Research Assistant I

Makro Scientific; Swiftwater (Monroe County); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical staffing firm based in the United States seeks an analytical Professional to execute and analyze scientific experiments. The ideal candidate should hold a Bachelor's degree and have 1-3 years of relevant experience in a pharmaceutical setting. Key responsibilities include managing various projects, documenting results, and ensuring compliance with validation concepts. Strong communication skills are essential to succeed in this role.

Qualifications

• Candidate should possess Bachelor's degree in related field or comparable experience of 1-3 years.
• Experience in project management and technical writing is essential.
• Understanding of validation concepts, preferably in a pharmaceutical environment.

Responsibilities

• Responsible for the execution and analysis of experiments and analytical procedures.
• Integrates, compiles, and tabulates data, reporting results to supervisor.
• Contributes to completion of routine technical tasks and obtains data following standard practices.

Skills

Project management

Technical writing skills

Validation concepts understanding

Pharmaceutical environment experience

Strong written communication

Strong verbal communication

Education

Bachelor's degree in related field

Tools

Trackwise

e-doc

MASTER

Pharmnet

SAP

LIMS

ISOtrain

Job description

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

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

• 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 used include, but are not limited to: Trackwise, e-doc (author, reviewer, approver), MASTER, Pharmnet, SAP, LIMS, ISOtrain.

Qualifications

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