We feel our greatest asset is our people. We are looking for employees who possess the right attitude, dedication to their work, and a sense of urgency. We seek team players who understand nature of entrepreneurship and are willing to participate, learn, contribute and share the growth of the company. We offer ample opportunities for career development and advancement. Tulex is a place where contributions are recognized and rewarded.
How To Get Involved
If you are interested in joining the growing and exciting team at Tulex Pharmaceuticals and wish to begin a dialogue with us, simply email your resume to firstname.lastname@example.org and give a brief explanation as to what position you are looking for. We would be very excited to hear from you.
Current Positions Open
Analytical Chemist Qualified candidates should have:
a BS or MS degree in Chemistry, Pharmaceutical Science or related field with 1-5 years pharmaceutical industry experiences
Good time management skill, flexibility, and multi-tasking abilities
Hands-on experiences in USP Dissolution, UPLC, GC, UV, FTIR and other laboratory instruments
Ability to follow Good Laboratory Practice for notebook recording, protocol design and report writing
Ability to conduct experiments independently and also be a good team player
Excellent work attitude/ethics
Excellent oral and written communication
This is a 6-month contract to hire position. Please reply with resume and salary requirement.
Manager, Regulatory Affairs The candidate is responsible for the regulatory aspects of the projects primarily in the area of ANDA. The qualifications include a minimum BS degree in pharmacy, pharmaceutics or science related field with 3-6 years of pharmaceutical regulatory experiences. Duties include:
Preparation, compilation and submission of the ANDA
Experience with 505b(2) NDA process is a plus
Preparation of responses to FDA deficiency letter and information request
Preparation of control correspondence letter.
Involve and implement regulatory strategy including CBE, CBE30 and PAS
Create, maintain and update drug product label
Prepare annual report of drug products
Work closely with QA for any regulatory related issues.
Excellent work ethics and attitudes
Familiar with cGMP requirements
Must be a team player
Analytical Data Reviewer The Analytical Lab Data reviewer is responsible to assure the quality of laboratory data and reports. This is accomplished by reviewing chromatographic data and related notebooks as specified by Standard Operating Procedures.
Review the analytical method validation, verification and transfer testing and ensure that the testing is conducted as per approved protocols and methods
Review in-process, final product, Raw Materials, cleaning validation/verification test results for accuracy and completeness. Ensure that the work performed is compliant with applicable procedures, analytical methods and specifications
Ensures that all affiliated data including electronic data and respective notebooks/logbooks/worksheets are complete and reviewed
Review Product Specification Sheets/Raw Material Specification Sheets/Stability Specification Sheets for accuracy in data reporting/transcription and the correct entries of all associated references
Assist in writing method validation, verification and transfer reports
Discuss with analysts when necessary to resolve all required corrections to paperwork. Educate analysts to improve analytical data documentation & reporting
Communicate frequently with Lab Management to keep them informed of potential delays in data review as well as the reasons why the delay is occurring
Consult with Lab supervisor regarding priority of assignments. Provide immediate notification to Lab supervisor of any deviations/discrepancies noted during the review process.P9. Provide feedback and suggest ideas to management to improve the review process.P10. Perform any other duties as assigned by the management.
Pharmaceutical Operator The candidate will be working with formulators in oral solid and liquid dosage forms. The qualifications include a minimum Associate degree in Science, Engineering, Mechanics or Pharmaceutics related field with 2-5 years of pharmaceutical industry experiences. Duties include:
Work under the guidance of formulator to operate the equipment
Capable of summarizing and reporting experimental results
Can independently operate the R&D as well as production equipment
Familiar with equipment used for oral solid an liquid dosage forms
Experienced with granulation, milling, blending, drying, tableting, tablet coating, particle coating, encapsulation, and liquid mixing