Deputy Manage - Formulation & Development (Topical) Gracure Pharmaceuticals

7.0 - 10.0 years

0 - 1 Lacs

Bhiwadi

Work from Office

Role & responsibilities ead formulation and development activities specifically for topical dosage forms including creams, ointments, gels, lotions, and sprays. Design and execute experiments for product development, optimization, and scale-up . Conduct pre-formulation studies , selection of excipients, and establish product design strategy. Ensure compliance with regulatory requirements for domestic and international markets (e.g., USFDA, MHRA). Coordinate with Analytical Development , Regulatory Affairs , QA/QC , and Production teams to ensure smooth technology transfer. Prepare and review technical documents like MFCs, MDDs, protocols, and development reports. Ensure documentation as per cGMP and data integrity standards. Troubleshoot formulation or process-related challenges during development or scale-up. Preferred candidate profile Strong understanding of topical formulations

Posted 2 days ago

Apply

Walk In Interview at Ahmedabad For OSD & Transdermal facility Zydus Lifesciences

3.0 - 8.0 years

3 - 7 Lacs

Ahmedabad

Work from Office

Manufacturing (OSD) Officer/Executive: B. Pharma/M. Pharma with 2 - 7 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection. Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation). To handle manpower and allocate daily activities. Plant Operator / Technical Assistant: ITI / Diploma having 3 - 8 years of experience in operating machines like, Granulation (Glatt, GEA), Cadmach Roll Compactor, Compression machines (Cadmach-26STN). Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items. Semi-Solid : Tube Filling Operator: ITI / Diploma having 3 - 8 years of experience in operating machines like; Wimco. Taking care of Machine operations, Machine Set-up and Trouble shooting. Ensuring accurate measurements, proper mixing and precise reaction conditions. Packing Department Transdermal (Semi Solid) Plant Operator / Technical Assistant – Packing: ITI / Diploma with 3 - 8 years of experience in packing department. Candidates should have exposure to Cartonator machine operation / Track & Trace, Check Weigher, Vision inspection System. Quality Control Department: Officer / Executive/Sr. Executive (Analyst/Reviewer): B. Pharm / M.Sc. with 3 to 8 years’ experience in handling analytical instruments like HPLC, GC, dissolution apparatus and UV visible spectrometer and able to work in different sections like RM, FP, Stability and GLP. Candidates should also have experience in GMP compliance and self-inspection of analytical labs, document review and finished product release in LIMS. Candidates must have exposure of QMS trending for Lab review of various types of reports and protocols. Interview Date : 29th June 2025 Interview Venue: Zydus Healthcare Ltd, Block 2,3,4,5, Sigma Commerce Zone, Nr, Isckon Mandir, BRTS Bus Stand, Ambli Bopal Road, Ahmedabad - 380015. Interview Location: Ahmedabad Interview Timings: 9:00 AM – 04:00 PM Job Location: Pharmez – Matoda -Ahmedabad

Posted 4 days ago

Apply

Regulatory Affairs- CMC - SPD- US market Aurobindo Pharma

4 - 7 years

2 - 6 Lacs

Hyderabad

Work from Office

Key Accountabilities Process/ Operational: 1. Basic knowledge for Review of Pharmaceutical Development Report. 2. Basic knowledge / hands on experience of review of manufacturing documents like batch formula, batch manufacturing records, batch packaging records, yield and reconciliation, manufacturing summaries, in-process controls data, etc. 3. Basic knowledge / hands on experience of review of analytical documents like specifications, test procedures, method equivalency reports, method validation/verification reports and method transfer reports, dissolution protocols, stability protocols, extractable & leachable study reports, etc. 4. Basic knowledge / hands on experience for preparation, review and compilation of assigned ANDAs for submission. 5. Basic knowledge / hands on experience for preparation, review and compilation of Annual Reports (ANDAs/NDAs). Strategic: 1. Basic knowledge of ICH guidelines, FDA guidelines. 2. Knowledge of CTD modules 1,2 and 3.

Posted 1 month ago

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.