Avid Bioservices, Inc.

Sr. EHS Engineer

Avid Bioservices, Inc. • $104K — $130K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in environmental engineering, safety, industrial hygiene, or related field; equivalent experience considered.
  • 8+ years of relevant EHS experience in regulated environments like manufacturing or biotechnology.
  • Strong knowledge of occupational safety and environmental compliance requirements.
  • Experience in leading risk assessments, audits, and incident investigations.
  • Ability to analyze technical information and communicate risks effectively.
  • Willingness to work on-site and respond to urgent EHS matters.

Responsibilities

  • Lead and maintain site EHS programs to ensure compliance with safety and environmental regulations.
  • Act as the primary EHS technical resource for site leadership and employees.
  • Conduct risk assessments and develop control strategies for various site projects.
  • Plan and execute site inspections and audits, ensuring timely corrective actions.
  • Investigate incidents and EHS concerns using structured root-cause analysis.
  • Maintain EHS records and communicate risks and performance metrics to leadership.
  • Develop and deliver EHS training to ensure consistent understanding across the site.

Benefits

  • Comprehensive health, dental, and vision insurance.
  • 401(k) matching program.
  • Paid time off and opportunities for career growth.
  • Supportive and inclusive work environment.
Full Job Description
Your Role:
The Senior Environmental Health & Safety Engineer serves as the primary EHS technical resource for the assigned site and leads the day-to-day design, implementation, and continuous improvement of site EHS programs. The role partners with site leadership and functions including Manufacturing, Facilities, Engineering, Quality, and People to identify and control risk, maintain regulatory readiness, and support reliable operations. This position independently evaluates complex EHS issues, recommends practical solutions, and leads cross-functional actions through completion. The role provides site-level functional leadership and technical guidance without direct people-management responsibility. Material regulatory, legal, policy, and resource decisions are escalated to the appropriate functional leader.

Key Responsibilities:
  • Lead and maintain site EHS programs, procedures, and controls to support compliance with applicable environmental, occupational health, safety, and biosafety requirements.
  • Serve as the primary site EHS technical resource for leaders and employees, translating regulatory and company requirements into practical operating expectations.
  • Lead risk assessments, job hazard analyses, management-of-change EHS reviews, and control strategies for facilities, equipment, processes, materials, and site projects.
  • Plan and lead site inspections, audits, and regulatory-readiness activities; document findings, assign corrective actions, and verify timely and effective closure.
  • Lead investigations of injuries, illnesses, near misses, environmental events, and other EHS concerns using structured root-cause methods and risk-based corrective actions.
  • Maintain required EHS records, permits, plans, reports, and metrics; monitor trends and communicate material risks, obligations, and performance to site leadership.
  • Develop and deliver role-appropriate EHS training and communications that support consistent understanding and application of site requirements.
  • Partner with Manufacturing, Facilities, Engineering, Quality, Security, and emergency-response stakeholders to coordinate preparedness, incident response, and business continuity activities.
  • Provide EHS input for contractors, vendors, capital projects, new processes, and operational changes so risks are identified and addressed before implementation.
  • Mentor and guide employees and program owners on EHS practices, and lead continuous-improvement initiatives that strengthen compliance, risk reduction, and site culture.

Minimum Qualifications:
  • Bachelor's degree in environmental engineering, safety, industrial hygiene, occupational health, engineering, a life-science discipline, or a related field; equivalent relevant education and experience may be considered.
  • 8 or more years of relevant EHS experience, including demonstrated ownership of complex cross-functional programs in a regulated manufacturing, biotechnology, pharmaceutical, or comparable environment.
  • Demonstrated working knowledge of occupational safety and environmental compliance requirements applicable to site operations.
  • Experience leading risk assessments, audits or inspections, incident investigations, corrective actions, and EHS training.
  • Ability to analyze technical and regulatory information, make sound recommendations, communicate risk to varied audiences, and maintain clear records.
  • Ability to work on-site and respond to time-sensitive site EHS matters as required by business operations.

Preferred Qualifications:
  • Experience supporting biopharmaceutical, biotechnology, CDMO, laboratory, or GMP manufacturing operations.
  • Professional certification such as CSP, CIH, CHMM, PE, or another relevant EHS credential.
  • Experience with environmental permitting, hazardous materials or waste programs, biosafety, emergency preparedness, and contractor safety.
  • Experience supporting regulatory agency interactions and leading cross-functional compliance or risk-reduction initiatives.


Position Type/Expected Hours of Work:

This role is a full-time onsite position in Costa Mesa, CA. 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 $104,000 to $130,000 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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