EPICUR Jobs Hiring Now
EPICUR is hiring for 6 open roles on Migrate Mate as of July 16, 2026, concentrated in project management and manufacturing operations. Migrate Mate updates EPICUR's live openings daily. EPICUR is a pharmaceutical or life sciences manufacturing company with operations focused on compliance, production, and quality assurance.
Find EPICUR JobsOverview
EPICUR hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 6
- Top team
- Project Management
- Seniority
- Across all levels
- Work type
- 0% remote or hybrid
- Top location
- Mount Laurel
Open Roles at EPICUR
Showing 6 of 6+ EPICUR jobs
Stokes Healthcare is a privately-owned business comprised of three divisions: Stokes Pharmacy (503A pharmacy), Epicur Pharma (503B facility) and STEP labs. The these divisions operate out of separate facilities in Mount Laurel, NJ, following different regulations and are guided by different principles.
Stokes Pharmacy was founded in 1975. The pharmacy formulates custom prescription medicines for both humans and animals. The business has grown from a small, hometown operation in Medford, New Jersey, to a respected pharmacy serving the entire U.S., enabled by sophisticated online ordering and overnight shipping capabilities.
In 2016, Stokes Healthcare built a world-class facility (which became Epicur Pharma), as a testament to the commitment to providing the highest level of quality. Adding a unique offering to the veterinary industry, Epicur Pharma is an FDA Registered 503B Outsourcing Facility, producing drugs such as Tacrolimus Eyedrops, Buprenorphine Injection and Gabapentin tablets. Epicur follows Current Good Manufacturing Practices (cGMP) which are the same rules and regulations followed by commercial manufacturers.
Epicur Pharma is proud to be a pioneer in animal drug standards, offering the largest selection of manufactured drugs that are traditionally compounded. Epicur products are distributed directly to veterinary hospitals from our manufacturing facility and offered through Stokes Pharmacy for individual patient prescriptions.
STEP Labs is a GMP-compliant laboratory that delivers accurate, reliable analytical testing for manufactured pharmaceutical products. Equipped with advanced instrumentation and operated under strict regulatory standards, STEP Labs provides comprehensive services in microbiological and chemistry analysis with a focus on quality, data integrity, and timely results.
Stokes Healthcare has built a reputation for unwavering quality and superb service by holding fast to the founders’ commitment to traditional craftsmanship, combined with today’s most advanced knowledge and technologies. In a field where many corporate-owned pharmacies try to compete on price, Stokes has always put safety and quality first because patients’ lives depend on it.
At Stokes, we offer competitive salaries and a comprehensive benefits package that includes medical, dental and vision coverage, life insurance, Health Reimbursement Account, Flexible Spending Account, 401(K) retirement savings plan with a generous employer match, a bonus program, paid holidays, vacation and personal time, and an excellent working environment. We are conveniently located in Mount Laurel, New Jersey, just minutes from Philadelphia and the NJ shore.
Summary/Objective
Schedule
Monday - Thursday 10AM - 8PM Full time
Salary
Starting at $20.00 hourly depending on experience plus twice yearly bonuses.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Learn aseptic gowning and technique within a cleanroom environment
- Learn and apply GxP (GMP, GDP, GLP) to operations
- Perform viable/non-viable environmental monitoring and read/review microbial samples
- Assist in the media-fill process validations and inspection of filled units
- Perform document review of operation activities such as cleaning record, line clearance forms, and inventory/equipment checklist
- Document non-compliance and work with supervisor/lead if further investigation is needed
- Review production batch records and associated data for product release; determine if records are within cGMP regulations; review data obtained for compliance specifications and report abnormalities
- Perform audits on aseptic technique and operation documentation
- Ensure completeness and accuracy of information contained in all documents, document files, databases, and documentation systems
- Ensure timely assessment and closure of Change Controls
- Assist with equipment calibration program and maintenance record files
- Identify and assess quality risk in activities and processes according to regulatory guidelines and Standard Operating Procedures
- Assist in the training of new employees and other technical personnel
Required Education and Experience
- Bachelor’s degree in biology, microbiology, or other related field, or 1 year relevant experience in cGMP environment
- Must be capable of wearing all protective gear (gown, hair bonnet, mask, beard cover, gloves, goggles)
- Must be able to follow gowning/garbing procedures (cannot wear makeup, must remove jewelry before sterile compounding)
- Must learn and understand 21 CFR Part 210 and Part 211, along with other relevant cGMP regulations
- Must be capable of working with small, delicate pieces of machinery to complete appropriate dosage forms in a timely manner
- Must possess strong verbal, written, and oral communication skills
- Must be able to work independently and with a team
- Must possess problem-solving skills
- Ability to recognize priorities and take action; make productive use of time
- Must exhibit punctuality and low absenteeism
- Able to sit and/or stand 8-10 hours or more per day as needed
Competencies
- Communication
- Organizational Skills
- Problem Solving/Analysis
- Results Driven
- Technical Capacity
- Thoroughness
Supervisory Responsibility
This position has no supervisory responsibilities.
Work Environment
This job operates primarily in a controlled laboratory environment. This position requires the use of standard office equipment, and frequent standing and walking.
Language Skills
Mathematical Skills
Reasoning Ability
Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
- May need to lift up to twenty-five (25) pounds on occasion
- This position is moderately active and requires standing and walking for a majority of the shift. (8-10 hours)
Position Type and Expected Hours of Work
This is a full-time position. Because of the nature of the business, work schedules may vary at times.
Travel
No travel is expected for this position.
Disclaimer
The above job description is intended to describe the general nature and level of work being performed by employees assigned to this job. It is not designed to capture or illustrate a comprehensive list of all responsibilities, duties, and skills required of employees assigned to this job.
AAP/EEO Statement
Stokes Healthcare is a privately-owned business comprised of three divisions: Stokes Pharmacy (503A pharmacy), Epicur Pharma (503B facility) and STEP labs. The these divisions operate out of separate facilities in Mount Laurel, NJ, following different regulations and are guided by different principles.
Stokes Pharmacy was founded in 1975. The pharmacy formulates custom prescription medicines for both humans and animals. The business has grown from a small, hometown operation in Medford, New Jersey, to a respected pharmacy serving the entire U.S., enabled by sophisticated online ordering and overnight shipping capabilities.
In 2016, Stokes Healthcare built a world-class facility (which became Epicur Pharma), as a testament to the commitment to providing the highest level of quality. Adding a unique offering to the veterinary industry, Epicur Pharma is an FDA Registered 503B Outsourcing Facility, producing drugs such as Tacrolimus Eyedrops, Buprenorphine Injection and Gabapentin tablets. Epicur follows Current Good Manufacturing Practices (cGMP) which are the same rules and regulations followed by commercial manufacturers.
Epicur Pharma is proud to be a pioneer in animal drug standards, offering the largest selection of manufactured drugs that are traditionally compounded. Epicur products are distributed directly to veterinary hospitals from our manufacturing facility and offered through Stokes Pharmacy for individual patient prescriptions.
STEP Labs is a GMP-compliant laboratory that delivers accurate, reliable analytical testing for manufactured pharmaceutical products. Equipped with advanced instrumentation and operated under strict regulatory standards, STEP Labs provides comprehensive services in microbiological and chemistry analysis with a focus on quality, data integrity, and timely results.
Stokes Healthcare has built a reputation for unwavering quality and superb service by holding fast to the founders’ commitment to traditional craftsmanship, combined with today’s most advanced knowledge and technologies. In a field where many corporate-owned pharmacies try to compete on price, Stokes has always put safety and quality first because patients’ lives depend on it.
At Stokes, we offer competitive salaries and a comprehensive benefits package that includes medical, dental and vision coverage, life insurance, Health Reimbursement Account, Flexible Spending Account, 401(K) retirement savings plan with a generous employer match, a bonus program, paid holidays, vacation and personal time, and an excellent working environment. We are conveniently located in Mount Laurel, New Jersey, just minutes from Philadelphia and the NJ shore.
Summary/Objective
Schedule
Monday - Thursday 10AM - 8PM Full time
Salary
Starting at $20.00 hourly depending on experience plus twice yearly bonuses.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Learn aseptic gowning and technique within a cleanroom environment
- Learn and apply GxP (GMP, GDP, GLP) to operations
- Perform viable/non-viable environmental monitoring and read/review microbial samples
- Assist in the media-fill process validations and inspection of filled units
- Perform document review of operation activities such as cleaning record, line clearance forms, and inventory/equipment checklist
- Document non-compliance and work with supervisor/lead if further investigation is needed
- Review production batch records and associated data for product release; determine if records are within cGMP regulations; review data obtained for compliance specifications and report abnormalities
- Perform audits on aseptic technique and operation documentation
- Ensure completeness and accuracy of information contained in all documents, document files, databases, and documentation systems
- Ensure timely assessment and closure of Change Controls
- Assist with equipment calibration program and maintenance record files
- Identify and assess quality risk in activities and processes according to regulatory guidelines and Standard Operating Procedures
- Assist in the training of new employees and other technical personnel
Required Education and Experience
- Bachelor’s degree in biology, microbiology, or other related field, or 1 year relevant experience in cGMP environment
- Must be capable of wearing all protective gear (gown, hair bonnet, mask, beard cover, gloves, goggles)
- Must be able to follow gowning/garbing procedures (cannot wear makeup, must remove jewelry before sterile compounding)
- Must learn and understand 21 CFR Part 210 and Part 211, along with other relevant cGMP regulations
- Must be capable of working with small, delicate pieces of machinery to complete appropriate dosage forms in a timely manner
- Must possess strong verbal, written, and oral communication skills
- Must be able to work independently and with a team
- Must possess problem-solving skills
- Ability to recognize priorities and take action; make productive use of time
- Must exhibit punctuality and low absenteeism
- Able to sit and/or stand 8-10 hours or more per day as needed
Competencies
- Communication
- Organizational Skills
- Problem Solving/Analysis
- Results Driven
- Technical Capacity
- Thoroughness
Supervisory Responsibility
This position has no supervisory responsibilities.
Work Environment
This job operates primarily in a controlled laboratory environment. This position requires the use of standard office equipment, and frequent standing and walking.
Language Skills
Mathematical Skills
Reasoning Ability
Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
- May need to lift up to twenty-five (25) pounds on occasion
- This position is moderately active and requires standing and walking for a majority of the shift. (8-10 hours)
Position Type and Expected Hours of Work
This is a full-time position. Because of the nature of the business, work schedules may vary at times.
Travel
No travel is expected for this position.
Disclaimer
The above job description is intended to describe the general nature and level of work being performed by employees assigned to this job. It is not designed to capture or illustrate a comprehensive list of all responsibilities, duties, and skills required of employees assigned to this job.
AAP/EEO Statement
Job Roles at EPICUR
Working at EPICUR
EPICUR's 6 open roles are across all levels, and about 0% are remote or hybrid. The most active teams are project management, manufacturing operations, and business analysis. EPICUR operates in pharmaceutical or life sciences manufacturing, with positions spanning production operations, quality control, regulatory compliance, and laboratory functions. Roles range from hands-on manufacturing technicians working shift-based schedules to supervisory and analyst positions overseeing compliance and quality systems. Most EPICUR roles are based in Mount Laurel.
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Browse jobs by roleEPICUR Jobs: Frequently Asked Questions
How many jobs is EPICUR hiring for right now?
EPICUR is hiring for 6 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in project management and manufacturing operations. Current openings include positions in manufacturing, quality assurance, quality control, and compliance. Migrate Mate pulls live postings so the count reflects what EPICUR is actively recruiting for at any given moment.
What kinds of roles does EPICUR hire for?
The most active teams are project management, manufacturing operations, and business analysis. EPICUR posts roles across pharmaceutical or life sciences manufacturing operations, including manufacturing technicians on shift schedules, production supervisors, quality control analysts, quality assurance analysts, and compliance officers. Most postings are across all levels, covering both hands-on production work and professional-level oversight functions in regulated manufacturing environments.
Are EPICUR jobs remote or in-person?
Mostly on-site. About 0% of EPICUR's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Mount Laurel. Each EPICUR listing shows its work location so you can filter before applying.
How do I apply to a job at EPICUR?
Find a EPICUR role on Migrate Mate, then follow the listing through to EPICUR's own careers page or application portal to submit your application directly. EPICUR manages its own hiring process, including screening, interviews, and offers. Migrate Mate keeps listings current so you can identify open roles and apply without delay.
Does EPICUR hire entry-level?
Most of EPICUR's open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual EPICUR listings for stated experience requirements.
Where is EPICUR hiring?
Most EPICUR roles are based in Mount Laurel, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.