Job Title: Production Manager Location: Greater Noida Industry: Pharmaceuticals (Ointment Manufacturing) About the Role We are looking for an experienced Production Manager to oversee and manage the production operations of our pharmaceutical manufacturing facility. The ideal candidate must be an Approved Chemist in Ointment with extensive experience in managing production teams, ensuring compliance, and achieving productivity and quality targets. Key Responsibilities Manage end-to-end production operations of the ointment manufacturing unit. Ensure compliance with GMP, cGMP, and regulatory requirements . Plan, organize, and oversee production schedules to meet delivery timelines. Coordinate with Quality Assurance (QA), Quality Control (QC), and R&D teams. Monitor production efficiency, reduce downtime, and optimize resources. Train and lead production staff, ensuring adherence to SOPs. Handle audits and maintain proper documentation as per regulatory standards. Implement safety and hygiene protocols in the manufacturing area. Requirements Education: B.Pharm / M.Pharm / M.Sc or equivalent. Experience: 8–10 years of experience in pharmaceutical production. Mandatory: Must be an Approved Chemist in Ointment . Strong leadership, problem-solving, and team management skills. Thorough knowledge of pharmaceutical manufacturing processes and regulatory guidelines. Compensation: Competitive salary package, commensurate with experience. How to Apply: Interested candidates, please send your CV to HR@radiconlab.com Job Type: Full-time Pay: ₹36,954.23 - ₹70,742.96 per month Benefits: Health insurance Paid sick time Provident Fund Application Question(s): Are u approved ointment chemist?? Experience: ointment: 5 years (Preferred) Work Location: In person
Job Title: Officer / Senior Officer – Engineering Department Location: Greater Noida Industry: Pharmaceuticals About the Role We are looking for a dedicated Officer / Senior Officer for our Engineering Department . The ideal candidate should have hands-on experience in the pharmaceutical industry , with strong knowledge of documentation, SOP preparation, and engineering compliance . Key Responsibilities Prepare, review, and maintain engineering documentation and SOPs as per GMP/cGMP guidelines. Support preventive maintenance schedules and ensure minimal downtime of equipment. Coordinate with production and quality teams to ensure smooth plant operations. Maintain compliance with regulatory, safety, and environmental standards . Assist in audits and maintain proper engineering records. Identify and implement improvements in processes, safety, and efficiency. Requirements Education: ITI (Mandatory) – Mechanical / Electrical / Instrumentation. Experience: Minimum 3–6 years of experience in engineering within the pharmaceutical industry . Strong understanding of engineering systems, utilities, and documentation practices. Good knowledge of GMP compliance and equipment maintenance. Excellent communication and teamwork skills. Compensation: Competitive salary package based on experience. Job Type: Full-time Pay: ₹12,489.28 - ₹25,179.97 per month Benefits: Health insurance Paid sick time Provident Fund Experience: pharmaceutical : 1 year (Preferred) Work Location: In person
About the Role: We are looking for a motivated Trainee – Warehouse to join our pharmaceutical operations team. This role offers an excellent opportunity to learn warehouse operations in a GMP-compliant environment. Key Responsibilities: Assist in receiving, storing, and issuing materials. Support inventory management and stock reconciliation. Maintain documentation as per SOPs. Ensure cleanliness and compliance with safety standards. Requirements: Diploma/Graduate in any discipline (D-Pharma/ B-Pharma). Freshers are encouraged to apply. Basic knowledge of warehouse operations will be an added advantage. Perks & Benefits: On-the-job training. Exposure to pharmaceutical industry standards. Job Type: Full-time Pay: ₹10,401.62 - ₹13,137.30 per month Work Location: In person
About the Role: We are looking for a motivated Trainee – Warehouse to join our pharmaceutical operations team. This role offers an excellent opportunity to learn warehouse operations in a GMP-compliant environment. Key Responsibilities: Assist in receiving, storing, and issuing materials. Support inventory management and stock reconciliation. Maintain documentation as per SOPs. Ensure cleanliness and compliance with safety standards. Requirements: Diploma/Graduate in any discipline (D-Pharma/ B-Pharma). Freshers are encouraged to apply. Basic knowledge of warehouse operations will be an added advantage. Perks & Benefits: On-the-job training. Exposure to pharmaceutical industry standards. Job Type: Full-time Pay: ₹10,401.62 - ₹13,137.30 per month Work Location: In person
Job Description – Assistant Manager – Quality Assurance Company: Radicon Laboratories Ltd. Experience: 8–10 years Location: Greater Noida Position Overview: Radicon Laboratories Ltd. is seeking a highly skilled and experienced Assistant Manager – Quality Assurance to oversee and ensure compliance with quality standards, regulatory requirements, and company SOPs. The ideal candidate will play a crucial role in maintaining product quality, driving continuous improvement, and ensuring adherence to GMP guidelines. Key Responsibilities: Quality Management System (QMS): Implement and maintain QMS in compliance with regulatory requirements. Review and approve SOPs, deviations, change controls, CAPAs, and other quality documents. Regulatory Compliance: Ensure compliance with GMP, ISO, and other applicable regulatory standards. Prepare and support regulatory inspections and customer audits. Documentation & Record Control: Oversee preparation, review, and maintenance of quality documentation. Ensure timely approval and archiving of batch records, validation protocols, and reports. Audits & Inspections: Conduct internal audits and coordinate external audits. Address audit observations and implement corrective and preventive actions. Training & Development: Train and mentor the QA team on regulatory guidelines, SOPs, and best practices. Conduct periodic training sessions for employees on quality compliance. Deviation & CAPA Management: Investigate quality issues, deviations, and non-conformances. Implement corrective and preventive actions (CAPA) to mitigate risks. Validation & Qualification: Support process validation, equipment qualification, and method validation. Ensure compliance with validation master plans. Supplier & Vendor Management: Evaluate and approve suppliers/vendors for raw materials, packaging, and services. Conduct vendor audits and ensure supplier compliance. Continuous Improvement Initiatives: Identify areas for process improvement and implement best practices. Work closely with cross-functional teams to enhance overall quality performance. Key Skills & Competencies: Strong knowledge of GMP, ISO, and regulatory guidelines (USFDA, MHRA, WHO, etc.). Excellent documentation and compliance management skills. Experience in handling audits and regulatory inspections. Strong problem-solving, analytical, and decision-making abilities. Effective leadership, communication, and team management skills. Qualifications: Bachelor's/Master’s degree in Pharmacy, Chemistry, Microbiology, or a related field. 8–10 years of experience in Quality Assurance within the pharmaceutical industry. If you are a quality-driven professional with a keen eye for compliance and excellence, we invite you to apply and be a part of our growing team at Radicon Laboratories Ltd. Job Type: Full-time Pay: ₹50,000.00 - ₹70,000.00 per month Benefits: Health insurance Paid sick time Provident Fund Application Question(s): Current package?? Experience: QA/QC: 6 years (Preferred) pharmaceutical manufacturing: 5 years (Required) Work Location: In person
Job Description: Accountant (with Tally and Marg ERP Expertise) Position Title : Accountant Executive Location : Ecotech 12 Greater Noida Experience : 5-6 years Employment Type : Full-time Job Overview: We are seeking an experienced and detail-oriented Accountant with proficiency in Tally and Marg ERP operating systems. The ideal candidate should have a solid understanding of accounting practices, compliance deadlines, and basic knowledge of balance sheet finalization. You will be responsible for managing day-to-day accounting operations, ensuring timely submission of compliance documents, and supporting the preparation of financial statements. Key Responsibilities: Accounting and Bookkeeping: Maintain accurate and up-to-date financial records using Tally and Marg ERP . Process day-to-day accounting entries, including accounts payable, accounts receivable, journal entries, and bank reconciliations. Monitor and maintain petty cash and ensure proper documentation for all transactions. Compliance Management: Oversee and ensure adherence to statutory compliance deadlines, including GST filings, TDS, and other direct/indirect taxes. Liaise with internal and external stakeholders for timely submission of tax returns and filings. Prepare and submit compliance reports related to taxes, GST, and other relevant financial documentation. Financial Reporting: Assist in the preparation of monthly, quarterly, and annual financial statements. Work closely with senior accountants to ensure timely and accurate balance sheet finalization . Support the senior accounting team in the preparation of financial analysis and budgeting. Excel and Reporting: Prepare and maintain financial reports, Excel spreadsheets, and accounting summaries. Create reports based on Excel functions and formulas for better decision-making. Utilize advanced Excel tools (pivot tables, VLOOKUP, etc.) to streamline accounting and reporting processes. ERP System Management: Ensure accurate entry and retrieval of financial data from Tally and Marg ERP . Troubleshoot ERP system issues and work closely with IT teams to resolve discrepancies or issues. Audit and Documentation: Maintain and organize all accounting and financial documents for auditing purposes. Assist in the internal and external audit processes and ensure that all required documents are readily available. Balance Sheet Finalization (Partial): Assist in the preparation and review of balance sheet reports, including reconciliation of accounts. Work on year-end closing procedures and ensure compliance with accounting standards. Skills & Qualifications: Educational Requirements : Bachelor’s degree in Commerce (B.Com) or a related field. Certification in Accounting (e.g., CA, CPA, or equivalent) is a plus but not mandatory. Technical Skills : Proficiency in Tally ERP and Marg ERP is a must. Strong working knowledge of Microsoft Excel (advanced formulas, pivot tables, VLOOKUP, etc.). Basic knowledge of balance sheet finalization . Experience : Minimum 5-6 years of experience in accounting or finance, with hands-on experience using ERP systems like Tally and Marg. Familiarity with compliance processes such as GST, TDS, and other tax filings. Experience in financial reporting and the preparation of accounting documents. Soft Skills : Detail-oriented with strong analytical and problem-solving skills. Strong organizational skills and ability to manage deadlines effectively. Good communication skills and ability to work independently or as part of a team. Additional Requirements: Ability to work under pressure and meet tight deadlines. Knowledge of current accounting trends and tax regulations. Adabtable with timings Job Type: Full-time Pay: ₹20,680.36 - ₹40,080.99 per month Benefits: Paid sick time Provident Fund Work from home Work Location: In person
Job Overview We are seeking a Tally Operator – Accounts with 1–3 years of experience to manage routine accounting entries and support compliance tasks. The candidate should be proficient in Tally ERP and have a good grasp of basic accounting principles. Key Responsibilities Enter day-to-day accounting transactions in Tally ERP (sales, purchase, receipts, payments, journals). Maintain and update ledgers, vouchers, and invoices . Handle bank reconciliation and petty cash records. Support in GST, TDS, and tax filing documentation . Generate basic accounting reports and summaries. Assist senior accountants with month-end and year-end closing. Ensure proper documentation and filing for audits. Skills & Qualifications Education: Minimum B.Com or equivalent. Experience: 1–3 years in accounting, with hands-on Tally ERP usage. Technical Skills: Strong in Tally ERP; working knowledge of MS Excel preferred. Soft Skills: Attention to detail, accuracy, organizational ability, and time management. Job Type: Full-time Pay: ₹11,561.18 - ₹20,311.66 per month Benefits: Health insurance Paid sick time Provident Fund Work from home Work Location: In person
Radicon Laboratories Ltd is a renowned name in the pharmaceutical manufacturing industry, committed to producing high-quality and safe healthcare products. We pride ourselves on maintaining rigorous quality standards and fostering an environment of continuous improvement and innovation. Job Overview : We are seeking an experienced QC Chemist to join our quality control team. The successful candidate will have 8-10 years of relevant experience in a pharmaceutical manufacturing environment and must be comfortable working night shifts. The role involves overseeing quality checks, ensuring compliance with established standards, and contributing to the overall quality assurance process. Key Responsibilities : Perform routine and non-routine testing of raw materials, in-process samples, and finished products using standard QC methodologies. Analyze chemical, physical, and microbiological properties of pharmaceutical products to ensure adherence to company and regulatory quality standards. Prepare, review, and maintain quality control documentation, including SOPs, test records, and reports. Identify and troubleshoot any discrepancies in testing results and implement corrective measures as needed. Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and other laboratory equipment. Conduct stability studies and support validation activities for new product introductions. Ensure strict compliance with GMP (Good Manufacturing Practices), FDA, and other regulatory standards. Coordinate with production, R&D, and other departments to maintain seamless operations and effective quality checks. Participate in internal and external audits and implement required changes based on findings. Train and mentor junior QC staff as necessary, fostering a collaborative team environment. Monitor and maintain the laboratory environment to uphold safety and quality protocols. Qualifications : Educational Requirement : Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field. Experience : 2-4 years of experience in a QC Chemist role within the pharmaceutical industry. Proficiency in handling analytical instruments (e.g., HPLC, GC) and familiarity with data analysis software. Strong knowledge of GMP, ICH guidelines, and other relevant quality regulations. Demonstrated ability to work night shifts and adapt to the operational needs of a 24/7 manufacturing facility. Excellent attention to detail, problem-solving skills, and the ability to handle complex testing procedures. Preferred Skills : Experience in method development and validation. Knowledge of environmental monitoring and microbiological testing. Strong documentation skills and experience with laboratory information management systems (LIMS). Effective communication and teamwork skills. What We Offer : Competitive salary and shift differential pay. Comprehensive benefits package, including health insurance, paid time off, and professional development opportunities. A supportive and inclusive work environment with a focus on career growth and skill enhancement. State-of-the-art laboratory facilities and resources. Job Type: Full-time Pay: ₹20,577.48 - ₹30,037.98 per month Education: Bachelor's (Preferred) Experience: total work: 1 year (Preferred) Work Location: In person
Radicon Laboratories Ltd is a renowned name in the pharmaceutical manufacturing industry, committed to producing high-quality and safe healthcare products. We pride ourselves on maintaining rigorous quality standards and fostering an environment of continuous improvement and innovation. Job Overview : We are seeking an experienced QC Chemist to join our quality control team. The successful candidate will have 8-10 years of relevant experience in a pharmaceutical manufacturing environment and must be comfortable working night shifts. The role involves overseeing quality checks, ensuring compliance with established standards, and contributing to the overall quality assurance process. Key Responsibilities : Perform routine and non-routine testing of raw materials, in-process samples, and finished products using standard QC methodologies. Analyze chemical, physical, and microbiological properties of pharmaceutical products to ensure adherence to company and regulatory quality standards. Prepare, review, and maintain quality control documentation, including SOPs, test records, and reports. Identify and troubleshoot any discrepancies in testing results and implement corrective measures as needed. Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and other laboratory equipment. Conduct stability studies and support validation activities for new product introductions. Ensure strict compliance with GMP (Good Manufacturing Practices), FDA, and other regulatory standards. Coordinate with production, R&D, and other departments to maintain seamless operations and effective quality checks. Participate in internal and external audits and implement required changes based on findings. Train and mentor junior QC staff as necessary, fostering a collaborative team environment. Monitor and maintain the laboratory environment to uphold safety and quality protocols. Qualifications : Educational Requirement : Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field. Experience : 2-4 years of experience in a QC Chemist role within the pharmaceutical industry. Proficiency in handling analytical instruments (e.g., HPLC, GC) and familiarity with data analysis software. Strong knowledge of GMP, ICH guidelines, and other relevant quality regulations. Demonstrated ability to work night shifts and adapt to the operational needs of a 24/7 manufacturing facility. Excellent attention to detail, problem-solving skills, and the ability to handle complex testing procedures. Preferred Skills : Experience in method development and validation. Knowledge of environmental monitoring and microbiological testing. Strong documentation skills and experience with laboratory information management systems (LIMS). Effective communication and teamwork skills. What We Offer : Competitive salary and shift differential pay. Comprehensive benefits package, including health insurance, paid time off, and professional development opportunities. A supportive and inclusive work environment with a focus on career growth and skill enhancement. State-of-the-art laboratory facilities and resources. Job Type: Full-time Pay: ₹20,577.48 - ₹30,037.98 per month Education: Bachelor's (Preferred) Experience: total work: 1 year (Preferred) Work Location: In person
Job Description: Tally Operator Location: Delhi & Greater Noida Department: Accounts / Finance Job Type: Full-Time Key Responsibilities Enter day-to-day accounting entries in Tally ERP9 / Tally Prime Maintain sales, purchase, receipts, payments, and journal entries Prepare and maintain ledgers, invoices, debit/credit notes Handle bank reconciliation and maintain cash book Assist in preparing GST reports , TDS working , and other statutory documents Maintain stock records and coordinate with the store department Generate periodic reports: P&L, balance sheet, outstanding reports Support the finance team during audits Ensure accuracy and timely completion of accounting tasks Required Skills Proficient in Tally ERP9 / Tally Prime Knowledge of GST, TDS, MS Excel (VLOOKUP, Pivot Tables preferred) Basic understanding of accounting principles Good communication and documentation skills Ability to work with accuracy and attention to detail Qualifications 12th / Bachelor’s in Commerce (B.Com preferred) 1–3 years of experience as Tally Operator or Accounts Executive Freshers with good Tally knowledge may also apply Work Location Delhi Office Greater Noida Office (mention exact sector if needed) Job Type: Full-time Pay: ₹9,929.28 - ₹25,020.80 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person
Job Title: Regulatory Affairs (RA) Executive / Officer Experience: 1–5 years (Pharma Industry) Qualification: B.Pharm / M.Pharm / M.Sc. Job Purpose To prepare, review, and submit all regulatory documentation required for product registration and ensure compliance with local and international regulatory agencies (e.g., PICS, EU, ROW countries). Key Responsibilities Prepare and compile dossiers (CTD/eCTD, ACTD, country-specific formats) Coordinate with F&D, QA, QC, and Production teams to collect technical data Prepare and maintain Product Master Files (PMF), Site Master Files (SMF), Drug Master Files (DMF), and related documents Review and finalize Stability Data, Process Validation Reports, Specifications, and Test Methods Handle new product registrations, renewals, variations, and post-approval submissions Respond to regulatory queries and track submission timelines Ensure compliance with current regulatory guidelines (CDSCO, WHO, ICH, etc.) Maintain and update regulatory documentation databases and archives Support in obtaining and maintaining COPP, FSC, Manufacturing Licences, and Registration Certificates Required Skills Strong understanding of regulatory requirements and dossier preparation Proficiency in CTD/eCTD documentation Good knowledge of MS Office (Word, Excel, PowerPoint) Excellent communication and cross-department coordination skills High level of attention to detail and accuracy Key Competencies Analytical mindset with strong documentation precision Good organizational and project management abilities Ability to manage multiple regulatory submissions Team player with a proactive and responsible approach Job Type: Full-time Pay: ₹20,082.18 - ₹40,861.33 per month Benefits: Provident Fund Work Location: In person
Job Title: Regulatory Affairs (RA) Executive / Officer Experience: 1–5 years (Pharma Industry) Qualification: B.Pharm / M.Pharm / M.Sc. Job Purpose To prepare, review, and submit all regulatory documentation required for product registration and ensure compliance with local and international regulatory agencies (e.g., PICS, EU, ROW countries). Key Responsibilities Prepare and compile dossiers (CTD/eCTD, ACTD, country-specific formats) Coordinate with F&D, QA, QC, and Production teams to collect technical data Prepare and maintain Product Master Files (PMF), Site Master Files (SMF), Drug Master Files (DMF), and related documents Review and finalize Stability Data, Process Validation Reports, Specifications, and Test Methods Handle new product registrations, renewals, variations, and post-approval submissions Respond to regulatory queries and track submission timelines Ensure compliance with current regulatory guidelines (CDSCO, WHO, ICH, etc.) Maintain and update regulatory documentation databases and archives Support in obtaining and maintaining COPP, FSC, Manufacturing Licences, and Registration Certificates Required Skills Strong understanding of regulatory requirements and dossier preparation Proficiency in CTD/eCTD documentation Good knowledge of MS Office (Word, Excel, PowerPoint) Excellent communication and cross-department coordination skills High level of attention to detail and accuracy Key Competencies Analytical mindset with strong documentation precision Good organizational and project management abilities Ability to manage multiple regulatory submissions Team player with a proactive and responsible approach Job Type: Full-time Pay: ₹20,082.18 - ₹40,861.33 per month Benefits: Provident Fund Work Location: In person
Job Title: Formulation & Development (F&D) Executive / Officer Experience: 1–5 years (Pharmaceutical Formulation) Qualification: B.Pharm / M.Pharm (Pharmaceutics / Pharmaceutical Technology) Job Purpose To assist in the design, development, and documentation of new and existing formulations, and to prepare technical documentation required for regulatory submissions and product transfers. Key Responsibilities Prepare and maintain Formulation Development Reports (FDRs) and Product Development Reports (PDRs) Compile data for CTD Module 3 (Quality) in coordination with Regulatory Affairs Support preparation of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) Document and interpret stability studies, analytical method validation, and process validation data Support technology transfer to production units by providing technical documentation Coordinate with RA, QA, QC, and Production teams for data collection and documentation Prepare QbD/DoE reports, comparative dissolution profiles, and bioequivalence data summaries Maintain archives of development documents as per GDP and regulatory guidelines Assist in generating product justification and stability summary reports for submissions Required Skills Knowledge of formulation development (solid oral / liquid / semi-solid dosage forms) Familiarity with ICH guidelines and CTD structure Proficiency in MS Office and technical report writing Understanding of stability study design and analytical interpretation Strong collaboration skills with RA and QA departments Key Competencies Strong analytical and scientific thinking Excellent technical writing and documentation abilities Attention to detail with a compliance-focused mindset Team-oriented, proactive, and deadline-driven Job Type: Full-time Pay: ₹18,359.71 - ₹40,215.47 per month Benefits: Paid sick time Provident Fund Work Location: In person
Urgent Requirement – Radicon Laboratories Ltd. Location: Greater Noida Position: Warehouse Executive Job Purpose To manage warehouse operations related to receipt, storage, issuance, and control of materials in compliance with GMP and company SOPs. Key Responsibilities Receive, unload, and verify raw materials, packing materials, and finished goods as per approved documents. Ensure proper labeling and status identification (Quarantine / Approved / Rejected). Store materials under specified environmental conditions as per SOP. Issue materials to Production and QC as per approved requisitions, following FIFO/FEFO. Maintain accurate inventory records in registers and ERP systems. Perform periodic physical stock verification and reconcile discrepancies. Ensure compliance with cGMP, GDP, and safety guidelines. Maintain cleanliness and organization of warehouse areas. Handle rejected, returned, and recalled materials with proper segregation and documentation. Support internal, customer, and regulatory audits. Coordinate with QA, Production, Purchase, and EHS departments. Follow safety practices and use PPE as required. Qualifications & Experience Graduate / Diploma (Any discipline) 1–5 years of experience in pharmaceutical warehouse operations Knowledge of GMP, FIFO/FEFO, and inventory management Skills & Competencies Understanding of pharma materials and storage practices Good documentation and record-keeping skills Basic knowledge of ERP/SAP preferred Attention to detail and compliance-focused approach Good coordination and communication skills Accountability Accuracy of inventory and documentation Compliance with GMP and warehouse SOPs Job Type: Full-time Pay: ₹13,514.08 - ₹25,220.60 per month Benefits: Paid sick time Provident Fund Work Location: In person
Urgent Requirement – Radicon Laboratories Ltd. Location: Greater Noida Position: Warehouse Executive Job Purpose To manage warehouse operations related to receipt, storage, issuance, and control of materials in compliance with GMP and company SOPs. Key Responsibilities Receive, unload, and verify raw materials, packing materials, and finished goods as per approved documents. Ensure proper labeling and status identification (Quarantine / Approved / Rejected). Store materials under specified environmental conditions as per SOP. Issue materials to Production and QC as per approved requisitions, following FIFO/FEFO. Maintain accurate inventory records in registers and ERP systems. Perform periodic physical stock verification and reconcile discrepancies. Ensure compliance with cGMP, GDP, and safety guidelines. Maintain cleanliness and organization of warehouse areas. Handle rejected, returned, and recalled materials with proper segregation and documentation. Support internal, customer, and regulatory audits. Coordinate with QA, Production, Purchase, and EHS departments. Follow safety practices and use PPE as required. Qualifications & Experience Graduate / Diploma (Any discipline) 1–5 years of experience in pharmaceutical warehouse operations Knowledge of GMP, FIFO/FEFO, and inventory management Skills & Competencies Understanding of pharma materials and storage practices Good documentation and record-keeping skills Basic knowledge of ERP/SAP preferred Attention to detail and compliance-focused approach Good coordination and communication skills Accountability Accuracy of inventory and documentation Compliance with GMP and warehouse SOPs Job Type: Full-time Pay: ₹13,514.08 - ₹25,220.60 per month Benefits: Paid sick time Provident Fund Work Location: In person
Job Description – Assistant Manager – Quality Assurance Company: Radicon Laboratories Ltd. Experience: 8–10 years Location: Greater Noida Position Overview: Radicon Laboratories Ltd. is seeking a highly skilled and experienced Assistant Manager – Quality Assurance to oversee and ensure compliance with quality standards, regulatory requirements, and company SOPs. The ideal candidate will play a crucial role in maintaining product quality, driving continuous improvement, and ensuring adherence to GMP guidelines. Key Responsibilities: Quality Management System (QMS): Implement and maintain QMS in compliance with regulatory requirements. Review and approve SOPs, deviations, change controls, CAPAs, and other quality documents. Regulatory Compliance: Ensure compliance with GMP, ISO, and other applicable regulatory standards. Prepare and support regulatory inspections and customer audits. Documentation & Record Control: Oversee preparation, review, and maintenance of quality documentation. Ensure timely approval and archiving of batch records, validation protocols, and reports. Audits & Inspections: Conduct internal audits and coordinate external audits. Address audit observations and implement corrective and preventive actions. Training & Development: Train and mentor the QA team on regulatory guidelines, SOPs, and best practices. Conduct periodic training sessions for employees on quality compliance. Deviation & CAPA Management: Investigate quality issues, deviations, and non-conformances. Implement corrective and preventive actions (CAPA) to mitigate risks. Validation & Qualification: Support process validation, equipment qualification, and method validation. Ensure compliance with validation master plans. Supplier & Vendor Management: Evaluate and approve suppliers/vendors for raw materials, packaging, and services. Conduct vendor audits and ensure supplier compliance. Continuous Improvement Initiatives: Identify areas for process improvement and implement best practices. Work closely with cross-functional teams to enhance overall quality performance. Key Skills & Competencies: Strong knowledge of GMP, ISO, and regulatory guidelines (USFDA, MHRA, WHO, etc.). Excellent documentation and compliance management skills. Experience in handling audits and regulatory inspections. Strong problem-solving, analytical, and decision-making abilities. Effective leadership, communication, and team management skills. Qualifications: Bachelor's/Master’s degree in Pharmacy, Chemistry, Microbiology, or a related field. 8–10 years of experience in Quality Assurance within the pharmaceutical industry. If you are a quality-driven professional with a keen eye for compliance and excellence, we invite you to apply and be a part of our growing team at Radicon Laboratories Ltd. Job Type: Full-time Pay: ₹50,000.00 - ₹70,000.00 per month Benefits: Health insurance Paid sick time Provident Fund Application Question(s): Current package?? Experience: QA/QC: 6 years (Preferred) pharmaceutical manufacturing: 5 years (Required) Work Location: In person