Sr. Manager Quality Control

piramalpharma; Lexington (VA); On-site; USD 110,000 - 160,000; Full time

Job summary

Piramal Pharma Solutions in Lexington is seeking a Sr. Manager, Quality Control to lead Analytical Quality Control and Microbiology operations. You will provide strategic direction, drive process standardization, and ensure compliance with global regulatory standards.

Reporting to the Director of Quality, you will oversee QC laboratories, develop budgets, mentor staff, and implement CAPA programs while maintaining inspection readiness across the department.

Qualifications

• B.S. or B.A. in scientific field (biology, life science, chemistry) preferred.
• 10+ years in regulated cGMP industry, with 5+ years in management.
• Experience in GMP parenteral/sterile manufacturing; contract manufacturing a plus.
• Strong knowledge of cGMP regulations.
• Excellent technical writing and oral communication skills.
• Six Sigma Green Belt (or equivalent).

Responsibilities

• Direct oversight of QC laboratories activities.
• Monitor and align lab revenue goals to expectations.
• Develop and manage department budgets.
• Ensure compliance with FDA/EMA/PMDA and other guidelines.
• Lead CAPA, deviations, and LIR investigations.
• Maintain inspection readiness and safety; mentor QC staff.

Skills

cGMP knowledge

Technical writing

Oral communication

Six Sigma Green Belt

Parenteral manufacturing

GMP compliance

Education

B.A./B.S. in scientific field

Job description

Division

Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Sr. Manager Quality Control Job Description

Business

Pharma Solutions

Department

Analytical Quality Control (AQC)

Location

Lexington

Job Overview

Reporting to the Director of Quality, the Sr. Manager, Quality Control has responsibility for the Analytical and Microbiology Quality Control (AQC/MQC) laboratories. The position will provide strategic direction and leadership to improve quality, efficiency, process standardization, and capabilities of the Quality Control Department.

Reporting Structure

This position reports to the Director of Quality.

Key Responsibilities

• Direct oversight of activities performed within Quality Control Laboratories


• Monitor revenue goals ensuring that Laboratories meet or exceed expectations


• Develop and manage department budgets


• Regularly monitor applicable internet and written information published by US FDA, EMA, PMDA, Other Applicable Agencies as required, and pharmaceutical manufacturing and laboratory technology organizations for the purpose of review/incorporation of latest requirements and guidelines into routine PPS laboratory operations


• Establish short and long-range plans for the timely and efficient execution of the testing activities within scope of the business priorities and applicable regulatory requirements (FDA, OSHA, etc.)


• Apply necessary oversight to the stability study program and ensure current regulatory guidelines are followed


• Oversee laboratory instrumentation activities including procurement, qualification, preventative maintenance, and calibration


• Establish, implement, and manage Laboratory Programs and/or Policies, SOPs, and good record keeping practices that are compliant with current regulatory requirements


• Oversee all quality investigations within the departments (deviations, CAPA and LIR)


• Ensure Lab is a constant state of compliance and Sustains Permanent Inspection Readiness (PIR)


• Ensure suitable laboratory safety procedures are in place


• Ensure that there is a department training program in place so that department staff are continuously developing and are current with industry practice


• Ensure that department technical expertise and capabilities are constantly evolving and current with industry.


• Provides information regarding Quality Control systems and data to internal or external regulatory personnel during inspections or inquiries


• Analyse and trend sample results and perform statistical studies and evaluations of key performance indicators


• Develop mechanisms and structures to allow for adjustment in the laboratory testing schedules to meet changing priorities due to business needs.


• Serve as liaison with the corporate data, documentation, and review center.


• Interact directly with project managers, clients, consultants, and regulatory agencies


• Oversee the development, execution and implementation of quality improvement plans within the QC Department


• Oversee the identification, procurement, qualification and implementation of new laboratory equipment, and software platforms (i.e. LIMS, Empower, etc.) as needed


• Perform gap assessments and implement CAPAs as needed


• Support internal and external audits, agency inspections, responses and CAPAs


• Support Cross Functional Quality and Operational activities/projects as needed


• Create and support an environment where department members seek opportunities to improve current practices in terms of quality, efficiency and safety


• Lead and develop/mentor QC members


• Assign department resources so that company goals/timelines are achieved

Qualifications

• B.A. or B.S in scientific related field, Biology, Life Science, Chemistry, or related scientific discipline preferred


• Minimum of ten (10) years' progressive experience in a regulated cGMP industry is required, with five (5) years' management experience


• Must have experience working within a GMP parenteral/sterile manufacturing environment, contract manufacturing a plus


• Strong/demonstrated knowledge of cGMP regulations


• Possess excellent technical writing and oral communication skills


• Six Sigma Green Belt, Benc