Website Pioneer Data Systems
Pioneer Data Systems
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Company : Pioneer Data Systems
Our client, a world-leading Pharmaceutical Company in Sanford, NC is currently looking for a Quality Assurance Associate to join their expanding team.
Job Title: Quality Assurance Associate / Change Management / Pharma Manufacturing
Duration: 12 months contract, extendable up to 36 months
Location: Sanford, NC
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
Quality Assurance Senior Associate
The position will support the Sanford, NC Quality Systems and Compliance department by performing Quality Assurance activities associated with clinical and/or commercial product.
Key responsibilities are performing Quality review/approval of clinical and/or commercial change management documentation for facilities/equipment/processes; planning and executing monthly/quarterly reports; suggesting improvements and conducting continuous improvement activities; and providing guidance/coaching to less experienced colleagues.
In addition, the position will be responsible for ensuring alignment with the Vaccines Quality Systems roles.
The successful candidate will be responsible for developing processes and procedures to perform these responsibilities.
This will require working collaboratively with cross-functional groups within the facility, at the Sanford site and across the Pharmaceutical network.
Responsible for review/approval of change controls, Engineering Change Management Requests, and proceduralized change SOP documentation for computer systems/equipment/processes
Provide support for other QA functions, e.g. quality investigation review
Interface with the Manufacturing Quality Operations team to ensure consistent approaches and sharing of best practices
Responsible for knowing, understanding, role modeling, and ensuring others follow Pharmaceutical’s values and culture
Support initiatives that contribute to building and strengthening the quality culture within the Facility. Practices and encourages quality cultural behaviors within both Quality and business lines
Act as SME for department to support site audits/inspections
Interface with other parts of the organization such as Global Quality Operations groups and Pharmaceutical Research and development groups.
Bachelor’s degree with a minimum 3+ years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry OR;
Master’s degree with a minimum of 1+ years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry
Previous experience with change management is beneficial
Experience with Drug Substance and Drug Product commercial manufacturing preferred
Experience with Standard Operating Procedures (SOP)
Experienced and proficient with Microsoft Word and Excel
Document management system experience
Ability to act as a team player with strong interpersonal skills
This is a fully onsite position in Sanford, NC