Manufacturing Associate - Pharmaceutical Manufacturing Day/Night Shift

SRG; Vacaville (CA); On-site; USD 27,552 - 41,328; Full time

Job summary

A leading pharmaceutical company in Vacaville is looking for a full-time Manufacturing Associate. The role involves upstream and downstream manufacturing processes, including the operation of fixed vessel systems and compliance with cGMP standards. Candidates should possess a relevant college degree and laboratory experience. This position offers a contract role with flexibility for day or night shifts.

Qualifications

• Candidates must have a college degree in the Sciences.
• Experience as a manufacturing technician is preferred.
• Knowledge of GMP practices is a plus.

Responsibilities

• Perform cleaning, sterilization, and operation of fixed vessel systems.
• Operate and clean filtration systems.
• Prepare materials for production.
• Comply with cGMP and SOP guidelines.

Skills

Cell culture laboratory experience

GMP knowledge

Education

College degree in the Sciences

Job description

Overview

Manufacturing Associate - Pharmaceutical Manufacturing Day/Night Shift — SRG. The role is a full-time, contract Manufacturing Technician to join our client\'s pharmaceutical manufacturing team in Vacaville, CA.

This is a W2 contract only.

Candidates must be available to work either the day shift or the night shift.

Must Haves

• A college degree in the Sciences with cell culture laboratory experience or previous experience working as a manufacturing technician or in a laboratory
• GMP knowledge is a plus

Responsibilities

• Upstream Manufacturing (UM): Primary focus is the cleaning, sterilization and operation of fixed vessel systems for media preparations, etc in the laboratory
• Downstream Manufacturing (DM): Responsibilities include the operation and cleaning of fixed tank systems, the operation and cleaning of filtration systems, etc.
• Operate systems that clean and sterilize tanks and filtration systems.
• Prepare materials for the production process.
• Comply with cGMP, SOP and manufacturing documentation.
• Use automation to perform production and equipment operation

Only candidates selected to be moved forward in the recruitment process will be contacted by SRG\'s Recruitment Team to schedule a conversation.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting [e-mail] or fill out this form to request accommodations.

Seniority level

• Entry level

Employment type

• Contract

Job function

• Manufacturing, Research, and Science

Industries

• Pharmaceutical Manufacturing