Post Graduate Degree, including the integrated PG degrees, Masters in Pharmacology / M. Sc in Neurosciences / Life Sciences. NIMHANS, Bengaluru

Pharmacy, Nursing, Sports Medicine or related field with valid license/experience

Minimum M.Sc OR M.Tech OR in any field of science / Life science / Biotechnology/ Physiology / Biophysics / Biochemistry with a good academic record.  NIMHANS Bangalore

M.Sc. in life sciences with NET/DBT-JRF/GATE or equivalent exam cleared with Masters or equivalent degree. Regional Centre for Biotechnology

Masters degree in any branch of Biological / Life Sciences with 60% (or Equivalent) marks or an equivalent degree in any branch of Biological / Life Sciences with two years post-master’s degree experience in research are eligible to apply. BRIC-NIPGR

Post-Doctoral Fellowship (PDF) position is available at the Protein Engineering & Translational Neuroscience Laboratory (ProTEN), Centre of Health & Therapeutics Research, Manipal University Jaipur (MUJ).

B.Pharm/ M.Pharm for Officer & Executive (Sterile USFDA Exp.) Officer/Sr.Officer (Analytical Method Validation, RM/PM,HPLC)

Monitor and maintain documents & records related to the Integrated Management System and Energy Management System to ensure compliance with international standards and audit requirements. 

Compression/ Granulation/ Capsule Filling/ Coating Technical Assistant : B. Sc/ Diploma/ ITI/ Intermediate  Executives : B.Pharmacy / M.Pharmacy

Shodhana Laboratories is a pharmaceutical company specializing in Active Pharmaceutical Ingredients (APIs) and Intermediates. Established in 2000, they cater to both generic and custom requirements for well-known pharmaceutical brands.

Otsuka Pharmaceutical India Private Limited primarily manufactures IV and parenteral nutrition products across multiple markets and therapeutic segments.

Strong command of English and Bangla with excellent analytical and proWem-solving skills. Self-driven, result-oriented and decent communication skills.

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.