About us
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people’s health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company’s capabilities are instrumental in combating many of the world’s most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

Description

* Formulates monoclonal antibody reagents using established documentation.
*
Manufactures buffers and solutions using established procedures.
*
Uses equipment such as pipettes, micro-pipettes, balances, pH and conductivity meters, and UV/Visible spectrophotometers.
*
Performs cleaning, inspection, verification for calibration and assist in the maintenance of equipment. Maintains related logs and records. Performs equipment troubleshooting.
*
Promotes a safe work environment. Provides recommendations on maintaining the safety of the work environment. Follows safety procedures. Participates in Environment Health and Safety (EH&S) programs. Initiates a corrective action whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices.
*
Maintains inventory of chemicals and supplies required for manufacture. Completes material order transactions in SAP system and performs the required inventory control activities to maintain accuracy.
*
Maintains detailed production records.
*
Participates in the development and revision of Standard Operating Procedures (SOP’s).
*
Executes assigned manufacturing and communicates project status.
*
Provides in-process testing as required.
*
Keeps abreast of the basic requirements for compliance in own area of work and complies with those requirements. Participates as required in training on regulatory issues affecting own area of work. Brings regulatory compliance questions/issues to next level of management.
*
Participates in Continuous Improvement Projects.
*
Maintain good housekeeping practices.
*
Generates Quality Reports such as Deviations Reports, etc.
*
Performs other related duties and assignments as required.


Qualifications

*
Requires a Bachelor Degree in a related scientific discipline (such as Chemistry, Biochemistry, Biology or Microbiology) and one year of experience in a research laboratory or pharmaceutical/medical device/biotechnology environment or equivalent combination of related education and experience.
*
Knowledge in the manufacture of protein dilution, buffers and solutions.
*
Knowledge of the operation of related instrumentation such as micro-pipettes, pipettes, balances and spectrophotometers, pH meters and conductivity meters.
*
Strong Mathematics skills.
*
Knowledge of cGMP, FDA, ISO and OSHA requirements highly desirable.
*
Working knowledge of MS Windows environment software such as MS Office. Knowledge of SAP highly desirable.
*
Effective skills using analytical thinking, problem solving, interpersonal relationships, written and oral communication, and planning/organization.
*
Demonstrated ability to follow established policies and procedures.
*
Ability to write, speak and read in English and Spanish.
Profile
Job Category Manufacturing
Location United States-Puerto Rico-Cayey
Shift First Shift / Day Job



Sources:

To view links or images in this forum your post count must be 1 or greater. You currently have 0 posts.


Thanks,
Jalpa