Senior Executive, PD (Analytical)
Job Description
Title: Senior Executive, PD (Analytical)
Company Name: UNIDO Pharmaceuticals Limited
Vacancy: Not specific
Job Location: Narsingdi
Employment Status: Full-time
Educational Requirements:
∎ Master of Pharmacy (M.Pharm), Master of Science (MSc) in Chemistry
Experience Requirements:
∎ At least 4 year(s)
∎ The applicants should have experience in the following business area(s):
Pharmaceuticals
Job Responsibilities:
∎ Analytical feasibility study of new project/product and pre-determination of required reference/working standard, reagents, solvents, machines, accessories, etc.
∎ Taking initiatives to procure required reagents, machines, accessories for completion of analysis in targeted timeline.
∎ Operational capability of different analytical equipment e.g., FTIR, UV-VIS Spectrophotometer, HPLC, GC, AAS, Malvern Particle Analyzer, Potentiometer, Karl Fisher Titrator, Osmometer, Viscometer, etc.
∎ Receiving of raw/packaging materials from suppliers/manufacturers and update status.
∎ Analysis of raw/packaging materials and preparation of Specification/Method of Analysis (MOA) for them.
∎ Preparation of Purchase Specification of raw/packaging materials and performing their source validation to ensure the quality of the products.
∎ New Product Analytical Method Development & Validation of different dosage forms of sterile products, especially including aqueous eye drops, suspension eye drops, eye ointment/gel, etc. following ICH Guidelines/GLP/Local Regulatory Guidelines.
∎ Analysis of finished products (e.g., lab trial and pilot/stability batches).
∎ Preparation of Specification and Method of Analysis (MOA) for intermediate/bulk/commercial finished products, etc. and handover to Quality Control Department.
∎ Preparing stability study protocol for carrying out accelerated/intermediate/long term stability study of new products at different conditions following ICH Guidelines/GLP Guidelines, stability study data compilation and declaration shelf-life of the new products.
∎ Preparing DTL Sample for INN Molecules with necessary documents/ Reference or Working Standard (RS/WS). for submission to Drugs Administration for registration purpose.
∎ Performing analysis of process validation batches, cleaning validation batches, etc. and reporting accordingly.
∎ Preparing stability study protocol for carrying out real time stability study of commercial products following ICH Guidelines/GLP Guidelines to ensure stability and safety of the product throughout the shelf-life.
∎ Preparing Standard Operating Procedure (SOP) for analytical activities.
∎ Analysis of market sample for Comparative Study (CS).
∎ Troubleshooting, calibration and maintenance of analytical equipment.
∎ Preparations and management of Reference/Working Standard (RS/WS).
∎ Proper documentation for easy retrieval & preparing monthly report.
∎ Maintenance of general hygiene and proper house-keeping within the department.
Additional Requirements:
∎ Both males and females are allowed to apply
∎ Good communication skills both in English & Bengali.
∎ Able to work under pressure & to face any audit.
∎ Leadership capabilities.
∎ Mental strength to meet the timelines of new project/product.
∎ Skill-ness on different micro-soft office programs (Words, Excel, Power Point, Outlook, etc.)
Salary: Negotiable
Compensation & Other Benefits:
∎ Excellent working environment, Competitive salary and benefits packages opportunity to learn and performance-based career growth.
Job Source: Bdjobs.com Online Job Posting.
Application Deadline: 22 Jan 2022
Company Information:
∎ 16 Jan 2022
∎ UNIDO Pharmaceuticals Limited
Category: Medical/Pharma
Source: bdjobs.com
Deadline Expired on 22nd Jan 2022
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