Position Details :
Our client, a world-leading Pharmaceutical Company in Rocky Mount, NC is currently looking for an Quality Associate to join their expanding team.
Job Title : Quality Associate / Pharma Manufacturing
Duration : 18 months contract, extendable up to 36 months.
Location : Rocky Mount, NC
Hybrid Role : must go onsite 2-3 days / week
Note :
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description :
The Annual Product Record Review Associate is responsible for writing Annual Product Record Review (APRR) s according to pre-approved calendar, company procedures and our Quality Agreements.
The job duties include, but are not limited, to the following :
Establish the product matrix and the APRR calendar
Gather the required data and write APRR s according to the calendar
Analyze trends, make recommendations based on the data in order to improve processes or tools
Send approved s to clients according to applicable Quality Agreements
Must be able to work and communicate effectively with all levels of people within the other Pharmaceutical sites
Must be able to work and communicate effectively with all levels of people within the Pharmaceutical organization.
Must be able to work and communicate effectively with all types of suppliers to help resolve issues
Education
Bachelor’s Degree with 2+ years working in a GMP FDA regulated environment
Minimum of 1 years of experience in one or more of the following :
Quality Engineering / Compliance / Regulatory Affairs
Manufacturing / Technical experience in Pharmaceutical or GxP regulated environment
Technical Skills
Strong analytical skills and ability to summaries vast amounts of data
Capacity to manage several projects at a time
Knowledge of the local & international regulatory requirements and Quality Management standards & systems
Strong organizational, presentation, meeting facilitation and technical writing skills.
Possess attention to detail and good communication skills as verbal and written feedback to departments is required when issues are discovered during auditing.
Strong computer proficiency skills in MS Office, Word, Excel, Project, Trackwise (ER / LIR), and Empower LIMS System or equivalent.
ASQ Certification preferred.
Physical Position Requirements
Ability to work extended hours, especially during health authority inspections, assessments and audits.
Allow for flexibility in shifts to accommodate ad-hoc assignments on an as needed basis
Hybrid (Will need to Adhere to RETURN TO SITE POLICY)
Hard Skills :
Strong analytical skills and ability to summaries vast amounts of data
Capacity to manage several projects at a time
Communication (Verbal / Written)
Strong computer proficiency skills in MS Office, Word, Excel, Project, Trackwise (ER / LIR), and Empower LIMS System or equivalent.
Work Independently
Scientific Background
Soft Skills :
Team Environment (previously worked / works well in)
Meet aggressive timelines (provide examples of)
Adaptable to new challenges (Prioritize)
Interview : 1st – Phone Screen
1st – Phone Screen
2nd – WebEx
Hybrid (Will need to Adhere to RETURN TO SITE POLICY)
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