Qc Supervisor

QC Supervisor will work as part of the Quality team to support the QC of day-to-day operations and maintain detailed records for all the tasks assigned. The individual will inspect the products in different stages of manufacturing process such as incoming raw materials, intermediates, in-process and finished good. The individual will also participate in the investigation of nonconforming products and follow-up with the actions that arises from these inspections.

**Roles and Responsibilities**
- Supervise QC Technicians to ensure smooth execution of routine QC operations.
- Plan and schedule daily QC routine and ad hoc testing.
- Oversee QC lab housekeeping, including cleanliness, equipment maintenance, document archival, and reagent inventory tracking.
- Perform routine QC testing of raw materials, in-process materials and finished goods.
- Evaluate data, draft and/or review QC reports, highlighting deviations from standard operating procedures.
- Consolidate and monitor QC data trends.
- Troubleshoot QC failures and raise nonconformance reports when needed. Investigate nonconformance to determine root causes.
- Draft and update QC work instructions.
- Support validation and stability studies for lab development and diagnostic products as needed.
- Contribute to the continuous improvement of laboratory procedures and processes to ensure compliance to GMPs.
- Perform any other duties as assigned.

**Desired Skills and Competencies**
- Diploma/Bachelor/ Master of Science/ Engineering or equivalent in Biotechnology, Biochemical, Biochemistry, Analytical Chemistry, Molecular Biology/ Life Science related courses.
- Appropriate experience may substitute for education.
- Have qPCR knowledge and experience in using qPCR machine.
- Familiar with the basic laboratory procedures. Relevant experience with laboratory testing, and QC of assays-based workflow will be an advantage.
- Able to work independently with mínimal supervision and with others within and outside his/her function.
- Excellent organizational and time management skills.
- High degree of initiative and ownership.
- Possess a positive and willing-to-learn attitude.
- Good logical thinking and reasoning ability.
- Good Documentation Practices and ability to write protocols and procedures
- People management experience including training, development and mentoring/coaching of technical staff would be an added advantage.
- 2-3 years of relevant experience in quality control and preferably in medical device manufacturing industry.
- GMP and/or ISO 13485 experience would be an added advantage.

**Job Types**: Full-time, Permanent

Pay: $4,000.00 - $5,500.00 per month

**Benefits**:

- Dental insurance
- Health insurance

Schedule:

- Monday to Friday

Supplemental Pay:

- 13th month salary

**Experience**:

- Quality control: 3 years (required)

Work Location: In person