ZipRecruiter

Log In

1

Director Vector Jobs (NOW HIRING)

Multnomah County

Vector Program Supervisor

Portland, OR · On-site

$88K - $135K/yr

Under direction of the Environmental Health Director, the Vector Control Supervisor provides supervision and guidance for Vector control and Code Enforcement Staff and assists in managing and ...

Neion Bio

Viral Vector Scientist, Avian

New York, NY · On-site

$120/hr

... vector transduction of cells, ideally in non-model organisms. This is a hands-on role. Key ... or directed evolution * Perform transfections on primary cells, immortalized cells, and animal ...

Neion Bio

Viral Vector Scientist, Avian

New York, NY

$120/hr

... vector transduction of cells, ideally in non-model organisms. This is a hands-on role. Key ... or directed evolution * Perform transfections on primary cells, immortalized cells, and animal ...

Neion Bio

Viral Vector Scientist, Avian

New York, NY · On-site

$120/hr

... vector transduction of cells, ideally in non-model organisms. This is a hands-on role. Key ... or directed evolution * Perform transfections on primary cells, immortalized cells, and animal ...

next page

Showing results 1-20

All JobsBusiness JobsBusiness Services JobsBusiness Specialist JobsDirector Vector Jobs

Director Vector information

What are the roles and responsibilities of a director vector?

A Director Vector typically leads teams focused on vector graphics or vector-based technologies within a company, overseeing project planning, execution, and innovation. Their responsibilities often include managing creative or technical staff, setting strategic goals, and ensuring alignment with organizational objectives. They may also be involved in collaborating with other departments, budgeting, and representing the vector team in executive meetings. The role requires strong leadership, technical expertise, and a deep understanding of vector technologies or related fields.

What are the key skills and qualifications needed to thrive as a director vector?

To thrive as a Director of Vector, you need leadership experience in biotechnology or pharmaceuticals, expertise in gene therapy or vector development, and an advanced degree such as a PhD or equivalent in a related field. Familiarity with laboratory information management systems (LIMS), regulatory submission processes, and tools for genetic engineering is crucial. Excellent strategic planning, project management, and communication skills help foster innovation and collaboration among multidisciplinary teams. These qualifications ensure effective oversight of vector development, regulatory compliance, and successful execution of research programs.

What are some common challenges faced by a director vector, and how can they be addressed?

A Director of Vector Operations often encounters challenges such as coordinating multidisciplinary teams, managing large-scale projects, and staying current with evolving technologies in vector control or vector-borne disease research. Effective communication and strong leadership are essential for aligning diverse teams and ensuring project milestones are met. Proactively fostering collaboration between research scientists, field teams, and external partners helps address operational hurdles, while ongoing professional development ensures that best practices and regulatory requirements are consistently upheld.

What cities are hiring for Director Vector jobs?

Cities with the most Director Vector job openings:

What are the most commonly searched types of Vector jobs?

The most popular types of Vector jobs are:

What states have the most Director Vector jobs?

States with the most job openings for Director Vector jobs include:

Director Vector jobs near you
Infographic showing various Director Vector job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Director, Vector Production

Sangamo BioSciences, Inc.

Point Richmond, CA

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago

Job description

JOB SUMMARY: The Director, Vector Production will oversee activities related to the Process Development and in-house non-GMP/cGMP production of recombinant Adeno-associated Viral Vectors (rAAV), and cGMP vector production at contract manufacturing organizations (CMOs). ESSENTIAL FUNCTIONS: Manage the Process Development, GMP production, testing and fill finish of rAAV products at CMO's Manage internal activities related to the scale-up and production of rAAVs in house for use in R&D and pending facility decisions Lead in-house team producing rAAV Co-ordinate production activities with research, non-clinical development, QA, QC and clinical development Ensure the ongoing security of the supply chain for raw materials and intermediates to ensure the uninterrupted performance of rAAV operations Co-ordinate the transfer, qualification and implementation of process improvements and scale-up Lead the reporting, investigation and resolution of deviations encountered during GMP production activities Participate in the design, construction and commissioning of company manufacturing facilities Other activities as may be assigned EDUCATION, EXPERIENCE AND SKILLS REQUIREMENTS: The ideal candidate for this position will have in-depth experience of the large-scale cGMP production of rAAV, including upstream cell culture, downstream processing, and fill finish operations. Candidate must possess: MS or Ph.D in bioprocessing, chemical engineering, vector biology, or biological sciences Minimum of 10 years experience in the biotechnology or pharma industry with a primary focus on upstream cell culture process development and manufacturing operations for biologics Proven track record of managing in-house and CMO GMP production operations In-depth experience with: Mammalian cell, insect cell and microbial cell culture systems at both pilot-scale and at large-scale Different bioreactor production systems and scales, including disposable-based culture systems CIP, SIP, WFI In-depth knowledge of FDA, EMA, GMP and ICH regulatory requirements Knowledge of Quality Systems and QBD as they relate to GMP production operations and process optimization OTHER REQUIREMENTS: Experience of facility, and production equipment design and validation, including IQ, OQ & PQ a plus Proven managerial skills Outstanding organizational skills Excellent written and oral communication skills Ability to operate in a fast-paced, multi-disciplinary industrial environment The successful candidate will enjoy a competitive base salary and the opportunity to participate in incentive compensation programs, including bonus and stock option plans

Sangamo offers a comprehensive benefits program, including: medical, dental and vision care; paid vacation and holiday time; access to a voluntary 401(k) and Employee Stock Purchase Plan. Sangamo is an equal opportunity employer. Please send your resume/CV and a cover letter that specifically addresses this job posting as email attachments to: jobs@sangamo.com

Apply