Titan Laboratories Jobs in India

We are looking for a dynamic professional as Executive / Sr. Executive to manage international markets with strong exposure to semi-finished and finished dosage forms and will be based at Juinagar, Navi Mumbai. · ...

Key Responsibilities: · Operate FBE coating equipment as per standard operating procedures (SOPs). · Monitor and control pre-heating, powder spray, curing, and cooling stages of the coating process. · Ensure correct pipe surface preparation including cleaning, blasting, and inspe ...

The job is responsible for international sales for API and follows up with clients regarding orders, collections, product development and market development. · Must have travelled to Egypt and Iran at least 2-3 times. · Follow-up from client for order, collection, product develop ...

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 · -Problem solving · -Team Management · ...

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 ident ...

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. Refere ...

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 te ...

Job Overview: · We are seeking an experienced Regulatory Affairs professional with strong expertise in Bioequivalence (BE) activities. The candidate will be responsible for preparing and reviewing regulatory modules, BE protocols and reports, and managing documentation for BE NOC ...

Role & responsibilities · Plan and manage project timelines, allocate task, and ensure timely execution. · Lead formulation development project from concept to commercialization. · Supervise pre-formulation studies, excipient compatibility, and feasibility assessments. · Drive pr ...

The role involves hands-on responsibility for compilation and filing of regulatory dossiers in regulated markets with strong exposure to EU regulatory procedures. · Should have hands on experience about dossier filing compilation in regulated market. · Knowledge about EU procedur ...

Role & Responsibilities: · Formulation and development of pharmaceutical products for both emerging and regulated markets, ensuring compliance with relevant regulatory requirements. · Execution of lab-scale trial batches and supporting technology transfer activities at manufactur ...

+We are looking for Deputy Manager / Manager - Regulatory Affairs (Regulated market), where we are seeking a proactive and detail-oriented Regulatory Affairs professional to join our dynamic team · + Lead a stagnant regulatory submission project through strategy to address agenc ...

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 relat ...

We are seeking a dynamic and motivated Talent Acquisition Specialist to join our team. · Manage end-to-end recruitment for technical and non-technical job requirements and staffing needs. · Source candidates using job portals, professional networks, and employee referrals. · ...

We are looking for motivated and detail-oriented candidates to join our Regulatory Affairs team in the Pharmaceutical sector. · Role & responsibilities: · Preparation and review of regulatory documents · Compilation and submission of dossiers · Coordination with internal departme ...

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 · ...

+Around 7 -8 years of experience in ROW markets. · + · Maintain up-to-date knowledge of regulatory guidelines and changes in Latam region. · Work closely with R&D departments to ensure timely submissions of dossiers, samples and other full kit requirements of customers. · ...

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 · ...

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) acti ...

Dear All, · We are looking for Manager / Sr. Manager - Project Management for regulated market for Pharmaceutic projects only. Candidate will be based at Navi Mumbai. · Candidates from pharma experience / background should apply. · Role & Responsibility - · You will be responsibl ...