Manufacturing Associate I

Job Title: Manufacturing Associate I

Job Location: Fremont, CA

Job Type: Contract

Pay Range: $19.51hr - $24.51hr

Job Overview:

The candidate executes routine unit operations in Manufacturing Assembly and Packaging as assigned related to the manufacturing of drug product in a multi-product facility. This role performs duties under limited supervision and according to standard operating and manufacturing procedures, assisting senior staff in performing assembly and packaging in designated functional manufacturing areas.

Duties:

• Executes routine unit operations in Manufacturing Assembly and Packaging as assigned related to the manufacturing of drug product in a multi-product facility.
• Performs duties under limited supervision and according to standard operating and manufacturing procedures.
• The candidate is responsible for assisting the Senior Associate and Master Associate in performing assembly and packaging in designated functional manufacturing area.
• Support with troubleshooting to equipment.
• Assists in the setup of the automated autoinjector assembly machine, pre-filled syringe assembly machine and semi-automated tabletop machine. This assistance includes tasks such as gathering tools, machine parts and documents required for such activities. Retrieves components and equipment from storage.
• Assists with the equipment changeover.
• Assists with minor equipment repairs and adjustments.
• Assists with real-time identification and correction of problems. Problems may include, but are not limited to mechanical issues and component issues.
• Performs all work in accordance with Company Policies and Procedures. All work is documented in controlled documents (batch records, logbooks or SOP attachments) in accordance with SOP. All activities are to be documented in the batch record. All events are to be recorded in the batch record and brought to the attention of the production supervisor for further action.
• Assists with room cleaning in production areas. The candidate will transfer rubbish to the transfer zones and may empty transfer zones of rubbish when required. This includes removal of equipment, room sanitization and disposal of waste according to established safety requirements.
• Responsible for following controlled documents to ensure that the equipment identified for operations are used and documented. This includes verification of equipment calibration. Completes logbooks, as required.
• Responsible for performing assembly and packaging operations and assisting in visual inspection or filling operations, if required.
• Ensures components, materials and supplies are stocked prior to the start of the assembly and packaging operations.
• Movement of product and components within the assembly and packaging area.
• Transfer product, components and equipment within the CNC area.
• Communication and hand-off to relief personnel during shift change as appropriate.
• Maintains production areas according to predefined standards (5s).
• Adheres to safety standards, identifies unsafe situations or habits, and escalates appropriately.

Skills:

The position requires concentration as errors might cause minor to moderate delays, confusion, or expense to correct. The position has some contact with other departments and the candidate must be able to discuss issues and ideas with an open mind and even temper.

Level of Proficiency - Entry level in subject matter.

Attendance / Schedule - The schedule is dependent on the shift for which the candidate is hired. Attendance requirements are based on general attendance policies.

• Demonstrated ability to be organized and work well in small work groups.
• Demonstrated mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions.
• Detail-oriented. Demonstrated ability to read, comprehend, and follow written instructions.
• Strong verbal and written communication skills.
• Must be able to work in a team environment.
• Experiences in related GMP environment within biotechnology or pharmaceutical industry strongly preferred.
• Must be able to learn and perform basic computer operations such as MS Office and Outlook and other computer-based software.
• Must obtain and maintain qualifications, as required, to perform the assigned work.
• Must understand, will be held accountable for and must adhere to all SOPs, company Policies and Procedures.
• Must adhere to proper technique, proper documentation practices, and all other aspects of the cGMPs.

Education:

• High School degree plus minimum one (1) year work experience in a GMP-regulated industry.
• Associate or Bachelor s degree from an accredited institution or biotechnology vocational training preferred.

Physical Requirements(Due to nature of job, The candidate must have):

• Ability to perform almost constant standing.
• Ability to walk for prolonged periods.

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• Medical, Dental, and Vision Insurance
• 401(k) Retirement Plan
• Health Savings Account (HSA)
• Disability Insurance (Short-Term and Long-Term)
• Life and AD&D Insurance
• Paid Sick Leave (where required by applicable state or local law)
• Supplemental Insurance Plans
• Identity Theft Protection
• Pet Insurance
• Employee Wellness Programs
• Employee Assistance Program (EAP)
• Career Growth and Professional Development Opportunities