Adesis Inc. - a subsidiary of Universal Display Corporation (Nasdaq: OLED) , a global leader in organic light emitting diodes - is a premier contract development and manufacturing organization (CDMO) accelerating our clients’ success in the biotech, pharmaceutical and specialty chemistry industries through our innovative chemistry and solutions.
Adesis Inc. encompasses almost 100,000 square feet of state-of-the-art laboratory and manufacturing space in two U.S. locations - New Castle and Wilmington, DE, centrally located in the Mid-Atlantic biotech/ pharmaceutical hub. Our business model provides clients with organic chemistry services in three areas: early-stage research, scale-up and development, and specialty manufacturing. We specialize in organic and organometallic synthesis, from milligrams to multi-kilogram quantities, and our exceptional technical team prides ourselves in our ability to solve challenging chemistry problems for our growing client base. Adesis is an extraordinary company looking for extraordinary talent! Our mission is to accelerate our clients’ success through innovative chemistry and solutions, and we offer promising careers in an inclusive work environment aligned with our values of innovation, ownership and integrity. Job Summary The Analytical Chemist I will support the Quality Control laboratory by performing analytical testing of raw materials, in-process samples, intermediates, and finished products. The technician will ensure compliance with ISO-9001 Standards, internal procedures, and client-specific requirements while maintaining accurate documentation and supporting laboratory operations. Essential Duties and Responsibilities Include the following. Other duties may be assigned.Perform routine analytical testing using techniques such as HPLC, GC, LC-MS, UV-Vis, FTIR, and wet chemistry methods.
Execute raw material, in-process, release, and stability testing in accordance with SOPs and regulatory guidelines.
Prepare, standardize, and document test solutions and reagent.
Calibrate and maintain analytical instruments; promptly report malfunctions.
Maintain accurate laboratory records in compliance with Good Documentation Practices (GDP).
Identify and correct problems with instruments in QC lab. Identify and communicate problems and solutions related to process, procedure, and materials to Analytical team lead and QC Chemists.
Maintain cleanliness and organization of lab by following safety, regulatory, and chemical hygiene plan
Perform daily record keeping in electronic lab notebook,
Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste
Assist in OOS/OOT investigations and support root cause analysis.
Attend and participate in QC Team meetings. Develop team skills.
Participate in continuous improvement initiatives to optimize laboratory efficiency and data integrity.
Required Qualifications
Bachelor’s degree in chemistry, Pharmaceutical Sciences, or related field.
QC analytical laboratory experience in a pharmaceutical, biotech, or CDMO environment, preferred.
Technical Skills:
Hands-on experience with HPLC, GC, and spectroscopic techniques.
Familiarity with cGMP, ICH, and USP/EP guidelines preferred.
Strong analytical and problem-solving skills with attention to detail.
Other Skills:
Proficiency in Microsoft Office and laboratory data systems (e.g., Empower, Open Lab CDS, Mass hunter and LIMS) is a plus.
Excellent written and verbal communication skills.
Strong organizational skills and ability to work both independently and in a team setting.
Current Benefits at UDC:
Competitive base salary and annual bonus program
Medical/Prescription Drug coverage, Dental, and Vision for employees and family
Option between Flexible Spending account (FSAs) or Health Savings Account (HSA)
Group Term Life insurance, short term disability, and long-term disability benefits for employees
Employee Stock Purchase Plan (ESPP)
401(k) company contribution
Annual charitable matching gift
Generous Paid Time Off
Annual compensation range: $65k-$75k
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