Job Description

We are looking for recent graduates as well as those already in employment who are looking for advancement within the pharmaceutical manufacturing industry. In addition to working on manufacturing production lines, the individuals will be responsible for supporting the cGMP facility by performing equipment qualifications, maintenance, and calibration. Individuals will be actively involved in the review of Standard Operating Procedures, Batch Records, and documentation to enhance processing.

Responsibilities:

Comply with Current Good Manufacturing Practices (cGMP) Comply with company Standard Operating Procedures (SOP) Execute against Batch Records Dispense raw materials Blend materials using Process Analytical Technology (PAT) Operate, maintain, and troubleshoot equipment including: tablet presses, fluid beds, roller compactors, granulators, extruders, capsule fillers, and granulators Complete initial and on-going trainings

Keys to Success:

Be a self-starter capable of working with minimal oversight Create value for the position, the department, and our client Prioritize proactive Quality by Design, ensuring problems are anticipated and addressed before they arise Understand and participate in prevention and be able to improve systems and procedures Adapt and excel in a fast paced and dynamic environment. Know how to prioritize activities appropriately Possess a strong understanding of quality practices Demonstrate expertise in your role

Candidate Requirements:

Ability to work on-site 6am to 4pm Monday through Friday (50 hours per week) Pass a background and credit check Minimum education of a Bachelor's Degree or 3 years of related work experience Ability to demonstrate excellence in one or more technical skills

Benefits:

Competitive salary Performance-based bonus structure Company-paid comprehensive medical and dental care Company-paid life insurance 401(k) retirement savings with company match
Job Type: Full-time

Pay: $80,000.00 - $100,000.00 per year

Work Location: On the road