
Pharmaceutical Production Specialist
5 days ago
KamionP is a leading manufacturer of pharmaceutical products, committed to delivering high-quality solutions.
Job Title: Deputy Production ManagerThis role involves overseeing daily production activities, ensuring alignment with company goals, quality standards, and following safety protocols in controlled production areas.
Main Responsibilities:- Manage production schedules to meet customer demands while ensuring all processes comply with DRAP regulations, GMP, and FDA standards.
- Monitor and adjust production activities to maintain productivity, safety, and adherence to established procedures.
- Implement and maintain SOPs and quality control measures, addressing issues related to contamination control, equipment sterilization, and machine maintenance.
- Collaborate with the Quality Assurance team to address any issues or deviations from required quality standards.
- Train and manage production staff to maintain efficiency, safety, and adherence to established procedures.
- Identify and implement process improvements to increase efficiency, reduce waste, and ensure cost-effective operations through lean manufacturing practices.
- Oversee machine maintenance and ensure all necessary equipment is in working order to minimize production downtime.
- Coordinate with the Procurement Department to maintain optimal inventory levels.
- Prepare regular production reports for senior management and document production processes to maintain accurate records.
To succeed in this role, you will need:
- A Bachelor's degree in Pharmacy, biomedical or related field, preferably with a master's degree.
- A minimum of 5 years of experience in production management, preferably in a pharmaceutical or medical device manufacturing environment.
- Familiarity with wound care dressings, pain relief patches, and surgical bandages & tapes, as well as sterilization processes such as Electron Beam and Gamma Radiation.
- Knowledge of GMP/ISO standards and DRAP regulatory requirements.
- Proficiency in production planning software and Microsoft Office Suite.
- Excellent problem-solving and decision-making abilities, as well as strong leadership and communication skills.
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