Supervisor, QC Labs-2nd Shift

Job Title:      Supervisor, QC Labs

Location:      Columbus, Ohio

Job Type:     Full time

Req ID:          6503

 

About Us:

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ mission is to bring Better Health.  Within Reach.  Every Day ®  for millions of patients around the world.  We are a trusted, reliable partner and dependable source of over 750 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe.  Through our 32 manufacturing plants, eight R&D centers, and 8,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.

 

Description:

We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds.  We are seeking a talented and motivated Supervisor, QC Labs to join our team.  In this role, you will be responsible for leading, coaching, mentoring, developing and building a cohesive team of individual contributors. 

Provides leadership, mentoring and decision-making for laboratory investigations through driving investigations to root cause with associated documentation to support.

Supervises scientists and technicians in the performance of analytical testing.

You will work closely with QC, QAS, ARD, Manufacturing, EH&S.

 

Key Responsibilities:

•  Regular onsite, predictable attendance.
• Mentors, leads, coaches, and develops employees; manages and addresses performance issues; and makes hiring, firing and compensation decisions to ensure individual and organizational performance currently and in the future.
• Communicates site and department goals and expectations to staff.
• Sets goals and expectations for staff with their input.
• Ensures conditions (time, equipment, etc.) necessary for staff performance are met and barriers to performance are removed.
• Measures direct reports' core job/MAG performance and contribution to team performance.
• Communicates site and department performance to staff.
• Provides direct reports with feedback on core job/MAG performance.
• Collaborates with direct reports to identify and enable their skill and knowledge development.
• Rewards and recognizes staff and team performance to build engagement.
• Ensures direct report positions are filled timely with the best qualified candidate(s).
•  Facilitate effective interpersonal relationships and performance across DRA, Change Control, and laboratory Flow Groups
• Assigns testing of samples
• Schedules laboratory activities and supervises laboratory work
• Trains new staff on laboratory safety and cGMP compliance.
• Approves and performs disposition of raw materials, components, intermediates, finished products and stability samples for release to production and analytical services as needed.
• Monitors workgroup/defined shift for efficiency, compliance to procedures and productivity
• Communicates with internal and external customers to ensure quality and timelines are met.
• Drives process improvements within QC Labs relating to work instructions, analytical procedures, specifications, and job profiles.
• Share scientific knowledge for the evaluation of compendial changes.
• Provide quality oversight of the sampling process for incoming materials (if applicable)
• Reviews and approves analytical work, laboratory investigations, and ensures implementation of CAPAs as needed
• Ensures laboratory operates in a safe and compliant manner
• Provides leadership across functional groups and drives support teams to affect improvements