Biotechnology company is hiring a Quality Compliance Associate to support Quality Compliance processes including inspection readiness, self-inspection program, data integrity initiatives, and regulatory certification activities.
This is a 6-month contract.
Responsibilities
- Support or lead continuous improvement in quality systems (procedures and systems) to improve organizational effectiveness, quality assurance compliance, and regulatory and other requirements (cGMP, ICH).
- Adhere and follow cGMPs guidelines and procedures. Escalate non-compliance concerns to management.
- Interface with other departments (Manufacturing, Quality Control, Technical Development, Quality Assurance, etc.) and contractors as necessary.
- Interpret and apply 21CFR, USP, EP, JP and ICH regulatory guidelines and directives.
Qualifications
- Bachelors degree in a scientific discipline
- 4-6 years of experience in a biologics manufacturing environment
- Prior experience in Manufacturing, Quality Control, and Quality Management System processes.
- $27.49-$34.36 per hour
Why Choose R&D Partners?
As an employee, you have access to a comprehensive benefits package including :
- Medical insurance PPO, HMO & HSA
- Dental & Vision insurance
- 401k plan
- Employee Assistance Program
- Long-term disability
- Weekly payroll
- Expense reimbursement
- Online timecard approval
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering.
We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&D Partners is an equal-opportunity employer.
0704 Quality Compliance Associate
Support or lead continuous improvement in quality systems (procedures and systems) to improve organizational effectiveness, quality assurance compliance, and regulatory and other requirements (cGMP, ICH). Support Quality Compliance processes including inspection readiness, self-inspection program, d...
Quality Compliance Associate
Biotechnology company is hiring a Quality Compliance Associate to support Quality Compliance processes including inspection readiness, self-inspection program, data integrity initiatives, and regulatory certification activities. Support or lead continuous improvement in quality systems (procedures a...
Quality Compliance Associate
Support or lead continuous improvement in quality systems (procedures and systems) to improve organizational effectiveness, quality assurance compliance, and regulatory and other requirements (cGMP, ICH). Support Quality Compliance processes including inspection readiness, self-inspection program, d...
Quality Compliance Associate
Support or lead continuous improvement in quality systems (procedures and systems) to improve organizational effectiveness, quality assurance compliance, and regulatory and other requirements (cGMP, ICH). Support Quality Compliance processes including inspection readiness, self-inspection program, d...
Quality Compliance Associate
Support or lead continuous improvement in quality systems (procedures and systems) to improve organizational effectiveness, quality assurance compliance, and regulatory and other requirements (cGMP, ICH). Support Quality Compliance processes including inspection readiness, self-inspection program, d...
Quality Compliance Associate
Review executed batch records and associated documents to ensure compliance with approved procedures and cGMP expectations. Associate, QA Frontline (Overnight). Associate, QA Frontline (Overnight):. Respond to quality-related incidents or non-conformances on the floor and secure necessary documentat...
Quality Compliance Associate
Support or lead continuous improvement in quality systems (procedures and systems) to improve organizational effectiveness, quality assurance compliance, and regulatory and other requirements (cGMP, ICH). Support Quality Compliance processes including inspection readiness, self-inspection program, d...
Quality System Specialist II - Temporary
Working in Bio-Rad as a Quality Systems Specialist under the Northern California Quality Assurance Operations team, you will support manufacturing activities including investigations of product non- conformance and deviations, blocking of non- conforming material, batch record and CoA review and rel...
Quality System Specialist
Working as a Quality Systems Specialist under the Northern California Quality Assurance Operations team, you will support manufacturing activities including investigations of product non- conformance and deviations, blocking of non- conforming material, batch record and CoA review and release. You’l...
Regulatory Compliance Specialist
Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports).Review/approval of...