Salary: Competitive salary is offered based on qualifications and experience.
Job Description:
This position is responsible for ensuring the proper disposition of raw materials and compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Standard Requirement Documents. As an Associate QA Specialist in the Raw Materials department, a typical day may include reviewing release data, preparing release documentation, and completing vendor raw material releases. Additionally, this role involves performing AQL visual inspections, managing QA requirements of SCAR processes, supporting supplier quality, and initiating, editing, reviewing, and approving change control and SOPs. The individual in this position will also perform compliance monitoring of area operations and notify relevant teams of any observed non-compliance.
Required Skills and Qualifications:
To be successful in this role, you should have excellent written, oral, and interpersonal communication skills. You should be able to effectively interact with a broad spectrum of audiences and have strong GMP knowledge. A Bachelor's degree in Life Sciences is required, and 0-2 years of related industry experience is preferred.
Benefits:
We offer a comprehensive benefits package, which includes health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels. Regeneron is an equal opportunity employer and provides reasonable accommodation to known disabilities or chronic illnesses of otherwise qualified applicants for employment.
Others:
The Company conducts background checks as part of the recruitment process to verify certain information regarding candidates prior to commencement of employment.