Macleods Pharmaceuticals Released Job Openings On 28/07/2022.Macleods, India Fastest growing pharmaceutical company, with a strong R&D and own Bio-equivalence centre, manufacturing sites approved by USFDA & WHO Geneva, ranked among the top pharmaceutical companies with a strength of more than 10,000 employees, presently operating in more than 50 countries worldwide..
Vacancy Details:
Macleods Pharmaceuticals Recruiting M.Pharma,M.Sc Graduates with 02-07+ Years of Experience for Research Scientist Position.Complete Details for the Research Scientist as follows.
Important Details :
- Location : Mumbai
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: ₹ 4,00,000 – 9,00,000 P.A.
- Opening date for online Application:28/07/2022
- Mode of application :Online
- How To Apply: We have multiple roles on LCMS instrument for candidates with relevant experience ranging from 2 – 10 years.Interested candidates may share their resume with advaitc@macleodspharma.com with Application for LCMS – Research & Development as the subject.
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Job Description/Skills Required
 Responsible for the regulatory and scientific conduct of development, validation, stability projects, and/or other specialty technologies such as extractable/leachable studies, Unknown Peak Identification & Nitrosamine quantification. Performs multiple detection techniques, calculates and interprets data, and records data in adherence with SOPs.. Routinely acts as the technical project leader for multiple projects, regularly provide updates to internal stakeholders, reviews and evaluates data, writes reports and protocols.
Essential Functions:
- Independently performs analytical testing, method optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods, and protocols applicable to assigned tasks. Designs and executes experiments independently.
- Reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.
- Prepares and reviews study protocols, project status reports, final study reports and other project-related technical documents.
- Provides technical guidance and training to team members.
- Assists in preparation and implementation of SOPs and quality systems.
- Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, Regulatory criteria and Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
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