Top 8 Collabera Jobs | SimplyHired

Adverse Event Specialist
Collabera —Mundelein, IL
- $28 - $30 an hour
- Contract
- Background check
- Mid-level
- 3 years
- Paid parental leave
- Paid holidays
Quick Apply
6d
Paralegal
Collabera —St. Louis, MO
- $70,000 - $100,000 a year
- Background check
- 5 years
- Microsoft Office
- Paid parental leave
- Paid holidays
Quick Apply
Switch Engineer
Collabera —Edgerton, KS
- $55,000 - $60,569 a year
- Contract
- Background check
- Pass drug screening
- Mid-level
- Paid time off
- Retirement plan
Quick Apply
6d
Refrigeration Technician
Collabera —Seattle, WA
- $27 - $35 an hour
- Full-time
- Background check
- Mid-level
- Ability to lift 50 pounds
- Paid time off
- Retirement plan
Quick Apply
6d

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Adverse Event Specialist

Collabera
Mundelein, IL

Quick Apply

Job Details

Contract
$28 - $30 an hour
6 days ago

Benefits

Paid parental leave
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Parental leave
Vision insurance
Life insurance

Qualifications

FDA submissions
Incident reporting compliance
Adverse event reporting
Complaint handling
Document review
Biomedical regulatory compliance
Regulatory submissions

Full Job Description

Title: Adverse Event Specialist

Location: Mundelein, IL (Onsite Tuesday–Thursday, Remote Monday & Friday)

Pay Range: $28/hr-$30/hr

Benefits:

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable

Details:

Looking for an Adverse Event Specialist to review and process new product complaints in a high-volume environment.

This individual will read and evaluate complaint narratives, determine reportability based on established procedures and regulatory requirements, and document findings accurately within the complaint management system.

The specialist will be responsible for managing approximately 50–60 complaints per day while maintaining quality, compliance, and productivity standards.

Must Haves:

3–5 years of experience in complaint handling, adverse event processing, or a related quality/regulatory function
Hands-on experience with MDR reporting, including knowledge of 21 CFR Part 803 and completion/submission of FDA Form 3500A
Experience reviewing new complaints and determining reportability
Ability to analyze and interpret complaint narratives and supporting documentation
Experience working in a high-volume environment, processing 50–60+ complaints per day
Experience working within regulated healthcare, pharmaceutical, or medical device environments

Job Requirement

Complaint handling
MDR
FDA
CFR

Reach Out to a Recruiter

- Recruiter
- Email
- Phone
- Vikas Sharma
- [email protected]

Work Location: In person

Quick Apply

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