BaronHR

Job Responsibilities:

• Provide Quality support to Manufacturing (Bulk& Assembly production).
• Testing of incoming Raw Materials.
• Perform basic in-process and finished good testing.
• Maintain logs of release.
• Perform line clearance and FG shipment checks - (Quality Inspection of Bulk Product before packaging and filling, packaging of components, fill weights, labels, label codes, cap torque, etc.)
• Maintain test data of raw materials and bulk product.
• Record keeping/documentation of analysis.
• Review contact lab data for accuracy.
• Monitor QC lab supplies.
• Maintain accurate and current Quality records.
• Assist with investigations for customers complaints.
• Maintain current General Manufacturing Practices (cGMP) compliance.
• Perform other responsibilities as assigned.
• Responsible for documenting all lab work per cGMP and company standards.
• Management and ownership of laboratory systems such as laboratory analytical standards, calibrations, etc.
• Working with instrumentation such as Brookefield Viscometer, pH meter, and USP methodologies.
• Testing performed in a high quality and timely manner and meet s all procedure and regulatory requirements.

Skills:

• Posses basic background and understanding of cGMP/compliance requirements for Cosmetic and Pharmaceutical or Medical Device products.
• Knowledge of basic chemistry & microbiology laboratory techniques is preferable.
• Proficient computer skills, (MS Word, MS Excel,are essential).
• Strong attention to detail.
• Strong problem identification/analysis and solving sills with hands-on approach in resolving issues.
• Excellent verbal and written communication skills.
• Strong sense of accountability, responsibility, and ownership of projects and tasks.
• Exhibit a professional standard and strong work ethic.
• Excellent organizational skills and time management skills.
• Ability to multi-task and prioritize in a fast-paced environment.
• Ability to interface with all personnel levels within the company.
• Motivated self-starter with ability to work independently on multiple assignments in a team environment.
• Understand personal care manufacturing processes.
• Consistent performance with a sense of urgency and commitment.
• Experience in cGMP documentation.
• Knowledge of USP/NF/EP testing procedure.

Qualifications:

• Science degree or related scientific background.
• 0 - 3 years Quality experience.

• Perform all quality control tests
• Comply with the quality system
• Perform quality checks on pieces
• Coordinate findings with quality and production personnel to facilitate quality goals
• Adhere to quality control procedures
• Insure quality of customer service
• Manage the quality control documentation
• Ensure quality products and processes
• Identify quality problems and solutions
• Ensure compliance with customer quality standards
• Assist in conducting quality inspections on work
• Provide focused, hands on quality support and expertise for all plant related quality issues
• Maintain all quality control procedures and policies
• Aid in training of associates on quality requirements
• Maintain acceptable quality and effectiveness levels
• Eliminating unnecessary downtime and enhancing quality
• Bring unit within quality control specifications
• Complete quality documentation (deviation investigations)
• Ensure product meets quality control criteria
• Communicate quality related problems to operations and quality supervision, and other necessary parties