Quality Assurance Specialist, Aseptic Manufacturing

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); In loco; USD 60.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Benefits starting day 1

Paid volunteerism: 16 hours/year

PTO: up to 13 days/year

Wellness time off

Descrizione del lavoro

Grand River Aseptic Manufacturing (GRAM) seeks a Quality Assurance Specialist to support cGMP drug product manufacturing and testing. The role provides oversight for aseptic processes, deviation and CAPA systems, batch record review, SOP creation, and quality document reviews within the Quality Management System.

Non-negotiable requirements include a Life Sciences degree with 2–5 years GMP/related experience and proficiency in Word, Excel, and Outlook.

Competenze

• Bachelor's degree in Life Sciences or related field with 2–5 years GMP/related experience.
• Ability to complete tasks with accuracy and efficiency.
• Proficient in MS Word, Excel, and Outlook.

Mansioni

• Provide on-the-floor Quality oversight within manufacturing and warehouse areas.
• Review and approve batch records and other controlled documents.
• Perform QA review of in-process results, environmental monitoring, and material release for incoming materials.

Conoscenze

Microsoft Word

Microsoft Excel

Microsoft Outlook

Formazione

Bachelor's degree in Life Sciences or related field

Strumenti

GMP training

Descrizione del lavoro

Grand River Aseptic Manufacturing (GRAM) seeks a Quality Assurance Specialist to support cGMP drug product manufacturing and testing. The role provides oversight for aseptic processes, deviation and CAPA systems, batch record review, SOP creation, and quality document reviews within the Quality Management System.

Non-negotiable requirements include a Life Sciences degree with 2–5 years GMP/related experience and proficiency in Word, Excel, and Outlook.