3586 Biotechnology Jobs - Page 9

Greetings from CorroHealth ! We are Hiring Paramedical Graduates! We are pleased to invite you for a direct walk-in interview. If you are enthusiastic, eager to learn, and ready to kickstart your career, we would love to meet you! Walk-In Details: Time: 9am to 12pm Interview Venue: Venue - Kochi CorroHealth 4th Floor, Double Tree Properties, Opposite Ernakulan Medical Center, Eranakulam, Chakkaraparambu, Palarivattom, Ernakulam, Kerala 682025 Eligibility Criteria: Qualification: B Pharm / M Pharm / PharmD / Biotechnology / Microbiology only Year of Passing: 2024 / 2025 Percentage: Min 60% in all academic year (10th, 12th, UG & PG) Documents to Carry: * Updated Resume * Government-issued ID proof * Passport-size photograph Note: Only direct walk-in. Please Call or WhatsApp 9043979492 for registration or Mention Sushil on top of your Resume

Job Opening: Medical Coder (Fresher Opportunity) CorroHealth Are you a recent graduate in life science looking to kickstart your career in the healthcare industry? CorroHealth is offering an exciting opportunity to join as a Medical Coder and grow in one of the most in-demand domains. Eligibility Criteria Education : B.Pharmacy (UG), M.Pharmacy, Bsc Microbiology, Biotechnology, BE Biomedical, Allied Health Science Academic Performance : Minimum 60% in 10th, 12th, and UG Age Limit : Below 28 years Perks & Benefits Attractive Salary Among the best in the industry Certification Sponsorship Get trained and certified in medical coding Career Growth Fast-track your journey in the healthcare domain Location Work Mode : Work From Office (WFO) City : Kochi, Kerala How to Apply Interested candidates can reach out directly: Contact Person : Praveena (HR) Phone : 9789916033 Email : praveenakumari.pechiumuthu@corrohealth.com

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you’ll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning; bold ideas; courage and passion to drive life-changing impact to ZS. Our most valuable asset is our people . At ZS we honor the visible and invisible elements of our identities, personal experiences and belief systems—the ones that comprise us as individuals, shape who we are and make us unique. We believe your personal interests, identities, and desire to learn are part of your success here. Learn more about our diversity, equity, and inclusion efforts and the networks ZS supports to assist our ZSers in cultivating community spaces, obtaining the resources they need to thrive, and sharing the messages they are passionate about. Insights & Analytics ZS's Insights & Analytics group partners with clients to design and deliver solutions to help them tackle a broad range of business challenges. Our teams work on multiple projects simultaneously, leveraging advanced data analytics and problem-solving techniques. Our recommendations and solutions are based on rigorous research and analysis underpinned by deep expertise and thought leadership. What You’ll Do Leverage quantitative skills to derive answers to clients' ongoing business analytics and reporting questions Work collaboratively with client to ascertain the client's specific business information needs Upskill on concepts relevant to solve client problems across modalities Discuss and determine with clients which specific data may be best utilized in order to perform the necessary analysis Evaluate, assess and analyze the data necessary to provide solutions to the clients' particular business information needs Communicate the data results to the client, with an emphasis on answering the business question as opposed to the analytical and reporting processes used Gain immediate familiarity with client's internal processes Develop expertise within a client analytics area Be available for clients during regular working hours What You’ll Bring Bachelor's (and often graduate) degree in Chemical Engineering, Mechanical Engineering, Chemistry, Biotechnology or similar degree 6-8 years of experience working in a pharmaceutical CMC organization Hands-on experience with at least one of the functions in CMC development such as Process Chemistry, Process Engineering, Formulation, and Analytical Chemistry Knowledge of key concepts including unit operations, processes, quality by design (QbD), tech transfer, process validation, quality attributes, and regulatory milestones across pharma development Understanding of the different data and information systems such as ELN, LIMS, ERP systems, and LCM or PLM systems Understanding of the CMC related regulatory submission requirements Ability to translate the knowledge of concept in one modality to other modalities, if needed Experience presenting to senior leaders, executives, and audiences with CMC backgrounds Hands-on experience with data analytics with ability to generate insights from data from various sources Ability to lead multiple workstreams and demonstrate effective time and project management skills Experience with at least one tech transfer, exposure to analytics, AI and/or technology implementation in CMC preferred Perks & Benefits: ZS offers a comprehensive total rewards package including health and well-being, financial planning, annual leave, personal growth and professional development. Our robust skills development programs, multiple career progression options and internal mobility paths and collaborative culture empowers you to thrive as an individual and global team member. We are committed to giving our employees a flexible and connected way of working. A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections. Travel: Travel is a requirement at ZS for client facing ZSers; business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed. Travel provides opportunities to strengthen client relationships, gain diverse experiences, and enhance professional growth by working in different environments and cultures. Considering applying? At ZS, we're building a diverse and inclusive company where people bring their passions to inspire life-changing impact and deliver better outcomes for all. We are most interested in finding the best candidate for the job and recognize the value that candidates with all backgrounds, including non-traditional ones, bring. If you are interested in joining us, we encourage you to apply even if you don't meet 100% of the requirements listed above. ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law. To Complete Your Application: Candidates must possess or be able to obtain work authorization for their intended country of employment.An on-line application, including a full set of transcripts (official or unofficial), is required to be considered. NO AGENCY CALLS, PLEASE. Find Out More At: www.zs.com

An Analyst Intern typically has a wide range of responsibilities, which can include: Willing to familiarize yourself with the company's vision and mission, seeking to accomplish set goals and objectives. Lead generation and use of the LinkedIn Navigator. Evaluate these new clients and sell our services to them. Do follow up on sales Cultivating strong relationships with new clients while maintaining existing client relationships. Help to prepare a new sales plan for our current and upcoming services. We are promoting the company on the online platform. We want only Pharma Students (B. Pharma, B.Tech Biotechnology, B.Sc Biotechnology, M.Pharma, M.Tech, M.Sc)

About the Job: FutureX Global Learning is hiring a highly qualified and experienced Subject Matter Specialist to join our team in Kochi, Kerala, with a focus on training students in the field of Microbiology, Food Technology, Biotechnology, or Life Sciences. As a Subject Matter Specialist, you'll play a key role in designing, developing, and delivering high-quality training programs that equip students with the knowledge and skills required to excel in their chosen field. Key Responsibilities: - Train and mentor students in the subject area through workshops, hands-on sessions, and interactive learning modules - Design, develop, and deliver high-quality training programs for students in Microbiology, Food Technology, Biotechnology, or Life Sciences - Develop and curate high-quality content, training programs, and solutions for various audiences - Create engaging and interactive learning experiences that cater to diverse student needs - Conduct research and stay up-to-date with industry trends and developments - Collaborate with internal stakeholders to design and deliver training programs - Work with instructional designers to develop engaging and effective learning experiences - Provide subject matter expertise and support to various teams - Stay current with industry developments to ensure training programs remain relevant and effective Requirements: - Master's degree in Microbiology, Food Technology, Biotechnology, or Life Sciences - Industrial experience in a related field - Strong knowledge and expertise in the relevant field - Excellent research and analytical skills - Ability to work independently and collaboratively - Strong communication and interpersonal skills - Experience in developing and delivering training programs or content - Familiarity with instructional design principles and adult learning methodologies - Familiarity with Microsoft Office - Immediate Joiners are preferred Why Join Us: - Competitive compensation package - Opportunity to work with a dynamic global team and contribute to innovative learning solutions - Professional development and growth opportunities - Collaborative and supportive work environment Position Type: Full Time / Morning Shift Resume Receipt: Accumulate Online Automatic Packet Generation: Yes Job Function: Subject Matter Specialist

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. Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹60,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Health insurance Internet reimbursement Paid sick time Paid time off Work from home Schedule: Day shift Fixed shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Ability to commute/relocate: Ambala, Haryana: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Mention your CCTC [in LPA] Mention your ECTC [in LPA] Do you have any working experience in Research and Development in Food Science or Health Supplement Industry? [If yes, how many years?] Have you ever Developed a Pharmaceutical or Nutraceutical Product? [If yes, please mention the Product details in short] Are you aware of the Regulatory Compliances that are followed by FDA / FSSAI / AYUSH / Health Canada Guidelines [Yes / NO] Education: Bachelor's (Required) Location: Ambala, Haryana (Preferred) Work Location: In person Speak with the employer +91 8685858602

Position Summary - Experienced IT Risk & Compliance professional responsible for managing Electronic Document Management Systems (EDMS), ensuring regulatory compliance (FDA, ISO, HIPAA, SOC2), and supporting audits, system validation, and risk mitigation across global teams. Strong expertise in IT controls, privacy, business continuity, and document lifecycle management within GxP environments. Primary Skill : EDMS Management or auditing Secondary Skill : Understanding of general IT Control framework, Change control, ISO 9001, IT compliance, and CAPA systems. Key Responsibilities - Perform the following functions: Required to have an excellent understanding of the IT Control framework, in particular risk assessment and control selection Working experience in any two of the compliance programs (PCI DSS,HIPPA,ISO 27001,SOC2) Partner with DCO/DCM and service delivery leadership to both communicate and manage risk in delivery to an acceptable level Partner with DCO/DCM and delivery team to increase the level of awareness of compliance with policy and process Develops and provides appropriate guidance on solutions to mitigate risks and enhance system security Deep understanding of privacy and business continuity requirements and support R&C Privacy and BCM teams in execution of their respective program Serve as the primary administrator for the validated Electronic Document Management System (EDMS) platform, overseeing day-to-day operations, user support, and system maintenance. • Manage the end-to-end lifecycle of controlled documents including SOPs, Work Instructions, and Quality Policies, ensuring version control, periodic review, and audit readiness. • Lead and support the validation team with the activities related to the EDMS, including developing and executing IQ/OQ/PQ protocols and maintaining validation documentation. • Ensure the EDMS remains compliant with global regulatory requirements (e.g., FDA, EMA, ISO 13485), and support audit and inspection readiness. • Administer user access controls, security roles, and training programs to ensure proper system use and compliance. • Act as the first point of contact for document-related issues, troubleshooting, and escalation to technical teams when necessary. • Collaborate with cross-functional teams (Service Delivery, IT) to drive system improvements and manage change controls related to EDMS functionality. Participate in corporate initiatives, including internal audits, Software Development Life Cycle (SDLC) reviews, major system developments and other strategic initiatives Demonstrates ability to work in virtual team with help of tools and technologies Demonstrates ability to handle conflicting situation & should have strong verbal, written communication & analytical skills Must have systematic and pragmatic approach to problem solving Demonstrates good inter-personal skills, high standards of professional behaviour in dealings with business customers, colleagues and staff Have a good technical awareness and the aptitude to remain up to date with information security and IT developments Ability to communicate Risk to non-IT business owners and support function such as delivery, HR, GWS, Physical Security, Legal, Contracting and others Education Qualification - Graduate or master's degree in IT, Risk Management, Business Management, or a related field. Certifications Required - Certification such as ISO13485/ISO90001/ISO27001 are preferred. Attributes of Ideal Candidate – 10+ years of experience in in Electronic Document Management System or auditing. Knowledge of document control processes in support of GxP operations (GMP, GVP, GCP). Familiarity with change control, IT compliance, and CAPA systems. Strong understanding of system validation principles and regulatory guidelines including GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity standards. Experience supporting audits/inspections and preparing validation or compliance documentation. Excellent organizational, communication, and problem-solving skills. Ability to work independently and collaboratively across global teams. Experience in pharmaceutical, biotechnology, or medical device industry settings is preferred. Strong communication skills Ability to multi-task, prioritize, and meet timelines on deliverables Proficient in MS Office Team Management Skills Able to translate contractual terms into information security controls

Hi, We are having an opening for Manager- Global Alliance Management at our Mumbai location. Job Summary : This role belongs to the speciality/branded business vertical of Sun Pharma. Sun Pharma has licensed and acquired several commercial and early-stage proprietary programs (NCEs, Biologics) for global development and commercialization and currently total revenue as per IQVIA is more than USD 1 Bn from such proprietary assets and growing in double digit year on year. This role creates value through management of strategic partnership by working closely with a diverse set of internal and external stakeholders across geographies and functions. Areas Of Responsibility: Key Role and Responsibilities Manage a broad portfolio of partnerships at all stages of their lifecycle with a focus on mutual value creation. Manage and oversee the financial transaction with support for finance and taxation team for royalty payments, milestone transactions and withholding taxes. Manage the amendments of the contract with internal legal and Global BD team. Ensure that mechanisms are in place for the governance of partnerships. Ensure the internal team understands the expectation, deliverables and obligations of all the stakeholders. Ensure decision making is aligned with contract terms and governance. Proactively identify and drive the resolution of any disputes, risks and issues and facilitate cross functional win/win solutions for such disputes Maintain the latest updates of the development (Commercial, Regulatory, Intellectual Property and Technical) Facilitate CEO and JxC meetings, as well as global summits, to support strategic decision-making and organizational growth with senior management Collaborate with external stakeholders, corporate communications, and investor relations to ensure timely and accurate joint press releases and medical publications Educational Qualification : Post-graduation (MBA) from a reputed college / university along with bachelor in pharmacy or related science discipline (biotechnology, chemical) Experience : 3+ years Specific Experience : Alliance Management, Business Development, Portfolio or Project Management Skill (Functional & Behavioural): 3+ years of experiences in healthcare industry preferably in Alliance Management, Business Development, Portfolio Management, Project Management, Partner Management Healthcare/ Pharma industry basic domain knowledge about regulatory, drug development, business and therapies A desire to learn, contribute value, and make the role better Strong interpersonal skills and business acumen, excellence in building and managing relationships, ability to understand all perspectives, find common ground and effectively bridge significant differences Problem solving, negotiation, advocacy and influence skills Ability to operate on both strategic and tactical levels, to flex as needed in a fast-paced environment, and to work across various time zones Maintain high integrity with respect to maintenance of proprietary and confidential information

Job Description: We are seeking a highly skilled and experienced Senior Scientist with a proven track record in protein expression and purification within the industrial setting, preferably in a contract research organization. The ideal candidate will possess a strong background in biotechnology, biology, or a related field, along with extensive hands-on experience in protein purification techniques. Key Responsibilities Lead and execute protein expression and purification projects according to client specifications and timelines. Utilize expertise in protein expression systems to optimize production yields and quality. Perform protein purification using AKTA FPLC systems and Unicorn control software, with proficiency in automating standard purification processes. Develop and validate purification methods to meet project requirements, ensuring high purity and yield of target proteins. Conduct analytical characterization of purified proteins using various techniques such as SDS-PAGE, Western blotting, and HPLC. Implement aseptic techniques for handling mammalian cell cultures, ensuring sterility and integrity throughout the purification process. A thorough understanding of bacterial endotoxin limits and strategies for their elimination from purified proteins. Collaborate effectively with cross-functional teams to troubleshoot and solve technical challenges. Mentor junior team members, providing guidance and support to foster their professional development. Contribute to the continuous improvement of laboratory protocols, processes, and workflows to enhance efficiency and quality. Qualifications Master's degree (MSc. or M.Tech) in biotechnology, biology, or a related field. Ph.D. not required. 7 to 9 years of hands-on experience in protein expression and purification within an industrial setting, preferably in a contract research organization. Proficiency in protein expression systems such as bacterial, yeast, and mammalian cell cultures. Extensive experience with AKTA FPLC systems and Unicorn control software, including the ability to automate standard purification processes. Strong understanding of protein purification techniques and analytical methods. Familiarity with bacterial endotoxin limits and strategies for endotoxin removal. Excellent communication skills and ability to work collaboratively in a dynamic team environment. Demonstrated ability of proactive and problem-solving mindset. Ability to effectively prioritize and manage multiple projects simultaneously while meeting deadlines.

Job Description Summary Job Description Job Summary To achieve sales target & profitability in assigned territory by executing marketing strategies through personal contacts with key users, influencers and through education. To ensure timely collection of outstanding payments. Responsibility Achieve sales target & profitability in assigned territory by executing marketing strategies through personal contacts with key users, influencers and through education. To plan and execute marketing programs to meet customer needs and BD objectives. To maintain a detailed record of customer accounts (incl. key opinion leaders, Key Accounts, Key HCP’s) as per defined norms or requirements. Achievement of Personal Goals - Sales achievement of targets /IIGs/ KPI’s - S&P (Sales & Profit), Cash Collection Targets Timeliness in submission of Reports, Claims, Tour Plan, Secondary Sales Statements etc. SFDC tools, Organize, conduct in educational workshops and educate users on BD Biosciences products in assigned territory. Manage distributors / channel partners on aspects of stock planning, claim settlement and pricing Ensure regular customer visits as per defined norms. Qualification Master of Science in Biotechnology/Biochemistry/Microbiology. Or B.Tech. Biotechnology and/or MBA- Biotechnology Experience At least 5 years working experience in direct sales of Life sciences & Medical devices/ consumables Required Skills Optional Skills Primary Work Location IND Gurgaon - Aurbis Summit Additional Locations Work Shift

Job Opportunity: Medical Coder Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Qualification & Specifications : MBBS, BDS, BHMS, BAMS, BSMS, PHARMACY B.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDICAL, B.Tech (Biotechnology/Bio Chemistry). 2020-2025 passed out Skills Required: * Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). Role: To review US medical records Initial file review for identifying merits Subjective review and analysis to identify instances of negligence, factors contributing to it To review surgical procedures, pre and post-surgical care, nursing home negligence To prepare medical submissions To prepare the medical malpractice case Regards Contact: HR Anu: + 91 9500408540

About the Role We are seeking a highly motivated and experienced Techno-Commercial professional to join our team and drive the B2B growth of our herbal extract portfolio across global and domestic markets. The ideal candidate will have a strong background in herbal extracts, nutraceuticals, or phytochemicals, with a proven ability to bridge technical expertise and commercial strategy. This is a strategic and client-facing role that involves product presentations, client engagement, technical consultation, solution-building, and driving sales closures across industries like dietary supplements, functional foods, personal care, and pharmaceuticals. --- Key Responsibilities Client Engagement & Sales Support Interact with B2B clients (domestic and international) to understand requirements, recommend solutions, and provide technical validation. Conduct in-depth product discussions covering specifications, applications, dosage forms, and technical documents (COA, MSDS, TDS, etc.). Technical Consultation Act as the technical expert during the sales cycle. Provide guidance on product performance, formulation compatibility, and regulatory concerns. Address queries related to phytochemical content, standardizations (e.g., USP, HPLC), solubility, and extract grades. Commercial Strategy Support pricing, quotation, and negotiation processes in collaboration with business development and finance teams. Help evaluate customer requirements and recommend commercially viable product-customization options. Documentation & Compliance Ensure accurate preparation and timely delivery of all supporting technical and regulatory documentation. Assist clients in understanding and meeting compliance for target markets (e.g., USA, Europe, India). Cross-Functional Collaboration Coordinate with R&D, Quality, Operations, and Production to ensure feasibility and timely delivery of custom requirements. Support product development and innovation initiatives for new ingredient launches. Market & Competitor Intelligence Track market trends, client preferences, competitor offerings, and regulatory updates to contribute to the overall product strategy. --- Key Requirements Education: B.Sc / M.Sc in Life Sciences, Botany, Biotechnology, Chemistry, Ayurveda, or related disciplines. MBA or PGDM in Marketing/Business (preferred but not mandatory). Experience: Minimum 3–7 years of relevant experience in B2B sales, technical support, or business development in the herbal extract / phytochemical / nutraceutical industry. Skills: Strong understanding of herbal extract specifications (HPLC, UV, TLC, etc.), phytochemistry, and formulation compatibility. Excellent communication and presentation skills — both technical and commercial. Ability to build trust and credibility with formulators, procurement teams, and senior decision-makers. Self-motivated, detail-oriented, and capable of managing multiple projects and clients simultaneously. --- What We Offer A fast-growing, innovation-led workplace at the intersection of Ayurveda, science, and global wellness. Opportunity to work closely with leadership on global B2B expansion. Exposure to international markets, clinical trials, branded ingredients, and high-growth product categories. A collaborative, entrepreneurial culture focused on quality, transparency, and long-term partnerships. --- About Us Amaara Bioactives Pvt. Ltd. is a part of the Amaara Group — a global wellness manufacturing company with a legacy of quality, science, and innovation. Our extract division focuses on research-backed herbal ingredients, traceable sourcing, and clean, standardized actives for the global B2B market.

You will be joining a multinational food catering company operating in the B2B sector as a full-time General Manager - QHSE - Food Catering (MNC). In this role, your primary responsibility will be to oversee the Quality, Health, Safety, and Environment aspects of the food catering operations. This will involve the day-to-day management of operations, ensuring compliance with safety regulations, maintaining quality assurance, and driving environmental sustainability initiatives. To be considered for this position, you should hold a Graduation degree in fields such as Food Technology, Food Science, Hotel Management, Catering & Hospitality, or Bio-Technology. Additionally, having a good understanding of HACCP, ISO, and FSSAI compliances is essential. The ideal candidate for this role would have 10-12 years of experience in leading QHSE initiatives with a proven track record of team management in the Food and Beverages (F&B) industry, preferably within food services, catering, or restaurant chains. Proficiency in Excel and PowerPoint is required for this position. Key skills that will be crucial for success in this role include strong analytical abilities, effective communication, negotiation skills, relationship management with stakeholders, and excellent organizational skills.,

Job Description Able to perform independent sampling and analysis of water, compressed air. To perform microbiological environmental monitoring of clean area and compressed air with relevant records. Able to perform Microbiological limit test/method suitability testing and relevant data. Able to prepare media and perform GPT of media. Should have awareness of Caliber LIMS system operation. Should have knowledge of regulatory requirements and guidelines. Qualifications Should be M.Sc. in Microbiology or Biotechnology About Us Minimum experience of 1-3 Years in relevant department. Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion. About The Team The Human Resources team partners with all aspects of the organization, driving success through the effective and innovative management of people for both current and future business needs. Key Roles That The Human Resources Team Performs Executive Role: Specialists in all aspects of people management. High-level input at strategic level into all key business decisions. Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures. Facilitator Role: Close partnership to support, advise and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing. Consultancy Role: Provide expert advice to the organization and it’s managers on any aspect of workforce management and employee relations and performance. Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation, changes in the characteristics of the labor market.

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines. Roles & Responsibilities • Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. • Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy. • You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits. • Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification. • You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques. Qualifications Educational qualification: An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology Minimum work experience: 2 years Skills & attributes: Technical Skills • Basic understanding of the Biologics/Biosimilar industry, including processes, regulations, and trends. • Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques, including Size Exclusion, Reverse Phase, Ion Exchange chromatography, and Peptide mapping analysis, especially within the context of Analytics. • Hands-on experience in Biochemical analysis techniques, specifically Electrophoresis, Enzyme-Linked Immunosorbent Assay (ELISA), and Polymerase Chain Reaction (PCR), with a focus on Analytics. • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). • Basic knowledge in protein chemistry, including an understanding of protein structure, function, and relevant analytical techniques. • Basic knowledge and hands-on exposure to Microbiology techniques, particularly relevant for individuals working in Microbiology Labs. • Basic knowledge and hands-on exposure to cell culture techniques, specifically for working in Bioassay (BA) Labs. Behavioural skills • Prioritizes effective communication and demonstrates a performance-oriented mind-set. • Effective verbal and written communication skills. • Performance-oriented approach, consistently striving for high standards. • Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva, you will be able to continuously improve yourself working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Field Service Trainee for Cytiva is part of the India Equipment services organization located in Pune/Ahemdabad/Kolkata and will be a Remote customer facing role. At Cytiva, our vision is to advance future therapeutics from discovery to delivery. In this role, you will have the opportunity to: - Accompany the service engineers and help them in pre-installation work, equipment demo & other service activities. This will involve travel within the city and outside as well. - Ensure the delivery of operations - installing, troubleshooting, planned maintenance of the various range of Single use and Chromatography Equipment sold by CYTIVA Life Science to the customers in Biopharmaceutical Industries. - Required to attend independently or with a trained engineer and close the service calls as per CYTIVA Service Quality. - Support the team in service documentation work & be an active contributor. The essential requirements of the job include: - Bachelor's degree in biotechnology / Instrumentation / Electrical / Mechanical / Electronics/ Electrical & Telecommunications Engineering - Ability to learn quickly & demonstrate independent working straits - Interface and gel with both internal team members and external customers. - Should have knowledge about the basic tools used for service and repairs - Fluency in English language. - Ability to learn the processes in CYTIVA Life Sciences for reporting, escalations, travel. - Be a team player Who You Are - Bachelor's Degree / Diploma in Instrumentation/ Electrical/ Electronics/ Electrical & Tele-Communications Engineering fresh passed out from Institution. - Ability to learn the service and troubleshoot the equipment like Upstream Bio-reactors & Downstream Liquid Chromatography systems. - Interface and gel with both internal team members and external customers. - Ability to learn the processes in CYTIVA Life Sciences for reporting, escalations, revenue forecasting, travel. At Cytiva, we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.,

We are seeking ambitious publishing professionals to join our growing team supporting the peer review process. As a Reviewer Selection Editor, you will be responsible for efficiently managing peer review administration procedures, utilizing tools like Scholar One Manuscripts and PubMed Central to identify international experts suitable for reviewing cutting-edge medical research. Reporting to the Reviewer Selection Lead, you will work alongside a team of Reviewer Selection Editors. The ideal candidate will hold a postgraduate qualification in MTech/M.Sc. in areas such as Electrical and Electronics (ECE, EEE, VLSI, Embedded Systems, Power systems, Communication systems), Life Science (Biotechnology, Biochemistry, Microbiology, Molecular biology), Economics (Business Economics, Financial Economics, Applied Economics), Agriculture, or Horticulture. You should have a solid understanding of the journal peer review process, a keen interest in academic publishing, and knowledge of current market trends. Proficiency in English grammar, experience with process-driven workflows, and a background in customer-facing roles are essential. Your responsibilities will include managing the peer review process for journals, selecting appropriate reviewers through database research, ensuring compliance with ethical publication practices, communicating with reviewers, analyzing data for process improvements, maintaining records, and collaborating with international editorial teams. Strong organizational skills, the ability to handle multiple tasks efficiently, effective communication, and a commitment to excellent customer service are key qualities we are looking for. Flexibility, familiarity with Microsoft Office, and a willingness to adapt to changing work plans are also important. The selection process will involve an online assessment, technical discussion, and final HR-level discussion. This position requires working from our office in Chennai or Puducherry. Prior experience with platforms like Scholar One Manuscripts or Editorial Manager is advantageous but not mandatory, as full training will be provided.,

Job Summary: We are seeking a highly motivated and detail-oriented Quality Assurance Professional to join our laboratory team. This role is crucial in ensuring the continuous implementation, maintenance, and monitoring of our quality management system, adhering to national and international standards. The ideal candidate will play a pivotal role in upholding regulatory compliance, driving continuous improvement, and ensuring the integrity of all laboratory operations. Key Responsibilities: Quality System Management: Actively participate in and support all quality assurance-related activities. Implement, maintain, and monitor the effectiveness of the Quality Management System (QMS) in compliance with ISO/IEC 17025:2017, NABL guidelines, FSSAI, EIC, APEDA, AYUSH, GLP, Commodity Boards (e.g., Tea Board), and other relevant regulatory body requirements. Ensure systematic control and management of all QMS documents and records, including preparation, review, issuance, revision, and updates. Training & Development: Identify, plan, and execute internal and external training programs for laboratory personnel. Review and compile comprehensive training records. Corrective & Preventive Actions (CAPA): Monitor the effective implementation and verification of corrective actions (CA) and preventive actions (PA). Systematically resolve complaints and non-conforming work, actively participating in complaint closure actions. Technical Review & Oversight: Review and maintain records for method development, validation, and verification. Review test reports, calibration, and validation certificates for accuracy and compliance. Vendor & Equipment Management: Perform qualification and ongoing evaluation of vendors providing products and services to the laboratory. Plan, conduct, and monitor equipment calibration, validation, intermediate checks, and maintenance activities. Quality Control & Proficiency Testing: Plan, conduct, and participate in inter-laboratory comparison (ILC), proficiency testing (PT), and internal quality check (IQC) programs, ensuring meticulous record maintenance. Audits & Compliance: Assist and actively participate in the execution of internal and external audits, as well as Management Review Meetings (MRM). Support the preparation for and participation in customer and regulatory audits, visits, and inspections, ensuring successful closure of any non-conformances raised. Customer & Information Management: Review, assess, and evaluate customer feedback to drive improvements. Assist in LIMS (Laboratory Information Management System) operation and ensure its compliant implementation. Circulate critical regulatory and laboratory information, circulars, notices, newsletters, and recent updates/guidelines to all relevant company personnel. Risk Management & Continuous Improvement: Identify, assess, and mitigate risks, while also developing and verifying the implementation of opportunities for system and process improvement. General Support: Perform other duties as assigned by the Lab Head or Management. Qualifications: Education: Master's degree in Biotechnology/Microbiology/Food Technology/Chmeistry or a related discipline. Experience: 3-6 of progressive experience in Quality Assurance within a NABL accredited. Technical Knowledge: In-depth understanding and practical experience with ISO/IEC 17025:2017. Familiarity with NABL guidelines, FSSAI, EIC, APEDA, AYUSH, GLP, and other relevant regulatory requirements (e.g., specific to food, pharma, tea, etc.). Proficiency in laboratory quality control principles, method validation, and equipment calibration. Experience with LIMS operations is highly desirable. Skills: Strong analytical and problem-solving skills. Excellent communication (written and verbal) and interpersonal skills. Ability to conduct effective training programs. Meticulous attention to detail and strong organizational skills. Proficient in Microsoft Office Suite (Word, Excel, PowerPoint). Ability to work independently and collaboratively within a team.

Invitation Note Applications are invited from passionate candidates for one post of Research Coordinator. We look forward to applications from skillful candidates. Program Overview The HASP (Heart Attack and Stroke Predictability) study aims to develop risk prediction tools for heart attacks and strokes using analytical techniques, such as machine learning. By analyzing lifestyle, clinical, and molecular data, the project aims to elucidate the role of risk factors in the development of vascular diseases. HASP is designed to enable the early identification of at-risk individuals and guide effective prevention strategies, chasing meaningful marks on public health outcomes in India. Workplace Integrated Research on Neuroscience (IRoN) Unit Mazumdar Shaw Medical Foundation (MSMF) Bangalore-560099, India Webpage: https://www.msctr.org/integrated-research-on-neuroscience/ Funding Partner SKAN Research Trust Working Team Neuroscience Research Group Job Title Research Coordinator Job Type Contractual Emoluments Competitive Duration The initial appointment will be for six months (probationary period), extendable based on performance in the first six months. Key Responsibilities Coordination of participant enrolment: Identifying, screening, and enrolling eligible subjects into neuro-related research studies, ensuring informed consent is obtained. Coordination of health data management: Meticulously collecting, documenting, and maintaining accurate data on study participants, adhering to established protocols and regulatory requirements. Coordination of project activities: Organizing and overseeing various aspects of the research process, such as scheduling appointments, conducting assessments, and managing study supplies. Coordination of regulatory clearance: Ensuring strict compliance with institutional, consortial, local, and federal regulations governing the conduct of clinical research, including maintaining necessary documentation. Collaboration with multidisciplinary stakeholders: Fostering effective communication and coordination between physicians, nurses, laboratory personnel, and other stakeholders involved in the research. Coordination of participant sensitization: Providing study participants with detailed information about the research and offering guidance and resources to support their involvement. About Company: Mazumdar Shaw Medical Foundation is striving to bring more innovation in healthcare technologies and is inviting MedTech companies to join hands in solving the healthcare problems of the current world. In collaboration with the BIRAC, Department of Biotechnology, Govt. of India, Narayana Health, and Villgrow, Mazumdar Shaw Medical Foundation has established a BioNEST- Technology Business Incubator to provide technical, clinical, and business support to MedTech startups. We are looking for active interns to participate in activities to erect technologies to lay foundations for a strong technical support infrastructure for the incubator.

The position in Bangalore requires a candidate with 3 to 4 years of experience. The ideal candidate should hold a BE/B. Tech in Chemical Engineering, with preference given to those with an ME/M. Tech in Chemical Engineering. Knowledge of processes in Pharmaceutical, Biotechnology, Bio Pharma, Chemical, and Food Process industries is essential for this role. The scope of the job extends beyond business development. The incumbent will be responsible for identifying issues within industries related to processes and providing solutions to enhance productivity outcomes. Key responsibilities include: - Identifying and covering markets to develop potential clients and convert them into sales - Demonstrating a thorough understanding of Chromatography and Membrane technologies - Providing Chromatographic solutions for compound separation technology across various industries - Establishing and maintaining good relationships with industry stakeholders - Analyzing market feedback to devise effective strategies for business development and sales Key Result Areas (KRA) for this position include: - Identifying territories and industries for business expansion - Building long-term and profitable relationships with clients - Providing management with insights on technology development, new business ventures, and competitor activities - Monitoring clients" organizational developments, forthcoming ventures, and plans Personal attributes such as being proactive, possessing leadership qualities, having a presentable personality, and being focused and target-oriented are highly valued for this role. If you are interested in this position, please send your resume to hr@nilsan-nishotech.com.,

You will be responsible for providing strong leadership and managing all aspects of the Microbiological production facility in Visakhapatnam, Andhra Pradesh. This includes overseeing quality, costs, P&L, market development, performance, employee engagement, and technical development. The ideal candidate should have 10+ years of experience and a background in handling operations of medical devices. Experience in the field of Microbiology, Biotechnology, or related areas is preferred. A Master's degree, PhD, or equivalent experience is desired. Additionally, excellent communication skills and prior experience in leading a large team of more than 25 people are essential for this role. If you believe you possess the skills and experience we are looking for, we encourage you to reach out to us at hr@dnaxperts.com and share why you are the best fit for this position. We are always seeking to collaborate with top talent in the industry.,

School of Agricultural Biotechnology PAU, Ludhiana NOTICE Subject: Postponement of Interview for One post of Junior Research Fellow @ Rs 37,000/- + HRA 18% per month fixed on contractual basis. Please refer to this office advertisement no. 2145-215 dated 03.07.2025 vide which it was informed that the interview for one post of junior Research fellow at a fixed salary of Rs. 37,000/- + HRA 18% p.m. on contractual basis in the project entitled “Enriching the rust resistance of wheat by mapping the novel leaf rust and stripe rust resistance from multiple wild progenitor and non-progenitor species ” CSS-10 (PC-6436) financed by DBT, New Delhi. ” will be held on 28.07.2025 at 11.00 a.m. is hereby postponed due to some administrative reasons. The interview will now be held on 30.07.2025 at 11:00 a.m. in the office of undersigned. Only short listed candidates will be informed through email. Memo No: 2698 Dated: 17.07.2025 Director School of Agricultural Biotechnology PAU, Ludhiana

Business Development Executive (BDE) Great opportunity for someone looking for growth their career and is looking to enhance their knowledge in U.S. Business Development Job description: Role: Business Development Executive (BDE) Education: BBA, BCom, B.Sc, Biotechnology, Btech, BCA, BA, BPharm, MBA, MCom, MSc, MCA Experience: Freshers Job Location: Phase 8, Industrial Area, Mohali, Punjab Shift: Night Shift (US Shift) Timings: 8:00 PM to 5:00 AM Interview : In-Person *2025 PASS OUTS CAN ALSO APPLY* Notes: Cab facility to and from work is available for all female employees. One time Meal for all the employees Requirements: 0-2 year of experience in lead generation . Excellent communication and interpersonal skills. Ability to work independently and as part of a team. Creative thinking and problem-solving skills Impeccable Communication Skills (written and verbal both) Should understand US market Job Description Conducting market research to identify potential industries. Developing and executing lead generation strategies across multiple channels, including email, social media, and cold calling. Identifying and qualifying leads through research, outreach, and communication. Managing and updating customer and prospect databases. Analyzing lead generation data and metrics to improve strategies and tactics continually. Creating and delivering reports and updates to senior management. Staying up-to-date with the latest lead generation trends and technologies. Job Type: Full-time Pay: ₹21,000.00 - ₹24,000.00 per month Benefits: Food provided Paid sick time Paid time off Provident Fund Work Location: In person

BDE (Business Development Executive) Great opportunity for someone looking for growth their career and is looking to enhance their knowledge in U.S. Business Development Job description: Role: Business Development Executive (Finance) Education: B.Sc, M.Sc, Biotechnology, Microbiology, BBA, BA, Bpharma Experience: 0-2 Years ( Freshers can also Apply ) Job Location: Phase 8 Industrial Area, Mohali, Punjab Shift: Night Shift (US Shift) Timings: 8:00 PM to 5:00 A Interview : F2F *2025 PASS OUTS CAN ALSO APPLY* Notes: Cab facility to and from work is available for all female employees. One time Meal for all the employees Requirements: 0-2 year of experience in lead generation . Excellent communication and interpersonal skills. Ability to work independently and as part of a team. Creative thinking and problem-solving skills Impeccable Communication Skills (written and verbal both) Should understand US market Job Description Conducting market research to identify potential industries. Developing and executing lead generation strategies across multiple channels, including email, social media, and cold calling. Identifying and qualifying leads through research, outreach, and communication. Managing and updating customer and prospect databases. Analyzing lead generation data and metrics to improve strategies and tactics continually. Creating and delivering reports and updates to senior management. Staying up to date with the latest lead generation trends and technologies.

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Priya 9600450980 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund