Careers

Join The Team At Aspire Pharmaceuticals

Become an innovator in the pharmaceutical industry. Aspire is always looking for talented people to join its team. To be considered for a position, please email a cover letter and resume to Careers@aspire-pharma.com.

OPEN POSITIONS:

Quality Control Chemist – ICP

This position is primarily responsible for testing samples using a wide range of analytical methodology. Reviewing, preparation/maintenance of SOPs and STP’s, calibration and other controlled document, to ensure quality of the dietary supplement by performing the following duties.

Educational Qualification: At least a bachelor’s degree or master degree in the field; minimum 3-5 years related experience and/or training; or equivalent combination of education and experience.

Essential Duties and Responsibilities: Personal responsibility for following safety rules, SOPs and cGMPs guidelines. Experience in ICP-MS techniques required to test a Dietary Supplement for minerals and heavy metals. Must possess very high/expert knowledge of ICP-MS (Perkin Elmer preferred), Microwave Digestion, and its sampling procedures as well as general knowledge of elemental analysis. Testing of raw materials, in-process materials and the finished products. Including preparing reports. Operate and trouble shoots ICP-MS instrument. Be proficient with the ICP-MS instrumental analysis and data interpretation Responsible to prepare accurate daily records and documents that report the results of their lab work. Documentation of logbooks, in-house calibration records, temperature and humidity records, etc. Perform safety and housekeeping aspects of the job by following all safety rules, wearing required safety equipment, keeping work areas clean during and at completion of tasks, maintaining all workstations and equipment in an orderly and clean fashion. Maintain monthly inventory on supplies for QC for devices and reagents and standards. Ensures that all paperwork is properly documented. Keeps accurate attendance records; files proper reports (accident, probation, etc.). Will assist in QC stability testing, prepare and maintain stability records and summaries. Responsible for the preparation and review of Standard operating procedure or Standard testing procedure.

Posted: 07/21/17

 

Quality Assurance Associate – Raw Materials

This position is primarily responsible for raw material vendor qualification, raw material specifications, non-conformance materials, and material approval.

Educational Qualifications: Four year college degree or equivalent; and one to two years related experience and/or training; or equivalent combination of education and experience.

Essential Duties and responsibilities: Ensures compliance with cGMP, company SOPs and FDA requirements during all phase of operations. Prepares and maintains vendor qualification reports and its requalification reports. Prepares and maintains raw material specifications. Prepares and maintains analytical reports for raw material testing and retest. Performs documentation review and batch record review as needed. Organizes and ensures accurate and reliable filing systems for all paper-based GMP Documents. Performs inspections on packaged product as needed.

Posted: 07/21/17

 

Formulation Technical Manager

Prepare Master files and product Specification for OTC, ANDA and relevant Drugs related products.
Coordinate Laboratory scale testing of new OTC, ANDA and Drugs related formulations and scale up in manufacturing.
Provide support to Manufacturing departments for feasibility formulations.

Posted: 05/01/2017

Quality Assurance Associate

Ensures compliance with cGMP, Company SOP’s and FD requirements. Responsible for SOP biannual update. Maintains the records for calibration on process equipment, calibration on QA data logger and calibration on engineering equipment. Maintains and oversees documentation control of all regulated documents. Completes Quality Assurance operational requirements by scheduling or co-ordination with other departments. Executes and participates in internal audits. Bachelor’ s Degree or foreign equivalent in Pharmacy, Chemistry or related field plus 24 months of work experience in this field.

Posted: 12/14/2016

 

Quality Control Chemist 

This position is primarily responsible for testing samples using a wide range of analytical methodology. Reviewing, preparation/maintenance of SOPs and STP’s, calibration and other controlled document, to ensure quality of the dietary supplements.

Educational Qualification: At least a bachelor’s degree or master degree in the field; minimum one year related experience and/or training; or equivalent combination of education and experience.

Essential Duties and Responsibilities: Personal responsibility for following safety rules, SOPs and cGMPs guidelines. To prepare and conduct all chemical testing and various analytical testing procedures on samples from all phases (Raw material, Finished Product, In-Process and Packaged product) according to Standard testing procedure (STP). Responsible to prepare accurate daily records and documents that report the results of their lab work. Adapt, maintain and operate analytical instrumentation and minor trouble shooting of equipment. Documentation of log books, in-house calibration records, temperature and humidity records, etc. Perform safety and housekeeping aspects of the job by following all safety rules, wearing required safety equipment, keeping work areas clean during and at completion of tasks, maintaining all work stations and equipment in an orderly and clean fashion.  Maintain monthly inventory on supplies for QC for devices and reagents and standards.  Ensures that all paperwork is properly documented. Keeps accurate attendance records; files proper reports (accident, probation, etc.). Will assist in QC stability testing, prepare and maintain stability records and summaries. Responsible for the preparation and review of Standard operating procedure or Standard testing procedure.

Posted: 1/19/2016

 

PACKAGING SPECIALIST
Job responsibilities:

Posted: 04/27/2016

 

Other Positions:

In Process Quality Control Associate

Shifts available: 1st shift, 2nd shift, 3rd shift

Encapsulation operators

Shifts available: 1st shift, 2nd shift, 3rd shift

Facility Cleaning/Housekeeping

Shifts available: 1st shift, 2nd shift, 3rd shift

Maintenance Mechanics

Shifts available: 1st shift, 2nd shift, 3rd shift

Posted: 04/11/2016

 

We are always interested in hearing from individuals with experience as an  Encapsulation Operator, Dispensing Technician, IPQA, or QA Regulatory.