Quality Specialist
Company: BIO FILM INC
Location: Vista
Posted on: September 1, 2024
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Job Description:
Description: BioFilm Inc is Hiring!!Who We AreBioFilm
manufactures and distributes high-quality medical device and
personal care products that contribute to the well-being of our
consumers. Our flagship product, ASTROGLIDE, is one of the world's
leading personal lubricant brands. Our headquarters, in Vista, CA
is home to sales, marketing & consumer engagement, research &
development, insights & innovation, quality control, regulatory
affairs, and distribution. Although ASTROGLIDE is a global brand,
we are a small, private, family-owned company with an
entrepreneurial spirit.Why Work HereBioFilm is a growing company
with an expanding product line, offering ample opportunity for
professional growth and development for employees. Our culture is
inclusive and guided by our core values of Teamwork, Have Fun,
Exceed Expectations, Do the Right Thing, Respect, Accountability,
and Make a Difference. Our competitive compensation includes the
following excellent benefits:4-day work weeks - every Monday
off!Full health, dental, and vision insurance plus Health
Reimbursement Account and Flexible Spending Account options
availableMatching 401K and profit-sharingDiscretionary annual
bonuses based on profitsGenerous PTO and holiday schedule including
paid time off from Christmas Eve to New Year's DayAnnual
professional development opportunitiesTuition reimbursementThis
role is a temporary role for up to 12 months. The salary range
listed represents a general guideline; however, Biofilm, Inc
considers a number of factors when determining base salary offers
such as the scope and responsibilities of the position and the
candidate's experience, education, skills and current market
conditions. Our Quality Specialist collaborates with key internal
stakeholders to enhance the performance of the overall Quality
Management System (QMS). They analyze data to track quality trends,
identify issues, and offer actionable insights for product and
process improvements. They design, support and implement changes to
boost quality and operational efficiency. Assist with research,
design transfer, and design control for new products. Additionally,
they lead risk analysis, problem-solving, and root cause analysis
efforts to address quality issues effectively and drive continuous
improvement across the business. Promotes a culture of quality,
continuous improvement, and outstanding customer service. 1.
Initiated and Drive NCMRs, CAPAs, SCARs, Deviations, customer
complaints, product/process investigations and systems. 2. Design,
implement , and monitor QMS process improvements3. Design transfer/
Design Control 4. Document Review / Change Review. Document changes
Quality -- A quality mindset and commitment to Quality are
required-- Responsible for following all quality procedures and
standards in work area-- Monitor product quality and flag any
defects immediately to supervisor-- Identify and report potential
regulatory compliance issues (lack of cGMP conditions, quality
system non-compliance, etc)Requirements: QUALIFICATIONS AND
EDUCATION REQUIREMENTS: BS in Engineering, Chemistry, Biology,
Biotech, Chemical ENG, or other Science Related Field5+ years of
Experience in Quality Control/AssuranceSCAR, CAPA, NCMR, and
Customer Complaint Investigation and Root Cause Analysis experience
Required.Experience working in a regulated environment with a
strong knowledge of medical device FDA 21 CFR 820/ISO 13485:2016
requirements. Working knowledge of Quality Systems and quality
related tools, such as FMEA, SPC, Cpk, AQP, DOE.ASQ or Six Sigma
Green/Black Belt certification is preferred.AQL/Statistical
Sampling experience is preferred.Formal training/course work in
statistical techniques is preferred.Project Management skills
Preferred.Compensation details: 85000-100000 Yearly
SalaryPI5c28b1c98bcf-25660-35370199
Keywords: BIO FILM INC, Vista , Quality Specialist, Other , Vista, California
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