Mendine Pharmaceuticals Pvt Ltd

About the Company: Mendine Pharmaceuticals Pvt. Ltd. – operating with its glorified journey of eight decades since 1937 (the then Mendine Pharmaceutical Works) in India with a stretch of its business network in Eastern & North Eastern India and part of Eastern U.P. Our horizon of expertise expands from cutting edge allopathic to age-old traditions of India – the Ayurveda Drugs. We have an ISO:9001:2015, WHO GMP certified Manufacturing, Research and Development set-up of our own with a wide range of Pharmaceutical, Nutraceutical and Food Supplement Products. We have also an SBU (Strategic Business Unit) viz., Mendine Lifecare Products Pvt. Ltd. - which focuses on ethical products promotion. We, at Mendine, always believe in retaining the goodwill of customers and spreading knowledge about good health and life. Our ethos is to perform with integrity and we believe in competitive compliance by building a newer and healthier tomorrow with adequate and intensive research works. We consistently aim at tracking new technologies to augment the quality of life and bring smile to our consumers’ faces and also educating our employees for up-skilling with enhancement of knowledge in accordance with the same. Job Objective : A Regulatory Affairs Specialist's job description involves ensuring a company's products and operations comply with relevant regulations, laws, and guidelines. Responsibilities : Responsible for monitoring regulatory changes, preparing and submitting documents to regulatory agencies, and providing guidance to internal teams on compliance. This role also includes assessing compliance, recommending remediation, and acting as a liaison between the company and regulatory agencies. Responsible for preparing and submitting various documents, including product registration dossiers, clinical trial documentation, Endorsement approval COPP product wise approval and other regulatory submissions. Co-ordination for external audit with external Regulatory Agency with Regularity guideline awareness. Qualifications : B. Pharm/M pharm/MSc. Minimum 5-8 Yrs. Experience in RA Preferred Skills : Regulatory Affairs roles require a blend of technical and soft skills. Strong analytical and problem-solving abilities are crucial for interpreting regulations and addressing complex issues. Effective communication, including writing and presentation skills, is essential for interacting with regulatory bodies and internal teams. Additionally, strong skills are needed to coordinate submissions and ensure compliance with deadlines. Pay range and compensation package : Pay range and compensation package will be negotiable based on present package & Industry norms. Equal Opportunity Statement : We are committed to diversity and inclusivity in our hiring practices.

About the Company: Mendine Pharmaceuticals Pvt. Ltd. – operating with its glorified journey of eight decades since 1937 (the then Mendine Pharmaceutical Works) in India with a stretch of its business network in Eastern & North Eastern India and part of Eastern U.P. Our horizon of expertise expands from cutting edge allopathic to age-old traditions of India – the Ayurveda Drugs. We have an ISO:9001:2015, WHO GMP certified Manufacturing, Research and Development set-up of our own with a wide range of Pharmaceutical, Nutraceutical and Food Supplement Products. We have also an SBU (Strategic Business Unit) viz., Mendine Lifecare Products Pvt. Ltd. - which focuses on ethical products promotion. We, at Mendine, always believe in retaining the goodwill of customers and spreading knowledge about good health and life. Our ethos is to perform with integrity and we believe in competitive compliance by building a newer and healthier tomorrow with adequate and intensive research works. We consistently aim at tracking new technologies to augment the quality of life and bring smile to our consumers’ faces and also educating our employees for up-skilling with enhancement of knowledge in accordance with the same. Job Objective: An experienced and strategic Senior Procurement Manager to lead our procurement operations. The candidate will be responsible for managing the sourcing and purchasing of goods, services, and contracts to ensure cost-effectiveness, quality, and timely delivery. This role demands strong leadership, negotiation skills, and the ability to build relationships with suppliers and internal stakeholders. Responsibilities Strategic Sourcing & Vendor Management Develop and execute procurement strategies aligned with company goals. Identify, evaluate, and manage relationships with key suppliers and vendors. Negotiate terms, prices, and contracts to secure the best value. Operational Excellence Oversee day-to-day procurement activities ensuring compliance with internal policies and external regulations. Ensure timely availability of materials and services to meet business requirements. Monitor market trends and apply industry knowledge to improve sourcing and procurement. Cost Optimization & Budget Control Manage procurement budgets and deliver cost-saving initiatives. Analyze procurement spend and identify opportunities for consolidation and efficiency. Ensure all purchasing activities are within allocated budgets. Process Improvement & Compliance Implement procurement best practices, policies, and procedures. Ensure adherence to ethical procurement standards and company governance. Support digital transformation initiatives in procurement (e.g., ERP implementation). Team Leadership Lead, mentor, and develop a team of procurement professionals. Drive a culture of continuous improvement, collaboration, and high performance. Export Merchant Negotiate incoterms and contracts specific to export requirements, balancing cost, quality and delivery timelines. Collaborate with logistics, customs, and export documentation teams to ensure smooth end to end export fulfilment. Manage supplier audits to ensure readiness for export orders. Qualifications Master’s degree in Supply Chain Management (Preferred). Professional certification such as CPP, CPSM, or equivalent is a plus. Age criteria: 40 TO 45 Years Minimum 8–10 years of progressive experience in procurement, including 3–5 years in a leadership role. Required Skills Strong negotiation and contract management skills. Deep understanding of procurement regulations, supply chain practices, and sourcing strategies. Proficiency in ERP systems (e.g., SAP, Oracle) and procurement tools. Analytical mindset with excellent problem-solving capabilities. Outstanding interpersonal and communication skills. Ability to manage multiple projects and stakeholders under tight deadlines. Preferred Skills Excellent communication and interpersonal skills are critical, as the role requires frequent interaction and negotiation with suppliers, internal stakeholders, and cross-functional teams. Strong administrative skills to build and nurture strategic relationships is key to fostering long-term partnerships and ensuring supplier reliability. Leadership and team management skills are vital to guide and motivate a procurement team, set clear expectations, and promote a collaborative work environment. Critical thinking and problem-solving abilities, enabling the manager to navigate complex sourcing challenges and make sound decisions under pressure. A high degree of emotional intelligence helps in managing conflicts, understanding stakeholder needs, and adapting to diverse working styles. Adaptability and Resilience are important, as procurement often involves responding to market fluctuations, supply chain disruptions, and evolving organizational priorities with agility and a solutions-focused mindset. Pay range and compensation package: UPTO 10 LPA (It can be negotiable depends on present package & Industry norms)

JOB TITLE - DEPUTY MANAGER PRODUCTION EXPERIENCE - More than 10 years of experience in Pharmaceutical Production. JOB RESPONSIBILITY - 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. SKILLS REQUIRED - 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 SALARY - CTC package will be suitable and negotiable based on the present package and industry norms for the right candidate.

You will be joining Mendine Pharmaceuticals Pvt. Ltd., a renowned company with a rich history spanning over eight decades since 1937. Operating primarily in Eastern & North Eastern India and part of Eastern U.P., the company prides itself on a diverse range of products covering cutting-edge allopathic medicines to traditional Ayurveda drugs. Mendine Pharmaceuticals boasts an ISO:9001:2015, WHO GMP certified Manufacturing, Research and Development unit that produces Pharmaceutical, Nutraceutical, and Food Supplement Products. Additionally, Mendine Lifecare Products Pvt. Ltd., a Strategic Business Unit, focuses on the promotion of ethical products. The core values of Mendine revolve around customer satisfaction, health education, integrity, and innovation through extensive research and technological advancements for a brighter future. As a Senior Procurement Manager at Mendine Pharmaceuticals, you will play a crucial role in overseeing the sourcing and purchasing operations. Your responsibilities will include developing and implementing procurement strategies in alignment with company objectives, managing supplier relationships, negotiating contracts, ensuring operational excellence, optimizing costs, and maintaining compliance with regulations. You will lead a team of procurement professionals, drive process improvements, budget control, and strategic sourcing initiatives. Moreover, your role will involve export management duties such as negotiating export contracts, collaborating with logistics and documentation teams, and conducting supplier audits to facilitate smooth export operations. To excel in this role, you are expected to hold a Master's degree in Supply Chain Management (Preferred) and have a minimum of 8-10 years of progressive procurement experience, including at least 3-5 years in a leadership position. Strong negotiation skills, contract management abilities, procurement regulations knowledge, ERP system proficiency, and excellent interpersonal and communication skills are essential requirements. Additionally, certifications like CPP, CPSM, or equivalent would be advantageous. Your role will also require analytical thinking, problem-solving capabilities, multitasking skills, and the ability to lead and motivate a team towards achieving common goals. Adaptability, resilience, emotional intelligence, and critical thinking are key attributes that will help you navigate complex sourcing challenges, manage conflicts, and respond effectively to market dynamics and organizational priorities. In summary, the Senior Procurement Manager role at Mendine Pharmaceuticals offers an exciting opportunity to lead procurement operations, drive strategic initiatives, and contribute to the company's mission of fostering a healthier tomorrow through innovative procurement practices and ethical standards.,

As a Deputy Manager Production with more than 10 years of experience in Pharmaceutical Production, you will be responsible for overseeing various aspects of production to ensure the efficient manufacturing of specially liquid and ointment products. Your key responsibilities will include: Production Planning & Scheduling: Develop and implement production plans, schedules, and workflows to optimize resource allocation and minimize downtime in manufacturing processes. Equipment Management: Oversee the operation, maintenance, and troubleshooting of production equipment such as mixers and filling machines to ensure smooth production operations. Material Management: Ensure proper sourcing, storage, and handling of raw materials, including liquids, ointments, and packaging materials while adhering to inventory control procedures. Safety & Compliance: Enforce safety protocols, maintain a safe working environment, and ensure compliance with health, safety, and environmental regulations. Team Management: Supervise and motivate production staff, provide training, guidance, and performance feedback to ensure a high-performing team. Cost Management: Monitor production costs, identify areas for improvement, and implement strategies to optimize efficiency and minimize waste in production processes. Process Improvement: Identify opportunities to enhance production processes, improve efficiency, and reduce costs by implementing necessary changes. Documentation & Reporting: Maintain accurate production records, batch records, QMS, and other required documentation while preparing reports on production performance. To succeed in this role, you should have proven experience in liquid and ointment manufacturing processes, a strong understanding of production planning, scheduling, and control, proficiency in operating and maintaining production equipment, knowledge of regulatory requirements, and excellent leadership, communication, and interpersonal skills. Additionally, familiarity with safety regulations, proficiency in MS Office tools like Word, Excel, and PowerPoint, and strong problem-solving and decision-making abilities are essential. The salary for this position will be a CTC package suitable and negotiable based on your present package and industry norms for the right candidate. You are expected to adhere to the company's rules and regulations concerning health, hygiene, safety, and product quality. If you meet the requirements and are ready to take on this challenging role, we look forward to receiving your application.,

Job Summary : We are seeking a highly motivated and detail-oriented QMS professional to join our Quality Assurance team in Mendine Pharmaceuticals Pvt Ltd. The successful candidate will be responsible for ensuring compliance with regulatory requirements and company standards by implementing and maintaining effective quality management systems. This role involves managing various quality-related activities, including quality risk management, batch manufacturing record preparation, process validation, and deviation management. Key Responsibilities : 1. Quality Risk Management: Identify, assess, and mitigate quality risks associated with products and processes. Implement and maintain a quality risk management system in accordance with regulatory guidelines. 2. Batch Manufacturing Record (BMR) Preparation: Prepare and review BMRs for accuracy and compliance with regulatory requirements. Ensure BMRs are properly approved, controlled, and distributed. 3. Process Validation: Coordinate and execute process validation activities, including protocol preparation, execution, and reporting. Ensure compliance with regulatory requirements and company standards. 4. Packaging Material Specification Preparation: Develop and maintain packaging material specifications in accordance with regulatory requirements. Ensure specifications are properly approved, controlled, and distributed. 5. Annual Product Quality Review (APQR): Prepare and review APQRs for products, including trend analysis and recommendations for improvements. Ensure APQRs are properly approved and distributed. 6. Cleaning Validation: Coordinate and execute cleaning validation activities, including protocol preparation, execution, and reporting. Ensure compliance with regulatory requirements and company standards. 7. Deviation Management: Investigate and document deviations from established processes and procedures. Ensure deviations are properly approved, controlled, and closed out. 8. Change Control Management: Coordinate and execute change control activities, including assessment, approval, and implementation. Ensure compliance with regulatory requirements and company standards. 9. Batch Card Preparation: Prepare and review batch cards for accuracy and compliance with regulatory requirements. Ensure batch cards are properly approved, controlled, and distributed. 10. Technology Transfer: Coordinate technology transfer activities, including documentation, training, and execution. Ensure compliance with regulatory requirements and company standards. 11. Coordination with RA & R&D: Collaborate with Regulatory Affairs (RA) and Research & Development (R&D) teams on quality-related matters. Ensure effective communication and coordination on quality-related activities. Skill Requirements: Master's degree in Pharmacy. Minimum 3-7 years of experience in a QA/QMS role in the pharmaceutical industry. Strong knowledge of regulatory requirements, including cGMP, ICH, and ISO 9001. Excellent analytical, problem-solving, and communication skills. Ability to work independently and lead cross-functional teams. Salary & Benefits: Competitive salary based on present package & industry norms. Opportunities for professional growth and development. Collaborative and dynamic work environment. If you are an Eligible, motivated and detail-oriented professional with a passion for quality management, please submit your application.

We are seeking a highly motivated and detail-oriented Quality Management System (QMS) professional to join our Quality Assurance team at Mendine Pharmaceuticals Pvt Ltd. As a part of our team, you will play a crucial role in ensuring compliance with regulatory requirements and company standards by implementing and maintaining effective quality management systems. Your responsibilities will include managing various quality-related activities such as quality risk management, batch manufacturing record preparation, process validation, deviation management, and more. In your role, you will be expected to identify, assess, and mitigate quality risks associated with products and processes. You will also be responsible for implementing and maintaining a quality risk management system in alignment with regulatory guidelines. Additionally, you will prepare and review Batch Manufacturing Records (BMRs) to ensure accuracy and compliance with regulatory requirements, as well as coordinate and execute process validation activities while ensuring compliance with regulatory standards. Furthermore, you will develop and maintain packaging material specifications, prepare and review Annual Product Quality Reviews (APQRs), coordinate cleaning validation activities, manage deviations from established processes and procedures, oversee change control activities, prepare batch cards, and coordinate technology transfer activities. Collaboration with Regulatory Affairs (RA) and Research & Development (R&D) teams on quality-related matters will be essential to ensure effective communication and coordination on quality-related activities. To be successful in this role, you should possess a Master's degree in Pharmacy along with a minimum of 3-7 years of experience in a QA/QMS role within the pharmaceutical industry. Strong knowledge of regulatory requirements such as cGMP, ICH, and ISO 9001 is necessary, along with excellent analytical, problem-solving, and communication skills. The ability to work independently and lead cross-functional teams will also be vital for this position. As part of our team, you will receive a competitive salary based on your present package and industry norms, along with opportunities for professional growth and development in a collaborative and dynamic work environment. If you are an eligible, motivated, and detail-oriented professional with a passion for quality management, we invite you to submit your application for consideration.,