Assembly Quality Control Associate
3 weeks ago
At Innovative Skincare, we believe in a unique formula: the perfect blend of professional expertise and cultural harmony. This philosophy fuels our brand’s continuous growth and empowers each member of our team. We are more than a company; we are a community bound by passion, dedication, and a deep love for what we do, crafting an atmosphere that is as vibrant and energizing as our products.
Who we are: Discover a world where skincare innovation meets scientific excellence at Innovative Skincare, a globally acclaimed leader in high-performance cosmeceuticals. Our journey is rooted in the relentless pursuit of creating skincare products that are not only effective but transformative. At the heart of our brand is the iS CLINICAL line, renowned for its fusion of nature’s finest ingredients with cutting-edge science. We are driven by a deep understanding of skin biology and a passion for unlocking the secrets of skin health and rejuvenation.
Our ethos is built on the pillars of innovation, integrity, and excellence. Our team members at Innovative Skincare are part of a company that is shaping the future of skincare, where your work contributes to the well-being and confidence of people globally. Join us and be a part of this exciting alchemy where your talent meets our vision, creating a world of pure chemistry
About the role: We are seeking an Assembly Quality Control Associate that will report directly to our Quality Control Manager. This individual will provide support in all aspects of the Assembly and Production Quality Control process.
The role is on-site in our Burbank, CA facility.
Duties/Responsibilities:
- Check Work Orders prior to assembling products.
- Verify the components and Finished Goods (FGs) needed for Work Order.
- Maintain a clean, neat, and orderly work area per GMP’s and SOP’s.
- Make sure all the tables are sanitized and cleaned and have cleared from previous orders before working on a new Order.
- Fill out Assembly Table Clearance and Set-up Record (SOP.GMP.OP.0001.59A) before the start of each Work Order.
- Make QC Approved labels for components after they have been sorted by assembly and for Finished Goods (UB) products after Micro Submission results have been received and approved. Approved labels are also made for products that are packaged and components that are checked 100% for filling room.
- Verify Item # of label, lot # of label, description of label, and placement of label on product is correct and to company’s specifications before running label machine.
- Verify Lot Code and Expiration Date is correct, legible, and placed correctly before running Lot Code machine.
- Walk the assembly floor to verify if products are being assembled properly and to company’s specifications. Check on the coders as well.
- Reject components and Finished Goods. Fill out a QC Reject form for each component and Finished Good that is being rejected.
- Reports any safety issues, GMP violations, and/or any quality & process issue to their supervisor.
- Additional duties given by their supervisor or the Director of Manufacturing Operation.
- Experience with Microsoft Office Suite - Outlook, Excel, Word
- Strong Computer Skills
- Strong Math Skills
- Prior experience in a QC environment
- Must be able to lift up to 50 pounds without assistance
- Must be able to stand and walk for extended periods of time
Following the Fair Chance Initiative for Hiring Ordinance, our hiring process is inclusive of candidates with criminal histories, ensuring fairness and equality in accordance with California's employment laws.
Adhering to the requirements of California's law on salary transparency, the salary bracket for this role is set between $18.00 and $20.00 an hour. The offered rate may be adjusted based on various factors such as the applicant's qualifications, skills, and professional experience.
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