34 Job openings found

Formulation & Development of Injectable Drug Delivery Systems Should be able to perform the below activities Involving Literature Search involving reading relevant product-related patents, research articles & regulatory recommendations & guidelines. Based on the literature proposing strategy and planning batches Sourcing of raw materials & excipients as per requirement & specification from approved vendors. Planning ...

Experience: 4–10 Years Location: Delhi / NCR Language: Japanese – JLPT N2 or N1 preferred ✅ Must-Have Skills 🔬 Core Clinical Research Skills Solid knowledge of ICH-GCP guidelines Hands-on experience with clinical trial phases (I–IV) Experience in: Site identification, initiation, monitoring, and close-out Protocol adherence and regulatory submissions SAE/AE reporting & handling deviations Patient recruitment and site coordination Documentation handling ...

  Perform Extractables & Leachables (E&L) studies in line with BPOG and regulatory guidelines (USP , , ICH Q3D). Operate and maintain instruments like LC-MS/MS, GC-MS/MS, UHPLC, GC-FID. Conduct method development, optimization, and validation for targeted and non-targeted analysis. Interpret mass spectral, elemental, and chromatographic data for accurate reporting. Support wet chemistry tests (pH, conductivity, titrations) and documentation ...

Position:          QC Manager (Biosimilars) Location:          Bhopal Experience:       8 - 10 Year Industries:        Pharma              Responsibilities:   Manage QC activities raw materials, in-process, and finished biosimilar products. Oversee analytical and microbiological testing (e.g., HPLC, ELISA, SDS-PAGE, Western Blot). Ensure compliance with cGMP, GLP, ...

Job Description: We are seeking a skilled and experienced microbiology professional to lead microbial testing and environmental monitoring activities in an API manufacturing setup. The Assistant Manager will ensure compliance with regulatory standards, supervise microbiological operations, and support quality systems in the microbiology lab. Key Responsibilities: Oversee routine microbiological testing of raw materials, ...

Job Description: We are hiring an experienced QC professional to lead and manage quality control operations in our API manufacturing unit. The Assistant Manager will be responsible for supervising analytical activities, ensuring regulatory compliance, handling audits, and supporting continuous improvement initiatives. Key Responsibilities: Supervise routine analysis of raw materials, intermediates, and finished APIs Review ...

Job Description: We are looking for an IPQA Executive to monitor and ensure in-process quality during manufacturing and packing operations in our API facility. The ideal candidate will be responsible for real-time quality assurance, GMP compliance, and documentation control throughout the production lifecycle. Key Responsibilities: Perform in-process checks during various stages of API ...

Essential Duties and Responsibilities:We are seeking a dynamic technical documentation Executive with a minimum of 1 years of experiencein the Chemicals & Pharmaceuticals industries. The ideal candidate will be responsible for thepreparation and processing Key responsibilities include. A. Preparation of Technical documents like below:1. COA/ Certificate of Analysis2. MSDS3. Specifications/ TDS4. ...

  Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority. Well versed with the guidelines of ICH and other regulatory. Preparation of documents for license application. Preparation of documents for COPP, FSC and other legal documents including product permission Preparation of registration documents as per ACTD , CTD ...

  Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority. Well versed with the guidelines of ICH and other regulatory. Preparation of documents for license application. Preparation of documents for COPP, FSC and other legal documents including product permission Preparation of registration documents as per ACTD , CTD ...