Sterling-Hoffman Executive Search
Home
Our Story
Domain Expertise
Clients
Career Opportunities
Newsletter
Community
Contact Us
Submit your resume
Interviewing Guidelines








    
Sign-up
for the Sterling-Hoffman Life Sciences Journal to get the latest industry news and job postings.
Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
Career Opportunities
Back

To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

 Job #03167 Email this job to a friend
About our client
Our client is an expanding development-stage biopharmaceutical company with cutting-edge technology in the area of large molecule delivery systems. With an experienced management team and an established set of large pharma partners, this is a high visibility position that will expose the right candidate to some of the most intriguing programs in the life sciences sector.
Position Location
Scientist, Pharmaceutics New York
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Oversee formulation development using the company's drug delivery technology
2) Perform hands-on solid dosage form unit operation such as milling, granulation, drying, blending and compression
3) Perform equipment calibration and maintenance
4) Set up equipment such as table presses, blenders and drying ovens
5) Design experiments in support of formulation development and characterization
6) Write and review manufacturing instructions for research activities
7) Write formulation development and characterization work
8) Design and schedule in vivo animal experiments for formulation development
9) Prepare and give scientific presentations (as required)
10) Order laboratory supplies (as required)
11) Perform technology transfer for clinical supplies manufacture
12) Conduct process development and scale-up activities
13) Write reports and prepare CMC documentation
14) Assist in manufacture of clinical supplies
15) Conduct IQ/OQ of equipment as well as calibration and cleaning of equipment for cGMP operations
16) Review production instructions
17) Perform hands-on clinical supplies manufacture and post-production review of batch records (s required)
18) Work closely with contract laboratories for clinical supplies manufacture (as needed)
19) Perform technology transfer for clinical supplies manufacture
20) Conduct process development and scale-up activities
21) Design feasibility studies and prepare dosing materials to support the studies
22) Participate in team activities representing Pharmaceutics
Requirements
1) MS in a relevant field with 7 years of experience or Ph. D. with minimum 3 years of experience
2) Previous experience in designing feasibility studies
3) Expertise in formulation development for solid dosage products
4) Experience in designing in vivo animal experiments
5) Superb communication skills (written and oral)
6) Ability to perform technology transfer for clinical supplies manufacture

Back
Home | Our Story | Domain Expertise | Clients | Career Opportunities | Community | Contact Us