Schedule:
- M-F 8:30am-5:00pm
- May be required to work on holidays or scheduled manufacturing shutdowns to support business needs.
- This is a 24-month contract.
Responsibilities
- Perform Sample Management aspects (sample receipt, control, and disposal of samples).
- Perform stability study protocol generation.
- Perform stability and reference standard pulls.
- Maintain stability, lot release, reserve, retention sample inventory.
- Perform preventative maintenance on stability/sample chambers.
- Perform domestic and international shipments of samples and critical materials.
- Participation in laboratory project initiatives such as 5S, LEAN, and Six Sigma.
- Participate in inspection readiness, regulatory inspection support and self-inspection activities.
- Perform Quality System attributes such as but not limited to (i.e. Minor Deviations, CAPAs, Change Controls, Action Items).
Qualifications
- Associates degree required; Bachelors degree in science preferred.
- 1+ year of cGMP/GLP laboratory experience; quality control experience is preferred.
- Ability to follow written instructions and to perform tasks with direct or minimal supervision.
- Familiarity with use of a computer: e.g., Proficient in Windows, Microsoft Word, Excel.
Salary
Why Choose R&D Partners?
As an employee, you have access to a comprehensive benefits package including:
- Medical insurance, Dental and Vision insurance
- Sick Pay
- 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.