NOI Investigations Specialist
Amneal Career Sites
NOI Investigations Specialist
About this role
Description:
The NOI Investigations Specialist plays a critical role in ensuring product quality, compliance, and patient safety by conducting comprehensive investigations into quality events that may impact the manufacturing, release, distribution, or shelf life of commercial products. Leveraging strong analytical, technical, and interviewing skills, this individual independently and collaboratively gathers and evaluates data, identifies root causes, assesses product impact, and develops effective corrective and preventive actions (CAPAs) to prevent recurrence. The role requires sound judgment in determining product disposition, with decisions potentially affecting regulatory commitments, business performance, customer satisfaction, and product availability. The specialist is responsible for clearly documenting and communicating investigative findings, supported by scientific rationale and factual evidence, in a manner that withstands scrutiny from regulatory agencies, customers, and auditors. By reviewing manufacturing, testing, storage, handling, and distribution activities to ensure compliance with established requirements and quality standards, the NOI Investigations Specialist serves as a key contributor to continuous improvement efforts and the organization's commitment to delivering safe, effective, and high-quality products.
Essential Functions:
- Perform investigations independently to assess aberrant events impacting product quality that could prevent product release. Performs interviews and schedule follow-up meetings in response to investigations.
- Perform gap assessments and root cause analysis evaluations to determine RISK level utilizing root cause analysis tools such as FMEA, wishbone and/or 5 Why tools.
- Directly supports the business through schedule/timeline adherence of NOI closures to allow for timely ANDA submissions, new product launches, and batch releases.
- Recommend quality process improvements to increase efficiencies and performance of systems, operations and personnel and prevent reoccurrence of incident or event.
- Writes investigation reports in a clear and concise manner to withstand regulatory scrutiny, with sufficient detail to support decisions drawn and actions taken to resolve an event.
- Identify and resolve objectionable GMP issues which may impact product quality and escalate the issues to supervisor in a timely manner.
- Ensure all work is performed and documented in accordance with existing Company policies and procedures, as well as GMP and health and safety requirements in the markets where product is sold.
Additional Responsibilities:
- As required, adhere to gowning and safety protocols by wearing appropriate personal protective equipment (PPE) to maintain product quality, environmental compliance, and personal safety.
- Applies technical expertise and professional judgment to determine CAPA effectiveness, ensuring deficiencies are identified, communicated, and addressed through appropriate management channels.
Education:
- Bachelors Degree (BA/BS) Science or Engineering, Quality Management or related field - Required
Experience:
- 3 years or more in Working in the Pharmaceutical or Medical Device industry
- 3 years of Experience working in GMP/FDA regulated environment
- 3 years on Hands on experience in a production
Specialized Knowledge:
- Use of Risk Assessment tools
The base salary for this position ranges from $75,000 to $95,000 per year. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities.
Frequently Asked Questions
What is the salary for the NOI Investigations Specialist role at Amneal Career Sites?
The listed salary for this NOI Investigations Specialist position at Amneal Career Sites is USD 75K–95K. This is an Full time role.
Where is the NOI Investigations Specialist position at Amneal Career Sites located?
This NOI Investigations Specialist role at Amneal Career Sites is based in Piscataway, NJ, United States. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the NOI Investigations Specialist role at Amneal Career Sites full-time or part-time?
This is listed as a Full time position. It is posted as a NOI Investigations Specialist role at Amneal Career Sites.
How do I apply for the NOI Investigations Specialist position at Amneal Career Sites?
Click the "Apply Now" button on this page. You will be redirected to Amneal Career Sites's official application portal hosted on oraclecloud where you can submit your application directly.
When was the NOI Investigations Specialist job at Amneal Career Sites posted?
This NOI Investigations Specialist position at Amneal Career Sites was posted on Jul 13, 2026. Apply as soon as possible — early applications are often reviewed first.
NOI Investigations Specialist
Amneal Career Sites · 💰 USD 75K–95K
You'll be redirected to Amneal Career Sites's official application page on oraclecloud.