3619 Biotechnology Jobs - Page 21

Company Name Shri Baba Gorakhnath Kripaa Job Title Quality Executive Job Location: Uttar Pradesh Description The Uttar Pradesh State Rural Livelihood Mission (UPSRLM) and NDDB Dairy Services (NDS), a wholly-owned subsidiary of the National Dairy Development Board (NDDB), have established Shri Baba Gorakhnath Kripaa Milk Producer Organisation, Gorakhpur was setup under the Uttar Pradesh Government’s ‘Mahila Samarthya Yojana’ (MSY) for the Dairy Value Chain Development project in the districts of Gorakhpur, Deoria, Maharajganj and Kushinagar. The SBGK MPO was incorporated on 29 August 2022 with the financial support from UPSRLM and technical assistance from NDDB Dairy Services (NDDB’s wholly owned organisation). The company commenced operations on November 26, 2023, on the birth anniversary of Dr. Verghese Kurien, the Father of the White Revolution. Hon’ble CM Yogi Adityanath has inaugurated its 7 BMC centres on 21 December 2024. A transparent and fair system has been implemented at the village level for milk procurement. Using Data Processor-cum-Milk Collection Units (DPMCU), milk is weighed, tested, and priced in the presence of the producer. We’re Hiring: Quality Executive 🚨 Are you passionate about quality and committed to excellence? Join our growing team in the dairy and food industry! Position: Quality Executive Qualification: Graduate (Chemistry) / B.Tech in Dairy Technology, Food Technology, Biotechnology or IDD. Experience: 4–6 years in the Dairy or Food Industry Key Traits We’re Looking For Strong understanding of quality control systems Hands-on experience in dairy/food processing environments Commitment to maintaining hygiene and compliance standards Preference will be given to candidates with exposure to ISO 22000, FSMS, HACCP, and QA in milk procurement Apply Here hr@shrigorakhmilk.com

Job Description Position: Medical Coder Ct: HR HR Shanmugapriya - 8072891550 Adhere to Utilization Review Accreditation Commission (URAC), jurisdictional, and/or established MediCall best practice UM time frames, as appropriate. Adhere to federal, state, URAC, client, and established MediCall best practice WCUM time frames, as appropriate. Develop a complete understanding of the Medical management Procedures. Perform medical review assessment (MRA) on utilization of health services (eg healthcare plans, workers compensation products etc) in an accurate, efficient and timely manner while ensuring compliance with utilization management regulations and adherence to state and federal mandates. Provide succinct negotiable points based on the submitted medical records that identify necessary medical treatment, casually related care, response or lack of response to treatment, etc. Identify missing records and information that are necessary in the completion of the medical review assessment. Adhere to Department of Labor, state and company timeframe requirements. Coordinates physician reviewer referral as needed and follows up timely to obtain and deliver those results. Track status of all utilization management reviews in progress and follow up on all pending cases. Work closely with management team in the ongoing development and implementation of utilization management programs. Respond to inbound telephone calls pertaining to medical reviews in a timely manner, following client a established protocols. Process customer calls consistent with program specified strategies and customer satisfaction measurements to include but not limited to proper answering procedure, eg opening and closing remarks. Learn new methods and services as the job requires. Ct: HR KAMATCHI 8925264660

What We Want You To Do Analyze and manage the NGS / Nanopore data using relevant pipelines. Develop customized pipelines and workflows and tweak current pipeline filters for NGS and Nanopor analysis Help in developing and executing various data management strategies Identify the databases, tools, catalogs, and their reliability in future and help the research team in data collection strategies. Interpret genetic sequence variations identified through the pipelines Check quality and accuracy of the data Work in conjunction with team members to ensure consistent result generation Work in conjunction with wet lab and tech teams to ensure smooth operations and development work Troubleshoot issues related to data analysis tools and software Review literature for new technologies in the field of Bioinformatics Write grants and papers in the company Creating documentation and maintaining it What Are We Looking In You PhD in Genetics/Genomics or related fields or 8+ years of experience in the field of human genomics/genetics Experience with building bioinformatics pipelines for various kinds of NGS data Assisting in drafting and completing manuscripts for publication Experience with handling various different databases and tools Perform statistical analysis on the datasets Comfortable working on Linux OS system Ability to read, interpret and curate scientific literature Excellent communication skills (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow, instructions, complete deadlines, and comply with company policies Experience of 1-2yrs+ in Python & experience of 3-5 yrs in Bash scripting Experience with pipeline orchestration tools (Nextflow or Snakemake) will be a bonus

Experience - in Diagnostic | Pharma | Sequencing Domain - acute care, critical care, anti-infectives, clinical sales & hospital sales What We Want You To Do Understand the range of products offered by HaystackAnalytics. Identify, connect, and establish relationships with clinicians in critical care by visiting their clinics/hospitals. Become owners of your accounts and secure maximum business outcome from them. Meet and exceed sales targets and goals Keeps management informed by submitting activity and results reports, such as daily call reports, weekly work plans, and monthly and annual territory analyses. Analyze competitors' performance to safeguard and further promote our position in the market. What Are We Looking In You Sales experience in the healthcare industry, with a focus on critical care products, services, and tests Ability to work independently and as part of a team Strong connections with top clinicians in his/her region

1.To perform cleaning of Visual inspection equipment in fill finish facility. 2.To Perform visual inspection of Vials, PFS and Cartridge along with documentation. 3.Making entries in log books, batch packing record and status labeling. Required Candidate profile 1. Looking for smart and dynamic pharma fresher candidate. 2. Candidate should be very good in to written and oral english communication 3. Candidate should be very dynamic.

What We Want You To Do Analyze and manage the NGS / Nanopore data using relevant pipelines. Develop customized pipelines and workflows and tweak current pipeline filters for NGS and Nanopor analysis Help in developing and executing various data management strategies Identify the databases, tools, catalogs, and their reliability in future and help the research team in data collection strategies. Interpret genetic sequence variations identified through the pipelines Check quality and accuracy of the data Work in conjunction with team members to ensure consistent result generation Work in conjunction with wet lab and tech teams to ensure smooth operations and development work Troubleshoot issues related to data analysis tools and software Review literature for new technologies in the field of Bioinformatics Write grants and papers in the company Creating documentation and maintaining it What Are We Looking In You PhD in Genetics/Genomics or related fields or 8+ years of experience in the field of human genomics/genetics Experience with building bioinformatics pipelines for various kinds of NGS data Assisting in drafting and completing manuscripts for publication Experience with handling various different databases and tools Perform statistical analysis on the datasets Comfortable working on Linux OS system Ability to read, interpret and curate scientific literature Excellent communication skills (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow, instructions, complete deadlines, and comply with company policies Experience of 1-2yrs+ in Python & experience of 3-5 yrs in Bash scripting Experience with pipeline orchestration tools (Nextflow or Snakemake) will be a bonus Skills: pipelines,pipeline orchestration tools (nextflow, snakemake),python,genomics,communication skills,bash scripting,ngs data analysis,linux,quality control,bioinformatics pipeline development,ngs,nanopore data analysis,genetics,literature review,bioinformatics pipelines,linux os,pipeline orchestration tools (nextflow or snakemake),grant writing,statistical analysis,genetic sequence interpretation,scientific literature interpretation,human genetics,bioinformatics,data management strategies,pipeline

What we want you to do Work with diagnostic lab partners for smooth functioning of infectious disease test Work with partners to ensure timely upgrades to the test are done Liaison with partners for technical support as needed Document activities What are we looking in you MSc in Microbiology or Biotechnology Experience in DNA Extraction & RT PCR Ability to quickly prioritize and execute tasks Good oral and written communication skills. Strong analytical skills and attention to detail Strong documentation skills Compulsory rotation shift (i.e day shift, mid shift, night shift) 6 days working with rotational week off What you will gain Exposure of working with one of the leading companies in genomics Experience in working with advanced sequencing technology in diagnostic industry i.e NGS, WGS, Nanopore, and Illumina Gain skills in troubleshooting during sequencing. Skills: ngs,troubleshooting,biotechnology,documentation,data management,organizational skills,excel,rna isolation,data entry,dna extraction,analytical skills,record-keeping,rtpcr,communication skills,powerpoint,word,microsoft office,documentation skills,rt pcr

Education Qualification - Pursuing or completed BSc or MSc in Microbiology, Life Sciences, or Biotechnology What We Want You To Do Execute required activities as part of ISO 13485 and ISO 15189 compliance Undertake activities as part of manufacturing documentation under ISO 13485 Undertake activities in molecular kit development and kit packaging departments Preparation of regulatory document dossier Requirements The candidate must have the ability to execute tasks and document information independently. Have a basic understanding of quality assurance and quality checks Awareness of ISO 13485 and ISO 15189 Skills Keen attention to details. Ability to critically evaluate scientific literature and integrate information from multiple sources. Proficiency in Google & Microsoft Office Suite and other relevant software applications. Ability to work independently with minimal supervision as well as collaboratively in a team environment. Excellent organizational and time management skills with the ability to prioritize tasks effectively Strong interpersonal and communication skills with the ability to interact professionally with diverse stakeholders Note: This is a paid internship.Skills: time management, regulatory documentation,documentation,iso,regulatory affairs,molecular kit development,genomics,quality assurance processes, google suite,interpersonal skills,iso 13485,microsoft office suite, proficiency in google & microsoft office suite,iso 15189,attention to details,quality assurance,biotechnology, communication,communication skills,scientific literature evaluation, organizational skills

Experience - in Diagnostic | Pharma | Sequencing Domain - acute care, critical care, anti-infectives, clinical sales & hospital sales What We Want You To Do Understand the range of products offered by HaystackAnalytics. Identify, connect, and establish relationships with clinicians in critical care by visiting their clinics/hospitals. Become owners of your accounts and secure maximum business outcome from them. Meet and exceed sales targets and goals Keeps management informed by submitting activity and results reports, such as daily call reports, weekly work plans, and monthly and annual territory analyses. Analyze competitors' performance to safeguard and further promote our position in the market. What Are We Looking In You Sales experience in the healthcare industry, with a focus on critical care products, services, and tests Ability to work independently and as part of a team Strong connections with top clinicians in his/her region

What We Want You To Do Analyze and manage the NGS / Nanopore data using relevant pipelines. Develop customized pipelines and workflows and tweak current pipeline filters for NGS and Nanopor analysis Help in developing and executing various data management strategies Identify the databases, tools, catalogs, and their reliability in future and help the research team in data collection strategies. Interpret genetic sequence variations identified through the pipelines Check quality and accuracy of the data Work in conjunction with team members to ensure consistent result generation Work in conjunction with wet lab and tech teams to ensure smooth operations and development work Troubleshoot issues related to data analysis tools and software Review literature for new technologies in the field of Bioinformatics Write grants and papers in the company Creating documentation and maintaining it What Are We Looking In You PhD in Genetics/Genomics or related fields or 8+ years of experience in the field of human genomics/genetics Experience with building bioinformatics pipelines for various kinds of NGS data Assisting in drafting and completing manuscripts for publication Experience with handling various different databases and tools Perform statistical analysis on the datasets Comfortable working on Linux OS system Ability to read, interpret and curate scientific literature Excellent communication skills (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow, instructions, complete deadlines, and comply with company policies Experience of 1-2yrs+ in Python & experience of 3-5 yrs in Bash scripting Experience with pipeline orchestration tools (Nextflow or Snakemake) will be a bonus

Role Overview We are looking for a Scientific Content Writing Intern who can help translate complex scientific data into clear, accurate, and engaging content. This role is ideal for students or early-career professionals passionate about science communication, public health, and genomics. Key Responsibilities Assist in writing, editing, and proofreading scientific documents including: Scientific content for blog posts, case studies, product brochures, and posters Whitepapers and abstracts for scientific conferences Website and social media content related to genomics and diagnostics Conduct literature reviews and ensure content accuracy and alignment with current scientific understanding Collaborate with R&D, and clinical teams to gather data and insights Maintain referencing and citations in appropriate formats (e.g., AMA, Vancouver) Support development of visual science communication tools like infographics Requirements Masters or final year Bachelor's student in life sciences, biotechnology, microbiology, genetics, pharmacology, or a related field Excellent written and verbal communication skills Strong understanding of biology/genomics and interest in diagnostics or healthcare innovation Ability to interpret and simplify research findings for broader audiences Familiarity with literature databases (e.g., PubMed) and reference managers (e.g., Mendeley/Zotero)

Role Overview Were looking for a proactive and organized Marketing Intern to support project coordination and research activities for our identifi product line. This role is ideal for someone who is detail-oriented, curious, and passionate about applying marketing skills in a high-impact, science-driven environment. Key Responsibilities Project Coordination Assist in tracking and coordinating ongoing marketing projects for identifi products Liaise with internal teams (sales, clinical, design, operations) to ensure timely execution Maintain project trackers, timelines, and weekly status reports Follow up with vendors and creative teams for deliverables and approvals Market Research Conduct research on infectious disease diagnostics market, competitors, and new trends Analyze and summarize data on customer needs, testing protocols, and regional trends Benchmark product messaging, pricing, and campaigns across diagnostic brands Assist in creating presentations, research summaries, and product decks Requirements Pursuing or recently completed a degree in Marketing, Healthcare Management, Life Sciences, or Business Strong organizational and communication skills Proficiency in MS Excel, PowerPoint, and Google Workspace Comfortable working in a fast-paced, cross-functional setup Interest in healthcare, diagnostics, or genomics is a strong plus

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials Job Title: Scientist I, Protein Biology Job Location: India, Bangalore About Company: About The Company Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers About Team: Antibody team The antibody team in involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of team include antibody designing, purification, conjugation and testing of antibodies in a variety of immuno-applications using pioneering tools and technologies. The goal of the program is advanced product development and creation of product specific information to promote research use. Role & Responsibilities Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular biology methods. Responsibilities: Meticulous experimental planning and execution to meet program goals. Timely record keeping of results into data sheets and laboratory note-books. Regular mining of literature and keeping oneself up to date with developments in field of antibody development. Compilation and presentation of data in written and oral formats. Active participation in team meetings. Attention to detail and adherence to schedules. Candidate Requirement: Education & Experience levels: Applicants should have Masters with 0-3 years confirmed experience or a PhD in a life sciences field with a strong focus on molecular biology, immunology, biotechnology or biochemistry. Nature of experience: Project or work experience in support of relevant skills such as publications, project reports or thesis work Strong theoretical or practical experience in antibody development platforms, antibody design, engineering and/or conjugation Extensive experience in immunoassays such as Western blotting, Immunofluorescence, Immunohistochemistry, Flow cytometry or ELISA Experience with proteins, which could include but not limited to structure function or mutational analysis of proteins, and molecular biology expertise in handling nucleic acid extraction, PCR, and cloning. Proficient in MS Office applications such as Word, Powerpoint, Excel and possess a strong statistical knowledge and familiarity with statistical software such as Prism. The successful candidate will be self-motivated and a self-starter who is excellent at learning and applying new concepts for process or product improvements, possess excellent oral and written communication skills to connect to peers and leadership, and will be an excellent teammate with the ability to work with different colleagues. Thermo Fisher Scientific is an equal opportunity employer and value diversity at our company. All qualified applicants will receive consideration for employment without discrimination basis race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, protected veteran status, age, genetics, pregnancy, disability or any other legally protected status. Thermo Fisher Scientific aligns with all applicable equal employment opportunity legislation in each jurisdiction in which it operates We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials Job Title: Scientist I, Protein Biology Job Location: India, Bangalore About Company: About The Company Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers About Team: Antibody team The antibody team in involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of team include antibody designing, purification, conjugation and testing of antibodies in a variety of immuno-applications using pioneering tools and technologies. The goal of the program is advanced product development and creation of product specific information to promote research use. Role & Responsibilities Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular biology methods. Responsibilities: Meticulous experimental planning and execution to meet program goals. Timely record keeping of results into data sheets and laboratory note-books. Regular mining of literature and keeping oneself up to date with developments in field of antibody development. Compilation and presentation of data in written and oral formats. Active participation in team meetings. Attention to detail and adherence to schedules. Candidate Requirement: Education & Experience levels: Applicants should have Masters with 0-3 years confirmed experience or a PhD in a life sciences field with a strong focus on molecular biology, immunology, biotechnology or biochemistry. Nature of experience: Project or work experience in support of relevant skills such as publications, project reports or thesis work Strong theoretical or practical experience in antibody development platforms, antibody design, engineering and/or conjugation Extensive experience in immunoassays such as Western blotting, Immunofluorescence, Immunohistochemistry, Flow cytometry or ELISA Experience with proteins, which could include but not limited to structure function or mutational analysis of proteins, and molecular biology expertise in handling nucleic acid extraction, PCR, and cloning. Proficient in MS Office applications such as Word, Powerpoint, Excel and possess a strong statistical knowledge and familiarity with statistical software such as Prism. The successful candidate will be self-motivated and a self-starter who is excellent at learning and applying new concepts for process or product improvements, possess excellent oral and written communication skills to connect to peers and leadership, and will be an excellent teammate with the ability to work with different colleagues. Thermo Fisher Scientific is an equal opportunity employer and value diversity at our company. All qualified applicants will receive consideration for employment without discrimination basis race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, protected veteran status, age, genetics, pregnancy, disability or any other legally protected status. Thermo Fisher Scientific aligns with all applicable equal employment opportunity legislation in each jurisdiction in which it operates We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Job Title: Biotech Reader Location: Bodhgaya, Bihar (On-Site) or Varanasi, UP (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. Job Description: We are seeking a motivated Biotech Reader with a background in Biochemistry and a strong understanding of enzymes and metabolic pathways. The role involves assay development, biochemical analysis, and contributing to research efforts for advancing our diagnostic platform. The ideal candidate will bridge biochemical insights with our electrochemical detection systems. Responsibilities: Develop, optimise, and validate biochemical assays based on enzymatic reactions and metabolic pathways. Analyse metabolic and enzymatic data from electrochemical detection platforms. Work closely with the R&D team on integrating biochemical processes with microfluidic devices. Conduct literature reviews and apply biochemical knowledge to enhance assay design. Maintain accurate laboratory records and contribute to scientific reports. Support troubleshooting of biochemical protocols and data interpretation. Qualifications: Master’s degree in Biochemistry, Biotechnology, or a related life sciences field. Strong knowledge of enzymes, enzyme kinetics, and metabolic pathways. Hands-on experience with biochemical assays and analytical techniques. Preferred Qualifications: Experience in electrochemical biosensing or bioassay development. Familiarity with microfluidics or point-of-care diagnostic systems. Exposure to interdisciplinary research environments. Skills: Strong analytical and problem-solving skills. Ability to work collaboratively in a research team. Proficiency in experimental design and data analysis. Effective scientific communication (both written and verbal). Personal Attributes: Curiosity-driven with a passion for applied research. Detail-oriented with a commitment to quality and precision. Proactive, self-motivated, and adaptable. Open to learning new techniques and interdisciplinary approaches.

Job Description Job Title: Sr. Manager RA No of Vacancy: 1 Job Location: Andheri Years of Experience:10 - 20 years Working Days: Monday to Saturday Job Summary: We are seeking a dynamic and experienced Senior Manager – Global Regulatory Affairs to lead regulatory strategy, compliance, and market authorization activities across all regions (including India, USA, EU, MENA, LATAM, and APAC ). The ideal candidate will manage end-to-end regulatory submissions and ensure compliance with CDSCO , USFDA , EU MDR , MDSAP , and other country-specific requirements for our wide portfolio of dental devices and technologies . This role will also drive cross-functional alignment and strategic planning to ensure timely market access and post-market compliance for global operations. Key Responsibilities: Global Regulatory Strategy & Submissions Develop and lead global regulatory strategies for new product approvals, product changes, and renewals across multiple markets. Oversee preparation and submission of regulatory dossiers including: 510(k) submissions for USFDA Technical Files under EU MDR CDSCO applications via SUGAM/NSWS Market-specific files for LATAM, MENA, ASEAN, and Africa Manage the lifecycle of product registrations, including change notifications, renewals, and labeling updates. Documentation & Compliance Oversee compilation and maintenance of technical documentation, Design Dossiers, CERs, Risk Management Files, SSCP, UDI, and IFUs. Ensure that documentation complies with ISO 13485, 21 CFR Part 820, Schedule V – MDR 2017, and global GSPR requirements. Ensure global labeling, UDI, and registration tracking systems are up to date and compliant. Regulatory Intelligence & Risk Management Monitor and assess regulatory changes, standards, and emerging guidance across geographies and proactively address business impacts. Provide strategic guidance to product development teams on regulatory pathways and compliance implications. Lead regulatory due diligence in new market expansions and partnerships. Cross-Functional Leadership & Stakeholder Engagement Collaborate with R&D, Quality, Manufacturing, Legal, and Marketing teams to ensure product and process alignment with global regulatory expectations. Serve as regulatory representative in design reviews, change control boards, and product launch meetings. Act as the company’s lead interface with regulatory bodies, notified bodies, consultants, and distributors for all global markets. Team Management & Development Build, mentor, and manage a high-performing global regulatory affairs team. Establish global SOPs, templates, and best practices to ensure documentation quality and consistency. Lead training and awareness programs across departments for regulatory requirements and changes. Interdepartmental Coordination & Cross-functional Collaboration Act as a regulatory liaison between internal departments including R&D, Quality Assurance, Manufacturing, Supply Chain, Legal, and Marketing to ensure seamless alignment of regulatory requirements during product development, changes, and market launches. Participate in cross-functional meetings such as design reviews, risk assessments, CAPA boards, and change control committees to provide regulatory insights and approval. Lead regulatory readiness for product launches by aligning internal teams on documentation, labeling, and certification requirements. Vendor & Notified Body Communication Maintain strong working relationships with Notified Bodies, regulatory authorities, consultants, and authorized representatives in global markets to ensure smooth product registration and certification processes. Coordinate with external vendors, including regulatory consultants, testing labs, and CROs, for clinical evaluation, biocompatibility, performance testing, and regulatory submissions. Act as the primary regulatory point of contact during audits or inspections conducted by external parties or authorities. Required Qualifications: Bachelor’s/Master’s in Pharmaceutical Sciences, Biomedical/Mechanical Engineering, Biotechnology, or Life Sciences Advanced certifications in Global Regulatory Affairs, MDR/USFDA Compliance, or Clinical Evaluation preferred Key Skills & Competencies: Proven expertise in 510(k), EU MDR, CDSCO, and MDSAP regulations Excellent understanding of global regulatory landscapes (LATAM, GCC, APAC, Africa) Experience with e-submission portals: SUGAM, NSWS, EUDAMED, FDA ESG Strong skills in technical documentation, clinical evaluation, and risk assessment Ability to influence and communicate regulatory impact at the executive level Strong leadership and team-building capabilities in a matrixed, global environment Meticulous attention to regulatory detail, coupled with business strategy alignment Preferred Industry Background: Medical Devices (Class I/II/III) Dental Products Manufacturing (e.g., clear aligners, restorations, implants) Diagnostics or Life Sciences Company website: https://www.illusiondentallab.com/ https://www.laxmidentallimited.com/ https://www.illusionaligners.com/

Work Schedule Standard (Mon-Fri) Environmental Conditions Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed Job Title: Scientist III, Cell Biology Location: Bangalore Division: BID When you are part of the team at Thermo Fisher Scientific, you’ll do important work. Surrounded by collaborative colleagues, you’ll have the support and opportunities that only a global leader can give you. Our respected, growing organization has an exceptional strategy for the near term and beyond. Take your place on our strong team and help us make significant contributions to the world. Introduction to the Division /Function BioSciences Division is part of Life Science Solutions Group in Thermo Fisher Scientific and R&D group in Bangalore is involved in antibodies and immunoassay development using recombinant DNA technology. Role Description (Purpose Of The Role) Scientist III will be working on ongoing R & D projects related to recombinant antibody development and validation. Individual will be responsible to take care of Core Cell culture Facility which supports all the programs with biological samples. Also should be able to efficiently manage 5 to 7 people and their career and growth path. Responsibilities Should be able to design, initiate, plan, execute and oversee experiments related to cell biology Should be good in scientific writing in different formats according to the project requirement. Good understanding about mammalian cell culture and maintaining cell culture lab with correct specifications. Having experience in specific differentiations, cell based models for studying proteins Expertise in analytical/ biochemical techniques like western blotting testing, immunofluorescence testing, Flow cytometry, ELISA Keeping thorough record of results into data sheets and/or electronic databases and notebooks. Maintain and upgrade available databases as well. Responsible for data integrity and accuracy. Other functions such as writing technical protocols, maintaining SOPs and taking care of required ordering. Deliver high quality results according to project schedule in support of product commercialization during early feasibility, development and validation phases. Qualification Must have Ph.D in Biotechnology/Life Sciences or related discipline or Masters in cell biology/biotechnology, genetics or related fields with more than 7 years of experience in cell biology work flow or relevant industry. Skills And Experience Should have a clear understanding of mammalian cells and their culturing techniques. Strong understanding and hands-on experience of handling, designing cell biology and protein workflow experiments and model development Should have a clear understanding and laboratory skills in the area of cell biology, immunoassays like western blot, immunofluorescence, Flow and ELISA Should have good scientific writing skills Publications in peer-reviewed journals would be a bonus. Good understanding of research projects using standard techniques and protocols. Should be a good team player, ready to learn new techniques and innovative thinker. Industry experience, bioinformatics and grant writing skills will be considered as a bonus. Excellent organizational skills with attention to detail. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Work Schedule Standard (Mon-Fri) Environmental Conditions Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Scientist I, Single cell (New Hire) Textio score: 100% About Team: Antibody team The antibody team is involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of the team include design, development, purification, conjugation and testing of antibodies in a variety of immunoassay applications using pioneering tools and technologies. The goal of the program is advanced product development and creation of product specific information to promote research use. Role & Responsibilities Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods. Responsibilities: Work on single cell sorting. Meticulous experimental planning and execution to meet program goals. Timely record keeping of results into data sheets and laboratory note-books. Regular mining of literature and keeping oneself up to date with developments in field of antibody development. Compilation and presentation of data in written and oral formats. Active participation in team meetings. Attention to detail and adherence to schedules. Candidate Requirement: Education & Experience levels: Applicants should have Masters with 0-4 years experience or a PhD in a life sciences field (submitted within the last one year) with a strong focus on molecular biology, immunology, biotechnology or biochemistry. Nature of experience: Thorough in immunology and flowcytometry workflows. Experience in cell sorting is an added advantage. Working knowledge and experience in molecular biology workflows such as high-throughput molecular cloning, plasmid vector construction, PCRs, Restriction digestion, Ligation, Transformation, Mini and maxi preps, sequencing Ability to provide technical trouble shooting to resolve scientific problems. Proficient in software or platforms for flowcytometry and data analysis, FlowJo, FCSExpress, MS Office and statistical software such as GraphPad Prism. Theoretical or practical experience in antibody development platforms is desirable. Project or work experience in support of relevant skills such as publications, project reports or thesis work. The successful candidate will be self-motivated and a self-starter who is excellent at learning and applying new concepts for process or product improvements, possess excellent oral and written communication skills to connect to peers and leadership, and will be an excellent teammate with the ability to work with diverse colleagues. Thermo Fisher Scientific is an equal opportunity employer and value diversity at our company. All qualified applicants will receive consideration for employment without discrimination basis race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, protected veteran status, age, genetics, pregnancy, disability or any other legally protected status. Thermo Fisher Scientific aligns with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Career Category Information Systems Job Description Let s do this. Let s change the world. In this vital role you will collaborate with business partners, service owners and IS peers to develop predictive models and insights across the US Commercial Organization. This position will innovate and build significant business impact through the use of sophisticated analytics techniques to help Amgen with its mission to serve patients by helping them get the therapies they need. Flexible Commuter role to Amgen India office. You will work on-site 2-3 days a week. This position will be primarily responsible for: Working collaboratively with cross-functional teams on projects and/or programs with aims to systematically derive insights that ultimately derive substantial business value for Amgen and our patients Identifying business needs and proposing potential analytics approaches for solutions Crafting and deploying a framework to supervise the performance of various campaigns, and tactics at a granular level Leading measurement and tracking of various omnichannel CX enablement initiatives Supporting the development of data science, machine learning prototypes, proof of concepts and models for testing various omnichannel strategies Communicating analysis ideas, progress and results to leadership and business partners 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 ORdata science and/or analytics experience Master s degree and 4 to 6 years of data science and/or analytics experience OR Bachelor s degree and 6 to 8 years of data science and/or analytics experience OR Diploma and 10 to 12 years of data science and/or analytics experience Preferred Qualifications: Relevant work experience in campaign measurement, marketing analytics and resource optimization in the pharma domain Programming experience with Python, R, or SAS and experience with ML libraries like scikit-learn, MLib, or TensorFlow Experience working with large datasets, experience working with distributed computing tools (Spark, Hive, etc.) is a plus Ability to communicate analysis in a clear, detailed, and practical manner Passion for learning and staying on top of current developments in sophisticated analytics Biotech / Pharma experience 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 .

Position Overview We are seeking a passionate and highly skilled Computational Research Scientist specializing in deep learning to join our R&D team. This role will focus on developing and applying advanced AI and machine learning methods to solve biological problems, with an emphasis on enzyme optimization, metabolic engineering, and bio-process innovation. The successful candidate will collaborate closely with biologists, engineers, and data scientists to accelerate the design and production of sustainable bio-alternatives. Key Responsibilities Design, develop, and deploy deep learning models for predicting and optimizing enzymes, proteins, and metabolic pathways in microbial and cellular systems. Conduct computational modeling and simulations of metabolic networks to identify critical control points and engineering targets. Build robust data pipelines to integrate diverse biological datasets and enable scalable model training and evaluation. Present technical findings clearly to interdisciplinary teams through reports, presentations, and collaborative discussions. Stay current with advances in AI, synthetic biology, and computational methods to drive innovation at ThinkBio.Ai. Required Qualifications Ph.D. in Computer Science, Bioinformatics, Computational Biology, or a related field with a focus on deep learning applications. Hands-on experience with deep learning frameworks such as TensorFlow, PyTorch, or similar. Proficiency in programming languages including Python (preferred), R, or MATLAB. Strong written and verbal communication skills. Proven ability to work independently and collaboratively in a dynamic research environment. Preferred Qualifications Knowledge of metabolic engineering, synthetic biology, or systems biology concepts. Familiarity with metabolic flux analysis and constraint-based modeling techniques (e.g., Flux Balance Analysis, COBRA Toolbox). Experience with protein structure prediction and modeling. Background in industrial biotechnology or experience working in start-up environments. Desired Working Style Exceptionally organized with the ability to manage multiple projects and priorities simultaneously. Quick learner with a proactive, inquisitive mindset. Adaptable and comfortable with evolving roles and responsibilities typical in start-ups. Strong collaborator with excellent interpersonal and communication skills. Commitment to high standards of scientific integrity and professional ethics.

India - Hyderabad JOB ID: R-216753 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jul. 22, 2025 CATEGORY: Engineering [Role Name : IS Architecture] Job Posting Title: Data Architect Workday Job Profile : Principal IS Architect Department Name: Digital, Technology & Innovation Role GCF: 06A 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 role is responsible for developing and maintaining the data architecture of the Enterprise Data Fabric. Data Architecture includes the activities required for data flow design, data modeling, physical data design, query performance optimization. The Data Architect is a senior-level position responsible for developing business information models by studying the business, our data, and the industry. This role involves creating data models to realize a connected data ecosystem that empowers consumers. The Data Architect drives cross-functional data interoperability, enables efficient decision-making, and supports AI usage of Foundational Data. This role will manage a team of Data Modelers. Roles & Responsibilities: Provide oversight to data modeling team members. Develop and maintain conceptual logical, and physical data models and to support business needs Establish and enforce data standards, governance policies, and best practices Design and manage metadata structures to enhance information retrieval and usability Maintain comprehensive documentation of the architecture, including principles, standards, and models Evaluate and recommend technologies and tools that best fit the solution requirements Evaluate emerging technologies and assess their potential impact. Drive continuous improvement in the architecture by identifying opportunities for innovation and efficiency Basic Qualifications and Experience: [GCF Level 6A] Doctorate Degree and 8 years of experience in Computer Science, IT or related field OR Master’s degree with 12 - 15 years of experience in Computer Science, IT or related field OR Bachelor’s degree with 14 - 17 years of experience in Computer Science, IT or related field Functional Skills: Must-Have Skills : Data Modeling: Expert in creating conceptual, logical, and physical data models to represent information structures. Ability to interview and communicate with business Subject Matter experts to develop data models that are useful for their analysis needs. Metadata Management : Knowledge of metadata standards, taxonomies, and ontologies to ensure data consistency and quality. Information Governance: Familiarity with policies and procedures for managing information assets, including security, privacy, and compliance. Hands on experience with big data technologies and platforms, such as Databricks, Apache Spark (PySpark, SparkSQL), performance tuning on big data processing Good-to-Have Skills: Experience with Graph technologies such as Stardog, Allegrograph, Marklogic Professional Certifications Certifications in Databricks are desired Soft Skills: Excellent critical-thinking and problem-solving skills Strong communication and collaboration skills Demonstrated awareness of how to function in a team setting Demonstrated awareness of presentation skills Shift Information: This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required based on business requirements. 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.

Job Title: Compliance Manager Department: Legal / Regulatory / Compliance Reports To: Senior Management Location: Plot no.175,Road 74,Jubilee Hills, Hyderabad-500096 Employment Type: Full-time Job Summary: The Compliance Manager is responsible for ensuring that the organization operates in compliance with all applicable laws, regulations, standards, and internal policies. This role involves designing and implementing internal controls, audits, and compliance programs to reduce risk, ensure regulatory adherence, and foster a culture of ethics and integrity. Key Responsibilities: Ensure that all herbal products meet regulatory standards under FSSAI, AYUSH, GMP, and international regulations (e.g., USFDA, EFSA, TGA). Review and approve labeling, packaging, and marketing materials for regulatory compliance (including health claims, ingredients, and warnings). Manage documentation for product registrations, export certifications, and product dossiers. Liaise with government agencies, third-party labs, and regulatory consultants for inspections, audits, and certifications. Monitor changes in regulations related to herbal/natural health products and proactively implement required changes. Conduct internal audits to ensure process and documentation compliance across procurement, manufacturing, and packaging. Oversee complaint handling, product recalls, and non-conformance investigations. Train internal teams (production, R&D, sales) on compliance and regulatory updates. Maintain a robust documentation system including COAs, MSDS, batch records, and SOPs. Qualifications: Bachelor's or Master’s in Pharmacy, Chemistry, Botany, Biotechnology, or related life sciences. 0-1 years of experience in regulatory compliance within the herbal, nutraceutical, or food supplement industry. Knowledge of Indian and global regulations (FSSAI, AYUSH, GMP, USFDA, etc.). Strong understanding of labeling and permissible health claims in herbal products. Excellent communication, documentation, and training skills. Experience with product registrations and export documentation is a plus. Key Competencies: Attention to detail Critical thinking and decision-making Strong interpersonal skills Policy development and implementation Risk assessment and mitigation Communication and training Apply to this link : https://www.medikonda.com/pages/careers Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Cell phone reimbursement Paid time off Schedule: Day shift Morning shift Work Location: In person

Responsibilities Edit manuscripts for spelling, grammar, punctuation, clarity, and rephrase sentences as needed Ensure that manuscripts conform to the publisher style guides Review manuscripts copy edited by trainee editors and offer constructive feedback. The ideal candidate An undergraduate or postgraduate with a degree in Physics, Chemistry, Botany, Zoology, Bio-Technology, Plant Biology, Microbiology, Nutrition, Bio-Chemistry, BioScience, Polymer Science, Environmental Science, Bio-informatics, Food Technology, Dairy Technology, Pharma, EEE, ECE, E&I, or English Someone with a keen eye for detail, who possesses excellent verbal and written English skills Someone who is skilled with MS Word An enthusiastic learner with a passion for reading and editing Shift schedule 1st shift: 6.15 a.m.1.45 p.m. 2nd shift: 1.45 p.m.9.15 p.m.

Job Summary The main functions of this position are to assure that products and materials are matching with the quality standards through performing the required lab tests and examinations in raw material, semi finished goods and finished goods in order to minimize the defected and returned goods aiming to increase IFFCO customers’ satisfaction. Roles & Responsibilities Analyze RM and SFG samples from Process units periodically to examine its quality registering the results in SAP system to ensure the quality standards application. Analyze SFG samples from production department periodically registering the results in SAP system (line-by-line) to guarantee the compliance with the quality standards. Ensure the continuous monitoring of all production lines registering remarks concerning quality issues in the daily check report and inform the concerned party to avoid quality mismatching. Issue certificates of analysis “COA” for finished goods to verify and certify that IFFCO products are satisfactory for the customer’s needs or requirement assuring their acceptance by customers. KPIs Work experience requirement Minimum 3 years of relevant functional experience at the field Qualification Bachelor’s degree in (Food Technology, Biotechnology and Food Science’). Competencies Communicating effectively Self and Team Management Business Unit: Pristine Ingredients (PIPL) Business Group: Bakery (BK01)

Why join Stryker? Looking for a place that values your unique talents? Discover Stryker's award-winning culture. We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific. Job description We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific. What you will do Complaint handling and Product investigations of medical devices Perform Visual, functional, dimensional, functional inspection & RCA of field returned products. Maintain and ensure complaint files are complete and accurately reflect corresponding complaint activities. Risk management –Risk assessment Review of Process flow, DHR, Inspection plans, Measurement techniques, GRR’s etc. Review and analyze Literatures such as Clinical reports, PMCF reports, National register etc. to identify Complaints Create PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis. Other tasks as assigned by manager. What you need: Required skills: B. Tech / M.Tech Mechanical, Biotechnology with 2-5 years of work experience. Hands on experience of PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis. Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability. 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. 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. Preferred Skills: 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) Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.