Makro Scientific:

Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.

Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.

Job Description:

• Responsible for the execution and analysis of experiments and analytical procedures. 

• Provides assistance in the execution of experiments and analytical procedures by performing routine scientific procedures and experiments according to detailed protocols. Integrates, compiles, and tabulates data and reports results to supervisor. 

• Assignments are task-oriented with detailed instructions. 

• Follows standard practices to obtain data. Contributes to the completion of routine technical tasks. 

• Failure to achieve results can normally be overcome without serious effect on schedules and programs. 

Examples of projects are as follows:

• Validation Study to support the use of viable tubing at various lengths. The intent of this validation study would be to show that the length of tubing does not have an adverse impact on recovery rates for viable organisms.

• This task would involve assessing all site production areas to determine the length of tubing used, developing a study to validate both the shortest and longest length, documented and then driving a protocol through the review and approval cycle, conducting the study in an appropriate location on site, writing report containing the results and then driving through report review and approval cycles. 

• A change control may also be needed to ensure the report is referenced in appropriate documentation.

• Implementation of an alternate EM media to replace DE Neutralizing agar. 

Skills:

• Candidate should have experience in project management, technical writing skills (reports, protocols, documents), some experience in or at least an understanding of validation concepts with some experience in a pharmaceutical environment.

• should include, strong written and verbal communication skills. Systems to be use include, but are not limited to: Trackwise, e-doc (author, reviewer, approver), MASTER, Pharmnet, SAP, LIMS, ISOtrain.

• Candidate should possess Bachelor's degree in related field or comparable Experience 1-3 years

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