Job Description: R&D Chemist (Lifesciences)Experience: 1-5 yearsQualification: Masters in Organic Chemistry/Medicinal Chemistry/Chemistry Job Responsibilities: Research and Development:Conduct research and development for Ingredients.Develop and optimize formulations for new products and improve existing formulations. Laboratory Work:Perform laboratory experiments, synthesis, and chemical reactions as required for R&D projects.Analyze raw materials and finished products using analytical instruments. Documentation and Compliance:Maintain accurate documentation of experiments, procedures, and findings.Ensure compliance with regulatory and quality standards applicable to pharmaceutical and API development. Quality Control:Perform quality control tests on products to ensure consistency and adherence to specifications.Provide technical support to manufacturing teams for scale-up and production. Collaboration:Work closely with cross-functional teams including Quality Assurance, Production, and Marketing.Provide technical guidance and support for troubleshooting during production. Key Skills:Strong knowledge of organic chemistry principles.Experience in formulation development for fragrances and pharmaceutical applications.Proficiency in handling analytical instruments (e.g., GC, HPLC, FTIR).Excellent problem-solving skills and attention to detail.Ability to manage multiple projects simultaneously.Knowledge of Microsoft Tools Salary : Upto 6 LPA Benefits:Paid sick time
Job Title: Assistant Manager – Drug Regulatory Compliance Industry: Pharmaceuticals Experience Required: 3–5 Years Job Summary: We are seeking a detail-oriented and proactive Assistant Manager – Drug Regulatory Compliance to ensure compliance with regulatory standards applicable to pharmaceutical products. The role involves managing end-to-end regulatory submissions, monitoring compliance with REACH, FSSAI, CDSCO , and other relevant national and international guidelines. Key Responsibilities: Ensure compliance with drug regulations , REACH compliance , FSSAI guidelines , and applicable international standards. Prepare, review, and submit regulatory documents, dossiers, and product registrations. Liaise with regulatory authorities (CDSCO, FSSAI, etc.) for approvals, renewals, and queries. Monitor changes in global and domestic regulatory requirements and update internal processes accordingly. Coordinate with cross-functional teams (R&D, Quality, Manufacturing, Supply Chain) to ensure timely submissions and product compliance. Maintain regulatory documentation and records as per SOPs and audit requirements. Support audits and inspections by internal/external regulatory authorities. Provide training and guidance to teams on regulatory compliance updates and best practices. Desired Candidate Profile: Bachelor’s/Master’s in Pharmacy, Life Sciences, Chemistry, or related field. 3–5 years of regulatory compliance experience in the pharmaceutical/healthcare/food industry. Good knowledge of Drug Regulatory Affairs, REACH, FSSAI, CDSCO regulations. Strong understanding of regulatory documentation and submission processes. Excellent communication and liaison skills for interacting with authorities and internal stakeholders. Detail-oriented with strong organizational and analytical skills. Key Skills: Regulatory Affairs & Compliance REACH Compliance FSSAI Guidelines CDSCO Regulations Documentation & Dossier Preparation Audits & Inspections Handling Job Type: Full-time Pay: ₹400,000.00 - ₹600,000.00 per year Work Location: In person
Job Title: Assistant Manager – Drug Regulatory Compliance Industry: Pharmaceuticals Experience Required: 3–5 Years Job Summary: We are seeking a detail-oriented and proactive Assistant Manager – Drug Regulatory Compliance to ensure compliance with regulatory standards applicable to pharmaceutical products. The role involves managing end-to-end regulatory submissions, monitoring compliance with REACH, FSSAI, CDSCO , and other relevant national and international guidelines. Key Responsibilities: Ensure compliance with drug regulations , REACH compliance , FSSAI guidelines , and applicable international standards. Prepare, review, and submit regulatory documents, dossiers, and product registrations. Liaise with regulatory authorities (CDSCO, FSSAI, etc.) for approvals, renewals, and queries. Monitor changes in global and domestic regulatory requirements and update internal processes accordingly. Coordinate with cross-functional teams (R&D, Quality, Manufacturing, Supply Chain) to ensure timely submissions and product compliance. Maintain regulatory documentation and records as per SOPs and audit requirements. Support audits and inspections by internal/external regulatory authorities. Provide training and guidance to teams on regulatory compliance updates and best practices. Desired Candidate Profile: Bachelor’s/Master’s in Pharmacy, Life Sciences, Chemistry, or related field. 3–5 years of regulatory compliance experience in the pharmaceutical/healthcare/food industry. Good knowledge of Drug Regulatory Affairs, REACH, FSSAI, CDSCO regulations. Strong understanding of regulatory documentation and submission processes. Excellent communication and liaison skills for interacting with authorities and internal stakeholders. Detail-oriented with strong organizational and analytical skills. Key Skills: Regulatory Affairs & Compliance REACH Compliance FSSAI Guidelines CDSCO Regulations Documentation & Dossier Preparation Audits & Inspections Handling Job Type: Full-time Pay: ₹400,000.00 - ₹600,000.00 per year Work Location: In person
Job Title: Senior Executive – Regulatory Affairs Industry: Pharmaceuticals Experience Required: 3–5 Years Job Summary: We are seeking a detail-oriented and proactive Senior Executive – Regulatory Affairs to ensure compliance with regulatory standards applicable to pharmaceutical products. The role involves managing end-to-end regulatory submissions, monitoring compliance with REACH, FSSAI, CDSCO , and other relevant national and international guidelines. Key Responsibilities: Prepare, review, and maintain dossiers, Product Information Files (PIFs), SDS,COAs, toxicological reports, CPSRs, and compliance statements. Manage global regulatory submissions and compliance for international countries . Liaise with international consultants/partners for local dossier filings and registrations. Certifications & Sustainability Standards Regulatory Intelligence & Training Cross-Functional & Customer Support * Desired Candidate Profile: Bachelor’s/Master’s in Pharmacy, Chemistry, Life Sciences, or related field. 3–5 years of Regulatory Affairs experience in cosmetic ingredients / personal care. Strong knowledge of global cosmetic regulations: EU, US, Japan, Korea, China,ASEAN, LATAM, and Africa. Hands-on experience with certification management: EcoVadis, COSMOS, Halal, Kosher, Vegan, Fairtrade, SEDEX. Proven skills in dossier preparation, certification audits, and complianc submissions. Strong organizational skills with ability to handle multiple country requirements simultaneously. Excellent liaison and communication skills with consultants, auditors, and regulatory authorities. Key Skills: Global Regulatory Affairs (Cosmetics & Ingredients) LATAM & ASEAN Regulatory Submissions (ANVISA, MERCOSUR, COFEPRIS, ASEAN Guidelines) Certification Management (EcoVadis, COSMOS, Halal, Kosher, Vegan, Fairtrade, SEDEX) Audit & Inspection Handling (EcoVadis, GMP/ISO, Customer Audits) Documentation & Dossier Preparation (PIFs, SDS, CPSRs, Toxicology, Safety Reports) Cross-Functional Collaboration (R&D, Quality, Manufacturing, Sales) Job Type: Full-time Pay: ₹400,000.00 - ₹600,000.00 per year Work Location: In person
Roles & Responsibilities: Prepare and serve tea, coffee, and refreshments to staff and visitors. Ensure pantry area is clean, hygienic, and well-maintained. Maintain stock of pantry items (tea, coffee, milk, sugar, snacks, etc.). Assist in serving water and refreshments during meetings and office events. Wash and clean utensils, crockery, and pantry equipment regularly. Support office staff with small errands related to pantry and hospitality. Follow hygiene and safety standards at all times. Document Filling Requirements: Basic knowledge of cleaning and serving. Prior experience in pantry or hospitality work preferred. Polite, disciplined, and punctual. Ability to maintain cleanliness and handle basic pantry stock. Job Type: Full-time Pay: ₹12,000.00 - ₹15,000.00 per month Benefits: Provident Fund Work Location: In person
Roles & Responsibilities: Prepare and serve tea, coffee, and refreshments to staff and visitors. Ensure pantry area is clean, hygienic, and well-maintained. Maintain stock of pantry items (tea, coffee, milk, sugar, snacks, etc.). Assist in serving water and refreshments during meetings and office events. Wash and clean utensils, crockery, and pantry equipment regularly. Support office staff with small errands related to pantry and hospitality. Follow hygiene and safety standards at all times. Document Filling Requirements: Basic knowledge of cleaning and serving. Prior experience in pantry or hospitality work preferred. Polite, disciplined, and punctual. Ability to maintain cleanliness and handle basic pantry stock. Job Type: Full-time Pay: ₹12,000.00 - ₹15,000.00 per month Benefits: Provident Fund Work Location: In person
Job Title: Senior Executive – Regulatory Affairs Industry: Pharmaceuticals Experience Required: 3–5 Years Job Summary: We are seeking a detail-oriented and proactive Senior Executive – Regulatory Affairs to ensure compliance with regulatory standards applicable to pharmaceutical products. The role involves managing end-to-end regulatory submissions, monitoring compliance with REACH, FSSAI, CDSCO , and other relevant national and international guidelines. Key Responsibilities: Prepare, review, and maintain dossiers, Product Information Files (PIFs), SDS,COAs, toxicological reports, CPSRs, and compliance statements. Manage global regulatory submissions and compliance for international countries . Liaise with international consultants/partners for local dossier filings and registrations. Certifications & Sustainability Standards Regulatory Intelligence & Training Cross-Functional & Customer Support * Desired Candidate Profile: Bachelor’s/Master’s in Pharmacy, Chemistry, Life Sciences, or related field. 3–5 years of Regulatory Affairs experience in cosmetic ingredients / personal care. Strong knowledge of global cosmetic regulations: EU, US, Japan, Korea, China,ASEAN, LATAM, and Africa. Hands-on experience with certification management: EcoVadis, COSMOS, Halal, Kosher, Vegan, Fairtrade, SEDEX. Proven skills in dossier preparation, certification audits, and complianc submissions. Strong organizational skills with ability to handle multiple country requirements simultaneously. Excellent liaison and communication skills with consultants, auditors, and regulatory authorities. Key Skills: Global Regulatory Affairs (Cosmetics & Ingredients) LATAM & ASEAN Regulatory Submissions (ANVISA, MERCOSUR, COFEPRIS, ASEAN Guidelines) Certification Management (EcoVadis, COSMOS, Halal, Kosher, Vegan, Fairtrade, SEDEX) Audit & Inspection Handling (EcoVadis, GMP/ISO, Customer Audits) Documentation & Dossier Preparation (PIFs, SDS, CPSRs, Toxicology, Safety Reports) Cross-Functional Collaboration (R&D, Quality, Manufacturing, Sales) Job Type: Full-time Pay: ₹400,000.00 - ₹600,000.00 per year Work Location: In person
Company Description Trishveda Naturals Pvt Ltd specializes in producing a wide range of specialized oils and powders from fruits, vegetables, flowers, minerals, and seeds using a physical manufacturing process. These natural ingredients have diverse applications in various beauty and personal care products. Utilizing plant-based chemistry and biotechnology platforms, Trishveda Naturals develops high-value products, innovations, and new functions with natural ingredients. Job Title: Senior Executive – Regulatory Affairs Industry: Pharmaceuticals Experience Required: 3–5 Years Job Summary: We are seeking a detail-oriented and proactive Senior Executive – Regulatory Affairs to ensure compliance with regulatory standards applicable to pharmaceutical products. The role involves managing end-to-end regulatory submissions, monitoring compliance with REACH, FSSAI, CDSCO , and other relevant national and international guidelines. Key Responsibilities: Prepare, review, and maintain dossiers, Product Information Files (PIFs), SDS,COAs, toxicological reports, CPSRs, and compliance statements. Manage global regulatory submissions and compliance for international countries . Liaise with international consultants/partners for local dossier filings and registrations. Certifications & Sustainability Standards Regulatory Intelligence & Training Cross-Functional & Customer Support Desired Candidate Profile: Bachelor’s/Master’s in Pharmacy, Chemistry, Life Sciences, or related field. 3–5 years of Regulatory Affairs experience in cosmetic ingredients / personal care. Strong knowledge of global cosmetic regulations: EU, US, Japan, Korea, China,ASEAN, LATAM, and Africa. Hands-on experience with certification management: EcoVadis, COSMOS, Halal, Kosher, Vegan, Fairtrade, SEDEX. Proven skills in dossier preparation, certification audits, and complianc submissions. Strong organizational skills with ability to handle multiple country requirements simultaneously. Excellent liaison and communication skills with consultants, auditors, and regulatory authorities. Key Skills: Global Regulatory Affairs (Cosmetics & Ingredients) LATAM & ASEAN Regulatory Submissions (ANVISA, MERCOSUR, COFEPRIS, ASEAN Guidelines) Certification Management (EcoVadis, COSMOS, Halal, Kosher, Vegan, Fairtrade, SEDEX) Audit & Inspection Handling (EcoVadis, GMP/ISO, Customer Audits) Documentation & Dossier Preparation (PIFs, SDS, CPSRs, Toxicology, Safety Reports) Cross-Functional Collaboration (R&D, Quality, Manufacturing, Sales) Location : Kohara, Ludhiana.