QA Specialist I

QA Specialist I#26-09886 North Chicago, IL All On-site Job Description What are the top 3-5 skills, experience or education required for this position: 1. Bachelor's Degree in a relevant field of study. 2. Relevant educational experience or work experience in pharmaceutical field or product complaint field. 3. Critical thinking, critical reading, and clear communication skills. 4. Experience with the Microsoft suite of business programs (Outlook, Excel, Teams, PowerPoint, Word, etc). 5. Ability to focus and prioritize work tasks.

Onshore or Offshore Position:

Onshore. Must be able to commute 3 days a week (Tuesday to Thursday) to office in Waukegan, Illinois. Individual will work in global quality organization processing pharmaceutical, medical device and combination product complaints and inquiries. Interface with internal customers such as physicians, nurses, pharmacists, hospital personnel, risk managers, purchasing agents, sales representatives, general public, manufacturing sites, technical support, commercial organization and PV regarding product complaints. Responsible for product complaint documentation, investigations and identification of potential adverse events and potentially reportable events. Responsibilities may include creation and submission of regulatory reports, creation of customer communications and interface with various third parties.

Responsibilities:

• Assure complaint records meet global requirements.
• Product complaint documentation, investigation, and review of all non-medical complaint content. Responsible for reviewing Medical complaints that involve a non-medical quality related problem. Provide quality customer service through coordination of return samples for investigation and follow up activities such as replacement of product.
• Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GCP. This requires good analytical skills, technical writing and good documentation. Responsible that complaint files meet all regulatory requirements.
• Identification of potentially reportable events and notification to appropriate functional groups and management.
• Interface with Third Party Manufacturers, health care professionals, general public, internal customers, functional areas and regulatory agencies.

Qualifications:

• Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products.
• Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred.
• Ability to prioritize multiple projects to ensure compliance with regulations and standard operating procedures is preferred.
• Solid written/verbal communication and organizational skills.
• Knowledge and application of computer systems for word processing and complaint management.
• Ability to work with cross-functional teams and to interact effectively with peers, management, and customers.
• A Bachelor Degree required. Preferred degree in technology or scientific background (MLT, LPN, RN).
• 0-3 years' work experience in a cGMP related industry or in a clinical setting is preferred Work Schedule (Define days,# of hours)/ Is Overtime offered or required?

M-F 8-4:30/5

EEO:

"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."