Manager, Compliance
$106.8k - $120.15kPCI Pharma Services
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.We are PCI.Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.SUMMARY:The Manager, Compliance leads a team responsible for audit inspection readiness and quality audit policies & procedures in support of PCI Pharma’s clinical and commercial manufacturing facilities. This role oversees quality management system (QMS) activities such as risk assessments, audit follow-ups, and client contractual agreements to ensure compliance with U.S. and international regulatory requirements.ESSENTIAL JOB FUNCTIONS-OTHER DUTIES MAY BE ASSIGNED:Manages QA Compliance team activities encompassing all internal audits and external compliance and regulatory inspections, as well as vendor and customer audit programs.Develops technical acumen and decision-making skills in direct reports.Oversees PCI Pharma’s risk management program including implementation and integration of the relevant risk evaluation into the QMS process, as well as collaboration with Manufacturing and other internal stakeholders.Leads complex audit, deviation and CAPA investigations.In collaboration with SMEs, oversees the process impact of audit observations, and associated quality events, as well as adverse events to product quality.Manages quality event trend reports and metrics to measure key quality attributes.Accountable for departmental process and system improvement initiatives and collaborates in the enhancement of other key QMS and manufacturing processes to ensure compliance with applicable FDA guidelines and regulations.Develops and maintains relevant quality sections of contractual agreements with clients.Regular and reliable attendance on a full time basis (or in accordance with posted schedule).Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.Embodies PCI Pharma’s cultural values and aligns daily actions with department goals and company culture.EDUCATION AND EXPERIENCE:Bachelor’s degree in a Life Sciences or Engineering discipline, or equivalent.Minimum of 7 years of relevant QA experience in a regulated industry; biotech or pharmaceutical industries strongly preferred.Minimum of 3 years of leadership or supervisory experience.Experience with aseptic processing; experience with restricted access barrier systems (RABS) and isolators preferred.Working knowledge of cGMPs, FDA regulations, ICH Guidelines in drug/device, and familiarity with the European Community guidelines for cGMPs.Advanced-level understanding of regulatory requirements related to aseptic drug product manufacturing and testing.Knowledge and hands on experience with QMS data management software such as Track Wise, Master Control, ETQ, etc.Experience with process mapping, data analysis and presentation software such as Visio, Microsoft office, Excel, PowerPoint, etc.LEADERSHIP RESPONSIBILITIES:Directs and provides expert knowledge in the day-to-day function of QA Compliance.Identifies, recruits, and retains top-notch talent.Champions PCI Pharma’s culture and empowers employees to take responsibility for their jobs and goals.Coaches, mentors, engageand develop the team, including overseeing new employee onboarding and providing career development planning and learning opportunities.Sets performance standards and encourages employee engagement and results through delegation, continuous feedback, goal setting, and performance management.Maintains transparent communication. Appropriately communicates organization information through department meetings, one-on-one meetings, and appropriate email, and regular interpersonal communication.Provides oversight and direction to the employees in accordance with PCI Pharma’s policies and procedures.The hiring rate for this position is $106,800 - $120,150.00 plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors, including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), a flexible spending account, and a 401(k) plan.n.#LI-AC1Join us and be part of building the bridge between life changing therapies and patients. Let’s talk futureEqual Employment Opportunity (EEO) Statement:PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.SummaryLocation: San Diego, CA, USAType: Full time
$106.8k - $120.15k
...tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.SUMMARY:The Manager, Compliance leads a team responsible for audit inspection readiness and quality audit policies & procedures in support of PCI Pharma’s clinical...SuggestedFull timeWork at officeFlexible hours$106.8k - $120.15k
...This role leads a compliance team overseeing audit readiness, quality management systems, and regulatory inspections for clinical and commercial manufacturing facilities. The manager directs internal audits, manages risk assessments, and ensures alignment with FDA and...Suggested- ...preparing or reviewing Module 3/Quality content for clinical-stage submissions; small-molecule experience is preferred.Ability to manage multiple programs and workstreams, establish priorities, maintain submission timelines, and deliver high-quality work in a fast-paced...SuggestedWork at officeFlexible hours
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...decisions that accelerate product development while ensuring full compliance with applicable regulations and guidance. Responsibilities:... ..., from early development through post-approval lifecycle management Serve as the primary regulatory strategist on cross-functional...Full timeWork at officeFlexible hours- ...responsible for supporting multiple global regulatory projects, ensuring compliance with all relevant regulatory requirements and guidelines, and... ...requirements, regulations, and guidance. Proven ability to manage complex projects, priorities, and timelines within a...
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...working-with-us.The GRS-CMC Director is responsible for overseeing management of multiple development and life-cycle management projects of... ...preparation of CMC policies and proceduresEnsure Regulatory Compliance: Maintain oversight and promote the highest standards of...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$284k - $302k
...mentoring, developing, and influencing teams.Ability to lead through influence across functions without direct authority.Experience managing regulatory risk and translating requirements into practical development strategies.Excellent communication skills, with the...Full timeSummer workWork at officeRemote workRelocationRelocation packageShift work$132k - $172k
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- ...roadmaps from first-in-human through post-marketing lifecycle management Provides guidance on complex regulatory issues to cross-functional... ..., respectful, and inclusive work environment Governance & Compliance Ensures compliance with global regulatory requirements...
$38 - $56 per hour
...strong understanding of regulatory requirements, medical device compliance, and regulatory documentation. This role offers an hourly pay... ...documentation, organizational, and communication skills Ability to manage multiple priorities and meet deadlines in a remote environment...Hourly payContract workLocal areaImmediate startRemote workMonday to Friday- ...30 countries. The U.S. office serves as the hub for strategic management, administration, business development, and innovative research... ...development and review of labeling and promotional materials for compliance. Qualifications ~ Strong proficiency in Regulatory...Full timeWork at officeRelocation
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...Labor Compliance Specialist Pay Rate: $32 - $43/hr Looking for your next opportunity in labor compliance? We're partnering with a... ...~ Experience with LCPtracker or similar systems ~ Ability to manage multiple projects independently Why consider this role?...Temporary workFor subcontractorLocal area$140k - $180k
...Chief Compliance Officer Summary of Superior Planning: Superior Planning offers a full-service Wealth Management and Family Office group that provides highly tailored services for clients with complex financial matters. We go beyond traditional financial planning...Full timeContract workWork at office- ...Neurocrine Biosciences seeks an Executive Director of QA Compliance to lead strategic oversight of quality compliance, regulatory readiness, and risk management programs across GxP activities. The role provides advisory support to senior leadership on complex compliance...
$91.7k - $137.53k
...physician initiated studies. • Provide Regulatory support to on-going compliance and corporate initiatives.• Partner with Marketing and... ...as required. Review submission decisions/content issues with manager.• Provide assistance in planning, creating, organizing and interpreting...Full timeWork at office- ...laser technologies.We have an exciting opportunity for a Senior Compliance Specialist at our Torrey Pines, San Diego, CA location. The... ...of supplier administration, supply chain, purchasing, material management, price/cost analysis and/or production control principles, theories...Part timeFor contractorsWork at officeRemote workRelocation package
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