Senior Manager, Site Regulatory Affairs – Your Experience Needed!
Location: New York, NY
Salary: $120,000-$130,000 + Bonus
Our Regulatory Affairs team seeks an experienced RA professional to assume responsibility for two separate pharma manufacturing sites: one in New York, and one in North Carolina.
Our hiring manager seeks candidates who are capable of dealing effectively with conflicting priorities and meeting deadlines for these two separate sites. Anyone with previous site ...
Are you a QC/QA professional, experienced in manufacturing, who can demonstrate experience with designing quality systems, identifying SOPs, and training staff on specific requirements of marketing a pharmaceutical product. Are you an animal lover???
ARK SCIENCES is an entrepreneurial, biotech startup, and will be a game changer with animal welfare advocates! We have introduced the first nonsurgical neutering solution into the marketplace, Zeuterin, which is FDA approved for use in dogs 3-10 ...
We have been retained by one of the world's leading manufacturers of medical/surgical disposable products to assist them as they expand their sales organization.
You will be responsible to manage your own Brooklyn/Staten Island Territory for their existing business and develop new sales primarily in the acute care market.
With products that are clinically superior, you will call on various departments of the hospital, i.e. critical care, O.R., infection control and hospital administration to bring ...
A large pharmaceutical company in Pomona, NY is looking for a Microbiologist to work on a long term contract. Must have 2+ years of Pharmaceutical Microbiology experience and be local to the area.
•Perform routine microbiological testing and auditing to ensure compliance with cGMP regulations and guidelines as defined by FDA, ICH, USP, validated methods, protocols and internal SOPs.
•Conduct microbiological atests
•Conduct and USP water tests, and microbial examination tests
Sr. Design Quality Engineer
Minimum 5 years full time experience in a Lean Six Sigma Quality engineering role.
Extensive knowledge of product design activities
Three (3) years of practical medical device manufacturing experience is preferred.
Working knowledge of FDA, cGMP and ISO Standards/regulations.
Good working knowledge of upstream product development and validation experience, including protocol development.
Able to read and interpret mechanical ...
Jan 9 -
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