Manufacturing QMS Specialist

The Manufacturing QMS (Quality Management System) Specialist will be executing routine documentation work, which includes writing and reviewing deviations, change controls, investigation reports, batch records, SOPs, CAPA, etc. This position requires technical expertise in upstream and downstream processes of biologics (Cytokines, monoclonal antibodies manufacturing).

Essential Duties & Responsibilities

• Will be responsible for supporting the manufacturing team with a wide variety of documentation.
• Documentation includes reviewing executed batch records, logbooks, and other associated documents, both Upstream department and Downstream batch records.
• Will be responsible for filing change controls, deviations, and CAPAs for the 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 processes 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 campaigns, will support the manufacturing process (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.

Qualifications

Minimum Qualifications:

Education:

• A Minimum BA or BS in Biological Sciences or related technical field is required.
• Minimum 5 years of experience in Biopharmaceuticals.
• Knowledge of USP and DSP processes
  
  

Special Skills:

• Previous investigation training
• 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 spreadsheets
• Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review.
• Knowledgeable in cleaning verification/validation.

Work Environment & Physical Demands

Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines.

General Work Environment :

• Wear appropriate PPE to work in cleanrooms and/or laboratories that are adequately lit, ventilated, and temperature controlled.
• Desk/computer work (reading, editing, writing documents) required.
• Potential for chemical odor and dust exists.
  
  

Standing/Lifting:

• Must be able to move around the facility to reach various equipment.
• Physical lifting and shifting required for pushing and pulling pre-made buffer containers
• Must be able to lift at least 25 lbs. to lift weights onto scale for daily scale verification
• Must be able to stand for long periods of time. Occasional bending, squatting, kneeling, stooping, pushing, pulling, reaching, and walking.
  
  

The salary range for this position ranges from $65,000 - $80,000 per year. In addition, Kashiv BioSciences, LLC., offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months. Kashiv BioSciences, LLC., ranges reflect the Company’s good faith estimate of what Kashiv BioSciences, LLC., reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills.

At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life’s many other commitments and opportunities.

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at View email address on aiapply.co. Requests will be handled confidentially and in accordance with applicable laws.