Top 47 Pharmaceutical manufacturer Jobs in Raleigh Nc

Pharmaceutical Development Scientist II
CATO SMS —Cary, NC
- Full-time
- Bachelor of Science
- Business development experience
- Bachelor's degree
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Prior Authorization Specialist
Empowered Arthritis and Rheumatology Center PLLC —Cary, NC
- $23 - $28 an hour
- Full-time
- Private practice
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Dental insurance
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Health Services Supervisor
McKesson —Cary, NC
- $49,900 - $83,100 a year
- Mid-level
- Office
- 3 years
Mgr., Product Complaints (Hybrid)
Eisai —Raleigh, NC
- $104,900 - $137,700 a year
- Full-time
- Hybrid work
- 5 years
- Engineering
- Neurology
Business Development Associate - Pharmaceutical
Ecolab Inc. —Raleigh, NC
- $93,800 - $140,600 a year
- Overtime
- Research
- Mid-level
- Bachelor's degree
- Opportunities for advancement
Field Engineer
Eupry —Raleigh, NC
- Full-time
- Hospital
- Laboratory experience
- Mid-level
- Health insurance
- Dental insurance
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Device Engineer
GlaxoSmithKline —Zebulon, NC
- Full-time
- Hybrid work
- Engineering
- Analysis skills
- Travel
13d
Pharmacist Local Specialty
WALGREENS —Durham, NC
- $87,859 - $168,896 a year
- Bachelor of Science
- Mid-level
- Team management
Assembly Technician
PROSYS FILL LLC —Durham, NC
- Overtime
- Mid-level
- High school diploma or GED
- Manufacturing
- Profit sharing
- Health savings account
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Project Manager
Axon LLC —Raleigh, NC
- Full-time
- Microsoft Excel
- Inventory management
- Engineering
- Wellness program
- Disability insurance
Associate Engineer
Eurofins USA Consumer Product Testing —Cary, NC
- Overtime
- Mid-level
- Travel
- Mentoring
- Paid holidays
- Disability insurance
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12d
Associate Safety Engineer
Eurofins USA Consumer Product Testing —Cary, NC
- Overtime
- Laboratory experience
- Mid-level
- Travel
- Paid holidays
- Disability insurance
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Computer System Validation Engineer
Ofni Systems —Raleigh, NC
- Bachelor of Science
- Mid-level
- Communication skills
Computer System Validation Manager
Ofni Systems —Raleigh, NC
- Computer science
- Computer Science
- Bachelor of Science
DeltaV Engineer
Flexware Innovation —Raleigh, NC
- Full-time
- Mid-level
- Databases
- Bachelor's degree
Global CDMO Compliance Officer
FUJIFILM —Morrisville, NC
- $220,000 - $240,000 a year
- Hybrid work
- Office
- Bachelor's degree
- Travel
- Health insurance
- 401(k)
MSAT Drug Product Lead (Associate Director level)
GlaxoSmithKline —Zebulon, NC
- $125,250 - $208,750 a year
- Full-time
- Doctor of Philosophy
- In-person
- Training & development
- Paid holidays
- Health insurance
6d
Engineering Technician - Fire & Gas Detection
Novo Nordisk —Clayton, NC
- Monday to Friday
- OSHA
- Schematics
- CAD
- Paid holidays
- Disability insurance
Lead Automation Engineer, MES & Digital Systems - Project Farma
PerkinElmer —Raleigh, NC
- Full-time
- Remote
- 7 years
- Engineering
- Driver's License
EAP Program Manager - US
Uniphar Logistics USA LLC —Garner, NC
- Full-time
- Remote
- Mid-level
- 3 years
- Organizational skills
- Work from home
- Employee assistance program
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3d

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Pharmaceutical Development Scientist II

CATO SMS -
Cary, NC

Quick Apply

Job Details

Full-time

Qualifications

Desktop applications
Productivity software

Full Job Description

CATO SMS is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. CATO SMS is a non-laboratory environment.

We are currently recruiting for a Pharmaceutical Development Scientist (PD Scientist) to join our team in RTP. The PD Scientist is responsible for managing the pharmaceutical development activities for various drug, biologic or medical device products. Responsibilities may include drug substance synthesis, preformulation, formulation, manufacture, scale-up, process validation, analytical methods development and validation, packaging and labeling. Conducts GMP and GLP audits of contractors including analytical laboratories, manufacturing, and packaging and labeling facilities. Participates in FDA teleconferences and meetings. Prepares CMC-related regulatory submissions, including INDs, NDAs, 505b2s, and BLAs.

Location: RTP

Responsibilities:

Develops, designs and monitors pharmaceutical development (CMC) activities to meet regulatory agency and client requirements.
Areas of planning and oversight include analytical methods, preformulation, formulation, manufacture, scale-up, validation, packaging, labeling, distribution, and blinding of clinical materials as well as identification, selection, and management of suitable third-party manufacturing and laboratory service providers.
Responsible for management of staff scientists and specific project teams.
Provides CMC regulatory expertise including preparation and review of regulatory documentation as well as participation at various regulatory agency meetings.
Contributes significantly to strategic and CMC related discussions and associated documents regarding drugs, biologics, or medical devices development, with primary emphasis on product development aspects.
Performs GMP and GLP audits of various third party manufacturers and laboratory service providers.
Assists in the evaluation of potential technologies and in the preparation of business development proposals.

Qualifications and skills:

Requires a R.Ph., M.S., Ph.D., or equivalent degree, in a scientific area, or B.S., degree in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development. The ideal candidate will be a Ph.D. level scientist with previous experience in the development, manufacture and analytical testing of small molecule or biopharmaceutical products. Ideally this would include development and manufacture of products such as therapeutic vaccines, antibodies, peptides, proteins, and antibody drug conjugates, etc. utilizing various expression systems, i.e. microbial or mammalian.
Demonstrates attention to details. Plans and organizes with little supervision.
Proficiency with various computer applications such as Word, Excel, and Power Point, required.

Equal Employment Opportunity and Affirmative Action

Cato SMS is committed to Equal Employment Opportunity and Affirmative Action. We recruit, hire, train and promote qualified persons in all job titles and ensure that all other personnel actions are administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, marital status, military and/or veteran status, or disability. Furthermore, to the extent required by applicable laws and/or Executive Orders, we take affirmative action to ensure that minority group individuals, females, disabled veterans, recently separated veterans, other protected veterans, Armed Forces service medal veterans, and qualified disabled persons are introduced into our workforce and considered for promotional opportunities. Cato SMS is committed to providing reasonable accommodations to employees and applicants with disabilities to the full extent required by the Americans with Disabilities Act - ADA. If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at 919.361.2286.

Quick Apply

Refine Your Search

pharmaceutical manufacturer jobs in raleigh nc

Pharmaceutical Development Scientist II

Prior Authorization Specialist

Health Services Supervisor

Mgr., Product Complaints (Hybrid)

Business Development Associate - Pharmaceutical

Field Engineer

Device Engineer

Pharmacist Local Specialty

Assembly Technician

Project Manager

Associate Engineer

Associate Safety Engineer

Computer System Validation Engineer

Computer System Validation Manager

DeltaV Engineer

Global CDMO Compliance Officer

MSAT Drug Product Lead (Associate Director level)

Engineering Technician - Fire & Gas Detection

Lead Automation Engineer, MES & Digital Systems - Project Farma

EAP Program Manager - US

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