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Need USC GC GCEAD Onsite Sr. QA Associate at Lexington, Massachusetts, USA
Email: [email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=218815&uid=

From:

Manpreet,

Intime Infotech

[email protected]

Reply to:   [email protected]

Hi,

I am hiring a consultant for one of my client's requirement. Job Description for the same is written below. If you find yourself comfortable with the requirement please reply back with your updated resume. I would really appreciate if you can give me a call back at my contact # 302-401-6677 Ext- 533.

Job Title         Onsite Sr. QA Associate

Location         Lexington MA

Duration         6 months /Contract

JOB DESCRIPTION

USC/GC/GC-EAD

Interview mode Video

Onsite Position

Length of contract assignment:

6 months PO with ability to extend.

Work schedule/typical work week/daily start and end time:

3pm-11pm

They are pioneering long-acting oral therapies to treat mental health/opioid addiction, central nervous systems diseases.

Project description:

Perform assessment of different semi-automatic manufacturing operations. The client clears 1-2 operations per day.
QMS is Intellect
 Interact with small team of four in a second shift made up of Manufacturing Techs, Engineers, Supply Chain, Quality Assurance
Work with the manufacturing and QA team to review batch records and deviations, update SOPs.
It is important that this person realize how basic the manufacturing environment is. It is truly Phase I with minimal production of pre-commercial products.

Technology environment the consultant will be working in:

Intellect is new QMS

Consultants day to day responsibilities:

Be Person on the Floor to provide Quality Operations Oversight to the Manufacturing Team in combination products drug/device- CFR 210/211, oral solid dose, non-sterile, GMP environment.
Perform assessment of different semi-automatic manufacturing operations. The client clears 1-2 operations per day. Interact with Manufacturing Techs, Engineers, Supply Chain, Quality Assurance
Work with the manufacturing and QA team to review batch records and deviations, update SOPs.
This person will write /edit/ review SOPs.
Report up to Associate Director of Quality with updates on progress, problems that need to be escalated for prompt resolution.

Regards,

Manpreet

Technical Resource Specialist

InTime Infotech Inc

time matters

39962 Cedar Blvd., Ste 185, Newark CA 94560

Contact# : 302-401-6677 x 533

Direct : 510-455-8178

Fax : 510-201-2367

Keywords: quality analyst access management information technology computer associates purchase order
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11:01 PM 16-Dec-22


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Location: Lexington, Massachusetts