Quality Assurance Specialist II at Kashiv BioSciences, LLC

Piscataway, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Aug, 26

Salary

0.0

Posted On

22 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Data Interpretation, cGMP Compliance, Document Control, Raw Material Sampling, Quality Assurance Auditing, CAPA Management, Deviation Investigation, Change Control, Method Validation, Stability Studies, Microsoft Office, Technical Writing

Industry

Pharmaceutical Manufacturing

Description

Description SUMMARY: The Quality Assurance Specialist II is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway NJ. This employee will be responsible for supporting Kashiv BioSciences Quality Assurance management in reviewing, implementing, and managing the quality system to ensure overall product and process quality. As an integral quality team member, this individual will provide assurance that all products and quality system processes in the facility are in compliance with cGMP requirements and company policies and procedures. Assists in the direction and training of other quality team members. Position involves reviewing and assembling batch documentation, issuing and tracking controlled documents, reviewing raw material documentation and releasing material, reviewing deviations, CAPAs, chance controls, validation/qualification, facility preventive maintenance and calibration records. Position also involves the completion of manufacturing clearance activities to ensure requirements are met prior to and upon completion of manufacturing activities and to serve as the witness for critical steps in manufacturing records and quality control documents. ESSENTIAL DUTIES & RESPONSIBILITIES: Manage a broad spectrum of projects to support the needs of Quality Management. Issue, assembly and review of documentation supporting batch, laboratory, warehouse, metrology, engineering and validation activities, to ensure complete and in compliance with company policies and procedures and cGMP requirements. Quality system documentation to include SOPs, deviation/investigation reports, equipment/system qualification protocols and reports, change controls, as well as document control activities (training records entries, logbook issuances, logbook archival etc.) Interface with cross functional departments Perform quality assurance walk-through audits of manufacturing, laboratory and warehouse areas to ensure compliance with CGMPs and company procedures. Quality support of environmental/quality monitoring and release of controlled systems and environments. Support includes data review for release and support of investigation activities. Assist and provide input as part of a project team to resolve quality and manufacturing issues and identify and implement corrective and preventive actions in a timely manner. Perform Raw Material, water and gas sampling, In-process and Finish Product sampling and coordinate submission of samples to QC analysis. Receiving of external samples and log in internal quality system Quality release of raw materials and finished products. Provide back up for other Quality Assurance Specialist responsibilities. Perform other duties and responsibilities as delegated by Quality Management. Ensure adherence to GMP good documentation practices Complies with all company policies and standards Requirements PREREQUISITES: Education: A 4-year Bachelor degree, preferably in science or engineering discipline Experience: Quality Specialist: Quality Specialist I or II Key Responsibilities: Analytical & Lab Support Review and interpret analytical data (e.c. HPLC, UV, Bioassay test, etc.) Verify test results against specifications and standards Support method validation, stability studies, and investigations (OOS/OOT) Perform trend analysis and identify quality risks Raw Material Sampling (Additional Responsibilities) Perform sampling of raw materials, APIs Ensure compliance with sampling plans and GMP guidelines Handle materials in controlled environments (warehouse/cleanroom) Maintain proper sample labeling, traceability, and documentation Required Experience; 2–5 years in Quality / QC / Analytical roles Education : Bachelor’s or master’s degree in: Chemistry / Analytical Chemistry/ Pharmacy / Life Sciences Key Skills: Strong understanding of analytical data interpretation SPECIALIZED KNOWLEDGE AND SKILLS: Good communication skills, both written and verbal. Good organizational skills and detail oriented. Must be able to effectively manage time to complete assignments. Excellent computer skills in Microsoft Office applications. Ability to work independently or in teams both within department and cross-functionally. Must be able to organize, plan and manage assigned tasks to bring projects to completion. Direct experience in manufacturing QA support (sampling, room/line clearance, cleaning verification) preferable Understand the requirements and procedures related to document control and Quality Assurance. Experience in GMP document control Must be able to utilize technical information appropriately to ensure documents produced are consistently clear, concise, accurate, and complete. WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS: Typing, desk work and plant auditing. Must be able to read, write and understand English. Manufacturing clean rooms Some brief and/or minimal exposure to hazardous chemicals may occur, requiring personal protective equipment. Safety alertness is required due to work around hazardous equipment and conditions. 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. 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.

Responsibilities

Responsible for managing the quality system to ensure product and process compliance with cGMP requirements and company policies. Duties include reviewing batch documentation, performing facility audits, and managing deviations, CAPAs, and change controls.