About the Role: We are looking for a creative and detail-oriented Graphic Designer with hands-on experience in designing packaging materials and print-ready artwork. The ideal candidate should be proficient in creating visual content for cartons, foils, pack inserts, labels (LBLs), brochures, banners , and other marketing or regulatory design needs. Key Responsibilities: Develop and execute designs for product packaging such as cartons, foils, labels, and inserts. Create marketing collaterals including brochures, banners, and promotional materials. Prepare accurate print-ready files ensuring alignment with brand guidelines and print specifications. Collaborate with cross-functional teams such as marketing, production, and quality to ensure final output meets both design and regulatory standards. Review and revise artwork based on feedback and product updates. Maintain an organized archive of artwork files for reference and compliance. Requirements: Proven experience in packaging and print design (minimum 1–2 years preferred). Strong proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign, etc.). Excellent understanding of print production processes and specifications. Attention to detail and the ability to manage multiple design tasks simultaneously. Strong communication and time management skills. Degree or diploma in Graphic Design, Visual Arts, or a related field is preferred. Nice to Have: Experience in the pharmaceutical, nutraceutical, or FMCG industry. Familiarity with compliance or regulatory artwork formats. Contact: Mail: [email protected] Phone: 9892843278 Job Type: Full-time Pay: ₹144,000.00 - ₹216,000.00 per year Benefits: Provident Fund Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person
As the Procurement Manager in the pharmaceutical and nutraceutical industry, your primary responsibility will be to oversee the sourcing, purchasing, and management of raw materials, packaging materials, and third-party services in adherence to regulatory and quality standards. Your role will entail a comprehensive understanding of Good Manufacturing Practices (GMP), vendor qualification, and supply chain risk management to ensure a continuous supply of essential materials for formulation and production processes. Your key responsibilities will include strategic sourcing by identifying and qualifying suppliers globally for APIs, excipients, nutraceutical ingredients, and packaging materials while ensuring compliance with regulatory bodies such as USFDA, FSSAI, and WHO-GMP. You will be responsible for establishing and maintaining strong supplier relationships through periodic audits and performance evaluations. Additionally, you will negotiate contracts to secure favorable terms for cost, quality, lead time, and supply continuity. Compliance and documentation will be crucial aspects of your role, requiring you to ensure adherence to regulatory and quality guidelines for all procured materials. You will be responsible for maintaining documentation for audits and inspections, including Certificates of Analysis (COAs), Material Safety Data Sheets (MSDS), Drug Master Files (DMFs), among others. Collaborating with R&D, production, and planning teams, you will forecast material requirements and optimize inventory levels to prevent stock-outs or overstocking. Cost optimization will be a primary focus, where you will drive initiatives to reduce costs while upholding material quality and integrity. Identifying potential supply chain risks and developing mitigation strategies, such as alternate suppliers and dual sourcing, will also be part of your responsibilities. You will utilize ERP systems like SAP or Oracle to manage purchase orders, supplier records, and procurement analytics, generating reports on procurement Key Performance Indicators (KPIs). To qualify for this role, you should hold a Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or Supply Chain, with an MBA or PGDM in Supply Chain Management being preferred. You must possess 5-10 years of procurement experience in the pharmaceutical, nutraceutical, or related industries, along with a deep understanding of cGMP, regulatory requirements, and sourcing challenges in the pharma/nutra sector. Strong negotiation, communication, and vendor management skills are essential, as well as familiarity with ERP systems and procurement software. Preferred skills for this position include knowledge of global sourcing, import/export regulations, and supplier qualification processes. Experience in raw material planning and coordination with R&D and formulation teams would be advantageous, as would certification in procurement or supply chain (e.g., CIPS, APICS, CPSM). This is a full-time position with a day shift schedule and opportunities for performance and yearly bonuses. The work location is in person.,
We Meliorate Health would like to introduce ourselves as a registered Healthcare product manufacturer in Mumbai, India. Our products are, pharmaceutical formulation, food supplementary products & herbal products. We aim to provide one stop service center for all our global partners for hospital & medical needs. We have a nutraceutical manufacturing facility at Ahmednagar, Maharashtra. To know more about us kindly go through our website www.melioratehealth.com . We Meliorate Health are pleased to inform you that our company is offering Regulatory Affairs Executive designation to B. Pharm/M. Pharm candidates. Please read the JD mentioned below for more details about the role. Designation: Executive Regulatory Affairs Qualification: B Pharma / M Pharm Department: Regulatory Affairs Location: Goregaon East, Mumbai Joining CTC: Package around 3.00 lacs to 4.00 lacs per anum Job Responsibilities: 1) Dossier Preparation: Preparation and review of standard dossier, ACTD, CTD, ECTD as per Country specific guideline. 2) Query Response: Response to all dossier related queries to comply the requirement from Ministry of Health of different countries or Regulatory team from different countries. 3) FDA Department: CO-ordinate with FDA documentation department to apply for product approvals, COPPs, FSCs or any tender documents. 4) Co-ordination: Co-ordination with plants for arranging samples and working standards from plant as per Authority requirement. Co-ordination with Marketing Department and Export Department for various registration activities. Co-ordination with the plant and R&D for MFR and BMR required for dossier preparation. 5) Recording/Data Management: Responsible for maintaining proper records and storing all dossiers as per company Guidelines/Policies. 6) Miscellaneous /General: After receipt of sample from plant further processing at HO for printing and dispatching of sample. Developing art works for label/carton and leaflet in co-ordination with artist /designer Co-ordination with customer & site for artwork finalization & approval. Ensuring orders to get manufacture as per approved artwork, coordinate to get print proof & pre shipment sample approval from customer. Arranging market samples for new product required by ADL Department to prepare quality Data. Work as a team with all Regulatory colleagues. Supervising and reviewing documentation of dispatch samples and hard copy of dossiers/Legal document (MSDS, Invoice, Non-Hazardous certificate, Covering letter, Indemnity letter and proper packing of sample). Supervising and reviewing of Administrative documents for Notarization, Bombay chamber of commerce, Legalization and apostille as per country specific Embassy. Data Surfing related to Clinical & non clinical pertaining to product as well as dossier requirement. Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹400,000.00 per year Benefits: Commuter assistance Internet reimbursement Leave encashment Education: Bachelor's (Required) Experience: total work: 1 year (Required) Location: Goregaon East, Mumbai, Maharashtra (Required) Work Location: In person
We Meliorate Health would like to introduce ourselves as a registered Healthcare product manufacturer in Mumbai, India. Our products are, pharmaceutical formulation, food supplementary products & herbal products. We aim to provide one stop service center for all our global partners for hospital & medical needs. We have a nutraceutical manufacturing facility at Ahmednagar, Maharashtra. To know more about us kindly go through our website www.melioratehealth.com . We Meliorate Health are pleased to inform you that our company is offering Regulatory Affairs Executive designation to B. Pharm/M. Pharm candidates. Please read the JD mentioned below for more details about the role. Designation: Executive Regulatory Affairs Qualification: B Pharma / M Pharm Department: Regulatory Affairs Location: Goregaon East, Mumbai Joining CTC: Package around 3.00 lacs to 4.00 lacs per anum Job Responsibilities: 1) Dossier Preparation: Preparation and review of standard dossier, ACTD, CTD, ECTD as per Country specific guideline. 2) Query Response: Response to all dossier related queries to comply the requirement from Ministry of Health of different countries or Regulatory team from different countries. 3) FDA Department: CO-ordinate with FDA documentation department to apply for product approvals, COPPs, FSCs or any tender documents. 4) Co-ordination: Co-ordination with plants for arranging samples and working standards from plant as per Authority requirement. Co-ordination with Marketing Department and Export Department for various registration activities. Co-ordination with the plant and R&D for MFR and BMR required for dossier preparation. 5) Recording/Data Management: Responsible for maintaining proper records and storing all dossiers as per company Guidelines/Policies. 6) Miscellaneous /General: After receipt of sample from plant further processing at HO for printing and dispatching of sample. Developing art works for label/carton and leaflet in co-ordination with artist /designer Co-ordination with customer & site for artwork finalization & approval. Ensuring orders to get manufacture as per approved artwork, coordinate to get print proof & pre shipment sample approval from customer. Arranging market samples for new product required by ADL Department to prepare quality Data. Work as a team with all Regulatory colleagues. Supervising and reviewing documentation of dispatch samples and hard copy of dossiers/Legal document (MSDS, Invoice, Non-Hazardous certificate, Covering letter, Indemnity letter and proper packing of sample). Supervising and reviewing of Administrative documents for Notarization, Bombay chamber of commerce, Legalization and apostille as per country specific Embassy. Data Surfing related to Clinical & non clinical pertaining to product as well as dossier requirement. Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹400,000.00 per year Benefits: Commuter assistance Internet reimbursement Leave encashment Education: Bachelor's (Required) Experience: total work: 1 year (Required) Location: Goregaon East, Mumbai, Maharashtra (Required) Work Location: In person
As a Procurement Manager in the pharmaceutical and nutraceutical industry, your role involves sourcing, purchasing, and managing the supply of raw materials, packaging materials, and third-party services while adhering to regulatory and quality standards. Your responsibilities include: - Strategic Sourcing: Identify and qualify suppliers globally for APIs, excipients, nutraceutical ingredients, and packaging materials, ensuring regulatory compliance. - Supplier Management: Establish and maintain strong supplier relationships through audits and performance assessments. - Contract Negotiation: Negotiate terms for cost, quality, lead time, and supply continuity. - Compliance & Documentation: Ensure adherence to regulatory guidelines and maintain documentation for audits and inspections. - Forecasting & Inventory: Collaborate with R&D, production, and planning teams to forecast material requirements and optimize inventory levels. - Cost Optimization: Drive cost-reduction initiatives while upholding material quality. - Risk Management: Identify and mitigate potential supply chain risks. - ERP & Reporting: Utilize ERP systems for managing purchase orders, supplier records, and procurement analytics, and generate reports on procurement KPIs. Qualifications required for this role: - Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or Supply Chain; MBA or PGDM in Supply Chain Management preferred. - 5-10 years of procurement experience in pharmaceutical, nutraceutical, or related industries. - In-depth understanding of cGMP, regulatory requirements, and sourcing challenges in pharma/nutra. - Strong negotiation, communication, and vendor management skills. - Familiarity with ERP systems and procurement software. This is a full-time position with day shift and morning shift schedules. Performance bonus and yearly bonus are provided. The work location is in person, and the expected start date is 20/06/2025.,
About the Role: We are looking for a creative and detail-oriented Graphic Designer with hands-on experience in designing packaging materials and print-ready artwork. The ideal candidate should be proficient in creating visual content for cartons, foils, pack inserts, labels (LBLs), brochures, banners, poster and other marketing or regulatory design needs. Key Responsibilities: Develop and execute designs for product packaging such as cartons, foils, labels, and inserts. Create marketing collaterals including brochures, banners, and promotional materials. Prepare accurate print-ready files ensuring alignment with brand guidelines and print specifications. Collaborate with cross-functional teams such as marketing, production, and quality to ensure final output meets both design and regulatory standards. Review and revise artwork based on feedback and product updates. Maintain an organized archive of artwork files for reference and compliance. Requirements: Proven experience in packaging and print design (minimum 1–2 years preferred). Strong proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign, etc.). Excellent understanding of print production processes and specifications. Attention to detail and the ability to manage multiple design tasks simultaneously. Strong communication and time management skills. Degree or diploma in Graphic Design, Visual Arts, or a related field is preferred. Nice to Have: Experience in the pharmaceutical, nutraceutical, or FMCG industry. Familiarity with compliance or regulatory artwork formats. Contact: Mail: [email protected] Phone: 9892843278 Job Type: Full-time Pay: ₹180,000.00 - ₹240,000.00 per year Work Location: In person