Generic Pharmaceuticals - Senior Formulation and Technical Services - Solids, Semi-Solids, Steriles - Chartwell Pharmaceuticals : Job Details

Generic Pharmaceuticals – Senior Formulations and Technical Transfer Team

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Dear Candidates, please respect our position, experience, and location requirements before you apply to the position and we incur the cost. We will ONLY consider candidates that meet ALL of the requirements, so please apply if you do. Thank you for your interest and understanding.

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ABOUT CHARTWELL PHARMACEUTICALS:

Chartwell Pharmaceuticals, LLC is a privately-held, US-based generic pharmaceutical manufacturer with manufacturing in Congers, Carmel, and Amityville, New York. With 999+ ANDA listings in the FDA Orange Book, Chartwell is rapidly growing and transforming our business as a full-scale Generic Pharmaceutical Manufacturer and Distributor serving the Retail, State and Federal Government Markets under the “Chartwell Rx” labels. This is an excellent opportunity to build your career with a fast-growing and dynamic generic pharmaceutical company!

Senior Scientist

Provide scientific, technical and hands-on support of Formulations and Technical Transfers of previously approved dosage forms into the Chartwell Pharmaceuticals sites, or to 3rd party sites. This position may work with solids, liquids, semi-solids, ophthalmic/otic, and injectable products. Must have a current understanding of formulation development, QbD, and tech transfer process from kick-off through validation. Possess strong technical skills in pharmaceutical manufacturing, scale up and scale down processes and packaging, relevant process equipment, formulations, API characterization, pre formulation and excipients performance. Should have knowledge of analytical methods. High sensitivity to QA, RA, QC requirements for regulatory filings. Identify opportunities to improve the process or materials to achieve best cost and efficiency.

Responsibilities:

• Work independently to design, conduct and troubleshoot benchtop formulation experiments.
• Evaluate and document key ANDA/NDA approval details.
• Responsible for execution of lab scale, scale up and validation batches.
• Perform gap analysis and characterize the changes required for formulations.
• Record experiments in laboratory notebooks.
• Compile data, data presentations, prepare product development reports and author technical reports for submission/validation batches.
• Perform scale-up studies and prepare technical transfer report for cGMP manufacturing.
• Operate small scale up manufacturing equipment to replicate to full scale.
• Identify problems, troubleshoot and offer solutions to advance assigned projects.
• Work with operations team to ensure equipment and capacity readiness for all required work.
• Provide clear and accurate verbal and written reporting of technical activities.
• Provide product status, with relevant materials for decision support.
• Maintain Research and Development pilot plant equipment/instruments.
• Meet project timelines and performance standards as assigned.
• Carries out responsibilities in accordance with organizational policies and procedures.

Qualifications:

• Bachelor or Master's degree in a related scientific discipline desired.
• Minimum 8 years of Pharmaceutical formulation and process development, technology transfer and scale up experience supporting technical and operational activities in various dosage forms.
• Experience and working in cGMP environment and knowledge in regulatory guidance.
• Superior problem solving, organizational and analytical skills, highest attention to detail, and ability to proactively seek multiple internal and external data sources and insights and synthesize into meaningful observations and action plans.
• Be challenge driven, and flexible, willing to take on extra responsibility to achieve organizational goals.
• Superior communication skills (verbal, written and presentation).
• Highly ethical and transparent, with professional sensitivity and care for confidentiality.
• Must have proficient computer skills.

PLEASE NOTE:

• This position is based in AMITYVILLE (Long Island) NY and we only seek candidates from the New York Metropolitan area.
• Candidates must meet all of the criteria in the qualification questions.
• Sponsorship is not available for this position.
• Agency referrals are not accepted