Senior Associate Quality Control

2 weeks 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 Associate Quality Control with experience in pharmaceutical company/Life Science industries for a role in Singapore.

**Position Overview**
- Non-lab-based Quality Control role under Technical Support.
- Supports the implementation of a new Electronic Lab Notebook (ELN) system.
- Involves system design, configuration, validation, and data migration.
- Requires coordination with cross-functional and international teams.
- Hybrid work setup (partially on site and partially remote), and may require flexible hours, including a mix of daytime (8am-5pm) and and some working hours during the night time to support meetings and project activities during US office hours (e.g. 8pm to midnight), fulfilling a total of 8 working hours a day.
- Contract duration is 1 year and may extend.

**Key Responsibilities**
- Participate in process engineering and ELN system setup.
- Develop and review SOPs, forms, and templates.
- Manage and verify site master data and support user acceptance testing.
- Support instrument qualification planning and execution.
- Provide input for and review training materials.
- Ongoing support for ELN system usage and periodic data review.

**Qualifications**:
**Basic**:

- Bachelor’s + 2 years QC/Quality experience
OR Associate’s + 6 years
OR High School + 8 years

**Preferred**:

- GxP experience (esp. biopharma testing)
- Experience with validated software in GMP environments
- Knowledge of ELN systems (e.g., Biovia, Benchling, LabWare)
- Familiarity with Veeva, Empower
- Analytical method exposure
- Microsoft Office proficiencyStrong communication and teamwork skills

**_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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