Job summary
Job post source
This job is directly from United Pharma Technologies Inc
Job overview
The Manufacturing Oversight Consultant role at United Pharma Technologies Inc involves providing senior-level on-site oversight of gene therapy GMP manufacturing at third-party facilities to ensure compliance and quality.
Responsibilities and impact
The consultant will observe the entire manufacturing process, monitor GMP and aseptic compliance, verify operational readiness, document observations, review batch records, communicate risks through controlled channels, and complete necessary safety training.
Experience and skills
Candidates need 10+ years of GMP manufacturing experience in biologics or advanced therapy products, strong knowledge of aseptic processing and fill-finish operations, gene therapy or small-batch manufacturing experience, and excellent documentation and communication skills.
Job location and travel
The position is located in Massachusetts (MA) and requires on-site presence for consecutive production days with cleanroom gowning qualification.
Unique job features
The role is non-interventionist focusing on real-time observation and structured communication without direct production involvement, emphasizing compliance risk escalation and controlled site access.
Company overview
United Pharma Technologies Inc. is a pharmaceutical and biotechnology company specializing in the development, manufacturing, and distribution of innovative healthcare solutions. The company generates revenue through the production of proprietary drugs, contract manufacturing services, and partnerships with healthcare providers and research institutions. Founded with a mission to address unmet medical needs, United Pharma Technologies has a history of significant contributions to therapeutic advancements, particularly in oncology and rare diseases. Candidates should note its emphasis on cutting-edge research, regulatory compliance, and global market expansion strategies.
How to land this job
Position your resume to emphasize over a decade of GMP manufacturing expertise, specifically highlighting experience in biologics, gene therapy, or advanced therapy products relevant to United Pharma Technologies Inc.
Focus on showcasing your knowledge of aseptic processing, fill-finish operations, contamination control, and your ability to oversee third-party manufacturing sites while maintaining non-interventionist observation and structured communication.
Apply through multiple platforms including United Pharma Technologies Inc's corporate career site and LinkedIn to maximize your application's visibility and reach for the Manufacturing Oversight Consultant role.
Connect with current employees or consultants in the Quality or Technical Operations divisions at United Pharma Technologies Inc on LinkedIn; use ice breakers like commenting on recent company advances in gene therapy manufacturing or asking about their experience with CMO oversight protocols to initiate conversations.
Optimize your resume for ATS by incorporating keywords from the job description such as 'GMP manufacturing,' 'aseptic processing,' 'fill-finish operations,' 'gene therapy,' 'CMO oversight,' and 'compliance risk documentation' to ensure it passes initial screening filters.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application portals, and find LinkedIn contacts in relevant divisions, allowing you to focus your time on networking and preparing for interviews effectively.
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