QC Chemistry Supervisor, 2nd Shift

Be the First to Apply

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

QC Chemistry Supervisor, 2nd Shift

Job Description

The QC Chemistry Supervisor, 2nd Shift is responsible for leading day-to-day laboratory operations while ensuring the timely execution of testing activities, laboratory investigations, and compliance initiatives. This position supports the establishment of departmental goals, manages laboratory priorities, and serves as a key liaison for internal and external stakeholders regarding chemistry testing activities.

The incumbent is accountable for achieving laboratory performance metrics, coordinating finished product and stability testing schedules, overseeing analytical investigations, and supporting continuous quality improvement initiatives. The QC Chemistry Supervisor also provides leadership, coaching, and performance management for laboratory personnel while fostering a culture of safety, compliance, and operational excellence.

Key Responsibilities

Laboratory Operations & Testing

• Oversee physical, chemical, and microbiological testing of raw materials, in-process materials, finished products, stability samples, and special project samples.
• Ensure testing is completed in accordance with approved procedures and established timelines.
• Coordinate sample shipments and manage testing performed by external contract laboratories.
• Schedule laboratory activities and allocate resources to meet production and project commitments.
• Perform and oversee data review and auditing activities supporting product disposition decisions.

Investigations & Compliance

• Lead laboratory investigations, including Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and laboratory events.
• Support method validation, method verification, and technology transfer activities for new and existing products.
• Prepare, review, and approve validation and verification protocols and reports.
• Drive audit readiness initiatives to maintain a continuous state of inspection preparedness.
• Monitor laboratory systems, procedures, and practices to ensure compliance with GMP, regulatory, and internal quality requirements.

Leadership & People Management

• Provide leadership, coaching, and development opportunities for QC analysts and laboratory staff.
• Establish individual and team performance objectives aligned with departmental goals.
• Conduct performance reviews, talent assessments, and merit recommendations.
• Participate in recruiting, interviewing, and onboarding qualified laboratory personnel.
• Ensure appropriate technical, compliance, and safety training programs are executed.

Continuous Improvement & Project Support

• Lead initiatives focused on quality, operational efficiency, and process improvement.

• Represent Quality Control on cross-functional site projects and improvement teams.

• Support implementation of laboratory systems and strategic initiatives, including:

• Laboratory Information Management Systems (LIMS)

• TrackWise

• Equipment qualification activities (IQ/OQ/PQ)

• Laboratory modernization projects

• Identify opportunities to enhance laboratory productivity, compliance, and customer service.

Bachelor of Arts (BA)