Randstad, in partnership with a leading global pharmaceutical company is hiring for production roles on 6-18 month contracts with permanent potential. Day & night shift available!
This involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments, depending on the particular department
Document/Record and Review cGMP data and information, revise or create documents as instructed.
Key documentation includes batch records validation protocols, SLRs, and equipment logbooks.
Working hours: 6:00 PM - 6:00 AM
highly detailed oriented with excellent documentation skills.
Your confidence will allow you to execute manufacturing processing steps following SOPs, and/or manufacturing support activities, and monitor the process against the batch record and control system.
You may coordinate or lead process steps once you are fully trained.
Attention to detail with excellent documentation skills
Team player and ability to work independently
Flexible and adaptable to changing needs
Bachelor's Degree in science and/ or a BioWorks certificate, and experience in pharma production, you will be performing and documenting daily manufacturing operations in a cGMP environment..
Targeted biopharmaceutical training (Bio-works or equivalent) and/or 4 year degree in a science and/or related military training
Able to work a 12-hour shift, night shift These positions operate on a 2-2-3 twelve-hour shift schedule, (6pm-6am with pay differential).
Ability to lift up to 50 lbs and stand for up to 3 hours at a time is required
Please apply for consideration!
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