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Quality Control Scientist
Ref No.: 18-25728
Location: Andover, Massachusetts

Job Title: Quality Control Scientist/ Analytical Scientist III

Location: Andover, MA 01810

Duration: 12 Months (12-24 months Contract)

Additional Skills:

• Lab Experience in basic analytical methods: HPLC, UV, pH

• Knowledge of Advanced analytical methods: Peptide map and Oligosaccharide, ELISA, iCE, Bioassay, Client

• Strong oral and written communication skills

• Knowledge and understanding of cGMP and industry standards

• Proficiency with computer systems (Microsoft Office applications, LIMS, etc.).

• Experience working in cGMP, regulatory environment.

Job Description:

The Quality Control Analytical group is seeking a highly motivated candidate to support analytical testing activities for multiple products at the Andover site.

The work includes various HPLC, UV spectrophotometry, and ELISA methods

The candidate will also be responsible for supporting technical writing, investigations, and other QC analytical business activities at the site.

The qualified candidate will work in a cGMP Quality Control Analytical lab.

Responsibilities include:

Prepares and record buffers and reagents, etc., and maintain work area in a neat and orderly manner.

Perform and review analytical testing of in-process, drug substance, and drug product samples.

Identify basic technical issues, atypical or out-of-specifications test results, instrument malfunctions and methodology problems and participates in the investigation to resolve and correct.

Maintain all related data and records in compliance with cGMPs and quality procedures.

Support laboratory investigations

Perform laboratory support functions including method revisions and maintain work area in compliance with cGMP and quality procedures.

Participates in continuous improvement culture within labs. Utilizes continuous improvement tools such as DMAIC.

QC Analytical experience and GMP Lab Experience are a must

Resumes in the past were lacking: GMP Lab, GMP Knowledge,

Analytical Lab techniques include but not limited to: HPLC, ELISA, UV Spectrometry, etc.

Tasks: Run Routine assays, Analytical Lab work, electronic documentation, investigations.

Plus would be technical writing skills, documentation, electronic documentation, LIMS, investigation experience

    • BA in science related field

previous roles: Analyst, Lab Analyst, Associate Scientist, Analytical Scientist, etc.

Self motivator, team player

Support of the tech transfer department

What is the minimum education experience required?: B.S. in Biology, Chemistry or related scientific discipline with a minimum of 5 years of related laboratory experience

Job Title: Quality Control Scientist/ Analytical Scientist III

Location: One Burtt Road, Andover, MA 01810

Duration: 12 Months (12-24 months Contract)

Additional Skills:

• Lab Experience in basic analytical methods: HPLC, UV, pH

• Knowledge of Advanced analytical methods: Peptide map and Oligosaccharide, ELISA, iCE, Bioassay, Client

• Strong oral and written communication skills

• Knowledge and understanding of cGMP and industry standards

• Proficiency with computer systems (Microsoft Office applications, LIMS, etc.).

• Experience working in cGMP, regulatory environment.

Job Description:

The Quality Control Analytical group is seeking a highly motivated candidate to support analytical testing activities for multiple products at the Andover site.

The work includes various HPLC, UV spectrophotometry, and ELISA methods

The candidate will also be responsible for supporting technical writing, investigations, and other QC analytical business activities at the site.

The qualified candidate will work in a cGMP Quality Control Analytical lab.

Responsibilities include:

Prepares and record buffers and reagents, etc., and maintain work area in a neat and orderly manner.

Perform and review analytical testing of in-process, drug substance, and drug product samples.

Identify basic technical issues, atypical or out-of-specifications test results, instrument malfunctions and methodology problems and participates in the investigation to resolve and correct.

Maintain all related data and records in compliance with cGMPs and quality procedures.

Support laboratory investigations

Perform laboratory support functions including method revisions and maintain work area in compliance with cGMP and quality procedures.

Participates in continuous improvement culture within labs. Utilizes continuous improvement tools such as DMAIC.

QC Analytical experience and GMP Lab Experience are a must

Resumes in the past were lacking: GMP Lab, GMP Knowledge,

Analytical Lab techniques include but not limited to: HPLC, ELISA, UV Spectrometry, etc.

Tasks: Run Routine assays, Analytical Lab work, electronic documentation, investigations.

Plus would be technical writing skills, documentation, electronic documentation, LIMS, investigation experience

    • BA in science related field

previous roles: Analyst, Lab Analyst, Associate Scientist, Analytical Scientist, etc.

Self motivator, team player

Support of the tech transfer department

What is the minimum education experience required?: B.S. in Biology, Chemistry or related scientific discipline with a minimum of 5 years of related laboratory experience