AVP, Quality & Technical Operations

Hikma Pharmaceuticals; Cherry Hill Township (NJ); On-site; USD 182,000 - 331,000; Full time

Benefits offered by this job

Annual performance bonus

401(k) with match

PTO 20 days (prorated)

Personal days

11 company holidays

Benefits including health, dental, and

Job summary

Hikma Pharmaceuticals USA Inc. in Cherry Hill, NJ is seeking an Associate VP, Quality Operations to oversee Quality Assurance, Quality Control, Validation, and related functions across sites.

You will ensure compliance, drive quality systems, and partner with regulatory agencies to maintain industry-leading standards. The role requires 15+ years in pharma quality/manufacturing with 7+ years in leadership, deep cGMP knowledge, and a proven ability to lead complex audits, improvements, and

Qualifications

• Bachelor’s degree in Science or Engineering (advanced degree preferred).
• 15+ years in quality/manufacturing with 7+ years in leadership within pharmaceutical manufacturing.
• Experience supporting injectable manufacturing operations and familiarity with regulatory expectations.

Responsibilities

• Develop and deploy quality systems ensuring products conform to requirements.
• Lead Quality organization for Hikma’s injectable sites and act as the QMR.
• Manage regulatory inspections and ensure conformance to regulations.
• Review quality system effectiveness with executive management.
• Oversee site validation master plans and technical operations.
• Lead contract manufacturing programs including cost proposals and validation.

Skills

Quality systems

Regulatory compliance

cGMP knowledge

Leadership

Data analysis

Communication

Project management

Education

Bachelor’s degree in Science or Engineering

Advanced degree preferred

Job description

Job Title: Associate VP, Quality Operations

Location: Cherry Hill ,NJ

Job-Type:Fulltime

Job Id: 12833

About Us

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.

JOB PURPOSE

The Associate VP, Quality Operations oversees Quality Operations and Technical Affairs, which includes, Quality Assurance, Quality Control, Quality Systems, Validation & Metrology, and Quality Investigations at the Cherry Hill, NJ and Bedford, Ohio facilities. This encompasses Chemistry, Microbiology, Environmental Monitoring, QA In-Process, QA Investigations, QA Documentation, Media Fills, Sterility. Assurance, SOP Training, Aseptic Technique Training, Quality Compliance, Product and Equipment Validations, and Manufacturing Calibrations Instrument Services. This role also ensure that systems and procedures for regulatory compliance are established and deployed, periodically reviews the suitability and effectiveness of quality systems with executive management, and oversees regulatory inspections and technical activities for all or multiple segments of the validation function. Further, this role is responsible for managing, developing, and implementing validation processes to ensure that equipment, components, processes, and products comply with the applicable regulatory agency validation requirements, internal company standards, and current industry practices, sharing advice and expertise on multiple disciplines to meet business plans.

KEY ACCOUNTABILITIES

• Develop and deploy quality systems (e.g., management review, CAPA, process control) that ensure products conform to defined requirements
• Manages the Quality organization for Hikma’s injectable Sites, acting as the Quality Management Representative. Is responsible for results in terms of product quality and conformance to regulations and policies
• Understands and deploy processes to assure conformance to regulations at Hikma’s Sites, managing regulatory inspections
• Periodically review the suitability and effectiveness of the quality system with executive management
• Assesses and advise senior management concerning acquisition targets
• Interact frequently with all levels of internal management as well as across functions and business units
• Responsible for adherence to specifications and procedures that have been established to ensure product quality in area of responsibility
• Direct the Technical Services organization to be efficient, effective and compliant in the execution of Site validation master plans, including product development, client Management and all aspects of a compliant validation program in line with industry best practice
• Have responsibility for Site contract manufacturing programs, including cost proposals, validation strategy and plan, technical evaluation and feasibility, liaising with clients, and project management
• Initiate, develop, and lead technical feasibility analysis where new and unproven methods and technologies are required.
• Manage interactions with customers and regulators concerning the quality of products, systems and processes
• Identify and manage continuous improvement projects that may span multiple sections or departments with the objective of achieving quality, reliability and cost improvements
• Responsible for adherence to specifications and procedures that have been established to ensure product quality in area of responsibility
• Consistently develop and execute innovative theories and technologies
• Understand and integrate information from more than one discipline and apply to complex problems requiring innovative techniques
• Participate in global task forces and committees
• Accountable for critical strategic and operational decisions (e.g., milestones, technical due diligence)
• Develop budgets and ensures adherence
• Perform other duties as assigned
• Maintain regular, predictable onsite attendance and punctuality

QUALIFICATIONS & SKILLS

QUALIFICATIONS

• Bachelor’s degree in Science or Engineering; advanced degree preferred

EXPERIENCE

• Mininimum of 15+ years of progressive Quality, Manufacturing, or related field experience, with at least 7+ years of management or leadership experience within pharmaceutical manufacturing, including the following:
• Managing others both internally and externally
• Demonstrated experience supporting injectable manufacturing operations; oral, including solid dose, experience is a plus
• Establishing strategies and leading Quality organizations and technical operations
• Strong understanding of injectable and, more generally, generic pharmaceutical manufacturing environments and associated quality systems and operations

SKILLS

• Proven experience and process knowledge in pharmaceutical manufacturing / packaging technology, engineering, maintenance and technical operations
• In depth knowledge of the regulatory environment for the manufacture of pharmaceutical products
• Strong knowledge of cGMP requirements, validation principles, human factors, quality systems, regulatory expectations and industrial safety
• Proven ability to influence and collaborate with stakeholders at all levels, including executive leadership, regulatory agencies, suppliers, customers, and global teams
• Exceptional leadership, coaching, mentoring, and talent development skills, including guiding senior-level professionals and leading organizational transformation initiatives
• Results-oriented leader with a strong focus on safety, quality, compliance, delivery, and cost performance
• Strong analytical, problem-solving, and data-driven decision-making abilities
• Highly effective communicator with exceptional verbal, written, presentation, and executive communication skills; able to translate complex technical and quality information to a diverse audience
• Self-motivated, detail-oriented team player with the ability to work effectively in domestic and international environments

ADDITIONAL CONSIDERATIONS (IF ANY)

• Significant travel expected to support operational needs

Compensation

Base Salary:$ $182,000 to $331,250. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.

What We Offer

• Annual performance bonus, commission, and share potential
• Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
• A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
• 3 personal days (prorated based on hire date)
• 11 company paid holidays
• Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
• Employee discount program
• Wellbeing rewards program
• Safety and Quality is a top organizational priority
• Career advancement and growth opportunities
• Tuition reimbursement
• Paid maternity and parental leave
• Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.

Equal Opportunity Employer

Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.