Manufacturing Scientist

Quotient Sciences•Concord Township, PA

3d•Onsite

About The Position

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical 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. 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.

Requirements

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.
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.
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 effectively with Internal and External resources.
Apply concepts such as fractions, percentages, ratios and proportions to practical solutions.
Define problems, collect data, establish facts and draw valid conclusions.
Ability to perform multitude of tasks while maintaining speed of work and attention to detail without loss to productivity.
Ability to perform under stress in cases of emergency, critical or hazardous situations.
Ability to work with others in a team environment.
Ability to travel 50%

Nice To Haves

Experience in the pharmaceutical industry.
Experience with the contract pharmaceutical services industry.

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.
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.