Job Details

HonorVet Technologies (SDVOSB) provides specialized and scalable staffing solutions to pharmaceutical companies, medical device companies, biotech organizations, CROs, research laboratories, and life sciences organizations across the United States. With strong delivery capabilities and rapid turnaround times, we support contract, direct hire, project-based, and consulting staffing needs across clinical research, pharmacovigilance, regulatory affairs, quality assurance, quality control, medical affairs, manufacturing, validation, and scientific operations. Our dedicated recruitment team focuses on delivering qualified life sciences and pharmaceutical professionals efficiently while ensuring quality, compliance, and client satisfaction.

Job Title: Technical Writer/Manufacturing Specialist
Job Location: Rockville, MD
Job Duration: 06 Months (Temp to Perm)

Position Summary:
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 datadriven 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.

• 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, nonconformances, 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.

• 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

• 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.