Formulation Development Pharmacist job at Quality Chemical Industries Limited
Posted by: great-volunteer
Posted date: 2025-Jun-26
Location: Kampala, Uganda
Formulation Development Pharmacist 2025-06-25T17:11:03+00:00 Quality Chemical Industries Limited https://cdn.ugashare.com/jsjobsdata/data/employer/comp_5520/logo/Quality%20Chemical%20Industries%20Limited.png https://www.qcil.com/ FULL_TIME Kampala Kampala 00256 Uganda Health Science Healthcare 2025-07-03T17:00:00+00:00 Uganda 8 Key Objectives and Responsibilities - Initiate the introduction of Formulation Development products by doing due diligence, gap assessment (Gap Analysis) and performing and reviewing all risks associated with introduction of new products
- Carry out Formulation Development activities and trials on introduced products until successful development of the product before transfer to Technology Transfer team for full scale manufacturing
- Check and review statutory requirements as mentioned in this SOP FD-01 prior to introduction of new product in Formulation
- Oversee and co-ordinate with relevant sections for effective project planning, execution, project review to enable smooth operation of documentation and Formulation Development activities for new products
- Prepare and review all necessary documentation including Formulation Development protocol and reports, annex for Critical Process parameters to be demonstrated, Master Batch Records, SOPs, Equipment qualification documents, Equipment equivalence documents, Change Requests, etc
- Undertake and supervise the development and packing of the formulation batches as per the applicable SOPs and approve development process to ensure successful execution of Formulation Development
- Manage the requisitions, inventory of spares, tooling, consumables related to Formulation Development through close collaboration with OEM, Engineering, and SCM Departments, with emphasis on cost management, and stock management through stock/inventory management to eliminate downtime
- Prepare, review all QMS, Audits, Investigations, Corrective Action and Preventative Action (CAPA), effectiveness, compliance, reviews in regulatory requirements in relation to operations within the Formulation Development section that enable timely support and response to all CFT requirements
- Manage performance through effective goal setting, periodic performance appraisals, engagements, skills enhancement, manpower planning and scheduling and training to maximize efficiency and optimize production processes
Qualifications and Experience Required - Bachelor of Pharmacy Degree
- At least 3 years’ experience in a pharmaceutical manufacturing setup
- Experience in Research, Formulation and Process Development
- Excellent communication, leadership and supervisory skills
- Excellent organizational and time-management skills
- Commitment to quality and continuous improvement
- Ability to create clear, concise, and accurate documents/reports
- Ability to work collaboratively with others
- Understanding and adhering to relevant standards and regulations
- Detail oriented and with excellent analytical
- Self-started, flexible and able to work well under pressure
- Computer knowledge (proficiency in MS office)
Initiate the introduction of Formulation Development products by doing due diligence, gap assessment (Gap Analysis) and performing and reviewing all risks associated with introduction of new products Carry out Formulation Development activities and trials on introduced products until successful development of the product before transfer to Technology Transfer team for full scale manufacturing Check and review statutory requirements as mentioned in this SOP FD-01 prior to introduction of new product in Formulation Oversee and co-ordinate with relevant sections for effective project planning, execution, project review to enable smooth operation of documentation and Formulation Development activities for new products Prepare and review all necessary documentation including Formulation Development protocol and reports, annex for Critical Process parameters to be demonstrated, Master Batch Records, SOPs, Equipment qualification documents, Equipment equivalence documents, Change Requests, etc Undertake and supervise the development and packing of the formulation batches as per the applicable SOPs and approve development process to ensure successful execution of Formulation Development Manage the requisitions, inventory of spares, tooling, consumables related to Formulation Development through close collaboration with OEM, Engineering, and SCM Departments, with emphasis on cost management, and stock management through stock/inventory management to eliminate downtime Prepare, review all QMS, Audits, Investigations, Corrective Action and Preventative Action (CAPA), effectiveness, compliance, reviews in regulatory requirements in relation to operations within the Formulation Development section that enable timely support and response to all CFT requirements Manage performance through effective goal setting, periodic performance appraisals, engagements, skills enhancement, manpower planning and scheduling and training to maximize efficiency and optimize production processes Bachelor of Pharmacy Degree At least 3 years’ experience in a pharmaceutical manufacturing setup Experience in Research, Formulation and Process Development Excellent communication, leadership and supervisory skills Excellent organizational and time-management skills Commitment to quality and continuous improvement Ability to create clear, concise, and accurate documents/reports Ability to work collaboratively with others Understanding and adhering to relevant standards and regulations Detail oriented and with excellent analytical Self-started, flexible and able to work well under pressure Computer knowledge (proficiency in MS office) JOB-685c2da751039 Vacancy title:
Formulation Development Pharmacist Jobs at:
Quality Chemical Industries Limited Deadline of this Job:
Thursday, July 3 2025 Duty Station:
Kampala | Kampala | Uganda Summary
Date Posted: Wednesday, June 25 2025, Base Salary: Not Disclosed JOB DETAILS:
Key Objectives and Responsibilities - Initiate the introduction of Formulation Development products by doing due diligence, gap assessment (Gap Analysis) and performing and reviewing all risks associated with introduction of new products
- Carry out Formulation Development activities and trials on introduced products until successful development of the product before transfer to Technology Transfer team for full scale manufacturing
- Check and review statutory requirements as mentioned in this SOP FD-01 prior to introduction of new product in Formulation
- Oversee and co-ordinate with relevant sections for effective project planning, execution, project review to enable smooth operation of documentation and Formulation Development activities for new products
- Prepare and review all necessary documentation including Formulation Development protocol and reports, annex for Critical Process parameters to be demonstrated, Master Batch Records, SOPs, Equipment qualification documents, Equipment equivalence documents, Change Requests, etc
- Undertake and supervise the development and packing of the formulation batches as per the applicable SOPs and approve development process to ensure successful execution of Formulation Development
- Manage the requisitions, inventory of spares, tooling, consumables related to Formulation Development through close collaboration with OEM, Engineering, and SCM Departments, with emphasis on cost management, and stock management through stock/inventory management to eliminate downtime
- Prepare, review all QMS, Audits, Investigations, Corrective Action and Preventative Action (CAPA), effectiveness, compliance, reviews in regulatory requirements in relation to operations within the Formulation Development section that enable timely support and response to all CFT requirements
- Manage performance through effective goal setting, periodic performance appraisals, engagements, skills enhancement, manpower planning and scheduling and training to maximize efficiency and optimize production processes
Qualifications and Experience Required - Bachelor of Pharmacy Degree
- At least 3 years’ experience in a pharmaceutical manufacturing setup
- Experience in Research, Formulation and Process Development
- Excellent communication, leadership and supervisory skills
- Excellent organizational and time-management skills
- Commitment to quality and continuous improvement
- Ability to create clear, concise, and accurate documents/reports
- Ability to work collaboratively with others
- Understanding and adhering to relevant standards and regulations
- Detail oriented and with excellent analytical
- Self-started, flexible and able to work well under pressure
- Computer knowledge (proficiency in MS office)
Work Hours: 8 Experience in Months: 36 Level of Education: bachelor degree Job application procedure
Interested in applying for this job? qcil.com&form%5Bvalid-to%5D=Thursday,%20July%203%202025">Click here to submit your application now.
|