Total 4 job vacancies by Epic Medical Pte. Ltd.

About Us

Epic Medical is cutting-edge medical device company focused on the development of advanced medical devices and healthcare solutions. As part of our team, you will gain hands-on experience working on real-world projects that make a difference in patient care and medical innovation.

Position Overview

We are seeking a highly motivated Biomedical Engineering Intern to join our dynamic team. The intern will assist in the design, development, and testing of medical devices, as well as collaborate with cross-functional teams to ensure product quality and regulatory compliance. This is a unique opportunity to gain valuable experience in the biomedical engineering field and work on innovative technologies.

Key Responsibilities

• Assist in the design, prototyping, and testing of biomedical devices and systems.
• Support the development of technical documentation, including reports, protocols, and user manuals.
• Collaborate with engineering, quality assurance, and regulatory teams to ensure compliance with industry standards (e.g., ISO, FDA).
• Assist in the preparation of regulatory submissions and documentation.
• Work on projects related to improving existing medical products or developing new products.
• Participate in team meetings, project planning, and brainstorming sessions.
• Provide technical support to other departments, as needed.

Qualifications

• Currently enrolled or completed a Bachelor’s program in Biomedical Engineering or a related field.
• Basic knowledge of biomedical devices, materials, and regulatory requirements is preferred
• Strong analytical and problem-solving skills.
• Ability to work both independently and as part of a team.
• Detail-oriented with good organizational skills.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

What We Offer

• Hands-on experience in the medical device industry.
• Mentorship from experienced professionals in the field.
• Opportunity to work on innovative healthcare technologies.
• Potential for full-time employment based on performance.

How to Apply

To apply, please submit your resume, cover letter, and any relevant project portfolios. We look forward to having you as part of our team and contributing to the future of healthcare!

Job Description: Regulatory Affairs Intern

Location: Singapore
Department: Regulatory Affairs
Duration: 6 months

Position Overview:

We are seeking a highly motivated and detail-oriented intern to join our Regulatory Affairs team. As a Regulatory Affairs Intern, you will have the opportunity to gain hands-on experience in the preparation, submission, and monitoring of regulatory documents for healthcare/medical devices/pharmaceutical products. You will work closely with the Regulatory Affairs team to ensure compliance with local, regional, and international regulations.

Key Responsibilities:

• Assist in the preparation and submission of regulatory documents (e.g., product registration, amendments, and renewals).
• Review and compile necessary documentation to ensure regulatory compliance for products.
• Conduct regulatory research to stay up to date with current guidelines and requirements in target markets.
• Help in maintaining regulatory databases and records.
• Support the coordination and communication with regulatory bodies, health authorities, and notified bodies as required.
• Review product labeling and marketing materials to ensure compliance with applicable regulations.
• Assist in managing correspondence with internal stakeholders and cross-functional teams (e.g., R&D, Quality Assurance) regarding regulatory activities.
• Participate in department meetings and provide input as required.
• Perform other administrative duties and projects as assigned by the Regulatory Affairs team.

Qualifications:

• Currently pursuing or recently completed a degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, or a related field.
• Interest in regulatory affairs, healthcare regulations, or medical devices/pharmaceuticals.
• Strong organizational skills and attention to detail.
• Good written and verbal communication skills.
• Ability to work independently and as part of a team.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Previous internship or work experience in a related field is a plus but not required.

What We Offer:

• Hands-on experience in regulatory affairs within a dynamic and growing industry.
• Exposure to regulatory processes and international standards.
• Mentorship and guidance from experienced regulatory professionals.
• Potential for career advancement based on performance and availability of roles.

Interested candidates should submit their resume and a brief cover letter outlining their interest in regulatory affairs and relevant qualifications.

Tasks & responsibilities

a) Software coding, Ladder programming

b) Familiar with robotic control and PC integration

c) System control design and integration of sensor, servo, etc

d) Electrical hardware implementation, sizing and schematic design.

e) I/O assignment work.

f) Electrical schematic design.

g) Hardware and Software troubleshooting.

h) Commissioning

Qualifications & experience

a) Minimum Diploma in IT or Electrical Engineering.

b) Knowledge in PLC and SCADA system,

c) Minimum 3 years working experience in ladder.programming and SCADA integration

d) Familiar with commercial PLC.

Position Title: Compounding Pharmacist for Automation

Location: Singapore

Company: Epic Medical Pte. Ltd

Department: Pharmacy / Automation

Reports To: Director of Pharmacy Automation

Employment Type: Full-Time

Job Summary: We are seeking a detail-oriented and experienced Compounding Pharmacist to join our team with a focus on automation. The ideal candidate will have expertise in pharmaceutical compounding, coupled with a keen interest in leveraging automation technologies to enhance efficiency, accuracy, and safety in the compounding process. This role will involve collaborating with cross-functional teams to implement and optimize automated systems within our pharmacy automation, strategy and support the implementation of such globally.

Key Responsibilities:

1. Compounding and Quality Control:
   • Oversee the preparation and compounding of personalized medications, ensuring adherence to regulatory standards and best practices.
   • Conduct quality control checks on compounded medications to guarantee their safety, potency, and accuracy.
2. Automation Implementation:
   • Collaborate with technology vendors and internal teams to implement and optimize automated compounding systems.
   • Train pharmacy staff on the use of automated equipment and software, ensuring seamless integration into daily operations.
3. Process Improvement:
   • Identify opportunities to improve compounding processes through automation, enhancing efficiency and reducing errors.
   • Develop and document standard operating procedures (SOPs) for automated compounding workflows.
4. Regulatory Compliance:
   • Ensure all compounding activities comply with relevant regulations, including USP <795>, <797>, and <800> guidelines.
   • Maintain accurate and up-to-date records for compounded medications and automation systems.
5. Customer Service:
   • Provide exceptional service to patients and healthcare providers, addressing inquiries related to compounded medications and automation processes.
   • Collaborate with healthcare professionals to develop customized medication solutions.

Qualifications:

• Doctor of Pharmacy (Pharm.D.) degree from an accredited institution.
• Active pharmacist license is preferable
• Minimum of 3-5 years of experience in pharmaceutical compounding.
• Experience with automated compounding systems and technology is highly desirable.
• Strong understanding of regulatory requirements and best practices for pharmaceutical compounding.
• Excellent problem-solving skills and attention to detail.
• Effective communication and interpersonal skills.
• Ability to work collaboratively in a fast-paced, dynamic environment.

Preferred Skills:

• Certification in compounding pharmacy (e.g., Board Certification in Sterile Compounding).
• Familiarity with software and hardware used in pharmacy automation.

Benefits:

• Competitive salary and benefits package.
• Opportunities for professional development and continuing education.
• Collaborative and innovative work environment.

Company Description: Epic Medical’s corporate vision is driven by mega trends in healthcare attributed to aging population, rising cost and changes in healthcare needs. The goal of being relevant requires game changing initiatives in product strategies to achieve significant market share.

The mission statement, Being Relevant, is symbiotic with innovative solutions that our company provides in addressing healthcare trends brought about by aging demography and the continuous global need for quality healthcare at lower costs.

We engineer all our products with state-of-the-art processes that are trusted worldwide. Expect no less.

Equal Opportunity Employer: Epic Medical is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.