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Gmp Production Supervisor Jobs in Indiana (NOW HIRING)

The Production Supervisor is responsible for coordinating raw materials, equipment, and staffing to ... Maintain Good Manufacturing Practices (GMP) and Food Safety Protocols in accordance with company ...

The Production Supervisor is responsible for coordinating raw materials, equipment, and staffing to ... Maintain Good Manufacturing Practices (GMP) and Food Safety Protocols in accordance with company ...

The Production Supervisor is responsible for leading daily manufacturing operations to safely ... Ensure compliance with food safety, quality, GMP, sanitation, HACCP, and customer requirements.

Production Operator II

Brownsburg, IN · On-site

$16 - $19.25/hr

Work with Production Supervisor and Management team to improve the process * Collaborate with the ... Experience * Hands-on GMP production of sterile pharmaceuticals 2+ yrs * Cleanroom operations ...

Production Supervisor Position Summary The Production Supervisor reports to the Production Manager ... Knowledge of food safety standards, GMP's, and production processes * Strong leadership ...

Production Supervisor Position Summary The Production Supervisor reports to the Production Manager ... Knowledge of food safety standards, GMP's, and production processes * Strong leadership ...

Champion and participate in company safety, GMP, and CI efforts. * Direct daily activities of ... Troubleshoot production problems. * Manage employee hours, scheduling and payroll using UltiPro ...

Production Supervisor This position is responsible for maximizing productivity while showing ... GMP gear in designated areas of the plant * § Able to walk and/or stand on concrete floors for ...

Production Supervisor This position is responsible for maximizing productivity while showing ... GMP gear in designated areas of the plant * § Able to walk and/or stand on concrete floors for ...

... Practices (GMP's), performance of sanitation audits, food safety checks (HACCP), and product ... At least 3 years of supervisory experience in a manufacturing environment; bakery manufacturing ...

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Gmp Production Supervisor information

What is a GMP production supervisor?

GMP Production Supervisors are professionals responsible for overseeing manufacturing processes in facilities that adhere to Good Manufacturing Practices (GMP). They ensure that all production activities comply with regulatory standards, company policies, and quality control guidelines to ensure product safety and consistency. Their duties typically include supervising staff, managing workflow, maintaining documentation, and training employees on GMP protocols. The role is crucial in industries such as pharmaceuticals, biotechnology, and food production, where strict adherence to GMP is required to meet regulatory and safety standards.

What are the key skills and qualifications needed to thrive as a GMP production supervisor?

To thrive as a GMP Production Supervisor, you need strong knowledge of Good Manufacturing Practices (GMP), leadership abilities, and a background in life sciences or engineering, often supported by relevant experience or a related degree. Familiarity with manufacturing management systems, quality control tools, and compliance documentation is typically required, along with certifications like Six Sigma or Lean Manufacturing being advantageous. Excellent communication, problem-solving skills, and the ability to motivate teams help individuals excel in this role. These competencies ensure efficient production, regulatory compliance, and a safe, high-quality environment in pharmaceutical or biotech manufacturing.

What are some common challenges faced by GMP production supervisors, and how can they be addressed?

GMP Production Supervisors often face challenges such as balancing strict regulatory compliance with production efficiency, managing cross-functional teams, and ensuring consistent product quality. To address these challenges, supervisors should foster clear communication between quality assurance, production, and maintenance teams, prioritize ongoing training for staff on GMP guidelines, and implement robust documentation practices. Proactively identifying potential bottlenecks and encouraging a culture of continuous improvement can also help maintain high standards while meeting production targets.

What is the difference between Gmp Production Supervisor vs Quality Control Supervisor?

AspectGmp Production SupervisorQuality Control Supervisor
CertificationsGMP certification, production management trainingGMP certification, quality assurance training
Work EnvironmentManufacturing floor, production linesLaboratories, quality testing areas
Industry UsagePharmaceutical, biotech manufacturingPharmaceutical, biotech manufacturing
Primary FocusOverseeing production processes and staffEnsuring product quality and compliance

The Gmp Production Supervisor and Quality Control Supervisor roles are both essential in GMP-regulated industries like pharmaceuticals. The supervisor oversees production operations, while the quality control supervisor focuses on testing and quality assurance. Both roles require GMP-related certifications and work within manufacturing environments, but their core responsibilities differ: one manages production flow, the other ensures product quality compliance.

How much does a Gmp Production Supervisor make?

The average salary for a GMP Production Supervisor is approximately $70,000 to $85,000 per year, depending on experience, certifications, and the specific industry sector. Salaries can vary based on location, company size, and individual qualifications, with some supervisors earning over $90,000 in high-demand areas.

How much is the salary of a Gmp Production Supervisor?

The salary of a GMP Production Supervisor typically ranges from $60,000 to $90,000 annually, depending on experience, location, and company size. They often oversee manufacturing processes in regulated environments and may require certifications in Good Manufacturing Practices (GMP).

Is a Gmp Production Supervisor a high position?

A GMP Production Supervisor is a mid- to senior-level role responsible for overseeing manufacturing processes in a regulated environment. While it involves leadership and technical skills, it is generally not considered an executive or top-tier management position, but it can lead to higher supervisory or managerial roles with experience and additional responsibilities.

What cities in Indiana are hiring for Gmp Production Supervisor jobs?

Cities in Indiana with the most Gmp Production Supervisor job openings:

Production Supervisor - Night Shift (4pm - 4am)

Seymour, IN • On-site

Lannett Company Inc
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees

Other

Posted 3 days ago

New


Lannett rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

Description:

Summary

 The primary function of this position is to supervise departmental operations to ensure quality and safety standards are met and the operations are efficient and organized. Maintain facilities in the highest level of compliance and cleanliness and ensure standard operating procedures (SOP’s) are executed with all regulations. Provide direct supervision and coaching to Production Operators and Team Leaders and promote an open and collaborative work environment. Provide daily expectations to employees and ensure all necessary resources are available for employees to perform at the highest safety and quality levels. 


Scope of Job

The Production Supervisor position is within the Manufacturing department and is solely responsible for management of personnel and activities associated with the operations of equipment utilized in the production of oral solid dose products.


Responsibilities 

  •  Review operating staff performance regularly and develop individuals within operation function to continually enhance performance at individual and team levels
  •  Ensure plant personnel are working safely and have the necessary safety equipment for their duties.
  • Communicate operational objectives to achieve department strategy, specifically around quality, safety and operational efficiency.
  • Receive assignments in the form of objectives with goals to meet as outlined. Assign tasks and provide guidance to employees according to established policies and management guidance
  • Administer company policies that directly affect subordinate employees.
  • Adhere to all cGMP’s, compliance/regulatory mandates and quality requirements.
  • Write, review and approve documents relevant to management activities (e.g. procedures, deviations, work instructions, files, validation reports).
  •  Complete regular reporting duties such as: end of shift reports, corrective actions
  • Assess issues; analysis and evaluate options. Make sound recommendations for conclusions and/or improvements to support overall productivity.
  • Understand and assist in SAP transactional issues. 
  • Mentor and coach operators and team leaders on new concepts.
  • Manage skillsets within the team ensuring training is up to date.
  • Accurately evaluate achievements of the team based on current status vs. newly implemented standards.
  • Provide formal and informal leadership to promote a positive work environment and communicate overall business expectations to Operators, Team Leaders and peers.
  • Service as an advisor to employees and be actively engaged as required to meet schedules and resolve problems.
  • Promote an open and collaborative work environment with all leadership, peers and subordinates
  • Establish consistent work instructions in conjunction with other supervisors and managers.
  • Assist in identification and implementation of continuous improvement opportunities by evaluating and track recurring issues.
  • Participate in training and development of operator and team leader skills.
  • Identifies needs of Production team and develops KPIs for overall team activities. 
Requirements:

· A minimum of 5 years of experience in a GMP production environment.

· Must have in-depth understanding and application of GMP principles, concepts, practices and standards.

· Practical mindset relative to production operations and business processes.

· Process-oriented, data driven mindset for decision making and driving quality into the product.


What Lannett employees say

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About LANNETT

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Philadelphia, PA, US

Year founded

1942

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