2032 Biotechnology Jobs - Page 50

Title Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Cardiologist - Medical Director to join our Core Labs in Mumbai office. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. 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. Responsibilities Participate in oversight of assignments, training, and management of central reader s of cardiac imaging and EKG Collaborat e with Core Lab management on technical aspects of cardi ac study assessments Participat e in sponsor site visits and audits related to cardiac assessments as requested Participati e in training and subsequently demonstrating competency in the operation of independent central review of EKG and cardiac imaging for clinical trials Review protocols, Image Review Charters and associated clinical and technical study documents as required Complete source documents accurately and promptly, according to the specific protocol requirements and Medpace’s SOPs Blinded independent central review of EKG and cardiac imaging according to study endpoints as specified in clinical trial protocol, charter and according to GCP and standard Medpace SOPs Participate in IntraReader and InterReader variability assessments Participate in the development, review and evaluation of SOPs and study specific procedures. Other duties as assigned Qualifications Must have an M.D. and current medical licensure Board Certification preferred. Experience with EKG and most cardiac imaging modalities and expertise interpreting EKG, Holter-EKG and one or more cardiac imaging modality and therapeutic application Experience with various EKG and cardiac image analysis and viewing software (including PACS) Experience working with computer software including Word, Excel, Access and Project preferred Board Eligibility in Cardiology or equivalent training demonstrating competency People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

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. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

We blend care and creativity to nourish the world Griffith Foods is global product development partner; we specialize in high-quality food ingredients. We serve global food companies and regional food companies worldwide. As a family business, we’ve valued people above all else for 100 years. Griffith is renowned for true, collaborative innovation. Our people care. We’re committed to helping our customers create better products - and a better, more sustainable world. Learn more about Griffith Foods on https://griffithfoods.com/ime/ Position Summary: The Regulatory Specialist is responsible for executing and improving the Raw Material and Supplier Compliance program, ensuring documentation, risk assessments, and audits are carried out efficiently. The role supports R&D, QA and Purchasing functions and contributes to building a robust and future-ready raw material portfolio. Ensure raw materials meet local and international regulatory standards, including label, documentation, and import/export compliance. Key Roles & Responsibilities: Manage supplier documentation and certifications. Ensuring Raw Material (RM) compliance as per the standards. Liaison with R&D and Purchasing on the addition of new suppliers and new raw materials and packaging. Maintain supplier RM certifications and provide support for all risk assessment evaluations. Contact suppliers and coordinate the completion of a wide range of supplier assurance documentation, specifications, and supply chain information for all raw materials and packaging for the IMEA region. Managing the supplier documents in internal tool application. Support audits and sustainability. Functional Knowledge: Thorough knowledge of food science, regulatory compliance, supplier assurance processes, risk assessment, and raw material management in the food industry. Business Expertise: Understanding of India, Middle East, and Africa food market regulations. Knowledge of international standards like ISO 9000 and ISO 14000. Familiarity with customer-facing documentation and commercial import requirements. Local and global food regulatory frameworks, customer-facing regulatory support, import/export compliance. Leadership: Individual contributor with cross-functional collaboration. Influences internal teams and external partners to drive compliance and continuous improvement. Problem Solving: Strong analytical thinking required for conducting risk assessments, ensuring accurate regulatory documentation, and troubleshooting compliance or supply chain gaps. Impact: Ensures compliant, sustainable, and efficient raw material sourcing, supporting product quality, regulatory alignment, and customer satisfaction. Interpersonal Skills: Excellent communication and coordination skills for interacting with suppliers, internal stakeholders, and global customers. Ability to influence and engage with cross-functional teams. Job Requirements and Qualifications: Minimum Education: MSc in Food Science, Chemistry, Biotechnology, Biochemistry, Regulatory Affairs, or Nutrition. Minimum Experience: 6-8 years Preferred Experience: Handling global customer requirements, familiarity with digital systems for documentation and supplier management. Required Licenses/Certifications: None specified, but knowledge of international regulatory standards is essential. Working at Griffith Foods We are a caring family company where everyone has the opportunity to grow, follow their own personal “Purpose” and find fulfilment in their work. We support each other, demonstrate mutual respect and nourish people’s well-being . We believe in doing the right thing, especially when it is hard to do and recognize that our success depends on our customers’ success consequently, we work together, leveraging our skills, knowledge and ideas to create exceptional products and solutions. We value diversity at our company and celebrate our cultural and personal differences , knowing that together, we create a unique source of strength. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, or age. Show more Show less

Position: Sales Intern We’re seeking passionate and driven Sales Interns who are eager to learn, contribute, and grow. This internship offers a hands-on experience where you’ll get to connect science with people transforming products into stories that matter. Key Responsibilities Support regional business development and sales outreach efforts Assist in customer engagement, lead follow-ups, and field activities Participate in scientific discussions, product demonstrations, and promotional campaigns Collaborate with the marketing and product teams to gather customer insights and feedback Represent Uncoded at events, academic institutions, and conferences Track and report key metrics, learnings, and potential growth opportunities in your region Position Requirements Bachelor's or Master’s degree (B.Sc/B.Tech/M.Sc/M.Tech) in Life Sciences, Molecular Biology, or Biotechnology Strong communication and interpersonal skills Self-motivated, curious, and proactive in approach Ability to work independently and manage multiple priorities A passion for science, sales, and storytelling Internship Details Locations : Delhi | Mumbai | Bengaluru | Kolkata Duration : 3 to 6 months Perks : Certificate of completion, on-ground sales experience, and exposure to India's emerging life science landscape Stipend : Paid Internship Why Join Us At Uncoded, we don’t just offer internships, we offer impact. This is your chance to be at the forefront of India’s life science revolution, learning from experienced mentors while working on real challenges with real solutions. At Uncoded by Premas Life Sciences , we are democratizing access to cutting-edge multi-omics technologies by building affordable, high-quality, Made-in-India products. Our mission is to empower scientists, researchers, and clinicians through accessible tools in genomics, proteomics, and cell biology unlocking discoveries that go beyond DNA. As the innovation-driven brand from Premas Life Sciences, with 18+ years of leadership in the biosciences ecosystem, Uncoded brings together in-house R&D, local manufacturing, and trusted global collaborations to deliver real impact. Working at Uncoded means being part of something greater than yourself. Every idea and every interaction plays a role in shaping the future of life sciences in India. Show more Show less

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

About Us ClinoGenesis Research Organization is a premier institute offering clinical research training, placement services, and recruitment solutions. We specialize in shaping skilled professionals for the healthcare and research industries. We are currently hiring freshers for the position of Clinical Research Executive (CRE) - a perfect launchpad for your clinical research career. Role Overview As a Clinical Research Coordinator, you’ll be responsible for supporting clinical trial operations, managing site-level activities, and ensuring compliance with regulatory protocols. This is an ideal opportunity for fresh life science graduates looking to step into the dynamic world of clinical research. Key Responsibilities Assist in organizing and conducting clinical trials Maintain accurate trial records and documents Coordinate with investigators, participants, and sponsors Ensure compliance with GCP, ICH, and ethical standards Support subject recruitment, screening, and follow-up activities Manage and track clinical trial data and site documentation Eligibility Criteria Education: Open to all Life Science graduates and postgraduates, including: B.Sc./M.Sc. in Life Sciences, Biotechnology, Microbiology, Biochemistry, Genetics, etc. B.Pharm, M.Pharm, Pharm.D Nursing (B.Sc./M.Sc. Nursing) BPT, MPT, and other health science-related backgrounds Experience: Freshers only (Training in clinical research is an added advantage but not mandatory) kills: Excellent communication and coordination skills Strong attention to detail and willingness to learn Basic understanding of clinical trial processes and ethical guidelines Why Join ClinoGenesis? Career launchpad for freshers Industry-relevant training and real-world exposure Recruitment and placement support Work with reputed clinical sites and research sponsors Apply Now: Send your updated resume to info@clinogenesis.com Or apply directly via LinkedIn. Show more Show less

Role Description This is a full-time on-site role for a Fresher- Medical Coder at AGS Health located in Jaipur. The Medical Coder will be responsible for assigning diagnostic and procedural codes to patient records, ensuring accuracy and compliance with coding guidelines. The role also involves reviewing documents and medical records to abstract information for coding and billing purposes. Qualifications Strong attention to detail and analytical skills Experience working in a healthcare environment is a plus Ability to communicate effectively with medical staff and team members Bachelor's degree in Pharmacy, Biotech, Nursing, Health Information Management or related field

Click here to download form SCHOOL OF AGRICULTURAL BIOTECHNOLOGY PAU, LUDHIANA Applications Are Invited On Prescribed Form Along With The Application Fee Of Rs 200/In Shape Of Online Payment On Any Working Day From 9 00 A M To 5 00 P M In Favor Of Comptroller, PAU, Ludhiana Along With Attested Copies Of Certificates For These Positions In Project As Given Below: One post of Project Scientist-1 @ Rs 56,000/+ 16% HRA provided in the project Application of Bioinformatics and Computational Biology in Agriculture BIC at Punjab Agricultural University, LudhianaCSS-05 (PC-6352) (Financed by Govt of India, Ministry of Science & Technology, DBT, New Delhi) with Qualifications as under, Educational Qualifications: Sc Sc D Age Limit: 18 years to 35 Years Note-I The Candidates who does not possess Masters degree in the relevant subject but possess Ph D degree in the discipline required at Masters level, shall be eligible for the post, Note-IIDesirable Qualifications; Experience of working in Bioinformatics / NGS / Genomics / Machine Learning/ Database Designing and good experience in Programming Language as evident from good quality publications in peer reviewed journals, NoteIIIThe position is purely on contract/ temporary basis and co-terminus with the project The position will be initially awarded for a period of six months and will be extended further based on performance, One post Project AssociateI @ Rs 31,000/per month fixed + 16% HRA for in the Project entitled Molecular Mapping and transfer of jassid resistance in Okra esculents (L ) Moench CSS 49 (PC6371) Educational Qualifications: (i) b-sc with minimum OCPA 6 00/10 00 basis or 60% marks, (ii) m-sc in Biotechnology/Molecular Biotechnology & Biology/Plant Breeding and Genetics/ Vegetable Science with at least an OCPA 6 50/10 00 or 65% marks, Note-I: The candidates who does not possess Masters degree in the relevant subject but possess P hD degree in the discipline required at Masters level, shall be eligible for the post, Note-II: The candidate have passed NET/ GATE exam, Note-III:Posts will be filled @ Rs 25000/fixed + 16% HRA from among the candidates who fulfill all other required qualifications but have not cleared NET/NET-LS/GATE/other National level tests conducted by Central level departments and their agencies Note-IV: The Candidates should have passed Punjabi at Matriculation level Age Limit: Maximum Age 37 Years, Details for the payment of online application fee- Name of Account COMPTROLLER PAU RECRUITMENT, Saving Account No 29380100017259, Name of the Bank Bank of Baroda PAU, IFSC Code BARB0PAULUD (0 is zero), The last date for the receipt of applications (duly completed in all respects) in this office is 09 05 2025 Incomplete applications or unsupported by the requisite documents will not be entertained The candidate should appear for interview on 20 05 2025 at 11 00 a m in the office of the undersigned Only selected candidates will be informed through email No TA/DA will be paid for attending the interview The application form is available at PAU website pau edu, Director School of Agricultural Biotechnology PAU, Ludhiana

Role Overview PIC Europe, a Genus Company, has an exciting opportunity. We are looking for a highly motivated Genetic Program Sr. Specialist. In this role you will lead successful execution in Europe of PIC’s genetic program, including the Genetic Nucleus Crossbred Program. This program ensures our animals meet the demands of the commercial setting. You will have the ability to work in a culturally diverse, fast-paced environment, work autonomously as well as collaboratively across functional teams, and is able to identify, analyze and solve problems in a self-directed/managed work location. The preferred location for the position is Spain but there will be 40-50% travel including some international travel to our sites across Europe You Will Support the execution and communication of the genetic improvement strategy across the elite farm system and within Genetic Nucleus Crossbred program partners to encourage understanding and alignment to objectives and goals Ensure successful execution of genetic improvement protocols for routine and special projects Ensure successful execution of PIC’s Genetic Nucleus Crossbred program by Providing guidance to contract Genetic Nucleus Crossbred Partners with oversight Coordinate and manage activities related to trials and product testing Develop and implement statistical analysis and quality control of large datasets, including daily plant slaughter data and on-farm product performance Use knowledge of swine production practices to recognize data errors and validate large datasets Identify new methods to improve the accuracy of data collection Provide support for data acquisition, including troubleshooting software and hardware Uses existing procedures to solve standard problems; analyses information and standard practices to make judgments Travel approximately 40-50% Requirements Basic Qualifications: (required) University Degree in Animal or Meat Science, Animal Breeding and Genetics or related field A minimum of 3 years of experience within livestock production systems A minimum of 2 years of experience presenting and disseminating significant amounts of information to stakeholders with attention to detail and accuracy in an organized and concise manner. A minimum of 2 years of experience with Microsoft Office Suite and R as well as other software applications A minimum of 2 years of data analysis experience with understanding of experimental design and mixed modeling Must not co-habitat or live on the same premises with any person who works with swine and/or with people that are in routine contact with swine. Preferred Qualifications: Advanced Degree in Animal or Meat Science, Animal Breeding and Genetics or related field 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. 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 . 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Job Description Senior Manager, SAP Agile (Project Manager) The Opportunity Based in Hyderabad, join a global healthcare biopharma company and be part of a 130- year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products. Drive innovation and execution excellence. Be a part of a team with passion for using data, analytics, and insights to drive decision-making, and which creates custom software, allowing us to tackle some of the world's greatest health threats. Our Technology centers focus on creating a space where teams can come together to deliver business solutions that save and improve lives. An integral part of the company IT operating model, Tech centers are globally distributed locations where each IT division has employees to enable our digital transformation journey and drive business outcomes. These locations, in addition to the other sites, are essential to supporting our business and strategy. A focused group of leaders in each tech center helps to ensure we can manage and improve each location, from investing in growth, success, and well-being of our people, to making sure colleagues from each IT division feel a sense of belonging to managing critical emergencies. And together, we must leverage the strength of our team to collaborate globally to optimize connections and share best practices across the Tech Centers. Role Overview Within the EIT SAP Platform Team, the Senior Manager, SAP Agile (Project Manager) will have responsibility managing and delivering SAP projects using Agile methodologies. The Senior Manager, SAP Agile Project Manager is responsible for guiding the SAP Platform team through the Agile process, facilitating effective communication and collaboration among team members, and ensuring that projects are delivered within the defined scope, timeline, and budget. The incumbent plays a critical role in driving successful project delivery by enabling teams to embrace Agile principles and practices, delivering value to stakeholders in a fast-paced and collaborative manner. What Will You Do In This Role Facilitate Agile practices Guide teams in the adoption and implementation of Agile methodologies (such as Scrum, Kanban, etc.) to enhance collaboration and productivity. Facilitate Agile ceremonies lead meetings such as daily stand-ups, sprint planning, sprint reviews, and retrospectives to keep the team aligned, ensure progress, and identify areas for improvement. Stakeholder Communication Act as the primary point of contact for stakeholders, providing updates on project status, risks, and changes while also gathering feedback and requirements. Risk Management Identify potential risks and impediments, assess their impact, and implement mitigation strategies to reduce project risks. Managing project scope and priorities work closely with stakeholders to define project requirements and prioritize tasks, ensuring that the team focuses on delivering the most valuable features first. Monitoring project progress track team velocity, monitor project metrics, and provide regular updates to stakeholders, enabling transparency and informed decision-making. Removing obstacles and facilitating collaboration identify and address any impediments that are affecting team productivity, promote effective communication, and foster collaboration among team members and stakeholders. Continuous improvement encourage a culture of continuous improvement, facilitating retrospectives to identify lessons learned and implementing changes to optimize project delivery. What Should You Have Bachelor’s degree in Computer Science, Life Sciences, Engineering, or a related field. 5+ years of experience in project management leveraging various frameworks within the pharmaceutical or biotechnology industry. Strong understanding of Agile methodologies, principles, values, and practices such as Scrum, Kanban, or Lean required. This includes knowledge of Agile frameworks, roles, ceremonies, and artifacts. Proficiency in project management techniques and practices. Excellent communication and facilitation skills for effective and productive collaboration and fostering a culture of transparency and open communication within the team. Problem-solving and adaptability The ability to think critically, analyze complex situations, and adapt plans based on feedback and changing requirements. Stakeholder management understanding stakeholder needs, balancing competing priorities, and effectively communicating project progress and outcomes. Ability to manage multiple and competing priorities. Working knowledge of common tools used in this role - MS-Project, Spotfire, SharePoint and MS Office tools (Word, Excel, PowerPoint), Atlassian tools (Jira & Confluence), Planning tools such as Apptio for financial planning and TCO management (Total Cost of Ownership). Continuous learning and improvement embracing a growth mindset, seeking feedback, and identifying opportunities for process optimization and innovation. Conflict resolution The ability to identify and address conflicts within the team or with stakeholders. Certifications preferred (one or more, not all) PMI-Agile Certified Practitioner (PMI-ACP), Certified ScrumMaster (CSM), Professional Scrum Master (PSM), SAFe Agilist (SA), Project Management Professional (PMP) or any other relevant certification. Knowledge of various SAP ERP modules, and experience with licensing for ECC, S/4 HANA and cloud platforms, etc. preferred. Experience in Global SAP implementations in a project planning capacity preferred. Good understanding of business processes and ability to connect requirements from different groups preferred. Knowledge of Pharmaceutical industry and validated software environments preferred. Our technology teams operate as business partners, proposing ideas and innovative solutions that enable new organizational capabilities. We collaborate internationally to deliver services and solutions that help everyone be more productive and enable innovation. Who We Are We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world. What We Look For Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today. #HYDIT2025 Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Not Applicable Shift Valid Driving License Hazardous Material(s) Required Skills Data Engineering, Data Visualization, Design Applications, Software Configurations, Software Development, Software Development Life Cycle (SDLC), Solution Architecture, System Designs, Systems Integration, Testing Preferred Skills Job Posting End Date 06/27/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R336569 Show more Show less

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. Essential Functions With minimal supervision, authors (writes/edits) high-quality medical writing deliverables (i.e., clinical, safety, regulatory, device, diagnostics, or disclosures documents) across all phases of clinical research and in various therapeutic areas including but not limited to: protocols, protocol amendments, study reports, patient narratives, IBs, ICFs, CEPs/CERs, DSURs, and plain language summaries, as well as more complex documents (e.g., PBRER, IND, NDA, BLA, MAA, eCTD submission‑level documents). Supervises, trains, and mentors less experienced medical writers, as necessary. Adheres to established regulatory standards/guidelines including but not limited to: ICH E3/E6(R2), EU MDR/IVDR, Company standard operating procedures, client standards, and Company- and/or client-approved templates. Strives to complete medical writing deliverables on time and within budget. With minimal supervision, manages client expectations and interacts and communicates directly with clients, leads team meetings (e.g., project kickoff, comment review), and manages the deliverable timelines. Interacts and collaborates with subject matter experts in clinical operations, data management, biostatistics, regulatory affairs, etc., as needed, to produce writing deliverables. Coordinates QC reviews of documents and maintains audit trails of changes as applicable. Reviews statistical analysis plans and table/figure/listing shells (as applicable) for appropriate content, grammar, format, and consistency. If requested by supervisor, performs QC review (e.g., reviews in-text tables against statistical output). Performs peer review of documents written by other medical writers, as required. Assists with project-related administrative tasks (e.g., creates and maintains timelines, updates deliverable trackers, hosts internal/client meetings). Maintains familiarity with current industry practices, regulatory requirements, and guidelines related to medical writing. Understands budget specifications for assigned deliverables, works within the budgeted hours, and communicates out-of-scope tasks to medical writing leadership. Supports multiple medical writing deliverables/projects simultaneously and manages own workload with minimal intervention from management team. Brings issues and potential concerns to line manager/client oversight manager’s attention and proposes possible solutions for consideration by management team. Participates in departmental initiatives (e.g., process improvement, lunch and learns, etc.). Other duties as assigned. Necessary Skills And Abilities Advanced knowledge of clinical research principles and demonstrated ability to interpret and present clinical data and other complex information. Advanced understanding of FDA (and other regulatory bodies as relevant to their role) and applicable regulations and guidelines. Advanced understanding of regulatory submission requirements and processes. Computer technology proficiency and expert word processing skills in MS Word, including required proficiency with tables, graphs, and figures. Exceptional project management skills and strong communication skills with a high attention to detail and quality. English language proficiency and familiarity with American Medical Association (AMA) style. Strong experience in relationship building and strategic collaboration on key business accounts. Thinks proactively, takes initiative, and willingly takes on new challenges. Ability to identify areas of concern or inefficiency and propose solutions for consideration by the management team to improve overall efficiency and quality of deliverables. Works independently with exceptional time-management skills and contacts management team proactively when additional support and resources are needed. Works effectively in a collaborative team environment. Demonstrates a growth mindset and positive outlook in all work activities. Educational Requirements Bachelor’s degree or higher, preferably in medical or scientific discipline. Experience Requirements Minimum of 6 years of experience in writing clinical and/or regulatory documents for drugs, biologics, and/or medical devices/diagnostics for a contract research organization, pharmaceutical company, or biotechnology company. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case‑by‑case basis. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Show more Show less

Diagnose and treat cancer patients, providing personalized treatment plans including chemotherapy, radiation, and immunotherapy Conduct research and stay updated on the latest advancements in oncology treatments Collaborate with a team of surgeons, radiologists, and pathologists to ensure comprehensive patient care Must have an MD/MS/M.Ch degree with extensive experience in medical oncology Experience in clinical trials and cancer research publications is a plus

Diagnose and treat cancer patients, providing personalized treatment plans including chemotherapy, radiation, and immunotherapy Conduct research and stay updated on the latest advancements in oncology treatments Collaborate with a team of surgeons, radiologists, and pathologists to ensure comprehensive patient care Must have an MD/MS/M.Ch degree with extensive experience in medical oncology Experience in clinical trials and cancer research publications is a plus

Diagnose and treat cancer patients, providing personalized treatment plans including chemotherapy, radiation, and immunotherapy Conduct research and stay updated on the latest advancements in oncology treatments Collaborate with a team of surgeons, radiologists, and pathologists to ensure comprehensive patient care Must have an MD/MS/M.Ch degree with extensive experience in medical oncology Experience in clinical trials and cancer research publications is a plus

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Project Coordinator to join our Core Labs in Mumbai office. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. Responsibilities Compile and maintain project-specific status reports and project timelines associated with Imaging studies; Engage in Quality Assurance and Process Improvement on a day-to-day basis Maintain inventory of imaging supplies for study sites; and Interact with study sites and internal associates. Qualifications Bachelor’s Degree (required), Master's in Biomedical Engineering/ Biotechology Prior experience in handling Quality Assurance and facing any Quality Audits Prior research related experience is preferred; and Excellent computer, organizational and communication skills. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

About Immuneel Immuneel Therapeutics Private Limited is a pioneering start-up company leading the charge in cell therapy and personalized immunotherapy for patients in India. For more details, please refer www.immuneel.com We Pursue, with Purpose, to serve our Patients (3 Ps) by Connecting within, Collaborating globally and Creating (3 Cs) solutions. Our flexible, diverse, and vibrant team is bringing together best practices and innovations in the field of cell and gene therapy. Working at Immuneel promises the excitement of an agile start-up on a critical mission. Proudly Indian in solutioning, yet global in outlook, we are keen to collaborate. We value diversity including in experience and perspectives. We value work-life balance and believe that having fun on the job is integral to achieving the right results. We pride ourselves on providing an open environment and our mission resonates with humanity everywhere. At Work, we are: Passionate in driving patient outcomes: We are passionately committed to doing the RIGHT thing to achieve the best outcomes for our patients through innovation, agility and performance orientation. We put the impact on the patient above all else. Responsible and accountable: We demonstrate ownership and accountability for our actions. We make timely and well-informed decisions, learning from our performance. Transparent, honest, and supportive in how we work together: We insist on integrity and respect for the individual. We demand excellence. Our performance management is focused on excellence through timely and constructive feed-forward. Inclusive and flexible: We are full of life and embrace all opportunities to collaborate and work together. We are excited about the collective knowledge and expertise that we share. “Being and thinking different” is valued. Immuneel prides itself as an organization that is keeping pace with best practices in organization design. Our role-based organization incorporates global trends in human capital that promote focus on work and greater nimbleness. Our role-based structure allows you to be cherished by the work you do and bring value to your work rather than designations, our organization is simplified into a flat, non-hierarchical, millennial, organization where you may fully inherit the role you play in the organization and are recognized by the accountability you take and the work you deliver. Immuneel’s employees are integral to our quest to develop and deliver high quality engineered cell therapies in India. We believe that our culture provides an environment for employees to excel and find purpose. The strength of our team is every bit as important as our cutting-edge technology and we invest in clear compensation and comprehensive benefits for our employees. People for us, are not resources, but our capital. If you are a talented professional, an out-of-box thinker with a zeal to help change, and passionate about healthcare, we invite you to join us and be a part of a historic initiative in India. Interested to be a part of the next revolution in cancer treatment? Send your resume to careers@immuneel.com 1. Role Title: Legal Counsel 2. Department/Function: Finance & Investor Relations 3. Reporting Structure: Reports to : Finance Direct Reports : NA 4. Role Summary: The position of Legal Counsel is vital to ensuring the organization’s adherence to legal and regulatory standards while supporting its strategic and operational goals. As the primary legal advisor, the role involves providing expert counsel, managing legal risks, drafting and negotiating contracts, overseeing compliance, and liaising with external parties to safeguard the company's interests. This position is integral to maintaining the organization's integrity and enabling smooth operations within the highly regulated biotechnology sector. 5. Key Responsibilities: Provide accurate and timely legal advice to executives on a variety of topics, including labor law, intellectual Property, partnerships, international ventures, corporate finance, and other relevant areas. Draft, review, and negotiate contracts with customers, vendors, and other parties, including but not limited to Confidentiality Agreements, commercial/business agreements, licensing agreements, Term sheets, Services Agreements, Consultancy Agreements, MOUs, Master Service Agreements, Collaboration Agreements, Shareholders Agreements, and Investor Agreements. Policy Drafting and Review: Collaborate with internal stakeholders to develop new policies and regularly update policies, ensuring they comply with legal standards, meet operational requirements, while identifying and addressing gaps or outdated provisions. Risk Management and Accountability: Mitigate legal risks by managing policy updates, overseeing compliance, and collaborating with external stakeholders to address and resolve any issues effectively. Provide legal oversight into business processes and collaborate with internal teams to ensure regulatory compliance and risk mitigation in operations and partnerships. Liaise with external parties , such as investors, government officials, and service providers, to ensure timely delivery of expected outcomes and to protect the company’s interests. Maintain a repository of executed agreements and manage legal records effectively and efficiently to ensure accessibility and compliance. Compliance Oversight: and regularly monitor compliance with applicable laws, regulations, industry standards and audits to maintain company-wide compliance. Litigation Management and Dispute Resolution: Oversee and manage all litigation matters, including contractual disputes, labor law cases, and other conflicts. Collaborate with external advocates and consultants for effective resolution of litigation matters. 6. Primary Objectives: Ensure Legal Compliance Foster adherence to all relevant laws and regulations across areas such as clinical trials, data protection, employment, business operations, and industry standards, supporting risk mitigation and safeguarding the company's integrity and reputation. Manage Contracts to Support Strategic Goals Draft, review, and negotiate contracts with customers, vendors, collaborators, and other parties to ensure they align with the company’s interests and strategic priorities. Minimize legal risks in all agreements while facilitating smooth business operations and fostering positive relationships with key stakeholders. Develop new company policies and conduct periodic reviews of existing ones to ensure alignment with legal requirements and organizational goals. Provide Strategic Legal Advice for Informed Decision-Making Offer timely, accurate, and proactive legal counsel to executives on a range of issues, including partnerships, corporate finance, business, licensing, due diligence, employment law, and international ventures. Identify potential legal challenges early and provide solutions that support the company’s growth, innovation, and risk management strategies. 7. Competencies Required: Technical Competencies: Legal Expertise in Relevant Areas In-depth knowledge of contract law, employment law, and regulatory compliance, with a strong understanding of laws and regulations specific to medical research, clinical trials, and immunotherapy (e.g., data protection, patient privacy, and industry standards). Ability to interpret and apply complex legal frameworks to the company’s operations and strategic initiatives. Contract Drafting and Negotiation Proficiency in drafting, reviewing, and negotiating a wide range of contracts (e.g., Confidentiality Agreements, Services Agreements, MOUs, Collaboration Agreements, Investor Agreements) to protect the company’s interests. Skill in ensuring contracts are legally sound, clear, and aligned with the company’s goals while minimizing legal risks. Regulatory Compliance and Risk Management Strong understanding of the regulatory environment affecting the company, including laws related to clinical trials, data protection, and industry-specific compliance. Ability to identify potential legal risks, advise on mitigation strategies, and ensure the company’s adherence to all applicable laws and regulations. Soft Skills: Self-motivated Result oriented Independent & Team player Good listener Decisive Persistent Analytical & Detailed oriented Problem solver Initiative Continuous learner 8. Qualifications: Bachelor’s degree in law (LLB) or Master’s in law (LLM) At least 10 years of experience in law firm or in-house legal counsel positions, ideally within the biotechnology, life sciences, or pharmaceutical industries, with a strong grasp of the business operations and dynamics of these sectors. 9. Working Conditions: Role Type: Full Time and Onsite Work Hours: 9:00 AM to 6:00 PM for the General Shift and 2:00 PM to 11:00 PM for the Post-Noon Shift (on a rotational basis). There will be two days off each week, which may not necessarily fall on a Saturday or Sunday. Travel Requirements: Depends Base Location: Immuneel Therapeutics Private Limited, 8th Floor, Mazumdar Shaw Medical Center, Narayana Health City, Bommasandra Industrial Area, Bangalore - 560099 Show more Show less

Grow Your Career at Rephine – A Great Place to Learn & Thrive! At Rephine, we are global leaders in quality assurance and compliance for Life Sciences. Our mission? Ensuring the highest industry standards while safeguarding product quality in Pharmaceuticals, Biotechnology, Medical Devices, and Cosmetics. With offices in Stevenage, Shanghai, and India, we provide top-tier consulting services worldwide. Why Join Rephine? Here’s What Our Team Says: 💬 "Rephine is a great place to grow and expand your career." 💬 "You’ll find a positive and collaborative work environment here." 💬 "At Rephine, everyone is treated fairly and with respect." Now, we’re looking for an Administrative Assistant to provide crucial administrative support to our auditing department , specifically in completing contracts. This position is focused on administrative tasks like data entry, contract preparation, and document management—perfect for someone who enjoys supporting operations with precision and organization. We are not looking for a highly technical background, but rather someone who thrives in an administrative role and is eager to assist in the execution of tasks efficiently. What You’ll Do: Contract Preparation & Management 🔹 Draft, review, and process contractual documents, ensuring compliance with company policies and legal standards. 🔹 Maintain organized digital and physical records of contracts, agreements, and related administrative documents. Salesforce Data Entry 🔹 Accurately input and update client and contract information in Salesforce. Administrative Support 🔹 Assist with generating reports, managing databases, and coordinating document approvals. 🔹 Help prepare proposals, presentations, and client communications. Compliance & Confidentiality 🔹 Ensure all sensitive information is handled securely and in compliance with company policies. Collaboration 🔹 Work closely with the sales and operations teams to ensure contract accuracy and timely processing. What You Need to Succeed: ✅ Education & Experience • Bachelor’s degree or equivalent experience in administration, business, or a related field. Legal background is appreciated. • Previous experience in contract administration, data entry, or administrative roles (Salesforce experience is a plus). ✅ Skills & Mindset • Proficiency in Salesforce, Microsoft Office (Word, Excel, Outlook), and document management systems. • Strong accuracy in data entry and document preparation. • Excellent organizational and communication skills in English (other languages are a plus). • Proactive, self-motivated, and detail-oriented mindset. What We Offer: 💡 Competitive salary 🌍 A multicultural and dynamic international team. 🎉 A great work atmosphere. Ready to Grow Your Career? Be part of a company that values your growth, fosters a positive work environment, and ensures fairness for all. Apply now in English through our careers page! Show more Show less

Company Description Cipla Limited., Reputed Pharmaceutical Company Of India is a biotechnology company based in Lucknow, Uttar Pradesh, India. The company is known for its innovative pharmaceutical products and commitment to healthcare. Role Description This is a full-time on-site role for a Pharmacist at Cipla Limited. in Bhopal. The Pharmacist will be responsible for dispensing medications, providing drug information to patients and healthcare professionals, maintaining records, and ensuring compliance with regulatory requirements. Qualifications Pharmacy degree and valid pharmacist license Knowledge of pharmaceutical drugs and their effects Excellent communication and customer service skills Attention to detail and accuracy in dispensing medications Ability to work in a fast-paced environment Experience with pharmacy software systems Understanding of regulatory requirements in the pharmaceutical industry Previous experience in a similar role is a plus Show more Show less

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results. We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow. Learn about the Danaher Business System which makes everything possible. We are currently seeking a Flow Application Specialist at Chennai, who will be responsible for high-quality onsite customer support and represent the face of the company to our customers. Responsible for providing Instrument and application training to Beckman customers on site as per the requirement. To support the Sales Team in identifying market opportunities and assisting in actualizing market potential. Positioning of products and technology through presentations, product demonstrations, workshops, seminars, etc., in alignment with company values, business objectives, and marketing strategy. In this role, you will be responsible for: Application and Training Support: Provide Instrument and Applications training on Beckman coulter cell analysis range of products to ensure a high level of end-user satisfaction. Attend to resolve customer queries telephonically and over email and related applications and if necessary, planned visits to customers. Inclined to learn and improve technical knowledge and skills on existing and new Beckman Coulter products. Plan and organize training programs for Sales teams and the application team to raise and strengthen the technical bar and increase the capability of product knowledge. Marketing: Maintain active dialogue and interactions with key opinion leadership network in flow cytometry, immunology and cell biology. Sales support: Understanding the requirements of the customer’s experiment and provide appropriate technical and product solutions through discussions, presentations and/or product/application demonstrations to positively impact sales and increase productivity. Co-ordinate / support / lead awareness activities such as seminars, conferences, workshops etc in alignment with marketing team. Monitor your plan: Prepare and provide a monthly report to the supervisor on the training and marketing activities. Ensure timely submission of training and evaluation reports. Tracking of customer feedback on product quality and escalating product issues to the appropriate authority within the organization Activity: Work in coordination with sales, service, and other application associates towards achieving the business objectives. Support a culture of constructive feedback and continuous improvement within the organization. The required qualifications for the job include: B. Tech/ B. Pharma/ B.Sc. MLT with 2 yrs experience or MSc. With 1 year of experience in flow Cytometry or Ph.D. with experience in flow Cytometry publications. Minimum 2 years on a Beckman or other analyzer flow Cytometry platform and Sorter experience will be preferable. Two or more flow cytometry-focused publications (preferrable). Good interpersonal skills with the ability to communicate effectively both internally and externally at all levels. IT literate, good knowledge of Microsoft Office products & confidence with other IT applications. Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. At Beckman Coulter Life Sciences 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 Beckman Coulter Life Sciences can provide. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results. We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow. Learn about the Danaher Business System which makes everything possible. We are currently seeking a Flow Application Specialist at Bangalore, who will be responsible for high-quality onsite customer support and represent the face of the company to our customers. Responsible for providing Instrument and application training to Beckman customers on site as per the requirement. To support the Sales Team in identifying market opportunities and assisting in actualizing market potential. Positioning of products and technology through presentations, product demonstrations, workshops, seminars, etc., in alignment with company values, business objectives, and marketing strategy. In this role, you will be responsible for: Application and Training Support: Provide Instrument and Applications training on Beckman coulter cell analysis range of products to ensure a high level of end-user satisfaction. Attend to resolve customer queries telephonically and over email and related applications and if necessary, planned visits to customers. Inclined to learn and improve technical knowledge and skills on existing and new Beckman Coulter products. Plan and organize training programs for Sales teams and the application team to raise and strengthen the technical bar and increase the capability of product knowledge. Marketing: Maintain active dialogue and interactions with key opinion leadership network in flow cytometry, immunology and cell biology. Sales support: Understanding the requirements of the customer’s experiment and provide appropriate technical and product solutions through discussions, presentations and/or product/application demonstrations to positively impact sales and increase productivity. Co-ordinate / support / lead awareness activities such as seminars, conferences, workshops etc in alignment with marketing team. Monitor your plan: Prepare and provide a monthly report to the supervisor on the training and marketing activities. Ensure timely submission of training and evaluation reports. Tracking of customer feedback on product quality and escalating product issues to the appropriate authority within the organization Activity: Work in coordination with sales, service, and other application associates towards achieving the business objectives. Support a culture of constructive feedback and continuous improvement within the organization. The required qualifications for the job include: B. Tech/ B. Pharma/ B.Sc. MLT with 2 yrs experience or MSc. With 1 year of experience in flow Cytometry or Ph.D. with experience in flow Cytometry publications. Minimum 2 years on a Beckman or other analyzer flow Cytometry platform and Sorter experience will be preferable. Two or more flow cytometry-focused publications (preferrable). Good interpersonal skills with the ability to communicate effectively both internally and externally at all levels. IT literate, good knowledge of Microsoft Office products & confidence with other IT applications. Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. At Beckman Coulter Life Sciences 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 Beckman Coulter Life Sciences can provide. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

About: Sahajanand Medical Division Medical division is approved by state and central licensing authority and it delivers efficient performance to meet specific requirements. The SLTL brand stents embodies that bold spirit, offering a unique blend of our leading-edge technologies and time-tested engineering With Technical Collaboration & Patent Design, the company started indigenous manufacturing of Coronary products, since 2009. The company has dedicated in-house R&D department approved by DSIR (Department of Scientific and Industrial Research). We believe that every product we make, should stand for something. Something more than expected. And that’s why we don’t manufacture products for stereotypes. We build them for you. Kindly go through our websites mentioned below for further details. Website: www.sltlmedical.com Job Description: Designation: Executive Experience: 3 to 8 Years Department: QA Division: Medical Location: Gandhinagar Edu. Qualification: BSc/MSc - Biology/Biotechnology/Microbiology/Toxicology B.Pharma/M.Pharma Share CV on placement@sltl.com Show more Show less

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for a Sales Manager at Amnion Biosciences Pvt Ltd located in Amalāpuram. The Sales Manager will be responsible for leading and managing the sales team, achieving sales targets, developing sales strategies, building and maintaining client relationships, and analyzing sales data to improve performance. Qualifications Sales Management, Sales Strategy, and Client Relationship Management skills Strong negotiation and communication skills Experience in analyzing sales data and performance metrics Team leadership and management skills Ability to work in a fast-paced environment and meet sales targets Bachelor's degree in Business Administration, Marketing, or related field Previous experience in the biotechnology or pharmaceutical industry is a plus Show more Show less

Company Description Jananom is a premiere metabolic engineering company out of India. It has a flexible services model for its clients. The facility is located in Coimbatore in Tamil "Nadu Role Description This is a full-time on-site role located in Coimbatore for a Senior Scientist. The Senior Scientist will be responsible for designing and conducting experiments, analyzing and interpreting data, developing and optimizing processes, and preparing technical reports. The role requires collaboration with cross-functional teams, mentoring junior scientists, and staying updated with relevant scientific advancements. The Senior Scientist will also contribute to the development of new products and technologies. Qualifications Extensive experience in designing and conducting experiments in the area of metabolic engineering Strong data analysis and interpretation skills Experience in process development and optimization Proficiency in preparing technical reports and documentation Excellent collaboration, communication, and mentoring skills PhD or Master's degree in a relevant scientific field Experience in the biotechnology or pharmaceutical industry is a plus Ability to work independently and manage multiple projects Show more Show less

Title Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Medical Writer to join our Core Labs in Mumbai office. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. 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. Responsibilities •Generate, revise, and maintain clinical documents; •Coordinate quality control of documents and maintain audit trail of reviews and changes; •Provide input on data analysis planning and its impact on clinical document outcome ; and •Performs other duties and responsibilities as assigned. Qualifications Master’s degree in a health or science-related field; Possess strong communication skills (oral and written); Intermediate knowledge of medical terminology and clinical patient management; People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Biotechnology Full-Time Job ID: DGC00517 Chennai, Tamil Nadu 2-5 Yrs ₹03 - ₹06 Yearly Job description Role Purpose Assist in designing test plans, writing, executing and automating test cases for functional and/ or performance testing within the domain assigned Perform both guided and exploratory manual test executions following established processes Work as a member of the scrum team including planning, estimating, and verifying user stories and acceptance criteria Develop strong expertise in the assigned domain area Effectively communicate status, metrics, and issues on a regular basis Understanding and complying of/ to Revvity Signals practices Assist in creating test summary reports of high quality, written language and content Become a user expert on how our products work, gaining an understanding of the strengths and weaknesses, and championing customer issues in order to ensure they have a positive experience Qualifications Computer Science and/ or Science-based bachelors degree 7+ years of experience qualifying high-volume, scalable enterprise software Excellent experience working in an agile/scrum environment Excellent working knowledge of Windows/Linux operating systems Excellent understanding of Quality Assurance life cycle, methodologies and best practices Excellent knowledge in test case management and bug tracking systems such as Jira, Zephyr Minimum 2 years of experience with one of the automation tools like TestComplete, Selenium, VS Coded UI, or Playwright is necessary Experience with databases and data platforms Experience in testing systems at a large scale is a plus Experience with developing API test frameworks is a plus Experience with scripting languages like Python, TypeScript, and JavaScript Excellent experience in transforming manual test cases into automated test cases Experience in test documentation, defect analysis, tracking and reporting Knowledge and prior experience with BDD a plus Prior experience in the Chemistry/Biologics space is a nice to have Special Skills & Knowledge Solid experience in the domain assigned to Good English, written and verbal Key Competencies Passion for quality Ability to respectfully speak up on quality matters Strong emphasis on good UI design with meticulous attention to detail Self-motivated, independent thinker with excellent troubleshooting skills Ability to learn quickly and stay current with new technologies Ability to work within a multi-site, multicultural team Show more Show less