Pharmaceutical Technical Writer
Company: ProStaff Solutions
Location: New Brunswick
Posted on: April 1, 2026
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Job Description:
Are you looking to be a part of a growing pharmaceutical
company? One of our largest clients is currently seeking a
Pharmaceutical Technical Writer to join their New Brunswick, New
Jersey 08901 team . Our client is one of the leading pharmaceutical
companies specializing in developing and manufacturing solid dosage
products. If you believe you are qualified, we would be excited to
connect and discuss this opportunity in more detail. Full-time
Onsite Direct Hire Pay Rate: DoE Job summary: Perform
investigation’s and assist manufacturing and packaging operations
on investigations, Product quality complaints. Assist in cross
functional investigations for out of specification (OOS), out of
trend (OOT), Laboratory Events, CAPAs, and change controls. Areas
of responsibility: Ensure timely closure of all
manufacturing/packaging and Quality Management System records.
Organize and participate in and reviews of cross functional
investigation’s Represents Operations at cross-functional meetings.
Work with process owners and SMEs to implement agreed upon
procedural documentation and to develop cross-functional process
models Collect input from stakeholders and consolidate comments for
conflict resolution Drive the improvement in established KPI’s /
metrics for manufacturing and packaging departments Assist
operations in responses to any internal audit, corporate audit, or
regulatory audit observations involving manufacturing or packaging
Control. Travel Estimate: Up to 5% Required Qualifications:
Associate degree in Life Sciences, Pharmacy, or equivalent
required. Minimum of three (3) years working in a pharmaceutical
environment with at least two (2) years of experience within
manufacturing area. Demonstrated excellent communication: verbal,
written and presentation skills. A self-starter with a hands-on
approach and a can-do attitude. A team building champion driving
innovative cross functional synergies. Excellent project management
and problem solving skills. Excellent computer skills; MS Office
(Word, Excel, PowerPoint), Track wise, EDMS, Outlook. Knowledge of
GDP, GMP, QA Documentation, QA Batch records, Quality Systems,
Archiving, Retrieval, EDMS workflow, Document Life Cycle and Audit
Compliance. The requirement for English language proficiency for
this job role is Intermediate-B1 (comparable to Global CEFR
Independent B1) level based on the Common European Framework of
Reference for Languages (CEFR). Our client offers a competitive
compensation package as well as an excellent benefits package for
eligible candidates. About ProStaff Workforce Solutions We are a
fast growing and successful agency that treats all its clients and
candidates with a personal touch. ProStaff Workforce Solutions is a
group of industry experts—many hailing from larger agencies—who
know their business well and enjoy working in a more hands-on and
flexible environment, with attention to detail. Our mission is to
match quality people with quality jobs and quality companies to
maximize productivity and profitability. We develop long-term
relationships and provide a level of customer service and expertise
that instill confidence and trust in our client companies and
candidates. Our Values • Integrity • Commitment • Quality •
Diversity Please visit us at https://www.prostaffworkforce.com/ to
explore all opportunities. IND1
Keywords: ProStaff Solutions, Freeport , Pharmaceutical Technical Writer, Manufacturing , New Brunswick, New York
