Support initiatives to maintain or improve quality performance and compliance of Novartis PV activities including case processing, medical safety, risk management, Health Authority reporting, PV IT systems and device vigilance. Champion the quality mindset.
Responsible for developing, executing, and documenting qualification and validation protocols for equipment, utilities, and facilities in a regulated pharma setup.
Manage granulation, compression, coating, palletization and capsule filling area. Ensure compliance with SOPs, cGMP and regulatory standards. Maintain accurate documentation and support continuous improvement initiatives.
Responsible for ensuring that the study is conducted in accordance with AZ Procedures / Applicable SOPs and Guidelines, such as ICH and GCP as well as relevant local regulations.
Aspiro Pharma Specialities Pvt Ltd located at the worlds largest integrated pharma cluster hub of Hyderabad, requires the following personnel for our Injectable facility, located at Karkapatla