Expert Level Manufacturing Technician - Glass Family of Companies

Opportunity Details

Expert Level Manufacturing Technician

JOB-10042284

Anticipated Start Date

August 5, 2024

Location

Berkeley, CA

Type of Employment

Contract to Hire

Employer Info

As a global leader in agriculture enterprise, our client is recognized for their multiple brands and renowned reputation.

Their research and development teams combine knowledge and ingenuity to create the most innovative ideas. With their cutting-edge products, they have a common goal : improved quality of life for all.

Job Summary

If you’re interested in an Expert Level Manufacturing Technician, then this is the best role for you. The Manufacturing Technician are responsible for clinical manufacturing of cell therapy DS / DP within the Cell Culture Technology Center (CCTC).

Collaborates closely with biological development (BD) and Manufacturing Science and Technology (MSAT) for new product introductions and ensure platform alignment.

Job Description

• Responsible for all aspects of clinical manufacturing in the following areas cell expansion, cell culture, differentiation, filling, visual inspection, solution preparation and weigh / dispense.
• Employee will move with the process and work seamlessly across all areas.
• Ensures all activities are performed to schedule.
• Manufactures products in various phases of product life cycles from clinical thru launch. Clearly understands, communicates, and manages differences in terms of documentation, sample handling, automation and cGMPs etc.

for different phases of product life cycle.

• Provide feedback to handles and troubleshoots single use technology (SUT) from end to end in manufacturing process.
• Works cross functionally to ensure process is controlled and issues are escalated and investigated.
• Redlines and reviews-controlled documents for various equipment / processes.
• Effectively employs all methods of communication (oral, written, presentation) to ensure knowledge and information transfer across shifts, to management, and cross functionally.
• Raises and supports investigation of deviations.
• Participates in safety investigations for CCTC and always promotes safe behaviors.

Skills Required

• Must have minimum of 2+ years' experience.
• Responds easily to last minute changes to production schedule.
• Demonstrates strong tendency towards independent thinking and decision making.
• Able to make logical decisions independently for multiple process work streams with limited information or supervision available.
• Ability to lift 45 lb.
• Transferable skills will be considered or an equivalent combination of education and experience.
• Works with highest level of flexibility.
• Must be Experienced in cGMP and GDP requirements for pharmaceutical manufacturing.
• Preferences : Experienced with data integrity, regulatory, requirements for pharmaceutical manufacturing.Experienced in operation of bag filler, pumps, BSCs, welders / sealers, environmental monitoring equipment.

Experienced with business IT systems (Delta V, SAP etc. ).Experienced with Microsoft Office. Excellent computer skills.

Education / Training / Certifications

Minimum of BS in science related field is preferred.

Additional Requirements

• Must be able to pass drug screen and criminal background check.
• Must be able to change shift schedule based on business and process needs.
• Must provide off-hour (night and weekend including holiday) coverage to meet business requirements on short notice.
• Shift : 7 : 00 AM.

Pay Rate / Salary

Estimated Salary : $30.00 to $38.00 per hour based on qualifications.

We are an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity or any other factor protected by applicable federal, state, or local laws."