Associate II, Quality Assurance at Kincell Bio, LLC

Gainesville, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

15 May, 26

Salary

0.0

Posted On

14 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, GMP, GDP, Document Review, Deviation Management, CAPA, Change Control, Batch Record Review, SOP Review, Regulatory Audits, Data Tracking, Microsoft Word, Microsoft Excel, Communication, Prioritization

Industry

Pharmaceutical Manufacturing

Description

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance. For more information, please visit our website at www.kincellbio.com. Kincell is seeking a highly motivated Associate II who will be a key contributor to a dynamic and collaborative Quality Assurance team. Quality Assurance Associate II will primarily be responsible for supporting quality operation activities. This highly motivated member of the Quality Unit will promote a culture of compliance throughout the organization by reviewing all production-related documents and assisting with quality oversight of quality events. The Associate II oversees the generation and revision of product-related master documents to support GMP manufacturing of drug substances and drug products. Mature professional capable of working independently and in a team setting. Continually evaluate opportunities for improvement to increase efficiency while ensuring compliance with applicable regulatory requirements and standards. Requires the ability to produce results in a fast-paced environment to meet client deadlines and to prioritize based on criticality effectively. Essential Duties and Responsibilities Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all- inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document. Actively participates in fostering a positive, collaborative work Ensuring adherence to cGMPs across the Addresses all quality and compliance matters in an open and timely Evaluating standard operating procedures, master batch records, and test methods for alignment with GMPs. Performs review of all product-related documents such as production batch records, testing forms, logbooks, etc. Supports raw material and finish product release Supports deviation, CAPA, and change control Will work directly with all departments and across sites to review and track executed documents to meet timelines. Provide status updates and reminders when necessary. Maintains databases used for tracking various lot disposition Support regulatory (FDA, EMA) and client audits/inspections. Other duties as Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully. HS Diploma With 7+ years of relevant industry experience Bachelor’s degree preferred in life sciences with 2+ Years of relevant industry experience Prefer experience with FDA Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDP) in the pharmaceutical, biologic, medical device, or human tissue industries in a Document Control position, including the revision, issuance, and tracking of batch records, Standard Operating Procedures (SOP), Specifications, etc. Microsoft Word and Microsoft Excel experience An equivalent combination of education and experience may be Exposure to 21 CFR Parts 210 & 211, 21 CFR 820, and/or 21 CFR 1270, biotechnology, and electronic computer systems is desired Excellent communication skills, written and Team player with the ability to influence Detail-oriented, excellent written and verbal communication skills Effectively manages cross-functional communication Multitasks strategically and tactically in a fast-paced work Strong organizational skills; able to prioritize and manage complex processes/projects. Ability to define problems, collect data, establish facts, and draw valid conclusions Ability to function in a rapidly changing environment and balance multiple priorities Physical Demands Adjusting or moving objects weighing up to 25lbs Travel Requirements None Location This position is 100% on-site in Gainesville, FL #LI-Onsite Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

Responsibilities

The Associate II will primarily support quality operation activities, promoting a culture of compliance by reviewing production-related documents and assisting with quality oversight of quality events. Key duties include overseeing the generation and revision of master documents for GMP manufacturing and supporting raw material/finish product release.