Wishing You a Bright and Joyful Diwali! ✨ This Diwali, may your life be filled with light, health, and happiness. At Novamed, we celebrate the spirit of new beginnings — illuminating paths to better health, innovation, and well-being. Let’s continue to spread positivity and light up lives together. Happy Diwali from all of us at Novamed! 🌸
Novamed Laboratories Pvt. Ltd.
Pharmaceutical Manufacturing
Bahadurgarh, Haryana 1,099 followers
Delivering Innovation and Excellence in Transdermal Solutions.
About us
At Novamed Laboratories, we are revolutionizing the topical patch manufacturing industry with cutting-edge technology and an unwavering commitment to quality. Located in Sector 16, Bahadurgarh, Haryana, our facility is designed to meet the highest standards of regulatory and GMP compliance. Why Choose Novamed Laboratories? 1. Largest Manufacturing Capacity: Equipped with advanced machinery, our facility boasts the largest production capacity in the region for transdermal patches, ensuring efficiency and scalability. 2. Uncompromising Quality: Built with precision and adherence to global regulatory norms, we are setting new benchmarks in quality and innovation in the topical patch sector. 3. Industry Leadership: Our vision is to compete with and surpass top-notch companies in the topical patch manufacturing space, delivering exceptional solutions for global healthcare needs. At Novamed Laboratories, we are not just manufacturing patches; we are delivering trust, innovation, and excellence.
- Industry
- Pharmaceutical Manufacturing
- Company size
- 51-200 employees
- Headquarters
- Bahadurgarh, Haryana
- Type
- Privately Held
- Founded
- 2024
Locations
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Primary
Get directions
Plot No. 03, Sector 16
Bahadurgarh, Haryana 124507, IN
Employees at Novamed Laboratories Pvt. Ltd.
Updates
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✨🌸 Wishing You a Joyous Durga Puja & Navratri! 🌸✨ At Novamed Laboratories Pvt. Ltd., we celebrate the spirit of strength, devotion, and positivity that Goddess Durga embodies. May this festive season fill your life with happiness, prosperity, and good health. As we come together to honor the divine power of Maa Durga, let us also be inspired to move forward with courage, compassion, and unity. 🙏 Happy Durga Puja & Navratri to all! 🙏
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🌺✨ Shubh Vishwakarma Jayanti! ✨🌺 On this sacred day of Vishwakarma Jayanti, we bow to Lord Vishwakarma, the celestial architect and divine engineer of the universe. He symbolizes creativity, skill, innovation, and prosperity, guiding us to build a future with perfection and purity. At Novamed Laboratories, we draw inspiration from his divine craftsmanship and blessings, striving to create with dedication, precision, and responsibility. 🌸 May Lord Vishwakarma bless our efforts with success, harmony, and progress. 🌸 May every hand that works with sincerity be guided by his divine grace. 🌸 May this day bring prosperity and well-being to the entire Novamed family. 🙏✨ Wishing you and your loved ones a blessed Vishwakarma Jayanti! ✨🙏 — With Divine Blessings, Team Novamed
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Professional Summary: A dedicated and results-driven Purchase Executive with over 5 years of experience in handling procurement operations across diverse categories. Skilled in strategic sourcing, vendor management, price negotiation, and procurement planning, with a proven ability to ensure cost-effectiveness without compromising on quality. Adept at building strong supplier relationships, ensuring timely availability of materials, and aligning purchasing processes with organizational goals. Key Skills & Competencies: Strong negotiation skills to secure competitive prices and favorable terms. Expertise in vendor identification, evaluation, and management. Ability to handle procurement of all types of goods, raw materials, consumables, engineering spares, and services. Familiarity with pharma procurement practices, GMP compliance, and documentation. Experience in preparing purchase orders, contracts, and vendor agreements. Knowledge of inventory management and cost control strategies. Proficient in ERP systems, MS Excel, and procurement reporting tools. Strong communication, coordination, and decision-making skills. Educational Qualification: Bachelor’s Degree in Commerce / Business Administration / Supply Chain / Relevant Field (Preferred). Certification in Supply Chain Management / Procurement (added advantage). Apply: https://lnkd.in/g27hM_7C career@novamedlabs.in
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Position Summary: We are looking for a highly skilled and motivated Assistant Manager – Engineering to oversee critical engineering operations. The ideal candidate must have strong expertise in HVAC systems, water systems, and pharmaceutical utilities, with the ability to align engineering operations with QMS (Quality Management System) requirements. This role requires both technical and compliance leadership to ensure smooth facility operations, regulatory readiness, and continuous improvement. Key Responsibilities: Manage and maintain HVAC systems, water systems (WFI, Purified Water, Cooling Towers, Boilers), and other utilities. Ensure all engineering operations comply with USFDA, EU-GMP, and regulatory guidelines. Oversee preventive and breakdown maintenance of HVAC, utilities, and critical equipment. Support and implement validation and qualification of engineering systems. Participate in QMS activities such as deviations, CAPA, change control, and risk assessments related to engineering. Prepare and review SOPs, logbooks, checklists, and validation protocols. Ensure effective utility monitoring (temperature, humidity, differential pressure, water quality parameters, etc.). Coordinate with QA, Production, and QC to ensure uninterrupted operations and compliance. Lead and train engineering teams on cGMP compliance, safety, and engineering best practices. Drive energy optimization, cost reduction, and continuous improvement initiatives. Required Qualifications & Experience: Bachelor’s/Master’s degree in Mechanical or Electrical Engineering. 10–12 years of experience in engineering/maintenance within the pharmaceutical industry. Strong expertise in HVAC design, operation, and maintenance. Hands-on experience with water systems, utilities, and environmental control systems. Exposure to QMS compliance (deviations, CAPA, validation, change control). Familiarity with USFDA/EU-GMP standards. Strong leadership, analytical, and problem-solving skills. Key Competencies: Excellent technical knowledge of pharma utilities and HVAC systems. Regulatory awareness with ability to align engineering with GMP compliance. Hands-on execution in validation & qualification of utilities. Leadership and team management skills. Strong troubleshooting, decision-making, and documentation abilities. Apply: https://lnkd.in/g27hM_7C career@novamedlabs.in
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Position Summary: We are seeking a dynamic and detail-oriented Assistant Manager – Quality Control (QC) with a strong background in analytical techniques, regulatory audits, and laboratory compliance. The ideal candidate must have worked in a USFDA-approved facility and should have faced a USFDA inspection within the last 3 years. This role requires expertise in analytical instruments, validation, qualification, QMS, and vendor audits. Key Responsibilities: Ensure QC laboratory compliance with USFDA, EU-GMP, and international regulatory requirements. Manage day-to-day QC operations including sampling, testing, documentation, and release of raw materials, intermediates, and finished products. Perform and oversee validation and qualification activities for analytical instruments (HPLC, GC, UV, IR, Dissolution, etc.). Ensure compliance with data integrity requirements (21 CFR Part 11). Support and prepare for regulatory audits and inspections (USFDA, EU-GMP, WHO, etc.). Conduct and participate in vendor audits and internal audits. Review and approve QC documents including SOPs, protocols, STPs, COAs, and validation reports. Lead investigations for laboratory incidents, OOS/OOT, deviations, and CAPA implementation. Train and mentor QC analysts and executives to ensure high laboratory standards. Collaborate with QA, Production, and Regulatory Affairs for smooth operations. Required Qualifications & Experience: Bachelor’s/Master’s degree in Pharmacy, Chemistry, Biotechnology, or related field. 10–12 years of experience in Quality Control (QC) within the pharmaceutical industry. Mandatory: Experience in a USFDA-approved facility and must have faced USFDA inspection in the last 3 years. Strong knowledge of analytical method validation, instrument qualification, stability studies, and QMS. Hands-on expertise with HPLC, GC, UV, IR, and other analytical instruments. Experience in vendor audits, laboratory compliance, and data integrity practices. Excellent communication, leadership, and analytical skills. Key Competencies: Strong analytical and technical knowledge of QC operations. Regulatory mindset with ability to handle audits and inspections confidently. Hands-on execution in validation, qualification, and method transfer. Leadership and mentoring abilities. Ability to manage multiple projects and meet timelines. Apply: https://lnkd.in/g27hM_7C career@novamedlabs.in
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Position Summary: We are seeking a highly skilled and motivated Assistant Manager – Quality Assurance (QA) to join our pharmaceutical team. The ideal candidate must have hands-on experience in a USFDA-approved facility and should have faced a USFDA inspection within the last 3 years. This role requires strong expertise in Quality Management Systems (QMS), validation & qualification execution, and regulatory compliance. Key Responsibilities: Ensure strict compliance with USFDA, EU-GMP, and other international regulatory guidelines. Implement and maintain a robust Quality Management System (QMS), ensuring effective CAPA, deviation, OOS/OOT, and change control management. Perform and review validation and qualification activities (equipment, utilities, analytical instruments, processes, cleaning validation, and computer system validation) as per regulatory requirements. Plan, conduct, and support vendor audits, internal audits, and regulatory inspections. Review and approve critical quality documents, including SOPs, protocols, reports, and risk assessments. Provide hands-on support in preparation, execution, and documentation of validation protocols and reports. Coordinate with cross-functional teams (Production, QC, Engineering, Regulatory Affairs) to ensure operational excellence with quality compliance. Train and mentor QA executives and team members to enhance audit preparedness. Drive continuous improvement, data integrity compliance (21 CFR Part 11), and regulatory documentation. Required Qualifications & Experience: Bachelor’s or Master’s degree in Pharmacy, Biotechnology, Chemistry, or related field. 8–12 years of experience in Quality Assurance within the pharmaceutical industry. Must have faced USFDA inspection in the last 3 years and contributed to successful audit outcomes. Prior experience in a USFDA-approved company is mandatory. Strong knowledge of cGMP, ICH, WHO, USFDA, EU-GMP guidelines. Hands-on experience in performing validation & qualification (equipment, process, cleaning, analytical instruments, and utilities). Expertise in QMS, vendor/third-party audits, and regulatory compliance. Excellent communication, leadership, and analytical skills. Apply: https://lnkd.in/g27hM_7C career@novamedlabs.in
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