Specialist, Label Control and Material Operations

Core Responsibilities Issue clinical and commercial final drug product labels Verify the legibility and accuracy of drug product labels in accordance with approved procedures and label specifications Ensure areas are maintained in state of compliance to always be ready for health authority inspection or audits Perform basic troubleshooting; communicate and resolve discrepancies independently and escalate as required Author and review department owned documents Maintain compliance with assigned learning plan Support integration of newer team members Support internal and external inspections as required Assess discrepancies for entry into quality system and initiate deviations as applicable Participate in cross-department and cross-functional meetings, communicate in professional manner and share data/knowledge within team; build relationships with specialized functions Qualifications Ability to understand, follow and apply approved procedures Proficient computer skills with knowledge of MS Office Ability to understand problems and propose practical solutions Ability to communicate effectively with cross functional peers and various levels of cross functional management through written and verbal skills Ability to work in a fast‑paced team environment with changing priorities Detail oriented and task focused with ability to meet deadlines and prioritize assigned work Active listening skills and ability to understand varied perspectives Ability to independently make decisions and recognize the need for escalation of issues Ability to seek out opportunities for improvement Education / Experience Bachelor's degree preferred. High school diploma/Associate degree with equivalent combination of education and work experience may be considered. 2 years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. Experience with quality management systems preferred. Experience with electronic system and databases such as Manufacturing Execution systems (MES), Enterprise Resource Planning (ERP) preferred. Experience with labelling software and commercial label printers preferred. Reporting Relationship Reports to the Manager, Label Control and Material Operations Physical Demands : Standing and moving for extended period of time Travel required : No Onsite requirement : 100% Onsite Work Schedule : Panama alternative 2‑3‑2 pattern 12‑hour shifts, 6:00 am–6:00 pm (3 days on: Sat, Sun, Mon; 2 days off: Tue, Wed; 2 days on: Thu, Fri; 3 days off: Sat‑Mon) Starting hourly compensation : $47 – $50.35 per hour Equal Opportunity Employer ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws. Legal Notices California Applicant Notice: ASK Consulting is committed to complying with the California Privacy Rights Act (CPRA), effective January 1, 2023, and all relevant data privacy laws. Applicants with disabilities may request this notice in an alternative format by contacting View email address on click.appcast.io. Fair Chance Employment Notice: In accordance with all applicable federal, state, and local Fair Chance ordinances and laws, such as the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act, ASK Consulting considers qualified applicants with arrest or conviction records. #J-18808-Ljbffr Bristol-Myers Squibb