Mendine Pharmaceuticals

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.