Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Randstad USA

Supply Chain Technical Writer II

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
60
out of 100
Average of individual scores

Were these scores useful?

Job Description

supply chain technical writer ii.somerville, new jerseyposted today job detailssummary$45 - $49.65 per hourcontractbachelor degreecategorylife, physical, and social science occupations reference 54657 job details job summary: Join a top-tier global pharma leader in Branchburg, NJ, as a Supply Chain Technical Writer II. This 6-month extendable contract role offers an excellent opportunity to drive manufacturing excellence, facilitate CAPA closures, and streamline critical GMP documentation within a dynamic supply chain environment.
location:
Somerville, New Jersey job type: Contract salary: $45.00 - 49.65 per hour work hours: 9 to 5 education: Bachelors responsibilities: Partner with Supply Chain SMEs to author, revise, and manage GMP documentation, including SOPs, work instructions, specifications, and Change Controls.

Facilitate CAPA closures and actively participate in Operations-related process improvement initiatives. Develop standardized document formatting and content structures to ensure logical organization while minimizing gaps and duplication.

Collaborate with Quality and Supply Chain teams to ensure all documentation meets or exceeds compliance expectations.

Compile supporting change management documentation and follow up with reviewers and approvers to meet project timelines.
qualifications:
Required:
Bachelor's degree in a scientific discipline or 5+ years of equivalent experience.3-6 years of relevant experience in a pharmaceutical manufacturing environment.

Demonstrated experience authoring and revising GMP documentation and managing change controls.

Proficiency in Microsoft Office applications (Word, Excel, Access, PowerPoint).
Preferred:
Experience with advanced document management applications and process improvement techniques.

Strong cross-functional communication and meeting facilitation skills. #LI-AO1 skills: SOP Development, Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA),
Clinical Supply Chain Risk Mitigation 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.

Benefits

  • 401(k) Plans
  • Dental Insurance
  • Disability Insurance
  • Life Insurance