Upstream Biotech Manufacturing Associate - Night Shift

MedDeviceJobs; Juncos (PR); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Total rewards program

Retirement plan

Medical coverage

Stock incentives

Flexible work options

Job summary

Amgen in Puerto Rico seeks an Associate Manufacturing AML6 for the night shift to support 24/7 production of life-changing therapies. You will operate equipment, follow cGMPs, and collaborate with engineers and leads to maintain safety, quality, and throughput.

Ideal candidates hold a Bachelor's or related experience, are bilingual (English/Spanish), and can document activities accurately while following SOPs. Experience with GMP and data systems is a plus.

Qualifications

• Bachelor’s Degree required.
• Associate’s + 6 months manufacturing experience required.
• High school/GED + 2 years manufacturing experience required.
• Experience with GMP regulated manufacturing preferred.
• Good documentation skills and attention to detail required.
• Written and spoken English and Spanish capability preferred.

Responsibilities

• Operate manufacturing equipment per SOPs and post-training.
• Record activities and verify data in electronic systems.
• Adhere to cGMPs and safety protocols.
• Collaborate with engineers, mechanics, or leads for issues.
• Identify deviations and escalate per SOPs.
• Support investigations and root-cause analyses.

Skills

English

Spanish

Documentation

Attention to detail

Problem-solving

MS Office

Good communication

Education

Bachelor's Degree

Associate’s + 6 months Manufacturing work experience

High school/GED + 2 years Manufacturing work experience

Tools

SAP

SCADA

MS Office

CBT

Job description

Amgen in Puerto Rico seeks an Associate Manufacturing AML6 for the night shift to support 24/7 production of life-changing therapies. You will operate equipment, follow cGMPs, and collaborate with engineers and leads to maintain safety, quality, and throughput.

Ideal candidates hold a Bachelor's or related experience, are bilingual (English/Spanish), and can document activities accurately while following SOPs. Experience with GMP and data systems is a plus.