Get alerts for new jobs matching your selected skills, preferred locations, and experience range.
2.0 - 5.0 years
10 - 20 Lacs
Bareilly
Remote
Must Published 3-4 paper in SCI/Scopus Q1/Q2Unpaid Journals with their Expertise Must be able to write and can arrange the data by themselves in such manner so that paper can be published easily Required Candidate profile Must Be Phd Must Be published 3-4 Journals in sci unpaid Must be able to write the good quality paper
Posted 2 weeks ago
3.0 - 8.0 years
3 - 7 Lacs
Kolkata, Delhi / NCR, Mumbai (All Areas)
Work from Office
Key Responsibilities: Regulatory Compliance & Documentation: Ensure compliance with FSSAI, Codex, USFDA, EU, and other relevant regulatory bodies. Prepare and submit regulatory documents for product approvals, label claims, and ingredient compliance. Maintain up-to-date records of all regulatory submissions, licenses, and product dossiers. Collaborate with internal teams (R&D, Quality, Marketing) to ensure regulatory requirements are met during product development. Scientific & Technical Support: Evaluate and interpret food regulations to guide formulation, labelling, and marketing claims. Provide scientific validation for nutrition claims, health benefits, and ingredient functionalities. Conduct literature reviews and regulatory assessments for new ingredients, additives, and processing aids. Support clinical trials, stability studies, and food safety risk assessments as needed. Labelling & Claims Validation: Review and approve packaging artwork, ingredient declarations, and nutrition labels as per regulatory guidelines. Ensure accurate representation of claims (e.g., 100% Whole Wheat, High Fiber, No Artificial Additives). Monitor global trends and regulatory updates affecting product claims and advertising. Stakeholder & Government Liaison: Represent the company in discussions with regulatory authorities, industry bodies, and standard-setting organizations. Handle queries and compliance matters related to regulatory inspections and audits. Work closely with external consultants, legal teams, and government agencies on regulatory approvals. Training & Awareness: Conduct internal training sessions on food regulations, scientific developments, and compliance best practices. Develop regulatory guidelines and SOPs to ensure uniform adherence across departments.
Posted 3 weeks ago
2 - 4 years
4 - 5 Lacs
Noida
Work from Office
The Executive - PMT will play a critical role in product management and marketing within the nutraceutical or Ayurvedic industry. The role requires strong expertise in scientific research, formulation, regulatory compliance, business development, and training. Department: Product Management Team (PMT) Experience: Minimum 2+ years Industry: Nutraceutical / Ayurvedic Educational Qualification: Master's or Bachelor's in Nutrition, Food Science, Dietetics, or M.Pharm or BAMS Location: Sector 65, Noida Work Timings: 9:00 AM 5:30 PM (Alternate Saturdays off) Key Responsibilities: 1. Business Development Developing formulation propositions and spec sheets. Handling NPDI (New Product Development & Introduction) processes. Preparing product presentations, scientific research, comparison tables, and marketing data. Assisting the BD team with various queries related to formulations and regulatory aspects. 2. New Product Development (NPD) Conducting technical research and feasibility studies for new product development. Coordinating with R&D and other teams for data collection and correspondence. 3. Regulatory Compliance Reviewing artwork, validating scientific claims, and ensuring compliance with regulatory guidelines. 4. Training & Development Conducting monthly training sessions for the BD and regulatory teams. Preparing training materials including PPTs, quizzes, and other learning resources . 5. Event Management Planning and managing events, sponsorships, and exhibitions . Booking stalls, overseeing fabrication, and providing branding materials. Managing bills, payments, and vendor coordination. 6. Social Media & Marketing Collaterals Providing content for brochures, flyers, and leaflets . Proofreading and ensuring accuracy in marketing or promotional materials. 7. R&D Coordination Conducting feasibility checks and gathering product information. Collaborating with the R&D team for product development insights. 8. Business Development (Domestic & Exports) Attending client meetings and supporting the BD team with technical expertise. Assisting in market analysis, competitive research, and strategy development . Key Skills & Competencies: Strong knowledge of Nutraceuticals, Ayurveda, and Functional Foods . Expertise in scientific research, product development, and regulatory compliance . Ability to create engaging presentations and conduct training . Experience in event planning and marketing support . Excellent communication and cross-functional collaboration skills . Interested candidates can apply by sending their CV to hr3@zeon.co.in with the subject line Application for Executive - PMT.
Posted 3 months ago
5 - 10 years
14 - 19 Lacs
Mumbai
Work from Office
Principal Accountabilities & Expected Results: Develop and Implement Country Medical Plans in Focus Disease Areas: Collaborate with local and global medical teams to provide country input into medical plans and translate strategy into country activity plans. Maintain audit-trailed records of inquiry requests and responses. Define key performance indicators and metrics to track progress of activities planned by designated MSLs. Develop and Provide Credible Scientific & Research Expertise: Build and maintain "Medical-to-Medical" scientific relationships with key thought leaders in healthcare, academia, and government organizations as per TAE plans and requests. Represent the company at external meetings including scientific symposia and group discussions. Lead the setup, delivery, and management of Phase IV and non-interventional studies, ensuring compliance with global and local SOPs. Maintain scientific plans timely, accurately, and compliantly, including cross-border interactions. Design and Implementation of Best-in-Class Scientific Research Activities: Collaborate with TAEs and investigators to identify areas of shared scientific interest and advance partnerships in line with the Country Medical Head's guidance. Maintain high-quality scientific interactions with external customers. Respond Effectively to Requests for Scientific Exchange: Coordinate responses to unsolicited inquiries from HCPs and other stakeholders, ensuring quality and timely communication. Develop appropriate responses to inquiries, such as presenting scientific evidence and providing medical education. Support Local Team Disease Area and Product Knowledge Through Scientific Training: Contribute to the medical training of field-based commercial personnel as assigned. Track and record training activities per established SOPs. People Management: Provide MSLs with individual coaching, mentoring, and feedback to support their development. Conduct annual developmental reviews and performance management for team members. Foster continuous learning and improvement within the team. Maintain Personal and Medical Team Expertise in Relevant Disease Areas: Keep up-to-date with scientific expertise on assigned disease areas and products. In coordination with the Country Medical Head, train MSLs on fundamental disease area knowledge and emerging evidence. Skills & Knowledge: Educational Qualifications: MBBS / MD with a minimum of 2 years experience in pharma oncology-hematology segments. Relevant Experience: 5+ years of total experience in pharma (oncology/hematology experience is an advantage). Experience in practicing medicine is an advantage. Skills & Personal Characteristics: Focused on personal accountability and continuous performance improvement. Strong ability to establish credible relationships and engage respectfully and professionally. Effective communicator, able to manage challenging conversations and objections. Customer and patient-focused. Ability to collaborate effectively with multidisciplinary and virtual teams. Strong listening skills and effective communication (both written and verbal). Medical Research Best Practices: Knowledge of applicable pharmaceutical guidelines and regulations (e.g., ICH, GCP, Code of Ethical Practices). Skilled in medical literature appraisal and staying current with scientific publications. Attendance and reporting on relevant scientific and patient advocacy meetings as assigned. Conduct training sessions for field force on medical and scientific topics at conferences and national briefings. Patient-In Affairs: Lead the development of Patient-In strategies in line with local regulations. Drive patient awareness initiatives, both physical and digital, for designated therapy areas. Set up Patient Support Programs (PSPs) to enable better patient outcomes. Medical Information Support: Handle and respond to medical queries related to designated products. Maintain up-to-date records of all medical queries per SOPs. Share updates from the global medical information team with relevant departments.
Posted 3 months ago
4 - 9 years
10 - 14 Lacs
Bengaluru
Work from Office
Position Summary: Thermo Fisher Scientific Inc. is seeking an inventive Project Manager II to drive the strategy, management, and lifecycle of the companys corporate standard Electronic Lab Notebook (ELN) . This established product serves as a cornerstone of our R&D digital ecosystem, enabling global research teams to enhance productivity and innovation. This role combines product management, collaborating with customers and partners, and operational excellence to meet the evolving requirements of the organization and our customers. Primary Responsibilities: Develop and maintain the product roadmap, ensuring alignment with organizational goals and evolving R&D needs. Develop clear performance indicators and success metrics to assess the impact and value of the product. Serve as the main point of contact with vendors, handling relationships, contracts, and blocking issues, while prioritizing the company's needs and concerns. Drive continuous improvement by identifying, prioritizing, and implementing new features, workflows, and integrations. Collaborate with other functions (i.e., Validation, Quality, IT, Legal, Finance) to address key aspects of the implementation including validation, tracking cost savings, and legal and IP considerations. Work with the Steering Committee to ensure timely reporting of progress, risk management, and support future growth and vision of the program. Essential Skills: Project Management Excellent project management skills within large, matrixed organizations with diverse collaborators. Strong background in tracking financial impacts of process improvements; Lean Six Sigma preferred. Critical and analytical thinking, data-driven decision-making, and a customer-focused approach. Effective at communicating risks and potential countermeasures. Proven track record of exhibiting Thermo Fisher Scientific values Integrity, Intensity, Innovation, and Involvement. Collaborative Support and Engagement Partner with cross-functional teams to address technical, compliance, and operational requirements. Lead communication and change management efforts, including developing and delivering training materials. Engage with R&D users worldwide to collect feedback, identify difficulties, and make improvements that improve adoption and happiness. Operational Oversight Coordinate configuration and administration of the product, ensuring consistent and efficient operations across regions and teams. Support integration with other systems in the R&D ecosystem, including data management and collaboration platforms. Manage risk and ensure timely reporting of progress to the Steering Committee, including advancing obstacles and proposing solutions. Program Leadership & Other Champion the product as a foundational tool for R&D efficiency, advocating for its role in driving innovation. Develop strategies to scale and expand the program as the organization grows. Demonstrated interest in digital transformation and building a program that helps global and diverse R&D teams achieve better results. Comfortable with recommending workflow process improvements. Comfortable learning new information management systems and software tools necessary for responsibilities. Comfortable working across geographies and time zones, navigating multiple languages and cultures. Qualifications 4+ years of experience in project and program management of significant software implementations at large organizations. Background in scientific or lab research, innovation and design thinking, software product management, and software development lifecycle, especially for the life sciences industry is highly desirable. Experience in vendor/technology evaluation and management is a plus.
Posted 3 months ago
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Accenture
36723 Jobs | Dublin
Wipro
11788 Jobs | Bengaluru
EY
8277 Jobs | London
IBM
6362 Jobs | Armonk
Amazon
6322 Jobs | Seattle,WA
Oracle
5543 Jobs | Redwood City
Capgemini
5131 Jobs | Paris,France
Uplers
4724 Jobs | Ahmedabad
Infosys
4329 Jobs | Bangalore,Karnataka
Accenture in India
4290 Jobs | Dublin 2