Location: Santa Fe Springs site – Santa Fe Springs, CA

Onsite

Company Summary:

Vytalogy is a modern wellness company, - we bring a vibrant energy to life. Headquartered in Sherman Oaks, CA, Vytalogy markets products across multiple channels and categories in vitamins, minerals, and supplements (VMS). Our incredible brands, Natrol and Jarrow Formulas, are recognized and trusted as industry leaders for over 85 years. We bring together exceptional talent and harness diverse backgrounds and perspectives to make life more vibrant for everyone, every day.

Summary:

The Quality Engineer will monitor and improve Vytalogy Wellness operational processes and documented outputs. The primary responsibilities include establishing and documenting quality engineering operations related to inspecting materials, equipment, processes, and dietary supplement products.

The Quality Engineer will also work with inter-plant quality and operations management to implement measures for ensuring continuous improvement of quality systems, processes, and commercialized products. A successful quality engineer should have excellent troubleshooting skills and be able to ensure that processes and products consistently meet established quality standards.

Your primary activities will include but are not limited to:

The Quality Engineer will provide engineering and technical support to ensure dietary supplement product quality is built into processes. Primary focus will be to maintain the Vytalogy Wellness Quality Management Systems (QMS) and provide support for process improvements to prevent deviations or discrepancies from occurring. Detailed duties, as follows:

1. Focusing in areas of quality engineering, such as facility commissioning, incoming material, process control, product evaluation, product reliability, inventory control, metrology, automated testing, software, technology operations, and administrative applications.

2. Collaborating closely with cross functional teams, including Research and Product Development, Technology and Manufacturing Operations, Facility Engineering and Technical Services to identify and mitigate quality/compliance risks.

3. Collaborating with manufacturing process engineers to develop and implement controls and improvements, and initiative-taking identification of areas for process improvements.

4. Developing and implementing functional quality control systems; and as well as monitoring and analyzing quality key metrics related to process and product efficiency.

5. Encompassing quality operations including deviations, CAPAs, customer complaints and out-of-specification results, risk managements and change controls.

6. Conducts root cause analysis using the Define, Measure, Analyze, Improve and Control (Six Sigma DMAIC) principles for defects, non-conformities, or other quality failures.

7. Performs analytical, statistical and trending analyses on relevant data to support timely management review and initiative-taking response or corrective action reviews. E.g. out of specification, deviation and customer complaint trending.

8. Supports supplier quality management including evaluation of supplier quality data to identify procurement process improvements and opportunities.

9. Establishing quality engineering program to evaluate precision and accuracy of production equipment and testing, measurement, and analytical equipment and facilities. Quality oversight of the validation/qualification quality engineering projects to ensure quality and compliance requirements are met in an efficient and effective manner.

10. Auditing internal operational processes for quality and regulatory compliances, or external contract manufacturing organizations, suppliers/vendors to ensure that established quality agreements and quality system standards are met.

11. Write training material and conduct training sessions on quality engineering and related control activities

12. Works closely with site quality managements to support the training program and compliance to Good Documentation Practices and Good Manufacturing Practices; and ensure adherence to health and safety guideline

13. May be responsible for ensuring compliance with formal external quality standards, such as ISO 9001, USP, NSF, and Oregon Tilth Certification

14. The job function listed is not exhaustive and shall also include any responsibilities as assigned by the quality managements from time to time.

You’ll need the following (minimum qualifications):

1. Degree from an accredited higher learning institution with studies in quality, math, industrial, chemical, or mechanical engineering related fields. ASQ certification preferred.

2. 3+ years of experience in quality engineering, quality assurance, or a similar role.

3. Knowledgeable in regulatory aspects of the dietary supplement industry, and with working knowledge of cGMP, FDA, USP, NSF, Oregon Tilth, Non-GMO Project, and California Proposition 65 guidelines.

4. Ability to work effectively and collaboratively in a cross-functional team within a demanding environment. This position communicates with all levels of internal personnel and vendors. Strong oral communication skills are required to establish interpersonal relationships across the organization.

5. Ability to complete and present technical analysis and assessments.

6. Occasional business travel required, and ability to work non-standard schedule as needed.

Vytalogy Wellness, LLC is an Equal Opportunity Employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law.

Job Type: Full-time

Pay: From $2.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Health insurance
• Life insurance
• Paid time off
• Referral program
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Ability to commute/relocate:

• Santa Fe Springs, CA 90670: Reliably commute or planning to relocate before starting work (Required)

Experience:

• quality engineering: 3 years (Preferred)
• quality assurance: 3 years (Preferred)
• vitamin / pharma: 3 years (Preferred)
• process improvement: 1 year (Preferred)

Work Location: One location

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