Combines scientific expertise, customer focus, and laboratory leadership to develop and optimize formulations, solve complex technical challenges, and deliver impactful solutions for our customers and business partners.
Responsibilities
Independently designing, executing, and analyzing laboratory experiments to develop, optimize, and validate household care formulations and application concepts.
Leading technical investigations and troubleshooting formulation, stability, compatibility, and performance challenges.
Planning and delivering performance evaluations, demonstrations, and technical studies related to enzymes and active ingredients.
Interpreting experimental data and translating findings into actionable recommendations for internal and external stakeholders.
Supporting Household Care projects through reliable technical execution aligned with business and project objectives.
Leading 2-5 projects in a pharmaceutical/CDMO manufacturing environment, managing lifecycle from specification to turnover, including product launches.
Responsibilities
Leading 2-5 projects each with 4-10 team members
Delivery of assigned projects on budget, on schedule, and on scope
Organizing, managing and leading projects from specification to way for processes and equipment
Leads cross-functional teams comprising Production, Process Engineering, Pharmaceutical Development, Quality Assurance, and more
Generating and maintaining project charts, plans, schedules, and documentation
Lead scientists and engineers developing robust, scalable upstream processes and technologies for a diverse biologics portfolio, providing scientific, technical, and people leadership across cell culture and bioreactor development.
Compensation
The annual base salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Leads an upstream process development group with accountability for people leadership, technical strategy, portfolio delivery, innovation, and technology transfer.
Influences project teams and partner functions and advances capabilities within the group and discipline.
Lead and develop a team of scientists and engineers delivering upstream processes and technologies across multiple biologic development programs.
Establish priorities, allocate resources, and provide scientific direction to meet project and portfolio objectives; coach and develop colleagues while fostering an inclusive, collaborative, and high-performing environment.
Lead the design, optimization, scale-up, characterization, and transfer of upstream processes using strong biological and engineering fundamentals, high-throughput experimentation, automation, advanced sensing, modeling, and data-rich experimental approaches.
Requirements
Ph.D. in Chemical Engineering, Biochemical Engineering, Biotechnology, Microbiology, Cell Biology, Biochemistry, or a related field
The Method Validation Scientist will support the Global Bioanalytical team by performing method validation and testing in compliance with SOPs and regulatory guidelines.
Compensation
Pay Range: $25- $36
Responsibilities
Organize and perform routine to moderate level of method validation/testing (and all associated activities) with relative independence and efficiency in compliance with appropriate SOPs and regulatory agency guidelines.
Capable of executing advanced level of method validation activities with guidance.
Provide downstream support of methods to associated groups and serve as a bioanalytical resource to the broader business
Displays intermediate data interpretation and analytical instrumentation skills and works through procedural and scientific routine problems and issues with minimal assistance.
Assists in review of reports, methods, protocols, and SOPs and maintains complete study documentation in compliance with regulatory guidelines (e.g. GLP and GCP) and department processes.
Requirements
Bachelor’s degree in a science related field (e.g., chemistry biology, molecular biology, immunology, biochemistry etc.)
Analytical Development Lead responsible for characterizing ingredients (bioactive proteins, HMOs, functional lipids) and building analytical methods to measure them from R&D to pilot and regulatory batches.
Compensation
Competitive salary, ESOP, part health insurance coverage, part transportation and lunch coverage.
Responsibilities
Define and deliver Nūmi's analytical strategy across the ingredient portfolio.
Build the full characterisation package of each ingredient: identity, purity, composition, isoforms, and post-translational modifications.
Benchmark ingredients against human milk counterparts and marketed references.
Characterise the process-related impurities (host cell proteins, residual DNA, media components).
The Pre-Clinical Medical Device Manager will oversee outsourced pre-clinical animal studies supporting medical device development, serving as the primary liaison between internal teams and external contract research organizations (CROs).
Compensation
For U.S.-based positions only, the annual base salary range for this role is $130,400.00 - $195,650.00
Responsibilities
Develop and manage pre-clinical study plans in collaboration with R&D, Regulatory, and Quality teams.
Serve as primary point of contact for CROs, ensuring adherence to protocols, timelines, and Good Laboratory Practices (GLP)/non-GLP requirements.
Coordinate logistics for outsourced animal studies, including protocol approvals, material shipments, and data transfer.
Review and approve study protocols and endpoints for relevance to device performance and safety.
Evaluate biostatistical methods and results to ensure robust data interpretation and regulatory compliance.
Requirements
Master’s degree in scientific, biomedical, or engineering field
Nice to have: PhD in relevant scientific discipline
Nice to have: DVM/VMD
Nice to have: AALAS Certification
Nice to have: experience managing outsourced studies and vendor relationships
A Scientist I in Quality Control Microbiology is responsible for an intermediate level of expertise of microbiological test methods, and instrumentation. A Scientist I participate in the mentoring and training of less experienced analysts in the group.
Compensation
Hourly Range: $29.31 - $41.20
Responsibilities
Understands department priorities and importance of planning ahead.
Performs peer review of data for accuracy, completeness and conformance to specifications.
Keeps supervisory personnel informed of all relevant events impacting the operations and performance of the department including discrepancies and out of limit conditions.
Be able to articulate work related issues clearly and effectively to management and peers.
Maintains knowledge of cGMPs and GLPs. Maintains knowledge of current compendial methods.
An intermediate level role in Quality Control Microbiology responsible for microbiological test methods, instrumentation, mentoring junior analysts, and performing environmental monitoring and product testing.
Compensation
Hourly Range: $29.31 - $41.20
Responsibilities
Performs peer review of data for accuracy, completeness, and conformance to specifications.
Keep supervisory personnel informed of all relevant events impacting department performance.
Maintain knowledge of cGMPs, GLPs, and current compendial methods.
Teach or coordinate teaching of training modules and laboratory techniques to new analysts.
Lead and manage global quality management and compliance programs for Amneal’s pharmaceutical manufacturing operations.
Compensation
The salary range for this position ranges from $200,000 - $245,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months.
Responsibilities
Lead network wide regulatory commitments monitoring and implementation of associated corrective and preventive actions (CAPAs).
Identify compliance risks and implement corrective and preventive actions.
Support external audits and inspections from regulatory agencies.
Coordinate with site leaders in addressing inspection findings including draft response.
Implement quality system compliance intelligence enabling proactive monitoring of changes in the worldwide drug, biologics, device regulations and guidance.
Requirements
Bachelor's Degree in Chemistry, Biology, Pharmacy, Engineering or other technical fields
Master's Degree in Chemistry, Biology, Pharmacy, Engineering or other technical fields
Director, Quality ManagementNewAmneal · Piscataway, US