Top 891 Pharmaceutical product development Jobs in New York, Ny

Consultant - Product Quality & Safety - Life Sciences & Healthcare
Deloitte —New York, NY
- $88,700 - $170,900 a year
- Full-time
- Up to 50% travel
- Bachelor's degree
- Product management
Medical Director (Lung focus)
BioNTech AG —Berkeley Heights, NJ
- $168,100 - $268,700 a year
- Full-time
- Background check
- 6 years
- Bachelor's degree
- Health savings account
- AD&D insurance
Director, US Medical Information & Medical Review
BioNTech AG —Berkeley Heights, NJ
- $168,100 - $268,700 a year
- Full-time
- Background check
- Medicine
- 8 years
- Health savings account
- AD&D insurance
Sr. Quality Engineer, Quality Operations - Wayne, NJ
Getinge —Wayne, NJ
- $115,000 - $120,000 a year
- Full-time
- 7 years
- Microsoft Excel
- Engineering
- Commuter assistance
- Disability insurance
Pharmaceutical Field Sales Representative
Inizio Engage —New York, NY
- $60,000 - $90,000 a year
- Full-time
- Background check
- Clean driving record
- No experience needed
- Paid parental leave
- Paid holidays
11d
Pharmaceutical Field Sales Representative
Inizio Engage —Queens, NY
- $60,000 - $90,000 a year
- Full-time
- Background check
- Clean driving record
- No experience needed
- Paid parental leave
- Paid holidays
11d
Sr. Operational Safety Manager
Balchem Corporation —Montvale, NJ
- $125,000 - $165,000 a year
- Full-time
- Hybrid work
- 8 years
- Travel
- Senior level
Quick Apply
Nurse Manager- Infusion
Amerita —New Hyde Park, NY
- $150,000 - $165,000 a year
- Full-time
- CPR Certification
- Nursing
- RN License
Quality Control Inspector - 1st Shift
PL Developments LLC —Westbury, NY
- From $19 an hour
- Writing skills
- Basic math
- English
- Paid holidays
- Health insurance
Pharmacy 340B Compliance Coordinator
Wyckoff Heights Medical Center —New York, NY
- $100,000 a year
- Monday to Friday
- Bachelor's degree
- 1 year
- Senior level
Field Service Representative
Inizio Engage —New York, NY
- $46,000 - $85,000 a year
- Full-time
- Background check
- Data analysis skills
- Analysis skills
- Paid parental leave
- Paid holidays
7d
Pharmacy 340B Compliance Coordinator
Wyckoff Heights Medical Center —New York, NY
- $100,000 a year
- Full-time
- Bachelor's degree
- 1 year
- Senior level
Rapid Deployment Representative
Inizio Engage —New York, NY
- $63,000 - $117,000 a year
- Full-time
- Background check
- Clean driving record
- Research
- Paid parental leave
- Paid holidays
7d
Field Service Representative
Inizio Engage —Brooklyn, NY
- $46,000 - $85,000 a year
- Full-time
- Background check
- Data analysis skills
- Analysis skills
- Paid parental leave
- Paid holidays
7d
Medical Science Liaison, Neuro-Oncology, Mid-Atlantic
Jazz Pharmaceuticals —New York, NY
- $160,000 - $240,000 a year
- Medicine
- RN License
- English
- Health insurance
- Dental insurance
Line Material Handler
PL Developments LLC —Westbury, NY
- From $18 an hour
- Basic math
- Ability to lift 75 pounds
- Entry level
- Paid holidays
- Health insurance
Nurse Hospital Diagnostic Sales Specialist
Inizio Engage —New York, NY
- $91,000 - $169,000 a year
- Full-time
- Background check
- Nursing
- Hospital
- Paid parental leave
- Paid holidays
7d
Associate Director Access & Reimbursement
CSL Seqirus —Summit, NJ
- $210,000 - $250,000 a year
- Full-time
- Bachelor's degree
- Contracts
- Budgeting
Clinical Sales Executive - Infusion
Amerita —Totowa, NJ
- $90,000 - $115,000 a year
- Full-time
- Nursing
- RN License
- Hospital
- Continuing education credits
- Health savings account
Associate Director, US Brand Marketing
CSL Seqirus —Summit, NJ
- $180,000 - $205,000 a year
- Full-time
- 7 years
- Marketing
- Analysis skills

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Consultant - Product Quality & Safety - Life Sciences & Healthcare

Deloitte -
New York, NY

Apply Now

Job Details

Full-time
$88,700 - $170,900 a year

Qualifications

AI tools proficiency
Employee relationship building
Reporting and dashboarding tools
Bachelor's degree
Management consulting experience
Managing projects
Cross-functional collaboration
Data-driven decision making
Data analytics technologies
Cross-functional communication

Full Job Description

Consultant - Product Quality & Safety - Life Sciences & Healthcare

Enterprise Operations & Risk

Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organizations. Join our team and use advanced data, AI, and emerging technologies-combined with industry insight-to help clients bring clarity from complexity and accelerate their path to value creation.

Work You'll Do

As a Consultant, you will support the delivery of client projects while continuing to grow your subject matter expertise and consulting skills. You will work with teams helping life sciences clients address quality, regulatory, operational, and technology-related challenges across pharmaceutical, biotech, and medical device environments. This could include:

Support clients in pharmaceutical and medical device Regulatory Affairs and Quality Assurance strategy, process, operating model, and governance improvements
Assist with quality and regulatory due diligence for mergers and acquisitions, including document review, evidence gathering, interview support, risk tracking, and diligence summaries
Support separation and integration activities for QA/RA functions, including Day 1 planning, governance coordination, TSA support, and cutover readiness activities
Help assess quality management system and regulatory compliance gaps across areas such as SOPs, training, deviation management, CAPA, change control, complaints, and audit readiness
Support inspection readiness efforts, including mock inspection preparation, issue tracking, and remediation planning support
Assist with QA/RA technology enablement efforts, including business requirements gathering, process documentation, test script development, validation support, training coordination, and deployment activities
Support implementation and optimization of systems such as eQMS, document management systems, learning management systems, complaint handling, CAPA, change control, audit management, supplier quality, and regulatory information management platforms
Develop portions of client-ready deliverables, including assessments, process flows, requirements, status reports, business cases, and implementation plans
Track project activities, risks, dependencies, and action items, and support stakeholder coordination across workstreams
Continue building subject matter knowledge in Regulatory Affairs, Quality Assurance, and Commercial/Medical Content Management

The successful candidate would possess these skills

Ability to work independently and collaborate as part of a team
Effective written and verbal communication skills
Meticulous attention to detail and quality of work product
Ability to build and sustain professional relationships
Ability to lead projects or workstreams
Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
Strong interpersonal skills and professional demeanor
Ability to meet deadlines
Ability to provide clear guidance to others

The Team
Our Enterprise Operations & Risk offering enables clients to achieve profitable growth and competitive advantage by optimizing the heart of the business. We leverage deep domain expertise to extend enterprise resilience, agility, and remediation. Our professionals address client needs that span the organization and impact strategy, operations, performance, and reputation.

Qualifications

Required:

Bachelor's degree required
2+ years of experience focused on Life Sciences in a consulting and/or industry role
Experience or exposure to the use of data, analytics, and/or AI-enabled tools to support business processes or decision-making
Foundational experience in pharmaceutical QA/RA (e.g., GMP, quality systems, compliance support) and/or medical device QA/RA (e.g., design controls, risk management, post-market processes)
Working knowledge of common regulatory and quality requirements applicable to pharmaceutical and/or medical device organizations
Experience supporting the translation of regulatory and quality requirements into business processes, documentation, or controls
Experience supporting project delivery in areas such as compliance remediation, process improvement, system implementation, diligence, or integration planning
Familiarity with quality and regulatory systems and capabilities such as document control, training, deviations, CAPA, change control, audits, complaints, supplier quality, and/or submission or product registration data management
Experience supporting data analysis, reporting, dashboards, KPI tracking, or process monitoring
Experience in project management, PMO support, or workstream coordination
Ability to manage multiple assignments and work effectively in a deadline-driven environment
Strong attention to detail and ability to produce polished, client-ready deliverables
Strong written and verbal communication skills and ability to work effectively in cross-functional teams
Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future
Ability to travel up to 50%, based on the work you do and the clients and industries/sectors you serve

Preferred

Experience in the pharmaceutical, biotech, and/or medical device industries
Experience supporting eQMS, RIM, DMS, LMS, or related quality/regulatory technology initiatives
Experience with compliance assessments, inspection readiness, remediation, or QA/RA process improvement

Information for applicants with a need for accommodation: https://www2.deloitte.com/us/en/pages/careers/articles/join-deloitte-assistance-for-disabled-applicants.html

The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $88700 - $170900.

You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various fac tors, including, without limitation, individual and organizational performance.

Apply Now

Refine Your Search

pharmaceutical product development jobs in new york, ny

Consultant - Product Quality & Safety - Life Sciences & Healthcare

Medical Director (Lung focus)

Director, US Medical Information & Medical Review

Sr. Quality Engineer, Quality Operations - Wayne, NJ

Pharmaceutical Field Sales Representative

Pharmaceutical Field Sales Representative

Sr. Operational Safety Manager

Nurse Manager- Infusion

Quality Control Inspector - 1st Shift

Pharmacy 340B Compliance Coordinator

Field Service Representative

Pharmacy 340B Compliance Coordinator

Rapid Deployment Representative

Field Service Representative

Medical Science Liaison, Neuro-Oncology, Mid-Atlantic

Line Material Handler

Nurse Hospital Diagnostic Sales Specialist

Associate Director Access & Reimbursement

Clinical Sales Executive - Infusion

Associate Director, US Brand Marketing

I want to receive the latest job alert for pharmaceutical product development in new york, ny

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