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Gmp Manufacturing Supervisor Jobs (NOW HIRING)

Manufacturing Supervisor

Bangor, PA Β· On-site

$54K - $73K/yr

S.-based manufacturer of GMP pharmaceutical-grade ingredients, including API's, excipients, GMP ... A supervisor reviews the daily production schedule, assigns work to their team, coordinates plant ...

New

Manufacturing Supervisor

Oakland, NJ Β· On-site

$75K - $95K/yr

Position Summary/ Objectives The Manufacturing Supervisor is responsible for supporting daily operations in a GMP-regulated medical device manufacturing environment, ensuring the safe, compliant, and ...

New

NY Β· On-site

$59K - $81K/yr

Manufacturing Supervisor (20965) Requisition ID 20965 -Posted - Processing - Processing - FL-M ... Establish and maintain compliance to current GMP, safety programs * Communicate any safety issues ...

Manufacturing Supervisor

San Jose, CA Β· On-site

$70K - $96K/yr

Manufacturing Supervisor - Berkeley Yeast - San Jose, CA We are seeking an experienced ... Exposure to one or more quality or food safety systems (e.g., GMP, HACCP, PCQI, SQF, ISO)

Manufacturing Supervisor

Richmond, VA Β· On-site

$65K - $85K/yr

Job Title : Manufacturing Supervisor Supervisor's Title : Manufacturing Manager Department ... Coaches production workers on food safe production and adherence to GMP's. Knowledge, Skills and ...

Manufacturing Supervisor

Midway, FL

$52K - $72K/yr

Manufacturing Supervisor Department: Processing Reports to: Manufacturing Manager FLSA Status ... Establish and maintain compliance to current GMP, safety programs * Communicate any safety issues ...

Manufacturing Supervisor

Midway, FL

$52K - $72K/yr

Manufacturing Supervisor Department: Processing Reports to: Manufacturing Manager FLSA Status ... Establish and maintain compliance to current GMP, safety programs * Communicate any safety issues ...

Manufacturing Supervisor

Midway, FL Β· On-site

$52K - $72K/yr

Manufacturing Supervisor Department: Processing Reports to: Manufacturing Manager FLSA Status ... Establish and maintain compliance to current GMP, safety programs * Communicate any safety issues ...

Manufacturing Supervisor

Midway, FL Β· On-site

$52K - $72K/yr

Manufacturing Supervisor Department: Processing Reports to: Manufacturing Manager FLSA Status ... Establish and maintain compliance to current GMP, safety programs * Communicate any safety issues ...

Showing results 21-40

Gmp Manufacturing Supervisor information

See salary details

$34.5K

$71.4K

$108K

How much do gmp manufacturing supervisor jobs pay per year?

As of Sep 13, 2026, the average yearly pay for gmp manufacturing supervisor in the United States is $71,398.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $82,500.00 per year, depending on experience, location, and employer.

What is a GMP manufacturing supervisor?

GMP Manufacturing Supervisors are professionals responsible for overseeing the production processes in facilities that follow Good Manufacturing Practices (GMP). They ensure that manufacturing operations comply with regulatory standards to guarantee the quality, safety, and consistency of products, often in the pharmaceutical, biotechnology, or food industries. Their duties include supervising staff, maintaining documentation, monitoring production lines, and troubleshooting issues to ensure smooth and compliant operations. They also collaborate with quality assurance teams to enforce protocols and train employees on GMP requirements.

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

To excel as a GMP Manufacturing Supervisor, you typically need experience in pharmaceutical or biotech manufacturing, a solid understanding of Good Manufacturing Practices (GMP), and a relevant degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and compliance auditing tools is crucial. Strong leadership, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure that production processes meet regulatory standards and quality expectations while maintaining team productivity and safety.

What are some common challenges faced by GMP manufacturing supervisors, and how can they be effectively managed?

GMP Manufacturing Supervisors often encounter challenges such as maintaining strict compliance with regulatory standards, managing diverse teams across different shifts, and ensuring production timelines are met without compromising quality. Effective management involves fostering clear communication, regular training on GMP protocols, and proactive problem-solving to address equipment issues or process deviations. Supervisors who build strong relationships with quality assurance and production staff are better positioned to quickly resolve issues and maintain smooth operations.

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

AspectGmp Manufacturing SupervisorGmp Quality Control Supervisor
CredentialsTypically requires a Bachelor's in Life Sciences or related field; GMP certification preferredSimilar credentials; often requires GMP or QC-specific certifications
Work EnvironmentOversees manufacturing lines, ensures production meets GMP standardsManages QC labs, reviews testing procedures, ensures product quality
Industry UsageCommonly employed in pharmaceutical and biotech manufacturingUsed in quality assurance departments within similar industries

The Gmp Manufacturing Supervisor focuses on overseeing production processes to ensure GMP compliance, while the Gmp Quality Control Supervisor concentrates on testing and quality assurance. Both roles require similar credentials and work within GMP environments, but their primary responsibilities differβ€”one manages manufacturing, the other quality control.

What states have the most Gmp Manufacturing Supervisor jobs?

States with the most job openings for Gmp Manufacturing Supervisor jobs include:

What are popular job titles related to Gmp Manufacturing Supervisor jobs?

For Gmp Manufacturing Supervisor jobs, the most frequently searched job titles are:

Infographic showing various Gmp Manufacturing Supervisor job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $71,398 per year, or $34.3 per hour.

Manufacturing Supervisor

Bangor, PA β€’ On-site

Biospectra Inc
Pharmaceutical and Medicine ManufacturingΒ β€’Β 51 - 200 employees

$54K - $73K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New


Job description

Join our team at BioSpectra, Inc., where we lead the way in delivering high-purity ingredients to the top 25 pharmaceutical companies globally. We are dedicated to maintaining the highest standards of excellence in the industry. Currently, we are looking for a Manufacturing Supervisor. As a key player in our organization, you will lead a manufacturing shift within our Bangor Manufacturing facility but be open to assist when required at our Stroudsburg facility. We are looking for a detail-oriented individual with strong leadership skills to drive operational excellence and foster team success.  BioSpectra, Inc. is a privately held, family-oriented organization and a U.S.-based manufacturer of GMP pharmaceutical-grade ingredients, including API’s, excipients, GMP process chemicals, and bulk GMP buffers and solutions. BioSpectra, Inc. currently has facilities located in Bangor, Wind Gap, Stroudsburg, PA, and Scarborough, Canada.  


Why should you join BioSpectra, Inc.?

  • Support our current customers who are the top 25 pharmaceutical companies in the world
  • Develop your career with a growing organization with ample opportunities for professional and personal development
  • Comprehensive Benefits Package (Medical, Dental, Vision, Company paid Life Insurance, Tuition Reimbursement)
  • 401K Retirement Savings Plan – Company matches $2 per $1 of employee contribution on the first 4%  
  • Excellent Paid Time Off Programs include vacation, sick, & personal time, plus paid holidays

Job Summary: 

The Manufacturing Supervisor leads their team to accomplish the safety, quality, delivery and cost objectives of the manufacturing department. A supervisor reviews the daily production schedule, assigns work to their team, coordinates plant activities, ensures their team is trained and inspects chemical operator activity throughout the shift. Responsible for ensuring finished goods meet the production schedule and are in compliance with quality standards set for the facility. Leads by example and holds their team accountable for performance/results. 

Essential Duties and Responsibilities: 

  • Ensures team compliance with all current quality/cGMP and safety systems
  • Tracks, records and reports production data / KPI’s on a daily basis.
  • Leads shift change meeting. Clearly communicates management priorities to team.
  • Maintains operational/batch data. Reads and analyzes charts, work orders or production schedules to determine production requirements.
  • Ensures new employees are trained, coached and evaluated.
  • Continuously assesses team performance on production floor and verifies compliance with cGMP/SOP requirements.
  • Ensures team members are trained, coached and developed to maintain coverage of critical tasks/functions in support of manufacturing operations.
  • Maintains training records for team. Schedules/facilitates training as required.
  • Executes daily production schedule as planned.
  • Initiates discrepancies as they occur and provides input on root cause and preventative actions.
  • Consults with Manufacturing Department Managers to coordinate operations and activities within and between departments.
  • Confers with management and/or subordinates to resolve worker problems and complaints.
  • Reviews and provides feedback for SOP/TOI revision documents.
  • Inspects materials, products or equipment to detect defects or malfunctions.
  • Routinely inspects documentation, processing rooms, equipment and finished good packaging during their shift to ensure compliance with cGMP manufacturing.
  • Monitors gauges, dials, and other indicators to ensure operations conform to production or processing standards.
  • Sets up and adjusts machines and equipment.
  • Monitors production area and enforces safety or sanitation regulations.
  • Inspects process rooms
  • Conducts batch record review and reconciliation.
  • Completes work order forms.
  • Utilize ERP system to issue, track and record manufacturing operation.
  • Other duties may be assigned as deemed appropriate by management

Qualifications: 

  • High School diploma or equivalent.
  • Minimum of two years of supervisory experience in the chemical manufacturing industry: candidates with less experience may be selected at the discretion of management.
  • Demonstrated ability to lead and supervise employees to achieve production goals while ensuring that quality, regulatory, safety, and environmental requirements are met.
  • Capability to lead, coach, inspire, and motivate employees to develop effective teamwork and achieve outstanding performance standards.
  • Demonstrated capabilities to diagnose and solve problems, assess situations and take appropriate actions, make decisions effectively, and communicate to employees at all levels of the organization.
  • Mechanical reasoning and critical thinking skills required in order to troubleshoot chemical manufacturing process.
  • Proficient with ERP system use.
  • Proficient in Microsoft Office (Excel, Outlook, PowerPoint, Word)
  • Must be able to read, write, speak, and understand English.

Work Hours: 

  • Exempt Position
  • Shift:  12-Hour Alternating 3 days on/3 days off (7:30pm-8:00am)
  • Minimum of 40-45 Hours Week, or other agreed upon documented schedule
  • Ability and willingness to work from all BioSpectra facilities- Primary Location: Bangor, PA

If you are ready to take on a challenging role, make an impact, and grow with a dynamic company that values innovation and quality, this position is for you! Apply now to be a part of our dedicated team and contribute to our ongoing success! 



7:30Pm to 8:00am, Rotating 3 Days on & 3 Days Off