Top 70 R&d/manufacturing development Jobs in Eatontown Nj

Associate Project Manager-Pharmaceutical Manufacturing
CMIC CMO USA —Cranbury, NJ
- $80,000 - $90,000 a year
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health savings account
- Health insurance
Quick Apply
Research Scientist
Colgate-Palmolive —Piscataway, NJ
- $86,000 - $121,000 a year
- Hybrid work
- Mid-level
- 3 years
- Databases
- Profit sharing
- Paid parental leave
4d
Research Scientist (175242)
Colgate-Palmolive —Piscataway, NJ
- $86,000 - $121,000 a year
- Hybrid work
- Mid-level
- 3 years
- Databases
- Profit sharing
- Paid parental leave
5d
Research Scientist/Sr Research Scientist (175055)
Colgate-Palmolive —Piscataway, NJ
- $96,800 - $137,000 a year
- Hybrid work
- Microsoft Office
- Master's degree
- Bachelor's degree
- Profit sharing
- Paid parental leave
9d
Specialist, Raw Materials (173409)
Colgate-Palmolive —Piscataway, NJ
- $96,800 - $130,000 a year
- Hybrid work
- 5 years
- Bachelor of Science
- Laboratory experience
- Profit sharing
- Paid parental leave
R&D/MANUFACTURING DEVELOPMENT ENGINEER
TE Connectivity —Middletown, NJ
- $143,500 - $179,300 a year
- 8 years
- Senior level
- No travel
- Employee stock purchase plan
- Disability insurance
Senior Scientist, Product Development – Life Science & Biotech Reagents
GenScript/ProBio —Piscataway, NJ
- $125,000 - $155,000 a year
- Full-time
- Master's degree
- Doctor of Philosophy
- Senior level
- Commuter assistance
- Paid parental leave
R & D Scientist
BERJE INCORPORATED —Carteret, NJ
- $100,000 - $110,000 a year
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Sr. Specialist, R&D Procurement
Merck —Rahway, NJ
- $96,200 - $151,400 a year
- Full-time
- Mid-level
- 3 years
- Analysis skills
- Paid holidays
- Health insurance
6d
Industrial Designer (173259)
Colgate-Palmolive —Piscataway, NJ
- $86,000 - $121,000 a year
- Hybrid work
- Mid-level
- 3 years
- Presentation skills
- Profit sharing
- Paid parental leave
Regulatory Affairs Specialist
Sunrise Pharma —Rahway, NJ
- Monday to Friday
- 5 years
- Master's degree
- Senior level
Principal Scientist, Technical Project Leader
Experic LLC —Cranbury, NJ
- $135,000 - $175,000 a year
- 3 years
- Math
- Doctor of Philosophy
Quick Apply
Principal / Senior Principal Scientist - Spectroscopy
Colgate-Palmolive —Piscataway, NJ
- $124,000 - $180,000 a year
- Hybrid work
- Doctor of Philosophy
- Senior level
- AI
- Profit sharing
- Paid parental leave
Program Manager
Safran —Township of Wall, NJ
- $115,486 - $147,245 a year
- Full-time
- Bachelor of Science
- Engineering
- Office
Associate Director, Internal Auditing- Hybrid
Merck —Rahway, NJ
- $129,000 - $203,100 a year
- Full-time
- Word processing
- 8 years
- Travel
- Paid holidays
- Health insurance
6d
Associate Principal Scientist, Downstream Process Development
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- Bachelor of Science
- 3 years
- Master's degree
- Paid holidays
- Health insurance
8d
SENIOR RESEACH AND DEVELOPMENT ENGINEER
TE Connectivity —Middletown, NJ
- $115,400 - $144,200 a year
- 5 years
- Master's degree
- Travel
- Employee stock purchase plan
- Disability insurance
R&D Project Manager
Tekni-Plex —Eatontown, NJ
- $100,000 - $120,000 a year
- Word processing
- Bachelor of Science
- Writing skills
- Health savings account
- AD&D insurance
Quick Apply
Account Manager
Hovione —East Windsor, NJ
- $120,000 - $192,000 a year
- Overtime
- 5 years
- English
- Mid-level
- Health insurance
- Dental insurance
Manager, Supply Network Design & Operations - PTB & Floss (175322)
Colgate-Palmolive —Piscataway, NJ
- $109,600 - $155,000 a year
- Hybrid work
- Engineering
- Analysis skills
- Product management
- Profit sharing
- Paid parental leave
2d

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r&d/manufacturing development jobs near eatontown nj

Associate Project Manager-Pharmaceutical Manufacturing

CMIC CMO USA -
Cranbury, NJ

Quick Apply

Job Details

Full-time
$80,000 - $90,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Parental leave
Vision insurance
401(k) matching
Life insurance
Referral program

Qualifications

Customer communication
Teamwork
Interpersonal skills
Project planning
Basic math
Manufacturing facility experience
Bachelor's degree
Attention to detail
Pharmaceutical company experience
Project task coordination
Organizational skills
Collaboration with manufacturing teams
Manufacturing
Cross-functional team management
FDA regulations
Time management
Pharmaceutical manufacturing facility experience

Full Job Description

Job Overview

CMIC CMO USA is seeking an Associate Project Manager with experience in pharmaceutical manufacturing, contract manufacturing (CDMO), or a regulated life sciences environment. This role serves as the primary coordinator between pharmaceutical clients and internal departments to ensure successful execution of oral solid dose manufacturing and packaging projects from project initiation through commercial delivery. Candidates without pharmaceutical manufacturing, CDMO, or FDA-regulated industry experience will not be considered.

Duties

Independently managing small- to medium-sized projects while supporting larger and more complex programs as assigned.
Coordinating and supporting cross-functional project activities throughout the project lifecycle, tracking deliverables, action items, milestones, and timelines to ensure successful project execution and alignment with project objectives and client expectations.
Serve as the primary liaison between clients and internal stakeholders, providing timely communication of project status, risks, issues, milestones, and other project-related information.
Collaborating with Operations, Quality Assurance, Regulatory Affairs, R&D, Supply Chain, Finance, and other stakeholders to support project objectives and deliverables.
Identifying project risks, challenges, and potential delays and assist in implementing mitigation strategies.
Supporting project financial activities, including revenue forecasting, invoicing coordination, budget tracking, and change management, as applicable.
Preparing and maintaining project documentation, meeting minutes, action item logs, project schedules, and status reports.
Developing and maintaining a working knowledge of oral solid dose manufacturing processes, packaging technologies, and services offered by CMIC CMO USA.
Ensuring compliance with company policies, procedures, SOPs, cGMP requirements, and applicable regulatory standards.

Technical Skills

Strong organizational, planning, and time management skills with the ability to manage multiple priorities and deadlines.
Excellent verbal and written communication skills, with the ability to effectively interact with clients, team members, and cross-functional stakeholders.
Strong interpersonal skills with the ability to build collaborative working relationships across all levels of the organization.
Proficiency in Microsoft Office applications including Excel, Word, PowerPoint, Outlook, Teams and project tracking tools.
Ability to analyze information, identify issues, and assist in developing practical solutions to support project objectives.
Maintain positive customer relationships through responsive communication and proactive follow-up.
Strong attention to detail and ability to maintain accurate project documentation and records.
Ability to work independently while contributing effectively within a cross-functional team environment.
Basic understanding of project management principles, including scheduling, action item tracking, risk identification, and stakeholder communication.
Familiarity with cGMPs.

Qualifications

Education:

Bachelor’s degree in Pharmaceutical, Biological, Chemical sciences, Life Sciences, Business, Project Management or a related field required.

Experience:

Two (2) to five (5) years of relevant experience in project coordination, project management, pharmaceutical manufacturing, contract development and manufacturing (CDMO), or a related industry.
Experience supporting FDA-regulated manufacturing environments.
Experience coordinating cross-functional teams supporting manufacturing, quality, regulatory, supply chain, and operations.
Certified Associate in Project Management (CAPM) certification preferred but not required.

Candidates with experience limited to IT, software development, construction, marketing, telecommunications, banking, or other non-regulated industries are not a fit for this position.

Mental & Physical Requirements:

Ability to perform basic math and reasoning functions.
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Must be able to sit or stand for prolonged periods.
Ability to occasionally lift up to 20 lbs.
Must be able to enter manufacturing and lab areas wearing appropriate PPE.
Visual requirements include the ability to read documents and view computer screens.

Pay: $80,000.00 - $90,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave
Referral program
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

r&d/manufacturing development jobs in eatontown nj

Associate Project Manager-Pharmaceutical Manufacturing

Research Scientist

Research Scientist (175242)

Research Scientist/Sr Research Scientist (175055)

Specialist, Raw Materials (173409)

R&D/MANUFACTURING DEVELOPMENT ENGINEER

Senior Scientist, Product Development – Life Science & Biotech Reagents

R & D Scientist

Sr. Specialist, R&D Procurement

Industrial Designer (173259)

Regulatory Affairs Specialist

Principal Scientist, Technical Project Leader

Principal / Senior Principal Scientist - Spectroscopy

Program Manager

Associate Director, Internal Auditing- Hybrid

Associate Principal Scientist, Downstream Process Development

SENIOR RESEACH AND DEVELOPMENT ENGINEER

R&D Project Manager

Account Manager

Manager, Supply Network Design & Operations - PTB & Floss (175322)

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