Job Summary
We are looking for a meticulous and self-motivated Pharmaceutical Production Assistant to assist with manufacturing and packaging processes in a pharmaceutical production setting. The ideal candidate will operate production machinery, manage raw materials, uphold rigorous hygiene protocols, and adhere to Good Manufacturing Practice (GMP) standards.
Oversee and execute a broad spectrum of critical duties, including the systematic planning, organization, and supervision of project activities to ensure alignment with strategic objectives. Collaborate with cross-functional teams to facilitate seamless communication, foster innovation, and drive project milestones. Monitor progress through detailed tracking and reporting mechanisms, identifying potential risks or deviations to implement timely corrective actions. Maintain compliance with organizational policies, industry regulations, and quality standards while optimizing resource allocation for maximum efficiency. Serve as a key liaison between stakeholders, providing clear updates and facilitating decision-making processes to support overall business goals. Additionally, contribute to the development and refinement of operational processes to enhance productivity and sustainability.
Install, calibrate, and oversee pharmaceutical production and packaging equipment, ensuring optimal functionality while adhering to strict cleanliness and maintenance protocols.
Accurately measure, weigh, and combine raw materials in strict adherence to approved formulas and specified ratios.
Oversee production operations to verify that products adhere to established quality benchmarks.
Perform thorough visual assessments of completed products to identify and document any deviations or irregularities.
Accurately prepare and maintain Batch Manufacturing Records (BMRs) and ensure precise reconciliation of labeling documentation.
Uphold a pristine, sterile, and contamination-free production environment at all times.
Conduct regular cleaning and sterilization procedures for all equipment and work areas to maintain optimal hygiene standards.
Compliance with Standard Operating Procedures (SOPs), safety standards, and Good Manufacturing Practices (GMP) regulations must be rigorously maintained at all times.
Seeking a highly motivated professional with a minimum of five years of experience in a similar role, preferably within the technology or engineering sector. The ideal candidate must possess strong analytical skills, exceptional problem-solving abilities, and proficiency in data analysis and interpretation. A bachelor’s degree in a relevant field, such as computer science, engineering, or mathematics, is essential. Additionally, experience with programming languages like Python or Java, as well as familiarity with database management systems, is required. Excellent communication and teamwork skills are also mandatory to collaborate effectively with cross-functional teams. The ability to work under pressure and meet tight deadlines is crucial for success in this position.
A diploma or certificate in pharmaceutical production, chemistry, biotechnology, or a related discipline is required.
Must possess a fundamental grasp of Good Manufacturing Practice (GMP) guidelines.
Demonstrates meticulous attention to detail and a commitment to maintaining high standards of accuracy in documentation and production workflows.
Possesses strong hand-eye coordination and demonstrates proficiency in performing fundamental mathematical calculations.
Capable of maintaining prolonged standing positions and thriving in a high-velocity manufacturing setting.
Proven ability to work effectively within collaborative environments and manage tasks with a high degree of organization.
Submit an updated CV to talentsourcing@sheerlogicltd.com by May 25, 2026, ensuring the subject line of your application clearly states “Pharmaceutical Production Assistant.”
Qualifications
Diploma , Professional Certificate
