Job Description
Job Description
Benefits :POSITION PURPOSE
The Quality Manager at Bayport Laboratories is responsible for developing, enhancing, and enforcing current Good Manufacturing Practices (cGMP) to ensure full compliance with federal and state regulations, as well as specific customer and industry requirements. This role plays a critical leadership function in both Quality Assurance (QA) and Quality Control (QC), ensuring the integrity, safety, and quality of all products manufactured and released
ESSENTIAL FUNCTIONS AND BASIC DUTIES
Ensure compliance with federal, state regulations, and customer specifications related to the quality of the products
Execute and manage closure of quality systems related records such as Deviations, CAPAs, NCMR, Complaints, and Recalls
Color matching and innovation
Execute and manage review and approval of quality operation documents such as batch records, Quality Control Data
Execute and manage implementation of quality systems and processes
Support implementation of cGMP
Support customer and regulatory audit preparation, facilitation, and follow up
Execute Internal Audit Program
Responsible for disposition of raw materials, components, WIP, bulk, and finish goods
Reviews equipment calibration records to ensure that are performed as indicated in the Bayport Laboratories Standard Operating Procedure
Assist on manufacturing processes as needed
Participate in team meetings
Conducts risk assessment and implement corrective actions
Utilize Hands on approach in performing all functions
Prepares quality documentation and reports by collecting, analyzing, and summarizing information and trends
Work with purchasing to ensure approved supplier use
Implement and performs training
Educate employees on preventing work related health problems and perform EHS training
Ensure compliance with EHS procedures
Responsible for identifying and remediating hazardous workplace conditions
PERFORMANCE MEASUREMENTS
Yearly reviews to asses success and determine areas of improvement
QUALIFICATIONS
EDUCATION / CERTIFICATION :
BS or MS degree in Chemistry, Biology, Cosmetic Science
REQUIRED KNOWLEDGE :
Familiarity with regulatory standards including cGMP, FDA, and ISO 22716 (2007)
EXPERIENCE REQUIRED :
Proficiency in developing and delivering GMP training
A minimum of 5 years of experience in Cosmetic manufacturing as Quality Manager
SKILLS / ABILITIES :
Excellent communication skills
Detailed oriented with strong analytical and problem-solving skills
Experience in Quality Systems
Bilingual in Spanish
Quality Manager • Houston, TX, US