Lupin Pharmaceuticals USA Vacancies Senior Manager, Pharmaceutical Development, MDI

LUPINLUPIN PHARMACEUTICALS,INC.
Senior Manager, Pharmaceutical Development, MDI
Job Locations :US-FL-Coral Springs
Category: R&D

More information about this job:
Lupin Pharmaceuticals Inc. is a specialty pharmaceutical company marketing generic and branded pharmaceutical products as well as Active Pharmaceutical Ingredients (APIs) from its sales and marketing headquarters in Baltimore, MD.
Lupin Inc. has established a new Research and Development Center in the US located in Coral Springs, FL. This center will focus on the development of generic and branded pharmaceutical products.

Responsibilities:
Manages a team of laboratory scientists conducting standard and advanced laboratory activities. Independently designs, conducts, leads and supervises characterization studies for pressurized Metered Dose Inhalers (pMDIs) products. Supports evaluation and selection of raw materials (APIs, excipients, primary and secondary packaging material, device component material etc.); pre-formulation, formulation and process development studies for pMDIs following cGMP, Lupin EH&S and other relevant guidelines. Leads the development and evaluation of new aerosol analytical technologies where required. Initiates investigations and data reviews. Manages resources and assure progress of project activities on a daily basis. Coaches, mentors and trains team members.

  • Manage a group of laboratory scientists conducting standard and advanced laboratory activities.
  • Independently design, conduct, lead and supervise characterization studies for pressurized Metered Dose Inhalers (pMDIs) products.
  • Provide leadership in CMC activities and represent CMC on global project teams.
  • Act as subject matter expert (SME) on aerosol analytical characterization methodologies for orally inhaled and nasal products (OINDPs).
  • Lead characterization studies for evaluation and selection of raw materials (APIs, excipients, primary and secondary packaging material, device component material etc.); pre-formulation, formulation and process development studies for pMDIs following cGMP, EH&S and other relevant guidelines of Lupin, FDA and other governing bodies.
  • Supervise and lead the execution of analytical activities required for regulatory submission including method transfer protocols and validation of analytical methods. Participate in laboratory activities as required.
  • Write protocols, methods, reports, standard operation procedures, and submission documents when required.
  • Analyze data, identify trends and perform statistical analysis. Present data, recommendations and conclusions to senior management on a regular basis.
  • Lead project activities, support project timelines and proactively contribute to meeting the team objectives. Communicate effectively with team members and internal or external customers. Work and communicate effectively with other functional groups.
  • Troubleshoot technical issues, analyze data, identify solutions, and implement recommendations.
  • Plan laboratory activities and resources on a weekly basis and ensure that project timelines are met consistently.
  • Develop and communicate project plans, goals and strategies to the group.
  • Propose and implement processes and new technologies that lead to increased efficiencies and quality of laboratory activities. Drive the continuous improvement process.
  • Develop and implement appropriate training programs for analytical activities across all respiratory development sites.
  • Mentor and assist junior scientists.
  • Ensure that members of the group are trained on relevant methods, policies and procedures. Verify that training records of group members are updated at least twice a year. Conduct quarterly performance reviews of group members and provide them with regular feedback. Support the personal development of group members.
  • Influence decisions within team.

Qualifications:

  • PhD in Pharmaceutics/Pharmaceutical Technology/Pharmaceutical Chemistry/Analytical Chemistry or related fields with a minimum 8 years of relevant experience; Minimum 12 years experience in pharmaceutical technology or related fields without a PhD.
  • In depth knowledge of pharmaceutical and inhalation technology.
  • Relevant experience in characterization of pressurized Metered Dose Inhalers (pMDIs) products and other OINDPs.
  • Extensive knowledge of analytical chemistry methodologies (UPLC/HPLC, GC, UV, FTIR etc.) and aerosol characterization methodologies (Cascade Impaction, Laser Diffraction techniques etc.).
  • Experience in supervising 6-10 laboratory scientists.
  • Experience in planning, organization and project management.
  • Knowledge and detailed understanding of the FDA cGMP requirements as they apply to the Pharmaceutical industry. Good understanding of USP methodologies and ICH guidelines.
  • Strong English language skills including writing ability and oral communication.

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Lupin Pharmaceuticals USA Vacancies Senior Manager, Pharmaceutical Development, MDI

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