Manufacturing Scientist

nical pharmacology, clinical trials, and commercial product manufacturing.

Our proprietary and disruptive platform – “Translational Pharmaceutics®” – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs
, improves outcomes, and significantly accelerates drug development times.
Why Join Us

Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.
The Role

We are looking for a Manufacturing Scientist to join our team in Garnet Valley. In this role, you will play a key part in supporting both lab‑scale formulation development and clinical‑stage GMP batch manufacturing. You will work hands‑on with a wide range of pharmaceutical dosage forms and contribute directly to the development and manufacture of products that support clinical trials and ultimately impact patient outcomes.
Key Responsibilities
• Conduct lab work as planned by the supervisor that involves development of pharmaceutical formulations such as tablets, capsules and liquids.
• Conduct pharmaceutical manufacturing of oral dosage forms using small to large scale equipment for development and process scale up and for clinical supplies.
• Review and write master batch records with input from supervisor. Prepare executed batch record folders.
• Comply with cGMPs, SOPs and Company policies.
• Operate manufacturing equipment’s with Operator for development clinical manufacturing.
• Maintain planned training schedule and record.
• Completion of clinical batch manufacturing as per timeline
• Ability to perform physical work while using a respirator.
Additional Tasks / Responsibilities
• Carries out duties in compliance with all state and federal regulations and guidelines including FDA, EPA, OSHA and DEA.
• Complies with all company and site policies and procedures.
• Remains current in profession and industry trends.
• Makes a positive contribution as demonstrated by:
• Making suggestions for improvement
• Learning new skills, procedures and processes.
• Is available for other duties as required.
Qualifications and Experience Required for Competent Performance
• B.S. Degree in Chemical Engineering, Pharmacy/Pharmaceutical Sciences or other related field or High School Diploma with 2-3 years’ experience in the pharmaceutical industry or appropriate combination of education and experience
• Read and interpret documents such as batch records, SOPs, policies, and safety rules, read and write business correspondence.
• Define problems, collect data, establish facts and draw valid conclusions.
• Interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
• Basic knowledge of physicochemical concepts and theories.
• Familiarity with the production process.
• Familiar with a variety of in-process equipment, such as disintegration, friability, particle size, etc.
Computer Skills
• Enter data into computer using software applications for data entry and word processing.
• Work and be proficient with e-mail systems
• Ability to perform repetitive tasks while maintaining speed of work and attention to detail without loss to production.
• Apply basic concepts such as fractions, percentages, ratios, proportions and significant figures to practical solutions.
• Work with basic statistical concepts such as average and standard deviation.
• Skills:

The effective use of knowledge and abilities in performance.
• Read and interpret documents such as RFP’s (request for proposals) Analytical methods, Formulation reports, MSDS’s, SOP’s (Job Standard Operating Procedures).
• Write routine reports and business correspondence, work orders, etc.
• Ability to communicate…