Top 98 Specialist ii, qa complaints Jobs in Columbus

Specialist II, QA Complaints
Hikma Pharmaceuticals PLC —Columbus, OH
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Paid parental leave
- Paid holidays
1d
Inventory Control Specialist 2
State of Ohio - Public Safety —Columbus, OH
- $23.65 an hour
- Full-time
- Background check
- Pass drug screening
- Mid-level
- Free parking
- Paid holidays
5d
IT Support Specialist II
THE VILLAGE NETWORK —Columbus, OH
- $60,000 - $65,000 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Paid holidays
- Paid time off
Quality Assurance Specialist - Complaints
BI Pharmaceuticals, Inc. —Columbus, OH
- Full-time
- Hybrid work
- Microsoft Word
- 7 years
- Microsoft Excel
QA Specialist - Virtual Hub
Gifthealth Inc —Columbus, OH
- $65,000 - $79,000 a year
- Full-time
- Remote
- Mid-level
- Communication skills
Quick Apply
8d
Claims Specialist II, First Party Medical
Branch Insurance —Columbus, OH
- $59,500 - $85,000 a year
- Full-time
- Remote
- Mid-level
- US work authorization
- In-person
- Health insurance
- Dental insurance
12d
Document Control Specialist II
HNTB Corporation —Columbus, OH
- $66,406.79 - $99,610.19 a year
- Full-time
- Mid-level
- Office
- 3 years
12d
Securities Operations Specialist I or II
State Teachers Retirement System of Ohio —Columbus, OH
- $30.98 - $39.21 an hour
- Full-time
- Pass drug screening
- Mid-level
- Office
- Free parking
- Health insurance
Quality Assurance Associate
The Axel Group LLC —Columbus, OH
- $50,000 - $60,000 a year
- Continuous improvement
- In-person
- Entry level
Quick Apply
3d
Retail Collections Specialist II Bilingual English and Spanish Required
JPMorganChase —Columbus, OH
- Weekends as needed
- Computer literacy
- Mid-level
- High school diploma or GED
- Health insurance
- Tuition reimbursement
Quality Assurance Supervisor - 3rd Shift
The Marzetti Company —Columbus, OH
- Full-time
- Bachelor of Science
- Mid-level
- Warehouse
4d
THCE Imaging Equipment Specialist II
Trinity Health —Westerville, OH
- Full-time
- Anatomy knowledge
- Hospital
- Customer service
Quick Apply
4d
QA Change Control Specialist II
American Regent, Inc. —New Albany, OH
- Overtime
- Microsoft Excel
- Mid-level
- Office
9d
Quality Assurance Specialist
Hims & Hers —New Albany, OH
- Full-time
- Remote
- Mid-level
- 3 years
- Analysis skills
- Employee stock purchase plan
- Health insurance
3d
IT Support Specialist II
WESTINGHOUSE OUTDOOR POWER EQUIPMENT —Columbus, OH
- Microsoft Outlook
- Research
- Mid-level
- Health savings account
- Disability insurance
Quick Apply
Grants Specialist (2 Positions)
State of Ohio - Public Safety —Columbus, OH
- $31.47 an hour
- Weekends as needed
- Background check
- Mid-level
- Office
- Free parking
- Paid holidays
Inventory Control Specialist 2 (PN 20015086)
State of Ohio - Health —Columbus, OH
- $23.65 - $24.27 an hour
- Full-time
- Background check
- Mid-level
- Microsoft Office
- Paid holidays
- Health insurance
Remote Physician Coding Specialist II
Mount Carmel —Columbus, OH
- Full-time
- Remote
- Surgery
- Mid-level
- High school diploma or GED
Claims Specialist II, First Party Medical
Branch Financial, LLC —Columbus, OH
- $59,500 - $85,000 a year
- Full-time
- Remote
- Mid-level
- US work authorization
- 1 year
- Health insurance
- Dental insurance
Quick Apply
12d
Pharmacovigilance Specialist I, II, III
Gifthealth Inc —Columbus, OH
- $68,000 - $92,000 a year
- Full-time
- Hybrid work
- Nursing
- Mid-level
- Bachelor's degree
Quick Apply

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Specialist II, QA Complaints

Hikma Pharmaceuticals PLC -
Columbus, OH

Apply Now

Job Details

Full-time
1 day ago

Benefits

Paid parental leave
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Vision insurance
Employee discount
Life insurance
Prescription drug insurance

Qualifications

High school diploma or GED
Pharmaceutical company experience
Manufacturing company experience
Customer complaint resolution

Full Job Description

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Description:
Job

Location: Columbus, Ohio

Job Type: Full time

Req ID: 12231

About Us:
As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our 32 manufacturing plants, eight R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.

Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Specialist II, QA Complaints to join our team.

In this role, you will be responsible for ensuring quality and compliance to regulations with respect to investigation of atypical events, i.e. Investigate and document atypical events – resulting in a recommendation of final disposition for goods, while identifying appropriate Corrective Action-Preventative Action (CAPA).

Key Responsibilities:
Conducts investigations on atypical events and documents accordingly to meet a Code of Federal Regulations requirement:

Locates the batch record
Interviews the people involved with the process in question
Documents all facts in the investigation form
Determine the root cause of atypical event and CAPA
Makes recommendations

Conducts meetings to discuss findings and obtain resolution/commitments from customers. Ensures agreement on investigation findings and appropriate CAPA has been identified with appropriate department.

Emails investigation form to possible involved personnel to ensure all required people are involved
Schedules meetings with appropriate personnel

Works directly with peer customers to resolve issues

Gather and document factual data that is used in written investigations to justify disposition of material
Interviews employee and asks questions about incident report

Recommends corrective actions as part of the atypical events investigation and follows up/becomes involved with department to provide guidance

Appropriate CAPA will help eliminate/minimize recurrence of atypical events
Sets up meeting with all affected departments
Determines appropriate CAPA

Makes recommendations with assistance of supervisor related to go/no-go decisions which impact production.

Keeps production moving with timely responses. Consult with supervisor to ensure knowledge is passed on, up and down the chain.
Assesses situation to determine if production should be continued or interrupted after an atypical event
Contacts managers to ensure all information is passed up and down the chain

Coaches and trains others on basic quality investigations for procedures and basic regulations

Ensure all parties involved understand why we have to do what we do
Conducts peer reviews of others investigator’s work
Answers any questions and directs fellow investigators

Writes/revises Quality Assurance Departmental Procedures, Standard Operating Procedures, and documentation to ensure compliance to requirements and efficient standardize practices.

Goes out on floor and researches step-by-step walkthrough of process
Conducts mock implementation
Recommends changes to procedures after investigations

Communicates clearly to peers, customers, and supervision. Communication is key to identifying root cause of the atypical event and appropriate CAPA

Communication imperative so that all operating units understand impact of atypical event at all stages of the investigation

Other duties as assigned

Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:

High school diploma or GED required, along with 3-5 years of experience in the pharmaceutical industry.
Strong verbal and written communication skills.
Excellent planning, organizational, and time management abilities.
Ability to adapt to changing priorities, deliverables, and work environments.
Proficiency in Microsoft Office applications, including Word, Excel, and Outlook.
Strong attention to detail with a commitment to accuracy, quality, and continuous improvement.

Preferred Qualifications:
Bachelors Degree in scientific or engineering discipline with 1-3 years of relevant experience in a Quality function.
Quality Assurance experience, including conducting reviews, identifying process gaps, and ensuring compliance with established standards.
Experience conducting investigations, analyzing information, documenting findings, and making objective, evidence-based recommendations.

What We Offer*:
Annual performance bonus, commission, and share potential
Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
A generous paid time off (PTO) bank ing with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
3 personal days (prorated based on hire date)
11 company paid holidays
Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
Employee discount program
Wellbeing rewards program
Safety and Quality is a top organizational priority
Career advancement and growth opportunities
Tuition reimbursement
Paid maternity and parental leave

Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.

Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma’s Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.

Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.

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Location:
Columbus, OH, US, 43228

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Nearest Major Market: Columbus

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Refine Your Search

specialist ii, qa complaints jobs in columbus

Specialist II, QA Complaints

Inventory Control Specialist 2

IT Support Specialist II

Quality Assurance Specialist - Complaints

QA Specialist - Virtual Hub

Claims Specialist II, First Party Medical

Document Control Specialist II

Securities Operations Specialist I or II

Quality Assurance Associate

Retail Collections Specialist II Bilingual English and Spanish Required

Quality Assurance Supervisor - 3rd Shift

THCE Imaging Equipment Specialist II

QA Change Control Specialist II

Quality Assurance Specialist

IT Support Specialist II

Grants Specialist (2 Positions)

Inventory Control Specialist 2 (PN 20015086)

Remote Physician Coding Specialist II

Claims Specialist II, First Party Medical

Pharmacovigilance Specialist I, II, III

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