Lead Quality Control for biologics programs, overseeing QC strategy, regulatory compliance, and cross-functional teams.
Compensation
The salary range for this position is: $182,070.00 - $235,620.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Responsibilities
Serve as QC Lead and primary QC point of contact for assigned biologics programs
Develop and maintain phase-appropriate QC strategies
Provide QC oversight for testing performed at internal laboratories, CMOs/CDMOs, and contract testing laboratories
Provide scientific and quality guidance for deviations and regulatory content
Lead cross-program initiatives for QC governance and harmonization
Lead validation initiatives for manufacturing equipment, processes, cleaning and computerized systems to ensure compliance with regulatory and quality standards.
Compensation
The estimated salary range for this position is $72,080.00 - $108,120.00 CAD annually, which reflects base salary as well as estimated target payout under the Management Incentive Compensation Plan.
Responsibilities
Lead the development, execution, and completion of validation programs for manufacturing equipment, processes, cleaning and computerized systems to ensure a validated state of control.
Author validation protocols and reports, analyze validation data, and apply statistical techniques to demonstrate compliance with regulatory and quality requirements.
Partner with Engineering, Production, Quality Control, and external vendors to plan, coordinate, and execute qualification activities including IQ, OQ, and PQ protocols.
Serve as a validation subject matter expert by providing technical guidance on process validation, cleaning validation, equipment qualification, computerized systems validation, and data integrity practices.
Support change control and quality system activities by assessing validation impacts, contributing to investigations, and leading resolution of validation-related non-conformances and corrective actions.
Requirements
Bachelor's degree in engineering, Chemistry, Microbiology, Pharmacy, Life Sciences, or a related scientific discipline.
The Process Engineer II is responsible for providing 1st shift engineering production support including implementing process and technology improvements, regular on-the-floor manufacturing support, collecting, monitoring, analyzing, troubleshooting, and reporting manufacturing data related to performance in the areas of quality, cost, and speed/service to market, investigating non-conformances, CAPAs, process performance drifts and implementing corrective and preventative actions, conducting technical assessments of change orders and Supplier Change Requests, and responsible for the initiation and follow-through of the change control processes.
Responsibilities
Implementing process and technology improvements
Regular on-the-floor manufacturing support
Collecting, monitoring, analyzing, troubleshooting, and reporting manufacturing data related to performance in the areas of quality, cost, and speed/service to market
Investigating non-conformances, CAPAs, process performance drifts and implementing corrective and preventative actions
Conducting Technical assessments of change orders and Supplier Change Requests
Lead technical workstreams and contribute to program outcomes by developing actionable methods and analyses, collaborating with cross‑functional partners to integrate technical solutions throughout the lifecycle, and advising on complex technical decisions and risks.
Responsibilities
Design site‑level processes and improvements by defining operating ranges, critical parameters, and acceptance criteria that support efficient, high‑quality production.
Lead process improvement and optimization workstreams, defining the technical approach, coordinating trial execution with production, and documenting results.
Conduct process validation and troubleshooting for manufacturing processes by analyzing performance data, investigating deviations, and drafting corrective actions and supporting documentation for review and approval.
Establish technical standards for process documentation and change execution, ensuring methods, assumptions, and evidence are complete.
Guide engineers through technical decisions by running working sessions, documenting decision logic, and tracking actions to closure.
Requirements
Bachelor’s degree in engineering discipline (Mechanical, Electrical, Chemical)
Supervisor, Product Engineering leads the Product Engineering team and is responsible for supporting customer products throughout the manufacturing lifecycle, from New Product Introduction (NPI) through sustaining production.
Compensation
Competitive salary package with 401K and company match
Responsibilities
Lead and supervise Product Engineering personnel, providing coaching, mentoring, development, and performance management.
Serve as the primary technical interface for customers regarding product implementation, manufacturing readiness, engineering changes, and technical concerns.
Lead New Product Introduction (NPI) activities to ensure successful product launches and manufacturing readiness.
Develop, optimize, and maintain manufacturing processes that support quality, efficiency, and customer requirements.
Evaluate customer product designs and provide Design for Manufacturing (DFM), Design for Test (DFT), and Design for Excellence (DFx) recommendations.
Requirements
Bachelor's degree in Engineering or related technical discipline
Lead the battery manufacturing process engineering organization, overseeing cell assembly, electrolyte filling, formation, aging, and related manufacturing processes while driving process innovation, equipment development, quality improvement, and organizational growth.
Compensation
Salary range of $160,000-180,000 with stock incentives
Responsibilities
Lead process engineering activities for Cell Assembly, Electrolyte Filling, Formation & Aging, Degassing and Final Sealing, and Process Validation and Qualification
Develop and implement manufacturing and processing strategies to improve product quality, throughput, yield, and cost
Drive continuous improvement initiatives using statistical analysis and data-driven decision-making
Lead root-cause investigations and corrective actions for process and manufacturing quality issues
Establish and optimize process parameters, control plans, and manufacturing standards
Supervisor, Quality Control (Chemistry) overseeing method transfer and quality processes at Cardinal Health.
Compensation
Anticipated salary range: $82,100.00-$117,200.00
Responsibilities
Coordinates and supervises the daily activities of Chemists or business support staff in the performance of technology transfer, method validation/verification and method optimization
Serves as the liaison between Cardinal Health Quality Control and Client Quality Control in the performance of technology transfer, method validation/verification/development/optimization
Is a quality lead for the QC Chemistry team
Identifies quality events and works with QA/QC management to ensure each event is handled in accordance with site procedures and regulatory requirements
Oversees chemists and contractors who operate analytical equipment, perform analytical tests, interpret results and documents findings in accordance with SOPs and regulatory requirements
Requirements
Bachelor’s degree in chemistry or related science field
Lead the Manufacturing Science & Technology organization at the Halle radiopharmaceutical production site, driving process robustness, validation, and technical excellence.
Compensation
Expected Annual Base Salary Range for role: € 97,900 to € 146,900
Responsibilities
Set strategic direction for Manufacturing Science & Technology
Serve as key partner for site and platform leadership
Strengthen knowledge management and technical standards
Ensure robust product stewardship and oversight
Drive manufacturing process robustness and continuous improvement
Requirements
Master’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or related scientific discipline
Ready to shape the technical future of a manufacturing site? As Site MS&T Head (m/f/d), you will lead the Manufacturing Science & Technology organization in Halle and play a key role in strengthening product and process performance across the site.
Compensation
Expected Annual Base Salary Range for role: € 97,900 to € 146,900
Responsibilities
Set the strategic direction and objectives for Manufacturing Science & Technology at the Halle radiopharmaceutical production site.
Serve as the key Manufacturing Science & Technology partner for site and platform leadership.
Strengthen knowledge management, technical standards and inspection readiness across the department and site functions.
Ensure robust product stewardship and end-to-end technical oversight throughout the commercial product lifecycle.
Drive manufacturing process robustness, capability and continuous improvement in collaboration with site and global teams.
Requirements
Master’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or a related scientific discipline
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