The Quality Control Specialist is responsible for generating and/or reviewing data under cGMP guidelines. Experience is running ELISA/microplate-based assays is a plus.
The Quality Control Specialist must be able to read and understand technical documents including, training documents, standard operating procedures, work instructions, safety protocols, and quality manuals, and should be able to explain the contents of these documents to any employee. The Quality Control Specialist is expected to perform technical, mathematical and statistical calculations such as buffer formulations, standard deviations, etc.
Responsibilities may include:
- Follow established protocols to run specialized assays (HPLC, ELISA, etc)
- Provide technical assistance in generation of protocols
- Edit protocols as assigned
- Perform maintenance and/or calibration of equipment as assigned
- Initiate deviation and CAPA reports in a timely manner
Education and/or Experience:
A B.S. degree in either chemistry, Biochemistry or Biology is required. In addition basic quality management system knowledge is preferred.
The Quality Control Specialist must have a strong command of the English Language.
The Quality Control Specialist must have strong basic math skills with emphasis on data entry (alpha numeric), and common scientific calculations. The Quality Control Specialist must also have strong basic statistic skills. Required Statistic skills include calculations of Means, standard deviations, percent error as well as probabilities.
The Quality Control Specialist must demonstrate good problem solving and reasoning skills.
How to Apply to Haemtech Biopharma:
Please send a cover letter and resume to firstname.lastname@example.org, and put the position you are applying for in the subject line. You may also mail your application documents to:
Haemtech Biopharma Services
57 River Road, Unit 1010
Essex Junction, VT 05452
Attn: Human Resources
Please, no telephone calls!