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Quality Control Analyst II (Analytical)
Описание вакансии
Текст:
TL;DR
Quality Control Analyst II (Analytical): Testing raw materials, in-process samples, and finished products to ensure quality and safety of life-changing therapies with an accent on cGMP compliance and analytical data review. Focus on delivering accurate laboratory results, documenting quality records, and supporting manufacturing operations.
Location: Onsite in Portsmouth, NH, USA
Company
is a global leader in the manufacture of medicines with over 30 sites across five continents.
What you will do
- Perform testing of raw materials, in-process samples, finished products, and stability samples to support product quality.
- Deliver accurate and timely laboratory results to support manufacturing operations and product release.
- Review analytical data and documentation to ensure compliance with quality standards.
- Document laboratory activities, investigations, and quality records in accordance with established procedures.
- Maintain laboratory materials, supplies, and organization to support efficient operations.
- Collaborate with Quality and Manufacturing teams to support continuous improvement and operational excellence.
Requirements
- Associate's degree in Life Sciences or a combination of education and relevant experience.
- Experience working in a regulated laboratory or cGMP environment.
- Ability to analyze data and identify trends or issues.
- Experience using laboratory systems, quality systems, or related software tools.
- Strong organizational and communication skills.
- Ability to work the night shift: Sunday through Wednesday, 8:00 PM to 6:30 AM.
Culture & Benefits
- Medical, dental, and vision insurance.
- Inclusive and ethical workplace culture.
- Compensation programs that recognize high performance.
- Opportunities for professional growth and technical skill development.
- Collaborative environment across Quality and Manufacturing teams.