3586 Biotechnology Jobs - Page 10

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Rubini-9600405840 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Data Engineer What You Will Do Let’s do this. Let’s change the world. Amgen India will be an integral part in driving growth & innovation, improving efficiency and creating enterprise value – supporting our mission “To Serve Patients”. The Amgen India Digital Technology & Innovation Data Engineer for Clinical Data Hub will be responsible for end-to-end design, development and DevOps of data pipelines for clinical data domain across technology platform and stacks. This role will leverage the latest technology to develop advanced data engineering pipeline and system solution to enable advanced data analytics for Amgen Clinical trial design and development. across various global clinical development business functions. As the results, comprehensive clinical domain datasets and systems are up-to-date and ready for advanced clinical trial design and development insight generation analytics Design, develop, and deploy data pipeline for clinical domain dataset As an infrastructure programmer, continuously develop and support Data Scientist R-Platform and integration with various technology (Kubernetes Container, HashiCorp Vault, SAS Storage, and Data Science Work Bench) Design and build various reusable program components using innovative technology (NLP, AI, Python, R, etc) to transform and harmonize clinical dataset for insight generation Collaborate with Data Architects, Business SME’s, and Data Scientists to capture the business requirement and translate into Agile product backlog Serve as primary data engineer to manage and support AWS, Databricks, RStudio platform, and cloud AI based system production DevOps Align to best practices for coding, testing, and designing reusable code/component Explore new tools and technologies that will help streamline data pipeline and add new durable capability for clinical development Participate in sprint planning meetings and provide estimations on technical implementation Collaborate and communicate effectively with the product teams What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. What We Expect Of You Basic Qualifications: Master's degree / Bachelor's degree and 5 to 9 years [Job Code’s Discipline and/or Sub-Discipline] Must Have Skills: Advanced skills in SQL, Python, and R languages programing; AWS cloud technology and databricks data lake technology stacks Proficient skills and knowledge on common AI/Machine Learning technologies. Data modeling skills, and software development lifecycle knowledge and standard processes Learning ability of new technology in the information field Skill of using DevOps CI/CD tools, such Git, Jenkins and front UI Visualization technology Good to Have Skills: Work experience in the biotechnology or pharmaceutical industry. Experience using and adopting Scaled Agile Framework (SAFe) Ability to work effectively in a fast-paced, dynamic environment. Experience with data modeling for both relationship databases, hands-on experience with SQL (PostgreSQL and Hive SQL is preferred) Experience with UI Visualization technology (Dash, RSConnect, Tableau preferred) Knowledge and experience in clinical trial design and development process and technology landscape, familiar with clinical trial data standards and structures Certification: SAFe for Teams certification (preferred) Soft Skills: Strong communications skills in writing, speaking, presenting and time management skills Strong transformation and change management experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. What You Can Expect Of Us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Manager - International Regulatory Lead Role Name: Manager – International Regulatory Lead (IRL) Department Name: International Regulatory Team, Global Regulatory Affairs Role GCF: 5A 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 The International Regulatory Lead (IRL) Manager will provide regulatory leadership & expertise for International countries for one or more Amgen products. This role involves collaboration with various functions and local regulatory teams to optimize product development and regulatory approvals in International countries develop international regulatory strategy and provide regulatory support for in-country product registrations and life cycle management. Roles & Responsibilities Advises Global teams on regulatory implications and requirements relevant to the global clinical development, Marketing Applications plans and objectives. Provides regulatory direction/expertise on the international regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, expedited regulatory designations, regulatory reliance mechanisms, compassionate use and pediatric plans). Under general supervision, plans regulatory submissions (e.g. clinical trial, marketing authorization applications and lifecycle management) for products within Amgen's portfolio. Under general supervision, contributes to the development of international regulatory strategy documents (regulatory product filing plan, strategies, risks associated with the potential Agency outcomes and contingency planning, estimate likelihood of success) and communicates to others, as appropriate. Provides and maintains clinical trial and/or marketing application documentation (excluding Chemistry, Manufacturing & Controls documentation). May author documents/redact such documents to support a regulatory filing. Directs development of and manages the international label submission strategy, leads the negotiation activities with cross-functional teams and is accountable for the label deviation requests and outcomes. Supports local regulatory teams in triaging queries from health authorities, and where appropriate, helps identify existing responses to same or similar questions, leveraging knowledge management. Participates as a member of the Global Regulatory Team (GRT), and various global clinical and labelling focused teams. Shares regulatory information and implications with the GRT and other global teams on an ongoing basis and provides advice on international considerations. Partners with peers to agree on product strategy including projected submission and approval time. Maintains regular communications with the local teams to ensure alignment on strategy and to share product development status. Builds effective relationships and communication paths across the global, regional and local elements of the global regulatory affairs function. Maintains an awareness of new and developing legislation, regulatory policy and technical regulatory guidance relating to Amgen products. Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement. Basic Qualifications And Experience Doctorate degree OR Master's degree and 3 years of relevant regional regulatory experience OR Bachelor's degree and 5 years of relevant regional regulatory experience OR Associate degree and 10 years of relevant regional regulatory experience OR High school diploma/GED and 12 years of relevant regional regulatory experience. Functional Skills Must-Have Skills Knowledge and experience in the international regulatory environment of clinical trial applications, non-clinical and/or clinical variations to marketing authorizations and product labelling relevant for biotechnology and/or oncology products Comprehensive knowledge of regulatory principles and understanding of regulatory activities, and how they impact other projects and/or processes General awareness of the registration procedures/challenges in International countries for Clinical Trial Applications, Marketing Applications and lifecycle management activities. Good-to-Have Skills Ability to resolve conflicts and develop a course of action leading to a beneficial outcome Cultural awareness and sensitivity to achieve results across country, regional and international borders. Soft Skills Strong communication skills, both oral and written Ability to understand and communicate scientific/clinical information Ability to work effectively with global, local and virtual teams High degree of initiative and self-motivation Planning and organizing abilities Ability to manage multiple priorities successfully Team-oriented, with a focus on achieving team goals Good negotiation and influencing skills. 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 Associate QC – QC Systems Templating Role Name: Sr Associate QC Department Name: Quality Control Role GCF: 4 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: Let’s change the world. Amgen is hiring for a Senior Associate to support the Electronic Lab Notebook (ELN) and consumable inventory system infrastructure in the Quality Control (QC) network. This candidate will primarily work a shift-based schedule to enable the business in delivering Amgen’s mission to serve patients. The candidate may need to work outside of his/her routine workday to support business needs. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN), and provide remote support from AIN to Amgen sites across multiple time zones globally. Roles & Responsibilities: This position will be responsible for creating, revising, peer-reviewing and qualifying templates for analytical method executions in ELN which includes ELN interfaces with other systems such as LIMS, Empower, and Chromeleon. Creation and revision of consumable templates, and supplementary master data will also be in the scope of responsibility. In addition, this position will collaborate with the US-based Master Data Group (MDG) and will also be involved in ELN template administration/registration activities, ensuring tasks align with procedures, best practices, and service level agreements for QC standardization. Coordination with site representatives and other ELN template builders and qualifiers is required to convert QC source documents into ELN templates accurately. Coordination with members within the team at AIN on the same shift and members of the team at AIN on different shifts will be critical in ensuring deliverables are met in accordance with schedule. To effectively provide support, candidates must demonstrate proficiency in virtual communication tools and have experience managing remote collaborations. Secondary responsibilities may include cross-training into LIMS, Empower, and Chromeleon. The following are some examples of tasks for the position Creation and revision of ELN templates Peer reviewing templates built by colleagues Qualification of ELN templates Creation and revision of consumable templates Collaboration with method subject matter experts, template builders and template qualifiers throughout the QC network Ensuring training is up to date Additional responsibilities may involve: Providing performance metrics Driving global QC system alignment Understanding prioritization of requests with the QC network Basic Qualifications and Experience: Any degree with 5-8 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience Functional Skills: QC lab testing experience Proficiency in ELN applications Knowledge of Data Integrity Requirements for QC systems Microsoft Office proficiency Familiarity with Good Manufacturing Practices Soft Skills: Excellent English verbal and written communication skills Problem-solving and troubleshooting abilities Independence in delivering right first time 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.

Company Name VM Bakery Products Pvt Ltd Job Title Production & Quality Internship Job Location: Vijayawada Description We are inviting passionate students to apply for stipend-based internships in Production and Quality Control at our bakery unit in Vijayawada. 📍 Location: Vijayawada 📆 Duration: 6 months to 1 year 💰 Stipend: Based on performance and duration 🎓 Eligibility B.Tech / B.Sc / M.Sc – Food Technology, Biotechnology, Microbiology Basic knowledge of GMP, FSSAI preferred No. of vacancy – 08 Experience – Freshers 🔧 Departments Production – Mixing, Baking, and Packing Operations Quality – QC/QA, Documentation, Food Safety ⸻ 🔹 Key Learning Areas ▪ Production line operations ▪ Mixing, baking & packing flow ▪ Hygiene & food safety practices ▪ Quality testing & internal audits ▪ FSSAI, HACCP, GMP systems ▪ Documentation & traceability Apply Here hr@justbreads.co.in

We currently have exciting opportunities available for Business Development Specialist on behalf of our esteemed biosupplier client. Position: Business Development Executive (Lab Instruments) Location: Pune Education & Experience: Qualification: Advanced Science degree in Molecular Biology, Biochemistry, Biotechnology, Life Sciences , or a related field. Experience: 3 – 6 years of relevant experience in scientific product sales. Role Overview: We are seeking a dynamic Business Development Specialist for our esteemed biosupplier client . The ideal candidate will be responsible for promoting scientific products, providing technical assistance, and driving sales in academia, pharma, biotech, CROs, and allied industries. Key Responsibilities: Sales & Business Development: Promote scientific products to institutes, academia, industries, pharma, biopharma, CROs, and allied customers . Generate leads for all company lab products and develop new business opportunities. Represent the company at local/regional vendor shows , delivering seminars and poster presentations . Customer & Technical Support: Provide product training to customers and ensure proper usage of sold equipment. Offer scientific and technical assistance to users, addressing queries and troubleshooting issues. Communicate via phone and email to support customers with Data Analysis software . Product & Market Knowledge: Develop in-depth expertise on Channel Partner products such as Agilent, Syngene, Nuaire, AES, GESIM, etc. Stay updated on new assays and industry advancements to provide the best solutions to customers. Reporting & CRM Management: Maintain daily/weekly reports using the CRM system , detailing customer visits, lead generation, sales demonstrations, and other field activities. Required Skills & Competencies: Excellent verbal and written communication skills with strong presentation abilities. Moderate knowledge of ELISA, PCR, Flow Cytometry, Electrophoresis, Imaging, Fluorescence, and Luminescence assays , gained in an academic or industrial lab. Ability to diagnose complex instrumentation and application issues . Strong computer proficiency and experience with data reduction tools . Willingness to travel as required.

LIMS Master Data Specialist What You ll Do As a LIMS Master Data Specialist you will: Review source documentation for master data objects such as laboratory methods and analysis Create/ build master data objects in the LIMS, including test methods, specifications, sample plans, and instruments Produce builds in an iterative manner Conduct demo / review sessions with key stakeholders, provide support and answer questions from business Ensure data consistency, accuracy, and compliance with internal SOPs and external regulatory requirements (e.g., FDA, ISO, GxP) Support LIMS validation activities, including documentation and testing. Troubleshoot and resolve data-related issues within the LIMS Collaborate with a team of master data builders working across various sites for the LIMS deployment What We re Looking For: 2+ years of experience working with LIMS platforms (Ideally, LabVantage, at a minimum, LabWare, STARLIMS, Thermo Fisher SampleManager) Strong understanding of laboratory operations and data management principles Experience with master data configuration for LIMS systems Excellent attention to detail and problem-solving skills Strong communication and collaboration abilities Experience in a regulated industry (e.g., pharmaceuticals, biotech, food safety) Knowledge of GxP, 21 CFR Part 11, and other regulatory frameworks Bachelor s degree in Life Sciences, Information Technology, or a related field

Job Summary: We are seeking a dynamic and results-oriented Business Development Manager to drive growth in our Pharmacovigilance services sector, with a special focus on integrating Artificial Intelligence (AI) solutions. The ideal candidate will possess strong knowledge of pharmacovigilance processes, regulatory compliance, and AI-driven innovations, coupled with a proven track record in business development and client relationship management within the life sciences industry. Key Responsibilities: 1. Strategic Growth Development: Identify, evaluate, and pursue new business opportunities in the pharmacovigilance domain, including AI-powered solutions. Develop and implement strategies to expand the company’s market presence and client portfolio. 2. Client Engagement: Build and maintain long-term relationships with pharmaceutical companies, biotech firms, and regulatory agencies. Understand client needs and propose tailored PV and AI solutions. 3. AI Integration in PV Services: Promote AI-driven tools and solutions for adverse event reporting, signal detection, and risk management. Stay updated on emerging AI trends and translate them into business opportunities. 4. Cross-functional Collaboration: Work closely with technical teams, including pharmacovigilance, AI, and data science experts, to develop customized service offerings. Collaborate with marketing to craft compelling proposals, presentations, and campaigns. 5. Market Analysis and Competitive Intelligence: Conduct market research to identify trends, competitive landscape, and emerging needs in PV and AI. Leverage insights to refine business strategies and solutions. 6. Revenue Growth and KPI Achievement: Achieve revenue and sales targets through consistent business development efforts. Monitor and report on sales performance and market dynamics. Qualifications: Educational Background: Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field. Advanced degree (MBA, MPH, or MSc) preferred. Experience: 5+ years of experience in business development within pharmacovigilance, life sciences, or healthcare. Hands-on experience with AI tools or services applied to PV is highly desirable. Skills and Competencies: Deep understanding of pharmacovigilance processes, regulations (e.g., FDA, EMA, ICH guidelines), and compliance standards. Familiarity with AI applications such as natural language processing, machine learning, and automation in pharmacovigilance. Excellent communication, negotiation, and presentation skills. Ability to work in a fast-paced, goal-oriented environment. Preferred Certifications: Certification in pharmacovigilance (e.g., Advanced Pharmacovigilance by DIA) or AI-related courses. What We Offer: Competitive salary and performance-based incentives. Opportunity to work with cutting-edge technologies in PV and AI. A collaborative and inclusive work environment.

Job description: Eligibility Criteria: Designation: Trainee Medical Coder Qualification: B.Pharma & M.Pharma (No Standing Arrears) Should have 60% in all the academics Work From Office only Work Location: Kochi, Kerala Shift: Day Age limit: 28 Yrs Salary: As Per Industry Interested Candidates share your resume durgadevi.chandrasekaran@corrohealth.com Durga HR 8248059972

Job Title: Electrocatalysis Scientist Location: Bodhgaya, Bihar (On-Site) Job Type: Full-time Joining Type: Immediate preferred About Us Technoculture Research is re-imagining how the world measures health. We build micro-scale electrochemical laboratories that place lab-grade accuracy directly in the hands of clinicians, community health workers and even patients at home. Our platform fuses microfabricated electrodes, novel surface chemistries and microfluidics to run protein, nucleic-acid and metabolite assays within minutes. By replacing costly optical detection with electron sensing, we slash instrument and per-test costs by roughly an order of magnitude, making precision diagnostics truly accessible. Our mission is clear: make diagnostics abundant so that every critical health decision is guided by immediate, affordable results, wherever care happens. Looking Ahead: Bio-Energy R&D Leveraging the same core strengths in electrochemistry, biotechnology and process miniaturisation, Technoculture Research is now exploring bio-energy technologies—from electrochemical green-hydrogen and ammonia synthesis to sustainable liquid-fuel production. This expansion will allow us to apply our platform science to the urgent challenge of low-carbon energy and chemicals, while staying true to our ethos of cost-compressed, data-rich solutions. www.technoculture.io Job Description We are seeking a PhD-level Electrocatalysis Scientist with deep expertise in electrolysis and electrocatalytic systems . The ideal candidate will have strong theoretical and experimental foundations in electrochemical reaction optimisation and a demonstrated interest in CO₂ electroreduction and cell-free enzymatic systems . This role is central to our efforts in building integrated electrochemical-biochemical platforms for sustainable fuel and chemical production. Responsibilities Design, execute, and optimise electrocatalytic processes for applications like CO₂ electroreduction , water electrolysis , and nitrogen reduction . Analyse and model electrochemical systems for improved reaction kinetics , selectivity , and energy efficiency . Explore the integration of cell-free enzymatic cascades within electroenzymatic reactor systems . Evaluate new electrode materials , catalysts , and electrochemical cell designs . Conduct literature and patent reviews to support innovation in hybrid catalytic systems. Closely document experimental setups, procedures, and data. Collaborate with enzyme scientists, materials engineers, and simulation experts across projects. Participate in candidate evaluations by reviewing PhD theses and prior academic work. Qualifications PhD in Electrocatalysis , Electrochemistry, or a closely related field. Strong understanding of electrochemical fundamentals , including reaction kinetics, mass transport, and cell design. Preferred Qualifications Hands-on experience with CO₂ electroreduction , water splitting, or similar electrocatalytic processes . Familiarity with cell-free enzyme cascades or electroenzymatic systems. Demonstrated ability to work with electrode materials , potentiostats , and custom electrochemical reactors . Scientific publications or thesis work related to CO₂ conversion , electrocatalysis , or hybrid bio-electrochemical systems. Personal Attributes Technically strong with a keen interest in cross-domain research . Analytical thinker with deep attention to experimental detail. Self-motivated and comfortable working in multidisciplinary teams. Excellent documentation, data interpretation, and communication skills. Willingness to review candidate research (especially PhD theses) critically during hiring.

Be the First to Apply Summary Job Description The Senior Manager, Business Development will develop and maintain business relationships with existing and potential clients. This individual is also responsible for managing existing business in the US for Piramal’s medicinal chemistry services business. Experience Minimum requirement of a BS/ MS in any Life Sciences (Preferably Chemistry, Pharmacy) PhD and or MBA desired 5 to 10 years of experience selling Medicinal Chemistry services to the pharmaceutical / biotechnology industry in the US, or in a project manager role managing chemistry collaborations in a large pharma or biotech. Skills And Competencies Solid demonstration of negotiation and sales skills including strategic thinking and key account management Solid and demonstrable experience of selling medicinal chemistry, preclinical research services into biotech, mid-size and large pharmaceutical companies or Sr. Scientist / Principal Scientist (Medicinal Chemistry) who have managed CRO collaborations looking to transition to a sales role. Should have a good network within US biotech/ pharma community Strong communication skills Willingness and ability to learn and grasp new ideas both independently and collaboratively Highly organized with an ability to work effectively to deadlines. A high attention to detail with an ability to follow through on commitments Key Roles Selling Piramal Pharma Solutions Medicinal Chemistry Support (Synthesis & in-vitro DMPK) & Route scouting Services in the US Identify and engage with new prospective clients and maintain existing business Coordinate initial client visits to the Piramal’s Discovery Services facility in India Prepare and deliver client proposals in collaboration with Program Managers Negotiate agreements of sale and achieve yearly sales objectives Managing Sales activities on a CRM platform Contribute to the implementation of marketing initiatives including providing market information, attending relevant tradeshows Develop and maintain a current understanding of the external marketplace (e.g. conditions, trends and competitors) as well as internal capabilities and technologies Maintain a current knowledge of sales and project management skills and techniques Job Info Job Identification 9172 Job Category Business Development Posting Date 07/28/2025, 01:18 PM Job Schedule Full time Locations Ash Stevens LLC, Riverview, MI, 48193, US

We are looking for a highly skilled and experienced MD Dermatologist Consultant Doctor to join our team at Skinfinity Derma Clinic. The ideal candidate will have 2-7 years of experience in dermatology. Roles and Responsibility Conduct thorough medical examinations and diagnose various skin conditions. Develop and implement effective treatment plans for patients with different skin conditions. Perform surgical procedures, such as biopsies and excisions, as needed. Provide guidance on preventive measures to minimize the risk of skin cancer and other diseases. Collaborate with other healthcare professionals to ensure comprehensive patient care. Stay updated with the latest developments in dermatology through continuous learning and professional development. Job Requirements Hold an MD degree in Dermatology from a recognized institution. Possess strong knowledge of dermatological procedures and treatments. Demonstrate excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment and prioritize tasks is essential. Strong analytical and problem-solving skills are required. Commitment to providing high-quality patient care and maintaining confidentiality.

Responsibilities: * Conduct biochemistry, biotech, biomedical tests with IVD equipment * Prepare samples for ELISA assays and RT-PCR analysis * Ensure quality control through documentation and QA processes

Job Title: Enzyme Development Scientist Location: Bodhgaya, Bihar (On-Site) Job Type: Full-time Joining Type: Immediate preferred About Us Technoculture Research is re-imagining how the world measures health. We build micro-scale electrochemical laboratories that place lab-grade accuracy directly in the hands of clinicians, community health workers and even patients at home. Our platform fuses microfabricated electrodes, novel surface chemistries and microfluidics to run protein, nucleic-acid and metabolite assays within minutes. By replacing costly optical detection with electron sensing, we slash instrument and per-test costs by roughly an order of magnitude, making precision diagnostics truly accessible. Our mission is clear: make diagnostics abundant so that every critical health decision is guided by immediate, affordable results, wherever care happens. Looking Ahead: Bio-Energy R&D Leveraging the same core strengths in electrochemistry, biotechnology and process miniaturisation, Technoculture Research is now exploring bio-energy technologies—from electrochemical green-hydrogen and ammonia synthesis to sustainable liquid-fuel production. This expansion will allow us to apply our platform science to the urgent challenge of low-carbon energy and chemicals, while staying true to our ethos of cost-compressed, data-rich solutions. www.technoculture.io Job Description We are seeking a highly skilled Enzyme Development Scientist with a strong foundation in enzyme production , molecular cloning , and protein analysis . The ideal candidate will be technically robust, with working knowledge or deep interest in cell-free enzymatic cascades or electroreduction of CO₂ . You will contribute to projects spanning diagnostics, sustainable chemistry, and synthetic biology, playing a key role in enzyme design, production, and optimisation workflows. Responsibilities Design and optimise enzyme production pipelines , including microbial overexpression and purification. Perform molecular cloning , plasmid construction, and strain development for high-yield enzyme expression. Analyse enzymes using molecular biology and bioinformatics tools , including sequence analysis and structural modeling. Contribute to the development of cell-free enzymatic systems , especially those relevant to electroenzymatic reactors . Participate in the design of enzyme mimics and evolutionary strategies . Collaborate with teams working on CO₂ electroreduction and hybrid electro-biocatalytic platforms . Maintain meticulous documentation of protocols, results, and findings. Qualifications Master’s or PhD in Biotechnology, Molecular Biology, or Microbiology . Demonstrated experience in enzyme production and bacterial expression systems . Preferred Qualifications Proficiency in molecular cloning , expression vector design, and strain engineering. Strong understanding of bioinformatic analysis , including protein sequence alignment, motif identification, and structure-function prediction. Exposure to or interest in cell-free enzymatic cascades or electrochemical applications of enzymes . Familiarity with enzyme evolution tools like error-prone PCR , site-directed mutagenesis , and recombinant library screening . Personal Attributes Technically rigorous, with a scientific mindset and problem-solving ability. Detail-oriented and organised in experimental execution and data interpretation. Strong collaboration and communication skills in cross-disciplinary teams. Curious, adaptable, and motivated to explore hybrid biochemical-electrochemical platforms . Open to feedback and able to think critically about their own and others' research work.

Job Title: Regulatory Affairs & Quality Assurance Executive Location: Devine Meditech – e.g., New Delhi / Okhla / Industry: Medical Devices (e.g., Ophthalmic Products, IOLs) Salary: ₹40,000 to ₹60,000 per month (based on experience) Experience Required: 3 to 5 years in RA/QA in a medical device manufacturing company Key Responsibilities: Regulatory Affairs Preparation and submission of regulatory dossiers for Indian (CDSCO) and international (e.g., CE, ISO 13485) approvals Handle device registration, license renewals , and technical file creation Ensure compliance with Indian Medical Device Rules (IMDR) and applicable global regulations Liaise with regulatory authorities and consultants for product approvals and clarifications Maintain and update Device Master Files (DMF) and regulatory databases Quality Assurance Implement, monitor, and maintain ISO 13485:2016 QMS Conduct and document internal audits, CAPA, and risk assessments Draft, review, and control SOPs, BMRs, validation protocols (IQ/OQ/PQ) Manage change control , non-conformance (NC), and customer complaint handling Coordinate training programs for employees on QMS and regulatory practices Candidate Profile: Educational Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc / B.Tech in Biotechnology, Biomedical, or related science Experience: 3 to 5 years in QA/RA for medical devices (especially Class B or C preferred) Sound knowledge of: ISO 13485:2016 Indian Medical Device Rules (IMDR) 2017 Technical File and Design Dossier compilation Regulatory inspections and audits Familiarity with ophthalmic products / surgical implants / IOLs is a plus Key Skills: Regulatory documentation Quality Management Systems Problem-solving and critical thinking Technical writing and communication Internal and external audit readiness Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹57,873.20 per month Benefits: Paid sick time Work Location: In person

ILA BIOAMRINE founded in 2007 is purpose driven company, a leading marine biotech ingredients and formulation importer & distributor in personal care, health care, feed & agri input industry . With our Blue Biotechnology expertise, we offer the perfect combination of innovative, natural, organic & sustainable solutions to multiple leading personal care brands. Be part of ILA BIOMARINE – a purpose-led business as you work to impact the business and the world; we'll work to help you become a better you! Job Description: Marketing & Sales Executive – Personal Care Ingredients & Formulations Location: NCR, New Delhi Experience: 5–7years in B2B sales within personal care, cosmetics, or specialty ingredients sectors Education: B.Tech Cosmetics or B.Sc./M.Sc. in Microbiology, Biotechnology, Pharmacy or Chemistry Salary Range: ₹6–9 Lakhs per annum CTC (based on experience) Reporting To: Business Head / COO Key Responsibilities · Business Development: Identify and engage potential B2B clients in the personal care industry, including cosmetic brands, contract manufacturers and R&D labs. · Client Relationship Management: Maintain and nurture existing client relationships, ensuring high levels of customer satisfaction. · Technical Consultation: Provide clients with technical insights and recommendations on marine biotech ingredients and formulations. · Market Analysis: Monitor industry trends, competitor activities, and customer feedback to inform sales strategies. · Reporting: Prepare regular sales reports, forecasts, and market analysis for management review. Desired Skills & Attributes · Industry Knowledge: Familiarity with personal care ingredients, formulations, and industry standards. · Sales Acumen: Proven track record in B2B sales and client acquisition. · Technical Proficiency: Ability to understand and communicate complex technical information effectively. · Digital Savvy: Experience with digital marketing tools and platforms is a plus. · Communication Skills: Excellent verbal and written communication abilities. · Team Player: Collaborative mindset with the ability to work cross-functionally. . Ready to Travel extensively Job Types: Full-time, Permanent, Freelance Pay: ₹50,000.00 - ₹75,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Internet reimbursement Work from home Supplemental Pay: Performance bonus Experience: B2B Marketing: 3 years (Required) Work Location: Remote

Location: Patparganj, Delhi Duration: 2 Months Internship Stipend: 10 k Department: Marketing / Communications About the Role: We are looking for a passionate and creative Marketing Intern with a B.Sc. background and strong exposure to scientific writing and content creation . The ideal candidate will support our marketing team by crafting clear, engaging, and informative content tailored to our scientific audience. Key Responsibilities: Write, edit, and publish scientific blogs, articles, and web content . Create content for social media posts, newsletters, and marketing campaigns . Translate complex scientific topics into easy-to-understand content. Collaborate with the marketing and product teams to generate creative content ideas. Assist in developing and executing content calendars. Perform research and ensure scientific accuracy in all written materials. Requirements: Bachelor’s degree in Science (B.Sc.) – Biology, Chemistry, Biotechnology, or related fields preferred. Strong scientific writing and editing skills . Experience in blog writing, content creation , or academic writing. Good command of English communication and strong attention to detail. About Company: Introduction Video link: https://youtu.be/YKWbPCGFMzw?feature=shared Job Type: Internship Contract length: 2 months Pay: ₹9,000.00 - ₹10,000.00 per month Schedule: Day shift Work Location: In person

About Turing: Turing is one of the world’s fastest-growing AI companies accelerating the advancement and deployment of powerful AI systems. Turing helps customers in two ways: Working with the world’s leading AI labs to advance frontier model capabilities in thinking, reasoning, coding, agentic behavior, multimodality, multilinguality, STEM and frontier knowledge; and leveraging that work to build real-world AI systems that solve mission-critical priorities for companies. Role Overview. In this role, you will be working on projects to help fine-tune large language models (like ChatGPT) using your strong analytical and english comprehension skills The ideal candidate should have a solid foundation in Biology, particularly at the level expected in engineering entrance exams, as well as graduate or PhD-level programs. You should be able to break down complex biological concepts into simple, clear explanations and work efficiently. The projects will also help you learn how to leverage AI to be a better analyst. This is your chance to future-proof your career in an AI-first world! What does day-to-day look like: Design and solve challenging Biology problems to probe the limitations of large language models. Develop high-quality, step-by-step solutions with clear and rigorous reasoning. Collaborate with LLM researchers to align problem types with evaluation goals, especially in areas where models typically struggle (e.g., conceptual abstraction, multi-step reasoning, and data interpretation). Contribute to defining new evaluation benchmarks based on Biology curricula spanning early undergraduate to PhD-level topics. Requirements: Candidates pursuing a Master’s/Ph.D./Postdoctoral degree in Biology, Biotechnology, Biochemistry, or a related field are eligible and encouraged to apply. Good research and analytical skills Ability to provide constructive feedback and detailed annotations. Creative and lateral thinking abilities. Excellent structured communication and collaboration skills in a remote setting. Self-motivated and able to work independently in a remote setting. Desktop/Laptop set up with a good internet connection. Note: This position is open only to candidates who have completed or are currently pursuing a Ph.D.; applications that do not meet this criterion will not be considered. Preferred Qualifications: Ability to analyze and solve complex biological problems with a structured approach. Ability to explain Biology concepts clearly using simple language, visuals, and simulations when needed. Perks of Freelancing With Turing: Work in a fully remote environment. Opportunity to work on cutting-edge AI projects with leading LLM companies. Potential for contract extension based on performance and project needs. Selection Process: Shortlisted experts may be asked to complete an assessment. If you clear the assessment, you will be contacted for contract assignments with expected start dates, durations, and end dates. Some contract assignments require fixed weekly hours, averaging 20/30/40 hours per week for the duration of the contract assignment.

*Product Specialist- Biotech/Bio Pharma* Life Technologies India Pvt. Ltd., one of the premier suppliers in the biotech industry serving science for over 23 years, is looking to hire a Product Specialist with 3–5 years of experience. The ideal candidate must hold an M.Sc. in Biotechnology and have proven experience in product management, marketing, or digital promotions. This role demands strong technical and analytical capabilities, along with a customer-focused mindset tailored to R&D, biopharma, and biotech segments. Please note this is not an entry-level position. *Salary will be commensurate with the best in the industry*. Job Type: Full-time Pay: ₹500,000.00 - ₹500,001.00 per year Expected Start Date: 01/08/2025

Work Flexibility: Hybrid or Onsite What you will do Independently processing results of PFA assessments. Initiate, organize and coordinate global containment actions Ensure that data is documented for the different sites. Together with the PFA specialist create a communication to affected parties. Provide necessary information to regulatory compliance team for reporting. Presenting PFA/commercial hold relevant processes and cases during audits Preparing weekly, monthly and quarterly Commercial Hold relevant statistics Performing training of colleagues and managers by procedural changes What you need Required Skills: B. Tech / M.Tech Mechanical, Biotechnology with hands on experience of working on PFAs, and Commercial Holds. Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability. Poses the ability to lead colleagues in other departments to perform the necessary actions for a timely Containment action Hands on experience of Risk Management process as per ISO 14971 Demonstrated ability to work effectively with various work groups to assure conformance to regulatory requirements, internal processes, and policies. Sound knowledge on complaint handling process of medical devices will be an added advantage Applied understanding of GDP, ISO 9001 & ISO 13485 (Good to have).Good understanding of FDA 21CFR Part 822 / 820 (Good to have) Preferred Skills: Demonstrated ability to self-motivate, ability to prioritize tasks in a deadline-driven environment. Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams. Travel Percentage: 20%

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. What you will do Let’s do this. Let’s change the world. In this vital role you will as a Senior Associate IS Business Systems Analyst with strong data science and analytics expertise to join the Digital Workplace Experience (DWX) Automation & Analytics product team. In this role, you will develop, maintain, and optimize machine learning models, forecasting tools, and operational dashboards that support strategic and day-to-day decisions for global digital workplace services. This role is ideal for candidates with hands-on experience building predictive models and working with large operational datasets to uncover insights and deliver automation solutions. You will work alongside product owners, engineers, and service leads to deliver measurable business value using data-driven tools and techniques. Roles and Responsibilities Design, develop, and maintain predictive models, decision support tools, and dashboards using Python, R, SQL, Power BI, or similar platforms. Partner with delivery teams to embed data science outputs into business operations, focusing on improving efficiency, reliability, and end-user experience in Digital Workplace services. Build and automate data pipelines for data ingestion, cleansing, transformation, and model training using structured and unstructured datasets. Monitor, maintain, and tune models to ensure accuracy, interpretability, and sustained business impact. Support efforts to operationalize ML models by working with data engineers and platform teams on integration and automation. Conduct data exploration, hypothesis testing, and statistical analysis to identify optimization opportunities across services like endpoint health, service desk operations, mobile technology, and collaboration platforms. Provide ad hoc and recurring data-driven recommendations to improve automation performance, service delivery, and capacity forecasting. Develop reusable components, templates, and frameworks that support analytics and automation scalability across DWX. Collaborate with other data scientists, analysts, and developers to implement best practices in model development and lifecycle management. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The vital attribute professional we seek is with these qualifications. Basic Qualifications: Master's degree / Bachelor's degree and 5 to 9 years in Data Science, Computer Science, IT, or related field Must Have Skill Experience working with large-scale datasets in enterprise environments and with data visualization tools such as Power BI, Tableau, or equivalent Strong experience developing models in Python or R for regression, classification, clustering, forecasting, or anomaly detection Proficiency in SQL and working with relational and non-relational data sources Nice-to-Have Skills Familiarity with ML pipelines, version control (e.g., Git), and model lifecycle tools (MLflow, SageMaker, etc.) Understanding of statistics, data quality, and evaluation metrics for applied machine learning Ability to translate operational questions into structured analysis and model design Experience with cloud platforms (Azure, AWS, GCP) and tools like Databricks, Snowflake, or BigQuery Familiarity with automation tools or scripting (e.g., PowerShell, Bash, Airflow) Working knowledge of Agile/SAFe environments Exposure to ITIL practices or ITSM platforms such as ServiceNow Soft Skills Analytical mindset with attention to detail and data integrity Strong problem-solving and critical thinking skills Ability to work independently and drive tasks to completion Strong collaboration and teamwork skills Adaptability in a fast-paced, evolving environment Clear and concise documentation habits EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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. What you will do Let’s do this. Let’s change the world. In this vital role we are seeking a skilled and proactive Mobility Engineer with hands-on experience managing mobile and Apple devices using JAMF and other Mobile Device Management (MDM) solutions. This role is responsible for configuring, securing, deploying, and supporting enterprise mobility systems to ensure seamless and secure device operation across the organization. The ideal candidate will also have a solid background in automation, scripting and app integration to improve mobile infrastructure performance and streamline deployment processes Roles & Responsibilities: Administer and manage Apple devices using JAMF Pro and other MDM platforms. Design and implement mobile device configurations, policies, and profiles to support business needs. Develop automated workflows for device provisioning, software deployment, patching, and compliance checks. Integrate third-party and internal applications with MDM tools for seamless app delivery and management. Collaborate with developers and IT teams to build or support custom scripts, APIs, and internal apps tailored for the mobile environment. Monitor and support mobile infrastructure to ensure high availability and performance. Ensure mobile devices align with corporate security and usage policies. Create and maintain technical documentation, including architecture, SOPs, and deployment guidelines. Troubleshoot and resolve issues related to mobile device deployments, applications, and integration workflows. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The vital attribute professional we seek is with these qualifications. Basic Qualifications and Experience: Master's degree / Bachelor's degree and 5 to 9 years in a Mobility Engineer or Systems Administrator role Functional Skills: Deep expertise with JAMF Pro and Apple ecosystem (macOS, iOS). Solid understanding of MDM tools (e.g., Intune, AirWatch, MobileIron, Meraki). Proficiency in scripting and automation (e.g., Bash, PowerShell, Python). Experience building or supporting automation and app integration pipelines. Understanding of API integrations and mobile application deployment. Ability to work cross-functionally in a fast-paced environment with minimal direction. AMF 200, 300, or higher certification. Familiarity with Apple Business Manager, DEP, and VPP. Knowledge of CI/CD tools or platforms related to mobile app deployment. Background in enterprise mobility within regulated industries (e.g., healthcare, finance). Experience with security and compliance frameworks in mobile environments. Professional Certifications: S caled Agile Framework (SAFe) for Teams (preferred) Soft Skills: High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Excellent verbal and written communication skills. Team-oriented with a focus on achieving team goals. Excellent analytical and troubleshooting skills. Ability to work effectively with global and virtual teams. 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.

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. What you will do Let’s do this. Let’s change the world. In this vital role you will as an Endpoint Management Architect be responsible for designing, managing, and evolving enterprise device management solutions within the Digital Workplace Experience team. This includes shaping end-user computing platforms, setting technology standards, managing roadmaps, and developing solutions aligned with business strategy—driving a flawless, secure, and outstanding experience for our users . The role involves close collaboration with Managed Service Providers, vendors, and internal teams to deliver and showcase both existing and emerging device management capabilities. Actively partnering with IS and business process teams, the architect will drive innovation and stability through best-practice solutions. The Device Engineering team supports global users by providing architecture and delivery for PC and device management, desktops, mobility, print, remote access, and security. Roles & Responsibilities: Serve as the domain expert driving business value from Amgen’s device technologies by defining, architecting, operating, and maintaining end-user computing platforms—including PCs, mobile devices, tablets, printers, and virtual desktops (W365 VDI)—while establishing and managing short- and long-term strategies and roadmaps for all device modalities. Define architectural solutions by analyzing business needs, reviewing current environments, and integrating industry-leading standards in collaboration with operations, enablement, and enterprise architecture teams. Establish standards, deployment methods, and supported configurations for IS-provisioned Windows, Mac, and iOS devices, in alignment with Amgen IS device lifecycle policies and procedures. Design and define next-generation desktop management platforms and processes, focusing on Modern Device and Unified Endpoint Management. Define hardware standards to meet current needs and guide future device selection with a strong understanding of enterprise IT. Provide data-driven feedback and testing on new devices (Windows, Mac, iOS) to ensure compliance and audit alignment. Develop and maintain systems, tools, policies, and processes to deploy and support applications and workforce services on end-user devices enterprise wide. Partner with IT teams including Cyber Security, Network Administration, and Deskside Services to gather requirements and support the procurement of end-user computing devices. Define, track, publish, and manage key metrics to demonstrate improvements in stability, usage, and efficiency. Oversee testing and qualification of all desktop and laptop software and updates, ensuring compliance with audit and regulatory requirements. Build strong vendor relationships, leverage beta programs and user feedback forums, provide technical oversight, and guide vendor roadmap alignment. Actively engage in critical outages, issue resolution, and capacity/availability planning sessions. Lead strategic IS projects and initiatives. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The vital attribute professional we seek is a type of person with these qualifications. Basic Qualifications: Doctorate degree / Master's degree / Bachelor's degree and 8 to 13 years in Information Systems experience Degree in Computer Science, Information Systems, Engineering, or Life Sciences. Functional Skills: Skilled in designing solutions for Digital Workspace technologies, including mobility, virtualization, and end-user devices. Experience creating strategic execution plans to address gaps between current and future business goals. Expert in applying enterprise architecture frameworks to enhance reliability and support cross-functional decisions. Proficient with iOS, iPadOS, macOS, Windows 10/11, and virtualization technologies. Experienced in collaborating with DevOps and Agile teams Strong background in system orchestration and integration. Proven UEM expertise (Intune, Microsoft Endpoint Manager, Jamf) in provisioning, deployment, updates, and policy management. Skilled in automation using PowerShell and Bash scripting. Experienced in packaging software for large-scale deployment on Windows and Mac. Track record of delivering business-aligned solutions that drive digital transformation across functions. Professional Certifications: S caled Agile Framework (SAFe) for Teams (preferred) Soft Skills: Excellent verbal and written communication with customers, team members, and management. Positive, proactive attitude focused on service improvement and exceeding expectations. Proven experience working closely with outsourced partners for device deployments, OS updates, and quality testing. Self-starter who thrives in fast-paced, high-pressure environments. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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. What you will do Let’s do this. Let’s change the world. In this vital role you will on the Automation team, serve as the primary lead for system integrations and associated automation initiatives. As such, you will require a proven understanding of the underlaying APIs, best practices, and ability to explain key information to those desiring an integration. Extensive automation experience is a must to be successful. Additionally, this is a dynamic role that will require a lot of flexibility along with the desire to help others achieve agreed upon goals. The ideal candidate should have a passion for automation, operational excellence, and building smart engineering solutions. They work well with others in a global team environment and bring a strong sense of drive and curiosity, quickly adapting to fast-paced situations and picking up new technologies along the way. They're comfortable managing multiple tasks across a wide range of tools and systems, and they know how to prioritize effectively. They're also not afraid to dive into areas outside their comfort zone and can communicate clearly—both in writing and conversation—with technical and non-technical teammates alike. Roles & Responsibilities: Reviewing and analyzing business processes, functions, and procedures to determine the most effective business systems software to meet the collaboration and productivity needs of the organization by using OOTB features Establishing systems specifications and objectives, based on business requirements and cost-effectiveness, and provides recommendations to management personnel The coordination of testing and implementation of the system software, including conversion of data to the new system, and working with application support personnel to resolve system problems Participate in writing and maintaining SOPs Creating awareness of the vendor product release plans and how they affect integrations Facilitating customer-focused interaction to ensure objectives are realized and expectations are properly managed. Coordinates activities and programs with other departments to improve service performance What we expect of you We are all different, yet we all use our unique contributions to serve patients. The vital attribute professional we seek is an engineer with these qualifications. Basic Qualifications: Doctorate degree / Master's degree / Bachelor's degree and 8 to 13 years in Information Systems experience 2+ years of direct experience with Office 365 as an admin, utilizing the Graph API 2+ years of Power Platform experience, particularly Power Automate and an understanding of Microsoft licensing 2+ years of automation utilizing AWS technologies such as Lambda functions & knowing how to properly secure such solutions Must Have Skills Experience with ServiceNow and an understanding of its abilities Extensive problem solving, debugging, and troubleshooting skills are required Excellent verbal communications and documentation skills are required Able to work independently and provide recommendations on strategies for meeting client needs Thorough understanding of REST, SOAP, OAuth and other relevant technologies Ability to bring consistency and quality assurance across various projects Functional Skills: Experience with Agile methodologies and JIRA Experience with RPA platforms such as UiPath (preferably Studio by using scripts and APIs) Working knowledge of SSO providers such as Okta Project Management experience within an enterprise environment Hands on experience working with ServiceNow (building integrations, workflows, etc.) Experience using Smartsheet Scripting knowledge using PowerShell, Python, JavaScript Experience working with OCM teams and following Change procedures/processes Microsoft, or other relevant certifications are a plus Professional Certifications: S caled Agile Framework (SAFe) for Teams (preferred) Soft Skills: High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Excellent verbal and written communication skills. Team-oriented with a focus on achieving team goals. Excellent analytical and troubleshooting skills. Ability to work effectively with global and virtual teams EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

About Turing: Turing is one of the world’s fastest-growing AI companies accelerating the advancement and deployment of powerful AI systems. Turing helps customers in two ways: Working with the world’s leading AI labs to advance frontier model capabilities in thinking, reasoning, coding, agentic behavior, multimodality, multilinguality, STEM and frontier knowledge; and leveraging that work to build real-world AI systems that solve mission-critical priorities for companies. Role Overview. In this role, you will be working on projects to help fine-tune large language models (like ChatGPT) using your strong analytical and english comprehension skills The ideal candidate should have a solid foundation in Biology, particularly at the level expected in engineering entrance exams, as well as graduate or PhD-level programs. You should be able to break down complex biological concepts into simple, clear explanations and work efficiently. The projects will also help you learn how to leverage AI to be a better analyst. This is your chance to future-proof your career in an AI-first world! What does day-to-day look like: Design and solve challenging Biology problems to probe the limitations of large language models. Develop high-quality, step-by-step solutions with clear and rigorous reasoning. Collaborate with LLM researchers to align problem types with evaluation goals, especially in areas where models typically struggle (e.g., conceptual abstraction, multi-step reasoning, and data interpretation). Contribute to defining new evaluation benchmarks based on Biology curricula spanning early undergraduate to PhD-level topics. Requirements: Candidates pursuing a Master’s/Ph.D./Postdoctoral degree in Biology, Biotechnology, Biochemistry, or a related field are eligible and encouraged to apply. Good research and analytical skills Ability to provide constructive feedback and detailed annotations. Creative and lateral thinking abilities. Excellent structured communication and collaboration skills in a remote setting. Self-motivated and able to work independently in a remote setting. Desktop/Laptop set up with a good internet connection. Note: This position is open only to candidates who have completed or are currently pursuing a Ph.D.; applications that do not meet this criterion will not be considered. Preferred Qualifications: Ability to analyze and solve complex biological problems with a structured approach. Ability to explain Biology concepts clearly using simple language, visuals, and simulations when needed. Perks of Freelancing With Turing: Work in a fully remote environment. Opportunity to work on cutting-edge AI projects with leading LLM companies. Potential for contract extension based on performance and project needs. Selection Process: Shortlisted experts may be asked to complete an assessment. If you clear the assessment, you will be contacted for contract assignments with expected start dates, durations, and end dates. Some contract assignments require fixed weekly hours, averaging 20/30/40 hours per week for the duration of the contract assignment.