About Kashiv BioSciences
Sourced by ZipRecruiter
Industry
Manufacturing
Company size
201 - 500 Employees
Headquarters location
Piscataway, NJ, US
Year founded
2011
Full-time
Medical, Dental, Vision, Retirement
Posted 22 days ago
Job description
Job Type
Full-time
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
Requirements
Education:
Special Skills:
Work Environment & Physical Demands:
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:
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.
Full-time
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
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.
kashivbiosciences.com
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Frequently asked questions
Q: What skills or qualities help someone succeed as a Manufacturing Specialist?
A: To succeed as a Manufacturing Specialist, key technical skills include proficiency in computer-aided design (CAD) software, knowledge of manufacturing processes and equipment, and experience with quality control and assurance methodologies. Soft skills such as strong communication and problem-solving abilities, attention to detail, and adaptability are also crucial, as they enable effective collaboration with cross-functional teams and quick response to production issues. By combining these technical and soft skills, a Manufacturing Specialist can drive efficiency, quality, and innovation in the production process, ultimately supporting career growth and effectiveness in the role.
Q: What is the career path for a Manufacturing Specialist?
A: A Manufacturing Specialist typically starts as an entry-level Production Technician or Quality Control Inspector, progressing to mid-level roles such as Manufacturing Engineer or Process Improvement Specialist, where they develop expertise in optimizing production processes and implementing quality control measures. As they gain experience, they can move into senior roles like Operations Manager or Manufacturing Manager, overseeing entire production facilities and making strategic decisions to drive efficiency and productivity. Throughout their career, Manufacturing Specialists can develop skills in areas like lean manufacturing, Six Sigma, and supply chain management, which can lead to opportunities in related fields like operations management, quality assurance, or even entrepreneurship.
