313 Biotech Jobs

Ct: HR GAYATHRI:7358125888 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM and CPT code Eligibility:Any lifescience,paramedical & medical UG/PG

Ct: HR SHANMUGAPRIYA -8072891550 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM and CPT code Elig:Any lifescience,paramedical & medical UG/PG

Role - Trainee Mode - Internship Qualifications MSC - Organic Chemistry A Trainee Research Scientist in Discovery performs hands-on organic chemistry, synthesizing and characterizing new molecules for drug discovery, working in a lab under supervision, documenting results, and collaborating with teams, focusing on practical skills in synthesis (TLC, column purification) and analysis

Seekout Online..... is an organized head hunters and staffing partner specialized in Oil & Gas, Power, Offshore in design engineering and construction area. To know more about us visit our website http://www.seekoutonline.com which will update you about our services and activities. One of our clients an Engineering Consultancy company having their based office in Bangalore are looking for following professionals:- Designations :- 1. Senior Piping Designer 2. Piping Autocad Plant 3d Admin Job Location: Bangalore Location (Permanent WFH) Experience:-10+ yrs Job Type:-Permanent Qualification:-B.E/B.Tech ,Diploma Candidates meeting the above profile can rush their detailed CV immediately to aksh...

Carry out the assigned Lean projects / transformations independently with zero conflicts by utilizing change management and project management skills Own, manage and track local Lean implementation plan (both short term during the Lean project but also long-term for continuous improvement) Ensure appropriate local resources are involved and trained during the Lean project and ensure sustenance Support in managing performance management infrastructure, namely the definition, tracking and reporting of KPIs, adequate structure of meetings and performance dialogues and definition and implementation of corrective action Coach/ train local Lean teams in Lean methodology and toolset following the L...

Please find the JD below. Planning and traveling for Food Safety audits Conducting Food Safety Audits as per FSSAI Schedule 4 requirements Generating the audit reports Submission of Audit Pack. Correction of audit reports as per technical review process Qualifications Minimum B.Tech/BE/B.SC- Food sciense/Biotech/ Foodtech/Food processing/Dairy Tech etc. Minimum 2-3 years of experience in the industry Candidates having ISO/FSSC 22000 lead Auditor certification and Minimum 20-30 audits experience, will be given preference.

Finding new business opportunities Potential to analyze opportunities and develop sales plans for each target account. Working exposure to multiple geographies (EU, USA, India etc.) Meet /exceed the business closure targets that are assigned based on budgets Experience in budget planning and management. Contacts in the Global Pharma / Biotech industry Experience of working in different geographies globally Sound knowledge in preparing annual, quarterly and monthly marketing plans with strategies Opportunities to learn and deliver these opportunities through the sales cycle to successful closure Qualifications 10+ years of overall Business Development, Marketing, and Business strategy experie...

In-depth scientific expertise in Genotoxicology, with significant experience in designing, executing, and interpreting genetic toxicology studies in both regulatory (FDA, EMA, ICH, and OECD guidelines) and non-regulatory environments. Responsible for the execution, planning, performance, reporting/archiving, and management of studies such as the Bacterial Reverse Mutation Test (Ames Test), Bone Marrow Micronucleus Test, Chromosome Aberration Test, and In Vitro Micronucleus Test etc. Preparation of study plans, protocols, amendments to study plans, study reports, creation, and review of SOPs. Lead and manage a team of genetic toxicologists, providing mentorship and guidance to achieve departm...

Leadership role to manage team size of 10+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Managing multiple instruments (LC-MSMS, GC-MSMS, ICP-MS, IC etc.) Method development experience in LC-MSMS, GC-MSMS and ICPMS instrument Preparation and Implementation of SOPs related to E& L , general laboratory processes and best guidance. Good knowledge of 21 CFR part 11, Data Integrity principals, good documentation practices in cGMP lab Monitor and management of day-to-day laboratory activities Extensive knowledge of preparation, reviewing and approval capability for standard operatin...

Ct: HR LAVANYA : 9566157632 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM & CPT code Eligibility:Any lifescience,paramedical & medical UG/PG

Ct: HR SHANMUGAPRIYA -8072891550 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM and CPT code Elig:Any lifescience,paramedical & medical UG/PG

Ct: HR DEEPA:7200179732 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM and CPT code Eligibility:Any lifescience,paramedical & medical UG/PG

Ct: HR LAVANYA : 9566157632 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM & CPT code Eligibility:Any lifescience,paramedical & medical UG/PG

Role Overview: You will be responsible for achieving defined revenue and cost goals in the Medical Devices sector. Your main tasks will include building proposals, actively participating in business development, leading and mentoring a team, and handling client communication. Strong communication skills, analytical mindset, and technical background will be essential for this role. Key Responsibilities: - Strive to achieve defined revenue and cost goals. - Build proposals with minimal support, including gathering requirements, formulating research solutions, designing commercial framework, and presenting solutions effectively. - Actively participate in business development tasks, articulate r...

Position Summary The Global Systematic Literature Review (SLR) Senior Associate provides expertise in designing, executing, and managing literature review services within Amgens Global HEOR function. The SLR Senior Associate will collaborate closely with team lead and Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen''s therapies through the generation of high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities Refine literature review questions in alignment with team lead and prepare research protocols. Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey li...

What you will do: We are seeking a detail-oriented and highly organized Content Metadata and Tagging Associate to join our content operations team. This role is critical to ensuring content is structured, discoverable, and aligned with brand standards through accurate tagging and metadata practices. The ideal candidate will have a strong grasp of content systems, metadata management, and interdepartmental collaboration. Key Responsibilities: Brand Information Management: Collect and document key brand messages, positioning statements, and content goals from stakeholders to inform metadata and tagging strategies. Metadata & Tagging Strategy Execution: Ensure all content meets defined tagging ...

Position Summary The Global HEOR Economic Modeling Senior Associate plays a critical role in supporting Amgens global market access and health economics strategy through the development of health economic models. This role will partner closely with team lead and Global HEOR Product Leads to ensure strong alignment with product strategy. The Economic Modeling Senior Associate will develop cost-effectiveness, budget impact, and other health economic models that reflect clinical and real-world data to inform HTA and payer decision-making. Key Responsibilities Design and develop hands on global core health economic models for products at all stages of development and launch, using cost-effective...

You are looking for a creative and confident STEM writer to join Diverge Communications, a specialized agency offering design and communication solutions tailored for life sciences and deep tech. They work with deep-tech, biotech, and science-forward organizations, helping them translate innovation into powerful stories. If you enjoy scientific storytelling and have proven writing experience, this role is perfect for you. **Key Responsibilities:** - Background in STEM (Biotech, Life Sciences, Engineering, or related fields) - Excellent writing skills and ability to simplify complexity - Experience writing blogs, explainers, video scripts, social media posts, technical content, or science com...

As an Specialist SAP Architect at Amgen, you will play a vital role in designing, configuring, and integrating SAP Production Planning and Manufacturing processes within S/4HANA across all Amgen manufacturing sites. Your focus will be on leveraging SAP technologies to streamline and enhance Manufacturing processes, ensuring alignment with business needs and industry best practices. Your responsibilities will include: - Designing, configuring, and implementing SAP S/4HANA PP and PP-PI modules aligned with life sciences clinical manufacturing best practices - Designing, configuring, and implementing SAP S/4HANA Quality Management processes - Supporting integration with QM, MM, WM/EWM, and PM m...

Quality Compliance Manager What you will do Lets do this! Lets change the world! We are hiring a Quality Compliance Manager, which will operate within the General Medicine & Obesity Quality Therapeutic Area. In this vital role you will provide proactive end to end quality support for the development and implementation of a risk-based quality assurance strategy that advances quality by design principles for the full clinical development program. (protocol development, database lock, and regulatory submissions/ approvals). Reporting to the Quality Compliance Associate Director, you will oversee quality management and ensure compliance for global and local clinical trials by supporting study te...

Position Summary The Global HEOR Economic Modeling Senior Associate plays a critical role in supporting Amgens global market access and health economics strategy through the development of health economic models. This role will partner closely with team lead and Global HEOR Product Leads to ensure strong alignment with product strategy. The Economic Modeling Senior Associate will develop cost-effectiveness, budget impact, and other health economic models that reflect clinical and real-world data to inform HTA and payer decision-making. Key Responsibilities Design and develop hands on global core health economic models for products at all stages of development and launch, using cost-effective...

Senior Associate, Incentive Compensation Inquiry & Data Operations What you will do In this vital role the Senior Associate, Incentive Compensation Inquiry & Data Operations will focus on managing inquiries, solving complex data challenges, maintaining data stewardship standards, and delivering ad-hoc analytics to support field and leadership decisions. Responsibilities Inquiry Management: Act as the primary point of contact for inquiries related to incentive metrics, payouts, and plan interpretation. Investigate and resolve inquiries promptly with clear, data-backed communication. Track and analyze inquiry trends to identify process or data improvement opportunities. Demonstrated ability to...

What you will do In this vital role you will [support the maintenance of organizational designs and execution of organizational design projects within Amgen. This role will involve partnering with HR, Finance, and functional organizations to develop and maintain organizational designs tailored to organizational objectives. Responsibilities: Utilize organizational design software and modeling tools to analyze and model organizational designs aligned with organizational strategies Support organizational design initiatives by providing advice and guidance and driving the creation of supporting materials. Generate scenario analyses and engage with in-house analytics capabilities on implications ...

What you will do The Global Mobility Manager is responsible for developing, managing, and executing relocation and immigration strategies that support the international talent mobility needs of a rapidly growing biotech company This role ensures compliance with immigration laws and regulations, delivers a seamless relocation experience, and supports talent acquisition and retention efforts across multiple countries Key Responsibilities Include: Immigration Management Oversee all global immigration processes, including work permits, visas, green cards, and permanent residency for employees and their families. Partner with external immigration counsel to ensure timely and compliant case manage...

What you will do The Manager, Incentive Compensation, Squad plays a vital role in ensuring the accuracy, transparency, and operational excellence of Amgens Incentive Compensation (IC) programs This role serves as the end-to-end IC project lead and point of contact for US Team for an assigned business unit, responsible for managing IC processes, coordinating cross-functional activities, and ensuring the delivery of high-quality outputs across all incentive workstreams Responsibilities End-to-End Incentive Compensation Project Management: Serve as the IC project lead and point of contact for US Team, overseeing all aspects of the IC lifecyclefrom plan design inputs to final payout delivery. De...