Job Details

Supervisor, QA Disposition – Hikma Pharmaceuticals

Location: Columbus, OH

Job Type: Full time

Job ID: 9923

About Us: Hikma Pharmaceuticals USA Inc. is a developer, manufacturer, and supplier of essential medicines committed to making high-quality medicines accessible to the people who need them across North America, the Middle East, North Africa and Europe.

Description: We are seeking a talented and motivated Supervisor, QA Disposition. In this role, you will be responsible for leading, coaching, and mentoring direct reports to accomplish organizational and department priorities. You will oversee the QA batch disposition team and processes to ensure compliance with batch disposition procedures and cGMP. You will schedule activities to support the supply chain, manage batch review and final disposition, and author and approve departmental procedures.

Key Responsibilities

• Mentors, leads, coaches, and develops employees; manages and addresses performance issues; and contributes to hiring, firing, and compensation decisions.
• 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 performance and contribution to team performance.
• Provides direct reports with feedback on 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).
• Supports audit readiness.
• Manages a team responsible for batch disposition, including on the floor batch record review, for internally and externally produced product. Must schedule resources to ensure batch disposition timelines support the supply chain process.
• Establishes/maintains a QA presence on the production floor, including ensuring physical presence of QA during manufacturing times and online batch record review.
• Responsible/accountable for batch review and final disposition. This includes the review of technical service reports, deviations, investigation, and repackaging instructions.
• Responsible/accountable for batch review and final disposition of batch records from third parties, including incoming finished goods from other Hikma sites and CMOs for distribution.
• Authors, reviews, and approves departmental and supply chain procedures.
• Regular onsite attendance required.
• Other duties as assigned.

Qualifications

• Bachelor's degree (preferably in a scientific discipline).
• 5+ years combination of quality, production, engineering and/or laboratory experience with demonstrated accomplishments in implementing cGMP requirements.

Preferred Qualifications

• 1+ years of supervisory experience.

What We Offer

• Annual performance bonus, commission, and share potential.
• Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay; Hikma matches 100% of the first 6% of eligible pay.
• A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date).
• 3 personal days (prorated based on hire date).
• 11 company paid holidays.
• Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and voluntary benefits.
• Employee discount program.
• Wellbeing rewards program.
• Safety and Quality is a top organizational priority.
• Career advancement and growth opportunities.
• Tuition reimbursement.
• Paid maternity and parental leave.
• Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.

Equal Opportunity Employer

Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.