Quality Control Analyst - Environmental Monitoring - mid shift

Stokes Pharmacy

Mount Laurel Township (NJ)

On-site

USD 42,000 - 55,000

Full time

14 days+

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Benefits offered by this job

Medical, dental, and vision coverage
401(K) retirement with employer match
Bonus program
Paid holidays, vacation and personal时间

Job summary

Stokes Pharmacy in Mount Laurel, NJ is seeking a quality-focused professional to join our sterile operations team. The role emphasizes aseptic gowning, GxP applications, environmental monitoring, and documentation to ensure regulatory compliance.

You will work Monday–Thursday 10AM–8PM, full-time, with a starting wage of $20.00 per hour plus annual bonuses. Candidates should have a biology/microbiology background or related cGMP experience and be able to wear full protective gear.

Qualifications

  • Bachelor’s degree in biology, microbiology, or related field or 1 year relevant experience in a cGMP environment.
  • Must be capable of wearing all protective gear (gown, hair bonnet, mask, beard cover, gloves, goggles).
  • Must follow gowning/garbing procedures and avoid makeup or jewelry in sterile environments.
  • Must learn 21 CFR Part 210 and 211 and other cGMP regulations.
  • Ability to work with small, delicate machinery to complete dosage forms.
  • Strong verbal, written, and oral communication skills.
  • Must be able to work independently and with a team.
  • Must possess problem-solving skills and be punctual with low absenteeism.

Responsibilities

  • 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 media-fill process validations and inspection of filled units.
  • Perform document review of operation activities such as cleaning records and inventories.
  • Document non-compliance and coordinate with supervisor for further investigation.
  • Review production batch records for cGMP compliance and report abnormalities.
  • Perform audits on aseptic technique and operation documentation.
  • Ensure completeness and accuracy of documents and systems.
  • Assist with Change Controls and calibration program maintenance.
  • Identify and assess quality risk per SOPs and regulatory guidelines.
  • Assist in training new employees and technical personnel.

Skills

Gowning procedures
GxP knowledge
Environmental monitoring
Documentation
Team communication

Education

Bachelor’s degree in biology or microbiology
1 year relevant cGMP experience

Job description

Why Stokes?

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

This position requires an individual who can work collaboratively with production personnel to optimize quality aspects of operations.

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

Must be able to read, write, speak and understand English fluently and have the ability to read and interpret documents such as operating and maintenance instructions and procedure manuals.

Mathematical Skills

Uses addition, subtraction, multiplication and the division of numbers including decimals and fractions when checking of reports, forms, records and comparable data where interpretation is required involving basic skills knowledge.

Reasoning Ability

Must have the ability to solve practical problems and deal with a variety of concrete variables in situations where substantial standardization exists. Must be able to interpret instructions furnished in written, oral, and diagram or schedule form.

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 an Equal Employment Opportunity and Affnitive Action Employer.

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