QA Specialist II: GMP Compliance & Quality Assurance

Quality Talent Group

Lititz (Lancaster County)

On-site

USD 60,000 - 90,000

Full time

7 days ago
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Benefits offered by this job

Benefits package
Paid time off
Health insurance
Retirement plan
EAP & mental well-being

Job summary

Quality Talent Group is seeking a Quality Assurance professional to uphold GMP standards across production records, manufacturing, packaging, and laboratory documents. The role focuses on product release conformity and adherence to established quality measures.

You will collaborate with Operations to address quality and compliance issues, conduct GMP walkthroughs, and apply QA processes and improvements in a global consumer health environment.

Qualifications

  • Minimum of a Bachelor's Degree.
  • At least 2 years of GMP experience in Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements Production.
  • Basic working knowledge of cGMP requirements and current FDA enforcement issues.
  • Ability to communicate thoughts and ideas effectively – verbal and written.
  • Demonstrated ability to accomplish work goals.

Responsibilities

  • Perform quality review of production records including manufacturing, packaging, and laboratory documents.
  • Responsible for releases of finished product based on conformance to established standards.
  • Apply quality assurance processes, procedures, and activities.
  • Conduct walkthroughs and assessments of GMP areas.
  • Partner with Operations to address quality/compliance issues and improvements.

Skills

GMP experience
cGMP knowledge
Quality assurance
Verbal and written communication
Goal oriented

Education

Bachelor's Degree

Job description

Quality Talent Group is seeking a Quality Assurance professional to uphold GMP standards across production records, manufacturing, packaging, and laboratory documents. The role focuses on product release conformity and adherence to established quality measures.

You will collaborate with Operations to address quality and compliance issues, conduct GMP walkthroughs, and apply QA processes and improvements in a global consumer health environment.

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