Job Description Template - Vesta Therapeutics Page 2

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13.
Perform other duties as assigned.
QUALIFICATIONS
Bachelor’s degree in science or related life science field. Must have >2 years supervisory/management
experience in clinical cell production with a sound knowledge of aseptic processing, cell culture and GMP
compliance.
The candidate also must have the following:
-
a working knowledge of cGMP, GLP, FDA and other regulatory requirements (standards).
Knowledge of EU-GMP requirements would be an extra qualification.
-
technical understanding of the manufacturing process and equipment
-
experience in writing scientific protocols, reports and compilation of documents required for
regulatory submissions.
-
Organizational skills and the ability to analyze and manage complex projects often without
line authority
-
Ability to drive projects to completion under pressure
-
Strong interpersonal, communication and technical writing skills
-
Ability to manage and organize time effectively
-
Good scientific judgement
SUPERVISORY RESPONSIBILITY
2 staff members
ENVIRONMENT
PHYSICAL
On the job the employee must:
(x) Sit
(x) Stand
(x) Walk
(x) Push/Pull
(x) Kneel
(x) Handle objects (manual dexterity)
(x) Reach above shoulder level
(x) use fine finger movements
(x) Other: bend at the waist
Must carry/lift loads of : (x) Light (up to 25lbs.)
( ) Moderate (25-50lbs.) ( ) Heavy (over 50lbs)
MENTAL
On the job the employee must be able to:
Prepared By: __________________________
Date:_____________
Supervisor:
__________________________
Date:_____________

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