Functional Responsibilities:

• Responsible for safety & compliance in all the work activities performed.
• Follow the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment and adhere to the highest standards of quality, integrity & compliance for every work activity.
• Complete the assigned training courses in a timely manner and comply with the training procedure & training calendar.
• Attend all assigned mandatory training related to data integrity, health, and safety measures.
• Compliance with Current Good Manufacturing Practices and Good Documentation Practices.
• Adherence to Standard Operating procedures, Operational control Procedures.
• Participate in & support the training on procedures, protocols, and On-the-Job activities.
• Follow the discipline of reporting structure at times of escalation.
• Report nonconformities & deviations to the respective supervisor(s) and/or line manager(s).
• Participate in & support for on-time initiation & closure of deviations, investigations, CAPA and change controls.
• Adhere to organizational policies & procedures on EHSS, POSH, Data Integrity and IT security.
• Always wear the applicable PPEs and adhere to any other Environment, Health, and Safety (EHS) requirements in the workplace for individuals & lab/plant safety.
• Understand all necessary safety protocols and always follow the same to ensure safety for all.
• Proactively identify near-misses & potential incidents and communicate to supervisor and/or line manager or through the respective web portals.

Primary Responsibilities:

1. Analytical method development and validation (MDR and MQR) for new drug molecules.
   Operation and calibration of HPL CE , pH meter, analytical balance, etc.
2. Knowledge of good laboratory practices (GLP), good documentation practices and safety.
   Preparation of standard testing procedures (STPs), standard operation procedures (SOPs) for equipment and instruments installed in R & D (Biologics).
3. SOP Preparation, SOP Revisions, Method development report , Qualification report ,Risk Assessment report and Qualification Plan.
4. Determination of protein concentration and protein content ,SDS PAGE,IEF-Method
5. Affinity Chromatography method (Protein-A)and RP-HPLC Method (Peptide Mapping Method, Quantative Method)
6.  Hands on experience on UV Spectroscopy (Microplate Reader), UPLC with Empower3Software, IEX, SEC, Glycan Method and Troubleshooting of UPLC.

Apply: https://careers.syngeneintl.com/job/Bangalore-ASSOCIATE-SCIENTIST/1252300600/