Quality Tech 2nd Shift

Trison Wells LLC; Walterboro (SC); Presencial; USD 42.000 - 64.000; Jornada completa

Descripción de la vacante

Trison Wells LLC in Walterboro, SC seeks a Quality Assurance professional to oversee quality throughout the manufacturing process, from raw materials to final packaging. You will perform inspections, run analytical checks, and facilitate information flow across teams to ensure compliance with standards.

The role involves maintaining lab records, validating COAs, and contributing to SOP development, with emphasis on safety and GMP adherence in a fast-paced environment.

Formación

• Associate degree or equivalent in Life Sciences or Industrial Technology.
• Understanding of GMP and safety policies.
• Experience with lab equipment and calibration standards.

Responsabilidades

• Perform quality inspections from raw materials through final packaging.
• Review batch records for completeness and accuracy.
• Conduct in-process checks of packaging components and labeling.
• Verify product attributes and publish COAs per lot.
• Maintain digital quality records and external lab results.

Conocimientos

Lab equipment

Calibration

GMP knowledge

Safety awareness

Detail oriented

SOP development

Communication skills

Educación

Associate degree or equivalent

Herramientas

ERP systems

Document management

Excel

Outlook

Descripción del empleo

Job Description

Job Description

** Job Summary:**

This position is responsible for ensuring that quality standards are being met throughout the entire manufacturing process (raw material, batch blending, filling, to final product packaging and storing) by performing quality inspections, analytical testing, and facilitating the flow of information across teams.

Main Responsibilities:

• -Follow safety rules, wear required PPE, and report any safety incident or accident.
• -Maintain a clean and organized work area.
• -Review production batch records for completeness and accuracy. Use of general laboratory equipment (i.e. pH meter, balance, densitometer, etc.)
• -Conduct in-process checks of packaging components, labeling, and lot coding.
• -Verify product attributes against specifications and publish COAs per lot.
• -Collect water samples using aseptic technique and process for external testing.
• -Verify calibration of production scales and maintain certification of weight standards.
• -Maintain digital daily quality records and external lab results.
• -Monitor production environment for safety hazards as well as for GMP compliance.
• -Collaborate in development of SOPs for new quality/lab equipment or methods.
• -Participate in company mandated training and operational meetings as required.

Skills:

• -Experience with general laboratory equipment, controls, and calibration standards.
• -Basic knowledge of microbiological principles and aseptic collection technique.
• -Use of enterprise resource systems and document management software.
• -Microsoft Excel and Outlook email. Basic laboratory mathematics (i.e. dilutions, molecular weight, unit conversions, etc.)
• -Active awareness for safety.
• -Detail oriented.
• -Development of methods and SOPs.
• - Communicating effectively with employees across the entire organization, from helper to manager.

Education:

• -Associate’s degree in Life Sciences or Industrial Technology field, or Equivalent relevant proven experience.

** Requirements:**

• -Understanding of and adherence to basic GMP principles
• -Follow all applicable safety requirements while assisting in identification of hazards and maintaining a safe working environment for self and others
• -Understanding of and commitment to Trison Wells Health, Safety, Environmental, and Quality Policy
• -Understanding of and adherence to basic Quality Principles

Additional requirements :

• -Lifting Demands: Lift up to 40 lbs. on an occasional basis floor to waist.
• -Carry up to 40 lbs. on an occasional basis up to 50 feet.

Postural Demands:

• Sitting: frequent
• Standing: frequent
• Walking: frequent
• Bending/stooping: frequent