechnology, Life Sciences, or Engineering. MBA is a plus. Minimum 5 years of relevant B2B sales experience in pharmaceutical consumables, cleanroom accessories, or single-use technologies. Sound knowledge of aseptic manufacturing processes, GMP standards, containment systems, and cleanroom practices. Strong network and existing customer base in pharma-biotech manufacturing environments. Proven ability to handle Pan India travel and territory management. Excellent communication, negotiation, and organizational skills. Preferred: Experience working with or selling products from well known suppliers for India. Understanding of validation protocols, vendor audits, and documentation for regulatory compliance. Familiarity with CRM tools, reporting, and sales forecasting. Travel: 50–70% across India