Seabird Staffing Solution Jobs in India

This Pharma Microbiology- Executive role involves testing and analysis of raw materials in-process samples finished products identifying analyzing microorganisms environmental monitoring method development validation quality assurance documentation reporting investigation trouble ...

Perform routine microbiological testing on raw materials, · in-process samples and finished products. · Identify and analyze microorganisms present to ensure they are within acceptable limits.Conduct environmental monitoring of manufacturing areas and laboratories. · Maintain acc ...

+h2>Job summary · pAssistant Manager – Regulatory Affairs (OSD & Injectables) needed by Seabird Staffing Solution for state-of-the-art Pharmaceutical leader in Chhatrapati Sambhajinagar. · +h2>Qualifications · B. Pharm / M. · +p+ · + · +Responsibilities · ,pDossier Preparation (C ...

This job involves leading formulation development from concept to commercialization conducting literature searches tech transfers and scale-up batches managing OSD solid oral liquid oral injectable dry syrup projects. · Lead formulation development from concept to commercializati ...

Collaborate with cross-functional teams on GMP compliance. · ...

+Quality Assurance Assistant Manager job opening. · + · Create and implement quality systems to ensure all products and processes meet regulatory requirements. · Ensure all activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations. · Review and approv ...

This is an opportunity to work as a microbiology executive in the pharma industry. · M.Sc.- Microbiology · ...

This is a Quality Control - Executive position at an unspecified company located in Chhatrapati Sambhajinagar, Maharashtra. · ...

We are looking for an experienced Microbiology Executive to join leading OSD pharma company in Chhatrapati Sambhajinagar. · Expertise in QMS, environmental monitoring and regulatory audits required. · ...

Conduct analytical research using HPLC and develop and validate analytical methods. · ...

Create and implement quality systems to ensure all products and processes meet regulatory requirements. Ensure all activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations. · Review and approve all necessary documents, including batch records, SOPs, ...

Literature search/study and development trials strategies preparation execution pre-formulation study market/innovator/reference product characterization/execution trial batches -prototype formulation development technology transfer activities at site coordination with relevant c ...

Formulation R & D Assistant Manager for OSD / Injectable position required. M. Pharm qualification and experience in formulation development of solid orals, liquids; semisolids, dry syrup dosage forms aimed for export/ROW and domestic market. · ...

Develop solid oral formulations for OSD products. · ...

The Trainee- HR -Talent Acquisition will assist in recruitment strategies design and future hiring needs identification. · Create and post job descriptions on various platforms. · ...

The Assistant Manager Formulation R will be responsible for literature search/study and preparing development trials strategies. · ...

Pharmaceutical company seeking experienced microbiology executive to oversee quality control and assurance in manufacturing processes. · ...

+Job summary · We are hiring an experienced Microbiology Executive/ Assistant Manager to join a pharma organization in Chhatrapati Sambhajinagar. · +Qualifications · M.Sc. Microbiology · +ResponsibilitiesRoutine testing (Raw materials/Finished products) · Method development & val ...

We are seeking a Quality Control Executive to perform physical chemical and instrumental analysis on raw materials packaging intermediates and finished products. · Prepare review and maintain batch records COAs SOPs and calibration records Ensure all lab activities adhere to GMP ...

Create and implement quality systems to ensure all products and processes meet regulatory requirements. Ensure all activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations. · Review and approve all necessary documents, including batch records, SOPs, ...