Biotechnology company is hiring a part time hybrid Data Coordinator on a 12-month contract to create, revise, and implement procedures, best practices for the Biologics Process Validation program. 20-25 hours per week hybrid schedule.
Responsibilities
- Act as a Project Manager to track and monitor Process Validation progress and deliverables.
- Coordinate Process Validation documentation: Prepare, edit, proofread, coordinate and adjudicate reviewer comments with author and subject matter experts.
- Perform Data Verification of completed Process Validation studies and reports.
- Create study templates to drive alignment.
- Work across Quality Assurance, Process Development, MSAT, and Contract Manufacturing Organizations.
Qualifications
- Bachelor's degree in life sciences or related field.
- 4+ years of experience in biotechnology, process validation, Quality or related field.
- Must have understanding and application of GMP principles, concepts, and practices.
- Knowledge of biochemical and manufacturing process and terminology.
- Knowledge and experience in process validation in highly regulated manufacturing environments.
- Strong quality mindset and project management skills.
Pay:
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.