সতর্কীকরণ
স্কিল জবস একটি অনলাইন জব পোর্টাল হিসেবে নিয়োগদাতা এবং চাকরি প্রার্থীদের মধ্যে যোগাযোগের মাধ্যম হিসেবে কাজ করে। নিয়োগদাতা এবং চাকরি প্রার্থীদের মধ্যে যে কোনো আর্থিক লেনদেনের জন্য স্কিল জবস দায়বদ্ধ নয়। কোন নিয়োগদাতা যদি আপনার কাছে অর্থ চায়, তাহলে আমাদের সাথে দ্রুত যোগাযোগ করুন।
আপনার নিরাপত্তা ও সুরক্ষা আমাদের সর্বোচ্চ অগ্রাধিকার। যদি আপনার কোনো প্রশ্ন থাকে বা সহায়তার প্রয়োজন হয়, দয়া করে আমাদের সাথে যোগাযোগ করুন।
Position Summary
Responsible for supporting pharmaceutical research and development activities, product improvement, and ensuring compliance with industry standards and regulations.
Job Responsibilities
Formulation:
- Develop and optimize pharmaceutical formulations (Tablets, Capsules, Liquids, Creams, or Ointments) as per cGMP and regulatory guidelines.
- Execute pre-formulation studies including compatibility, solubility, and excipient evaluation for new drug product development.
- Prepare and review Master Formula Records (MFR), batch manufacturing records, and formulation development reports.
- Support pilot batch manufacturing, scale-up trials, and technology transfer to commercial production.
- Design and monitor stability studies for drug products as per ICH Q1A guidelines and interpret results accordingly.
Analytical:
- Perform analytical method development and validation for APIs and finished pharmaceutical products as per ICH Q2(R1) guidelines.
- Conduct routine and advanced analytical testing using HPLC, GC, UV-Vis Spectrophotometry, KF Titration, and dissolution apparatus.
- Analyze raw materials, in-process samples, and finished products to ensure compliance with pharmacopeial standards (IP, BP, USP).
- Maintain and calibrate analytical instruments and ensure proper documentation as per GLP and GMP requirements.
- Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results and prepare deviation and CAPA reports.
Required Educational Qualifications
- Master of Philosophy (M.Phil) in Chemistry
Additional Qualifications
- Proficient in formulation development of solid, liquid, and semi-solid dosage forms including pre-formulation studies and excipient-API compatibility evaluation as per cGMP.
- Hands-on experience in operating HPLC, GC, UV-Vis Spectrophotometer, Dissolution Apparatus, and KF Titrator for routine and advanced pharmaceutical analysis.
- Capable of performing analytical method development, validation, stability studies, and investigation of OOS and OOT results with proper CAPA documentation.
- Familiar with ICH guidelines, pharmacopeial standards (IP, BP, USP), and preparation of SOP, MFR, BMR, and analytical reports as per GLP and GMP requirements.
Education
- Master of Pharmacy (M.Pharm)
- Master of Science (MSc) in Chemistry
Experience
- 2 to 4 years
- The applicants should have experience in the following business area(s): Group of Companies
- Freshers are also encouraged to apply.
Required Skills
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Strong motivation and commitment for work
