Senior Scientist I, Bioanalytical

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Cranbury, NJ, USA
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Leads complex DMPK and non-GLP bioanalytical method development, qualification, sample analysis, reporting, and study coordination. Supervises and mentors scientists, serves as study director or project coordinator, reviews technical work, develops SOPs, communicates with sponsors, and supports pharmaceutical bioanalysis involving small and large molecules across biological matrices.
Summary Generated by Built In
Overview

The Senior Scientist I is responsible for the day-to-day coordination and supervision of the team operation to ensure the successful implementation of the DMPK Non-GLP Bioanalytical method development, method qualification, sample analysis, report writing, and metrics in order to deliver outstanding customer satisfaction in the field of drug discovery and development.

Responsibilities
  • Designs, plans and carries out the more complex research studies including method development for the analytes and its metabolites in various matrices. Provides multiple approaches during the planning step.
  • Trains, coaches, or mentors others on technical, personal development or business issues.
  • Works on extremely complex problems in which analysis of situations or data requires an evaluation of intangible variables. Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results.
  • Functions as a study director, principle investigator, or project coordinator including serving as a primary contact for sponsors, responsibilities include planning and supervising more complex and exacting research studies.
  • Supervises personnel. Ensures optimum personnel performance through leading by example, motivation, and performance recognition.
  • Conducting quick PK sample analysis in variety of biological matrices, including but not limited to stock solution preparation, sample extraction, small or large molecule sample analysis, and report writing.
  • Reviews other scientists’ calculations, records, and reports. Writes comprehensive reports, recommending application of finings, and presents clear and concise oral reports of processes and accomplishments.
  • Complies with all safety rules, practice good housekeeping, and maintain safe workplace without supervision.
  • Learns, enhances, and shares technical knowledge of pharmaceutical areas, DMPK, ADME, In Life, Metabolism, and Bioanalysis.
  • Participates in writing and review of Standard Operating Procedures (SOPs) and suggest practical changes.
  • Promotes company’s safety policies, practices and procedures in order to maintain a safe work environment.
  • Other duties as assigned.
Qualifications
  • PhD or Master’s degree in chemistry, Biology, or related Physical science degree. PhD with 3+ years related work experience.  Or Master’s degree with 10+ years related work experience. 

Knowledge / Skills / Abilities:

  • An expert in the use of advanced experimental methods, concepts and techniques relevant to scientific discipline and specific area, such small or large molecule bioanalytical, including LC-MS, ELISA/MSD, PCR, flow cytometry, western blotting, etc,
  • Demonstrated experience in the independent development of LBA and/or LC-MS bioanalytical methods.
  • Emerging skills in novel experimental methods, concepts and techniques
  • Demonstrates independent thought and scientific creativity
  • Demonstrates technical success and proficiency in projects
  • Utilizes expert knowledge of scientific principles and concepts
  • Collaboratively researches and proposes methodologies for projects
  • Acts independently to research and propose new research projects and methodologies and implement them
  • Good time management skills in order to perform multiple projects within deadlines
  • Expected to initiate external publications and presentations
  • Effective oral and written communication and interpersonal skills
  • Good time management skill in order to perform of multiple projects within deadlines
  • Ability to work in a team environment
  • Follow and adhere to nonGLP guidelines/SOPs consistent with WuXi AppTec requirement

 

Physical Requirements: 

  • Must be able to work in an office environment with minimal noise conditions.
  • Must be able to work in Lab setting with exposure to biohazards / chemicals
  • Must be able to wear appropriate PPE
  • Must be able to work in environment with variable noise levels
  • Ability to stand /Sit/walk for long periods of time
  • Ability to Lift 15 lbs routinely
  • Ability to crouch, bend, twist, and reach
  • Ability to push/pull 15 lbs routinely
  • Clarity of Vision
  • Ability to identify and distinguish colors
  • Must be able to perform activities with repetitive motions
  • Ability to work in variable temperatures high to freezing

 

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability


This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.  Employees holding this position will be required to perform any other job-related duties as requested by Management.


Skills Required

  • PhD in chemistry, biology, or a related physical science with 3 or more years of related work experience
  • Master's degree in chemistry, biology, or a related physical science with 10 or more years of related work experience
  • Expertise in advanced bioanalytical methods and techniques, including small- or large-molecule analysis
  • Independent development of ligand-binding assay and/or LC-MS bioanalytical methods
  • Expert knowledge of scientific principles and concepts
  • Ability to independently research, propose, and implement research projects and methodologies
  • Ability to manage multiple projects and meet deadlines
  • Effective oral, written, and interpersonal communication skills
  • Ability to work collaboratively in a team environment
  • Ability to follow non-GLP guidelines and standard operating procedures
  • Ability to work in laboratory environments with biohazard and chemical exposure while wearing appropriate PPE
  • Ability to routinely lift and push or pull up to 15 pounds
  • Emerging skills in novel experimental methods, concepts, and techniques
  • Initiation of external publications and presentations
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The Company
Couvet
430 Employees
Year Founded: 2000

What We Do

WuXi Chemistry, a business division of WuXi AppTec, provides contract services for new drug development from discovery to commercial. Our unique CRDMO model offers an integrated solution combining traditional CRO (contract research organization), CDMO (contract development and manufacturing organization) and CMO (contract manufacturing organization) services under one roof. As a world leading chemistry service organization, WuXi Chemistry have over 24,000+ employees from our 16 research, development or manufacturing sites worldwide, serving over 2,000+ clients from top pharma to virtual biotech companies. Our services cover all categories for all synthetic molecular modalities, meeting any material requirement at any scale. Visit STA, CRDMO for small molecule drugs: https://stapharma.com Visit WuXi TIDES, CRDMO for oligonucleotide, peptide, and conjugates: https://tides.wuxiapptec.com/

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