Job Responsibilities :
  • To Execute Analytical Method Development activities of drug products under development, based on QbD principles and regulatory requirements.
  • Execution of Analytical Method validation activities for drug products as per the regulatory requirements.
  • Execute routine Analytical Research activities of drug products.
  • Establishing In-house systems and procedures to ensure cGLP practices & regulatory requirements for analytical activities at in-house R & D Facilities.
  • Profile Description & Ability:
  • Strong conceptual, analytical development and validation skills.
  • Good communication (verbal, writing) and presentation skills.
  • Must have ability to work under pressure, meet deadlines, and work on multiple projects simultaneously.
  • Must be a team player and be able to interact with staff at all levels of the company and with external parties as well.
  • Must have ability to work independently.
  • Adequate Job knowledge and exposure to different Analytical methods and instrumentations.
  • Adequate Job knowledge and exposure to QbD, DoE and statistical interpretation etc.,
  • Trouble shooting related to Testing methods, Stability studies, test results and designing of additional experimentations as necessary
  • Execution & coordination for Analytical method transfer activities of drug products.
  • Calibration of the Analytical instruments as per the master calibration schedule.
  • Technical assessment & Analysis of drug substances (API) for projects execution.
  • Review & clearance of technical documents leading to dossier batches executions and registrations.
  • Preparation and review of Specifications, Method of analysis procedures and Analytical development reports.
  • Preparation and review of analytical protocols and reports (Analytical method validation, Method feasibility, Analytical method transfer, etc.).
  • Technical assessments of projects (Screening, pipeline and development projects stages) & Literature search).
  • Preparation of analytical technical documents for dossier / Technology transfer executions / Regulatory submissions of projects.
  • Assisting and resolving technical queries raised during Technology transfer activities & regulatory submissions.
  • Assisting in establishment of In-house Infrastructure (Analytical equipment's Qualifications and preparation of SOP's).
  • Assessment & coordination on regulatory deficiencies.
  • Assisting with analytical requirements in finalization of project costings.
Educational Requirements :
  • Master of Pharmacy (M.Pharm) in M. Pharm
  • The candidate should be an M.Pharm / B.Pharm with thesis in relevant R&D work.
Experience Requirements :
  • At least 5 year(s)
  • The applicants should have experience in the following area(s): Pharmacist
  • The applicants should have experience in the following business area(s): Pharmaceuticals
Additional Requirements :
  • Age 25 to 45 years
  • Only males are allowed to apply
  • Candidates who are applying for the senior officer post should have working experience as officer at least 03 years.
  • Candidates who are applying for the Assistant Manager post should have working experience as senior officer at least 03 years.
Compensation & Other Benefits :
  • Provident fund
  • Salary Review: Yearly
  • The Successful Candidates will get oriented remuneration package and excellent working environment for rapid career growth.
How to Apply
Primary Information
Published on:

Vacancy:

Not specific

Employment Status:

Full-time

Gender:

Male

Age:

Age 25 to 45 years

Job Location:

Gazipur

Salary:

Negotiable

Application Deadline: