Supervisor, Training
Hikma Pharmaceuticals
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Benefits offered by this job
Job summary
Hikma Pharmaceuticals USA Inc. in Columbus, OH seeks a Supervisor, Training to oversee development and implementation of training programs across departments.
You will lead onboarding, ongoing training, and regulatory compliance activities, mentoring a team of contributors and shaping a cohesive training strategy. You will ensure programs meet cGMP standards, collaborate with department heads, and drive continuous improvement in training effectiveness and documentation.
Qualifications
- Five years of pharmaceutical/regulatory operations or quality experience.
- Proficiency with GMP/DEA regulatory requirements.
- Strong computer skills using Word, Excel, PowerPoint, Outlook and site systems (LMS, QSDB, Trackwise, Veeva Vault).
- Experience developing and delivering training for adults and managing training programs.
- Ability to prioritize multiple priorities and communicate clearly.
Responsibilities
- Mentor, lead and develop staff; manage performance and hiring decisions.
- Oversee training program design, delivery, and effectiveness across departments.
- Ensure training activities comply with industry regulations and company standards.
- Collaborate with department heads to identify training needs and track progress.
- Maintain training records and drive continuous improvement in onboarding.
Skills
Education
Tools
Job description
Job Title: Supervisor, Training
Location: Columbus, OH
Job Type: Full time
Req ID: 10641
This position will cover 1st & off‑Shifts.
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 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.
We are seeking a talented and motivated Supervisor, Training to join our team. In this role, you will oversee the development and implementation of training programs for employees across various departments. This role ensures that all individual contributors are equipped with the necessary knowledge and skills to perform their duties effectively and in compliance with industry regulations. You will provide leadership, mentoring and decision‑making for company NEO and technical onboarding training, lead, coach, mentor, develop, and build a cohesive team of individual contributors.
- Mentors, leads, and develops employees; manages and addresses performance issues; and makes hiring, firing and compensation decisions to ensure individual and organizational performance.
- Communicates site and department goals and expectations to staff.
- Sets goals and expectations for staff with their input.
- Ensures conditions necessary for staff performance are met and barriers to performance are removed.
- Measures direct reports' core job performance and contribution to team performance.
- Communicates site and department performance to staff.
- Provides direct reports with feedback on core job 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).
- Facilitates effective interpersonal relationships and performance across the site (including Operations, Warehouse, Regulatory, and Laboratory).
- Schedules technical training activities and monitors work‑group for efficiency, compliance to procedures and productivity.
Manages comprehensive training programs for new and existing employees.
- Reviews training materials and modules in DMS as part of the quality unit, as well as e‑learning modules and presentations.
- Conducts training sessions and workshops on company policies, procedures, and best practices.
- Collaborates with department heads to identify training needs and tailor programs accordingly.
- Monitors and evaluates the effectiveness of training programs and makes necessary adjustments.
- Ensures all training activities comply with industry regulations and company standards.
- Provides ongoing support and mentorship to employees to facilitate continuous learning and development.
- Maintains accurate records of training activities and employee progress.
- Drives consensus in teams toward solutions that are effective and compliant.
- Creates and implements CAPAs in a timely fashion.
- Communicates with internal and external customers to ensure quality and timelines are met.
- Provides leadership across functional groups and drives support teams to affect improvements.
- Interacts with various regulatory authorities and provides support for audit requests, as applicable.
- Capable of working independently and with minimal supervision and training.
- Proven competency with general functions of the site training program.
- Must be proficient in computer applications including Microsoft Word, Access, Excel, SAP, and LMS.
- Must be able to prioritize multiple priorities and assess contingency plans.
- Must have good written and oral communication.
- Demonstrated teaching and mentorship skills.
- Thorough knowledge of cGMPs and DEA material operations.
- BA/BS, preferably in scientific, quality, or education field.
- Other BA/BS programs may be considered provided that the applicant has successfully completed fundamental college math and science coursework.
- Five (5) years of pharmaceutical/regulated industry operations or quality experience.
- Demonstrated proficiency in regulatory compliance requirements (GMP, DEA).
- Demonstrated proficiency in computer skills as a business tool, including work experience with Microsoft applications (Word, Excel, PowerPoint, Outlook) and site systems (LMS, QSDB, Trackwise, and Veeva Vault).
- Experience developing and delivering pharmaceutical manufacturing, packaging, and/or quality control training.
- Experience developing and delivering training for adult learners using different methodologies.
- Experience leading projects.
- Minimum of five (5) years of demonstrated experience developing and delivering training.
- Experience in Pharmaceutical.
- Annual performance bonus, commission, and share potential
- Auto enrollment in a Hikma-sponsored 401(k) program at a pre‑tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
- A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
- 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 a variety of 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.
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.
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