Avid Bioservices, Inc.

Associate Director, Utilities & Site Development Workstream

Avid Bioservices, Inc.$147K — $184K *
Energy & Utilities
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering, facilities management, construction management, or related field, or equivalent experience.
  • 10+ years of relevant experience in utilities, facilities engineering, site development, or related areas in a regulated environment.
  • Proven track record of managing complex cross-functional workstreams.
  • Knowledge of utility infrastructure and operational readiness processes.

Responsibilities

  • Own the Utilities & Site Development workstream plan and ensure timely execution.
  • Translate technical requirements into actionable design inputs and acceptance criteria.
  • Coordinate with engineering and operational teams for effective project execution.
  • Monitor workstream metrics (scope, schedule, cost, quality) and manage escalations as needed.
  • Facilitate critical technical decisions across diverse project domains.
  • Lead the planning for operational readiness and transition of facilities management.
  • Maintain governance documentation and provide concise progress reports.

Benefits

  • Full-time onsite role with Monday to Friday schedule.
  • Opportunity for overtime and weekend work as needed.
  • Comprehensive health, dental, and vision insurance.
  • 401(k) matching program.
  • Paid time off and career development opportunities.
Full Job Description
Your Role:
The Associate Director, Utilities & Site Development Workstream provides owner-side leadership for utility infrastructure and site-development scope within Project AMPLIFY. The role integrates business, technical, permitting, construction, and operational requirements into an executable workstream plan through design, installation, startup, readiness, and handover. The position is accountable for workstream scope, schedule, cost, risk, and technical readiness while coordinating internal subject-matter experts, engineering partners, contractors, and operating teams. The role operates with substantial day-to-day independence and escalates material commitments or changes through the appropriate project governance channels.

Key Responsibilities:
  • Own the integrated Utilities & Site Development workstream plan, milestones, dependencies, risks, and deliverables through operational handover.
  • Translate facility, utility, infrastructure, site, and operating requirements into clear design inputs and acceptance criteria.
  • Coordinate engineering partners, contractors, subject-matter experts, Quality, EHS, and operating stakeholders to support execution.
  • Monitor workstream scope, schedule, cost, quality, safety, and readiness, escalating material issues with clear options and recommendations.
  • Facilitate technical decisions and interfaces across civil, utility, facility, automation, and operational systems.
  • Lead readiness and transition planning for startup, procedures, maintenance strategies, training, and operating ownership.
  • Maintain workstream governance, decision records, risk documentation, and concise stakeholder reporting.
  • Support commissioning, startup, and stabilization through successful transition to the Facilities & Engineering organization.

Minimum Qualifications:
  • Bachelor's degree in engineering, facilities management, construction management, or a related field, or equivalent relevant experience.
  • 10 or more years of relevant experience in utilities, facilities engineering, site development, construction, or capital-project delivery in a regulated environment.
  • Demonstrated ownership of complex cross-functional technical initiatives or workstreams.
  • Working knowledge of utility infrastructure, technical design coordination, operational readiness, and change control.

Preferred Qualifications:
  • Professional Engineer, project management, or construction management credential.
  • Experience supporting biotechnology or pharmaceutical manufacturing facilities.
  • Experience with facility startup, commissioning, or operational handover.


Position Type/Expected Hours of Work:

This role is a full-time onsite position. Days and hours of work are Monday through Friday 8:00 a.m. to 5:00 p.m. unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.

Compensation:

We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.

The compensation range for this role is $147,200 - $184,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.

Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:

In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

About Avid Bioservices, Inc.

Avid Bioservices, Inc. is a contract development and manufacturing organization (CDMO) focused on development and CGMP manufacturing of biopharmaceutical drug substances derived from mammalian cell culture. The company provides a comprehensive range of process development, high quality CGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. With 25 years of experience producing monoclonal antibodies and recombinant proteins in batch, fed-batch and perfusion modes, Avid's services include CGMP clinical and commercial drug substance manufacturing, bulk packaging, release and stability testing and regulatory submissions support. The company also provides a variety of process development activities, including cell line development and optimization, cell culture and feed optimization, analytical methods development and product characterization.
Learn more about Avid Bioservices, Inc.
Size
321 employees
Market Cap
$873.5 million
Industry
Net Income
$4.4 million
5 Year Trend
+15.7%
Revenue
$80.8 million
NASDAQ

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