QA Specialist II

Quality Talent Group; Hopeland (PA); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive benefits

Paid time off

Health insurance

Retirement plan

EAP & well-being

Well-being reimbursement

Parental leave

Volunteer time

Learning & development

Job summary

Quality Talent Group is seeking a Quality Assurance professional with at least 2 years of GMP experience across Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements Production. A Bachelor’s degree is required, and basic knowledge of cGMP is essential.

You will perform quality review of production records, authorize releases based on standards, apply QA processes and conduct walkthroughs of GMP areas, while partnering with Operations to address quality and

Qualifications

• Bachelor's degree required.
• Minimum 2 years GMP experience.
• Basic working knowledge of cGMP requirements.
• 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

Verbal & written communication

Goal-oriented

Documentation proficiency

Education

Bachelor's degree

Job description

Overview:

Recognized in 2024 by Seramount as one of the 100 Best Companies for Working Parents and Caregivers, the company also earned a place on the 2024 US Inclusion Index and Global Inclusion Index across 7 countries - Brazil, Canada, China, Germany, India, Japan, and the UK.

This is a global organization in the consumer health and personal care industry, with 135+ years of heritage, 22,000+ employees, and a presence across 100+ countries. Its portfolio includes iconic consumer health and personal care brands used by millions of people worldwide.

Benefits:

• Competitive benefits package.
• Paid time off.
• Health insurance benefits, including coverage for doctor visits and mental health care.
• Retirement program.
• Employee Assistance Program (EAP) and mental well-being resources.
• Global exercise/well-being reimbursement.
• Adoption, fertility, and surrogacy benefits.
• Global parental leave.
• Paid company holidays and volunteer time.
• Learning and development opportunities.

Qualifications

• A minimum of a Bachelors Degree
• A minimum of 2 years of GMP experience in either 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.