Production Supervisor - 2nd Shift

Sun Pharmaceutical IndustriesNew Brunswick, NJ
32d$79,000 - $87,500

About The Position

Sun Pharma is the world's fourth largest generics company with presence in Specialty, Generics and Consumer Healthcare products. Supported by more than 40 manufacturing facilities, we provide high-quality medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S., and we are rapidly ramping up our presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology. Are you ready to take on a leadership role where your expertise drives operational excellence? We're looking for a Production Supervisor to lead our 2nd shift team and ensure smooth, efficient, and compliant manufacturing operations. This is a hands-on leadership opportunity for someone who thrives in a fast-paced environment and is passionate about quality, safety, and team development. As a Production Supervisor, you'll play a critical role in overseeing daily production activities and ensuring adherence to cGMP standards. You'll lead a team of Operators and Team Leads, guiding them to meet production targets while maintaining the highest standards of quality and safety.

Requirements

  • High School Diploma or equivalent required; B.S. in a related field preferred.
  • 2-3 years in a manufacturing environment (pharmaceutical experience a plus).
  • Strong knowledge of granulation, blending/mixing, compression (AWC machines), coating, and encapsulation equipment.
  • Excellent communication (verbal and written), problem-solving, and decision-making abilities. A positive, hands-on leader with a can-do attitude.
  • Proficiency in MS Office applications
  • Ability to work under pressure and meet tight deadlines
  • Sound knowledge of cGMP, SOPs, FDA guidelines, and safety regulations
  • Ability to lift 50-75 lbs and navigate manufacturing environments
  • Willingness to work extended hours when needed
  • The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).

Nice To Haves

  • pharmaceutical experience a plus
  • B.S. in a related field preferred.

Responsibilities

  • Manage daily and weekly production schedules based on planning requirements. Set priorities and ensure timely completion of tasks.
  • Ensure all processes follow SOPs, batch records, and quality protocols. Conduct periodic document checks and take corrective actions to prevent deviations.
  • Prepare and train employees on manufacturing SOPs and best practices.
  • Apply your expertise to resolve routine and complex manufacturing challenges.
  • Work closely with other supervisors and departments to maintain alignment and operational excellence.
  • Participate in internal audits and FDA/customer inspections. Suggest process improvements and support continuous improvement initiatives.
  • Promote and enforce GMP and safety standards at all times.

Benefits

  • Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program.
  • Employees also receive various paid time off benefits, including vacation time and sick time.
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