Location: Allendale,NJ, USA
QC Microbiology Manager – Allendale, NJ
The Manager, QC Microbiology plans, organizes, schedules, and directs the department to effectively utilize employees and equipment to meet and exceed GMP requirements, established KPIs, and material utilization while adhering to quality control-microbiological and technical standards. The Manager provides direct on-site analysis of the day-to-day operation including adjustment of workflow, test performance, and quality compliance.
Essential Functions and Responsibilities:
Devising sound hiring strategies based on business needs (S&OP and LE). Maintaining adequate staffing by interviewing, hiring, training, and performing the competency assessment of personnel.
Performing scheduling, planning, staffing, and monitoring of workflows based on business needs.
Providing staff development through feedback aimed towards performance development and review.
Performing corrective counseling, when necessary.
Procuring appropriate supplies and equipment to maximize department efficiency while adhering to established budgetary and quality goals.
Lead equipment life cycle management &asset/investment optimization process. Evaluate and purchase equipment based on S&OP demand within the aliquoted budget.
Assure the qualification of the laboratory equipment and validation of microbial methods, approving the protocols and/or respective reports.
Overseeing or initiating in-sourcing of microbial methods to attract clients as well as generate revenue.
Work with the BD group for initiation of W.O. for any out-of-scope work done for the clients.
Providing technical oversight of area(s) of responsibility; Serving as a technical resource for problem solving and process improvement to ensure accurate test performance.
Form project teams and champion the execution of agreed projects using project management, problem- solving and operational excellence tools
Investigating and documenting non-conforming events and environmental excursions. Serving as approver in investigations while overseeing timely closure of deviation reports, change controls, CAPAs, and applicable batch records.
Monitoring effectiveness of quality systems, change control activities and their completion, for both, internal, client, and regulatory agency audit findings
Troubleshooting and recommending process improvements to achieve greater efficiency and meet quality goals.
Lead strategy to simplify &standardize equipment software architecture, enabling digital integration.
Identify and execute Continuous Improvement Projects for the department. Lead and develop best practices in the laboratory.
Leading/participating in department and cross functional meetings.
Supporting, implementing, and ensuring compliance amongst all departments, company policies, and procedures.
Ensuring compliance with regulatory agency requirements by enforcing a quality culture throughout the department.
Interacting with internal and external customers to ensure proper sampling, reporting, and resolution of questions and concerns.
Authoring/revising Standard Operating Procedures, Work Instructions, Forms, and Protocols to accurately reflect current practices.
Performing microbiological and environmental monitoring data review and trending of data within established timelines
Developing and maintaining Key Performance Indicators (KP|s) for laboratory testing.
Participating in and tracking group budget setting and cost containment drives.
Ensuring completion of all client QC Microbiology requirements related to GMP cellular products and/or materials.
Interface with Regulatory Agency Inspectors/Auditors and participate in external and internal audits.
Participate in BLA filings by providing review and compilation of Analytical data required for filings. Competencies
Qualifications:
BA/BS in Microbiology or relevant field required
Biotechnology certificate and/or cGMP experience
Minimum 7-10 years of experience in environmental monitoring or within the biopharmaceutical industry
Multiple years of previous management experience including interviewing, hiring, and training. Planning, assigning, and directing work. Rewarding and Disciplining employees. Addressing complaints and resolving problems.
Proficient with computer software (Microsoft office, MODA, visio)
Clear understanding of compliance regulations 21CFR 210/211, 21CFR 610, 21CFR 1271, 21CFR11, EDU annex 1, cGMPs, FDA guidance on Sterile Drugs Produce by Aseptic Processing
Strong knowledge of microbiological test methods, philosophies, method validation and method transfer.
Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review