Scientist / Method Development / Pharma Industry / REMOTE WORK

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Posted 10 days ago United States Salary undisclosed
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Job Description

Our client, a world-leading Pharmaceutical Company in Cambridge, MA is currently looking for a Scientist / Method Development / Pharma Industry / REMOTE WORK to join their expanding team.

Position Details:
Job Title: Scientist / Method Development / Pharma Industry / REMOTE WORK
Duration: 12 months contract, extendable up to 36 Months
Location: Cambridge, MA

Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan

Job Description:
Candidate can sit anywhere within US & work any time zone: fully remote flexible hours within reason
3+ years of pharma/biotech experience
Biotech/ pharma experience required)
Ideal candidate Bachelors or Masters 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.

Job Requirements:
Responsibilities:
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.

Requirement:
Pharma or Biotech
Bachelor's or Master's degree and 3 years of Operations or Scientific experience
Degree 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
Client is an Equal Opportunity/Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.

Top 3 Must Have Skill Sets:
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

Day to Day Responsibilities:
Write protocols and reports from templates
Compile and verify data
Statistical analysis of data

Employee Value Proposition:
The person in this role will do all method transfers and validations globally. You will get a full view

Red Flags:
Lack of biotech/pharm industry experience
Lack of good writing skills
Only research experience