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Senior Process Chemist
2 months ago
Job Overview
Porton Pharma Solutions Ltd. stands as a premier global entity delivering extensive process research and development along with manufacturing services tailored for the pharmaceutical sector. Our expertise lies in providing comprehensive solutions for small molecule active pharmaceutical ingredients (APIs), dosage forms, and biologics. With a strong emphasis on innovation and client satisfaction, we are dedicated to producing high-quality products and services that align with the dynamic requirements of the industry. Our skilled team of professionals is committed to ensuring that every project is executed punctually, within budget, and to the utmost standards of quality.
Key Responsibilities
- Execute process chemistry research and development for clients, focusing on the exploration of synthetic pathways for active pharmaceutical ingredients and chemical intermediates through route discovery, process enhancement, safety assessments, and the application of enabling technologies.
- Formulate safe, efficient, and timely chemical processes utilizing established and innovative methodologies.
- Oversee analytical chemistry techniques in relation to process and catalysis discovery, development optimization, and troubleshooting.
- Uphold a steadfast commitment to quality, documentation, confidentiality, and scientific rigor.
- Engage in the generation of ideas for targeted proposals to clients and ensure successful execution of accepted proposals.
- Facilitate interdepartmental communication to develop synchronized research and development schedules and deliverables.
- Lead and engage in scientific discussions with colleagues and clients to strategize, execute, and resolve challenges.
- Maintain transparent and timely communication with clients, management, and peers.
- Participate in regular client updates, prepare weekly reports, contribute to campaign reports, and assist in process chemistry technology transfer.
- Coordinate and draft professional campaign reports, research summaries, and technical documentation.
- Adhere to all company, site, and laboratory Environmental, Health, and Safety (EHS) protocols, processes, guidelines, and standard operating procedures. Actively engage in EHS discussions with peers and management to foster continuous improvement.
- Ensure a clean and organized workspace, advocating for these principles and positively influencing others.
Qualifications
- Demonstrated success in achieving ambitious targets related to safe and timely synthetic organic chemistry projects.
- Experience in a c-GMP environment is preferred but not mandatory.
- Exceptional written, verbal, and presentation abilities.
- Background in small molecule drug development is advantageous but not essential.
- Proven scientific achievements as evidenced by publications and presentations.
- Capacity to prioritize and manage multiple tasks concurrently.
- Able to interact effectively with diverse groups.
- Experience contributing positively to scientific teams.
- Capability to meet the physical demands of the role.
- Proficient in Microsoft Office applications.
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 8-hour shift
- Monday to Friday
Experience:
- CDMO: 5 years (Preferred)
- Organic chemistry: 8 years (Required)
Work Location: In person
