Responsibilities:
assess, evaluate and review manufacturing operations to determine if current GMP is met, ensure compliance with all applicable regulations and resolve GMP issues, perform internal audits for compliance of regulations and company policies, author and execute process, packaging and cleaning validation protocols and prepare reports, validate SOPs, control analytical records and review batch production records, sample incoming materials and in process samples.

Applicant must have a Masters Degree in Drug Regulatory Affairs/Pharmacy/Pharmaceutics/Industrial Pharmacy/Pharmaceutical Manufacturing with 3 months of experience.

40 hr/wk. M-F.

Send Resume referring to job #MSVP001 Sunrise Pharmaceutical, Inc. 665 East Lincoln Ave., Rahway, NJ 07065.