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Medical Device Production/Quality Management Specialist
₱20-25K[Monthly]
Great PerksNo Resume NeededOn-site - Bulacan1-3 Yrs ExpBachelorFull-time

Morishita-Segg’s Pharmaceutical, Inc.
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Medical Device Production/Quality Management Specialist
₱20-25K[Monthly]
Great PerksNo Resume NeededOn-site - Bulacan1-3 Yrs ExpBachelorFull-time

Morishita-Segg’s Pharmaceutical, Inc.
Medical Device Production/Quality Management Specialist
Morishita-Segg’s Pharmaceutical, Inc.₱20-25K[Monthly]
On-site - Bulacan1-3 Yrs ExpBachelorFull-time
Job Description
Benefits
- Government Mandated Benefits
13th Month Pay, Employee Loan, Pag-Ibig Fund, Paid Holidays, Philhealth, SSS/GSIS
- Insurance Health & Wellness
Accidental Death & Dismemberment Insurance, Health Care On-Site
- Professional Development
Employee Assistance Program, Professional Development
- Time Off & Leave
Sick Leave, Vacation Leave
Read More
Description
As the QA Officer for Pharmaceutical, you will play a crucial role in ensuring the quality and compliance of our products and processes.
This full-time role is based in Bulacan and will be a pivotal part of our growing team.
What you'll be doing
- Developing, implementing and maintaining quality assurance systems, processes and procedures to meet regulatory requirements and industry standards
- Managing quality control activities, including product inspection, testing and release
- Conducting internal audits and coordinating external audits to identify and address quality issues
- Collaborating with cross-functional teams to resolve quality-related problems and implement corrective actions
- Providing training and guidance to production, engineering and other teams on quality assurance best practices
- Staying up-to-date with pharmaceutical and medical device regulations, guidelines and industry trends
- Preparing and reviewing quality-related documentation, reports and records
Requirements
- 2-3 years of experience in quality assurance or quality control in the pharmaceutical or medical device industry
- Strong knowledge of good manufacturing practices (GMP), good laboratory practices (GLP) and other relevant quality standards and regulations
- Excellent problem-solving, critical thinking and decision-making skills
- Proficient in data analysis and quality management software
- ·Strong communication and interpersonal skills to effectively collaborate with cross-functional teams
- Bachelor's degree in a relevant field (e.g. Pharmaceutical Sciences, Biomedical Engineering, Quality Assurance,Chemist)
pharmacychemist

Joedelyn Iglesia
HR SupervisorMorishita-Segg’s Pharmaceutical, Inc.
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