QA Documentation II || Framingham, MA || Type-16-month Contract ||$30/hr

Job title- QA Documentation II

Location: Framingham, MA

Pay Rate: $25-30 per hour

Description:  

Records Management ensures that cGMP records used at Framingham are managed and protected during their life-cycle (issuance, reconciliation, archival and destruction) in compliance with business needs and regulatory expectations. The overall goal is to ensure that record management policies, procedures, and processes meet applicable regulations. Additionally, record management provides life-cycle guidance to records users.
Position Summary
The Record Management Specialist is responsible providing Record Management related quality support and guidance to ensure continued compliance to cGMP and company expectations.

Core Responsibilities
•       Perform record issuance and reconciliation activities.
•       Interact/update/maintain the record management database.
•       Initiate/perform periodic record audits.
•       Point of contact for customer record management discussions.
•       Point of contact for record off-site storage and retrieval.
•       Interact/update offsite records management vendor database.
•       Assist with record destruction.

Qualifications

  • Bachelor’s degree in Life Science
  • 3 – 6 Years experience
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QA Documentation II || Framingham, MA || Type-16-month Contract ||$30/hr

Job title- QA Documentation II

Location: Framingham, MA

Pay Rate: $30 per hour

Description:  

Track and review change control documentation. Assist with the editing of quality documents (SOPs, guidelines, validation master plans, etc.) to ensure compliance with regulator requirements. Must be able to work quickly with a high degree of accuracy. Must possess sound interpersonal and information gathering skills, be able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.    Prepare and/or maintain documentation pertaining to programming, systems operation, and user documentation. Translate business specifications into user documentation. Plan, write, and maintain systems and user support documentation efforts; including online help screens. Knowledgeable of commonly used concepts, practices, and procedures within a particular field. Rely on instructions and pre-established guidelines to perform the functions of the job..

Years of Experience: 3 – 6 Years

Qualifications

  • Bachelor’s degree in Life Science
  • 3 – 6 Years experience
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QA Documentation || Framingham, MA || Type-6-month Contract ||$25/hr

QA Documentation

Location: Framingham, MA

Pay Rate: $25 per hour

Responsibilities

  • Track and review change control documentation. Assist with the editing of quality documents (Master Batch Records, SOPs, guidelines, etc.) to ensure compliance with regulator and internal quality requirements. Must be able to work quickly with a high degree of accuracy. Must possess sound interpersonal and information gathering skills, be able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others. Prepare and/or maintain documentation pertaining to programming, systems operation, and user documentation. Translate business specifications into user documentation. Plan, write, and maintain systems and user support documentation efforts; including online help screens. Knowledgeable of commonly used concepts, practices, and procedures within a particular field. Rely on instructions and pre-established guidelines to perform the functions of the job

Qualifications

    • Bachelor’s degree in Life Science
    • 0-2 years of QA Documentation experience.
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Seniority Level

Entry level

Industry
  • Staffing & Recruiting  
  • Biotechnology  
  • Pharmaceuticals
Employment Type

Contract

Job Functions
  • Quality Assurance
  • Documentation