Supervisor is responsible for preparation, review, revision, control and implementation of standard operating procedures activity, Change control and CAPA of Sterile manufacturing department
Responsible for independent management, review, and approval of Quality Assurance activities. Ensures implementation of quality systems, drives regulatory compliance, leads investigations, and collaborates with cross-functional teams to maintain cGMP standards and inspection readiness.
Contribute to a culture of continuous improvement using Lean, Six Sigma, and Design for Six Sigma principles. Explore new tools and methodologies to enhance project execution and process efficiency.
Design and synthesize novel small molecules based on biological and medicinal chemistry objectives. Develop and execute multi-step organic synthesis routes, including reaction optimization and scale-up.
Communicate with headquarter regulatory team on local regulation changes with impact assessment. Assist in communications with global regulatory representatives to assist in filings and responses to inquiries from health authorities.
Aspiro Pharma is one of the leading USFDA-approved pharmaceutical companies with global outreach and requires personnel for its Injectable facility, located at Karkapatla (V), Markook (M), Siddipet (Dist.), Telangana.
B. Pharma. / B.Sc. (Medicinal Chemistry) / B.Sc. (Pharmaceutical Chemistry). (MBA in Sales & Marketing is a desirable qualification). Pharmaceuticals & Medical Devices Bureau of India
Pharmacy qualifications obtained before the Pharmacy Council of Indias Education Regulation, 1991, as amended by the Education Regulation Amendment 1994, came into force in the State of Uttarakhand will also be considered eligible. Veterinary Pharmacy Officer in government veterinary hospitals, Uttarakhand
Graduate degree in Science B.pharm, Life Sciences, Biotech, Zoology, Botany, etc. with PG Diploma in Clinical Research is mandatory with minimum 1 years’ experience in Clinical Trials is desirable.