Manufacturing QMS Specialist at Kashiv BioSciences, LLC

Chicago, Illinois, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Aug, 26

Salary

0.0

Posted On

05 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

QMS, Deviation Writing, Change Control, CAPA, Batch Record Review, SOP Authoring, Upstream Processing, Downstream Processing, Biologics Manufacturing, GMP, 5Why Method, 6M Method, Cleaning Validation, Technical Writing, Interpersonal Skills, Microsoft Office

Industry

Pharmaceutical Manufacturing

Description

Description The Manufacturing QMS Specialist , is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC. This position is located in Chicago, IL. Under the direction of Manufacturing Management, the Manufacturing QMS Specialist will be executing routine documentation work which includes writing and reviewing deviations, change controls, investigation reports, batch records, SOPs, CAPAs etc. This position requires technical expertise in the upstream and downstream process of biologics (Cytokines, monoclonal antibodies manufacturing). Essential Duties & Responsibilities Will be responsible for supporting the manufacturing team with all kinds of documentation. Documentation includes reviewing executed batch records (both Upstream department and Downstream batch record). Will be responsible for filing change controls, Deviation, and CAPA for manufacturing department. For all critical / major investigation, will have to use investigation tools like 5Why or 6M method. Attend daily meetings with both upstream and downstream process to get all the documentation requirements for the day. Will meet weekly with QA to avoid any delay in the QMS closure. Will author batch records, SOPs and associated forms / formats required for the manufacturing process. Will be responsible for requesting / submitting all GMP documents to QA. During critical campaign, will support manufacturing process (rotating shifts) Wet lab work will not be more than 10 % of your time. Performs other functions as required or assigned. Complies with all company policies and standards. Requirements Education: A Minimum BA or BS in Biological Sciences or related technical field is required. Minimum 5 years of experience in Biopharmaceuticals. Knowledge in USP and DSP process Special Skills: Ability to work with other team members and independently - good interpersonal skills. Good communication skills: verbal and written, good computer and organization skills, detail oriented. Basic computer skills, including knowledge of Word, Excel and spread sheet Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review. Knowledgeable in cleaning verification/validation. Work Environment & Physical Demands: Noise: No extraordinary noise levels. Standing/Lifting: No extraordinary requirements. Visual: No extraordinary requirements. Stress: High-paced demanding environment to meet ambitious project goals. Travel: None General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines. Some travel may be involved. Supervisory Responsibility, if any: No Benefits/Perks: Medical Dental Vision 401K FSA HSA Commuter/Transit Benefits Student Loan Assistance Program Monthly Cell Phone Allowance Free Parking (Company Paid) Conveniently located next to the Metra, Green and Red Line One block east of the Chicago White Sox Stadium < 10 minutes away from Downtown Chicago This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization. Kashiv Biosciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Kashiv Biosciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, and transfer, leaves of absence, compensation and training.

Responsibilities

The specialist is responsible for executing routine QMS documentation, including writing and reviewing deviations, change controls, and SOPs. They will support the manufacturing team by managing GMP documents and conducting investigations using tools like 5Why and 6M.