Analytical Development Scientist II - Method Validation

MilliporeSigma; Rockville (MD); On-site; USD 36,000 - 55,000; Full time

Benefits offered by this job

Health insurance

Paid time off (PTO)

Retirement contributions

Other perquisites

Job summary

MilliporeSigma is seeking an Associate Scientist 2 - Analytical Development to support analytical method development/validation and feasibility/transfer within the Analytical Laboratory. You will ensure scientific integrity of work, maintain thorough documentation, and apply industry standards to clinical and commercial products.

Responsibilities include GMP awareness, method development/validation, transferring studies on schedule, performing analytical testing per SOPs and cGMP, and

Qualifications

• Master’s Degree in a scientific discipline with 6+ months of lab experience.
• Or Bachelor’s Degree with 1+ year lab experience.
• Or Associate’s Degree with 2+ years lab experience.
• Or High school diploma with 5+ years of lab experience.

Responsibilities

• Understand GMP requirements for analytical method validation and transfer.
• Support method development/validation and feasibility transfer activities.
• Perform analytical testing with SOPs and cGMP.
• Maintain complete study records and documents.
• Create and revise protocols, reports, SOPs and lab records.
• Assist with training of laboratory personnel.
• Communicate deviations and progress to SME.
• Operate and maintain lab equipment per SOPs.
• Use Word, Excel, Oracle, LIMS in testing.
• Contribute ideas to improve techniques and equipment.

Skills

GMP experience

Analytical testing

Documentation

Lab teamwork

Problem solving

Education

Master's degree in life sciences

Bachelor's degree in life sciences

Associate's degree in life sciences

High school diploma or GED

Tools

Oracle

LIMS

BRIQS

Microsoft Word

Microsoft Excel

Job description

MilliporeSigma is seeking an Associate Scientist 2 - Analytical Development to support analytical method development/validation and feasibility/transfer within the Analytical Laboratory. You will ensure scientific integrity of work, maintain thorough documentation, and apply industry standards to clinical and commercial products.

Responsibilities include GMP awareness, method development/validation, transferring studies on schedule, performing analytical testing per SOPs and cGMP, and