Date: 1 week ago
City: East Brunswick, New Jersey
Salary:
$55,000
-
$65,000
per year
Contract type: Full time

Job Description
Primary responsibilities of this role include the following:
Primary responsibilities of this role include the following:
- With Supervision, review documents/records and provide batch release authorization to 3PL service provider for products manufactured outside of the US.
- Support Drug Product Complaint management; forwarding to respective drug product manufacturing site and coordinate with corporate QA for investigations.
- Support Drug Product Recall/Field alert management.
- Assist with review of Quality Agreements.
- For applicable products, coordinate with Contract Testing Laboratories for Analytical Method Transfer activities, Drug Product testing, any OOS results, and test method issues.
- With supervision, review deviations/investigations related to Strides Pharma Inc. (Strides) frontend products.
- Assist with SOP management for Strides’ US corporate office.
- Support with quality matters for disposition of product returns.
- Assist during FDA inspections and local regulatory inspections at Strides’ US corporate office.
- Excellent verbal and written communication skills are necessary.
- With supervision and direction, effectively prioritizes competing tasks in a fast-paced and dynamic environment.
- Motivated, results driven with attention to detail, accuracy and clarity.
- BS degree in Pharmacy, Chemistry, Biology or Microbiology is preferred. 1-2 years of Quality Assurance or related pharmaceutical industry experience is preferred. Recent graduates will be considered for this role.
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