Roles and Responsibility: Managing operations: Overseeing the website, product listings, inventory, orders, payments, and customer service Improving customer experience: Ensuring a consistent and high-quality experience for users Analyzing data: Studying sales and market trends to identify growth opportunities Developing strategy: Working with management to develop a digital marketing strategy Managing content: Ensuring the company's website content is current and relevant Creating partnerships: Establishing relationships with other businesses to create cost-effective partnerships Content Creation: Research and organize sources and information. Collaborate and brainstorm with the team for new strategies and ideas. Write well-researched and keyword-driven content to boost organic traffic. Create optimized, engaging title tags and meta descriptions to increase click-through rate. Create clear and innovative headlines and body copy. Produce high-quality blog posts on industry-relevant topics and address user queries in detail. Write a wide variety of topics for podcasts, e-books, websites, blogs, social media, case studies, whitepapers, banners, etc. Create, execute, and maintain a content calendar. Ensure consistency in writing style, fonts, images, and tone. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Benefits: Provident Fund Education: Bachelor's (Preferred) Experience: total work: 1 year (Required) Language: English (Preferred) Work Location: In person
Job Summary: We are seeking a motivated and knowledgeable Quality Assurance (QA) professional to manage compliance activities related to third-party pharmaceutical manufacturing and packaging sites. The ideal candidate will ensure that all contract manufacturing organizations (CMOs) operate in alignment with current regulatory guidelines (cGMP, ICH, WHO, etc.) and internal quality systems, from production to release. Key Responsibilities: Coordinate with third-party manufacturing (TPM) and packaging sites to ensure adherence to company and regulatory quality standards. Review and approve batch manufacturing records (BMRs) and batch packaging records (BPRs) from TPMs. Monitor and support investigation of deviations, change controls, and CAPAs for timely resolution. Conduct periodic quality audits and site visits; prepare audit reports and follow up on observations. Review and approve quality documentation (SOPs, protocols, reports) submitted by TPMs. Ensure timely QA product release by coordinating with site QA teams and internal departments. Maintain and update Quality Agreements with third-party manufacturing partners. Support customer audits and regulatory inspections (WHO, MHRA, USFDA, etc.) at TPM sites. Track and report key quality metrics to management related to third-party operations. Provide training and support to QA/QC teams at third-party sites when required. Collaborate with internal teams including Regulatory Affairs, Production, R&D, and Supply Chain for smooth operations. Manage new product registration processes and associated documentation. Oversee brand registration on Trade Safe platform. Handle NPPA/DPCO-related compliance and submissions. Coordinate with labs for sample testing activities and ensure timely Certificate of Analysis (COA) issuance. Qualifications: B.Pharm / M.Pharm / M.Sc. in Life Sciences. 2–5 years of QA experience in the pharmaceutical industry, preferably in a corporate QA or third-party manufacturing role. Sound knowledge of cGMP, ICH guidelines, and Indian regulatory frameworks. Hands-on experience in batch record review, documentation control, and vendor compliance. Familiarity with NPPA/DPCO requirements and regulatory processes. Desired Skills: Experience working with multiple third-party manufacturers and packagers. Strong communication and coordination skills across cross-functional and external teams. Proficiency in MS Office and quality documentation tools. Willingness to travel to TPM sites for audits, training, or compliance support. Job Types: Full-time, Permanent Pay: Up to ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person
Job Summary: We are seeking a motivated and knowledgeable Quality Assurance (QA) professional to manage compliance activities related to third-party pharmaceutical manufacturing and packaging sites. The ideal candidate will ensure that all contract manufacturing organizations (CMOs) operate in alignment with current regulatory guidelines (cGMP, ICH, WHO, etc.) and internal quality systems, from production to release. Key Responsibilities: Coordinate with third-party manufacturing (TPM) and packaging sites to ensure adherence to company and regulatory quality standards. Review and approve batch manufacturing records (BMRs) and batch packaging records (BPRs) from TPMs. Monitor and support investigation of deviations, change controls, and CAPAs for timely resolution. Conduct periodic quality audits and site visits; prepare audit reports and follow up on observations. Review and approve quality documentation (SOPs, protocols, reports) submitted by TPMs. Ensure timely QA product release by coordinating with site QA teams and internal departments. Maintain and update Quality Agreements with third-party manufacturing partners. Support customer audits and regulatory inspections (WHO, MHRA, USFDA, etc.) at TPM sites. Track and report key quality metrics to management related to third-party operations. Provide training and support to QA/QC teams at third-party sites when required. Collaborate with internal teams including Regulatory Affairs, Production, R&D, and Supply Chain for smooth operations. Manage new product registration processes and associated documentation. Oversee brand registration on Trade Safe platform. Handle NPPA/DPCO-related compliance and submissions. Coordinate with labs for sample testing activities and ensure timely Certificate of Analysis (COA) issuance. Qualifications: B.Pharm / M.Pharm / M.Sc. in Life Sciences. 2–5 years of QA experience in the pharmaceutical industry, preferably in a corporate QA or third-party manufacturing role. Sound knowledge of cGMP, ICH guidelines, and Indian regulatory frameworks. Hands-on experience in batch record review, documentation control, and vendor compliance. Familiarity with NPPA/DPCO requirements and regulatory processes. Desired Skills: Experience working with multiple third-party manufacturers and packagers. Strong communication and coordination skills across cross-functional and external teams. Proficiency in MS Office and quality documentation tools. Willingness to travel to TPM sites for audits, training, or compliance support. Job Types: Full-time, Permanent Pay: Up to ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person
Roles and Responsibility: Managing operations: Overseeing the website, product listings, inventory, orders, payments, and customer service Improving customer experience: Ensuring a consistent and high-quality experience for users Analyzing data: Studying sales and market trends to identify growth opportunities Developing strategy: Working with management to develop a digital marketing strategy Managing content: Ensuring the company's website content is current and relevant Creating partnerships: Establishing relationships with other businesses to create cost-effective partnerships Content Creation: Research and organize sources and information. Collaborate and brainstorm with the team for new strategies and ideas. Write well-researched and keyword-driven content to boost organic traffic. Create optimized, engaging title tags and meta descriptions to increase click-through rate. Create clear and innovative headlines and body copy. Produce high-quality blog posts on industry-relevant topics and address user queries in detail. Write a wide variety of topics for podcasts, e-books, websites, blogs, social media, case studies, whitepapers, banners, etc. Create, execute, and maintain a content calendar. Ensure consistency in writing style, fonts, images, and tone. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Benefits: Provident Fund Education: Bachelor's (Preferred) Experience: total work: 1 year (Required) Language: English (Preferred) Work Location: In person
Job Summary: We are seeking a motivated and knowledgeable Quality Assurance (QA) professional to manage compliance activities related to third-party pharmaceutical manufacturing and packaging sites. The ideal candidate will ensure that all contract manufacturing organizations (CMOs) operate in alignment with current regulatory guidelines (cGMP, ICH, WHO, etc.) and internal quality systems, from production to release. Key Responsibilities: Coordinate with third-party manufacturing (TPM) and packaging sites to ensure adherence to company and regulatory quality standards. Review and approve batch manufacturing records (BMRs) and batch packaging records (BPRs) from TPMs. Monitor and support investigation of deviations, change controls, and CAPAs for timely resolution. Conduct periodic quality audits and site visits; prepare audit reports and follow up on observations. Review and approve quality documentation (SOPs, protocols, reports) submitted by TPMs. Ensure timely QA product release by coordinating with site QA teams and internal departments. Maintain and update Quality Agreements with third-party manufacturing partners. Support customer audits and regulatory inspections (WHO, MHRA, USFDA, etc.) at TPM sites. Track and report key quality metrics to management related to third-party operations. Provide training and support to QA/QC teams at third-party sites when required. Collaborate with internal teams including Regulatory Affairs, Production, R&D, and Supply Chain for smooth operations. Manage new product registration processes and associated documentation. Oversee brand registration on Trade Safe platform. Handle NPPA/DPCO-related compliance and submissions. Coordinate with labs for sample testing activities and ensure timely Certificate of Analysis (COA) issuance. Qualifications: B.Pharm / M.Pharm / M.Sc. in Life Sciences. 2–5 years of QA experience in the pharmaceutical industry, preferably in a corporate QA or third-party manufacturing role. Sound knowledge of cGMP, ICH guidelines, and Indian regulatory frameworks. Hands-on experience in batch record review, documentation control, and vendor compliance. Familiarity with NPPA/DPCO requirements and regulatory processes. Desired Skills: Experience working with multiple third-party manufacturers and packagers. Strong communication and coordination skills across cross-functional and external teams. Proficiency in MS Office and quality documentation tools. Willingness to travel to TPM sites for audits, training, or compliance support. Job Types: Full-time, Permanent Pay: Up to ₹40,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Job Summary: We are seeking a motivated and knowledgeable Quality Assurance (QA) professional to manage compliance activities related to third-party pharmaceutical manufacturing and packaging sites. The ideal candidate will ensure that all contract manufacturing organizations (CMOs) operate in alignment with current regulatory guidelines (cGMP, ICH, WHO, etc.) and internal quality systems, from production to release. Key Responsibilities: Coordinate with third-party manufacturing (TPM) and packaging sites to ensure adherence to company and regulatory quality standards. Review and approve batch manufacturing records (BMRs) and batch packaging records (BPRs) from TPMs. Monitor and support investigation of deviations, change controls, and CAPAs for timely resolution. Conduct periodic quality audits and site visits; prepare audit reports and follow up on observations. Review and approve quality documentation (SOPs, protocols, reports) submitted by TPMs. Ensure timely QA product release by coordinating with site QA teams and internal departments. Maintain and update Quality Agreements with third-party manufacturing partners. Support customer audits and regulatory inspections (WHO, MHRA, USFDA, etc.) at TPM sites. Track and report key quality metrics to management related to third-party operations. Provide training and support to QA/QC teams at third-party sites when required. Collaborate with internal teams including Regulatory Affairs, Production, R&D, and Supply Chain for smooth operations. Manage new product registration processes and associated documentation. Oversee brand registration on Trade Safe platform. Handle NPPA/DPCO-related compliance and submissions. Coordinate with labs for sample testing activities and ensure timely Certificate of Analysis (COA) issuance. Qualifications: B.Pharm / M.Pharm / M.Sc. in Life Sciences. 2–5 years of QA experience in the pharmaceutical industry, preferably in a corporate QA or third-party manufacturing role. Sound knowledge of cGMP, ICH guidelines, and Indian regulatory frameworks. Hands-on experience in batch record review, documentation control, and vendor compliance. Familiarity with NPPA/DPCO requirements and regulatory processes. Desired Skills: Experience working with multiple third-party manufacturers and packagers. Strong communication and coordination skills across cross-functional and external teams. Proficiency in MS Office and quality documentation tools. Willingness to travel to TPM sites for audits, training, or compliance support. Job Types: Full-time, Permanent Pay: Up to ₹40,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Interested candidate put your CV on this mail * [email protected] * Note . Required Skills: Attention to Detail: Meticulous attention to detail is crucial for ensuring data accuracy. Computer Literacy: Proficiency in using computer systems, databases, and relevant software is necessary. Organizational Skills: Strong organizational skills are needed to manage data and tasks effectively. Time Management: Ability to manage time effectively and meet deadlines is important. Communication Skills: Good communication skills are helpful for collaborating with colleagues and addressing data-related issues. Basic Understanding of Database Structure: Familiarity with database structures and queries can be beneficial. Job Type: Full-time Benefits: Health insurance Life insurance Paid sick time Provident Fund Language: English (Preferred) Work Location: In person
Interested candidate put your CV on this mail * hr@smartwaywellness.com* Note . Required Skills: Attention to Detail: Meticulous attention to detail is crucial for ensuring data accuracy. Computer Literacy: Proficiency in using computer systems, databases, and relevant software is necessary. Organizational Skills: Strong organizational skills are needed to manage data and tasks effectively. Time Management: Ability to manage time effectively and meet deadlines is important. Communication Skills: Good communication skills are helpful for collaborating with colleagues and addressing data-related issues. Basic Understanding of Database Structure: Familiarity with database structures and queries can be beneficial. Job Type: Full-time Benefits: Health insurance Life insurance Paid sick time Provident Fund Language: English (Preferred) Work Location: In person
As a candidate for this role, you will be responsible for coordinating with clients, performing bank reconciliation, and entering invoices and cheques into the system. Qualifications required for this position include: - Minimum 1 year of experience in bank reconciliation - Proficiency in English is mandatory Please note that the job is full-time with a day shift schedule. The company offers benefits such as health insurance, life insurance, provident fund, and a yearly bonus. The work location is in person.,
Responsibilities Prepare and review financial statements and reports Ensure compliance with tax regulations and filing requirements Manage accounts payable and receivable processes Assist in the preparation of budgets and financial forecasts Conduct internal audits to ensure regulatory compliance Collaborate with external auditors for annual audits Monitor and analyze accounting data to produce financial insight Skills Tax compliance Financial reporting Budgeting and forecasting Accounts payable/receivable management Internal auditing Regulatory compliance Excel Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Provident Fund Education: Bachelor's (Preferred) Work Location: In person