Samantha M Ryan
Harrisburg,PA
Summary
Detail Oriented, friendly, loyal and clearly dedicated individual who has an ambition to succeed in any given environment. I have experience in biotech sterile packaging, secondary OTC, pharmaceuticals ,consumer/beauty goods, Flexo Printing Quality and SQF practices. I am always up to a challenge whenever the situation, I work well within a team environment, and get along well with others while also working efficiently on my own. I am seeking a position where I can develop and excel while giving my best to achieve success and develop within an organization.
Overview
7
7
years of professional experience
Work History
Quality Supervisor
CP Flexible Packaging
York, PA
08.2020 - Current
- Developed Weekly reports showing inspections, improvements and heldware.
- Supported audits and led teams to fully investigate quality control processes and root out deficiencies.
- Supervised and directed quality control personnel through effective mentoring, coaching and work delegation.
- Validated new methods to properly integrate improved strategies into quality control processes.
- Trained personnel in proper sampling techniques, raw materials testing protocols and finished product inspection and testing strategies.
- Coordinated disposal of discrepant materials not suitable to be salvaged.
- Oversaw Payroll
- HCCP,SQF Edition 9 Certified
- SSGI Green Belt (enrolled)
- Reduced heldware by 27% in once year
Quality Technician
CP Flexible Packaging
06.2019 - Current
- Responsible for the Quality coming off of the Press, Lamination & finishing departments
- Verification & approval of each press to determine if the material meets CP & Customer requirements
- Preforming correct & timely inspections on the floor (picking up samples)
- Reviewing press & lamination samples for any discrepancies that include but does not limit to; Color variance, UPC issues, Incorrect measurements, incorrect lamination, print defects ect.
- Filing QC, Press, Lamination, and finishing records in their proper area
- Auditing Press check forms (Must be GMP compliant)
- Preforming Testing on lamination samples ( C.O.F, Bond test, basis weight, Gauge, correct lamination , and visual representation)
- Data entry on Access Data base
- Initiating NCMR ( Non Conformance Material Record) for any discrepancy that is not acceptable or questionable
- All discrepancies found will be tagged & all personnel is notified by QC for a description and further steps for each HOLD
- Creating COC (Certificate of Compliance) & COA (certificate of Analysis)
- Supports and has a good attitude with production personnel
- Reviews work orders against Customer specifications
Quality Packaging Specialists International, QPSI
07.2018 - 06.2019
- Responsible for Inbound outbound shipments
- Examine incoming trailers and material for any contamination, infestation, odor and damage
- Review Bill of Ladings, packing slips, trailer tags for correctness, completion and security
- Verify the quantity and correctness of incoming materials (bulk cases, any incoming count for correctness) and documents any discrepancies
- Verification of finished goods criteria, per release criteria
- Verification and approval of incoming goods as required
- Place incoming product on hold/quarantine status until incoming inspection is complete
- Perform required inspections (incoming sampling inspection) and complete incoming Inspection Reports, inspect incoming material per customer and QPSI specification
- Any discrepancy in material or documentation will be tagged as HOLD pending disposition
- Complete receiving (Quality Inbound) and shipping (Quality Outbound) records ensuring compliance and quality
- Enter all receivers into the inventory system for inventory accuracy
- Assisted the Quality Assurance Inspector on an as needed basis
- Assure that “HOT” priority inbound materials/products are inspected quickly and accurately
- Interacts with warehouse management and personnel for continuous improvement
- Initiate NCR – Non-Conformance Reports as they occur
- Filing of QA inbound and out bound records.
Sanofi Pasteur
01.2016 - 12.2017
- Packaging and filling of sterile biological products
- Inspect finished goods for particulates and defects
- Verify correct lot code/expiration date
- Sterile filling room training
- Class 1000 gowning
- GMP compliant
- Audited batch records to verify accurate documentation
- Batch records and specifications
- CFR 210/211 FDA guidelines
Education
Business Management
Northampton Community College
Tannersville, PA2018
Pocono Mountain High School
Swiftwater, PA06.2016
Skills
Problem solving
Communication
Attention to detail
Documentation
Time Management
Critical Thinking
Patience
Adaptability
Computer skills
Timeline
Quality Supervisor
CP Flexible Packaging
08.2020 - Current
Quality Technician
CP Flexible Packaging
06.2019 - Current
Quality Packaging Specialists International, QPSI
07.2018 - 06.2019
Sanofi Pasteur
01.2016 - 12.2017
Business Management
Northampton Community College
Pocono Mountain High School
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