TP Operator

Quotient Sciences: Molecule to Cure. Fast.

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.

The Role

Are you hands-on, detail‑driven, and passionate about contributing to high‑quality pharmaceutical development? Join our team in Garnet Valley as a TP Operator, where you will play a key role in the execution of CMC/GMP operations, supporting small‑scale development, clinical manufacturing, hand‑packaging activities, and critical sanitization and equipment processes. This is a great opportunity for someone who thrives in a fast‑paced, regulated environment and enjoys working across a wide range of operational tasks that directly impact patient-focused clinical programs.

Main Tasks and Responsibilities

• Facility Sanitization & Equipment Cleaning Procedures
• Weighing and Manufacturing of GMP, R&D and Clinical Batches
• Hand-packaging and labelling of clinical batches and R&D samples
• Equipment Staging, Setup, Operation, Disassembly and Cleaning with no supervision
• Performance Verification/Calibration of Instruments
• Material Handling (API and excipients)
• Execution of GMP, R&D and Clinical batch records with minimal or no supervision
• Authors and reviews GMP equipment Standard Operating Procedures (SOPs)
• Proficient in Batch Record Review
• Ability to work with secondary containment when manufacturing as needed

Additional Responsibilities Include

• Execution of manufacturing batch records and material sampling
• 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
• Makes a positive contribution as demonstrated by:
• Making suggestions for improvement
• Providing overtime as needed
• Learning new skills, procedures and processes
• Is available for other duties as required
• Occasional interaction with clients to discuss process/manufacturing observations

The Candidate

• Qualifications include HS diploma (or GED) with 2-5 years experience of GMP manufacturing and/or equipment maintenance/calibrations.

Language Skills

• Read and interpret documents such as safety rules, equipment operating and maintenance instructions, and standard operating procedure & MSDS
• Write internal business correspondence and standard operating procedures.

Mathematical Skills

• Apply concepts such as fractions, percentages, ratios and proportions to practical solutions.
• Proficient in the use of a calculator

Reasoning Ability

• Define problems, collect data, establish facts and draw valid conclusions.
• Spatial Management

Other Skills, Abilities, Qualifications

• Organizational skills
• Computer skills:
• Familiarity with Microsoft Office Suite
• Windows Operating System
• Demonstrates Mechanical Aptitude
• Ability to work with others in a team environment
• Ability to work with minimal supervision
• Attention to detail

Physical Demands

• While performing the duties of this job, the employee is frequently required to stand, walk, use hands to finger, handle or feel, and talk or hear
• The employee is occasionally required to sit, reach with hands and arms, climb or balance, stoop, kneel, and crouch
• The employee must occasionally lift and/or move up to 50 pounds
• Must be able to qualify for respiratory protective equipment use

Application Requirements

When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.

Our Commitment to Diversity, Equity and Inclusion

Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.

Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.

This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.