Top 9 Hplc Jobs in Griffith In

Stability Coordinator
Aquestive Therapeutics Inc. —Portage, IN
- Background check
- Bachelor of Science
- Pass drug screening
Quick Apply
13d
Senior QC Chemist
Aquestive Therapeutics Inc. —Portage, IN
- Background check
- 5 years
- Word processing
Quick Apply
Chemist 1
Merieux NutriSciences —Crete, IL
- $21.50 - $23.00 an hour
- Full-time
- Ability to lift 50 pounds
- Analysis skills
- Computer skills
- Health insurance
- Dental insurance
Chemist III
Merieux NutriSciences —Crete, IL
- $60,000 - $70,000 a year
- Full-time
- Customer service
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
14h
Senior Scientist, Quality CMC
Aquestive Therapeutics Inc. —Portage, IN
- Background check
- Bachelor of Science
- Pass drug screening
Quick Apply
6d
Analytical Chemist
Frontage Laboratories —Chicago, IL
- $65,000 - $80,000 a year
- Full-time
- Management
- Bachelor of Science
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
Quality Control (QC) Analyst II
Kashiv BioSciences, LLC —Chicago, IL
- Extended hours
- Writing skills
- Master's degree
- Bachelor's degree
9h

More jobs to discover

Find similar jobs that you might be interested in.

Senior QC Chemist
Aquestive Therapeutics Inc. —Portage, IN
Actively participates and/or leads technical transfer of methods from development phase to validated phase. Continually reviews programs and systems to develop…
Quick Apply

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

QC Chemist - 1st Shift
kdc/one —Groveport, OH
Sample and inspect incoming raw materials from chemical tankers and palletized deliveries. High school diploma or GED required; Bachelor’s in Chemistry or…
Quick Apply
Chemist - Third Shift - kdc/one Columbus Laboratory
kdc/one —New Albany, OH
Sample and inspect incoming raw materials from chemical tankers and palletized deliveries. High school diploma or GED required; Bachelor’s in Chemistry or…
Quick Apply

Show more jobs in cities nearby

I want to receive the latest job alert for hplc in griffith in

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

hplc jobs near griffith in

Stability Coordinator

Aquestive Therapeutics Inc.
Portage, IN

Quick Apply

Job Details

13 days ago

Qualifications

Statistics
High-performance liquid chromatographs
Minitab
Pharmaceutical analysis
Desktop applications
Statistical analysis tools

Full Job Description

Job Summary:

This position is responsible for planning, coordination, oversight of the execution and completion of the Stability Program for both Aquestive owned products as well as non-Aquestive owned products. This includes setting testing strategy, initiating and managing all stability studies.

Responsibilities:

Subject Matter Expert on ICH guidelines.
Perform statistical analysis, tracking and trending of all data points associated with stability studies.
Creates, maintain and manage changes to stability set down and pull schedule, ensuring compliance with internal SOPs and ICH standards.
Manages stability scheduling tools and ensures timely communication between all internal and/or external parties to ensure on time testing, data reporting and report generation.
Establish requirements/general strategy for stability batches and communicate to Production and other necessary parties, ensuring annual commitments are met.
Author stability protocols per applicable annual commitments and ICH guidelines, agency filings and business rules.
Author all stability summary reports in a timely manner, ensuring all data is statistically analyzed, and any trends noted throughout the stability program are appropriately addressed.
Perform data entry for stability control charts; identify trends (including OOS and ATR) and lead investigations real-time as necessary.
Create data packages to fulfill Statements of Work with external business contracts, ensuring on-time delivery.
Draft Statements of Work related to stability for external business contracts, coordinating with both internal and external parties through to execution.
Author stability summary requirements for inclusion in Annual Product Quality Review reports for all products.
Work closely with Analytical R&D and CMC Development to author, review and report stability data for developmental products, including clinical batches, bulk stability and pivotal/registration batches.
Aid in stability sample testing or data analysis/review if necessary.
Aid in data analysis for non-stability complex QC investigations and/or process improvements.
Monitor and maintain the stability chamber room for adherence to established environmental requirements and audit/review stability chamber documentation (i.e., logbooks).
Authors and maintains all Standard Operating Procedures (SOPs) for the Stability Program.

Qualifications:

3+ years of experience in a pharmaceutical analytical laboratory.
A BS/BA degree in a scientific discipline or higher required.
Experience utilizing statistical analysis tools required (i.e., Minitab).
Experience with Stability systems or LIMS systems.
Proficient knowledge of analytical testing equipment and procedures required, including HPLC and Chromeleon.
Proficient in GMP regulations, as they apply to manufacturing analytical laboratory.
Strong attention to detail and ability to handle multiple projects with competing priorities.
Excellent technical writing skills.
Excellent oral and written communication skills with strong interpersonal skills.
Highly motivated and self-directed with strong organizational skills.
Able to exercise independent intellectual judgment using data driven decision making.
Highly proficient and advanced in computer use (Word, Excel, PowerPoint, etc.) with ability to learn and master new computer applications.

The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position. This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary.

As part of Aquestive’s employment process, final candidate will be required to complete a drug test and background check prior to employment commencing. Please Note: Aquestive is a drug-free workplace and has a drug free workplace policy in place.

Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

Quick Apply

Refine Your Search

hplc jobs in griffith in

Stability Coordinator

Senior QC Chemist

Chemist 1

Chemist III

Senior Scientist, Quality CMC

Analytical Chemist

Quality Control (QC) Analyst II

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for hplc in griffith in

Explore jobs in more locations

Job Summary:

Responsibilities:

Job Seeker Tools

Employer Tools

Browse

Stay Connected