We are looking for candidates for Executive / Sr. Executive / Manager / Sr. Manager - International BD handling ROW / LATAM / Asia / CIS and will be based at Juinagar, Navi Mumbai. Job Description as below - Role & responsibilities : Responsible for Business Development of pharma formulations for International Business .Identify New Sales opportunities and Increase New Business in Regulated or Semi Regulated markets.To understand and monitor the registration guidelines & Process, and to obtain the registration of the productsTo identify and finalize the agreements with appropriate business partners in various countries.Monitoring export marketing, regulatory affairs, costing, negotiation, executions, logistics and export documentations.Interaction with manufacturer for product sourcingMaintain up to date data on competitive productsManaging distributors / Vendors in International marketTo ensure proper coordination with CFT Interested candidates can mail / WhatsApp your resume or if you have good references you can share - Thanks & Regards,Vaibhavi BehereHR DepartmentTitan Laboratories Pvt Ltdvaibhavi.b@titanpharma.com

Role & responsibilities :1. Sales order processing2. Reviewing incoming sales orders for accuracy, including product details, quantities, and delivery dates.3. Collaborating with the operational team to communicate order status updates to customers.4. Generating reports on sales order processing metrics like lead times, on-time delivery.5. Ensure effective communication with the respective departments to manage order expectations.6. Familiarity with enterprise resource planning (ERP) software to manage sales orders Desirable Skills & Competencies:1. Strong coordination and communication skills2. Attention to detail and ability to manage multiple tasks3. Basic knowledge of inventory management.Interested candidates can mail their updated resume & CTC on vaibhavi.b@titanpharma.com.Thanks & Regards,Vaibhavi BehereHR DepartmentTitan Laboratories Pvt Ltd

Key Responsibilities:Preparation and submission of DMF (Drug Master Files) and other regulatory documents.Handling regulatory queries and compliance with global regulatory agencies.Coordination with R&D, QA, and production teams for regulatory submissions.Maintaining up-to-date knowledge of regulatory guidelines (USFDA, EDQM, TGA, etc.).Ensuring smooth regulatory approvals and post-approval compliance.

Candidate will be based at Navi Mumbai and will be responsible for as below - Ensure accurate preparation and submission of import-related documentation for smooth customs processing.Monitor and maintain records of invoices to ensure timely payments and accurate financial reporting.Manage the acquisition and submission of GSP certificates to secure preferential tariff benefits.Prepare and verify commercial documents to meet international trade compliance requirements.Review and approve shipping bill checklists to confirm accuracy before customs submission.Facilitate the timely approval of Bills of Entry to expedite the customs clearance process.Generate and manage E-Way Bills in compliance with regulatory requirements for goods movement.Oversee the end-to-end customs clearance process to ensure timely release of goods.Desirable Skills & Competencies:•Analytical and problem-solving abilities to handle discrepancies and resolve issuespromptly.•Attention to detail for accurate documentation and compliance checks.•Strong communication and interpersonal skills for effective collaboration.Interested candidates can mail / whatsApp their updated resume & CTC on contact details below - Thanks & Regards,Vaibhavi Behere HR Department Titan Laboratories Pvt Ltdvaibhavi.b@titanpharma.com

Key Responsibilities: Conduct Literature Search, Pharmacopoeia & Patent Search, and document findings Apply for NOC, Test License, Manufacturing & Import Licenses Perform Reference Product Characterization, Reverse Engineering & Prototype Development Conduct Preformulation studies & bench-scale trials Prepare & manage stability batches Optimize manufacturing process, scale-up & submission batches Develop Bill of Material (BOM) & Master Formula Record (MFR) for submission batches Prepare Product Development Reports for regulatory filing Ensure compliance with EU/UK/Canada regulatory requirements Apply QbD & DOE principles in formulation & process development Coordinate with DQA, Clinicals, Regulatory, Technology Transfer & Production teams Work on IR/MR solid oral dosage forms

Job description1. Production DepartmentDesignation/Position: OfficerRequired Qualification: B.Pharma/M.Pharma,M.Sc/B.ScExperience: Min. 2Yrs. and aboveKey Skill: Documentation2. Production DepartmentDesignation/Position: Operator/TechnicianRequired Qualification: ITI/12th/AOCP/DiplomaExperience: Min. 2Yrs. and aboveKey Skill: Pellet Coating( FBE operator wruster coating)/Coating Pan/Auto coater/Capsule Filling/Compression Operator3. Packing DepartmentDesignation/Position: Operator/TechnicianRequired Qualification: ITI/12th/AOCP/DiplomaExperience: Min. 2Yrs and aboveKey Skill: Blister/Bottle/ Cartonator/Labelling 2D & ATD4. Packing DepartmentDesignation/Position: Officer/Executive/Shift In chargeRequired Qualification: B.Pharma/M.Pharma,M.Sc/B.ScExperience: Min 3 Yrs. and AboveKey Skill: Line Supervisor/ BPR/Shift In Charge5. Quality Control (QC) DepartmentDesignation/Position: OfficerRequired Qualification: B.Pharma/M.Pharma,M.Sc/B.ScExperience: Min. 3 Yrs. and aboveKey Skill: Knowledge of HPLC, GC, UV, Dissolution and all other instrument6. Quality Assurance DepartmentDesignation/Position: Officer/Executive/Sr. ExecutiveRequired Qualification: B.Pharma/M.Pharma, M.Sc/B.ScExperience: Min. 3 Yrs. and aboveKey Skill: IPQA, QMS, AQA,

Role & Responsibility -You will be responsible for anchoring end to end Project Management of New product launches in regulated markets like EU, UK, Australia. Titan own products and CMO products.Responsible for end-to-end project management of all project phases (Initiation, planning, execution, monitoring. and dossier submission) of commercial generics for in-house and customers projects.Tracking from development of product, licencing, procurement of RM and PM for RND trials and commercial, artworks approvals, documentation etc to its first commercial dispatch.Manage and coordinating with cross-functional teams to support milestone achievement and ensuring projects are on time, on budget and within scope.Closely monitoring and overseeing the risk management throughout the duration of project.Coordinate resource planning including documentation, procurement, invoicing & budgeting.Desirable Skills & Competencies:Candidate should be B.Pharma & MBA/M.Sc/M.Pharma with 10 - 12 yrs of experience in Project Mangement for Regulated Market.You should be strong in Planning, coordination and communication skills.Attention to detail and ability to manage multiple tasks.Should be strong in Project management & Decision Making .Manage and coordinate with cross-functional teams.Interested candidates can mail their updated resume & CTC on vaibhavi.b@titanpharma.com.Thanks & Regards,Vaibhavi BehereHR DepartmentTitan Laboratories Pvt Ltd

Role & responsibilities Online monitoring of QC analysis along with respective raw data.Review of Analytical Test Reports for Raw Material, Packing Material, In-Process, Finished Product, Stability, and Working Standards.Review of analytical testing reports for validation, hold time study, cleaning validation, method validation, and method verification.Final review of Finished Product COA along with raw data.Review of Master Specifications for Raw Material, Packing Material, In-Process, Finished Product, Stability, MOA, Test Protocols, and Test Reports.Monitoring the withdrawal and analysis of stability samples as per the planner.Oversight of stability chamber-related activities.Monitoring the calibration of QC instruments as per the planner and SOPs, ensuring compliance and completion of calibration reports.Responsible for the review of QMS documents, including Change Control, Deviation, Incident, and Investigation.Initiation of Change Control, Deviation, Incident, and CAPA.Responsible for initiation of document Ratification and Errata.Investigation of OOS, OOT, and incidents in the QC laboratory.Review of metadata & Audit Trail in software as well as reports.Ensuring the maintenance of data integrity for documents and systems.Compliance with cGMP norms and regulatory requirements.

* Experience - 3 Years + In Formulation QC* QC - Finish Product - GC/HPLC/ Dissolution/AAS/UV* QC- In process- HPLC/UV/Dissolution/GC* QC - Validation- HPLC/UV/GC/Dissolution* RM - HPLC* Stability HPLC GC UV Dissolution

We are looking for Manager / Sr. Manager handling International Sales & Business Development and will be based at Juinagar, Navi Mumbai. Roles & Responsibilities:Creating new Market, New clients for the company.Make sure of good profitable and sustainable business for the companyFollow-up from client for order, collection, product development & market developmentRegistration of the products in given territoryImplementation of identified Business Models & Sales TargetPreparation of Budget planning and Annual TargetDevelop strong working relationships with internal team and clientsMaintain sales and registration records. Education: B pharm and MBA (Preferred)Desirable Skills & Competencies:Strong communication skills for effective client and team interactions.Excellent negotiation skills to close profitable deals.Strategic thinking for market expansion and business growth. Interested candidates can apply or mail your resume. If you have good references you can share - Thanks & Regards,Vaibhavi BehereHR DepartmentTitan Laboratories Pvt Ltdvaibhavi.b@titanpharma.com

We are looking for Regulatory Affairs - Officer / Sr. Officer handling Reg, CIS, Africa and Asia and will be based at Juinagar, Navi Mumbai. Roles & Responsibilities: 1. Dossier Preparation and Submission: Compile and review regulatory submissions in ACTD, CTD and formats.Ensure all regulatory documents are accurate, complete, and compliant with regulatory requirements.2. Review of Plant and R&D Data:Review R&D data to confirm compliance with regulatory expectations and assist in developing effective submission strategies.3. Regulatory Compliance and Updates:Stay informed of changes in Asian and CIS market regulations, ensuring timely implementation of updates to maintain compliance. Provide regulatory insights to internal teams on best practices for data management and documentation.4. Documentation and Record Keeping:Maintain well-organized records of submissions, communications, and approvals.Use regulatory software and systems for document tracking, version control, and report generation. Education: B pharm and MBA (Preferred)Desirable Skills & Competencies:Strong communication skills for effective client and team interactions.Excellent negotiation skills to close profitable deals.Strategic thinking for market expansion and business growt Interested candidates can apply or mail your resume. If you have good references you can share -Thanks & Regards,Vaibhavi BehereHR DepartmentTitan Laboratories Pvt Ltdvaibhavi.b@titanpharma.com

Role & responsibilities 1. Lead API projects from concept to final delivery, ensuring timely execution. 2. Collaborate with R&D, Regulatory Affairs, QA, and Manufacturing teams. 3. Develop project timelines, resource plans, and risk management strategies. 4. Ensure compliance with GMP, GLP, FDA, EMA, and ICH regulations. 5. Manage project budgets, resources, and resolve any issues proactively. 6. Provide regular project updates to senior management and stakeholders. 7. Maintain communication with external vendors and suppliers. 8. Oversee API documentation accuracy and compliance. 9. Conduct post-project reviews for continuous improvement.Preferred candidate profile - Desirable Skills & Competencies:1. PMP certification or equivalent. 2. Understanding of API manufacturing technologies and supply chain management. 3. Experience in risk management and quality control processes.4. Strong problem-solving skills with the ability to handle complex, cross-functional issues.5. Familiarity with project management tools (MS Project, Jira, Asana) and pharmaceutical development documentation.6. Strong understanding of API development, manufacturing processes, and regulatory requirements.Perks and benefits