About the Job :
Syngene, an internationally reputed pharmaceutical contract research organization and manufacturing body that established its journey in 1993. This company serves the purposes in the areas of medicinal chemistry, in vivo pharmacology, biology, toxicology, Process R&D, cGMP manufacturing, analytical development and custom synthesis
The firm has accreditations like iso 9001:2008. It has also animal facilities authorized by Indian authorities. Syngene serves for 331 clients globally including start-up companies. Large pharma/biotech, chemical, animal health and nutritional companies from 25 years.
The company focuses on client satisfaction areas of safety, quality, integrity and ethics. Recently it made an agreement with GSK in the area of advanced drug delivery system. Received PMDA accreditation, expanded collaboration with baxter till 2024. This has been awarded with CMO Leadership awards by life science leader magazine in Newyork.
About the Job :
For Sr. Executive in QC
Experience : Msc/M.pharma with 3-5 years of experience in ARD or QC
Job role :
• Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
• Planning of day to day activities and reviewing of documents.
• To prepare draft investigation report for the deviations, Incidents, Out of Control (OOC), and Out of Specification (OOS).
• Review of document generated on stability analysis, validations, method transfers and calibrations.
• Execution of validation protocols and routine analysis.
• Preparation of validation and stability protocols and reports.
• Preparations of Standard Operating Procedures (SOPs), Emergency Operating Procedures (EOPs) and IOPs and provide training whenever required.
• To execute stability analysis, validations and method transfers on Flame emission spectrometry (FES), Atomic Absorption Spectrophotometer (AAS), Inductively coupled plasma Optical Emission Spectroscopic (ICP-OES) and Inductively coupled plasma mass spectrometry (ICP-MS) techniques as on required within timeline.
• To ensure the entire instrument for intended use meets the 21 CFR part 11 compliance.
• To oversee the quality aspects of stability operations and ensure the compliance for stability testing and Laboratory information management system LIMS
• Attend training on environment, health, and safety (EHS) measures imparted company
2. For Assistant manager in QC
Experience : 9-12 years
Location : Bangalore
3. For Peptide R&D
Experience : 5-7 years
Experience in handling automated peptide synthesizer and skills in peptide and Should be familiar with concepts of peptide synthesis & modifications purification/characterization techniques would be preferred
Familiar with operations of relevant apparatus - instrument / equipment and Good Knowledge of analytical techniques and analytical data interpretation.
Good written and verbal communication skills.
Send resumes to [email protected]