Top 56043 Pharmaceutical Jobs

Stability Coordinator I
Norwich Pharmaceuticals Inc —Norwich, NY
- $62,354 a year
- Full-time
- Computer literacy
- Organizational skills
- 1 year
- Wellness program
- Health savings account
Quick Apply
Manufacturing Specialist
SpectronRx —South Bend, IN
- $28 - $35 an hour
- Background check
- Customer service
- Mid-level
Quick Apply
Quality engineer and NC CAPA Manager
Hydrox Laboratories —Elgin, IL
- $100,000 - $120,000 a year
- Extended hours
- Analysis skills
- Presentation skills
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Supervisor, Non-Sterile Compounding
Empower Pharmacy —Houston, TX
- 5 years
- Office
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
6d
Associate Scientist-Analytical R&D
Ascendia Pharmaceuticals —North Brunswick, NJ
- $40,000 - $70,000 a year
- Temporary
- Bachelor of Science
- Laboratory experience
- Mid-level
- Health savings account
- Health insurance
Quick Apply
DRUG SAFETY ASSOCIATE (multiple openings)
Zenith LifeScience —South Plainfield, NJ
- $111,925 a year
- Full-time
- Mid-level
- Travel
- Scripting
Safety Scientist
FATHOM LIFE SCIENCES & TECHNOLOGY SERVICES —Wilmington, NC
- Full-time
- Mid-level
- Bachelor's degree
- 1 year
QA Associate- Micro Reviewer
RK PHARMA INC —Pearl River, NY
- $55,000 - $95,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Communication skills
Quick Apply
Process Engineer
Charlotte Extraction Labs LLC —Pineville, NC
- $85,000 - $115,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- 3 years
PRINCIPAL INVESTIGATOR PHARMA TECH/PROCESS DEVELOPMENT
Teksky LLC —Colorado Springs, CO
- Full-time
- Management
- Master's degree
- Doctor of Philosophy
Quick Apply
4d
Validation Technician
eTeam Inc —Indianapolis, IN
- $30.00 - $39.95 an hour
- Contract
- In-person
- Manufacturing
- Senior level
Quick Apply
Pharmaceutical Territory Rep
Prism Biotech —Fresno, CA
- $84,120 - $115,372 a year
- Full-time
- Mid-level
- Continuous improvement
- Commercial
Quick Apply
Sales Representative – Biotech
Prism Biotech —Riverside, CA
- $87,550 - $118,802 a year
- Full-time
- Mid-level
- Analysis skills
- Experience equivalent to degree accepted
Quick Apply
Sales Rep – BioPharma
Prism Biotech —Boise, ID
- $85,266 - $116,518 a year
- Full-time
- Mid-level
- Analysis skills
- Experience equivalent to degree accepted
Quick Apply
Sales Representative – Biotech
Prism Biotech —Redmond, WA
- $87,550 - $118,802 a year
- Full-time
- Mid-level
- Analysis skills
- Experience equivalent to degree accepted
Quick Apply
Pharmaceutical Rep – Oncology
Prism Biotech —Springfield, MO
- $85,606 - $118,828 a year
- Full-time
- Mid-level
- Continuous improvement
- Commercial
Quick Apply
Account Representative – BioPharma
Prism Biotech —Fremont, CA
- $89,155 - $120,407 a year
- Full-time
- Mid-level
- Analysis skills
- Experience equivalent to degree accepted
Quick Apply
Primary Care Pharma Sales Rep
Prism Biotech —Champaign, IL
- $87,980 - $121,202 a year
- Full-time
- Primary Care
- Mid-level
- Analysis skills
Quick Apply
Regional Account Liaison - BioPlus Specialty Infusion- Ohio
Elevance Health —Columbus, OH
- $95,040 - $142,560 a year
- 6 years
- Bachelor of Science
- Mid-level
- Employee stock purchase plan
- Paid holidays
Oncology Detail Rep – Pharma
Prism Biotech —Santa Rosa, CA
- $89,265 - $120,517 a year
- Full-time
- Organizational skills
- Leadership
- Communication skills
Quick Apply

I want to receive the latest job alert for pharmaceutical

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

pharmaceutical jobs near

Sales Representative jobs in Redmond, WA

Principal jobs in Colorado Springs, CO

Sales Representative jobs in Boise, ID

Pharmaceutical Sales Representative jobs in Springfield, MO

Sales Representative jobs in Riverside, CA

Liaison jobs in Columbus, OH

Primary Care Physician jobs in Champaign, IL

Quality Engineer jobs in Elgin, IL

R&d Engineer jobs in Los Angeles, CA

Cloud Engineer jobs in Orlando, FL

R&d Engineer jobs in Oklahoma

R&d jobs in Chicago, IL

R&d Engineer jobs in Savannah, GA

R&d Engineer jobs in Indianapolis, IN

Business Development Representative jobs in Las Vegas, NV

Remote Sales Part Time jobs in Florida

Sales Representative jobs in Hartford, CT

Sales Representative jobs in Sacramento, CA

Sales Representative Base Salary Plus Commission jobs in Tampa, FL

Sales Representative jobs in Fort Wayne, IN

Stability Coordinator I

Norwich Pharmaceuticals Inc -
Norwich, NY

Quick Apply

Job Details

Full-time
$62,354 a year

Benefits

Wellness program
Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Vision insurance
Life insurance
Prescription drug insurance

Qualifications

Computer operation
Customer communication
Laboratory standard operating procedures
Desktop applications
Productivity software
Standard operating procedures (SOPs)

Full Job Description

SUMMARY OF POSITION

The Stability Coordinator I is responsible for all aspects of the stability sample program. The Stability Coordinator initiates and manages stability studies, including protocol development and maintenance, sample handling, and data reporting.

ORGANIZATION STRUCTURE

The Stability Coordinator I reports to a QC Manager or Team Leader.

RESPONSIBILITIES

Primary responsibilities of this role include the following:

1. Master Stability Protocol Management

a. Create and maintain Master Stability Protocols based on the registered requirements and in compliance with all current ICH/FDA regulatory guidance.

b. Work directly with project team to define stability commitments for study design, testing requirements, and material specification references.

c. Calculate the number of samples required per study based on pack types and storage conditions.

d. Review specification changes for products to assess impact to Master Stability Protocols and revise protocols as needed using appropriate change management systems.

2. Study Protocol Management

a. Create, review, and/or approve stability study protocols and summary report tables.

b. Submit sample request forms to be included with the production records for individual stability studies.

c. Assign stability study identification numbers and stability sample quantities to individual study protocols.

d. Ensure stability samples are labeled properly and placed in the correct conditioned chamber(s) for storage.

e. Revise stability study protocols as needed throughout study lifetime.

3. Study Scheduling and Implementation

a. Perform stability study sample pulls according to daily pull schedule.

b. Review and ensure the correct samples are pulled and delivered to the appropriate NPI laboratory when due.

c. Provide stability data to customers when applicable.

d. Dispose of stability samples when study is completed or discontinued.

e. Work with metrology department on chamber monitoring and maintenance.

f. Participate in stability improvement projects.

4. Compliance Activities

a. Complete corrective and preventive actions when assigned.

b. Prepare stability data tables and summary reports as needed for customer Annual Reports or ongoing regulatory and/or stability data review processes.

c. Review stability summary data tables for compliance and possible trends. Ensure any stability issues or potential issues are appropriately communicated to laboratory management.

5. Additional duties as required

QUALIFICATIONS

1. A degree in life sciences, plus 1-3 years of pharmaceutical experience, or equivalent combination of education and experience.

2. Excellent oral and written communication skills.

3. Proficient in computer use (Word, Excel, PowerPoint, internet) with ability to learn new computer applications.

4. Ability to comprehend and follow standard operating procedures and test methods.

5. Strong attention to detail and ability to multitask.

6. Operates with a sense of urgency in a fast-paced environment.

7. Strong organization, communication, and interpersonal skills.

GMP DECISION-MAKING AUTHORITY

1. Authors regulatory documents and reports.

2. Authors and revises stability protocols.

3. Maintains and implements stability sample pull schedule.

4. Reviews and reports stability data.

5. Participate in audits as required.

The anticipated base salary for this position is $62,354.00. This position is eligible for Alvogen’s annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage (two PPO plans and an HDHP with Health Savings Account and employer contribution), dental, vision, flexible spending accounts. Alvogen’s benefits package also includes a retirement savings program, long-term care coverage, paid time off (176 hours per year, prorated to hire date) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on [Posting Date] and remain open for at least 20 days. To apply, select the apply button and submit your application.

An Equal Opportunity Employer, including disability/vets

Quick Apply

Refine Your Search

pharmaceutical jobs

Stability Coordinator I

Manufacturing Specialist

Quality engineer and NC CAPA Manager

Supervisor, Non-Sterile Compounding

Associate Scientist-Analytical R&D

DRUG SAFETY ASSOCIATE (multiple openings)

Safety Scientist

QA Associate- Micro Reviewer

Process Engineer

PRINCIPAL INVESTIGATOR PHARMA TECH/PROCESS DEVELOPMENT

Validation Technician

Pharmaceutical Territory Rep

Sales Representative – Biotech

Sales Rep – BioPharma

Sales Representative – Biotech

Pharmaceutical Rep – Oncology

Account Representative – BioPharma

Primary Care Pharma Sales Rep

Regional Account Liaison - BioPlus Specialty Infusion- Ohio

Oncology Detail Rep – Pharma

I want to receive the latest job alert for pharmaceutical

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected