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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.

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.

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
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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

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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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