Temp-QA Associate

Alkermes • Wilmington, OH

29d

About The Position

This function is responsible for supporting the daily activities related to the investigations of product complaints. Functions include investigating, batch record review, discrepancy identification, logbook review, and TrackWise Digital trending. This function manages events with Senior Associate for approval of the complaint records. The position will perform general QA work, using their ability as a skilled contributor in completing tasks where judgement is required in resolving problems and making recommendations. Works on problems of a diverse scope where analysis and problem solving is required. Receives general oversight and guidance on approaches to complete project related tasks. Applies job related skills and understanding of policies and standards in completing tasks.

Requirements

• Requires a bachelor's degree in a scientific discipline or equivalent experience.
• Working knowledge of US Drug Product GMP requirements and associated guidelines.
• Experience in Pharmaceutical Quality Assurance, including the ability to identify and resolve compliance issues.
• Ability to increase others knowledge of US end European GMP regulations and guidance.
• Strong written and oral communication skills.
• Experience in administration of quality systems for drug product manufacturing and quality control operations.
• Strong written and oral communication skills.
• Team Player committed to quality; motivated self-starter; detail and results oriented; Well organized, efficient worker with good communication skills; innovative thinker and problem solver; flexible and can embrace change; can manage multiple duties and tasks.
• Ability to utilize knowledge and interpersonal skills to provide leadership, direction and development of others
• Good computer skills.
• Good work ethic, dependable, punctual, and flexible.
• Good motivator of personnel.
• Good team player with a can-do attitude.
• Can get things done on the basis of influence.
• Can work in a fast-paced environment with multiple issues open simultaneously.
• Highly organized.
• Attention to detail.
• Identifies opportunities to improve and contributes to problem solving.

Responsibilities

• Authority to approve written procedures and other documents
• Develop Standard Operating Procedures and other quality related documents.
• Evaluation of batch manufacturing records and testing records
• Follow-up on preventive and corrective actions associated with deviations
• Interact with plant personnel to insure CGMP compliance.
• Prepare and maintain trend analysis
• Provides back up for other QA and plant site personnel as appropriate.
• The monitoring of compliance with the requirement of GMP
• Investigate complaints

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Chemical Manufacturing
• Number of Employees: 1,001-5,000 employees