Top 43 Program director/pd Jobs in Los Angeles, Ca

Director / Sr. Director, Manufacturing Sciences
Angitia Incorporated Limited —Los Angeles, CA
- $210,000 - $265,000 a year
- Remote
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
- AD&D insurance
- Paid holidays
Quick Apply
13d
Administrative Assistant
City of Roseville (CA) —Vernon, CA
- $31.30 - $41.94 an hour
- Full-time
- Background check
- Customer service
- Mid-level
- Paid holidays
- Health insurance
2d
Supervisory Health System Specialist (Corporate Compliance Chief)
US Veterans Health Administration —Los Angeles, CA
- $146,632 - $190,627 a year
- Online Application
- Hybrid work
- Background check
- Writing skills
- Pass drug screening
3d
Global Merchandising Manager, Sportswear
Wilson Sporting Goods Co. —Los Angeles, CA
- $125,000 - $140,000 a year
- Microsoft Excel
- Marketing
- Merchandising
- Paid parental leave
- Health insurance
Program Director, Occupational Therapy (OT)
Lifepoint Rehabilitation —Glendale, CA
- $135,000 - $145,000 a year
- Full-time
- Working with individuals with disabilities
- Hospital
- Customer service
- Disability insurance
- Health insurance
Quick Apply
Program Coordinator, CAP Fellowship
Charles R. Drew University of Medicine and Science —Los Angeles, CA
- Full-time
- Microsoft Excel
- Psychiatry
- Writing skills
Quick Apply
Program Director of Pre-Clinical Education, Los Angeles College of Chiropractic
Southern California University —Whittier, CA
- $130,000 - $140,000 a year
- Full-time
- Hybrid work
- Microsoft Outlook
- Customer service
- Windows
Quick Apply
Director of Biology & Biochemistry
Eli Lilly —Pasadena, CA
- $163,500 - $281,600 a year
- Full-time
- Continuous improvement
- Doctor of Philosophy
- Mentoring
- Health insurance
- Dental insurance
9d
Psych EM Team Clin PD
AHMC Healthcare —San Gabriel, CA
- From $46.28 an hour
- Weekends as needed
- LMFT
- Psychiatry
- RN License
Global Merchant, Sportswear
Wilson Sporting Goods Co. —Los Angeles, CA
- $100,000 - $120,000 a year
- Microsoft Excel
- Marketing
- Merchandising
- Paid parental leave
- Health insurance
After School Program Coordinator: Mid-San Fernando Valley
After-School All-Stars Los Angeles —Los Angeles, CA
- $22 - $26 an hour
- Weekends as needed
- School experience
- Current TB test
- Pass drug screening
Quick Apply
After School Program Coordinator: Full-Time, Commerce 90040
After-School All-Stars Los Angeles —Los Angeles, CA
- $22 - $26 an hour
- Weekends as needed
- School experience
- Current TB test
- Pass drug screening
Quick Apply
After School Program Coordinator: Full-Time, Los Angeles 90026
After-School All-Stars Los Angeles —Los Angeles, CA
- $22 - $26 an hour
- Weekends as needed
- School experience
- Current TB test
- Pass drug screening
Quick Apply
Program Supervisor
Help Group —Inglewood, CA
- $80,000 - $84,000 a year
- 8 hour shift
- LMFT
- Master of Social Work
- Psychiatry
- Health insurance
- Dental insurance
Quick Apply
Sr. Director, Product Lifestyle & PMO Ops
MGA Entertainment, Inc. —Los Angeles, CA
- $160,000 - $200,000 a year
- Agile
- Senior level
- Communication skills
Quick Apply
Bilingual (English-Spanish) Professional Development Specialist (Per Diem)
Catapult Learning —Los Angeles, CA
- Per diem
- School experience
- Classroom
- Spanish
- Paid training
- Opportunities for advancement
Quick Apply
After School Program Coordinator: Full-Time, South LA
After-School All-Stars Los Angeles —Los Angeles, CA
- $22 - $26 an hour
- Weekends as needed
- Current TB test
- Pass drug screening
- Mid-level
Quick Apply
After School Program Coordinator: Full-Time, East LA/Montebello
After-School All-Stars Los Angeles —Los Angeles, CA
- $22 - $26 an hour
- Weekends as needed
- School experience
- Current TB test
- Pass drug screening
Quick Apply
After School Program Coordinator: Full-Time, South LA 90003
After-School All-Stars Los Angeles —Los Angeles, CA
- $22 - $26 an hour
- Weekends as needed
- School experience
- Current TB test
- Pass drug screening
Quick Apply
After School Program Coordinator: Full-Time, South Gate 90280
After-School All-Stars Los Angeles —Los Angeles, CA
- $22 - $26 an hour
- Weekends as needed
- School experience
- Current TB test
- Pass drug screening
Quick Apply

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Director / Sr. Director, Manufacturing Sciences

Angitia Incorporated Limited
Los Angeles, CA

Quick Apply

Job Details

$210,000 - $265,000 a year
13 days ago

Benefits

AD&D insurance
Paid holidays
Disability insurance
Health insurance
Dental insurance
Employee assistance program
Vision insurance
401(k) matching
Life insurance
Paid sick time

Qualifications

GMP
ICH Q9
Pharmaceutical company experience
ICH Q10
Bioprocessing
Chemistry, manufacturing & controls
Lean management
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

Position: Director / Sr. Director, Manufacturing Sciences
Department: CMC
Location: Remote with up to 20% global and domestic travel
Reports To: VP, CMC Operations

Position Summary

The Director / Sr. Director, Manufacturing Science & CMC Operations will support the cross-functional technical and operational work that connects Drug Substance Process Development (PD), Analytical Development (AD), and our external manufacturing partners across the late-stage development of bispecific monoclonal antibody programs.

Angitia operates a fully outsourced model. In this environment, much of the work that connects our science to the manufacturing involves sponsor-side oversight of CDMO execution, integration of process and analytical data and documentation, and hands-on support of manufacturing readiness. In this role, you will provide drug substance (DS) technical expertise, support day-to-day technical oversight of the CDMOs, and help ensure the programs are manufacturing- and submission-ready as they advance into Phase 3, process validation, and commercial supply.
You will work within a lean, US-based CMC team, partnering with Process Development, Analytical Development, Program Management, Quality, and Regulatory CMC. This role will suit someone who brings late-stage and process validation rigor but is energized rather than slowed by a lean, still-maturing organization – someone who can raise the bar while making sound, pragmatic decisions where structure is still being built.

Responsibilities

Manufacturing Science & CDMO Technical Oversight

Serve as a sponsor-side technical point of contact for manufacturing executed at CDMOs, providing technical oversight
Provide on-site technical presence (person-in-plant) during key manufacturing activities — engineering runs, process performance qualification, and process change implementation
Review CDMO-generated batch records, in-process data, deviations, and investigations with a sponsor lens; contribute technical assessments for deviations, CAPAs, and change controls
Establish and own a continued process verification (CPV) / process monitoring program, trending process and analytical data across campaigns to monitor consistency, robustness, and ongoing comparability
Identify process improvement opportunities arising from this monitoring and from manufacturing experience, and support their development in partnership with PD

CMC Documentation Integration & Technical Writing

Support the integration, consistency, and quality control of the CMC document set across PD and AD inputs — including Module 3 sections of INDs, CTAs, and IMPD updates, with review and QC of CDMO-generated content
Review and integrate CDMO-generated documents (e.g., tech transfer plans and reports, process validation documentation, and other technical summaries) into clear, defensible regulatory content
Draft and help finalize responses to health authority RFIs and CMC questions
Ensure consistency, scientific accuracy, and regulatory alignment across all CMC documents for both programs

Technology Transfer & Phase 3 / PPQ Readiness

Coordinate and support technology transfer activities as the Phase 3 processes are defined and implemented at CDMOs
Support manufacturing readiness and process performance qualification (PPQ) planning, and author or contribute to PPQ protocols and reports from a sponsor-side technical standpoint
Plan, execute, and interpret process and analytical comparability as drug substance processes move between sites and scales, building defensible bridges from earlier clinical material to Phase 3 and commercial supply

Cross-Functional Collaboration

Contribute to control strategy and specification justification for drug substance and drug product quality attributes, in partnership with AD and QC
Partner across PD, AD, Program Management, Quality, and Regulatory CMC to advance CMC deliverables
Support inspection and submission readiness from a CMC technical and documentation standpoint

Qualifications

Experience with monoclonal antibodies or complex biologics required; bispecific antibody experience a strong plus
Advanced degree (MS or PhD) in biochemistry, chemistry, chemical/biochemical engineering, or a related life sciences discipline; BS with extensive relevant industry experience considered
10–12 years of CMC development experience for biologics, including hands-on background in drug substance process development, analytical development, or manufacturing science / technical operations
Solid command of ICH guidelines (Q6B, Q8, Q9, Q10, Q11) and GMP requirements for biologics
Familiarity with control strategy principles and specification setting for biological products
Strong technical judgment, with the ability to manage external technical relationships and to influence cross-functionally without direct authority
Self-directed and effective operating with autonomy in a lean, fast-moving organization
Effective in both structured late-stage / commercial environments and lean, earlier-phase or small-company settings
Willingness to travel to CDMO sites (~10–20% of time); international travel likely

Preferred Experience

Experience working in or with a fully outsourced (CDMO-based) development model
Direct MSAT or technical operations experience supporting late-stage or commercial biologics manufacturing
Prior involvement in BLA or MAA submissions for biologics
Experience supporting process performance qualification (PPQ) and process validation for biologics

Salary Range: $210,000 to $265,000

About Angitia

Established in June 2018, Angitia Biopharmaceuticals is a clinical-stage biotechnology company focused on the discovery and development of innovative therapeutics for serious musculoskeletal diseases. Angitia is currently studying 3 biologic product candidates in the clinic for the treatment of osteoporosis, osteogenesis imperfecta (OI), and spinal fusion. Leveraging the team's extensive experience and scientific acumen in novel drug development, Angitia is committed to providing groundbreaking therapies to satisfy key unmet medical needs. The founder and the core team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. The company has built an organization with offices in Westlake Village, CA and Guangzhou, China that is distinguished by world-class scientists with talents that are proficient in the pathophysiology of musculoskeletal diseases. We utilize cutting-edge technologies of genetics and molecular biology to uncover new mechanisms, signal transduction pathways and their interactions combined with computer aided drug design to identify new drug targets, and to discover and develop new biological and small molecule medicines. The company is committed to serving patients in need by carrying out innovative science including internal research and external collaborations with academics and global biopharmaceutical companies. We are seeking talented individuals who are innovative, ambitious, and great team players to join our vibrant group.
Learn more at www.angitiabio.com.

Benefits:

Medical, dental, and vision coverage for employees and their eligible dependents
401(K) Retirement Plan with Company match
Company paid Long Term Disability Coverage
Company-paid life Insurance & AD&D Coverage
Voluntary Life Insurance & AD&D Coverage
Employee Assistance Program (EAP)
Company-paid Holidays
Vacation
Paid Sick Leave
Telecommunication Monthly Stipend
Work-From-Home Equipment Reimbursement

Quick Apply

Refine Your Search

program director/pd jobs in los angeles, ca

Director / Sr. Director, Manufacturing Sciences

Administrative Assistant

Supervisory Health System Specialist (Corporate Compliance Chief)

Global Merchandising Manager, Sportswear

Program Director, Occupational Therapy (OT)

Program Coordinator, CAP Fellowship

Program Director of Pre-Clinical Education, Los Angeles College of Chiropractic

Director of Biology & Biochemistry

Psych EM Team Clin PD

Global Merchant, Sportswear

After School Program Coordinator: Mid-San Fernando Valley

After School Program Coordinator: Full-Time, Commerce 90040

After School Program Coordinator: Full-Time, Los Angeles 90026

Program Supervisor

Sr. Director, Product Lifestyle & PMO Ops

Bilingual (English-Spanish) Professional Development Specialist (Per Diem)

After School Program Coordinator: Full-Time, South LA

After School Program Coordinator: Full-Time, East LA/Montebello

After School Program Coordinator: Full-Time, South LA 90003

After School Program Coordinator: Full-Time, South Gate 90280

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