Job Description
NO C2C please
OPT stem OPT are welcome
What are the top 3-5 skills, experience or education required for this position:
• Masters in biomedical engineering
• Relevant educational experience or work experience in pharmaceutical field or product complaint field.
• Critical thinking, critical reading, and clear communication skills.
• Experience with the Microsoft suite of business programs (Outlook, Excel, Teams, PowerPoint, Word, etc).
• Ability to focus and prioritize work tasks.
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
OPT stem OPT are welcome
What are the top 3-5 skills, experience or education required for this position:
• Masters in biomedical engineering
• Relevant educational experience or work experience in pharmaceutical field or product complaint field.
• Critical thinking, critical reading, and clear communication skills.
• Experience with the Microsoft suite of business programs (Outlook, Excel, Teams, PowerPoint, Word, etc).
• Ability to focus and prioritize work tasks.
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
💡 Quick Summary
Seeking a career-building opportunity? The Quality Complaints Specialist position is now open for candidates interested in the Health Jobs sector. This role in Chicago offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Health Jobs is a plus.
