Sovereign
Pharmaceuticals is an equal opportunity employer that offers many
benefits if you join our team.
JOB OPENINGS
Analytical Scientist - R&D
Must be able to develop and validate analytical methods and operate HPLCs.
Required Skills:
- Problem solving
- Organized
- Project management
Required Education/Training:
- Chemistry degree
- One year of experience in a laboratory environment
Product Analyst
Prepares samples for analysis. Prepares solutions for use in laboratory. Works up data and checks results. Analyzes samples by operating and calibrating instruments.
Required Skills:
- Ability to understand and follow laboratory procedures
- Ability to follow verbal and written instructions
- Knowledge of laboratory operations as they apply to pharmaceutical analysis
- Chromatographic interpretation
Required Education/Training:
- College degree
- Math, Science, or Chemistry background
- Experience in GMP environment
Quality Assurance Inspector
Inspects and approves packaging lines. Approving/rejecting raw materials. Assigning shelf life/retest dates for raw materials. Perform and document in process checks. File paperwork with accuracy and in a timely matter.
Required Skills:
- Basic Math
- Written and oral communication
- Ability to work independently
- Computer literate
- Attention to details
- Organized
- Work well in a team environment
Required Education/Training:
- Some college (prefer college degree)
- Experience in GMP environment
- Experience in Quality setting prefer not required
Quality Assurance Stability Technician
Responsible for maintaining accurate up to date stability reports. Maintain current expiration date data. Compare formula sheets. Perform stability testing. Assist in some Laboratory functions when needed.
Required Skills:
- Basic Math
- Written and oral communication
- Ability to work independently
- Computer literate
- Attention to details
Required Education/Training:
- Some college (prefer college degree)
- Experience in GMP environment
- Minimum 6 months Pharmacueticals environment
- Minimum 6 months Laboratory environment
Raw Materials Chemist
Performs raw material tests in accordance with current USP, EP, and JP testing methods (i.e. Identification and Monograph Procedures). Prepares and maintains solutions for raw material testing. Prepares detailed documentation of tests performed and solutions prepared. Performs preventative maintenance on instruments.
Must be a self starter, organized, detailed oriented, dependable, goal oriented, and be able to handle multiple projects simultaneously.
Required Skills:
- Knowledge of chemical reactions
- Knowledge of apparatus setup for chemical reactions (i.e. distillation)
- Ability to follow oral and written instructions
- Ability to perform tasks in compliance with cGMP's, cGLP's, and safety guidelines
- Knowledge of HPLC and GC preferred
Required Education/Training:
- College chemistry degree
- Experience in GMP environment
Regulatory Affairs Specialist
Works with Regulatory Affairs Manager to play a key role in supporting the transition to electronic ANDA submissions utilizing the eCTD format. Responsible for the production, assembly, document management and electronic submissions. Responsible for the collection, scanning, filing, and submission preparation of documents for paper and/or electronic submissions. Working with regulatory counterparts, responsible for ongoing maintenance of submissions, preparation of general day-to-day submission filings. Responsible for data entry, filing, archiving, and maintenance of submission tracking databases for several active filings. Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.
Required Skills:
- Computer skills related to regulatory software applications
- Attention to detail
- Excellent communication skills, written and verbal
- Presentation skills
- Reasoning skills
Required Education/Training:
- Bachelor's Degree from an accredited college or university
- 4 years pharmaceutical industry experience, 2 of which must be in Regulatory or equivalent combination of education and experience
- Knowledge of current FDA regulations and guidelines
Validation Specialist
Performs process validation for solid dose, liquid dose, and other products. Performs installation and operational qualifications for manufacturing and packaging equipment. Prepares master production records.
Must be a self starter, organized, detailed oriented, dependable, goal oriented, and be able to handle multiple projects simultaneously.
Required Skills:
- Basic math
- Written and oral communication
- Computers
- Pharmaceutical manufacturing processes and formulations
- Problem solving
- Innovating new ideas
Required Education/Training:
- Four year college degree
- One or more years experience in the pharmaceuticals industry
BENEFITS
- Health insurance. Sovereign pays
a portion of employee and
family premium.
- Vision, Supplemental Life & Dental
Insurance
- 401k with employee match
- Employer pays Basic Life.
- Long term disability offered.
- Paid Vacation
- Sick Leave
- Holiday Pay
CONTACT INFORMATION
Human Resources
Sovereign Pharmaceuticals
(817) 284-0429
Jobs@sovpharm.com
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