Top 264 Technical writer contract Jobs

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Technical Writer

Maxonic, Inc. -
Rockville, MD

Quick Apply

Job Details

Contract
Up to $31 an hour
7 days ago

Qualifications

AP style
Operational analysis
Doctoral degree in life sciences
Policy & process development
Training & development

Full Job Description

Maxonic maintains a close and long-term relationship with our direct client. In support of their needs, we are looking for a Technical Writer.

Job Description:

Job Title: Technical Writer

Job Type: Contract

Job Location: Rockville, MD

Work Schedule: On-site

Pay Rate: $31, Based on experience

Description:

The Manufacturing Specialist is a key technical contributor responsible for process optimizations, manufacturing troubleshooting, continuous improvement initiatives to ensure Manufacturing consistently produces quality product. This role sits at the intersection of operational excellence, quality, training & development, and MSAT supporting efficient, compliant, and ever improving operations. The ideal candidate will have a strong understanding of cGMP compliance, quality event investigation, lean production methodologies, and process technology to drive reliability in operations.

Key Responsibilities and Duties:

Process Improvement & Optimization
Identify and implement continuous improvement projects using Lean methodologies to improve and stabilize yield, efficiency, and process success.
Partner with MS&T and Process Development to monitor process performance to identify data driven solutions and enhancements.
Support technology transfer, process scale-up, and process validation to ensure smooth transitions into manufacturing.
Partner with MS&T and Engineering to optimize equipment utilization, automation strategies, and data analytics for real time adjustments and support. Compliance & Manufacturing Support
Conduct timely batch record reviews and deviation investigations, ensuring long term resolution of documentation/instructional issues.
Lead root cause analysis and corrective/preventive action (CAPA) for process deviations, non-conformances, and quality issues.
Work close with Quality and Manufacturing teams to ensure documentation supports data integrity & good documentation practices (GDP) incompliance with FDA, EMA, guidelines.

Training and Documentation Management

Develop and maintain SOPs, training materials, and documentation systems for manufacturing compliance and process improvements.
Partner with MS&T and Training to conduct training programs for manufacturing staff to ensure adherence to cGMP, process guidelines, and quality requirements.
Work cross-functionally to ensure employees remain qualified and up to date on process and compliance expectations.

Qualifications:

Bachelor’s degree in relevant Science or Engineering discipline preferred.
Minimum 3 years working within industry. Strong technical writing capabilities a plus.
Experience within cell/gene therapies, biologics, and/or cGMP regulated environment preferred
Knowledge of process improvement and lean methodologies preferred.
Ability to interpret and present complex scientific data in a clear and concise manner.
Proficient in Microsoft office suite and document management systems.
Strong organizational and project management skills.

About Maxonic:

Since 2002 Maxonic has been at the forefront of connecting candidate strengths to client challenges. Our award winning, dedicated team of recruiting professionals are specialized by technology, are great listeners, and will seek to find a position that meets the long-term career needs of our candidates. We take pride in the over 10,000 candidates that we have placed, and the repeat business that we earn from our satisfied clients.

Interested in Applying?

Please apply with your most current resume. Feel free to contact Harkirat Singh ([email protected]/(408) 400-2319) for more details.

Pay: Up to $31.00 per hour

Work Location: In person

Quick Apply

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