PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking for a Project Engineer with experience/internship in pharmaceutical engineering for a role in Singapore.
Job Summary:
The Project Engineer will work closely with the Project Engineer and cross-functional teams to assist in the planning, execution, and coordination of engineering projects within the pharmaceutical manufacturing plant. This is an excellent opportunity for a motivated individual with a strong interest in pharmaceutical engineering to gain hands-on experience and contribute to the production of critical vaccines.
Responsibilities:
- Support the Project Engineer in developing project plans, timelines, and budgets.
- Participate in project meetings and contribute to project status updates.
- Coordinate with various teams to gather project-related information.
Documentation and Reporting:
- Assist in preparing project documentation, including reports, drawings, and specifications.
- Maintain accurate and organized project records.
- Generate progress reports and updates for review by the Project Engineer.
Cross-Functional Collaboration:
- Work closely with cross-functional teams, including production, quality control, maintenance, and regulatory affairs, to support project objectives.
- Communicate effectively with team members to ensure project goals are met.
Regulatory Compliance:
- Assist in ensuring that engineering projects comply with cGMP and other regulatory standards.
- Contribute to the preparation and maintenance of documentation required for regulatory submissions.
Quality Assurance Support:
- Collaborate with the quality control team to implement quality assurance protocols for engineering projects.
- Support regular quality audits and compliance activities.
Learning and Development:
- Actively participate in training programs to enhance knowledge of pharmaceutical manufacturing processes and regulatory requirements.
- Stay informed about industry trends and advancements.
Skills and Qualifications:
- Bachelor's degree in Engineering, preferably in Chemical Engineering, Mechanical Engineering, or a related field.
- Strong interest in pharmaceutical manufacturing and project management.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a team-oriented environment.
- Detail-oriented with a focus on accuracy in documentation and reporting.
- Eagerness to learn and contribute to the success of engineering projects.
Why PharmEng Technology?
Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.
EEOC Statement
At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.
