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Title:  Supervisor, Manufacturing

Date:  Jul 22, 2026
Location:  New Brunswick, NJ
Company:  Ohm Laboratories Inc , USA

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.

 

Job Summary:

Monday–Friday | 3:15 PM – 11:45 PM
Pharmaceutical Manufacturing | Onsite

We are seeking an experienced and motivated Manufacturing Supervisor to lead our 2nd shift production team in a fast-paced pharmaceutical manufacturing environment. This critical leadership role is responsible for overseeing daily manufacturing operations, ensuring production goals are achieved safely and efficiently while maintaining the highest standards of quality, compliance, and operational excellence.

The ideal candidate is a hands-on leader with strong technical knowledge of pharmaceutical manufacturing processes, a passion for developing teams, and a commitment to maintaining cGMP and safety compliance.

 

What You'll Do:

Production Leadership & Operations

  • Coordinate and supervise daily and weekly manufacturing activities based on production schedules and business priorities.
  • Lead Team Leads and Operators to ensure production targets, quality standards, and operational objectives are consistently achieved.
  • Prioritize work activities and coordinate with other supervisors and departments to ensure seamless execution of manufacturing schedules.
  • Monitor productivity, identify process improvements, and drive operational efficiency.

Compliance & Quality Oversight

  • Ensure manufacturing processes are performed in accordance with batch records, SOPs, protocols, and cGMP requirements.
  • Conduct periodic reviews of manufacturing documentation to ensure accuracy, completeness, and compliance.
  • Take corrective actions to prevent deviations and maintain audit readiness.
  • Initiate and support investigations, deviations, and change controls as required.
  • Oversee the execution of:
    • Scale-up batches
    • Exhibit batches
    • Characterization studies
    • Validation batches
    • Cleaning verification and validation activities

Team Development & Training

  • Train and mentor employees on manufacturing procedures, SOPs, and compliance requirements.
  • Foster a culture of accountability, collaboration, and continuous improvement.
  • Build confidence, engagement, and respect through a positive and energizing leadership style.
  • Ensure team members understand and support operational excellence initiatives.

Problem Solving & Continuous Improvement

  • Apply technical expertise to resolve routine and complex manufacturing challenges.
  • Lead troubleshooting efforts and support risk-based decision-making.
  • Collaborate with team members to identify opportunities for process improvements and enhanced efficiency.
  • Effectively build alignment and consensus when addressing difficult operational issues.

Safety & Regulatory Compliance

  • Promote and maintain a safe working environment by ensuring adherence to all safety policies and procedures.
  • Follow DEA Controlled Substance SOPs and immediately report violations or concerns to management.
  • Maintain compliance with FDA regulations, company policies, and industry standards.

 

Work Schedule:

  • 2nd Shift: Monday–Friday, 3:15 PM – 11:45 PM
  • Travel: Up to 0%

 

Work Environment:

This role operates within a manufacturing, production, and laboratory environment and may involve exposure to:

  • Moderate to high noise levels
  • Dust, fumes, odors, gases, and airborne particles
  • Manufacturing equipment and machinery
  • Industrial and production-related hazards

Strict adherence to safety procedures and PPE requirements is required at all times.

 

Physical Requirements:

  • Frequent standing, walking, sitting, bending, stooping, kneeling, crouching, crawling, pushing, and reaching.
  • Ability to lift, move, and/or carry 50–75 pounds.
  • Ability to navigate manufacturing, warehouse, laboratory, and office environments.
  • Must be able to wear required PPE, including:
    • Respirators
    • Safety glasses/goggles
    • Safety shoes

 

What You Bring:

Education & Technical Skills

  • High School Diploma, GED, Trade School, or Vocational School Diploma required.
  • Bachelor’s degree in a related field preferred.
  • Extensive knowledge of pharmaceutical manufacturing operations, including:
    • Granulation
    • Blending and mixing
    • Compression (AWC machines)
    • Coating
    • Encapsulation
  • Proficiency with Microsoft Office applications.

Leadership & Professional Skills

  • Strong leadership and team development capabilities.
  • Excellent communication skills (verbal, written, and presentation).
  • Ability to work under pressure and meet demanding production schedules.
  • Strong problem-solving and decision-making skills.
  • Demonstrated ability to influence, motivate, and engage employees.
  • Self-starter with a hands-on, results-driven approach.
  • Willingness to work extended hours when business needs require.

Compliance Knowledge

  • Strong understanding of:

    • cGMP requirements
    • SOP compliance
    • FDA regulations
    • Pharmaceutical manufacturing standards
    • Workplace safety requirements
  • English language proficiency at CEFR Intermediate B1+ level.

 

Experience:

  • Minimum 7 years of pharmaceutical manufacturing experience required.
  • Prior leadership experience required.

 

Why Join Us?

  • Lead a critical 2nd shift manufacturing operation that directly impacts product quality and business success.
  • Manage and develop a dedicated production team in a highly regulated pharmaceutical environment.
  • Play a key role in operational excellence, process improvements, and manufacturing performance.
  • Work in a collaborative culture focused on quality, compliance, safety, and continuous improvement.
  • Opportunity to make a meaningful impact while advancing your leadership career within pharmaceutical manufacturing.

 

If you're an experienced manufacturing leader who thrives in a fast-paced environment and is passionate about developing people, driving results, and maintaining the highest standards of quality and compliance, we'd love to hear from you.

 

 

The presently-anticipated base compensation pay range for this position is $75,000 to $87,500. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan, and may be eligible for the Long Term Incentive Plan. 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.

The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.

Notice to Agency and Search Firm Representatives:

Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.

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