Manufacturing Technician - II

Job Description

Immediate need for a talented Manufacturing Technician - II . This is a 06+months contract opportunity with long-term potential and is located in Oceanside, CA(Hybrid). Please review the job description below and contact me ASAP if you are interested.

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Job ID:26-31448

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Pay Range: $28 - $31/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

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Key Responsibilities:

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• Execute manufacturing processes under supervision, adhering to batch records, standard operating procedures (SOPs), and Current Good Manufacturing Practice (cGMP) regulations.
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• Ensure right-the-first-time performance for all process steps and promote a safety-first culture.
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• Collaborate with Manufacturing Science and Technology (MSAT), Facilities and Engineering (F&E), and Quality departments during GMP runs.
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• Perform weighing of raw materials and electronic inventory transactions using Manufacturing Execution Systems (MES) and Enterprise Business System (EBS).
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• Conduct cell culture and filling unit operations for viral vector products in a cGMP environment, employing proper aseptic techniques and Good Documentation Practices (GDP).
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• Maintain mammalian cell culture in flasks, CellSTACK chambers, and single-use bioreactor systems.
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• Assist with the transfection of cells and the harvest of viral vectors, as well as the manual and/or automated filling of harvested materials.
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• Escalate processing and equipment issues as necessary and assist in the revision of SOPs and Manufacturing Production Records (MPRs).
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• Review in-process cGMP documentation for completeness, accuracy, and compliance.
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• Work effectively in an inclusive, cross-functional, team-based environment and be available for off-shift hours and weekends.
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• Perform additional duties as assigned.
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Key Requirements and Technology Experience:

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• 2+ years of experience in a manufacturing or laboratory setting.
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• Strong understanding of cGMP regulations and Good Documentation Practices (GDP).
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• Familiarity with Manufacturing Execution Systems (MES) and Enterprise Business System (EBS).
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• Ability to work collaboratively in a team-oriented environment.
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• Nice to have: Experience with viral vector manufacturing processes and cell culture techniques.
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Our client is a leading Biopharmaceuticals Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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