Quality Assurance QA Associate Full Time
Quality Assurance QA Associate Full Time
Posted on :
11-04-2025
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1 Vacancy
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Job Description
Are you a detailoriented Quality Assurance professional looking to advance your career in the health and beauty care manufacturing industry We are seeking a Quality Assurance (QA) Associate to play a vital role in ensuring compliance continuous improvement and product quality in accordance with Good Manufacturing Practices (GMP)
WHY JOIN APOLLO HEALTH AND BEAUTY CARE
- Work with a leading contract manufacturer in the health and beauty sector producing highquality products for top global brands.
- Be part of a collaborative and innovative team dedicated to excellence in quality and compliance.
- Gain handson experience in a fastpaced highgrowth environment where your contributions make a real impact.
YOUR ROLE & RESPONSIBILITIES
As a QA Associate you will support quality management systems (QMS) and ensure compliance with regulatory standards. Your key responsibilities include:
Deviation & CAPA Management: Review deviation records track corrective and preventative actions (CAPA) and ensure timely resolution of issues.
Deviation & CAPA Management: Review deviation records track corrective and preventative actions (CAPA) and ensure timely resolution of issues.
Annual Product Reviews (APR): Gather data from batch records investigations product changes and complaints to complete APR reports on schedule.
Internal Audits & Compliance: Conduct internal audits across production validation laboratories and facilities to ensure QMS compliance and support external audits.
Documentation & SOP Management: Generate and review applicable standard operating procedures (SOPs).
Documentation & SOP Management: Generate and review applicable standard operating procedures (SOPs).
Batch Record Review: Assist with reviewing batch records to support timely product release.
Collaboration & Continuous Improvement: Work crossfunctionally with Manufacturing Process Development Regulatory Affairs and other departments to drive quality initiatives.
Collaboration & Continuous Improvement: Work crossfunctionally with Manufacturing Process Development Regulatory Affairs and other departments to drive quality initiatives.
WHAT YOU BRING TO THE TEAM
Education & Experience:
- 5 years of GMPrelated experience in pharmaceutical biopharmaceutical health and beauty care cosmetics or personal care product manufacturing.
- Bachelors degree or diploma in Chemistry Biology Engineering or a related field.
- Strong knowledge of cGMP/GDP international regulatory compliance and QMS.
Skills & Competencies:
- Ability to analyze data solve complex quality issues and drive continuous improvement.
- Strong organizational skills to prioritize tasks in a fastpaced environment.
- Excellent written and verbal communication skills for internal and external collaboration.
- Attention to detail with the ability to manage confidential and sensitive information.
Apollo is committed to providing accommodation for people with disabilities in all parts of the hiring process. Apollo will work with applicants to meet accommodation needs that are made known to Apollo in advance.
We thank all applicants for their interest however only those meeting the minimum qualifications will be interviewed.
Required Experience:
IC
Employment Type
Full-Time
Key Skills
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