Quality Control Analyst I - Pharma Manufacturing

EPICUR; Mount Laurel Township (NJ); In loco; USD 23.000 - 32.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical Insurance

Dental Insurance

Vision Coverage

Life Insurance

401(k) with match

Paid holidays

Vacation

Descrizione del lavoro

Epicur Pharma in Mount Laurel, NJ is seeking a Quality Control Analyst I to ensure materials and finished drug products meet cGMP standards. The role involves material inspection, in-process checks, and accurate documentation in a fast-paced manufacturing setting.

Starting at $20/hour with bonus opportunities twice a year, the position requires PPE proficiency, teamwork, and strong communication skills. This full-time role offers competitive benefits and growth within our FDA-registered facility.

Competenze

• High school diploma or GED required.
• Familiar with cGMP and 21 CFR Parts 210 & 211 preferred, but not required.
• Ability to wear protective gear and follow gowning procedures.
• Strong communication, teamwork, and time-management skills.
• Must be punctual with low absenteeism and able to stand 8–10 hours.

Mansioni

• Perform quality inspection on incoming materials for drug manufacturing.
• Conduct in-process quality checks to ensure standards are met.
• Document inspection results and maintain samples and logs.
• Review batch records for quality release of finished product.
• Assist CAPA and change controls and participate in quality audits.

Conoscenze

Communication

Organizational Skills

Results Driven

Technical Capacity

Thoroughness

Formazione

High school diploma or GED

Descrizione del lavoro

Epicur Pharma in Mount Laurel, NJ is seeking a Quality Control Analyst I to ensure materials and finished drug products meet cGMP standards. The role involves material inspection, in-process checks, and accurate documentation in a fast-paced manufacturing setting.

Starting at $20/hour with bonus opportunities twice a year, the position requires PPE proficiency, teamwork, and strong communication skills. This full-time role offers competitive benefits and growth within our FDA-registered facility.