Address
Form of workImmediate need for a talented Global Product Quality Complaints Associate. This is a 5+Months contract opportunity with long-term potential and is located in New Brunswick, NJ(Hybrid). Please review the job description below and contact me ASAP if you are interested.
Job ID: 23-18612
Pay Range: $20 - $25.64/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Responsibilities:
- Support the Global Product Quality Complaint (PQC) process for the biosterile, pharmaceuticals and combination drug/device products with respect to Product Quality Complaints.
- Analyze, identify and execute continuous improvement initiatives within the process while collaborating within the PQC headquarters team as well as with key stakeholders, including internal and external sites and in-market supply chain quality.
- This individual will be a valued team member of one of several cross-functional, multi-divisional teams which are responsible for developing and executing Global Quality Systems (GQS) initiatives and strategies for Client, with focus on the global PQC process.
- Provide ongoing management for PQCs ensuring compliance to global framework of GMP policies and Client procedures
- Support the Global Product Quality Complaint (PQC) processing activities at PQC Headquarters.
- Participate in PQC HQ team meetings for the processing of, and improvements to, global Client PQC processes,
- including but not limited to: PQC case intake, triage, due diligence activities, product replacements and patient
- reimbursements/refunds; metrics generation and slide presentation; PQC training delivery and management;
- new product launches; PQC related Quality Management System (QMS)
- Support tracking, trending and other ancillary activities for controlled documents (SOPs/Job Aids/Templates);
- record archivals; quality deviations and CAPA involving PQC HQ and provide quality and compliance support for these processes.
- Assist in implementation of Quality Risk Management principles in evaluation and investigation of PQCs.
- Support PQC related audits and inspections as necessary. Participate in QMS business process requirements development and validation activities as necessary.
- This opportunity is cross functional and will involve the management of mid-size projects between PQC HQ and
Key Requirements and Technology Experience:
- BS/BA in Sciences (i.e Chemistry, Biology, Biochemistry, Microbiology, Pharmacy), engineering, business.
- Enrolled in Bachelor's, Masters or MBA degree program. Preferred Completion of Bachelors and enrolled in graduate studies.
- Microsoft Office (Power point, Excel, Word, Outlook)
- Project Management expertise with advanced PowerPoint preferred
- Basic statistics/analytics; clear communications
- Ability to manage deliverables within target timelines
- Must have strong analytical, interpersonal, communication, organization, and project management skills and passion to learn and grow within the biopharmaceutical industry
Our client is a leading Telecom organization and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
#DEL
