At Guardian we are committed to providing the best environment for our employees. We have the advantages of a small company combined with the heritage of being an established leader in the OTC pharmaceutical manufacturing industry since 1984.
GDC provides employees with the opportunity to grow and exercise responsibility to realize their full potential. Creativity, innovation and superior quality are at the core of our business and team members.
Along with an exciting and diverse working environment, Guardian Drug Company offers its employees a competitive salary and benefits* plan including:
- A comprehensive Medical program
- Company paid short and long term disability
- Paid vacations
- Personal and sick days
- Bonus program
*Please note that employee benefits may change at the company's discretion.
Current Oppenings:
Job Title: PRODUCTION CHEMISTS
Requirments:
Experience in planning and execution of production activities starting from
dispensing raw materials to finished product; experience with validation and
qualification of products and processing equipment; exposure to federal and
state regulations.
Job Title: RESEARCH SCIENTIST
Requirments:
Development and validation of analytical methods, test raw materials and
finished products and assist with dev. of OTC formulations. Candidate must
coordinate with Q&C and Production, and utilize knowledge of controlled
production, sampling techniques & testing procedures.
Job Title: SYSTEM & PROCESS DEVELOPMENT ANALYST
Requirments:
Maintain and validate computerized systems as per Federal regulations and
develop validation life cycle documents including master plan,
IQ/OQ/PQ/SOP’s, and traceability; experience w/ performing architecture
analysis and developing pharmaceutical process procedures.
Job Title: QUALITY ASSURANCE MANAGER
Requirments:
Oversee testing and quality maintenance of pharmaceutical active and
inactive ingredients utilized in manufacturing; evaluate and qualify sources
of raw materials; inspect and audit drug manufacturing facilities and drug
master files; supervise mixing and processing of raw materials according to
cGMP; ensure efficient production as per cGMP.
Send resumes to:
HR Dept.
Guardian Drug Company
P. O. Box 915
Dayton, NJ 08810
