Manufacturing Technician III / Laboratory Technician III

PSG Global Solutions; La Verne (CA); On-site; USD 45,000 - 60,000; Full time

Job summary

A leading biotechnology firm is seeking a Manufacturing Technician in La Verne, CA. This role requires 3-5 years of experience in pharmaceutical manufacturing, with a focus on aseptic processing and equipment operation. Responsibilities include performing routine assignments as well as more complex tasks, maintaining documentation, and ensuring compliance with good manufacturing practices. An excellent opportunity to contribute to innovative biotechnological processes within a confidential work environment.

Qualifications

• 3-5 years of experience required in manufacturing, preferably in pharmaceutical or biotechnology.
• Experience with aseptic processing and equipment operation is essential.

Responsibilities

• Work on routine assignments following established procedures and good manufacturing practices.
• Perform complex tasks related to aseptic processing and equipment operations.
• Maintain documentation related to assigned work and manufacturing processes.

Skills

Pharma Experience

Aseptic Processing

Equipment Operation

Troubleshooting

Tools

Oracle

MES

Cleanroom Equipment

Job description

Company Description

Prominent Biotechnology Company

Job Description

JOB TITLE: Manufacturing Technician

CLIENT: A prominent Biotechnology Company.

CONTRACT: 6 months initial contract - with a possibility of extension - possibility to be an employee based. (05/15/2017 to 11/10/2017)

LOCATION: La Verne CA USA 91750

Pay: To be discussed over the phone

First Shift: 8:00am to 5:00pm

PHARMA Experience required / Degree Optional

Mandatory 3-5 years experience required

• Works on basic to routine assignments following established Standard Operating Procedures (SOPs), Master Batch Records and current Good Manufacturing Practices (cGMPs).
• Performs moderately complex tasks associated with aseptic processing, dispensing, compaction, granulation, milling and coating.
• Reports to Team Lead on a regular basis on line performance and reports any issues that need to be resolved.
• Performs more complex troubleshooting unassisted; works on more complex manufacturing processes and assignments; assembles, disassembles and operates aseptic filling equipment and lyophilizer autoloading equipment in classed cleanroom environments.
• Prepares equipment and components for sterilization; operates processing equipment including autoclaves, ovens, vial washers, and depyrogenation tunnel.
• Cleans (manually and clean-in-place) and assembles equipment for production; performs clean-in-place and sterilization-in-place of tanks.
• Performs annealing and sterile filtrations of products.
• Operates vial capper, unloads product from lyophilizers, and packs off unloaded vials from lyophilizers and liquid fill line; performs detailed /Oracle and MES transactions in resolving inventory discrepancies.
• Cleans manufacturing areas, including walls, ceilings and floors; creates purchase orders for consumables.
• Completes and maintains documentation related to assigned work, including logbooks and batch records.
• May act as point of contact for a compliance audit; operates drum coater and compression equipment; dispenses ingredients for batches.
• Performs MBR Manufacturing batch report updates.
• Performs manual handling of product loads and unloads tablets.

Additional Information

All your information will be kept confidential according to EEO guidelines.