CMC Technical Writer

About Nexinfo:

Nexinfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges such as inventory management, product lifecycle management, demand management, forecasting, sales and operations planning, business intelligence, security compliance, and financial alignment.

Job Title: CMC Technical Writer

Location: Santa Monica, CA (REMOTE)

Type: Contract

We are seeking a highly motivated individual with late-phase CMC technical experience, including technical and regulatory submission experience. This position is part of the Process Development organization and in this role, this individual will be supporting the internal Process Development teams. In the near-term, this role will support time critical CMC Regulatory submissions. Longer-term, this individual will be embedded in technical teams within the Process Development department supporting CMC aspects of our growing pipeline projects.

Responsibilities (include but are not limited to):

• Author and Finalize appropriate Module 3 documents and Response to Agency Questions in collaboration with Regulatory CMC and Technical Subject Matter Experts

• Experience in analytical method development of vector and T cell, extended characterization of vector and T cell products, awareness of ICHs and global compendial requirements governing analytical development and characterization/comparability of Advanced Therapy Medicinal Products and vector intermediates.

Requirements:

• Bachelor's, Master's Degree, or PhD in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, Biology, Biochemistry or equivalent with 7 years (Bachelors), 5 years (Masters), 3 years (PhD) of relevant experience

• Experience CMC/Module 3 regulatory submissions

• Experience in technical writing and proficient in high quality writing

• Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing and analytical and process development

• Thorough knowledge of biologics analytical and process development is essential. Cell therapy process development experience is highly desired

• Knowledge of product lifecycle – Product and process development, clinical trials, validation and regulatory submissions, commercial GMP manufacturing

• Working knowledge of regulatory requirements for biologics, pharmaceuticals and medical devices

• Must be able to function and contribute as part of a team, have excellent communication skills and contribute to team based decisions

• Ability to think critically, and demonstrated troubleshooting and problem solving skills

• Self-motivated and willing to accept temporary responsibilities outside of initial job description

• Well-developed computer skills and fluent with Microsoft office applications

• Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment

Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities

Thanks & Regards,

Joseph Thambi

Senior Executive - Talent Acquisition