Associate Scientist Biopharma HPLC - JP10491
Associate Scientist Biopharma HPLC - JP10491
Posted on :
11-04-2025
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Job Description
Job Title:Associate Scientist Biopharma HPLC (JP10491
Location: Cambridge MA. 02138
Employment Type: Contract
Business Unit: Pivotal DPT
Duration: 3 years
Posting Date: 6/24/2022
Notes: 100 onsite.3 years contract. Must have lab experience and HPLC. Masters degree or Bachelors degree & 2 YOE
3 Key Consulting is hiring an Associate Scientist for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
To 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. Responsibilities include:
Top Must Have Skills:
Day to Day Responsibilities:
Analyze samples from Drug product related studies and process the data output according to known SOPs and protocols. All data is then transcribed into a lab notebook for compliance.
Basic Qualifications:
Minimum BS degree in Biology Biochemistry Analytical Chemistry or related discipline and 2 years experience in a Biopharmaceutical working environment.
Red Flags:
Interview process:
Virtual (phone/Webex) thenPanel
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our websitewww.3keyconsulting/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Location: Cambridge MA. 02138
Employment Type: Contract
Business Unit: Pivotal DPT
Duration: 3 years
Posting Date: 6/24/2022
Notes: 100 onsite.3 years contract. Must have lab experience and HPLC. Masters degree or Bachelors degree & 2 YOE
3 Key Consulting is hiring an Associate Scientist for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
To 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. Responsibilities include:
- 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
- Works efficiently in a matrix team environment and collaborates with coworkers
- 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 (HPLC CE...
- Effectively troubleshoots equipment and experimental difficulties
- Contributes to internal/external reports papers presentations regulatory documents invention disclosure submissions and/or patents
- Participates in departmentwide support efforts such as safety recruiting and committees
- May train staff and/or supervise others
- Coordinates and organizes resources needed to complete the task
- Understands when to seek input and when to make independent judgments.
Top Must Have Skills:
- Masters degree or Bachelors degree & 2 YOE ideal candidate
- Experience in HPLC in application to proteins including SEC CEX RPHPLC and capillary electrophoresis (CE) able to operate process data and report findings into electronic lab notebook.
- Good documentation practices bonus would be GMP/QC experience
- Lab experience hands on
Day to Day Responsibilities:
Analyze samples from Drug product related studies and process the data output according to known SOPs and protocols. All data is then transcribed into a lab notebook for compliance.
Basic Qualifications:
Minimum BS degree in Biology Biochemistry Analytical Chemistry or related discipline and 2 years experience in a Biopharmaceutical working environment.
Red Flags:
- Lack of experience in HPLC and lab work.
- Needs to be handson experience; not theoretical.
- Must show hands on HPLC and lab experience***
Interview process:
Virtual (phone/Webex) thenPanel
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our websitewww.3keyconsulting/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Regards
3KC Talent Acquisition Team
Required Experience:
IC
Employment Type
Full Time
Key Skills
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