Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us. Your Role In this role, the hire will engage in activities related to Large Data handling, including data maintenance, updates, reporting, and more MDGM Data maintenance, PRM/PRP updates, Back-order reporting, Sales reporting, and more Training to be on site, 3 days work from office Who You Are Conduct data Analysis, management & visualization. Advance knowledge of MS Office especially in MS Excel & Access Proficient in SAP & ERP system navigation Utilize tools like Power BI and Palantir for reporting and data visualization. Problem Solving ability - Identifying and resolving data related issues and discrepancies. Strong verbal and written communication skills Planning, time management, organization, and attention to detail Work with stakeholders to define and set priorities, deadlines, and deliverable schedules. Basic/ Minimum Qualifications Proficient in navigating SAP: PRE, PRD. Excellent Excel skills. Knowledge of Master data management. Preferred Qualifications Education: University post-graduate degree: MSc in Life science, Biology or related fields Biotechnology, Biochemistry, Microbiology, Genetics, Molecular Biology, Zoology, Botany. Experience: 3-5 years of experience in Product management Operations, Master Data, Supply chain. Note Based on the experience and skills of the candidate, we are open to offering a higher role as well. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! Show more Show less

Role Overview We are looking for a Senior Sales Manager to join our team, reporting to the Commercial Director for Southern Europe you will ideally be based in the “Bretagne & Pays de Loire” area You will develop and implement a strategy for selling and driving the PIC Value proposition in France. You will also develop, manage, and support a team of Sales Representatives to identify new commercial opportunities, drive business growth, profitability, and drive market share growth in the area. You will promote and sell a portfolio of technical and/or nontechnical products and/or services and solutions directly to current and new customers and inform customers of new product/service introductions and prices, and create, monitor and revise lead generation plans to ensure a substantive sales opportunity pipeline, with responsibility for overall P&L delivery. You Will Supports Regional Commercial Director in the development of the strategic customer initiatives to deliver profit targets and lifetime customer value. Develops and maintains relationships with new and existing customers and business partners to deliver a profitable business model. Grow and develop and create a high performing team of Sales Representatives. Motivate and lead the team to increase revenue, profitability and market share. Prepares sales forecasts and revenues for area of responsibility. Negotiates, sustains and renews customer contracts. Prepare and manage the annual budget for area of responsibility, monitor and adjust sales operations as appropriate to meet forecasts. Establishes and maintains relationships with key industry influencers and customers and communicating the value proposition. Works with all customer interfaces within accounts to influence, develop and implement improved ways of realizing the full genetic performance potential in customer farms. Develops strong relationships with enabling functions; Marketing; Supply Chain; Technical Services, Genetic Services, Health Assurance HR and Finance to ensure success of the region and the delivery of the strategic goals. Requirements Minimum of Bachelor’s Degree; Agricultural or Animal Sciences preferred. Extensive sales experience in the industry; modern pork production experience desired. Strong negotiation skills and constructing contracts that mitigate risk and result in “win-win” relationships with customers. Understanding of working in a Matrix Management organization an advantage Innovative, highly self-motivated with the ability to respond to changing demands are key requirements for success in this role. Excellent IT skills - Microsoft office proficient including excel and PowerPoint. Domestic and some international travel will be a key part of this role. Strong verbal and written English skills essential. Excellent communication and influencing skills and the ability to coach and mentor. Understands own leadership style and varies it to gain hearts and minds. Encourages and respects different styles. Business Overview PIC is the swine division of Genus PLC. PIC currently supplies over 70% of the world’s top pork producers. We directly employ people in 18 countries worldwide and our products are available in more than 50 countries across the globe. We are a diverse team, ranging from scientists to sales teams, production personnel to customer service, and are all united by a passion for producing nutritious, affordable pork and a commitment to continuous improvement. Genus PLC is an agricultural biotechnology pioneer. We are a global FTSE 250 company, headquartered in the UK, and listed on the London Stock Exchange. Genus PLC has a presence in over 70 countries and a global workforce of over 3,000 employees and growing. We are a worldwide leader in porcine and bovine animal genetics, partnering with farmers to transform how we nourish the world – a mission that is important to a sustainable future. Our vision is clear: Pioneering animal genetic improvement to sustainably nourish the world. Our Values Collaborate as One Team Create Value for Customers Innovate with Purpose Never stop improving DEI Genus is a place where you can be yourself and be part of a growing global team. We have a culture of respect, openness and fairness for all. Whatever your background, your role or your area of work, you will have the chance to thrive in an environment that inspires, challenges and supports you to succeed. Tackling climate change: Monitor and identify goals for the reduction of our GHG emissions from our own operations. Drive porcine and bovine genetic improvements which support productivity gains and improve feed efficiency, enabling a reduction in the production of greenhouse gas (GHG) emissions per unit of milk or meat produced Identify facility and other opportunities for reductions in GHG emissions, consistent with our goals Partner and advocate for policies that advance positive climate goals and identified United Nations Sustainable Development Goals (SDGs). Tackling PRRS: Developing pigs through gene editing that are resistant to PRRSv (Porcine Reproductive and Respiratory Syndrome Virus), a deadly disease that causes animal death and suffering as well as the loss of billions of dollars in farm production worldwide.* Equal Employment Opportunities Genus is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. Genus prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Genus conforms to the spirit as well as to the letter of all applicable laws and regulations. Recruitment Fraud Warning Genus plc will never ask you to provide fees or payment for computer, software, or other equipment or supplies during the recruitment and/or onboarding process. If you have any questions about your individual application, please contact the Genus Talent Acquisition team at recruiting@genusplc.com . Show more Show less

Job Description: Sales Head Company : Pinnacle Biosciences Location : Remote (Work from Home) with monthly travel to HQ in Kanyakumari, Tamil Nadu, India Department : Sales & Marketing Reports To : Managing Director Employment Type : Full-Time Compensation : Up to ₹2,00,000/month + attractive incentives and performance-based bonuses About Pinnacle Biosciences Pinnacle Biosciences, an 11-year-old biotechnology startup, is a leader in algae-based innovation, headquartered in Kanyakumari, Tamil Nadu. Our team of energetic and intellectually driven biologists is dedicated to developing sustainable, high-quality algae-based products for agriculture, aquaculture, animal husbandry, and human health care. Recognized as the "Renaissance of the Future," our algae-based solutions, including organic input fertilizers, animal/aqua feed additives, and food-grade algal polysaccharides are backed by robust in-house manufacturing and a proactive R&D team. With a solid product portfolio and a focus on sustainability, we are poised to convert prospects into long-term partners in both domestic and international markets (Canada, Japan, UAE, UK, US). Job Summary As a fast-growing startup ready to dominate the field, Pinnacle Biosciences is seeking a dynamic Sales Head to lead our sales strategy and drive revenue growth in institutional, bulk B2B, and international markets. This role will focus on closing high-value deals, building strategic partnerships, and expanding our market presence for algae-based products. The Sales Head will work closely with the Managing Director, leveraging leads provided and proactively identifying new opportunities in a dynamic, high-growth startup environment. key Responsibilities ● Strategic Sales Leadership : Develop and execute a comprehensive sales strategy to achieve revenue targets, focusing on institutional and bulk B2B sales for algae-based products, including organic fertilizers, feed additives, and health care solutions. ● Lead Conversion & Prospecting : Close leads provided by the Managing Director and proactively identify new sales opportunities with institutional buyers, agri-input distributors, and industry partners in domestic and international markets. ● Market Expansion : Drive domestic market penetration while supporting exports to key regions (Canada, Japan, UAE, UK, US). Build long-term partnerships with farmers, aquaculture businesses, and health care distributors, leveraging our 5,000+ satisfied farmer base. ● Client Relationship Management : Nurture relationships with key accounts, ensuring client satisfaction and repeat business. Understand client needs and collaborate with R&D and manufacturing teams to deliver customized, seaweed-based, naturally chelated product solutions. ● Product Positioning & Customization : Work with internal teams to position Pinnacle’s innovative, eco-friendly products as premium solutions. Support job-work-based offerings and third-party formulations, ensuring compliance and market fit. ● Industry Representation : Represent Pinnacle Biosciences at agro fairs, exhibitions, and B2B networking events to enhance brand visibility and forge strategic partnerships. ● Sales Performance & Reporting : Set and track sales targets, analyze market trends, and provide regular performance reports to senior management. Use market feedback to identify demand trends and support product expansion. ● Team Leadership : Build and manage a high-performing sales team, fostering a culture of accountability, innovation, and results in a startup environment. ● Sustainability Advocacy : Promote Pinnacle’s commitment to sustainability, highlighting our algae-based solutions for environmental challenges like methane mitigation and carbon utilization. Qualifications & Skills ● Education : Bachelor’s degree in business administration, marketing, biotechnology, agriculture, or a related field. An MBA is preferred. ● Experience : ○ 8+ years of experience in B2B sales or business development, with at least 4 years in a leadership role, preferably in agriculture, biotechnology, chemicals, or allied sectors. ○ Proven track record of closing large deals and managing key accounts in institutional or bulk sales. ○ Experience in international market expansion (e.g., Canada, Japan, UAE, UK, US) is highly desirable. ● Skills : ○ Strong leadership, communication, negotiation, and relationship management skills. ○ Strategic thinker with a solution-oriented mindset and the ability to work independently in a fast-paced startup environment. ○ Knowledge of biotechnology, agriculture, or algal technology is a plus. ○ Proficiency in CRM tools, sales forecasting, and data-driven decision-making. ○ Willingness to travel 3-4 days per month to HQ in Kanyakumari and frequently attend agro-related events and fairs. ● Personal Attributes: Self-driven, persuasive, results-oriented, and passionate about sustainability and innovation. Why Join Pinnacle Biosciences ● Impactful Role in a Growing Startup : Lead sales for an 11-year-old organization with a solid product portfolio, ready to convert prospects and scale rapidly. ● Competitive Compensation : Attractive package of up to ₹2,00,000/month, plus incentives and performance-based bonuses. ● Innovative & Sustainable Mission : Join a pioneering team revolutionizing nutrition and sustainability through algae-based solutions. ● Dynamic Work Environment : Work remotely with the flexibility to collaborate with an energetic team and leverage in-house manufacturing and R&D capabilities. ● Global Opportunities : Drive growth in domestic and international markets, contributing to Pinnacle’s vision of a brighter, sustainable future. Show more Show less

🔊 It’s Time. Join Us at PCJ LAW PARTNERS. PCJ LAW PARTNERS — a boutique law firm known for excellence in Corporate & Commercial Law , with a specialised focus on: 🏗️ Infrastructure 🚢 Logistics 🏢 Real Estate 🖥️ Data Centres 🌐 International Trade & Commerce 💡 IT, ITES & Startups — is now inviting Partners to lead from the front. What We’re Looking For: We’re building a dynamic, forward-thinking leadership team. We seek trailblazers who can: ✅ Drive their own P&L ✅ Lead practice areas with vision ✅ Spearhead client acquisition & relationship management ✅ Forge partnerships with international firms entering India Who Should Apply? This is a gender-neutral opportunity for professionals with passion, presence, and purpose . 📌 Experience matters — but it’s not everything. 📌 Bright, young minds with a flair for business development and a knack for client engagement are highly encouraged to reach out. If you’re ready to take ownership, innovate boldly, and help shape the future of legal services in India, we’d love to hear from you. 📩 Write to us at: pcj@pcjlaw.in 📞 Or call: +91-9319337377 Let’s make the law dynamic again. Let’s lead. Together. #lawfirm #legalcareer #partnership #lawjobs #india #businessdevelopment #corporatelaw #startuplaw #internationaltrade #genderneutral #PCJLawPartners #Business #Trade #Investment #Economy #EmergingMarkets #Entrepreneurship #Innova:on #Leadership #GlobalBusiness #Interna:onalTrade #Uruguay #La:nAmerica #LAC #GRULAC #Mercosur #IndiaBusiness #IndiaTrade #SouthAmerica #AsiaLatam # #GlobalPartnerships #TradeAgreements #ForeignInvestment #IT #ITServices #DigitalTransforma:on #CloudComputng #ArtficialIntelligence #MachineLearning #Blockchain #CyberSecurity #BigData #SoIwareDevelopment #Outsourcing #ITConsul:ng #GlobalCapabilityCenters #GCCIndia #SharedServices #BusinessProcessOutsourcing #CorporateExpansion #Nearshoring #FutureOfWork #GlobalOpera:ons #DataCenter #CloudInfrastructure #DigitalInfrastructure #RenewableEnergy #CleanEnergy #SolarEnergy #WindEnergy #SustainableDevelopment #EnergyTransi:on #GreenEnergy #NetZero #Decarboniza:on #Transporta:on #Logis:cs #SupplyChain #SmartMobility #ElectricVehicles #UrbanMobility #Mari:meLogis:cs #RailwayInfrastructure #Engineering #InfrastructureDevelopment #SmartCi:es #CivilEngineering #Construc:onTechnology #ManufacturingInnova:on #IndustrialAutoma:on #AerospaceEngineering #Pharmaceu:cals #HealthcareInnova:on #Biotechnology #MedTech #HealthcareInvestment #Business #Trade #Investment #Economy #EmergingMarkets #Entrepreneurship #Innovation #Leadership #GlobalBusiness #InternationalTrade #Uruguay rmaceuticals #HealthcareInnovation #Biotechnology #MedTech #HealthcareInvestment Show more Show less

India - Hyderabad JOB ID: R-216700 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jun. 04, 2025 CATEGORY: Human Resources 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. ABOUT THE ROLE Role Description: Amgen is seeking a Sr Associate HR Data Analysis (Visier Admin). The Sr Associate HR Data Analysis (Visier Admin) will report to the Associate Director HR Technology. The successful incumbent will have previous Visier reporting tool Admin experience. Roles & Responsibilities: Hands on experience supporting Visier Previous experience with Vee Administrative tasks associated with Visier such as role assignments and creating roles Visier Security configuration, data integration, and data exports Ability to analyze, troubleshoot and resolve Visier data issues Must have previous experience handling large datasets and sensitive HR data Basic Qualifications and Experience: 5 years minimum experience in human resources with hands on experience with Visier Master’s degree, OR Bachelor’s degree and 5 years of HR IS experience Functional Skills: Must-Have Skills: Strong working knowledge of Visier 5+ years’ experience in human resources and corporate service center supporting Workday Soft Skills: Excellent analytical and troubleshooting skills Strong quantitative, analytical (technical and business), problem solving skills, and attention to detail Strong verbal, written communication and presentation skills Ability to work effectively with global, virtual teams Strong technical acumen, logic, judgement and decision-making Strong initiative and desire to learn and grow Ability to manage multiple priorities successfully Exemplary adherence to ethics, data privacy and compliance policies 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 an accommodation.

Sr Executive/Asst Manager Role: 5–8 years of procurement experience in a pharmaceutical/CRO/CDMO - preferably in the biology domain. Key Responsibilities: Source and procure biology-related consumables, reagents, lab supplies, assay kits, cell lines, as per project requirements. Interact with scientific stakeholders (biology team) to understand technical requirements and ensure procurement aligns with research timelines. Identify, evaluate, and onboard qualified suppliers while maintaining compliance with regulatory and internal procurement standards. Request and evaluate quotations, negotiate with vendors, and raise purchase orders in the ERP system (Oracle). Track order status, coordinate logistics, and ensure timely delivery. Maintain procurement documentation, including quotations, order confirmations, delivery challans, and invoices. Work closely with Sai Boston procurement team ,Stores and Finance teams for MRNs, invoice processing, and vendor payment follow-ups. Monitor vendor performance and develop supplier relationships to ensure continuous quality improvements and cost savings. Required Skills and Qualifications: Bachelor’s or master’s degree in science (preferably Biology/Biotechnology) or equivalent. Knowledge of sourcing lab consumables, reagents, instruments, and equipment. Familiarity with procurement tools - ERP Oracle Strong negotiation, communication, and vendor management skills. Ability to work independently and collaboratively with cross-functional teams. Basic MS office reporting skills

We are inviting applications for two research positions under a Ministry of Earth Sciences (MoES), Government of India funded Deep Ocean Mission project in the Department of Marine Biotechnology at AMET University, Chennai. 🔬 Project Title: Exploring Marine Bioresources as Potential Natural Antifoulants: An In-depth Study on Secondary Metabolites of Marine Actinomycetes 🧪 Open Positions: Senior Project Associate – Ph.D. in Life Sciences – Experience in microbiology, biofilm, and antifouling studies – Fellowship: ₹42,000 + 24% HRA Project Associate-I – M.Sc. in any Life Science discipline – Preference for those with experience in marine-related fields – Fellowship: ₹25,000 + 24% HRA 📅 Last Date to Apply: 15 June 2025, 5:30 PM 📧 Apply via email: jayaprakashvel.m@ametuniv.ac.in 📍 Interview will be conducted in physical mode only. The selected Project Associate may also enroll in the Ph.D. program as per University norms. Interested and eligible candidates are encouraged to apply. For further details, feel free to reach out. 🔹 Dr. M. Jayaprakashvel Principal Investigator, MoES–DOM Project Professor, Department of Marine Biotechnology AMET University, Chennai #DeepOceanMission #MarineBiotechnology #MoES #ResearchOpportunity #LifeSciences #PhD #HiringNow #MarineEcology #BiofilmResearch #Actinomycetes #ProjectPositions #ChennaiJobs #AcademicJobs #ResearchCareers Show more Show less

India - Hyderabad JOB ID: R-216693 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jun. 04, 2025 CATEGORY: Human Resources 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. ABOUT THE ROLE Role Description: Amgen is seeking a Senior Associate of Human Resources – Workforce Administration who will work on our HR Technology group. The Senior Associate of Human Resources – Workforce Administration will work out of Amgen’s Capability Center in Hyderabad, India. The successful incumbent will have experience within the many aspects of human resources administration to provide customer service support to staff members and managers as a member of our service delivery team. The Senior Associate will also monitor worker data in the Human Resources (HR) system, Workday, and liaise with other groups on processes and analyzing HR system functionality. Roles & Responsibilities: Receives and responds to inquiries and issues related to Amgen’s HR system, Workday, that have been escalated from HR Associates Provides excellent customer service as measured by Service Level Agreements (SLAs) Assigns and balances HR system security roles Provides analysis and documentation to support the quarterly SOX process for Workday Security role assignments and removals. Analyze HR system functionality, identify gaps, perform system testing, and support the configuration of HR system to meet business goals Handles and maintains the content in the team’s knowledgebase program and suggests improvements for ongoing development Generates and creates Workday reports and performs audits on transactional work and other processes Performs transactional work in Workday using mass upload tool and correcting data discrepancies Fosters relationships and service levels through enthusiastic communications as well as timely and effective responses Contributes to knowledge sharing within the team, providing on-floor support and training the call center representatives on HR system processes while providing feedback on process and technology improvements Leads other projects/activities, as needed, and participate in other cross-functional process improvements Basic Qualifications and Experience: Strong working knowledge of Workday 4+ years’ experience in human resources and corporate service center Strong working knowledge of Workday including generating Workday reports, EIBs, Mass Operations Management Strong quantitative, analytical (technical and business), problem solving skills, and attention to detail Functional Skills: Must-Have Skills: 4+ years’ strong working knowledge of Workday including using tools such as EIBs, Mass Operation Management, data audits Experience in creating and using Workday reports 3+ years’ experience in human resources and corporate service center supporting Workday Soft Skills: Excellent analytical and troubleshooting skills Strong quantitative, analytical (technical and business), problem solving skills, and attention to detail Strong verbal, written communication and presentation skills Ability to work effectively with global, virtual teams Strong technical acumen, logic, judgement and decision-making Strong initiative and desire to learn and grow Ability to manage multiple priorities successfully Exemplary adherence to ethics, data privacy and compliance policies 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 an accommodation.

India - Hyderabad JOB ID: R-216490 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jun. 04, 2025 CATEGORY: Finance 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. ABOUT THE ROLE Role Description: We are seeking a proactive and empathetic Manager, Wellbeing Programs to lead the development, implementation, and evaluation of initiatives that promote the health, wellbeing, and resilience of our employees. This role plays a key part in fostering a culture of wellness, prevention, and support across the organization. This role will work cross-functionally to design and manage programs that support physical, mental, emotional, and financial wellbeing—aligned with our values and business goals. The ideal candidate is passionate about employee wellbeing and supporting programs that enhance the overall employee experience. Roles & Responsibilities: Program Design & Implementation: Develop and execute a comprehensive employee wellbeing strategy covering physical, mental, emotional, and financial wellness. Design and launch targeted programs and initiatives based on employee feedback, health trends, and organizational priorities. Partner with benefits, HR, and leadership teams to integrate wellbeing into company culture and policies. Stakeholder & Vendor Management: Collaborate with internal teams (e.g., HRBPs, DEI, Facilities) and external partners (e.g., EAP providers, wellness vendors) to deliver holistic wellbeing services. Manage relationships with wellness partners, negotiate contracts, and monitor service quality. Education & Engagement: Lead company-wide wellness campaigns, events, and awareness initiatives (e.g., Mental Health Month, fitness challenges, workshops). Promote utilization of wellbeing resources through engaging communications and events. Provide training and tools to leaders and teams to support wellbeing in daily work. Measurement & Continuous Improvement: Track and analyze utilization, engagement, and outcome data to assess program effectiveness. Use surveys, focus groups, and health data to continuously refine and enhance offerings. Prepare reports and presentations for leadership to highlight impact and recommend improvements. Basic Qualifications and Experience: 5+ years of experience managing corporate wellness or wellbeing programs. Strong knowledge of health promotion, workplace wellness trends, and behavior change strategies. Knowledge of current wellbeing trends and evidence-based practices. Experience with wellness platforms, employee assistance programs (EAPs), and health benefits integration. Excellent communication, project management, and cross-functional collaboration skills. Ability to analyze data and translate insights into actionable program improvements. Strong project management skills and ability to manage multiple initiatives. Exceptional interpersonal and communication skills. Experience working in a large, diverse, global organization. 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 an accommodation.

India - Hyderabad JOB ID: R-216510 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jun. 04, 2025 CATEGORY: Human Resources HOW MIGHT YOU DEFY IMAGINATION? You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role. Human Resources Senior Associate - Remote Live What you will do Let’s do this. Let’s change the world. In this vital role you will support Amgen’s efforts in driving employee listening programs across the organization and surface the voice and pulse of Amgen staff. Additionally, this role will assist with the integration of MS analytics tools across listening platforms to help understand and illuminate decision making about employee’s experience and well-being across the company. This role works in a global HR Center of Excellence (COE), part of the HR Insights and Analytics team. You will partner with business leaders, managers and HR partners across the globe to ensure our listening strategy is advising key organizational priorities, answering critical organizational questions, addressing employee needs, and adopting new working norms. Responsibilities: Support the design and implementation of core survey programs and ad hoc surveys that address emerging business needs Contribute to the transformation of the employee listening strategy in alignment with organization priorities Respond to data needs, create dashboards, and generate analyses to assess overall listening program impact against key talent indicators Collaborate with IS/Data/Tech teams to support the evolution of the technology and platforms used to build a connected and unified listening strategy Assists with the creation and execution of the overarching change management roadmap and associated activities related to the broader employee listening strategy Coordinate the development and delivery of communications, training materials, tools, and resources for both HR and the broader organization Partner with HRBPs, functional and regional HR and talent leaders, senior business leaders, and other stakeholders to advise and socialize the employee listening program Collaborate with third party vendor partner to configure and manage the listening platform Lead and oversee internal platforms (i.e. SharePoint, Yammer, Outlook Mailbox, etc.) for employee listening resources and communication Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The outstanding professional we seek is a candidate with these qualifications.

Responsible for in process Quality Assurance activities Responsible for In process Quality Assurance checks during Manufacturing, packing operations. Responsible for line clearance of manufacturing, Packing and dispensing activities. Responsible for assurance of cleaning, sterilization and aseptic manipulations of components Responsible for Sampling of Cleaning Validation & Compilation of the records. Responsible for sampling and coordination during validation studies (process / cleaning validation). Responsible for routine monitoring of Manufacturing Areas. Responsible for Review of Batch Manufacturing Record (BMR) & Batch Packing Records (BPRs). Responsible for the routine GMP Inspection & review of Quality Records of other departments. Responsible for monitoring in Aseptic process simulation study. Responsible for Preparation and Compilation of Media Fill Protocol , Report Involve in Initiation of Change Control ,Deviation and Participate in Failure Investigation. Responsible for environmental monitoring (Viable) in liquid, lyophilized and dry powder manufacturing areas Responsible for preparation and implementation of SOP's Good Documentation recording and updation Responsible for Preparation and Implementation of SOP's. Viable monitoring in clean area of manufacturing and warehouse as per the defined schedule. Responsible for personnel monitoring. Responsible to participate in qualification, requalification, area qualification activities. Responsibilities other than defined in the JD are to be done as per instruction of HOD Bachelor's Degree in Pharmacy, Microbiology, Biotechnology, Chemistry, or a related field. Master's Degree in Quality Assurance, Regulatory Affairs, or a related field (preferred but not mandatory). 3-5 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry. Hands-on experience with GMP inspections , environmental monitoring , and aseptic process simulations . Proven track record in sampling . Experience in reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) . Familiarity with SOP preparation and implementation . Involvement in change control , deviation management , and failure investigations .

Job Summary: We are seeking a dynamic and knowledgeable Product Specialist in Biotechnology to join our team. The Product Specialist will be responsible for promoting and selling our biotechnology products, providing technical support to customers, and contributing to the overall growth of the company's biotechnology division. The ideal candidate will have a strong background in biotechnology, excellent communication skills, and a passion for helping customers solve their technical challenges. Key Responsibilities: Product Promotion and Sales: Promote and sell biotechnology products to existing and potential customers. Develop and execute sales strategies to achieve sales targets. Identify and cultivate new business opportunities in the biotechnology sector. Technical Support: Provide technical support and product information to customers and sales teams. Conduct product demonstrations and presentations to customers. Assist customers in troubleshooting and resolving technical issues related to our products. Customer Relationship Management: Build and maintain strong relationships with key customers and stakeholders. Regularly communicate with customers to understand their needs and provide appropriate solutions. Gather and report customer feedback to improve products and services. Market Research and Analysis: Conduct market research to identify trends, competitive products, and potential opportunities. Analyze market data to inform product development and marketing strategies. Monitor industry developments and advancements in biotechnology. Training and Education: Provide training and educational support to sales teams and customers. Develop training materials and programs to enhance product knowledge and sales skills. Stay updated with the latest advancements in biotechnology and share knowledge with the team. Collaboration: Collaborate with the product development team to provide customer insights and feedback. Work closely with marketing teams to develop promotional materials and campaigns. Participate in trade shows, conferences, and other industry events to promote products. Qualifications: Master's degree in Biotechnology, Life Sciences, or a related field. Proven experience in sales or technical support in the biotechnology industry. Strong understanding of biotechnology products and applications. Excellent communication and presentation skills. Ability to work independently and as part of a team. Strong problem-solving skills and customer-focused mindset. Willingness to travel as needed. Preferred Qualifications: Experience with CRM software and sales analytics tools. Previous experience in product management or marketing in the biotechnology sector. Job Types: Full-time, Permanent Pay: ₹400,000.00 - ₹500,000.00 per year Benefits: Cell phone reimbursement Health insurance Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Application Question(s): We must fill this position urgently. Can you start immediately? Education: Master's (Preferred) Experience: Sales: 2 years (Preferred) Biotechnology: 4 years (Preferred) Willingness to travel: 100% (Preferred) Work Location: In person

We are seeking a motivated Content Editor to join our talented Zoological Records (ZR) team in Chennai/Hyderabad. This is the team of 11 member. As a Content editor in the ZR team you will select, analyze and interpret, and summarize scientific research and, as such, you should have comprehensive knowledge in a life sciences subject. Your role will require you to be target-driven and to meet defined quality standards. About You – Experience, Education, Skills, And Accomplishments Work experience (Fresher or at least 1 year of experience in content editing in a science-related field Knowledge on animal classification, systematic taxonomy & Nomenclature will be added advantage. Education M.Sc. Zoology or related life science streams Knowledge in performing end of production cycle completeness, and accuracy tasks as assigned. Good scientific research and analytical skills, with attention to detail General computer proficiency (MS Office) and ability to quickly learn new software tools Good oral and written communication skills, with excellent command of English A good team player with the ability to work independently. Ability to set priorities and be flexible in a changing environment. Effective time management Self-motivated with the ability to deliver consistently. It would be great if you also had . . . Fresher or 1 year of experience Masters in life science (Zoology, Microbiology, Biotechnology). Knowledge on animal classification, systematic taxonomy & Nomenclature will be added advantage. What will you be doing in this role? Apply zoology, systematic taxonomy, ICZN Nomenclature, microbiology, genetics and molecular biology concepts to curate animal and its biological related data from research articles in line with editorial policies Achieve weekly production volumes and consistently meet quality targets. Take active role within the team to ensure targets are met Maintain a flexible and adaptable approach towards process change Take initiative by raising, discussing, and resolving subject matter and production issues Maintain and develop scientific knowledge and skills training as required to complete work and stay current on scientific trends and developments related to your editorial responsibilities About The Team ZR is a comprehensive source of animal information with mainly related animal classification, systematic taxonomy & Nomenclature coming from academic literature and covers all aspects of animal biology. As an Content editor in the ZR team you will select, analyse and interpret, and summarize scientific research and, as such, you should have comprehensive knowledge in a life sciences subject. Your role will require you to be target-driven and to meet defined quality standards. In addition, this team and its processes and workflows are about to undergo huge transformation which will offer opportunities to rethink how the team operates and identify synergies with similar teams so the ideal candidate will be comfortable with change and someone able to offer ideas and think creatively. Hours of Work Full-time Permanent role Team working hours – 9 am to 6 pm IST At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations. Show more Show less

Position Title: Bioprocess Engineer Department: Process Reports To: Director Job Overview: We are seeking a highly skilled Bioprocess Engineer to design, optimize, and scale up biotechnological processes for industrial applications. This role involves developing efficient bioprocessing workflows, troubleshooting technical challenges, and ensuring compliance with regulatory standards. The Bioprocess Engineer will collaborate with R&D, production, and quality teams to translate laboratory-scale processes into scalable manufacturing solutions. Key Responsibilities: 1. Process Development and Optimization: Design and execute experiments to develop, optimize, and validate bioprocesses (e.g., fermentation, cell culture, downstream purification). Analyze data to identify critical process parameters (CPPs) and optimize yield, efficiency, and product quality. Scale up processes from laboratory to pilot and commercial production scales. 2. Technical Collaboration: Work closely with R&D, manufacturing, and quality assurance teams to ensure seamless technology transfer and process validation. Provide technical support to resolve process deviations, equipment malfunctions, and production bottlenecks. 3. Compliance and Documentation: Ensure all processes comply with industry regulations, including GMP, FDA, ISO, and environmental/safety standards. Prepare and maintain detailed technical documentation, including SOPs, batch records, and validation reports. 4. Equipment and Technology Integration: Evaluate, select, and implement bioprocessing equipment and automation systems. Train operations staff on new equipment and process workflows. 5. Continuous Improvement: Identify opportunities for process innovation, cost reduction, and sustainability. Stay updated on emerging bioprocessing technologies and industry trends to drive continuous improvement. Required Qualifications: Ph.D. in Biotechnology, Biochemical Engineering, or a related field. Minimum 3–5 years of hands-on experience in bioprocess development, preferably in pharmaceuticals, biofuels, or biomanufacturing. In-depth knowledge of upstream (fermentation, cell culture) and downstream (purification, filtration) processes. Familiarity with bioreactor systems, chromatography, and process analytical technology (PAT). Desired Skills and Competencies: Excellent problem-solving skills with a focus on root-cause analysis and troubleshooting. Project management experience, including timeline adherence and cross-functional coordination. Ability to present technical data clearly to both technical and non-technical stakeholders. Personal Attributes: Innovative and analytical mindset with a strong attention to detail. Collaborative team player with excellent interpersonal skills. Self-driven and adaptable to fast-paced, dynamic environments. Committed to safety, quality, and ethical standards. Work Environment: Primarily lab and pilot plant settings, with occasional office work. Occasional travel to vendor sites or manufacturing facilities may be required. Application Instructions: Interested candidates should submit a resume on WhatsApp on +917888780061 detailing their relevant experience and qualifications for this role. Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Life insurance Schedule: Day shift Morning shift Work Location: In person

**READ THE JD CAREFULLY BEFORE APPLYING!!! Key Responsibilities and Tasks: Data Analysis and Interpretation: Analyzing large datasets, identifying patterns, and drawing meaningful conclusions from the data. Research and Experimentation: Conducting experiments, collecting data, and analyzing results. Report Writing and Presentation: Preparing detailed reports and presentations for internal and external stakeholders. Collaboration: Working with cross-functional teams, including researchers, scientists, and other analysts. Staying Current: Keeping up-to-date with the latest advancements and trends in the biotechnology field. Regulatory Compliance: Ensuring adherence to regulatory standards and company policies in research methodologies. Model Development: Developing and maintaining statistical models to predict outcomes and trends. Industry Knowledge: Understanding the dynamics of the biotechnology industry, including market trends, company performance, and competitive landscape. Skills and Qualifications: Strong analytical and problem-solving skills: Ability to analyze data, identify trends, and draw meaningful conclusions. Excellent communication skills: Ability to communicate research findings effectively through written reports and presentations. Knowledge of biotechnology principles: Understanding of key concepts and techniques in molecular biology, cell biology, and other relevant areas. Data analysis and statistical software proficiency: Familiarity with tools like Excel, R, Python, or other statistical software. Scientific writing skills: Ability to clearly and concisely communicate research findings in scientific reports. Proficiency in relevant software and tools: Familiarity with software and tools used in data analysis, modeling, and research. Strong communication and presentation skills: Ability to effectively communicate research findings and insights to both technical and non-technical audiences. =========>>>please note: FULL TIME JOB OFFER AFTER INTERNSHIP BASED ON PERFORMANCE ENCOURAGING FINAL YEAR STUDENTS TO APPLY (B.sc/M.sc Biotechnology,microbiology,fisheries) * **CANDIDATES AIMING FOR HIGHER EDUCATION OR PHD CAN WORK WITH OUR PROJECTS THAT WILL HELP THEM SECURING GOOD RANK (SCHOLARSIPS)IN REPUTED UNIVERSITIES(INDIA OR OUTSIDE) Job Types: Fresher, Internship Contract length: 3 months Pay: ₹5,000.00 - ₹6,000.00 per month Benefits: Flexible schedule Leave encashment Paid time off Provident Fund Schedule: Day shift Fixed shift Supplemental Pay: Performance bonus Quarterly bonus Yearly bonus Ability to commute/relocate: Patia, Bhubaneswar, Orissa: Reliably commute or planning to relocate before starting work (Required) Application Question(s): when can you come for interview? when can you join us if selected? What is your aim in Life? Education: Bachelor's (Preferred) Location: Patia, Bhubaneswar, Orissa (Preferred) Work Location: In person Application Deadline: 28/06/2025 Expected Start Date: 28/06/2025

The Opportunity: Avantor is looking for a dynamic, forward-thinking, and experienced Associate - Cross Reference EU, who will be responsible for delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of IND- Coimbatore. If you are passionate about solving complex challenges and driving innovation – let’s talk! Our organization is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We are looking for an associate who can work on data management strategies by investigating and resolving data quality issues in enterprise applications via deletion and merging, while safeguarding against data loss. MAJOR JOB DUTIES & RESPONSABILITIES: Adhere to the workflow instructions/standard operating procedure provided by the business. Extract, analyze, update data, and implement of process improvement. Liaise with both internal and external customers and provide resolution with a customer centric approach. To provide alternatives through Branding Strategy promoting sales of Private label products. To enrich the SAP database by providing alternatives for Competitor codes. Responsible for the content of the cross-reference data in SAP. Building up knowledge of our product portfolio and know the preferred suppliers in different segments. Works with large amounts of data and regularly audits, research, analyzes, makes modifications to, and communicates about all the above tasks. Maintains accurate tracking of open and closed requests to ensure smooth workflow and accurate reporting. Perform other duties as assigned. SKILLS, KNOWLEDGE & EXPERIENCE: Results oriented and works with a sense of urgency. Assertive, responsible for his/her own work and has a strong affinity for defining work in deliverables and is willing to commit to deadlines. Focused and versatile team player that is comfortable under pressure. Knowledge of distribution, project management skills, critical thinking, data analysis. Experienced level in MS Excel & knowledge of MS Access, SAP, SQL & basic VBA skills are a plus. Excellent communication skills, oral and written. Results driven, self-sufficient and highly motivate. Must be able to work effectively with all levels of the organization. Must be able to develop excel reports as well as PowerPoint presentations. Knowledge of Avantor systems. Logical thinking and ability to analyse, standardize and improve fragmented processes. Independent thinker Affinity with large data sets and analytics EDUCATIONAL QUALIFICATIONS : Education: Bachelor's /master’s degree preferably in Biology, Chemistry / Life Science (Microbiology, Biotechnology, Biochemistry) or an equivalent subject. Experience: 0 to 5 years of experience in manufacturing and distribution environment preferred. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd party non-solicitation policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation

INSIDE SALES EXECUTIVE (Fresher - Biotech) | On-site at Cloudnine Hospital, Kompally 📍 Location : Cloudnine Hospital, Kompally, 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 Benefits Performance Incentives Cryoviva Biotech Private Limited, founded in 2006 by RJ Corp, is a leading provider of high quality umbilical cord blood stem cell processing and storage for private and public donation purposes. Show more Show less

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description About Company: Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers. Responsibilities: Facility Operations and Maintenance Coordinate day-to-day operations of the facility, ensuring all infrastructure and utilities (HVAC, purified water systems, cleanrooms, etc.) meet operational requirements. Perform routine maintenance, inspections, and solving of facility systems to ensure efficient performance and compliance with industry standards. Support the installation, qualification, and validation of equipment and systems used in single-use biomanufacturing. Develop and implement preventive and predictive maintenance programs to minimize downtime and operational disruptions. Regulatory Compliance and Safety Ensure facility operations adhere to cGMP, OSHA, and other regulatory requirements. Conduct risk assessments and ensure compliance with environmental, health, and safety (EHS) standards. Maintain comprehensive documentation for audits, including maintenance logs, calibration records, and operational procedures. Support the preparation and execution of internal and external inspections and audits. Utility Management Manage critical utilities supporting the bioprocess design center, including steam systems, water purification systems, and air handling units. Monitor utility performance and implement measures to optimize energy efficiency and sustainability. Troubleshoot utility-related issues and coordinate repairs or upgrades with contractors and vendors. Project Management Lead facility improvement projects, including upgrades, expansions, and new system installations, to support evolving biomanufacturing needs. Develop project plans, timelines, and budgets, ensuring completion within scope and schedule. Collaborate with external vendors and contractors to procure and install equipment and materials as needed. Single-Use Technology Support Support the integration and operation of single-use systems within the facility, including bioreactors, filtration systems, and storage solutions. Ensure facility infrastructure is compatible with single-use technologies and flexible for future process changes. Collaborate with process development teams to address facility-related challenges associated with single-use biomanufacturing. Continuous Improvement Identify and implement innovative solutions to improve facility performance, reduce operational costs, and bolster sustainability. Stay updated on the latest technologies and standard methodologies in facility engineering and biomanufacturing. Propose and complete projects that enhance efficiency and reliability in facility operations. Experience: Bachelor’s or master’s degree in mechanical engineering, Electrical Engineering, Facilities Management, or a related field. 3+ years of experience in facility engineering or operations, preferably in the biopharmaceutical, biotechnology, or healthcare industries. Familiarity with single-use technologies and bioprocessing systems is highly desirable. Experience with cGMP facilities, cleanroom operations, and critical utility management. Strong knowledge of HVAC, purified water systems, cleanroom operations, and facility management systems. Proficiency with CMMS (Computerized Maintenance Management Systems) and facility monitoring tools. Strong analytical and problem-solving skills with a hands-on approach to troubleshooting. Excellent organizational and project management skills with the ability to prioritize multiple tasks. Effective communication and collaboration skills to work with cross-functional teams and external vendors. Certification in facility management (e.g., CFM, PMP) is a plus. Knowledge of automation systems, Building Management Systems (BMS), and environmental monitoring systems. Experience in sustainability initiatives, energy management, and green building practices. At Thermo Fisher Scientific, our mission is to enable customers to make the world healthier, cleaner, and safer. We achieve this with a distributed team of over 125,000 colleagues who embody the values of Integrity, Intensity, Innovation, and Involvement. Together, we accelerate research, solve complex scientific challenges, drive technological innovation, and provide support to patients. Join us and start your story today! Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our +100,000 extraordinary minds have a unique story to tell. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status .

Education & Relevant Experience: Postgraduate degree in Biotechnology/Pharmaceuticals/Science with 2 to 4 years of relevant experience, preferably in the pharma/life sciences Sector/associated industries. Competencies: Technical (Knowledge, Skills, Attitude) Skilled in conducting both primary and secondary research for various projects. Understanding of dynamics and key issues in the Pharma industry. Basic understanding of working with Central and State Governments, industry players, representatives, and other stakeholders. Capable of coordinating events/business meetings/delegations. Generic/Managerial Highly motivated and passionate, with a strong interest in international affairs. Excellent research and analytical abilities. Effective communication and writing skills. Multi-tasking and the capability to thrive under pressure and tight deadlines. A team player with good Interpersonal Skills. Technical Proficiency in MS Word, Excel, PowerPoint, and other relevant software applications. PRINCIPAL ACCOUNTABILITIES: Thought Leadership/Policy Advocacy work in Pharma Sector Monitor key developments in the pharmaceutical and life sciences sectors, particularly in the Indian context. Conduct in-depth research and data analysis on sectoral issues, policy developments, regulatory changes, and market trends. Draft formal representations, consultation responses, and advocacy documents for submission to relevant government ministries, regulatory authorities, and other stakeholders. Prepare briefings, reports, policy papers, and position documents with actionable insights and recommendations. Draft talking points, presentations, and background notes for internal and external meetings. Stakeholder Engagement Interface with mid-to-senior-level stakeholders across government bodies, regulatory authorities, academia, and industry. Support engagement with FICCI’s Pharma Committee leadership and senior government officials. Maintain and regularly update a comprehensive database of key stakeholders. Task Force & Committee Coordination Organize and manage periodic committee meetings, including agenda setting, documentation of minutes, and follow-ups. Form and coordinate specialized Task Forces/expert groups to address sector-specific issues. Collaborate with Task Forces to develop policy papers, execute targeted projects, and provide strategic inputs. Events Management Plan and execute roundtables, webinars, B2B meetings, and large-scale conferences. Support in designing thematic sessions and curating content for FICCI’s annual Pharma Summits and other sectoral events. Prepare event-related materials such as concept notes, agendas, post-event reports, and presentations. Fundraising & Partnerships Support in raising sponsorships and forging partnerships with relevant organizations. Generate revenue through value-added services and strategic alliances. Develop partnerships with external partners and generate revenue for the organization. Show more Show less

Company Description Biology Career Insights (BCI) is a platform and podcast dedicated to exploring the diverse and evolving landscape of careers in life sciences, particularly biotechnology. BCI bridges the gap between scientific training and real-world career opportunities through insightful conversations with scientists, biotech founders, investors, policy makers, and industry leaders. The BCI podcast provides practical wisdom, inspiring stories, and actionable advice for navigating the biotech ecosystem. Whether you are a graduate student, a postdoc, or a professional in biotech, BCI offers valuable perspectives on thriving in this dynamic field. 🎬 We’re Hiring a Video Editor Intern for our Podcast! 🎬 BCI Podcast is on the lookout for a creative and detail-oriented Video Editor who can turn raw footage into scroll-stopping content. 🔹 Role: Video Editor (Internship) 🔹 Type: Remote, India 🔹 Content: Long-form (Podcasts, Interviews) +Short-form (Reels, Shorts) 🔹 Tools: Adobe Premiere Pro, Final Cut, or similar 🔹 Start: ASAP If you're passionate about visual storytelling and want to work with a fast-moving content team, we'd love to hear from you! 👉 Tag someone who might be interested 📩 Apply now or DM for more details! #Hiring #VideoEditor #Internship #RemoteWork #CreativeJobs #BCIpodcast #ReelsEditor #BiologyCareerInsights #PodcastEditing #VideoInternship Show more Show less

We are seeking enthusiastic and driven candidates to join our Molecular Biology & Strain Engineering team. As an interdisciplinary group with expertise spanning research, business, and food science, we are committed to revolutionizing sustainable food production through cellular agriculture . If you are innovative, proactive, and entrepreneurial —with a passion for leveraging molecular biology to make a meaningful impact—we’d love to hear from you! Key Responsibilities Utilize molecular biology techniques to engineer strains for protein expression in bacterial and yeast host systems. Design and conduct experiments, actively contributing to hypothesis testing and optimization. Perform high-throughput screening to identify clones with enhanced protein expression levels and yields. Conduct thorough molecular analysis of transformants to ensure quality and functionality. Identify, apply, and innovate new molecular tools for strain development. Independently design, execute, and analyse experiments. Collaborate closely with cross-functional teams (e.g., Fermentation & DSP ) to optimize expression strains for enhanced protein functionality . Maintain accurate documentation of research, findings, and product development efforts. Ideal Candidate Profile Educational Background: PhD or Master’s degree in Molecular Biology, Biotechnology, Synthetic Biology, Microbiology, Biochemistry , or related fields. o Experience Requirements: o Research Scientist: 3+ years of experience o Senior Research Associate: 1–3 years of experience o Research Associate: 6 months – 1 year of experience Strong expertise and passion for molecular cloning and strain improvement techniques . Experience with protein expression in prokaryotic and eukaryotic hosts ( bacteria & yeast ). Eagerness to develop innovative strategies for strain engineering and collaborate with team members. Knowledge of protein expression, bioprocessing, and protein analysis techniques (a plus). Passionate about food science, health, sustainability, and climate-focused innovation . What We Offer Career Acceleration within an early-stage startup. Continuous Learning Opportunities in a highly innovative environment. Competitive Compensation and flexible working hours . Long-term Growth Potential and wealth creation opportunities. Location 📍 Surat, India How to apply? hr@zerocowfactory.com Show more Show less

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Desktop Systems Engineer to join our Information Technology team. Responsibilities As our team has several openings at different levels and in different skill areas, the list below are samples of some of the technologies that we work with. While we desire candidates with experience in these specific technologies, we also understand that each of them have market alternatives, so the most important skillset a candidate can have is a good attitude and have a strong work ethic. Top candidates will have an aptitude to learn new technology and have a “do what it takes” attitude. Designing and implementing mobile device management (MDM) policies and procedures Configuring and deploying mobile applications using Intune Monitoring and managing Medpace’s end user computing applications, deployments, and devices for compliance. Keeping up to date with the latest end user hardware and software best practices, technologies, and methodologies specifically around Microsoft tooling and services as well as other third party tools Expert experience in administrating, creating, and packaging applications and operating system security patches for deployments using Microsoft Configuration Manager tools and associated Powershell scripting Ensure secure operations of infrastructure technologies (security updates, vulnerability management, role access management, configuration hardening) Expert experience in support of Windows Operating System, MacOS, and other desktop operating systems environments Strong background in scripting using SQL, PowerShell, VBScript, WMI Scripting, and Python Demonstrated aptitude around task automation and process documentation. Creating, and maintaining policies and training for end users and other IT teams Advanced OS and Microsoft management experience Experience working directly with hardware manufacturers and software publishers to resolve problems. Experience with Active Directory, Azure Active Directory, Group Policy, Intune, and Autopilot technologies strongly desired. Working knowledge of asset management tools, processes, and procedures Prior experience with Conference Room technologies, Collaboration Tools, and A/V Support is a plus Provide off-hours support (24 x 7) as required Qualifications Bachelor's degree in Information Systems or a related field; Proficient in enterprise desktop management; Solid experience in Microsoft Intune; Solid experience in scripting; Desire to learn and grow, with a solid foundation of experience; Aptitude to manage many different projects, applications, and priorities effectively and simultaneously; Ability to communicate effectively with peers, end users, as well as all levels of management; and Demonstration of strong communication, decision making, self management, and teamwork capabilities. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. Show more Show less

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Software Engineer to join our Information Technology team. The Software Engineer position will work on Administrative Systems and modernization of aging applications. Strong attention to detail, desire for process ownership, and interest in implementing new technology are highly valued. This is an incredible opportunity to join, contribute, and shape a new team, while also being a part of a large, fast-growing organization. You will be joining an organization where your contribution makes a significant impact in positively impacting people's lives, as new treatments and therapeutics are developed. Responsibilities Collect, analyze and document user requirements; Design, modify, develop and support software applications; Participate in software validation process through development, review, and/or execution of test plan/cases/scripts; Create software applications by following software development life-cycle, which includes requirements gathering, design, development, testing, release, and maintenance; Communicate with team members regarding projects, development, tools, and procedures; Utilize skills in development areas including object oriented programming (C#), databases (SQL) web applications (ASP.NET); Potential opportunities to lead software development projects. Qualifications Bachelor's Degree in Computer Science; At least 2 years of software development experience using technologies such as C#, Angular, Webservices, GraphQL, Git, relational databases; Experience in Entity Framework, Azure DevOps is advantageous; Understanding of software development life cycle (SDLC) and software release management; Prior experience modernizing systems to a cloud-based platform (Azure) is a plus; Excellent analytical, written and oral communication skills in English. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, US, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. Show more Show less

Company Profile : NewLife Medicals offers solutions that help pharmaceutical, CROs, nutraceutical, and biotechnology companies to accelerate business growth through clinical development, manufacturing, drug development and commercialization process. Our operations are spanning in more than 42 countries across the globe. We are supporting Sponsors, Research & Development centers, and Clinical Research Organization’s to build their drug development capabilities, by supplying the comparator drugs or RLDs from global markets. Job Overview : As the Senior Executive - Global Sourcing, you will play a pivotal role in executing and shaping the company's aggressive growth-oriented Sourcing/Procurement strategy. Job Description : • Responsible for Sourcing of RLD/Comparator drugs from the global market. • Maintain existing suppliers and add new suppliers across targeted global market. • To coordinate with Internal team members & ensure timely completion of tasks. • Review weekly progress of sourcing plan vs actual and devise tactics to ensure no gap in monthly achievement. • Responsible for negotiating contracts for sales/purchases and managing and reviewing contracts as required enabling effective operations, and customer/supplier relations. • Build good rapport with the Key Suppliers across the globe. • Manage/liaise with facility/warehouse team members on inventory levels, stock control, warehousing and distribution activities etc. • Support logistics team in identification of 3PL service providers in targeted markets and conduct meetings for finalization of service agreements. • Coordinate with logistics team and oversee that committed TAT is achieved. • Maintain monthly MIS & work with documentation team for day-to-day operations, archiving of all invoices wrt each transaction. • Planning of day-to-day shipment pick up or collection. • Maintaining & Tracking supplier wise activities in CRM/SAP • Monitor and track supplier wise, provide feedback for each supplier accounts for timely action. • To analyze the SAP data and derive the supplier wise strategy in line to achieve the target. Show more Show less

ROLES & RESPONSIBILITIES: LEADS GENERATION: Identify prospective clients & arrange meetings to understand their requirements and provide solutions (related to research, lab instruments & chemicals) to promote our products. Conduct technical discussions & provide demos of our products as per the requirement. Provide detailed information about lab setup and research work that can help him/her to complete the project/research. Send brochures/catalogues to clients so that he/she can get clarity on the product range. KEY RESPONSIBILITIES: New Prospect generation. Increasing reach and business geography. Take follow-up from the client to get the order. Understand queries of clients on technical and commercial terms and provide necessary data/information to resolve queries. Update process flow and costing details. Responsible for sales and receipt of payment. Provide demonstrations of instruments or chemicals, as per the requirements of the client. MISC & REPORTING: Compile client data and use it for brand promotion activities. Provide reports to Management as per requirement. Daily Activity Report on WhatsApp/Microsoft Teams and CRM Daily, Weekly, Monthly, and Quarterly sales plan, Lead report, sales report in CRM. REQUIRED KNOWLEDGE: Marketing & Sales A clear understanding of Biology concepts Good knowledge of instruments and consumables used in biotechnology and life sciences. BEHAVIOURAL SKILLS: Leadership skills, Planning & Organisation Skills, Business Communication, Presentation Skills, Time Management, Result Orientation & Innovative Thinking. BASIC REQUIREMENTS: Immediate Joiner Experience: 0 - 1 Years Educational Qualification: B.Sc. / B. Pharm. / Any Graduate in Life Science. Great Communication Skills. Able to speak fluent - Marathi, Hindi and English Role: Business Development Executive (BDE) Industry Type: Biotechnology & Life Sciences Department: Sales & Business Development Employment Type: Full Time, Permanent Role Category: BD / Pre Sales Mandatory Education UG: B.Tech/B.E. in Bio-Chemistry/Bio-Technology, Biomedical, B.Sc in Bio-Chemistry, Biology, Microbiology Key Skills Lead Generation, Prospecting, Lead Management, Strong Communication Skills, Lead Qualification, Presentation Skills, Written Communication, Client Meeting, Sales, Lead Generation, Verbal Communication, Market Research Show more Show less