Role & responsibilities : An experienced Production Manager with a strong background in the pharmaceutical manufacturing industry with a track record of effectively managing production processes, ensuring compliance with GMP standards, and optimizing productivity and quality. Who has leadership qualities, long-term vision, and a desire for growth within the Organization. Production Planning & Scheduling : Develop and implement production plans, schedules, and workflows for Specially liquid and ointment manufacturing, optimizing resource allocation and minimizing downtime Equipment Management: Oversee the operation, maintenance, and troubleshooting of production equipment, including mixers, filling machines, and other relevant machinery. Material Management: Ensure the proper sourcing, storage, and handling of raw materials, including liquids, ointments, and packaging materials, adhering to inventory control procedures. Safety & Compliance: Enforce safety protocols, maintain a safe working environment, and ensure compliance with all relevant health, safety, and environmental regulations. Team Management: Supervise and motivate production staff, providing training, guidance, and performance feedback. Cost Management: Monitor production costs, identify areas for improvement, and implement strategies to optimize efficiency and minimize waste Process Improvement: Identify opportunities to enhance production processes, improve efficiency, and reduce costs, implementing changes as needed. Documentation & Reporting: Maintain accurate production records, batch records, QMS, and other required documentation, and prepare reports on production performance. Preferred candidate profile : In-depth knowledge of GMP guidelines and regulatory requirements in the pharmaceutical industry. Strong understanding of production processes, Quality control, Quality assurance and supply chain management. Proven experience in especially liquid and ointment manufacturing processes. Strong understanding of production planning, scheduling, and control. Proficiency in operating and maintaining production equipment. Knowledge of regulatory requirements. Fluent Knowledge of Word and Excel. Excellent leadership, communication, and interpersonal skills. Ability to manage and motivate a team. Strong problem-solving and decision-making abilities. Familiarity with relevant safety regulations and procedures. Proficient in MS Office (Word, Excel, PowerPoint) Follow the rules and regulations of company with respect to Health, Hygiene, safety and quality of product & personnel Perks and benefits : Salary : CTC package will be suitable and negotiable based on the present package and industry norms for the right candidate Interested & eligible candidates may send their profile in - piyali.basu@mendine.com, atrayee.mandal@mendine.com
Role & responsibilities Provide a safe, stimulating, and nurturing environment Plan and engage in age-appropriate educational and developmental activities Assist with potty training, feeding, and hygiene routines Maintain consistent routines and schedules Communicate regularly with parents regarding progress and daily activities Light nursery duties (tidying up toys, organizing children's belongings) Preferred candidate profile Minimum 3 years of experience caring for toddlers, ideally twins B.Sc./MSc. and a Background in early childhood education or similar qualification preferred Fluent in English (additional languages a plus) CPR and First Aid certified Energetic, warm, and highly reliable Non-smoker with a clean background check
JOB PROFILE OF SR. TECHNICAL OFFICER-QUALITY ASSURANCE MENDINE PHARMACEUTICALS PVT LTD Job Title / Designation- SENIOR TECHNICAL OFFICER - QA Qualifications- M.PHARM Experience- 5 to 6 years experience in QUALITY ASSURANCE Job Objective- The ideal candidate will be responsible for implementing and maintaining quality systems, ensuring compliance with cGMP guidelines, conducting internal audits, reviewing batch records, and supporting regulatory inspections. This role demands strong documentation skills, a sound understanding of pharmaceutical quality standards, and the ability to work collaboratively across departments to uphold product integrity and safety throughout the manufacturing process. Job Responsibilities 1) Quality Risk Management 2) Batch Manufacturing Record preparation 3) Process Validation 4) Packaging Material Specification Preparation 5) APQR 6) Cleaning Validation 7) Regulatory Affairs activity 8) Dossier preparation 9) Application of ONDLS system 10) Form 29 & Form 30 preparation 11) Endorse documents preparation 12) New drug application 13) COPP application in ONDLS.
SENIOR QUALITY CONTROL ANALYST Job Objective: The Quality Control (QC) Analyst specializing in Method Validation and Method Development is responsible for developing, validating, and transferring analytical methods for pharmaceutical raw materials, intermediates, and finished products. The role ensures compliance with regulatory requirements and contributes to continuous improvements in analytical methodologies. Qualifications: Bachelors/Masters degree in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or related field. Experience: More than 8 years of experience in method validation, method transfer, and regulatory compliance within a pharmaceutical QC or analytical development environment. Job Responsibilities: Method Development & Optimization: Develop and optimize analytical methods for assay, dissolution, related substances, and residual solvents using techniques like HPLC, GC, UV-Vis, FTIR. Establish and refine chromatographic conditions, mobile phases, and detection parameters for improved sensitivity and reproducibility. Conduct forced degradation and stability-indicating method development as per ICH Q1A guidelines. Method Validation & Transfer: Perform method validation as per ICH guidelines covering accuracy, precision, specificity, linearity, robustness, and system suitability. Prepare and review method validation protocols and reports. Execute method transfer activities between R&D, QC, and manufacturing sites following GMP requirements. Regulatory Compliance & Documentation: Ensure analytical methods meet US FDA, EU GMP, MHRA, WHO, and other regulatory expectations. Maintain accurate documentation as per Good Documentation Practices (GDP). Support regulatory filings by preparing analytical method validation reports and technical dossiers. Assist in responding to regulatory queries and audits related to analytical methods. Instrumentation & Troubleshooting: Operate and maintain analytical instruments such as HPLC, GC, UV-Vis, FTIR, and dissolution testers. Troubleshoot chromatographic issues related to retention time shifts, peak tailing, and resolution problems. Participate in instrument qualification (IQ/OQ/PQ) as needed. Collaboration & Process Improvement: Work closely with R&D, Manufacturing, and Quality Assurance teams for seamless method transfer. Investigate out-of-specification (OOS) and out-of-trend (OOT) results to identify root causes. Contribute to continuous improvements in analytical techniques and laboratory efficiency. Technical Skills: Strong expertise in HPLC, GC, UV-Vis, FTIR
JOB PROFILE OF SR. TECHNICAL OFFICER-QUALITY ASSURANCE MENDINE PHARMACEUTICALS PVT LTD Job Title / Designation- SENIOR TECHNICAL OFFICER - QA Qualifications- M.PHARM Experience- 5 to 10 years experience in QUALITY ASSURANCE Job Objective- The ideal candidate will be responsible for implementing and maintaining quality systems, ensuring compliance with cGMP guidelines, conducting internal audits, reviewing batch records, and supporting regulatory inspections. This role demands strong documentation skills, a sound understanding of pharmaceutical quality standards, and the ability to work collaboratively across departments to uphold product integrity and safety throughout the manufacturing process. Job Responsibilities 1) Quality Risk Management 2) Batch Manufacturing Record preparation 3) Process Validation 4) Packaging Material Specification Preparation 5) APQR 6) Cleaning Validation 7) Regulatory Affairs activity 8) Dossier preparation 9) Application of ONDLS system 10) Form 29 & Form 30 preparation 11) Endorse documents preparation 12) New drug application 13) COPP application in ONDLS.
Job Objective Supply Chain Executive will be responsible for overseeing supply chain operations, ensuring smooth coordination between vendors, clients, and internal teams. The role involves managing distribution activities, building strong vendor-client relationships, and travel requirements. Experience 2 to 3 years experience in supply chain management/logistics (Pharma + SCM preferred) Role & responsibilities Assist in managing end-to-end supply chain operations including procurement, logistics, and distribution. Coordinate with vendors and clients to ensure timely delivery of materials and products. Maintain accurate records of inventory, purchase orders, and delivery schedules. Support vendor selection , negotiation , and performance monitoring. Travel as required for vendor/client interactions, (across India) Work closely with internal teams (sales, production) to align supply chain operations with business needs. Skills Required Strong knowledge of supply chain processes Good communication and interpersonal skills for client & vendor coordination Basic understanding of pharmaceutical distribution and compliance requirements Flexibility and willingness to travel for business needs (across India) Proficiency in MS Excel/ERP tools for data handling and reporting Negotiation and relationship management skills Salary Suitable and negotiable based on current package and industrial norms
Job Objective Senior Scientist with expertise in oral liquid formulation development, manufacturing, and regulatory compliance, driving innovation and quality in pharmaceutical product development. With a passion about formulation and development for oral liquid. Age: 35 to 45 years Education: P.hd or related field Mandatory experience in Pharmaceutical Oral Liquid Formulation Role & responsibilities 1. Formulation Development: - Design, develop, and optimize oral liquid formulations for new and existing products. - Conduct pre-formulation studies, solubility testing, and stability assessments. 2. Product Development: - Lead cross-functional teams to develop and launch new oral liquid products. - Collaborate with R&D, Quality, and Manufacturing teams to ensure smooth technology transfer. - Develop and implement product development plans, timelines, and budgets. 3. Regulatory Compliance: - Ensure compliance with regulatory requirements, guidelines, and standards (e.g., USP, EP, JP). - Prepare and review regulatory documents, including DMFs, ANDAs, and NDAs. - Collaborate with regulatory teams to address regulatory queries and issues. 4. Process Optimization: - Optimize manufacturing processes for oral liquid products, including mixing, filling, and packaging. - Identify and implement process improvements to enhance efficiency, quality, and yield. - Develop and implement process controls, including in-process testing and release criteria. 6. Technical Support: - Provide technical support to manufacturing, quality, and regulatory teams. - Troubleshoot technical issues and provide solutions to ensure product quality and compliance. - Conduct training and knowledge-sharing sessions to enhance team capabilities. 7. Innovation and Continuous Improvement: - Identify opportunities for innovation and continuous improvement in oral liquid formulation and development. - Evaluate and implement new technologies, processes, and methodologies to enhance product quality, efficiency, and competitiveness. Skills Required: 1. Pharmaceutical formulation development: Expertise in developing oral liquid formulations. 2. Regulatory knowledge: Understanding of regulatory guidelines and compliance. 3. Analytical skills: Ability to analyze data, identify trends, and troubleshoot issues. 4. Problem-solving: Strong problem-solving skills to address formulation and manufacturing challenges. 5. Communication: Effective communication and collaboration with cross-functional teams. 6. Project management: Ability to manage multiple projects, prioritize tasks, and meet deadlines. 7. Technical expertise: Strong knowledge of pharmaceutical sciences, chemistry, and pharmacology. 8. Quality assurance: Understanding of quality standards, procedures, and protocols. 9. Innovation: Ability to think creatively and implement new technologies and processes. 10. Leadership: Experience in leading teams and mentoring junior scientists.
Sales Management and Strategy Development skills, Strong Leadership and Team Management abilities, Excellent Communication and Interpersonal skills along with good presentation skill, Proficiency in Market Analysis and Sales Reporting, Problem-Solving and Decision-Making skills, Ability to handle the product effectively scientifically analysing the Products along with competitions. Zonal budget achievement, brand and market establishment through deep market penetration, market development through area sales managers, creating and implementing sales/marketing strategy, knowledge of window displays and merchandising at the retail level, establishing strategic alliances with channel partners, ensuring adequate inventory coverage and distribution, educating stockiests staff about the product, team building, mentoring, training and development of field functionaries, coordinating with cross-functional departments for smooth operations.
Technical: cGMP compliance, QA/QMS, Quality Risk Management, Process Validation, Cleaning Validation, APQR, BMR/BPR preparation and review, Packaging material/specification management, Dossier/NDA preparation, Change Control and Deviation Management, Technology transfer, Internal auditing, Documentation control and data integrity (ALCOA+). Soft: Attention to detail, strong documentation and communication skills, cross-functional collaboration, problem-solving, compliance mindset. Domain: Pharmaceutical manufacturing and regulatory inspection support. Quality Risk Management; Batch Manufacturing Record (BMR) preparation; Process Validation; Packaging Material Specification preparation; Annual Product Quality Review (APQR); Cleaning Validation; Batch card preparation; Dossier preparation; Change Control Management; Deviation Management; Endorse documents preparation; New Drug Application; Technology transfer
Strong Communication Quality Content Writing Digital Communication Media Relations Relationship Management Strategic Planning Stakeholder Management and Communication A Executive Communication Support 1 Draft and edit speeches, keynote addresses, and presentations for the MD at industry events, conferences, and internal forums Prepare detailed briefing documents, media responses, and executive summaries ahead of public appearances or meetings Develop and execute a communication calendar for the MD, aligned with corporate events, industry developments, and regulatory changes Ensure all public-facing communications comply with pharmaceutical marketing and communication regulations B External Communication Serve as a communication bridge between the MD and external departments, ensuring timely dissemination of key updates 6 Draft external announcements, newsletters, and strategic memos on behalf of the MD Coordinate town halls, leadership communication sessions, and internal forums led by the MD C Association & Stakeholder Management 8 Build and maintain strong working relationships with pharmaceutical associations, regulatory bodies, key opinion leaders (KOLs), and government stakeholders Schedule and coordinate the MD s participation in external committees, panels, and association meetings Maintain a stakeholder contact database and manage ongoing engagement strategy To manage, coordinate, and execute external communication strategies on behalf of the Managing Director (MD), ensuring consistent corporate messaging, maintaining professional relationships with key stakeholders (Pharmaceutical Associations), and enhancing company s public image within the pharmaceutical industry
Technical: Pharma brand management; market research and Rx data analysis; sales/portfolio analytics; promotional material development workflows (VA, LBL, product literature); MS Excel and PowerPoint; basic statistics; familiarity with CRM/reporting tools Soft: Communication and presentation; coordination and stakeholder management; time management and deadline adherence; analytical thinking; attention to detail; persuasion/negotiation; problem-solving; willingness to learn Domain-specific: Knowledge of pharmaceutical marketing processes, doctor surveys, and fieldwork; understanding of Indian pharma sales practices; product lifecycle basics in pharma - Brand Management: Sample and input planning; develop perceptive design/briefs for promotional inputs (VA, LBL, product literature); ensure timely dispatch of promotional inputs and physician samples; prepare launch brand plans; prepare market share presentations; brief and coordinate with creative agencies on VA/LBL; form and monitor promotional strategies (MPPL & RSE); telephonic follow-ups and reporting on strategy execution (RSE & MPPL); execute and follow up on rack displays (RSE) - Support to Sales Team: Coordinate promotional strategy implementation with sales; monitor depot-wise stock of products and spot gifts (MPPL & RSE); persuasion with RRWS; conduct cycle meetings (RSE & MPPL); update achievement vs target and communicate incentive schemes to field force (MPPL & RSE); prepare field visit reports; arrange and monitor retailer gift schemes (MPPL & RSE) - Market Research: Conduct market surveys; gather competitor information; analyze Rx survey reports circulated by external agencies - Portfolio Management: Track brand-wise target vs achievement; perform sales trend analysis; analyze competitor information; monitor ongoing activities (MPPL & RSE)
Sales Management, Strategy Development, Leadership, Team Management, Communication, Interpersonal, Presentation, Market Analysis, Sales Reporting, Problem-Solving, Decision-Making, Product Handling Overseeing sales activities, developing sales strategies, analyzing market trends, preparing sales reports, identifying new business opportunities, establishing strategic alliances, ensuring adequate inventory coverage, educating stockiests staff, handling stockiest Sales representatives & retail Brand Promoters, sourcing, mentoring, training and development of the field functionaries.
Mendine Pharmaceuticals Pvt. Ltd. is looking for TRAINER EDUCYTE MADHYAMGRAM to join our team Roles and Responsibility Develop and implement comprehensive training programs to enhance employee skills and knowledge. Conduct workshops, seminars, and other training sessions to promote learning and growth. Design and deliver customized training materials and content. Evaluate the effectiveness of training programs and recommend improvements. Collaborate with subject matter experts to develop high-quality training content. Manage and maintain accurate records of training activities and participant progress. Job Requirements Proven experience in training and development, with a minimum of years of experience. Excellent communication, presentation, and interpersonal skills. Strong analytical and problem-solving skills, with attention to detail. Ability to work independently and as part of a team. Experience with adult learning principles and instructional design models. Familiarity with e-learning platforms and online training tools. Educational qualification: Any Graduate or Postgraduate degree. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.
Computer & MS-Office Knowledge, Sales, Business Development, Customer Relationship Management, Supply Chain Management. Meet Day to day sale Target. Chemists and Stockiest visit to generate sales & achieve budgeted sales. Business Development through meeting with the doctors and making good relations with them. Meeting Doctors as per schedule to promote the products to generate the prescriptions. Meeting with Stockiest make the products availability. Chemist survey. Customer Relationship Management. Supply Chain Maintain. Reporting.
Strong programming skills in , JavaScript, C#, and NET MVC Knowledge of relational databases and SQL Excellent problem-solving, analytical, and creative thinking skills Ability to work in a fast-paced environment and manage workload effectively Strong communication and teamwork abilities Design, develop, and implement web applications as per requirements Ensure the performance, quality, and responsiveness of applications Collaborate with the team to define, design, and deploy new features Identify and correct bottlenecks and fix bugs Help maintain code quality, organization, and automatization
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