Qc Chemist

**QC Chemist**

Since 1998, Sigan Industries Group has been a premier private label manufacturer of health and beauty products. Sigan is known for its superior customer service, its firm commitment to quality control and its ability to innovate and deliver products that leave our customers satisfied.

**KEY DUTIES AND RESPONSIBILITIES**
- Ensures applicable standard operating procedures and GMP are followed for all activities.
- Testing bulk and finished products to ensure the product complies with specifications.
- Logging the batch has been fabricated in the appropriate log.
- Providing samples to QA if testing is required to be done by the contract lab as per the bulk and finished product specification.
- Providing samples for Micro testing.
- Arranging samples for clients (if needed)
- Providing status tags to compounders after bulk testing.
- Receive and issue the bulk in system and release the production work order from the lab for packaging.
- Updating equipment usage log book in a timely manner.
- Submitting the manufacturing documents received from compounders for QA review.
- Perform analytical testing.
- Executing method validation.
- Attending production meetings.
- Maintaining the log books for analytical testing.
- Calibrate the equipment’s used on time and logging them in the appropriate log books.
- To ensure that equipment, instruments and facilities within the laboratory are kept serviceable and to report any defect to QA.
- To ensure that safe working methods and practices are adopted at all times.
- Responsible for housekeeping, tidiness, and general cleanliness of the designated area.
- Reporting any deviation or OOS to QA/QC Director.
- Ensure retains are kept for all tested and bulk batches.
- Other duties as assigned.

**REQUIRED EDUCATION AND EXPERIENCE**
- Relevant education in Science/Chemistry/Biochemistry/Biology or another relevant field OR equivalent work experience is an asset
- Prior experience with GMP, US FDA and Health Canada regulations.
- Experience working in manufacturing, Pharmaceutical or cosmetic and/or GMP facility is an asset

**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
- In-depth understanding of Quality Control Procedures and Principles
- Excellent written and verbal communication skills
- Extremely well organized and detail-oriented
- Excellent time management skills
- Ability to prioritize and manage multiple concurrent projects in a dynamic and fast-paced environment
- Proficient in Microsoft Office programs
- Ability to perform duties with a high level of accuracy and with less supervision
- Advanced Experience in Quality Control, Analytical or product formulation preferred

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

**Benefits**:

- Dental care
- Life insurance

Schedule:

- 8 hour shift
- Night shift