Manufacturing Associate

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 PMRS

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 matchCompany Description

Pharmaceutical Manufacturing and Research Services Inc. (PMRS) provides cGMP contract manufacturing and analytical services for drug products in all stages of development, from early clinical development to commercial production. Our streamlined processes facilitate timely production of the highest quality products at the lowest possible cost.

Full-time