Title: Executive, Research & Development / Production Department (Pabna)
Company Name: SQUARE Pharmaceuticals PLC.
Vacancy: --
Location: Pabna
Experience:
∎ 1 to 3 years
∎ The applicants should have experience in the following business area(s):Pharmaceutical/Medicine Companies
Published: 21 Jan 2025
Education:
∎ Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm)
∎ M.Pharm / B.Pharm
Requirements:
Additional Requirements:
∎ 1-3 years experience in related work in reputed pharmaceutical company is preferable but fresh candidates are also encouraged to apply
∎ Good interpersonal and communication skills
∎ Candidate must possess excellent planning & execution skills as well as strong quantitative & qualitative analytical skills
∎ Well conversant with MS Office
Responsibilities & Context:
∎ Conduct analytical method development, validation/verification, and formulation development of herbal products.
∎ Prepare specifications and Methods of Analysis for raw materials, packaging materials, and products, ensuring seamless technology transfer to Quality Control.
∎ Perform re-formulation and formulation development for assigned new products, including all related subsequent activities.
∎ Prepare Process Optimization and Process Validation documents, as well as other necessary documentation, such as protocols, batch records, Drug Master Files, and Product Development Reports. Execute
∎ PO and PV batches in accordance with procedural requirements.
∎ Analyze stability samples of new products as per the defined schedule.
∎ Address troubleshooting for commercial products and perform cleaning validation activities in compliance with regulatory standards.
∎ Monitor and oversee herbal manufacturing processes, including line clearance, machine startup clearance, in-process controls, reconciliation, storage, cleaning, and changeovers, ensuring alignment with planning, guidelines, and Standard Operating Procedures for timely production.
∎ Ensure optimal utilization of resources as per the production plan.
∎ Maintain compliance with current Good Manufacturing Practices in all production activities.
∎ Prepare Batch Manufacturing Records, Batch Packaging Records, and other relevant documentation, including SAP-related records.
∎ Participate in cross-functional activities such as machine trials for new products, validation and qualification of environments, equipment, and products, as well as Quality Management System activities.
∎ Supervise and provide training to operators, helpers, and other production staff.
∎ Monitor and report on productivity metrics daily, monthly, and annually.
∎ For Research & Development
∎ Conduct analytical method development, validation/verification, and formulation development of herbal products.
∎ Prepare specifications and Methods of Analysis for raw materials, packaging materials, and products, ensuring seamless technology transfer to Quality Control.
∎ Perform re-formulation and formulation development for assigned new products, including all related subsequent activities.
∎ Prepare Process Optimization and Process Validation documents, as well as other necessary documentation, such as protocols, batch records, Drug Master Files, and Product Development Reports. Execute
∎ PO and PV batches in accordance with procedural requirements.
∎ Analyze stability samples of new products as per the defined schedule.
∎ Address troubleshooting for commercial products and perform cleaning validation activities in compliance with regulatory standards.
∎ For Production
∎ Monitor and oversee herbal manufacturing processes, including line clearance, machine startup clearance, in-process controls, reconciliation, storage, cleaning, and changeovers, ensuring alignment with planning, guidelines, and Standard Operating Procedures for timely production.
∎ Ensure optimal utilization of resources as per the production plan.
∎ Maintain compliance with current Good Manufacturing Practices in all production activities.
∎ Prepare Batch Manufacturing Records, Batch Packaging Records, and other relevant documentation, including SAP-related records.
∎ Participate in cross-functional activities such as machine trials for new products, validation and qualification of environments, equipment, and products, as well as Quality Management System activities.
∎ Supervise and provide training to operators, helpers, and other production staff.
∎ Monitor and report on productivity metrics daily, monthly, and annually.
Employment Status: Full Time
Job Location: Pabna
Apply URL::
Apply Procedure:
Company Information:
∎ SQUARE Pharmaceuticals PLC.
∎ 48 Mohakhali C/A. Dhaka-1212
∎ Square Pharmaceuticals Limited, the flagship company of Square group, is holding the 1st position in the pharmaceutical industry among all national and multinational companies of Bangladesh since 1985 and is now on its way to become a high performance global player.
Address::
∎ 48 Mohakhali C/A. Dhaka-1212
∎ Square Pharmaceuticals Limited, the flagship company of Square group, is holding the 1st position in the pharmaceutical industry among all national and multinational companies of Bangladesh since 1985 and is now on its way to become a high performance global player.
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Application Deadline: 30 Jan 2025
Category: Others