Graviti Pharmaceuticals

Company: Graviti Pharma Location: Hyderabad Duration: 1 to 3 Months Stipend: ₹10,000 + ₹5,000 incentives (performance-based) + Travel Allowance Working Days: Monday to Saturday Work Hours: 9:00 AM – 6:00 PM Mode: Field-based 🏢 About Graviti Pharma Graviti Pharmaceuticals, a sister concern of Yashoda Hospitals , is a rapidly growing healthcare company. 🔍 Role Overview We’re looking for passionate Market Research Interns to support our PACS radiology software initiative. This is a hands-on, field-based internship involving interaction with diagnostic centers and hospitals to collect insights, support demos, and drive early adoption. 📌 Key Responsibilities Conduct field market research in healthcare institutions Gather insights using structured questionnaires Support scheduling and demonstrations Document and qualify leads Submit regular reports with actionable data ✅ Eligibility Criteria MBA (Marketing / Healthcare / General Management preferred) Graduates from Pharmacy, Life Sciences, or Medical Devices background can also apply Must own a two-wheeler for local travel Strong communication and interpersonal skills Interest in healthcare technology and diagnostics 🎁 What You’ll Get Real-world experience in healthcare tech market research Mentorship from senior professionals Internship certificate Strong consideration for full-time roles based on performance Opportunity to contribute to an impactful project backed by the Yashoda Group legacy

The Group Product Manager is responsible for overseeing the strategic planning, development, and execution of marketing strategies for the cardio-diabetic product portfolio. You will need to have an in-depth understanding of the cardio-diabetic market, demonstrate strong leadership capabilities, and collaborate effectively with cross-functional teams to drive business growth and meet company objectives. Your key responsibilities will include developing and implementing marketing strategies to maximize market share, profitability, and revenue growth for the cardio-diabetic product portfolio. This will involve conducting thorough market research to identify trends, opportunities, and the competitive landscape in the cardio-diabetic sector. You will also collaborate with R&D and regulatory teams to guide the development of new products and enhancements to existing ones. In addition, you will be responsible for designing and executing effective marketing campaigns, including digital marketing, advertising, and promotional activities. Working closely with the sales team, you will provide training, tools, and support to drive product adoption and sales performance. Leading cross-functional teams, including medical, regulatory, and supply chain, will be essential to ensure alignment and successful execution of product strategies. As the Group Product Manager, you will manage the marketing budget for the cardio-diabetic portfolio, ensuring efficient resource allocation and ROI. Building and maintaining strong relationships with key stakeholders, including healthcare professionals, KOLs, and industry partners, will be a critical aspect of your role. You will also be responsible for tracking and analyzing the performance of marketing initiatives, providing regular reports and insights to senior management. The ideal candidate for this position should have an MBA or an equivalent degree.,

Graviti Pharmaceuticals Pvt Ltd is looking for Medical Representative to join our dynamic team and embark on a rewarding career journey Develop and maintain relationships with healthcare professionals and organizations Promote and sell our medical products and services to targeted customers Provide product demonstrations and education to customers Attend industry events and conferences to network and stay up to date on industry trends Maintain accurate records of sales activities and customer interactions Achieve sales targets and quotas Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying. Drive prescriptions and build doctor relationships in the cardio-diabetic therapy area. Achieve sales targets through strategic engagement and market insights.

Graviti Pharmaceuticals Pvt Ltd is looking for Business Analyst to join our dynamic team and embark on a rewarding career journey Evaluating business processes, anticipating requirements, uncovering areas for improvement, and developing and implementing solutions. Leading ongoing reviews of business processes and developing optimization strategies. Staying up-to-date on the latest process and IT advancements to automate and modernize systems. Conducting meetings and presentations to share ideas and findings. Performing requirements analysis. Documenting and communicating the results of your efforts. Effectively communicating your insights and plans to cross-functional team members and management. Gathering critical information from meetings with various stakeholders and producing useful reports. Working closely with clients, technicians, and managerial staff. Providing leadership, training, coaching, and guidance to junior staff. Allocating resources and maintaining cost efficiency. Ensuring solutions meet business needs and requirements. Performing user acceptance testing. Managing projects, developing project plans, and monitoring performance. Updating, implementing, and maintaining procedures. Prioritizing initiatives based on business needs and requirements. Serving as a liaison between stakeholders and users. Managing competing resources and priorities. Monitoring deliverables and ensuring timely completion of projects. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying. Analyze market data and financial models to optimize sales and supply chain Act as a liaison between business and technical teams, driving process improvements and regulatory compliance

Role & responsibilities Assist in manufacturing activities as per Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs). Operate and clean machines like granulators, mixers, tablet compression machines, coating pans, capsule fillers, etc. (depending on the formulation section). Maintain cleanliness and hygiene in the production area. Adhere to cGMP, safety protocols, and quality standards. Support in in-process checks and documentation under supervision. Coordinate with QA/QC and maintenance teams for process compliance and equipment handling. Participate in training programs related to production, quality, and safety. Record daily production activities and report any deviations to the supervisor. Preferred candidate profile Male Candidates

???? Were Hiring Scientist (Injectable R&D) ???? ???? Location: Hyderabad ???? Experience: 38 Years Graviti Pharmaceuticals Pvt Ltd (a fast-growing company and sister concern of Yashoda Hospitals Group) is looking for a Scientist Injectable R&D to join our Formulation R&D Injectables team, What were looking for: 38 years of experience in injectable formulation development (solutions, lyophilized products, suspensions, emulsions, complex injectables) Pharm (Pharmaceutics / Pharma Tech / Industrial Pharmacy) or PhD Experience with 505(b)(2) formulations, regulatory submissions (US/EU/Canada), tech transfer, and cGMP ?? Note: Candidates with only analytical experience or freshers are not eligible, ???? How to Apply: Send your CV to jijila v@gravitipharma with the subject line: Job Application Injectable Scientist, If this isnt relevant to you, please refer someone who fits the role,

As a Market Research Intern (Field Work) at Graviti Pharmaceuticals, a group concern of the prestigious Yashoda Group, you will have the opportunity to be part of a leading healthcare innovation and quality organization. Your role will primarily involve fully field-based market research activities for a duration of 2 months in Hyderabad. Key Responsibilities: - Engage in full-time fieldwork by visiting pharmacies and hospitals on a daily basis. - Check and report the stock availability of Graviti Pharma medicines. - Provide support to sales managers by offering valuable market insights. - Assist in understanding pharmacy/hospital buying trends and market behavior. Qualifications Required: - Any graduate or student from any semester can apply. - Availability to work from 9:00 AM to 6:00 PM, 6 days a week. - Possession of a two-wheeler (bike) and a valid driving license. - Comfortable with fieldwork and daily travel requirements. During this internship, you will gain hands-on experience in pharmaceutical market research, collaborate closely with senior sales and marketing teams, and have the opportunity to receive an Internship Certificate and Letter of Recommendation based on your performance.,

As Brand Director , you will be the strategic custodian of Graviti Pharma’s brand identity, positioning, and communication. You will lead cross-functional initiatives that elevate brand equity, drive emotional engagement, and ensure consistency across all touchpoints—from corporate messaging to employer branding and digital storytelling. Key Responsibilities • Define and execute a long-term brand strategy aligned with business goals and market dynamics • Lead brand architecture, visual identity, tone of voice, and messaging frameworks • Oversee integrated brand campaigns across digital, print, PR, and experiential channels • Build and manage a high-performing team of brand managers, designers, and content creators • Collaborate with marketing, HR, product, and leadership teams to ensure brand consistency and alignment • Champion employer branding and internal communication to strengthen culture and talent attraction • Manage external agencies, creative partners, and media vendors • Monitor brand health metrics, customer sentiment, and competitive positioning using data-driven insights Ideal Candidate Profile • 12–18 years of experience in brand management, strategic communication, or marketing leadership—preferably in any industry with strong brand-building exposure • Proven success in building and scaling brands across geographies and stakeholder groups • Strong team leadership experience with a track record of mentoring creative and strategic talent • Deep understanding of brand equity, consumer psychology, and integrated communication strategies • Excellent storytelling, stakeholder management, and cross-functional collaboration skills • Experience with employer branding, internal comms, and digital-first campaigns is a plus

Job Title: Regulatory Manager – Europe Market Location: Hyderabad, India Experience: 10–12 Years Industry: Pharmaceuticals / Healthcare Employment Type: Full-time About the Companys Graviti Pharmaceuticals is a sister concern of the prestigious Yashoda Group of Hospitals, Hyderabad. Focused on innovation and development , Graviti channels a significant share of its revenue into advanced research , driving the creation of next-generation therapies and high-impact pharmaceutical solutions. As part of our global expansion, we are now entering the European market to deliver high-quality healthcare solutions worldwide. Role Overview We are seeking a highly skilled and experienced Regulatory Manager (Europe Market) to lead and manage regulatory submissions and post-approval activities for our growing product portfolio. The role requires strong expertise in handling solid oral and sterile dosage forms and a deep understanding of European regulatory guidelines. Key Responsibilities Evaluate and implement regulatory submission strategies for the Europe market. Prepare, review, and submit dossiers (CTD/eCTD) in line with EMA and EU regulatory requirements. Handle post-approval regulatory activities , including variations, renewals, and lifecycle management. Coordinate with cross-functional teams — R&D, QA/QC, Production, and Supply Chain — to ensure compliance and timely submissions. Stay updated with evolving EU/EMA regulations and ensure company processes remain aligned. Coach and develop team members to strengthen their regulatory expertise and submission proficiency. Key Requirements 10–12 years of experience in pharmaceutical regulatory affairs , focusing on European market submissions. Proven experience in managing solid oral and/or sterile dosage forms. Strong knowledge of EMA guidelines , Module 1 regional requirements , and eCTD submission systems. Excellent communication, planning, and leadership skills. Ability to collaborate effectively with cross-functional teams and regulatory authorities. Educational Qualification Master’s degree in Pharmacy, Life Sciences, or a related discipline. Why Join Us Be part of a rapidly growing pharmaceutical company. Work in an innovation-driven environment contributing to global healthcare advancements. Opportunity to lead regulatory operations for the European market and shape our international growth journey.

As the Brand Director at Graviti Pharma, you will play a crucial role in overseeing the brand identity, positioning, and communication strategies. Your responsibilities will involve leading initiatives to enhance brand equity, drive emotional engagement, and maintain consistency across various touchpoints. - Define and implement a comprehensive brand strategy in line with business objectives and market trends - Supervise brand architecture, visual identity, tone of voice, and messaging frameworks - Manage integrated brand campaigns spanning digital, print, PR, and experiential channels - Build and supervise a proficient team consisting of brand managers, designers, and content creators - Collaborate with marketing, HR, product, and leadership teams to ensure brand alignment and consistency - Advocate for employer branding and internal communication efforts to reinforce company culture and attract top talent - Oversee relationships with external agencies, creative partners, and media vendors - Utilize data-driven insights to monitor brand health metrics, customer sentiment, and competitive positioning The ideal candidate for this role should possess: - 12-18 years of experience in brand management, strategic communication, or marketing leadership, preferably with a strong background in brand-building - Demonstrated success in expanding and enhancing brands across different regions and stakeholder groups - Proven ability to lead teams effectively and nurture creative and strategic talent - In-depth knowledge of brand equity, consumer psychology, and integrated communication strategies - Strong skills in storytelling, stakeholder management, and cross-functional collaboration - Experience in employer branding, internal communications, and digital-first campaigns would be advantageous,

Job Title: Production Planning Executive – OSD Manufacturing Location: Hyderabad Experience Required: Minimum 2 years in Production Planning Industry Preference: Plant experience compulsory FMCG or Non-Pharma preferred About the Role We are looking for a Production Planning Executive who will manage planning and scheduling activities for Oral Solid Dosage (OSD) manufacturing. The role requires strong coordination, analytical skills, and the ability to drive smooth production operations in a fast-paced plant environment. Key Responsibilities Develop and maintain detailed production schedules for OSD manufacturing processes including: Granulation Blending Compression Coating Packaging Monitor production progress and ensure schedules align with demand forecasts and capacity. Coordinate closely with Procurement, Quality, Manufacturing, and other departments to align production plans. Identify and resolve scheduling or material-related issues, making real-time adjustments as needed. Track material availability and ensure optimal inventory levels to prevent stockouts or excess holding. Expedite operations to minimize downtime and ensure timely completion of production batches. Requirements Minimum Graduate education. At least 2 years of experience in production planning at a manufacturing plant. Strong coordination, analytical, and time-management skills. Prior experience in FMCG or non-pharma manufacturing preferred. Interested candidates may apply or share profiles at rajesh.a@gravitipharma.com . Join us and be part of the growing Graviti team!

Senior GM | AVP | VP – Global Markets We are seeking an accomplished Commercial Head with extensive experience in the pharmaceutical industry to lead and drive global commercial strategies across US, Europe, and Rest of World (ROW) markets . Revenue Profitability management. Business Development market access Strategic Leadership Minimum 10 years Solid track record in commercial operations in pharma generic companies handling oral solids and injectables. Track record of successful product launches in multiple geographies and multiple dosage forms Email - nikhil.balaji@gravitipharma.com Mobile - 9666244474

Location: Hyderabad Experience: 12–18 Years Industry: Pharmaceutical Formulations (OSD, Injectables, Liquids, Pellets) About Graviti Pharmaceuticals Graviti Pharmaceuticals is a research-driven formulation company based in Hyderabad, specializing in complex generics, modified-release technologies, stability-sensitive molecules, and novel drug delivery systems. We maintain high-quality standards and strong scientific capabilities to support global regulatory expectations. Graviti Pharmaceuticals is a sister concern of the prestigious Yashoda Group of Hospitals , one of India’s most trusted healthcare institutions. With this strong foundation, we are expanding rapidly across regulated and global markets. About the Role We are seeking an experienced Development Quality Assurance (DQA) Manager / Senior Manager to lead quality oversight for new product development. The ideal candidate must have strong expertise in R&D QA, Technology Transfer, CMC documentation, analytical data review, and regulatory compliance for US/EU/ROW markets. Key Responsibilities 1. Development Quality Assurance Oversee all DQA activities for new product development, including pilot, exhibit, process validation, and qualification batches. Review and approve: Product Development Reports (PDR) Master Formula Records (MFR/MFC) Master Packing Records (MPR/MPC) Specifications, STPs, and analytical reports Compatibility and stability study protocols Ensure compliance for FRD, FARD, ARD, and PKD labs. Oversee DOE reviews, residual solvent assessments, elemental impurity evaluations, and stability plans. 2. Regulatory & Audit Preparedness Coordinate with Regulatory Affairs for ANDA, EU DCP, and global submissions. Support regulatory audits including USFDA, EMA, and other international inspections. Review CMC sections, analytical validations, and development data required for dossier filing. Lead internal audits, CAPA implementation, and continuous improvement initiatives. 3. Vendor & External Site Quality Evaluate and qualify vendors including CROs, API suppliers, excipient suppliers, and service providers. Lead and support vendor audits; ensure timely closure of audit observations. Oversee external manufacturing quality including batch reviews, packaging approvals, deviations, OOS/OOT, market complaints, and recall readiness. 4. Quality Management Systems Manage change controls, deviations, investigations, and CAPA. Maintain and support DMS and e-systems such as: SAP QM iLearn Training Module DOC-Hub KAROMI Artwork system Ensure strong QMS compliance across all development laboratories. Key Skills & Competencies Strong understanding of cGMP, GLP, ICH, USFDA, and EU guidelines Expertise in formulations including Tablets, Capsules, Injectables, Liquids, Ointments, Topicals, Pellets Strong skills in analytical method development, validation, and interpretation Excellent documentation, audit handling, and regulatory compliance skills Effective cross-functional coordination with R&D, RA, QC, QA, and Production teams Educational Qualification M.Sc (Chemistry) / B.Pharm / M.Pharm or equivalent Preferred Background Experience in Development QA within major pharmaceutical organizations Exposure to USFDA audit readiness and CMC documentation Experience in regulated market submissions (US/EU) Who Should Apply Professionals with 12–18 years of experience in DQA / QA / CQA / RA-CMC Candidates with strong documentation and formulation development QA experience Experience in both API and formulation QA is an added advantage

Company Description Graviti Pharmaceuticals, established in Hyderabad, India, is a research-driven company specializing in the production of high-quality and complex generic formulations. The organization focuses on developing modified-release formulations, bio, stability-sensitive molecules, and innovative drug delivery platforms. Known for its excellence in manufacturing, Graviti Pharmaceuticals adheres to and exceeds regulatory standards, ensuring superior-quality products. Our values of reliability, integrity, and transparency form the foundation of enduring partnerships and trust. Role Description This is a full-time, on-site role located in Hyderabad for a Regulatory Affairs Professional. In this role, you will manage the preparation, submission, and maintenance of regulatory documents to ensure compliance with applicable guidelines and regulations. You will collaborate with cross-functional teams to address regulatory requirements, monitor regulatory changes, and provide strategic guidance for product development. Other responsibilities include liaising with health authorities and managing dossier submissions and regulatory timelines effectively. Specialty in Europe and Us markets Experience : 5-8 years Qualifications Comprehensive knowledge of regulatory guidelines, dossier preparation, and submission requirements. Proficiency in regulatory documentation, compliance management, and interpretation of regulatory updates. Strong organizational, analytical, and project management skills to handle multiple tasks efficiently. Excellent communication, collaboration, and problem-solving skills to work with cross-functional teams and regulatory bodies. Ability to adapt to changing guidelines and anticipate regulatory challenges in the pharmaceutical industry. Bachelor's or Master's degree in Pharmacy, Life Sciences, or a related field is preferred. Prior experience in regulatory affairs within the pharmaceutical sector is highly desirable.

Hiring: Product Manager – CNS Division 📍 Location: Hyderabad 💼 Experience Required: 5-10 Years (CNS Segment) About the Role Graviti Pharmaceuticals is looking for an experienced Product Manager for our CNS (Central Nervous System) Division. The ideal candidate must have minimum 5-10 years of experience as a Product Manager in the CNS therapy area and be willing to relocate to Hyderabad. Key Responsibilities 1. Strategic Planning Develop and implement marketing strategies to maximize market share, revenue, and profitability for CNS products. 2. Market Analysis Conduct detailed market research to identify therapy trends, competitive landscape, and growth opportunities within the CNS segment. 3. Product Development Collaborate with R&D, Medical Affairs, and Regulatory teams to support new product development and lifecycle enhancement. 4. Marketing Campaigns Plan and execute marketing campaigns, digital initiatives, promotional materials, and branding activities. 5. Sales Support Provide training, scientific knowledge, and marketing tools to the sales team to drive product adoption and performance. 6. Cross-Functional Collaboration Work with teams such as Medical, Regulatory, Supply Chain, Finance, and Sales for seamless execution of product strategies. 7. Budget Management Manage the marketing budget, ensuring optimal resource allocation and strong ROI. 8. Stakeholder Engagement Build and maintain strong relationships with KOLs, healthcare professionals, and external partners to support product growth. 9. Performance Monitoring Track and analyze product performance metrics and provide insights and recommendations to senior management. Ideal Candidate Profile Minimum 5 years of experience as a Product Manager in the CNS therapy segment. Strong exposure to product strategy, marketing planning, digital promotion, and cross-functional coordination. Proven success in product launches and CNS portfolio management. Excellent communication, analytical, and presentation skills. Must be willing to relocate to Hyderabad.

Company Description Graviti Pharmaceuticals, established in Hyderabad, India, is a research-driven company specializing in the production of high-quality and complex generic formulations. The organization focuses on developing modified-release formulations, bio, stability-sensitive molecules, and innovative drug delivery platforms. Known for its excellence in manufacturing, Graviti Pharmaceuticals adheres to and exceeds regulatory standards, ensuring superior-quality products. Our values of reliability, integrity, and transparency form the foundation of enduring partnerships and trust. Role Description This is a full-time, on-site role located in Hyderabad for a Regulatory Affairs Professional. In this role, you will manage the preparation, submission, and maintenance of regulatory documents to ensure compliance with applicable guidelines and regulations. You will collaborate with cross-functional teams to address regulatory requirements, monitor regulatory changes, and provide strategic guidance for product development. Other responsibilities include liaising with health authorities and managing dossier submissions and regulatory timelines effectively. Specialty in Europe and Us markets Experience : 5-8 years Qualifications Comprehensive knowledge of regulatory guidelines, dossier preparation, and submission requirements. Proficiency in regulatory documentation, compliance management, and interpretation of regulatory updates. Strong organizational, analytical, and project management skills to handle multiple tasks efficiently. Excellent communication, collaboration, and problem-solving skills to work with cross-functional teams and regulatory bodies. Ability to adapt to changing guidelines and anticipate regulatory challenges in the pharmaceutical industry. Bachelor's or Master's degree in Pharmacy, Life Sciences, or a related field is preferred. Prior experience in regulatory affairs within the pharmaceutical sector is highly desirable.

Company Description Graviti Pharmaceuticals, headquartered in Hyderabad, India, is a research-driven formulation company dedicated to developing high-quality complex generics. Specializing in modified-release and stability-sensitive molecules, as well as innovative drug delivery systems, Graviti upholds stringent regulatory standards to ensure superior product quality. The company is committed to building trustworthy partnerships grounded in integrity, transparency, and responsiveness, with a focus on excellence in manufacturing. Role Description This is a full-time on-site role located in Patancheru for a Production Operator in the OSD (Oral Solid Dosage) function. Responsibilities include operating production machines, monitoring manufacturing processes, conducting quality checks, and maintaining production lines. Additional duties involve collaborating with team members to ensure efficiency and compliance with quality standards. Qualifications Proficiency in Machine Operation and managing Production Lines Knowledge of Quality Control practices in manufacturing Strong Communication skills for teamwork and reporting Ability to conduct and participate in Training activities as needed Attention to detail and commitment to adhering to safety and regulatory standards Prior experience in handling OSD production processes is a plus High school diploma or a relevant technical qualification