On-site, with occasional remote available.*. The candidate will perform downstream process development activities for a vaccine-related drug substance
Onsite. 35 hours per week Mon-Fri 9am- 4:30pm -OR- 8am-3:30pm. Review Emails for bills & payment notices. Enter bills into online bookkeeping system.
The incumbent is responsible that all finished goods are packed in accordance with specifications and for completing all packaging documentation required before
Position is day shift, but candidates should be flexible to work 2nd shift if required.*. The Training & Development Specialist is responsible for the
Keeps premises of account in clean and orderly condition to meet Clean All Services standards. Empty trash and replace liners. Empty and wipe ash trays.
Prepare laboratory reagents, solutions, and culture media. Perform lab-scale upstream processing of vaccine products and process intermediates (including
The Raw Material Testing group is seeking an enthusiastic Research Associate to act on development and execution of critical raw material performance testing
QA SHOP FLOOR SPECIALIST 1ST SHIFT*. 1st shift work schedule: M-F, *9 am*-*5:30 pm. The QA Shop Floor Specialist is responsible for quality activities
Night shift: 6pm to 6am. The primary role of the candidate is working on assignments that train for proficiency in the operation of primary production equipment
Reports To: Operations Manager / Asst. Operations Manager. Primary function is to ensure the Client Accounts in a designated geographic area are cleaned and
Hybrid - 3 Days in the office, 2 days remote.*. Some leadership or supervisory experience desired. Experience working in pharmaceutical company or CRO strongly
MEDICAL AFFAIRS SYSTEM OVERSIGHT WITH VEEVA *. Reporting to the Associate Director of R&D Business Systems for Clinical/Medical Affairs, the Sr.
Wipe off all surfaces such as baseboards after waxing. Sweeping hard Surface floors, Mopping hard surface floors, buffing hard surface floors.
Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices and standard operating procedures.
Generate scientific content for internal and external medical communications-related activities such as scientific slide decks and digital assets for use during
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