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Skills:

Research, Compliance, Legal

Job type:

Full-time

• Develop, supervise, and oversee testing in the areas of Microbiology and Biotechnology within the Research Laboratory and Services, ensuring accuracy and compliance with international standards and legal requirements. This is to support the needs of customers within the Innovation & Product Development Center, within SCGP, and external customers.
• Develop quality systems, conduct evaluations, and design new analysis and testing methods. Provide technical consultation to support research activities and respond to ...
• Assess employee risks and improve work processes in the microbiology and biotechnology laboratories to ensure safety in accordance with legal and relevant standard requirements.
• Job Description Manage and oversee testing/inspection operations in the scientific and technical/quality laboratory areas.
• Develop and maintain work systems to ensure smooth operations and testing accuracy to support SCGP customers.
• Supervise and manage routine and new test methods to ensure readiness and compliance.
• Oversee laboratory operations and provide test result reports.
• Prepare laboratory readiness for audits and customer visits.
• Monitor and maintain equipment efficiency to ensure availability and performance.
• Develop and maintain the laboratorys Quality Management System to meet required standards and customer expectations.
• Ensure laboratory staff are aligned with the scientific and technical/quality functions and operate according to SCGP requirements.
• Develop scientific and technical work systems and support operational changes.
• Review and recommend suitable methods for each type of test and business unit.
• Develop testing systems to comply with ISO/IEC 17025 and ISO 13485 (as applicable).
• Maintain and update documents required by ISO/IEC 17025.
• Manage and monitor annual testing, equipment maintenance, and calibration plans.
• Prepare laboratory operational plans.
• Prepare annual and medium-term plans.
• Maintain and develop ISO/IEC 17025 systems in the laboratory.
• Manage laboratory cost structure and support scientific/technical data for Innovation and Product Development Centers (IPDC) to comply with SCG Safety Framework.
• Perform other duties as assigned.
• QualificationBachelor's/Master's degree in Medical Technology, Health Sciences, or related fields (Bachelor's G.P.A. > 2.70, Master's G.P.A. > 3.30).
• Open for New Graduates.
• Experience in QA/QC lab testing in the food and healthcare industry is an advantage.
• Knowledge in Microbiology and Biotechnology.
• Knowledge in Standards or Compliance related to labolatory or healthcare (ISO/IEC 17025, ISO 13485).
• Good command in English (TOEIC score at least 550).
• Must obtain a Professional License for Medical Technology issued by the Medical Technology Council.
• Able to work on-site mode at Innovation and Product Development Center (IPDC), SCGP, Ratchaburi, Thailand.
• Contact: Pupat (Mac) Email: [email protected]

Skills:

System Administration, Research, Compliance, English

Job type:

Full-time

• Leading relationships with Health Care Professionals travelling across locations as well as providing support virtually.
• Gaining deep understanding of Health Care Professional needs, sharing expert medical advice, tailoring data, delivering medical to medical activities, connecting them to relevant internal Pfizer people whenever they need it.
• Provide objective and scientifically medical information regarding Pfizer's product portfolio and the diseases states treated. Incorporating the use of educational prog ...
• Develop, monitor and report KPIs in relation to field-based medical activity.
• External Collaboration Projects:Ensure timely and efficient communication to complete required internal/external process including system administration, maintain good documentation, tracking, payment, material, and drug shipment in a timely manner.
• Pfizer-Sponsored Research and Investigator-Sponsored Research:Coordinating with Medical Affairs Manager and/or other medical colleagues for medical stakeholder engagement in research and ensure compliance of operational requirements.
• Training and DevelopmentCapability development, building high performance field medical team, enhancing sharing of best practice and cross-BU/cross-functional collaborations.
• Ensure capability (excluding scientific knowledge) related to field medical execution, quality of operation and compliance.
• Solicit and consolidate feedback from external and internal stakeholders in relation to team effectiveness, quantify and communicate the value and effectiveness of field-based medical activities.
• Other Medical Affairs projects as defined by the Country Medical Lead
• QUALIFICATIONS Degree in Medical or advanced degree in Biological Sciences or Healthcare-related filed (e.g. Medicine, Dentistry, Veterinary Medicine, Pharmacy, Nursing, Medical Technology, Optometry, etc.).
• Industry, clinical, research or academic experience; with track record of publications preferred.
• Knowledge of clinical research and clinical development processes desirable.
• Experience in field-based medical role, clinical affairs, regulatory affairs, or field interaction in the pharmaceutical industry preferred.
• Good communication in Thai and English.
• Preferable Oncology background.
• Work Location Assignment: Hybrid Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical