• QA Associate (Pharmaceuticals)

    Astrix Technology (Wilmington, OH)


    QA Associate (Pharmaceuticals)

     

    Quality Assurance

     

    Wilmington, OH, US

    Pay Rate Low: 25 | Pay Rate High: 30

    + Added - 02/10/2025

     

    Apply for Job

     

    Our client, a global leader in pharmaceutical manufacturing, is seeking a QA Associate to join their operations team. This will be a long term contract assignment of 12-18 months.

     

    **Pay Range** : $25-30/hr

    **Terms** : 12-18 month contract

    Job Description

    This function is responsible for disposition of bulk product and release of raw materials. Functions include document review, TrackWise reporting, hold form review, discrepancy tracking, status reporting, resolution and escalation of raw material delays.

     

    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 related tasks. Applies job related skills and understanding of policies and standards in completing tasks.

    Key Duties:

    + Evaluation of raw material records and testing records

    + Disposition of raw materials and bulk batches per associated specifications.

    + Approve and/or author intermediate level written procedures and other documents

    + Interact with plant personnel to insure CGMP compliance.

    + Provides back up for other QA and plant site personnel as appropriate.

    + The monitoring of compliance with the requirement of GMP

    + Ability to excel in a team environment

    Preferred Skills/ Abilities:

    + 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

    Preferred Personal Attributes:

    + 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

    Required Education/ Experience:

    + Bachelor’s degree in a scientific discipline or equivalent

    + 2+ years relevant experience in a Quality Assurance role in the pharmaceutical industry

    + Working knowledge of US Drug Product GMP requirements and associated guidelines

    INDBH

    We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.