Job Summary
We seek a meticulous and self-disciplined Pharmaceutical Production Assistant to assist manufacturing and packaging operations in a pharmaceutical production setting. The ideal candidate will operate production equipment, manage raw materials, uphold stringent hygiene standards, and ensure adherence to Good Manufacturing Practice (GMP) guidelines.
Oversee daily operations to ensure efficient workflow, prioritize tasks, and meet established deadlines while maintaining high standards of quality. Collaborate with cross-functional teams to align on project goals, share updates, and address challenges proactively. Develop and implement policies and procedures to enhance productivity, safety, and compliance with regulatory requirements. Monitor performance metrics, analyze data trends, and provide reports to leadership to support data-driven decision-making. Supervise staff, including assigning duties, conducting performance evaluations, and fostering professional growth through coaching and mentorship. Manage budget allocations, track expenditures, and optimize resource utilization to maximize operational efficiency. Identify opportunities for process improvements, streamline workflows, and implement innovative solutions to drive continuous enhancement. Maintain open communication channels with stakeholders to ensure transparency, alignment, and timely resolution of issues. Represent the organization at industry events, conferences, or meetings as needed to represent its interests and build strategic partnerships.
Operate, clean, and perform routine maintenance on pharmaceutical processing and packaging machinery, ensuring all equipment is properly set up for production.
Responsibilities include precisely measuring, weighing, and blending raw materials in accordance with approved formulas and specified ratios.
Oversee manufacturing operations to verify that outputs align with established quality benchmarks.
Perform thorough visual evaluations of completed items and document any deviations from established standards.
Prepare Batch Manufacturing Records (BMRs) and label reconciliation documentation with precision and thoroughness.
Uphold a production environment that is consistently clean, sterile, and free from contamination at all times.
Conduct regular cleaning and sterilization of all equipment and work areas to ensure compliance with established health and safety protocols.
Strict compliance with Standard Operating Procedures (SOPs), safety protocols, and Good Manufacturing Practices (GMP) regulations is mandatory.
• Bachelor’s degree in Computer Science, Engineering, or a related technical field, or equivalent practical experience
• Minimum of 5 years of relevant work experience in software development, with proficiency in programming languages such as Python, Java, or C++
• Strong understanding of data structures, algorithms, and software design principles
• Experience with distributed systems, cloud platforms (e.g., AWS, GCP, Azure), and containerization technologies (e.g., Docker, Kubernetes)
• Demonstrated ability to troubleshoot complex technical issues and optimize system performance
• Excellent problem-solving skills and a passion for writing clean, maintainable, and efficient code
• Strong communication skills to collaborate effectively with cross-functional teams and stakeholders
• Ability to work independently and manage multiple priorities in a fast-paced environment
A diploma or certificate in pharmaceutical production, chemistry, biotechnology, or a related discipline is required.
Demonstrated familiarity with Good Manufacturing Practice (GMP) guidelines is required.
Meticulous focus on precision is essential, particularly in documentation and production workflows.
Requires proficient hand-eye coordination along with the capacity to execute fundamental mathematical computations.
Must be capable of standing for prolonged durations while operating efficiently in a high-paced manufacturing setting.
Exceptional ability to organize tasks efficiently and collaborate seamlessly with team members.
Qualified applicants should forward their latest CV to talentsourcing@sheerlogicltd.com by 25 May 2026, with “Pharmaceutical Production Assistant” clearly stated in the email subject line.
Qualifications
Diploma , Professional Certificate
