About this role
Second Shift Supervisor
Job Summary
This position is a 2nd shift role, 1:30PM - 10:00PM. Supervise and perform regularly the preparation, formulation and dispensing of pharmaceutical products according to our current Good Manufacturing (cGMPs) and utilize Standard Operating Procedures (SOPs) in a clean room environment. Write and complete investigations, CAPAs, deviations and change controls utilizing root cause analysis tools and reporting software.
Area Of Responsibility
- Supervise and perform the activities of technicians on the second shift in equipment and component preparation operations; dispensing API and excipients; formulation and filling and capping of parenteral drug products. Also responsible for overseeing the formulation and filling of dermatological drug products.
- Schedule weekly plan of floor activities for technicians on second shift
- Author and track to close investigations, CAPAS, deviations and change controls as required
- Troubleshoot and solve moderate to complex problems related to the equipment, processes; existing or new products
- Oversee inventory control in the production area and order supplies as needed for production to assure no delay in the manufacturing plan
- Use systems like SAP, Track Wise, EDMS etc.
- Evaluate team performance by conducting midyear and yearly reviews
- Review completed batch records to ensure product is made in accordance with specifications
- Review SOPs and Batch Records, and update through DCRs as needed
- Work under limited supervision and follows clearly described procedures
- Other duties as assigned
- Education in Life sciences or technical discipline
Travel Estimate Up to 0%
Education and Job Qualification
- Bachelor's degree in related field or equivalent experience
- 6 to 8 years of experience in pharmaceutical manufacturing
- Excellent verbal, written and interpersonal communication skills
- High level of initiative and self-motivation
- Strong computer skills
- Attention to detail
- Ability to plan, prioritize and organize diversified workload
- Team management skills
- Record keeping skills
- Safe chemical handling techniques
- Knowledge of SAP, GMP, GDP, FDA, and OSHA regulations and standards
Experience
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Minimum 2 – 5 years of supervisory or team lead experience
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5 to 7 years of aseptic processing and aseptic area techniques experience
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Experience with technical writing, root cause analysis and completing investigations, CAPAs, deviations and change controls
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About Us
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Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S. We are the eighth-largest generics pharmaceutical company in the U.S., and we are rapidly ramping up our presence in the specialty branded market, with dermatology, ophthalmology, and oncology as key target segments.
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Our Values
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Sunology, a combination of Sun and Ideology, is the way of life at Sun Pharma. We practice humility, integrity, passion, and innovation.
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How We Work
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With people at our core, Sun Pharma has built an inclusive and collaborative work culture, where all employees are empowered to pursue their dreams and professional aspirations.
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Create Your Own Sunshine
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Create Your Own Sunshine
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At Sun we empower our employees to be Better Everyday, Take Charge and Thrive Together.
Benefits
- Health & Wellness
- We offer comprehensive benefits, including medical, dental, and vision coverage, as well as health and wellness programs.
- Financial
- We provide a competitive 401(k) match program and financial wellness programs to support our employees’ short- and long-term financial goals.
- Life, Work & Family
- We provide work-life benefits that support our employees beyond their workday.
Benefits
- We offer extended health care, dental care, and life insurance.
- Financial
- We provide a competitive RRSP match and financial wellness programs to support our employees’ short- and long-term financial goals.
- Life, Work & Family
- We offer work-life benefits that support our employees beyond their workday.