Hiring Candidates for APITORIA PHARMA PRIVATE LIMITED (100% subsidary of Aurobindo Pharma Limited) Hyderabad Cluster to fill the following Positions in API Division.
Bharat Biotech International Limited (BBIL) has entered into a licensing agreement with GSK plc to take over the development of altSonflex1‑2‑3, GSK’s promising Shigella vaccine candidate.
Novartis announced promising results from its Phase IIIB APPULSE-PNH study, evaluating the twice-daily oral monotherapy Fabhalta® (iptacopan) in adults with paroxysmal nocturnal hemoglobinuria
M.Sc. in Analytical Chemistry, Applied Chemistry, M. Pharm Pharmaceutical Analysis, Chemistry, Biochemistry, Microbiology, Biotechnology, Botany from a recognized University or equivalent
Mahatma Gandhi College of Pharmaceutical Sciences, established & managed by Sri Laxmi Narayan Charitable Society is located at the ISI 15 (A) RIICO Institutional area ,Sitapura, Tonk Road, Jaipur just behind Mahatma Gandhi Medical College & Hospital.
Diploma in pharmacy from recognized institute. should have registered under Jharkhand state pharmacy council
Computer proficiency (MS Office) & internet
Post-graduate degree in Life Sciences, Biotechnology, Biochemistry, Microbiology, Toxicology, Molecular oncology, Bioinformatics, Genetics with two years of research experience in Biochemistry, Biotechnology, Immunology, Molecular Biology.
The candidate must have a first class Post-Graduate Degree in any branch of Life Sciences. Candidates with atleast one year experience in cell culture and molecular biology techniques.
Understanding of drug development processes and proficiency in quality principles driving drug development such as GMP and applicable regulations and policies.
Sound knowledge of analytical method development and Method validation using HPLC as per guidelines. Knowledge of calibration and operations of all equipment like balance, ph meter, in analytical operation.
Responsible for reviewing batch manufacturing, monitoring process steps, and reviewing documentation. Additionally, support in handling deviations, change control, and CAPA management, internal and external audits to maintain compliance.
Preparation and review of Protocol as per sponsor and various regulatory requirements. Preparation and review of Informed Consent Document in English and vernacular language according to protocol.
Developing India-specific Artwork, Support to Regulatory dossier preparation and submissions like New drug applications, Site registration, Clinical trials and Import licence. Managing Registration samples right from dispatch of samples till the report.