Job Actions

Job Information

Category: Manufacturing
  • We need you for Contract
  • This job pays $50.73 - $59.68 per hour per
  • **job details: **
    + reference: 25311

Job code: lhw-e0-90661626

Company Profile


Contact Company

Local Information

Laugh while you Look

Sponsored Ads


  Job posted:   Thu Jun 7, 2018
  Distance to work:   ? miles
  10 Views, 0 Applications  

job description**



**Job Responsibilities**

+ As a member of Analytical Development Method Development team, he/she will work on method development, qualification and characterization of drug substance, drug product and reference standards for biological programs.

+ Responsibilities include designing experiments per ICH guidelines, flawless execution of experimental studies, documenting results accurately in the laboratory notebooks, writing and reviewing technical reports, generating test methods to support high throughput and QC testing groups, participate in analytical, process development and QC meetings and discussions, etc.

+ Provide quality and regulatory support as needed and actively participate project teams

+ Applies technical knowledge under minimal supervision to independently execute method development and assay remediation activities

60% of Responsibilities

+ Execution of experimental studies

30% of Responsibilities

+ Documentation including writing protocols and reports

10% of Responsibilities

+ Training and presenting data

**Education & Qualifications**

+ BS with 6+ years of industry experience, or MS with 4-6+ years of industry experience in analytical chemistry, biochemistry or other biological/analytical discipline.

+ Experience in method development, qualification and validation of analytical methods for biologics.

+ Strong analytical and problem solving skills are required

+ In-depth knowledge of HPLC, UPLC, LabChip, SoloVPE, and enzyme activity measurements, including both theory and practice is required

+ Ability to work successfully in both a team/matrix environment as well as independently

+ Ability to work in a fast pace environment, manage priorities, and flexible to work on multiple projects

+ Knowledge of cGMPs, regulatory guidelines and good laboratory practice are essential

+ Excellent written and verbal communication skills are essential

+ Complex problem solving skills

+ Understanding of ICH, USP and GMP guidelines

+ Flexible to work on multiple projects

+ Available to participate in early or late meetings/teleconferences

+ Familiarity in Microsoft Office (word, excel, and powerpoint) and JMP


+ Medical, Dental, and Vision Insurance

+ 401K Plan with Company Match

+ Life and AD&D Insurance

More Information »