Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
Home View All Jobs (2,203,475)

Job Information

Randstad US quality documentation specialist in north billerica, Massachusetts

quality documentation specialist.

  • north billerica , massachusetts

  • posted today

job details

summary

  • $30 - $35 per hour

  • contract

  • bachelor degree

  • category life, physical, and social science occupations

  • reference49085

job details

job summary:

As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: North Billerica, Massachusetts

job type: Contract

salary: $30 - 35 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

The Quality Document Coordinator is an individual contributor who is responsible for conducting day to day processing of controlled documents for cGMP operations. Responsible for compliance in accordance with Document Management procedures and will assist with ongoing Quality documentation deliverables driven by business objectives and identified by management.

  • Coordinates, proofreads, formats, and troubleshoots issues for controlled documents supporting the manufacturing and testing of products.

  • Balances and prioritizes assigned documents to ensure meeting document change request due dates.

  • Aligns with all levels of the organization to meet the needs of documentation system users on site and at external facilities.

  • Manages multiple tasks in a fast paced and dynamic environment while maintaining focus on quality and compliance with local SOPs, policies and directives, and regulatory requirements.

  • Supports individual and group training sessions for system users on making document changes and reviewing electronic reference copies of documents.

  • Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety & environmental hazards.

  • Actively demonstrates the company values of accountability, quality, efficiency, customer service, collaboration and safety.

    • In the case of absence the reports to Manager above or a peer incumbent will function as a backup for this position.
qualifications:

  • AS in English or Science.

  • A combination of education, training and experience may be considered in lieu of the above stated qualifications.

  • 4-6 years of experience in the pharmaceutical industry, preferably within Quality or Documentation function

  • Prior experience with Electronic Documentation Management System is preferred

  • Proficient in Microsoft Office

  • Proficient in advanced functions of Microsoft Word.

  • Excellent verbal and written communication

  • Ability to work independently,

  • Able to identify and present solutions that will resolve issues and meet the required due dates for documents

  • Ability to work in a team environment

  • Attention to detail

skills: SOP, Quality Assurance, MS-WORD, MS-EXCEL, GMP (Good Manufacturing Practice), ERP System

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.

DirectEmployers