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 company Follow-up from client for order, collection, product development & market development Registration of the products in given territory Implementation of identified Business Models & Sales Target Preparation of Budget planning and Annual Target Develop strong working relationships with internal team and clients Maintain 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 Behere HR Department Titan Laboratories Pvt Ltd vaibhavi.b@titanpharma.com

Experience - 2 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 * RM Reviewer

1. Operations Management Trainee: Overseeing and directing all operational activities to ensure efficient and compliant manufacturing, distribution, and quality control. provides administrative and operational support to the management team, assisting in day-to-day tasks and learning company processes and procedures. Qualification: MBA + B. Pharma 2. Finance Management Trainee: Supports finance functions, learning about financial reporting, analysis, and budgeting while assisting with various finance-related tasks. Qualification: MBA (Finance) + Any Graduate 3. Project Management Trainee: Supports project managers and contributes to the efficient execution of projects, from drug development to regulatory processes. Qualification: MBA (Operations) + Any Graduate 4. Portfolio Management Trainee: Assisting senior portfolio managers with tasks like product lifecycle management, market research, and portfolio optimization. Qualification: MBA + B. Pharma 5. Order Management Cell (OMC): Responsible for ensuring the accurate and timely processing of customer orders, from initial receipt to final delivery. Qualification: MBA + Any Graduate

Role & responsibilities TTD Preparation GTI, Nitros, Elemental risk assessment Patent review & ROS Finalize Preferred candidate profile Male candidate

Role & responsibilities 1. Literature Search, Pharmacopoeia and Patent Search, Review and Discussion and Documentation. 2. Application of NOC, Test License, Manufacturing and Import License 3. Reference product Characterization, Manufacturing and Import License. 4. Reference product Characterization, Reverse Engineering and prototype development. 5. Preformulation study, Manufacturing of bench scale trials for formulation development. 6. Manufacturing of process optimization batches, scale up batches and submission batches. 7. Preparation of Bill of Material, Master Formula Record for manufacturing of submission batches. 8. Preparation of Product development Report for regulatory filing of products. 9. Should have knowledge on product development requirements for Regulated market (EU/UK/Canada). 10. Should have knowledge on QbD and DOE, formulation development and Process development of drug products. 11. Coordination with CFTs like: DQA, Clinicals, Regulatory, Technology transfer and production for smooth development and transfer of product from laboratory to Production floor. 12. Knowledge on IR/MR solid oral drug products. Preferred candidate profile Male candidate only

Role & responsibilities 1. Responsible to lead a team of 4-5 scientist for the development of drug products of Regulated Market (EU and UK) 2. Responsible for drug product development to exhibit batch execution and to support for regulatory filing. 3. Conduct Literature survey and compile the scientific data per product. Development of Rubust, bioequivalent formulation and processes through optimization by applying QbD principles. 4. Compilation and review of developmental data and exhibit batch stability data. 5. Should have good understanding on Reference Product Characterization, reverse Engineering, Bioequivalent Prototype development, Stability studies, Scale up activities. 6. Coordination with different cross functional team like ADL, IP, Project Management, SCM, Clinical and regulatory for smooth execution of the projects. 7. Execution of Tech Transfer and monitoring scale up / Exhibit batches. 8. Having well verse knowledge on Regulatory Guidelines for EU, Canada and TGA 9. Lab activities and team management experience is must. Preferred candidate profile Team Management, Formulation Development, Scale Up and Technology Transfer

Role & responsibilities 1. Formulation & Development for emerging & regulated market. 2. Execution of Lab Trial batches & Tech Transfer activities at site. 3. Lab note book writing & documentation ensuring compliance with regulatory guidelines \ Preferred candidate profile - Experience in Tablets, Capsule, Pellets, ER, SR, and DR product development for emerging market.

We are looking for Regulatory Affairs - Executive / Sr. Executive handling 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: 5 - 8 years of experience in regulatory affairs, focusing on Africa and Asian markets. Desirable Skills & Competencies: Attention to Detail: Ability to review and analyze technical documentation with precision. Collaboration: Effective communication skills for working with R&D, manufacturing, and quality assurance teams. Problem Solving: Proactive in identifying compliance issues and developing solutions to address regulatory challenges. Proficient in MS Office and regulatory documentation software. Interested candidates can apply or mail your resume. If you have good references you can share - Thanks & Regards, Vaibhavi Behere HR Department Titan Laboratories Pvt Ltd vaibhavi.b@titanpharma.com

Role & responsibilities - align MD meetings - participate in all MD meeting - prepare and share MOMs of the meetings - Follow-up on tasks and projects - Travel local and domestic as per business need Preferred candidate profile MBA + B. Pharm or Any Graduate

Role & responsibilities - Dossier preparation, review and submission in ACTD/CTD/ Country specific formate and also in ROW. - Review of technical documents - Responding to dossier - related queries. - License related activity. - Strong coordination with functional related department. Preferred candidate profile Dossier Preparation, Submission, Technical Review

Role & responsibilities To create designs for Primary & Secondary Packing Materials. 2. Handling CorelDraw/AI for artwork correction & Packaging Development of New Products for Product Registration, Registration samples & Commercial orders. 3. Artwork checking & give approval for 1 st stage Corel file of Primary & Secondary Packing Materials for Product Registration, Registration samples & Commercial orders. 4. Preparing Die Line Artwork of Primary & Secondary Packing for Initial Development. 5. Clarifying and solving Design, Primary and Secondary packing issues. 6. Generating new packaging in response to briefs & ensuring that packaging material meet set requirements and specifications. 7. Generating EAN-13 Barcode. 8. Initiate Item code & Pharm code form for Primary & Secondary Packing. 9. Giving the some ideas for cost reduction of Packing Materials. 10. Coordinate & follow up with Internal RA team, QA, Production, Purchase & Marketing team for Packaging Development. 11. Maintain records of all final Corel files of artworks. Preferred candidate profile Pharmaceutical Industry

Role & responsibilities : Responsible for Business Development of API International Markets. Identify New Sales oppurtunities and Increase New Business To understand and monitor the registration guidelines & Process, and to obtain the registration of the products To identify and finalise 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 sourcing Maintain up to date data on competitive products Managing distributors / Vendors in International market To ensure proper cordination with CFT Kindly send your resumes on vaibhavi.b@titanpharma.com

We are looking for Assistant Manager - International Business / Export Sales for Middle East market and will be based at Juinagar, Navi Mumbai. Role & responsibilities : Handled Egypt/Iran for API and Pellets & Iraq. Preferable - Travelled in those markets and have 1:1 personal contact with the customers / min he/she should have been to international exhibition (CPHI). Capability of business development taking the products from sampling to commercialization. Order execution, inter-departmental co-ordinate. Annual sales budget for its region. Develop a sound business plan to ensure seamless revenue generation & customer satisfaction. Conduct research to identify new customers / markets & their needs. Promote the products in respective markets from companys approved facilities. Arrange successful business meet with existing & prospective customers 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. Kindly send your resumes on vaibhavi.b@titanpharma.com

We are looking for Manager / Sr. Manager handling International Sales for Asia market 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 company Follow-up from client for order, collection, product development & market development Registration of the products in given territory Implementation of identified Business Models & Sales Target Preparation of Budget planning and Annual Target Develop strong working relationships with internal team and clients Maintain 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 Behere HR Department Titan Laboratories Pvt Ltd vaibhavi.b@titanpharma.com

Role & responsibilities Must have experience in Analytical Method Development. Must have Analytical Method Validation Handling HPLC Apply only API background candidate Preferred candidate profile Male candidate preferred

Role & responsibilities 1. SOP establishment, implementation of system process, note books, work books, protocols for testing and continuous monitoring of Quality Systems in R & D and ADL of Titan Laboratories and Titan Pharma Plus at various locations through SOPs and periodic inspections. 2. Documentation review , approval , Issuance, archival and control of all documents in R&D and ADL of Titan Laboratories and Titan Pharma Plus at various locations . Example Review and approval of MFR against the lab note books , specifications , MOA against analytical method validations , review of analytical method validation protocol and report. Review of ADL results against raw data. Calibration procedures and records of all equipment and instruments . Review of reference standards / working standards/impurities 3. Online review of R&D and ADL activities, daily in-process checks at RND+ADL , line clearances, all system similar to mfg. 4. ADL stability , method validation ,OOS, OOT , in process checks, method verification etc, 5. Review of documents for application of test licenses / manufacturing licenses of Titan Laboratories and Titan Pharma Plus 6. Review of PDR and all documents of R&D and ADL required for submission to regulatory authorities for Dossier registration for Titan Laboratories and Titan Pharma Plus 7. Establishment, implementation and continuous monitoring of Systems in various departments through SOP and periodic inspections 8. Timely escalations of issues impacting the development / testing of product 9. Support to all sites for audit preparations 10. Execution of any tasks assigned by Management from time to time basis Preferred candidate profile Apply formulation background only

Roles & Responsibilities: Creating new Market, New clients for the company. Make sure of good profitable and sustainable business for the company Follow-up from client for order, collection, product development & market development Registration of the products in given territory Implementation of identified Business Models & Sales Target Preparation of Budget planning and Annual Target Develop strong working relationships with internal team and clients Maintain 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.

Key Responsibilities: Operate machines and equipment such as granulators, tablet presses, coating machines, blenders, filling lines, or packaging lines (depending on the product and plant type). Set up and adjust machinery before starting the production run. Monitor the production process and report deviations or abnormalities to supervisors. Maintain equipment cleanliness and perform minor maintenance or cleaning as needed. Complete batch manufacturing records (BMR), logbooks, and other documentation accurately and on time. Ensure compliance with safety, hygiene, and quality standards. Assist in the changeover and cleaning of equipment between batches. Identify and escalate equipment malfunctions or quality issues. Participate in training sessions related to SOPs, GMP, and safety. Qualifications: ITI / Diploma / 10+2 with relevant technical or science background. 13 years of experience in pharmaceutical or manufacturing operations (preferred). Key Skills: Familiarity with manufacturing processes and SOPs. Understanding of cGMP and safety standards. Ability to follow written instructions and maintain accurate records. Physically fit and able to work in a shift-based environment. Team player with attention to detail.

Key Responsibilities: Prepare and execute validation protocols (IQ, OQ, PQ) for equipment, facilities, and utilities. Conduct cleaning validation and revalidation studies, including swab/rinse sampling and microbial testing coordination. Perform process validation (PV) activities for new and existing products. Coordinate with cross-functional teams (Production, QC, Engineering, R&D) for validation execution and troubleshooting. Review and update validation master plans (VMP), protocols, and reports as per regulatory requirements. Ensure calibration and qualification records are up to date and compliant. Maintain documentation in compliance with data integrity and ALCOA+ principles. Support audits and regulatory inspections by providing validation documentation and clarifications. Track and monitor validation schedules and ensure timely completion. Stay updated with latest regulatory trends, validation guidelines, and industry best practices (ICH Q8, Q9, Q10, Q12). Qualifications: B.Pharm / M.Pharm / B.Sc. / M.Sc. (Microbiology, Chemistry, Biotechnology) or related field. 25 years of relevant experience in validation within a pharmaceutical or healthcare manufacturing setup. Knowledge of cGMP, WHO, USFDA, EU, and other regulatory requirements. Key Skills: Sound knowledge of validation principles, risk assessment, and lifecycle approach. Proficiency in drafting validation protocols and technical documentation. Experience with computerized system validation (CSV) is an advantage. Good analytical, problem-solving, and organizational skills. Effective communication and ability to work in a team.

Key Responsibilities: Prepare, review, and format quality and regulatory documents including SOPs, batch manufacturing records (BMR), validation protocols/reports, regulatory dossiers, and audit reports. Maintain documentation control systems and ensure proper filing, archiving, and retrieval processes. Ensure compliance with Good Documentation Practices (GDP) and company policies. Coordinate document approvals and revisions through proper channels. Assist in document preparation for internal and external audits and inspections. Monitor document review cycles and ensure timely updates. Support cross-functional teams with document management and training. Maintain confidentiality and security of all documentation. Qualifications: Bachelor's degree in Pharmacy, Life Sciences, or related field preferred. 13 years of experience in documentation control in pharmaceutical or regulated industry. Knowledge of GMP, regulatory requirements, and quality management systems. Key Skills: Strong attention to detail and organizational skills. Excellent written and verbal communication. Proficiency in MS Office (Word, Excel, PowerPoint) and document management software. Ability to work under deadlines and manage multiple tasks. Understanding of GDP and regulatory document standards.