logo

View all jobs

Scientist, Biopharma - Remote (JP9940)

Providence, RI · Biotech/Pharmaceutical
Job Title: Scientist, Biopharma - Remote (JP9940)
Location: Providence, RI 

Employment Type: Contract
Business Unit: Method Stewardship 
Duration: 1 years with likely extensions or conversion to FTE
Job posting date: 3/14/2022

Note: 100% remote with 8 am - 5pm EST (some flexibility)

3 Key Consulting is hiring a Scientist for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.

Job Summary:

Ideal candidate Master in Biochemistry, Analytical Chemistry, Physical or Life Sciences. Strong understanding of method validation/transfer for methods within the following platforms Chromatography, Bioassay, PCR, Microbiology, Immunoassay, CE, Gel, Device, Viral, and General (compendia)

Biopharmaceutical leader founded on discovering, developing, manufacturing, and delivering innovative human therapeutics. Attribute Sciences group within Process Development is seeking a Scientist. The scientist will be responsible for the data verification, drafting, reviewing, and compilation for method transfer and method validation protocols and reports. The position will be a documentation centric role and the candidate will need to have experience with document management systems.

The Scientist role in Commercial Process Development will be part of a team responsible for authoring method transfer and method validation protocols and reports for late stage programs for the following method platforms: Chromatography, Bioassay, Device, PCR, Microbiology, Immunoassay, CE/Gel, Viral, and General. Protocols and reports will be authored according to regulatory and industry guidelines (i.e., ICH). This individual will support clinical and commercial locations throughout the company.


Top Must have Skill Sets:
  • 3+ years of pharma/biotech experience
  • Excellent writing skills
  • Capable of interfacing with multiple digital platforms simultaneously (MS teams, Document control systems)
  • Knowledge of method transfer and validation in biotech/pharma required
  • Ability to learn new systems quickly
  • Must have GMP Pharma experience (2-3+ plus years of experience)

Basic Qualifications: Pharma or Biotech
Master’s degree and 3 years of Operations or Scientific experience OR Bachelor’s degree and 3 years of Operations or Scientific experience

Preferred Qualifications:
  • Master in Biochemistry, Analytical Chemistry, Physical or Life Sciences
  • Strong understanding of method validation/transfer for methods within the following platforms Chromatography, Bioassay, PCR, Microbiology, Immunoassay, CE, Gel, Device, Viral, and General (compendia)
  • Direct experience with method transfer and method validation processes from a Pharmaceutical or Biotechnology Company.
  • Knowledge of analytical methods/technologies used in biologic and synthetic development and manufacturing
  • Excellent written and oral communication skills for the timely documentation, presentation, and discussion of scientific results in a fast-paced, multi-disciplinary, team-based environment
  • Demonstrated ability to critically analyze and interrogate various analytical data sets to drive and influence the process
  • Demonstrated ability to propose and drive new scientific initiatives

Top Must have Skill Sets:
  • 3+ years of pharma/biotech experience
  • Excellent writing skills
  • Capable of interfacing with multiple digital platforms simultaneously (MS teams, Document control systems)
  • Knowledge of method transfer and validation in biotech/pharma required
  • Ability to learn new systems quickly
  • Must have GMP Pharma experience (2-3+ plus years of experience)

Day-To-Day Responsibilities:
  • Write protocols and reports from templates
  • Compile and verify data
  • Statistical analysis of data

Employee Value Proposition:
Remote and flexibility
The client is a great company and gain experience in biotech industry
Work with a group that is leading industry in method transfers
Cross functional team

Red Flags:
Lack of biotech/pharm industry experience
Lack of good writing skills
Only research experience
PHD degree but no experience will not be required, BS/MS with years of experience (is ideal)
Must have GMP Pharma experience

Interview Process:
1/2 hour initial phone/video screen
Second round 1/2 hour with 2-3 team members (video, remote).

 We invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website https://3kc.catsone.com/careers/2010-General. You are welcome to also share this posting with anyone you think might be interested in applying for this role.

 
 
Regards,
 
3KC Talent Acquisition Team
 
 
Powered by