Quality Assurance Associate

Planet Pharma; Holly Springs (NC); On-site; USD 33,062 - 35,817; Part time

Benefits offered by this job

Medical insurance

Vision insurance

Job summary

A leading pharmaceutical company located in Holly Springs is seeking a Quality Assurance Associate to support inspections, sampling, and testing of raw materials. The role involves ensuring compliance with cGMP requirements, documenting test results, and participating in training efforts. Ideal candidates will have expertise in inspection techniques and RAMAN technology usage, along with a commitment to quality processes.

Qualifications

• Experience with inspecting materials and ensuring compliance with specifications.
• Understanding of cGMP regulations and processes.
• Ability to document results accurately and thoroughly.

Responsibilities

• Inspect materials to meet specification requirements.
• Document inspection and test results accurately.
• Support inspection readiness activities and training.

Skills

Inspection skills

Sampling techniques

RAMAN technology usage

Documentation and reporting

GMP compliance knowledge

Job description

The role will support the inspection, sampling, and testing of raw materials that are received at the North Carolina (ANC) site. This role will ensure that raw materials received for use in our cGMP manufacturing plants meet all specification requirements and master inspections characteristics required for use in our manufacturing process. This role will also demonstrate leadership skills in support of scheduling, coordination, and staff training. There will be opportunities to advance Quality learning through additional responsibilities and training.

Primary Responsibilities of the Role Include:

• Inspect materials including biobags, tubing, filters, and other components to ensure all inspection-related specification requirements and master inspections characteristics are met

• Remove samples from containers of medias and other chemicals to facilitate the testing of samples

• Use RAMAN technology with TruScan equipment to identify chemicals (must have)

• Ensure that inspection & sampling results are complete and detailed according to written procedures and cGMP requirements

• Responsible for accurately documenting inspection, sample, and test results in systems

• Responsible for ensuring that characteristics that could potentially impact product quality are assessed according to procedures

• Ability to determine the color of components match required attributes

• Support inspection readiness activities

• Supports Continual Improvement initiatives, programs and projects

• Assist area management with the prioritization and scheduling of tasks

• Serve as a trainer in tasks associated with raw material inspections, samples, and testing

• Own controlled documents for the area including SOPs and FORMs

• Initiate and own deviation records and CAPAs associated with events and projects in ANC’s raw material inspections, samples, and testing areas

• Provide QA oversight to Warehouse and ensure they are adhering to GMP regulations.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Quality Assurance and Science

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

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