This non-supervisory role in the Reference Standard Laboratory involves performing necessary project tests and maintaining a GLP-compliant environment. The incumbent leverages their technical expertise and pharmaceutical analysis knowledge to conduct collaborative testing and ensure efficient and effective laboratory operations.

Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export.

Candidate acquainted of Quality Management System Document like Change control, Deviation and their Investigations, CAPA and Audit Management. This role will focus on ensuring the highest standards of quality throughout the manufacturing process, specifically for active pharmaceutical ingredients

Bachelors Degree in Pharmacy or Pharmaceutical Science or Microbiology or Bio- Chemistry or Chemistry or Life Sciences from a recognised University or Institute.

Masters in Natural or Agricultural or Pharmaceutical Sciences/MVSc/Animal Sciences OR Bachelor’s degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement

Monitoring for Documents compilation activities for New product filing , Re-Registration, renewals from plant dossier filing , sample requirements etc. Participation in Action plan discussion for queries from different Regulatory agencies and monitoring for submission of data/documents from plant.

Performing post-submission processing activities such as receiving acknowledgment from authority of submission receipt; capturing and the electronic receipt and metadata in RIM; communicating submission receipt to key stakeholders

Develop and maintain a comprehensive understanding of the company's products, particularly in the cardiovascular therapeutic area, while staying updated on the latest medical advancements, clinical guidelines, and treatment protocols.

Master / Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences / MVSc / Animal Sciences OR Bachelor’s degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement

Knowledge in Computer Application. Sree Chitra Tirunal Institute for Medical Sciences and Technology is an Institution of National Importance under the Department of Science and Technology, Govt. of India.

MSc in Biotechnology / Zoology / Molecular biology / Microbiology or related field in Life Sciences from a recognized University. Looking for motivated and individuals with good academic standing who are interested to explore career opportunities in this innovative multi-organization initiative undertaken by NIBMG

PhD in bioinformatics, molecular biology, cell biology, biotechnology or relevant scientific discipline. Bachelor's or Master’s degree in Finance, Commerce, Business Administration, Public Administration, or Life Sciences with diploma/certification in project/financial management.

Masters in any area under biology, bioengineering, medical biotechnology, or life sciences disciplines. Individuals with experience in model system re-search or with wet lab experience in cellular or molecular biology, or bioengineering will be preferred. Freshers with fellowships will be preferred.

First class postgraduate degree including the integrated PG degrees OR second-class postgraduate degree including the integrated PG degree with Ph.D. OR for Engineering/ IT/CS-First Class Graduate Degree of 4 years.

Post Graduate Degree in Life Science or related subjects. The ideal candidate should have GATE or CSIR-NET qualification including LS, preferably with a rank below 70, and possess extensive experience in cell culture, fluorescence imaging of cells, along with proficiency in image processing.

M.Pharm, B.Pharm, M.Sc, B.Sc ; Must have experience in Granulation & Coating, Review BMR & BPR and follow QMS.

Ciron has carved a niche for itself in the sphere of operations of manufacturing Ampoules, Vials, Eye / Ear / Nasal drops, Lyophilized products and Lyophilized bulk

To ensure compliance of computerized systems, PLC, SCADA-controlled equipment, and automation systems with regulatory requirements 21 CFR Part 11, EU Annex 11, GAMP 5, etc. by executing validation activities as per approved procedures and maintaining validated states throughout the system lifecycle.

M.Pharm, B.Pharm, M.Sc, B.Sc ; QMS, Manufacturing, Ampoule Washing, Visual Inspection, Autoclave, Lyo, Filling & Sealing, Terminal Sterilization.