Top 1 Quality assurance associate Jobs in Wilmington, Oh

Temp-QA Associate
Alkermes, Inc. —Wilmington, OH
- Full-time
- Psychiatry
- Computer literacy
- Mid-level

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Temp-QA Associate

Alkermes, Inc. -
Wilmington, OH

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Job Details

Full-time

Qualifications

Computer operation
Quality records maintenance
Document control experience within pharmaceutical industry
Monitoring compliance data
Pharmaceutical regulatory compliance
Computer literacy
Preventive action implementation
Drug regulation
Production deviation management
TrackWise
Quality control preventive actions
Corrective and preventive actions (CAPA)
Mid-level
Trend analysis
Manufacturing standard operating procedures
Bachelor's degree
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Computer skills
Quality control experience within pharmaceutical industry
Production batch record review
Leadership
Standard operating procedures (SOPs)
Team motivation (leadership skill)
Communication skills
Product quality failure
Standard operating procedures drafting
Pharmaceutical manufacturing facility experience

Full Job Description

Summary

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.

Essential Functions

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

Required Education and Experience

Requires a bachelor’s degree in a scientific discipline or equivalent experience.

Competencies

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.

Why join Team Alkermes?

Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.

We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.

Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.

Degree LevelBachelor's Degree

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quality assurance associate jobs in wilmington, oh

Temp-QA Associate

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