Specialist, DS Manufacturing Programs

Job overview

The Specialist, DS Manufacturing Programs role is onsite in Juncos, PR. Compensation is not specified. The posting describes a six-month contract with possible extension and a Monday–Friday schedule, 8:00 AM–5:00 PM; overtime may be requested based on business needs. The role supports manufacturing and quality systems. The specialist helps maintain compliant, effective manufacturing operations by supporting process monitoring, investigations, corrective actions, validation, training, and new product introductions. The work contributes to process performance, documentation accuracy, and timely closure of quality issues.

What you'll do

• Initiate, revise, and approve manufacturing procedures
• assess process performance and improvement opportunities
• provide troubleshooting support
• assist with training materials
• support process monitoring parameters, data collection, deviation assessments, and quarterly reports
• triage non-conformances
• author investigation reports
• execute corrective actions and manage NC/CAPA closure
• review root-cause investigations
• support process validation and new product introduction activities
• assist with process or equipment modification projects.

What we're looking for

Skills & competencies

manufacturing programs

process support

quality systems

bioprocessing

gmp

process validation

capa

root cause analysis

juncos pr

monday–friday

8:00 am–5:00 pm

possible extension

Work arrangement

• Weekend coverage required

Benefits & perks

• Six-month contract with possible extension
• Monday–Friday, 8:00 AM–5:00 PM
• overtime may be requested based on business needs.

Why this role

The posting specifies a six-month contract with possible extension, weekday hours of 8:00 AM–5:00 PM, and possible overtime.

About the employer

BioPharma Consulting JAD Group is hiring for this role. Industry: Process, Physical Distribution, and Logistics Consulting Services. Sector: 54.