We have urgent opening for Executive/ Sr.Executive - FR&D (liquid orals) JD for Liquid Oral dosage form: 1. Experience in formulation & Development of liquid oral dosage form (Solutions & Suspensions) in regulatory market (US/EU/Aus). 2. To conduct literature search, patent search of assigned project and should be familiar with regulatory guidances. 3. To prepare application for form 29, form 11, RLD import license, form 25 etc. 4. To procure raw materials (API/Excipients), Packing material and Innovator samples in consultation with packaging/Regulatory & Purchase department. 5. To execute pre-formulation and formulation optimization trials with QbD approach and develop a robust formulation. 6. To manufacture batches for stability studies and perform other studies on optimized formulation. 7. To review analytical reports and prepare compilation sheet and discuss with superiors. 8. To co-ordinate with cross functional departments like Analytical, Regulatory, QA, MS&T etc. 9. To prepare Technology transfer documents like MFC, PDR, Stability Protocols, Risk assessment and execute scale up and Exhibit batches. 10. Address the regulatory queries. Interested Candidate may send their resume on email Id : audrey.fernandes@marksanspharma.com Regards, Audrey Fernandes Asst.Manager-HR
Urgent opening for Executive/Sr.Executive- FR&D (Topical Dosage) Roles & Responsibilities: 1. Experience on Topical dosage form formulation development Conduct Develop prototypes trials, proof-of-concept models, and experimental formulations to evaluate feasibility, performance Conduct literature reviews, patent searches, and market analyses to assess the feasibility Maintain accurate and detailed records of experimental procedures, results, and observations, and prepare technical reports like MFC, BMR, PDR, Stability protocol etc Experience on Technology transfer (TT) from R&D to commercial manufacturing site. Raw material indenting, packaging material, dies & punches stock management. Preparation & review of Scale up, Exhibit &Validation batch documents such as BOM, BMR, BPR, PVP & PVPR. Collaborate with cross-functional teams to gather and analyze data. Assist and support to plant team and cross functional team in scale-up of new products technology Summarize and document results in LNB , prepare technical reports Maintain clean working laboratory environment and suitable working equipment. Perform general lab assignments (e.g. raw material inventory review, lab instruments) as assigned. Interested Candidate may send their resume to audrey.fernandes@marksanspharma.com
We are hiring Research Officer/ Research Executive at our R&D (Preferably Male Candidate) Location: Navi Mumbai Job Responsibilities: Analytical Method Development and validation of Assay, Dissolution and Organic impurity by using HPLC. Chemical Analysis raw material / finished product. Qualifications, Calibration of all instruments and Equipments as and when required. Method transfer to plant. Monitoring and Maintaining of GLP, GDP & compliance to audit points. Support and coordination for activity related to Project and Lab responsibility. Coordination with service engineers for instrument and equipment maintenance and trouble shooting. Support for training to juniors & new joiner. Keeping track of Chemicals inventory and coordination with Store keeper and purchase department for receipt of the same. Interaction with departments - Project management, Regulatory affairs, R&D- QA, Goa plant and FD. Any other analytical related activity as per company requirement. Qualification: Must be M Pharma/B Pharma/ M.Sc Minimum 6-9 yrs of Experience. Interested Candidate can directly walk in for Interview on the below address: Marksans Pharma Limited D-185/186, TTC Industrial Area, T.B Road, MIDC Shirvane, Navi Mumbai-400706. Landmark: Opp to Courtyard Hotel Lane Date: 26th July 2025 Time: 10 am to 4:30 pm Contact Person: Mr. Vijendra Auti 022-62241200 / 022- 40012000
We are hiring Research Officer/ Research Executive at our R&D (Preferably Male Candidate) Location: Navi Mumbai Job Responsibilities: Analytical Method Development and validation of Assay, Dissolution and Organic impurity by using HPLC. Chemical Analysis raw material / finished product. Calibration of all instruments and Equipments as and when required. Method transfer to plant. Support for training to juniors & new joiner. Keeping track of Chemicals inventory and coordination with Store keeper and purchase department for receipt of the same. Any other analytical related activity as per company requirement. Qualification: Must be M Pharma/B Pharma/ M.Sc Minimum 2-5 yrs of Experience. Interested Candidate can directly walk in for Interview on the below address: Marksans Pharma Limited: D-185/186, TTC Industrial Area, T.B Road, MIDC Shirvane, Navi Mumbai-400706. Landmark: Opp to Courtyard Hotel Lane Date: 26th July 2025 Time: 10 am to 4:30 pm Contact Person: Mr. Vijendra Auti 022-62241200 / 022- 40012000
We are hiring Research Officer at our R&D. Location: Navi Mumbai Job Responsibilities: 1. Prepare and review documentation: Ensure accuracy, completeness, and compliance with regulatory requirements for documents such as analytical methods, study reports, and validation protocols. 2. Prepare SOPs and STPs: Develop, review, and maintain Standard Operating Procedures (SOPs) and Study Protocols (STPs) to ensure compliance with regulatory requirements. 3. Justification of queries: Prepare responses to queries and deviations, ensuring justification and compliance with regulatory requirements. 4. Maintain AMC records: Maintain and track records of Annual Maintenance Contracts (AMC) for instruments and equipment, ensuring timely renewals and compliance. 5. Maintain documentation: Ensure all documents are up-to-date, and revisions are properly tracked and approved. 6. Collaborate with teams: Work closely with analytical scientists, quality assurance, and regulatory affairs teams to ensure documentation meets requirements. 7. Ensure compliance: Familiarize yourself with regulatory guidelines (e.g., ICH, FDA) and ensure documentation complies with these standards. 8. Improve processes: Identify opportunities to improve documentation processes and implement changes as needed. 9. Strong attention to detail and organizational skills, Excellent written and verbal communication skills, Ability to work independently and collaboratively and Familiarity with regulatory guidelines and documentation requirements. Qualification: Must be M Pharma/B Pharma/ M.Sc Minimum 1-3 yrs of Experience. Interested Candidate can directly walk in for Interview on the below address: Marksans Pharma Limited: D-185/186, TTC Industrial Area, T.B Road, MIDC Shirvane, Navi Mumbai-400706. Landmark: Opp to Courtyard Hotel Lane Date: 26th July 2025 Time: 10 am to 4:30 pm Contact Person: Mr. Vijendra Auti 022-62241200 / 022- 40012000
We have urgent opening for Sr.Executive - FR&D (Oral Liquids & OSD) Job description: 1. Experience in formulation & Development of liquid oral dosage form (Solutions & Suspensions) in regulatory market (US/EU/Aus). 2. To conduct literature search, patent search of assigned project and should be familiar with regulatory guidance. 3 .Preformation Study and prototype formulation development. 4. Trail Batch Planning, Execution of trail batches, LNB writing. 5. RLD Characterization. 6. Stability protocol preparation, Stability charging, stability data compilation. 7. Documentation: MFC, PDR, scale up report & other relevant documents. 8. Scale up & Exhibit batches at plant. 9.Additional exposure to dietary supplements will be an added advantage. Other Skill Set: Handling of Instruments: Viscometer, DO Meter, pH meter etc. Interested Candidate may send their resume on email Id : audrey.fernandes@marksanspharma.com Regards, Audrey Fernandes Asst.Manager-HR 022 4001 2000
We have urgent opening for Research Associate/ Executive - FR&D (Oral Liquids & OSD) Job description: 1. Experience in formulation & Development of liquid oral dosage form (Solutions & Suspensions) in regulatory market (US/EU/Aus). 2. To conduct literature search, patent search of assigned project and should be familiar with regulatory guidances. 3 .Preformation Study and prototype formulation development. 4. Trail Batch Planning, Execution of trail batches, LNB writing. 5. RLD Characterization. 6. Stability protocol preparation, Stability charging, stability data complilation. 7. Documentation:TDR, MFC, PDR, scale up report & other relevant documents. 8. Scale up & Exhibit batches at plant. 9.Additional exposure to dietary supplements will be an added advantage. Other Skill Set: Handling of Instruments: Viscometer, DO Meter, pH meter etc. Interested Candidate may send their resume on email Id : audrey.fernandes@marksanspharma.com Regards, Audrey Fernandes Asst.Manager-HR 022-4001 2000
Job description: We have urgent opening for Manager-Supply Chain ( PPIC). Job Overview: The Supply Chain Manager will be responsible for overseeing and managing the company's overall supply chain operations within the pharmaceutical industry. This includes the efficient and effective procurement, production, and distribution of pharmaceutical products. The role will focus on optimizing processes to ensure that materials are procured and delivered in a timely manner, inventory levels are managed effectively, and costs are minimized while ensuring compliance with regulatory standards. Key Responsibilities: Supply Chain Strategy: Develop and implement supply chain strategies that align with business goals and ensure the availability of pharmaceutical products in the market. Procurement: Manage the procurement process, including supplier selection, negotiation, and contract management to ensure a reliable supply of high-quality raw materials and components. Inventory Management: Oversee inventory control and management, ensuring that stock levels are optimized to meet production demands while minimizing excess inventory. Logistics and Distribution: Coordinate logistics activities, including warehousing, transportation, and distribution to ensure timely delivery of products to customers and compliance with Good Distribution Practices (GDP). Demand Forecasting: Collaborate with sales and marketing teams to forecast demand and adjust supply chain activities accordingly to meet market needs. Need to add new manufacturer depend on products and market. Supplier Relationship Management: Build and maintain strong relationships with suppliers and third-party manufacturers to ensure continuity of supply and resolve any issues that arise. Regulatory Compliance: Ensure that all supply chain activities comply with relevant regulatory requirements, including Good Manufacturing Practices (GMP), and other industry-specific regulations. Continuous Improvement: Identify and implement opportunities for process improvements within the supply chain to enhance efficiency, reduce costs, and improve product quality. Risk Management: Develop and implement risk management strategies to mitigate supply chain risks, including disruptions, shortages, and quality issues. Qualifications: Education: Bachelors in Science or Supply Chain Management, Logistics, Business Administration, or a related field. Experience: Minimum of 5-7 years of experience in supply chain management within the pharmaceutical or healthcare industry. Technical Skills: Strong understanding of pharmaceutical manufacturing processes, GMP, GDP, and regulatory requirements. Proficiency in supply chain management software (e.g., SAP, Oracle, or similar). Leadership Skills: Proven experience in leading and managing teams, with strong interpersonal and communication skills. Analytical Skills: Excellent problem-solving and analytical skills, with the ability to interpret data and make informed decisions. Project Management: Experience in project management and the ability to handle multiple projects simultaneously. Attention to Detail: High attention to detail and accuracy, particularly in regulatory compliance and documentation. Negotiation Skill: Good communication & Negotiation Skill is must Preferred Qualifications: Experience working in a global supply chain environment. Knowledge of emerging trends in pharmaceutical supply chain management. Familiarity with cold chain logistics and handling of temperature-sensitive products. Work Environment: This position is based in an office setting with occasional travel to manufacturing sites, suppliers, and distribution centers as required. Interested Candidate may Send their resume to email ID: audrey.fernandes@marksanspharma.com Regards, Audrey Fernandes Asst.Manager- HR 022 4001 2000