Process Development Sr Associate Scientist 34994

Inteldot • Juncos, PR

6d

About The Position

Inteldot has over 14 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico . Administrative Shift Responsibilities: Perform experiments, organize data and analyze results under minimal supervision. With minimal supervision plans, conducts or monitors experiments, records and organizes data, analyses results. Generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision. Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data. Effectively transfers experimental methods from literature to the lab and makes modifications as necessary. Develops and implements new protocols with moderate review. Engages coworkers in scientific discussions. Communicates data and interpretation to work group. Skilled at developing systems to ensure quality data. Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques. Effectively troubleshoots equipment and experimental difficulties. Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents. Participates in department-wide support efforts such as safety, recruiting and committees. Understands when to seek input and when to make independent judgments.

Requirements

• Experience in manufacturing bio processes and technical writing
• Working knowledge of analytical methodologies and analytical instruments qualification programs.
• Excellent computer technical writing skills.
• Strong knowledge of cGMPs.
• Fully bilingual (English/Spanish).
• Master’s degree and 1 year of scientific experience or bachelor’s degree and 3 years of scientific experience
• Science background (Chemical Engineering, Industrial Biotechnology, Chemistry or Microbiology)

Responsibilities

• Perform experiments, organize data and analyze results under minimal supervision.
• Plans, conducts or monitors experiments, records and organizes data, analyses results.
• Generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
• Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision.
• Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data.
• Effectively transfers experimental methods from literature to the lab and makes modifications as necessary.
• Develops and implements new protocols with moderate review.
• Engages coworkers in scientific discussions.
• Communicates data and interpretation to work group.
• Skilled at developing systems to ensure quality data.
• Effectively troubleshoots equipment and experimental difficulties.
• Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents.
• Participates in department-wide support efforts such as safety, recruiting and committees.
• Understands when to seek input and when to make independent judgments.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level