Report this Job
BioPharma Consulting JAD Group has a great Manufacturing Associate role with an industry leader in Thousand Oaks, CA (link removed) This is a temporary position with the possibility of extension.
The candidate will work in a highly collaborative team environment and be responsible for both moderately-complex to complex nGMP and GMP manufacturing activities to support of our early phase clinical pipeline of synthetic drug products.
Job Responsibilities:
Hands-on cleaning, sanitization, and setup of processing equipment and process rooms
Support in manufacturing process readiness activities
Assist in the review of facility and equipment documentation (equipment/room logbooks)
Maintenance of Raw Materials & Consumables Inventory
Supporting the day to day operational needs of the facility
The candidate will collaborate in multi-disciplinary teams with Process Development scientists, engineers, EH&S, Quality, F&E, maintenance, and other supporting functions.
Preferred Qualifications:
Associates degree in science/pharmaceutical science-related area
Ability to adhere to current Good Manufacturing Practices cGMPs and follow Standard Operating Procedures SOPs.
Understanding of typical unit operations for the manufacture of synthetics drug product (i.e. granulation, roller compaction, drying, milling, blending, compression, encapsulation and film coating)
Strong technical skills to support problem solving exercises.
Strong interpersonal skills and a proactive leadership mindset
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
BioPharma Consulting JAD Group
