NOTE: This is a Temporary Role for about 3-4 months.
BioFilm Inc is Hiring!!
Who We Are
BioFilm is a subsidiary of Combe Incorporated that specializes in manufacturing Astroglide Personal Lubricant and other sexual wellness products.
With state-of-the-art faculties and a commitment to excellence and continuous innovation, we leverage advanced technologies and stringent quality control processes to ensure our products meet the highest industry standards and regulatory requirements.
Why Work Here
As a privately held family business, we have a uniquely caring culture. But even with our family-feel, we're all part of a high-performing team that loves to compete and win in the marketplace. To achieve that, we embrace a set of core attributes that guide our performance each day. We call these attributes C.A.R.E.
Collaborative. Accountable. Responsive. Entrepreneurial.
C.A.R.E. drives our success. We celebrate people for demonstrating C.A.R.E in their day-to-day work. We encourage our teams to give feedback to one another, so that we bring out the best in one another. We take a totally kind, totally honest approach to our communications with one another. We believe this makes for a more humane work environment where high-performers can thrive, work together effectively, and truly enjoy the work they do to drive our company forward.
- 4-day work weeks - every Friday off! 2 Shifts 6am-4:30pm or 7am-5:30pm
- Full health, dental, and vision insurance plus Health Reimbursement Account and Flexible Spending Account options available
- Matching 401K and profit-sharing
- Discretionary annual bonuses based on profits
- Generous PTO and holiday schedule including paid time off from Christmas Eve to New Year's Day
- Annual professional development opportunities
As our Temporary Quality Control Technician, you would handle sampling, inspections, testing, and scheduling for a wide range of samples, including raw materials, in-process items, and finished good products. Ensures that all materials and final products meet specifications and manages the release of materials. Oversees accurate status labeling, inventory transactions, and material segregation. Gathers, organizes, and analyzes data for monitoring and trend analysis. Continuously investigates products and processes, implementing changes and modifications as directed by management. Promotes a culture of quality, continuous improvement, and outstanding customer service.
Other duties include...
* Collects, prepares, schedules QC analytical testing for raw materials, bulk solutions, and finished goods while following all universal precaution, safety guidelines, while documenting test results.
* Performs microbiological, endotoxin, bioburden, and environmental monitoring testing.
* Notify quality team of potential problem areas or test results which do not meet specifications. Initiate and assist required out-of-specification (OOS) and Non-Conforming Material investigations.
* Prepare, maintain, and operate analytical instruments and equipment (e.g., ovens, viscometers, analytical balances, FTIR, osmometers, pH meters).
* Ensures accuracy of product, bulk, environmental, water-related monitoring databases for tracking and trending.
* Perform inspections for incoming materials, including first article inspections (as required).
* Performs all necessary activities related with the inspection of these items.
* Ensure proper status labeling, real-time inventory transactions, and segregation of all material based on inspection/testing status.
* Monitor production lines to maintain high quality and consistency in finished products, and promptly escalate any errors or delays to the quality team (as required).
* Complete non-conformance report with proper detail and accuracy for all materials/product that is not meeting specifications.
* Assists with root cause investigations and completes all investigational tasks on-time and in-full.
* Ensures proper follow up, closure and corrective actions based on inspection requirements and status.
* Understand the Quality Systems as it relates to your job function.
* Assists in the Quality Systems administration to include but not limited to the NCMR, CAPA, Calibration, and Customer Complaint systems.
* Responsible for gathering and organizing of data for analysis. Making informed disposition or supplier escalations based on data.
* Communicates potential quality problems promptly to manufacturing and quality management.
* Operates, programs, and maintains computer software, forms, reporting systems, and documentation.
* Record and track test numbers related to production information.
QUALIFICATIONS AND EDUCATION REQUIREMENTS:
* HIGH SCHOOL DIPLOMA OR EQUIVALENT.
* BACHELOR'S DEGREE IN BIOLOGY, CHEMISTRY, BIOTECH, OR OTHER SCIENCE RELATED FIELD PREFERRED.
* KNOWLEDGE OF CGMP/QSR REQUIREMENTS REQUIRED.
* WORKING KNOWLEDGE OF ISO 13485 REQUIRED.
* KNOWLEDGE OF ERP SYSTEMS REQUIRED.
* 1+ YEARS' EXPERIENCE IN QUALITY INSPECTION OR TESTING.
* 1+ YEARS' EXPERIENCE IN AN FDA REGULATED ENVIRONMENT.
* ASQ CQI CERTIFIED QUALITY INSPECTOR (PREFERRED).
Compensation details: 25-28 Hourly Wage
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