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SalaryPosition Summary
Manages the respective activities related to cGMP manufacturing, including the development and implementation of manufacturing methods, processes and operations for manufactured biopharmaceutical products. Ensures the effective use of material, equipment and personnel while producing products at high quality levels. Manages daily manpower requirements.
Position Responsibilities
- Execute manufacturing requirements by meeting or exceeding productivity, quality and capacity objectives as set forth by management. Manage daily schedules of production activities, outline staff assignments, material and equipment requirements, and training needs. Assist staff with on the floor execution of production tasks.
- In cooperation with customer representatives, process development and management personnel, look for opportunities to improve operations. Closely coordinate potential process improvements with quality and regulatory to assure cGMP compliance.
- Hire, develop and motivate manufacturing operators. Assure continual technical development of staff. Conduct bi-annual performance reviews for staff. Conduct more frequent reviews for new hires and personnel who have shown performance deficiencies.
- Assist with management of production/operation planning and scheduling
Position Requirements
Bachelor’s degree in a related scientific or engineering discipline and 5+ years industry experience (fermentation, cell culture, purification); or 7+ years related experience and/or training; or equivalent
Salary Range: 93,000 - 115,000
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate’s qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.
KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.
