Operational Compliance Specialist

About the Role

The Operational Compliance Specialist will ensure safe, efficient, innovative and cost‑effective operation of GMP buildings at Genentech’s Oceanside campus, maintaining full compliance with Good Manufacturing Practices, corporate policies, and quality standards. The role involves implementing compliance programs, conducting audits, delivering training, and investigating compliance issues to mitigate risk and uphold ethical standards. • Develop and implement compliance policies and procedures to meet regulatory standards. • Conduct audits and assessments to identify compliance gaps and risks. • Collaborate with internal teams to address issues and implement corrective actions. • Stay current on regulatory changes and ensure organization‑wide adherence. • Provide training and guidance on compliance matters to employees. • Maintain qualification as a Qualified OJT Trainer and verify frontline training status through periodic reports. • Investigate compliance violations and support supervisors with disciplinary actions. • Keep accurate records and documentation of all compliance activities. • Review documentation against area‑specific SOPs and ensure timely approvals. • Lead continuous‑improvement projects to enhance compliance processes. • Serve as backup GMP supervisor when needed and support the GMP pest‑control program, including audits and quarterly reporting.

Key Responsibilities

• ▸compliance audits
• ▸policy development
• ▸compliance training
• ▸record keeping
• ▸process improvement
• ▸gmp supervision

What You Bring

JLL empowers you to shape a brighter way by combining world‑class services, advisory and technology to transform real estate. The company is committed to hiring talented people, fostering career growth, and creating a sense of belonging across diverse roles. Whether you have deep commercial‑real‑estate experience, skilled‑trade expertise, or a technology background, JLL invites you to join its mission. Candidates must have at least two years of experience in compliance, risk management or regulatory environments within pharma, biotech, cosmetics or manufacturing, and be familiar with cGMPs and FDA guidelines. Strong written and verbal communication skills, self‑motivation, attention to detail, and the ability to work independently in a dynamic team are essential. Preferred qualifications include prior work with regulatory agencies, conducting examinations, and bilingual capabilities.

Requirements

• ▸2+ years
• ▸compliance
• ▸cgmp
• ▸fda
• ▸communication
• ▸bilingual

Benefits

This full‑time, on‑site, exempt position is based in Oceanside, CA, with a swing‑shift schedule and requires occasional after‑hours troubleshooting and clean‑room access. The estimated compensation range is $81,000‑$87,000 per year, and the role does not provide visa sponsorship. JLL offers a comprehensive benefits package that supports mental, physical and emotional well‑being, including a 401(k) match, medical/dental/vision coverage, paid parental leave at 100 % salary, paid time off, company holidays, and early wage access via Daily Pay. The company is an equal‑opportunity employer, committed to reasonable accommodations and inclusive hiring practices.

Work Environment

Onsite