 
                Indoco Remedies Ltd., is a fully integrated, research-oriented pharma company engaged in the manufacturing and marketing of Formulations (Finished Dosage Forms) and Active Pharmaceutical Ingredients (APIs). We have seven decades of presence in the Indian Pharma market and a strong foothold in the international market across 55 countries. Indoco has carved a place for itself in the international arena and is exporting a number of generic products in the Regulated and Emerging Markets.
DATE AND TIME:
- Date: Saturday, January 04, 2025
- Time: 9:00 am to 3:00 pm
- VENUE: INDOCO REMEDIES LIMITED, R&D Center, R-92/93, TTC Industrial Area, MIDC, Thane-Belapur Road, Near Fire Brigade, Rabale, Navi Mumbai – 400 701.
Contact Information:
- E-mail Ids: gauri.deo@indoco.com, sakshi.pande@indoco.com
- Website: http://www.indoco.com
- Position : Sr. Officer / Executive
- Department : Formulation & Development (Regulated Market)
- Specialization : Sterile (Emulsion) / Ophthalmic
- Qualification: M. Pharm
- Experience : 3 – 8 years
Job Details:
- Candidate should have through knowledge on regulatory guidance, literature search applicable for sterile formulation developments,
- Responsible for development and execution of complex Injectable, suspension, emulsion / ophthalmic formulations solution, suspension, emulsion for regulated market.
- Should be responsible for review of trials and stability data throughout product development.
- Candidate should have hands-on experience in transfer of technology from R&D to plant / GMP scale
- Responsible for drafting and review of documents like MFC, MPC, BMR / BPR, stability protocols, specific study protocols / reports, product development report, change controls, item code generations, etc.
- Responsible for all formulation / process related CMC documents drafting and review which will be part of regulatory filings.
- Responsible for execution of process optimization batches, exhibit batches at manufacturing site.
- Assure that all formulation and process development activities are documented in the notebook as per company procedures and cGLPs.
- Responsible for maintaining lab equipments and ensure lab practices as per defined SOP.
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