Scientific Technical Writer, QC Micro - Randstad USA

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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you!

 
location: Worcester, Massachusetts
job type: Contract
salary: $24.00 - 26.90 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:

• Collaborate with QC team members and SMEs to gather and interpret scientific data.
• Compile data and author validation reports and other technical documents in accordance with QC and regulatory requirements.
• Format and prepare reports for submission in PDF format for review and approval within the Document Management System.
• Ensure documentation meets compliance with GMP and GLP standards.
• Track and maintain timely completion of training requirements.
• Maintain a high level of attention to detail and accuracy in documentation.

 
qualifications:

• Minimum of 1 year of experience in technical writing within a scientific, QC, or pharmaceutical environment.
• BS degree-Life science/Biotech/chemistry
• Familiarity with GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices) guidelines.
• Familiarity with the Microsoft Office 365 suite of products
• Experience working with Document Management Systems is a plus. (OneVolt)
• Strong organizational and communication skills.
• Ability to work independently as well as part of a team.

 
skills: Quality control, Quality Assurance, Chemistry, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice)

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.