3619 Biotechnology Jobs - Page 38

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Key Responsibilities Drive advancement of Data Governance capabilities Partner with Product Master Strategy Lead to ensure alignment to Reference Data and Metadata strategies. Support Data Governance and Stewardship capabilities by developing Data Catalog - Business Glossary and Data Lineage requirements. Evaluate opportunities for integration of Data Governance platforms, such as Collibra. Partner with Data Governance and functional Business Leaders to identify Decision Intelligence use case opportunities. Work closely with Data Lifecycle Implementation Lead to ensure the future state of Data Governance capabilities are aligned to Lifecycle Processes. Develop a Data Strategy and Governance maturity assessment framework, with objective criteria for Business progression against the 2025-27 roadmap. Support the team in establishing a Data to Outcomes view for key Governance focus areas. Support Product Master functionality alignment to Enterprise and Network functionality Help retrofit the existing Enterprise Product Master capability to enable Functional Business use during data creation, including time-phasing of data and the appropriate governance controls for downstream consumption. Ensure key documentation, including SOPs, are maintained as necessary to stay current with our environment of Compliance. Ensure Product Master functionality aligns to the future state Enterprise Data Governance structure. Support expansion of Product Master capability across our target Business user-base. Implement new attributes and functionality consistent with Enterprise Data Governance Operating Model and in alignment with design outlined by Product Master Strategy lead. Provide Business Ownership oversight and guidance as a part of Product Master capability sustainment. Qualifications & Experience Education B.S. or BA in supply chain, management and/or engineering (biotechnology, biology, chemistry, pharmacy, engineering, or related disciplines). Experience across multiple Global Product Development and Supply business functions with a diverse set of data management applications desired. Operational excellence experience (Green/Black belt or equivalent) preferred. Experience 3-7 years of experience in Supply Chain, Manufacturing, Quality, or Regulatory Management. 3-5 years of experience in Strategic Data Management disciplines including Data Governance, Master Data Management, and Data Quality Management. Good understanding and exposure to current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirements. Exposure and experience in Biotech / Pharmaceutical manufacturing processes, principles, and practices. Additional professional and personal requirements include Business Acumen & Enterprise Mindset Strong understanding of the key business drivers of the industry/organization. Influences others with fact-based judgments pertaining to business situations. Understands the big picture, beyond their own functional area / discipline. Leads within the broader internal and external network and seeks to have an impact on organizational-wide performance. Embraces complexity but strives for simplicity. Shares resources and makes difficult trade-offs to benefit the organization at-large. Strong Problem Solving and Analytical Skills Effectively contextualizes and structures business problems. Leverages data (qualitative and quantitative) to identify insights and make informed recommendations. Leverages key matrix partners (i.e., Digital Leads). Conveys a sense of urgency and drives issues to closure. Leading Cross Functional Project Teams Holds themselves and other people accountable for agreed-to results. Identifies and keeps others focused on the most important metrics to drive the business. Builds effective, collaborative relationships & influences to drive our Business forward. Establishes credibility and earns respect with a diverse set of internal and external cross functional stakeholders. Communicates articulately and makes arguments in a clear and compelling manner. Has excellent negotiation skills and achieves win-win outcomes in demanding situations. Change Agility Creates a vision for the future by identifying strategic opportunities for breakthrough performance. Translates cases for change into actionable plans for the organization. Demonstrates smart risk-taking and personal resilience when implementing change. Enables others to navigate change with confidence in sustainable ways. Digital Dexterity Possesses powerful desire to exploit existing and emerging technologies for better business outcomes. Is a lead digital adopter and a flexible learner. Travel Requirements Travel is not currently required for this role. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About Amgen Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Role Description: The SOC Tier 2 Analyst serves as the primary escalation point for the Tier 1 SOC team, responsible for advanced threat detection, investigation, and incident response coordination. This role acts as a technical lead, ensuring that security incidents are properly triaged, investigated, and remediated while continuously improving security operations processes. The SOC Tier 2 Analyst plays a critical role in cybersecurity defense, supporting real-time monitoring, forensic analysis, and threat hunting. They will assist incident responders across all lifecycle phases, from detection to post-incident reviews, and contribute to SOC process optimizations. Roles & Responsibilities: Act as the primary escalation point for SOC Tier 1 analysts, providing technical expertise and guidance in incident handling. Perform deep-dive analysis of security events, leveraging SIEM, EDR, IDS/IPS, and other security tools. Identify common attack techniques (MITRE ATT&CK framework) and investigate anomalies to detect advanced persistent threats (APTs). Assist in security incident response, leading containment, eradication, and recovery efforts. Conduct artifact analysis to determine the root cause and scope of security incidents. Collaborate with Threat Intelligence and Threat Hunting teams to improve detection rules and incident response playbooks. Develop and refine SOC standard operating procedures (SOPs) to enhance security event triage and response. Work with engineering teams to fine-tune security controls and improve overall SOC efficiency. Mentor and train Tier 1 analysts to improve SOC maturity and ensure effective knowledge transfer. Support security audits, compliance initiatives, and reporting efforts as required. Basic Qualifications and Experience: Master’s degree in Information Technology or Cybersecurity OR Bachelor’s degree with 1 year of experience in Security Operations or related field OR Diploma with 2 years of experience in Security Operations or a related field Functional Skills: Must-Have Skills: Strong understanding of SOC operations, including event triage, escalation, and investigation. Experience analyzing cybersecurity threats and understanding attacker TTPs (Tactics, Techniques, and Procedures). Proficiency in security tools such as SIEM (Splunk, QRadar, Sentinel), EDR (CrowdStrike, Defender ATP), IDS/IPS, and firewall logs. Experience in incident response across all phases (detection, containment, eradication, recovery). Knowledge of Windows and Linux security, including log analysis, PowerShell, and Bash scripting. Good-to-Have Skills: Experience in 24/7 SOC operations and shift leadership. Knowledge of forensic tools (Volatility, Autopsy, FTK) and malware analysis techniques. Understanding of cloud security monitoring (AWS, Azure, GCP). Familiarity with MITRE ATT&CK, NIST Cybersecurity Framework, and CIS controls. Threat hunting experience to proactively detect unknown threats. Professional Certifications: CompTIA Security+ (preferred) CEH (preferred) GSEC (preferred) GCFA (preferred) MTA Security Fundamentals (preferred) CISSP (preferred) Soft Skills: Strong communication and collaboration skills, particularly when working with global teams. Ability to manage and prioritize tasks effectively in a high-pressure environment. Critical thinking and problem-solving abilities, especially in incident response situations. A commitment to continuous learning and knowledge sharing. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Job Title: Scientific Trainer – QA/QC & Regulatory Compliance Location: Remote / Online (Part-Time or Full-Time) Organization: Biotecnika About the Role: Biotecnika is looking for an experienced and motivated QA/QC professional to join us as a Scientific Trainer. This role is ideal for someone passionate about teaching and mentoring students in the fields of Biotechnology, Life Sciences, Chemistry, and Pharmaceutical Sciences. The trainer will be responsible not just for teaching, but also for designing complete course curricula, delivering interactive classes, and creating engaging learning materials. The goal is to prepare students for real-world industry roles in Quality Assurance and Quality Control, with a strong understanding of regulatory and compliance frameworks. Key Responsibilities: Design comprehensive course curricula for QA/QC in biotech, pharma, and chemical industries. Conduct live online classes for students in Biotechnology, Life Sciences, Chemistry, and Pharmacy. Organize and lead online workshops, YouTube webinars, and guest sessions. Provide virtual hands-on training using simulations, case studies, and tools relevant to QA/QC. Create student handouts, glossaries, reference articles, and reading material. Develop quizzes, assignments, and assessments to evaluate student progress. Explain core concepts such as GMP, GLP, ISO standards, ICH guidelines, documentation practices, batch records, and audit processes. Prepare students to understand and apply regulatory frameworks and quality control instrumentation and protocols. Collaborate with the content and academic teams to record educational videos, write articles, and develop visually engaging learning resources. Mentor students during project work and guide them in applying QA/QC knowledge to real-life scenarios. Eligibility & Skill Requirements: Master’s or PhD in Biotechnology, Chemistry, Pharmacy, Microbiology, or Life Sciences. Minimum 3 years of hands-on industrial experience in a QA/QC role. In-depth knowledge of regulatory compliance standards (GMP, GLP, ICH, WHO, ISO). Familiarity with QA/QC instruments & documentation practices (HPLC, GC, SOPs, audit reports, etc.). Prior experience in teaching/training/content creation preferred. Strong communication skills and ability to explain technical topics in a simple, engaging way. Proficiency with online teaching platforms, PowerPoint, and basic content tools. What We Offer: Remote work flexibility with options for part-time or full-time engagement. Exposure to multi-format teaching: live classes, recorded video content, webinars, and workshops. Opportunity to mentor future industry professionals in QA/QC. Competitive remuneration with additional incentives based on performance and deliverables. A chance to become a part of India’s leading life sciences training platform – Biotecnika.

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: 1. Pick Up & Drop Facility 2. Food Facility 3. Day Shift 4. 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

ct Us: HR Shanmuga Priya 8072891550 This Role is Open to Fresh Graduates with Excellent English Communication Skills. you should have At Least a Diploma/degree in Any Field DESCRIPTION Medical Coding is the Fastest-growing Profession in the Healthcare Industry Today. It is a Niche Specialization and the Demand for Trained and Certified Medical Coders is Increasing Exponentially and Bound to Increase in Upcoming Years, Especially in India. you Pay Strong Attention to Details and are Capable of Delivering Top-quality Work you are Goal-oriented and Thrive in Fast-paced Environments maintains a Working Knowledge of Cpt-4, Icd-10-cm, and Icd-10-pcs Coding Principles, Governmental Regulations, Uhdds (uniform Hospital Discharge Data Set) Guidelines, Aha Coding Clinic Updates, and Third-party Requirements Regarding Coding and Documentation Guidelines Methodology Identify cases eligible for medical reviews and assign these to appropriate reviewers. Reach out to the client for any problems identified in the cases for review. Adhere to Utilization Review Accreditation Commission (URAC), jurisdictional, and/or established MediCall best practice UM time frames, as appropriate. Adhere to federal, state, URAC, client, and established MediCall best practice WCUM time frames, as appropriate. Develop a complete understanding of the Medical management Procedures. Perform medical review assessment (MRA) on utilization of health services (eg healthcare plans, workers compensation products etc) in an accurate, efficient and timely manner while ensuring compliance with utilization management regulations and adherence to state and federal mandates. Provide succinct negotiable points based on the submitted medical records that identify necessary medical treatment, casually related care, response or lack of response to treatment, etc. Identify missing records and information that are necessary in the completion of the medical review assessment. Adhere to Department of Labor, state and company timeframe requirements. Coordinates physician reviewer referral as needed and follows up timely to obtain and deliver those results. Track status of all utilization management reviews in progress and follow up on all pending cases. Work closely with management team in the ongoing development and implementation of utilization management programs. Respond to inbound telephone calls pertaining to medical reviews in a timely manner, following client a established protocols. Process customer calls consistent with program specified strategies and customer satisfaction measurements to include but not limited to proper answering procedure, eg opening and closing remarks. Learn new methods and services as the job requires. Required Skills Medical Coding Freshers Medical Coder Pharmacy Physiotherapy, BPT, MPT Staff Nurse Biotechnology, Biomedical Engineer, Biochemistry Microbiologist, Biology HR Shanmuga Priya 8072891550

What is Medical Coding Job all about : Develop a complete understanding of the Medical management Procedures. Perform medical review assessment (MRA) on utilization of health services (eg healthcare plans, workers compensation products etc) in an accurate, efficient and timely manner while ensuring compliance with utilization management regulations and adheren ce to state and federal mandates. Provide succinct negotiable points based on the submitted medical records that identify necessary medical treatment, casually related care, response or lack of response to treatment, etc. Identify missing records and information that are necessary in the completion of the medical review assessment. DESCRIPTION Medical Coding is the Fastest-growing Profession in the Healthcare Industry Today. It is a Niche Specialization and the Demand for Trained and Certified Medical Coders is Increasing Exponentially and Bound to Increase in Upcoming Years, Especially in India. you have At Least a Diploma/degree in Any Field. this Role is Open to Fresh Graduates with Excellent English Communication Skills. you Pay Strong Attention to Details and are Capable of Delivering Top-quality Work you are Goal-oriented and Thrive in Fast-paced Environments Position: Medical Coder Medical Coding is the Fastest-growing Profession in the Healthcare Industry Today. It is a Niche Specialization and the Demand for Trained and Certified Medical Coders is Increasing Exponentially and Bound to Increase in Upcoming Years, Especially in India. you have At Least a Diploma/degree in Any Field. this Role is Open to Fresh Graduates with Excellent English Communication Skills. you Pay Strong Attention to Details and are Capable of Delivering Top-quality Work you are Goal-oriented and Thrive in Fast-paced Environments maintains a Working Knowledge of Cpt-4, Icd-10-cm, and Icd-10-pcs Coding Principles, Governmental Regulations, Uhdds (uniform Hospital Discharge Data Set) Guidelines, Aha Coding Clinic Updates, and Third-party Requirements Regarding Coding and Documentation Guidelines Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. ct Us: hr Shanmuga Priya 8072891550

Description External Job Description Working principles of field instruments, transmitters, in-depth understanding of operation of PLC, load cells and their troubleshooting, packing machines/ASRS troubleshooting, sensors, signal exchanges Calibration ABB 800XA, DCS ABB, Emerson, Honeywell, PLC Honeywell, Siemens, Field instruments - weigh bridge, Load cell, actuator, MES Manufacturing execution system • Attending line breakdowns • Executing the PM as per schedule and maintaining records • Adherence to SAP workflow for engineering• Executing the inspection as per SMS / EMS and maintaining records• Report generation and communicating to the relevant block incharge - Shift report• Implementation of the initiative such as 5S, TPM• SOP audits• Implementation and ensuring daily checklist of the machine are filled• Coordinating with the shift representative for prioritization of the jobs with mobilization and giving fast solution• Permit and LOTO for the job• Providing inputs for breakdown analysis and support in implementation of CAPA• Utility operations management through outsourced vendor•

Position - Intern - Business Expansion Type: Full-time, Work from Office Location - Navi Mumbai Who are we Based out of IIT Bombay, HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics-based diagnostic solution for Tuberculosis was recognized as one of the top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. What we want you to do Identify and research potential B2B partners in assigned geographic regions. Generate leads through cold outreach (emails, calls, WhatsApp) and schedule discovery meetings. Convert leads into clients by aligning their needs with company offerings. Collaborate with Marketing to design and execute targeted campaigns. Coordinate with Logistics and Lab Operations teams to ensure seamless service delivery. Assist in strategising and executing go-to-market (GTM) plans for new market entry. Conduct secondary market research to uncover expansion opportunities. Manage end-to-end business transactions, from negotiation to closure. What are we looking in you Current enrollment or recent graduation in a Bachelor’s program (Biotechnology, Life Sciences, Business, or related fields preferred). Excellent written and verbal communication abilities. Extrovert with excellent interpersonal skills. Basic understanding of biotechnology/life sciences (advantageous). Prior experience in client handling, sales, or stakeholder management (a plus). Creativity in outreach and persuasion. Strong organisational and multitasking skills with attention to detail. Proactive and solution-oriented with the ability to work independently and collaboratively. Familiarity with Excel, mailing and PowerPoint. What you will gain Exposure to end-to-end business development, from lead generation to deal closure. Training in sales funnel management, client negotiation, and cross-functional collaboration. Skills: multitasking,biotechnology,powerpoint,lead generation,collaboration,life sciences,organisational skills,client negotiation,b2b partnerships,mailing,stakeholder management,b2b partner research,communication,cold outreach,attention to detail,client handling,negotiation,problem-solving,market research,sales,excel,business expansion

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment. If someone asks for payment on our behalf, it is a scam. Please report the incident to the local police or cybercrime unit. Your trust and safety are important to us. Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations. The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world. Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare. The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world. Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA. Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare. At Intas, our success is fundamentally built on the strength of our people. Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence. This approach ensures that every employee plays a meaningful role in driving both the company’s growth and advancements in global healthcare. Job Title: Senior Executive - Quality Control Job Requisitions No.: 14048 Job Description Purpose of Job To handle the routine Documentation and analysis of ELISA PCR Lab Skill Required Roles and Responsibilites Overall Management of ELISA and PCR ( Sampling,Analysis,Report preparation/Review,SAP Release). 2. Support to IPQC,Finished Product and Stability testing. 3. Responsible for imparting Training as when required. 4. Responsible for involvement in QMS activity. 5. Responsible to perform other activity as and when assigned by Management. 6. Responsible for QC Document Preparation,Review and Batch release. Qualification Required M.Sc. - Biotechnology / B. Tech Biotechnology Relevant Skills / Industry Experience Relevant professional / Educational background Any Other Requirements (If Any) Compensation / Reward Location: Plasma Fractionation Unit, Ahm, GJ, IN, 382210 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people. Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success. We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape. Date: 14 Jul 2025

Vitaliz Biosciences JOB DESCRIPTION Position Title: National Sales Advisor – Pharma (Retired Professional) Reporting to : CEO NOTE: This document is an outline of the primary tasks assigned and may be changed at the discretion of the management, formally or informally, either verbally or in writing. All team members are expected to assist Vitaliz in achieving its goals even if such tasks are beyond the scope of this outline. The job description does not constitute an employment contract, implied or otherwise, other than an “at will” relationship and is subject to change by the management as the needs of the company and requirements of the job change. Position Overview: We are seeking highly experienced and seasoned Process Engineering Consultants from the pharmaceutical and biotechnology industry to support our precision fermentation project. A retired professional who possesses deep domain expertise in upstream and downstream areas and is interested in consulting engagements, to share their knowledge, provide mentorship, and contribute to process optimization, facility design, technology transfer, and regulatory compliance. Essential Duties and Responsibilities: Provide expert guidance on fermentation process design, development, and optimization for active ingredient production from microbial metabolites. Assist with GMP compliance, validation, and regulatory readiness for FDA, EMA, and other global regulatory bodies. Review and advise on technology transfer, scale-up, and commissioning activities. Contribute to facility design and layout planning for new or upgraded production sites. Identify and troubleshoot bottlenecks or inefficiencies in existing manufacturing processes, guide and oversee continuous improvement programmes. Mentor junior engineers and collaborate with cross-functional teams (QA, QC, RA, Operations). Support clients with risk assessments, gap analysis, and process improvement initiatives. Assist in developing or reviewing SOPs, URS, and validation protocols. Qualifications/Competencies/Position Requirements: Bachelor’s / Master’s Degree / Ph.D in Biotechnology/Chemical Engineering/Process Engineering Pharmaceutical Engineering, or related field. 25+ years of experience in Industrial Biotechnology and process engineering. Demonstrated knowledge of GMP regulations, ICH guidelines, and global regulatory standards. Proven experience in facility design, process scale-up, technology transfer, and validation. Excellent communication and documentation skills. Ability to work independently as a consultant or as part of a multidisciplinary team. Retired professionals from leadership roles (e.g., Director, VP, Principal Engineer) are strongly encouraged to apply. Location: Trivandrum Travel: Ability to travel as required by role. Remuneration: As per industry. Will consider higher for deserving candidates. Job Type: Freelance Pay: ₹100,000.00 - ₹200,000.00 per month Application Question(s): Are you currently retired and open to taking on a consulting or advisory role? Do you have 25 or more years of experience in pharmaceutical sales, including national team building and strategy? Have you built or led national pharmaceutical sales teams and structured territory operations? Have you held a senior leadership role (President/VP/Director) in sales and marketing at a leading pharmaceutical company in India? Have you been involved in launching pharmaceutical products and expanding sales channels across India? Please specify the Languages Known Willingness to travel: 25% (Preferred) Work Location: In person

MUST HAVE GRADUATION OR POST-GRADUATION IN BSC/MSC IN BIOLOGY OR MICROBIOLOGY, BIOTECHNOLOGY ROLES AND RESPONSIBILITES Identify new business opportunities. Generate leads through various channels. Build and maintain client relationships. Develop and execute sales strategies. Conduct market research and analysis. Collaborate with internal teams. Maintain accurate sales records. Achieve sales targets and revenue goals. Qualifications and Skills: Bachelor's degree in BSC, MSC in Biotechnology, Microbiology, Biology, B.TECH, Business Administration, Marketing, or related field. Proven track record of success in sales or business development roles. Strong communication, negotiation, and interpersonal skills. Ability to work independently and as part of a team. Proficiency in CRM software and Microsoft Office Suite. Knowledge of industry trends, market dynamics, and competitive landscape. These roles and responsibilities may vary depending on the company's industry, size, and specific business objectives. Benefits: Cell phone reimbursement Provident Fund Health Insurance Incentive Paid Leave Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹42,000.00 per month Job Types: Full-time, Fresher Pay: ₹18,000.00 - ₹32,000.00 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Quarterly bonus Yearly bonus Education: Bachelor's (Required) Experience: Pharma Sales: 1 year (Required) Work Location: In person Job Types: Full-time, Permanent, Fresher Pay: ₹18,000.00 - ₹42,000.00 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Work Location: In person

On-site at Cloudnine Hospital Nallagandla Location: Hyderabad 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: ₹20,000.00 - ₹25,000.00 per month Benefits: Food provided Health insurance Provident Fund Compensation Package: Performance bonus Schedule: Day shift Morning shift Work Location: In person Expected Start Date: 23/07/2025

India - Hyderabad JOB ID: R-208858 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jul. 14, 2025 CATEGORY: Information Systems ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Role Description: The SOC Tier 2 Analyst serves as the primary escalation point for the Tier 1 SOC team, responsible for advanced threat detection, investigation, and incident response coordination. This role acts as a technical lead, ensuring that security incidents are properly triaged, investigated, and remediated while continuously improving security operations processes. The SOC Tier 2 Analyst plays a critical role in cybersecurity defense, supporting real-time monitoring, forensic analysis, and threat hunting. They will assist incident responders across all lifecycle phases, from detection to post-incident reviews, and contribute to SOC process optimizations. Roles & Responsibilities: Act as the primary escalation point for SOC Tier 1 analysts, providing technical expertise and guidance in incident handling. Perform deep-dive analysis of security events, leveraging SIEM, EDR, IDS/IPS, and other security tools. Identify common attack techniques (MITRE ATT&CK framework) and investigate anomalies to detect advanced persistent threats (APTs). Assist in security incident response, leading containment, eradication, and recovery efforts. Conduct artifact analysis to determine the root cause and scope of security incidents. Collaborate with Threat Intelligence and Threat Hunting teams to improve detection rules and incident response playbooks. Develop and refine SOC standard operating procedures (SOPs) to enhance security event triage and response. Work with engineering teams to fine-tune security controls and improve overall SOC efficiency. Mentor and train Tier 1 analysts to improve SOC maturity and ensure effective knowledge transfer. Support security audits, compliance initiatives, and reporting efforts as required. Basic Qualifications and Experience: Master’s degree in Information Technology or Cybersecurity OR Bachelor’s degree with 1 year of experience in Security Operations or related field OR Diploma with 2 years of experience in Security Operations or a related field Functional Skills: Must-Have Skills: Strong understanding of SOC operations, including event triage, escalation, and investigation. Experience analyzing cybersecurity threats and understanding attacker TTPs (Tactics, Techniques, and Procedures). Proficiency in security tools such as SIEM (Splunk, QRadar, Sentinel), EDR (CrowdStrike, Defender ATP), IDS/IPS, and firewall logs. Experience in incident response across all phases (detection, containment, eradication, recovery). Knowledge of Windows and Linux security, including log analysis, PowerShell, and Bash scripting. Good-to-Have Skills: Experience in 24/7 SOC operations and shift leadership. Knowledge of forensic tools (Volatility, Autopsy, FTK) and malware analysis techniques. Understanding of cloud security monitoring (AWS, Azure, GCP). Familiarity with MITRE ATT&CK, NIST Cybersecurity Framework, and CIS controls. Threat hunting experience to proactively detect unknown threats. Professional Certifications: CompTIA Security+ (preferred) CEH (preferred) GSEC (preferred) GCFA (preferred) MTA Security Fundamentals (preferred) CISSP (preferred) Soft Skills: Strong communication and collaboration skills, particularly when working with global teams. Ability to manage and prioritize tasks effectively in a high-pressure environment. Critical thinking and problem-solving abilities, especially in incident response situations. A commitment to continuous learning and knowledge sharing. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Job Title: Production Manager – SDH Naturals Job Summary We are looking for an experienced Production Manager to oversee the manufacturing process of our Ayurvedic herbal and wellness products. The ideal candidate will ensure efficient production, maintain quality standards, optimize resources, and comply with industry regulations. Key Responsibilities Production Planning & Execution: Develop and implement production schedules to meet demand while optimizing efficiency and cost-effectiveness. Quality Control & Compliance: Ensure all products meet company and regulatory quality standards (GMP, ISO, FSSAI, etc.). Team Management: Supervise and train production staff to maintain high levels of efficiency and productivity. Process Optimization: Identify areas for improvement in production processes, machinery, and resource utilization. Inventory & Resource Management: Oversee raw material procurement, stock levels, and coordination with inventory management team. Safety & Compliance: Ensure all safety protocols and industry regulations are adhered to in the production facility. Collaboration: Work closely with QC/QA/ R& D, supply chain, and marketing teams to align production with product development and business goals. Reporting & Documentation: Maintain detailed records of production activities, efficiency reports, and quality control documentation. Experience & Qualifications Education: Bachelor's/Master’s degree in Pharmacy, Biotechnology, or a related field. Experience: Minimum 5-8 years of experience in production management within the herbal, Ayurveda, nutraceutical, or pharmaceutical industry. Industry Knowledge: Familiarity with GMP, ISO, AYUSH, and FSSAI guidelines for herbal and nutraceutical products. Job Type: Full-time Benefits: Provident Fund Schedule: Day shift Work Location: In person

We're Hiring! Assistant Product Manager – SDH Naturals Location: Amritsar, Punjab SDH Naturals is looking for a dynamic and driven Assistant Product Manager to join our growing team. This role is ideal for someone with a passion for herbal wellness, product innovation, and strategic marketing. If you have 2–4 years of experience in herbal, Ayurveda, nutraceutical, pharmaceutical, or FMCG industries, we want to hear from you. Key Responsibilities: Assist in new product development and conduct market research. Coordinate with R&D, production, procurement, and marketing teams. Ensure regulatory compliance with GMP, FSSAI, and AYUSH guidelines. Support branding, packaging, and promotional strategy execution. Analyze sales data and customer feedback to suggest improvements. Monitor industry trends and competitor products for insights. Prepare internal reports and assist in product lifecycle planning. Qualifications: B.Pharm, M.Pharm, Biotechnology, MBA (Marketing/Operations), or related field. 2–4 years of relevant experience in herbal, Ayurveda, nutraceutical, or pharmaceutical. Strong understanding of market trends and regulatory standards. Excellent coordination, analytical, and communication skills. Job Type: Full-time Benefits: Provident Fund Schedule: Day shift Work Location: In person

Job Title: Molecular Biologist – qPCR Consultant (Preclinical – In Vitro) Location: MS Clinical Research Pvt Ltd (MSCR) Department: Preclinical – In Vitro Employment Type: Consultant/Part-time Experience: Minimum 10 years in Molecular Biology with hands-on expertise in qPCR Role Overview: MSCR is seeking an accomplished Molecular Biologist – qPCR Consultant to support our preclinical (in-vitro) research team. The ideal candidate will bring deep technical expertise in qPCR assay development, optimization, and data analysis, specifically aligned with preclinical drug screening and mechanistic in-vitro studies. This is a strategic consulting role aimed at enhancing our molecular biology capabilities in gene expression, target validation, and biomarker discovery. Key Responsibilities: Provide technical leadership in the design, development, and validation of qPCR assays for in-vitro studies including cytotoxicity, gene expression profiling, and pathway analysis. Advise on sample preparation, RNA/DNA extraction, and quality control specific to in-vitro systems. Guide the team in primer/probe design, assay optimization, and standard curve generation. Troubleshoot experimental issues and recommend improvements to protocols and workflows. Ensure robust data integrity, statistical soundness, and scientific documentation of qPCR results. Review experimental designs to align with regulatory and scientific requirements for GLP-compliant preclinical studies. Train lab scientists on best practices for qPCR technique and data interpretation. Collaborate with research scientists and study directors to integrate molecular endpoints in preclinical study design. Stay updated with emerging trends, technologies, and best practices in molecular biology and qPCR. Qualifications: Ph.D. or Master’s in Molecular Biology, Cell Biology, Biotechnology, or a related field. Minimum 10 years of hands-on experience in molecular biology techniques, with a strong focus on qPCR in preclinical models. Excellent analytical, documentation, and communication skills. Desirable Skills: Knowledge of cell-based assay systems, molecular endpoints, and biomarker quantification. Exposure to RT-qPCR, miRNA analysis, or multiplex PCR. Engagement Type & Compensation: Consulting basis – Part-time, Remote, Hybrid Remuneration commensurate with experience and scope of involvement.

Greetings from pathnsitu biotechnologies pvt ltd......................... Job Description: This position involves 80% of travel within the given territory. The selected candidate will be given technical training at our regional office/lab in Hyderabad. 1. Onsite troubleshooting on company products. 2. Technical demos and presentations. 3. Conducting workshops, frequent follow-ups etc. 4. Assist sales personal in closing the leads. 5. Act as a link between customer and company. 6. Responsibly handle the critical situations at client site. Qualification Requirement: Candidate should have Bachelors Degree or Masters degree in Biotechnology/Biochemistry or any life science degree. Experience: Knowledge in immunology, basic dilution calculation, and antigen antibody reaction is must. Experience in immunohistochemistry is plus. Selected candidate will be called for interview. Company Profile: The PathnSitu teamconsists of world class scientific advisors and hands-on technical advisors that bring over two decades of global tissue diagnostics experience directly to the customer. The company is founded upon a fresh, dynamic perspective that brings energy and motivation to develop quality products for better patient care. Our dedication to your lab will streamline your staining process and reduce the turnaround time, all at affordable pricing. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Work Location: In person

We are hiring Production Executives for an exciting opportunity with our esteemed client – a global leader in in-vitro diagnostics with over 60 years of innovation, delivering solutions to enhance public health across the world. 📍 Location: Karkapatla, Hyderabad Role: Production Executive Responsibilities include: -Preparation & filling of reagents and purification of recombinant enzymes -Assembly & packaging of molecular diagnostic kits -Operation & maintenance of production equipment (laminar airflow, refrigerated centrifuge, shaker incubator, etc.) -Following GMP, ISO 13485, SOPs, and documenting production activities accurately -Working in ISO Class 8 cleanroom, following strict safety & biohazard protocols -Conducting in-process quality checks and reporting deviations -Supporting equipment calibration, preventive maintenance, and inventory tracking ✅ Ideal candidate should have: -Master’s degree in Biotechnology, Microbiology, Molecular biology, or related field -2+ years of experience in IVD medical device or biotech manufacturing (molecular diagnostics is a plus) -Strong skills in reagent preparation, pipette handling, cleanroom practices, and documentation -Familiarity with GMP, ISO 13485 standards Interested? Apply now or reach out to us to explore this opportunity! ✉ For details, DM or contact: 📧 abdul@prosapiens.in

Job description- Professor(Forensic Science) Qualification:- B Tech (Agriculture/Biotechnology/Biochemical Eng.) + M Tech ( Agriculture/Biotechnology/Biochemical Engineering) +Ph D ( any specialization) Teaching/Research Experience-10-12 years in a reputed University/College/Research institute Contact Details:- deepu.hr@peoplesuniversity.edu.in garima.hr@peoplesuniversity.edu.in Ph 9109115070, 07554005426 Job Type: Full-time Pay: ₹475,000.00 - ₹650,000.00 per year Schedule: Day shift Experience: total work: 1 year (Preferred) Work Location: In person

HIRING MICROBIOLOGIST Qualifications & Requirements Bachelor’s or master’s degree in microbiology, Food Technology, Biotechnology, or related field. 1–3 years of experience in a food microbiology lab (freshers with strong lab experience may be considered). Knowledge of food pathogens (e.g., Salmonella, Listeria, E. coli, etc.), spoilage organisms, and environmental monitoring. Familiarity with microbiological testing standards (ISO, BAM, APHA, etc.). Strong analytical, documentation, and communication skills. APPLY NOW - xpertzhr9@gmail.com Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Schedule: Day shift Experience: microbiologist: 1 year (Preferred) Work Location: In person

Job Overview Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditable adverse events to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. Responsible to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. He/she will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual. Summary Of Responsibilities Assist in the processing of Expedited Safety Reports (ESRs), Periodic Safety Reports (PSRs) and submission, including but not limited to: Maintenance of adverse event tracking systems. Set-up and maintenance of project files, and central files for documentation. Assist with the reporting of ESRs and PSRs to clients, Regulatory Authorities, Ethics Committees, investigators and Fortrea project personnel, as required, within study specified timelines. Ensure all incoming Adverse Event (AE)/ Serious Adverse Event (SAE) reports are appropriately logged into the departmental tracking application and forwarded to the centralized mailbox. Assist with processing of the adverse events, including but not limited to: Data entry of safety data onto adverse event tracking systems. Write patient narratives and code adverse events accurately using MedDRA (for Marketed products, if applicable). Assist in the listedness assessment against appropriate label (for Marketed products, if applicable). Generate queries for its collection of missing or discrepant information in consultation with medical staff, if needed. Submission of expedited SAE reports to clients, Regulatory Authorities, Ethics Committees, investigators, 3rd party vendors, Partners and Fortrea project personnel, as required within the agreed timelines. Maintenance of adverse event tracking systems Assist with peer/quality review of processed reports and support with trends and actions as needed. Assist in the reconciliation of databases, as applicable. Assist in the maintenance of files regarding adverse event reporting requirements in all countries. Work within the Quality Management System framework, including but not limited to Standard Operating Procedure (SOP), departmental Work Instructions (WIs) etc. as appropriate. Prepare and support coordination of safety study files for archiving at completion of projects. Arrange and schedule internal and/or external meetings/teleconferences. Train and mentor, the PSS Assistants or peers in their day-to-day activities. Build and maintain good PSS relationships across functional units. Ensure compliance of operations with governing regulatory requirements and applicable study/project specific plans. Assume responsibility for quality of data processed. Provide administrative support to PSS personnel. All other duties as needed or assigned. Qualifications (Minimum Required) PharmD/Mpharm/Bpharm + 1 year of relevant experience.. Degree preferred to be in one or more of the following disciplines: Pharmacy, Nursing, Medical Sciences, Life Sciences, or related area. * Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions. ** Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, working in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitoring, Regulatory Affairs, or Quality Assurance. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Speaking: English and local language. Writing/Reading: English and local language. Experience (Minimum Required) Good Team player and offer peer support as needed. Ability to set priorities and handle multiple tasks. Attention to detail. Good written and verbal communication skills. Logical and spelling skills, preferably with an aptitude for handling and proof-reading numerical data. Good keyboard skills, preferably with knowledge of MS office and Windows would be beneficial. Ability to operate standard office equipment. Physical Demands/Work Environment Office Environment or remote. Learn more about our EEO & Accommodations request here.

Learn and perform well-defined procedures within a GMP manufacturing setting Perform equipment monitoring & and basic 6S housekeeping Perform basic laboratory tasks (e.g. sampling, pH / conductivity / osmolality measurements etc.) Perform routine sanitization tasks to maintain facility standards Trained & signed off on Performance Measures (PMs) relating to CIP/ SIP/ basic tank & instrument operations Demonstrate aseptic technique in the handling of product / materials Perform basic process & equipment troubleshooting Multi-task on equipment preparations & operations to ensure adherence to schedule Display basic process & equipment troubleshooting ability under routine scenarios. Use Standard Operating Procedures (SOPs), logbooks & Batch Records (BRs) to perform operation Submit samples via Laboratory Information Management System (LIMS) Work duration: 8 months Work hour: 12 hours rotating shift in a 2-2 3-2 2-3 pattern. Day/night shift rotation is every 2 months. Transport: Preferably with own transport Remarks: Able to perform manual labor work to push 1000L pallet tank with a pair of 2 or 3 members, or charge raw material powder (12kg per bag) to the vessel. Requirements Bachelor’s degree in Biotechnology, Chemistry, Biology, Pharmacy, or Process engineering. 1-2 years experience in Biotech Industry or any related experience Competent in analyzing complex situations and show practical problem-solving capabilities. Ability to work independently and within a cross-functional team. Excellent communication skills to collaborate with internal teams and external teams.

Location: New Delhi (Remote) Salary: Paid internship - INR 28,000 to INR 35,000 per month Type: Full-time/ Internship Contract Contract Duration: 3 months (with the possibility of a full-time role) Start date: Immediate start Our client is a consulting firm specialising in the pharmaceutical and healthcare sector. It is part of a larger company, and we are hiring for its Asia Pacific Team, which is based in Singapore. The client offers healthcare-focused market and business intelligence, complemented by strategic advisory services. In addition, they assist top medical device, pharmaceutical, and biotechnology companies and government entities in furthering their understanding of the healthcare industry and providing pragmatic and innovative strategies to fulfil their business objectives. We are looking for a dedicated candidate who will be committed to a 3-month contract and understands how the pharmaceutical and healthcare industry functions. As a Market Analyst Intern, you have the opportunity to participate in the design, development and delivery of a spectrum of challenging healthcare-related projects. Accountabilities You will get to work closely with a team of market analysts, data analysts, and consultant analysts and have the opportunity to work on live projects and contribute to research reports that will help advance their careers, as well as gain great experience. Our client is looking for a Market Analyst Intern who is globally curious and has a profound interest in healthcare, market research and solving business issues. How will you contribute? Perform a range of tasks depending on the research project's needs Perform data analysis to generate insights for informed decisions Display critical thinking skills and be able to apply logic and rationale to solve healthcare-related business problems (this is evaluated using a case study) Demonstrate a willingness and ability to acquire domain knowledge and expertise quickly Perform primary research (QC surveys, set up interviews), as per project needs Write, proofread or fact-check reports (not essential, but possible for someone with the right skill set) Experience, skills and professional attributes The ideal skills for the role are: Good communication skills, both written and oral and attention to detail Qualification in any degree related to Healthcare Exposure and proficiency in Market Analysis and Market Research in healthcare/pharmaceutical A profound interest in healthcare, pharmaceutical, research and solving business issues Globally curious mindset Based in New Delhi, India Remote role for 3 months (with a possibility of a full-time role) Full-time availability (Monday to Friday) Must have completed studies, OR not be in full-time studies Immediate start

Job Title: Sales/Senior Sales Executive – General Laboratory Instruments Location: Ahmedabad, Hyderabad and Delhi Company: Spark Scientific Pvt. Ltd. About the Company: Spark Scientific Pvt. Ltd. is a well-established distributor of advanced scientific and laboratory instruments, serving research institutions, educational organizations, and industrial labs across India. We are an authorized partner for DLAB, a leading global brand specializing in high-quality laboratory equipment. Job Description: Spark Scientific Pvt. Ltd. is seeking a dynamic and motivated Sales/Senior Sales Executive for the Hyderabad region. This position focuses on promoting DLAB's comprehensive portfolio of laboratory instruments, including pipettes, centrifuges, vortex mixers, magnetic stirrers, and other essential lab equipment. Key Responsibilities: Represent DLAB’s product line and promote its range of laboratory instruments to research institutions, educational organizations, and industrial labs. Develop and maintain strong relationships with new and existing customers to understand their needs and offer suitable solutions. Conduct product presentations, demonstrations, and training sessions for prospective clients. Identify and qualify sales leads, actively working to meet and exceed sales targets. Collaborate with internal teams to ensure smooth order processing, delivery, and after-sales service. Participate in industry events, exhibitions, and trade shows to represent the brand and generate new leads. Maintain accurate customer and sales records, regularly reporting progress to the management. Qualifications & Requirements: Educational Background: B.Sc./M.Sc. in Life Sciences, Chemistry, Biotechnology, or a related field. Experience: 1-2 years in sales of laboratory instruments is preferred; fresh graduates with strong communication skills and enthusiasm for sales may also apply. Strong interpersonal, presentation, and negotiation skills. Self-motivated with a passion for scientific sales and customer interaction. Willingness to travel extensively within the assigned territory. Residency in or readiness to relocate to Hyderabad is required. What We Offer: Comprehensive training programs with a focus on DLAB products and solutions. Opportunities to work with a globally recognized brand in laboratory equipment. Career growth pathways tailored to your performance. Competitive salary package, including incentives and bonuses. Join Spark Scientific Pvt. Ltd. and play a pivotal role in delivering world-class laboratory solutions to the scientific community! To Apply: Send your updated resume to hrd@sparksci.in with the subject line “Application for Sales Executive – GLI” .

Location: Coimbatore, India | Type: Full‑time (On‑site) About Carbelim ( Linkedin ) Carbelim is a climate‑tech startup pioneering nature‑based carbon capture and utilisation (CCU) solutions powered by advanced microalgae biotechnology. We develop AI‑driven systems that purify polluted air, capture CO₂, and transform emissions into valuable bio‑based products. Incubated by IIT‑Madras and accelerated by IIM‑Lucknow, we unite biotechnology, sustainable engineering, and urban design to build a cleaner, climate‑positive future. Why Join Us  Mission‑driven hardware: build products that directly improve planetary health.  End‑to‑end ownership: take ideas from concept to certified, field‑ready devices.  Small, expert team: collaborate with scientists, designers, and entrepreneurs who value curiosity and initiative. What You'll Do  Own the complete lifecycle of IoT hardware products, from system architecture and component selection through prototyping, testing, certification, and pilot production.  Design electronics: create schematics, multilayer PCBs, and low‑power circuits; run DFM/DFT and bring‑up.  Develop embedded firmware (C/C++ or similar), including drivers, OTA updates, bootloaders, and power‑management features.  Interface sensors and connectivity, wiring up serial buses (I²C, SPI, UART) and wireless stacks (BLE, Wi‑Fi, LoRa, Zigbee, MQTT).  Prototype, test, and certify hardware, ensuring it meets functional, EMI, safety, and regulatory requirements before field deployment.  Collaborate on mechanics: work with industrial designers on enclosures, waterproofing, and ergonomic wearables.  Document & transfer: maintain BOMs, Gerbers, test procedures, and production hand‑off packages.  (Optional) Cloud linkage: hook devices to AWS IoT / Azure IoT Hub / custom back‑ends nice to have, not mandatory. Requirements (Must Haves)  B.E./B‑Tech in ECE, CSE, EE or related branch  3+ years delivering commercial embedded products  Hands‑on with MCUs such as ESP32, STM32, nRF52  Strong analog/digital design & PCB CAD (Altium/KiCad/Eagle)  Wireless protocol know‑how (BLE, Wi‑Fi, LoRa, Zigbee)  Power‑budgeting & battery‑powered design chops  Ability to showcase prior IoT hardware you built (demo units, photos, or repo links  (Nice to have) Cloud dashboards, Grafana, Node‑RED, etc.  (Nice to have) AWS IoT/Azure IoT Core integration Skills  Ownership mindset; able to drive schedules and unblock issues independently  Clear communicator who can document designs and mentor interns/juniors  Passion for sustainability and real‑world impact Compensation *Competitive; commensurate with experience.* How to Apply Apply with a cover letter including your résumé/CV, and links or photos of relevant projects. email us hr@carbelim.io