Quality Control Analyst I || Framingham, MA || Type-15 month Contract ||$28-30/hr

Job Title-Quality Control AnalystI

Location: Framingham, MA

Pay Rate: $28-30 per hour

Description:   
Position Summary
– This Quality Control Analyst I is responsible for performing routine testing of in-process
samples, stability samples and final products in accordance with SOPs for product
release.
Core Responsibilities
– Perform UV-Vis spectrophotometry, HPLC and Gel assays for in-process and final
product samples.
– Review of QC Data for compliance to procedures and specifications.
– Calculate and evaluate results.
– Successful completion of assigned training.
– Effectively demonstrate an understanding of cGMPs and application to specific
responsibilities:
– Follow accurate written procedures for testing of in-process and final product samples.
– Provide input to the technical composition of operating documentation.
– Work independently under general supervision and direction.
– Work in compliance with CGMPs.
– Practice safe work habits and adhere to Sanofi’s safety procedures and guidelines.
– Perform maintenance on basic laboratory equipment.

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Quality Control Analyst I || Framingham, MA || Type-15 month Contract ||$28-30/hr

Job Title-Quality Control AnalystI

Location: Framingham, MA

Pay Rate: $28-30 per hour

Description:   
– This Quality Control Analyst I is responsible for performing routine testing of in-process
samples, stability samples and final products in accordance with SOPs for product
release.
Core Responsibilities
– Perform UV-Vis spectrophotometry, HPLC and Gel assays for in-process and final
product samples.
– Review of QC Data for compliance to procedures and specifications.
– Calculate and evaluate results.
– Successful completion of assigned training.
– Effectively demonstrate an understanding of cGMPs and application to specific
responsibilities:
– Follow accurate written procedures for testing of in-process and final product samples.
– Provide input to the technical composition of operating documentation.
– Work independently under general supervision and direction.
– Work in compliance with CGMPs.
– Practice safe work habits and adhere to Sanofi’s safety procedures and guidelines.
– Perform maintenance on basic laboratory equipment

Apply here

Research Associate-II || Waltham, MA || Type-2-Year Contract ||$40-45/hr

Job Role- Research Associate II

Employment Type-2-year contract
Pay rate-$40-45/hr
Location-Waltham,MA

Job Specific Duties:

Perform formulation screening, prepare and characterize dosing formulations for animal studies. Conduct HPLC method development and samples analysis of small molecules in support of discovery formulation development. Measure protein concentration of monoclonal antibodies to support biotherapeutic programs. Troubleshoot analytical instrumentation and solve technical problems. Independently conduct formulation research and process improvement as needed. Interpret results and write technical reports. Responsible for general laboratory maintenance, buffer preparations, labeling, packaging and shipping of outgoing materials.

Skills:

HPLC, SEC, UV and LC/MS
Microscopy
Particle size analysis
Experience with solubility, stability studies and formulation screening.
Ability to multi-task and work efficiently in a fast paced and dynamic environment.
Ability to manage multiple projects while maintaining efficiency and effectiveness.
Ability to independently design experiments and conduct formulation research.
Excellent organizational and communication skills.
Ability to work independently and in a team environment.

Education:

MS (with 0-5 years related experience) in pharmaceutical sciences or analytical chemistry.

General Duties:

Responsible for the execution and analysis of experiments and analytical procedures. Display an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures. Investigate basic technical problems and performs routine scientific procedures and experiments under general supervision. Plan and prioritize concurrent experimental procedures. Integrate, compile, and tabulate data and assist supervisor in the analysis and interpretation of the results. May provide oral presentations on results to other department members. Contribute to the completion of milestones associated with specific projects. Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters. 

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