Senior Quality Control Associate

6 days ago

Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

**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 an experienced Senior Quality Control Associate with experience in pharmaceutical company/Life Science industries for a role in Singapore.

**Key Responsibilities**:

- Contribute to the planning, implementation, and optimization of process engineering initiatives.
- Lead or assist in the creation and revision of SOPs, forms, and manuals aligned with updated workflows and business processes.
- Support the definition of system requirements, and assist in software configuration and solution design efforts.
- Ensure accuracy and completeness of site-specific master data by performing review and verification activities.
- Collaborate with site Subject Matter Experts (SMEs) to oversee the development and review of templates.
- Assist in drafting, reviewing, and finalizing Operational Qualification documents for equipment or systems.
- Perform User Acceptance Testing and validate data migration processes to ensure system readiness and data integrity.
- Evaluate and contribute feedback on training content to ensure clarity, accuracy, and alignment with procedures.
- Collaborate in the development of training resources by offering technical input and conducting content reviews.Assist with the planning, coordination, and execution of site-level instrument qualification efforts.

**Qualifications**:

- Bachelor’s degree and 2 years of industry Quality Control or Quality experience **OR**Associate’s degree and 6 years of industry Quality Control or Quality experience **OR**High school diploma / GED and 8 years of industry Quality Control or Quality experience.
- Proficient in Microsoft Office (i.e., Outlook, Word, Excel, PowerPoint)
- Excellent written and verbal communication skills.
- Excellent problem-solving capabilities and attention to detail
- GxP experience, specifically practices and requirements in the testing of biopharmaceuticalsExperience in development and validation testing of software used in a GMP environment.

**_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.

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